71925 lines
2.6 MiB
71925 lines
2.6 MiB
C565588||epidermolysis bullosa with diaphragmatic hernia
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C567755|613097||tooth agenesis selective 6
|
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C567755|613097||sthag6
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C565584||epithelial squamous dysplasia keratinizing desquamative of urinary tract
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C565585||epiphyseal dysplasia of femoral head myopia and deafness
|
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C565587||epilepsy photogenic with spastic diplegia and mental retardation
|
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145250||hyperpigmentation familial progressive 2
|
|
145250||fph
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145250||fph2
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145250|266140|C563004||hpp
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145250|C564163||melanosis universalis hereditaria
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145250||muh
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D065008||scorpion stings
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D065008||scorpionism
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D065008||scorpionisms
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D065008||scorpion sting
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D065008||sting scorpion
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D065008||stings scorpion
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C566466|610508||maturity onset diabetes of the young type 7
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C566466|610508||mody7
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C567393|612225||maturity onset diabetes of the young type 9
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C567393|612225||mody9
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C567842|612955||long qt syndrome 12
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C567842|612955||lqt12
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C567296|115300||hypercarotenemia and vitamin a deficiency autosomal dominant
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C567296|115300||carotenoids plasma level of quantitative trait locus 1 included
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C565591||endothelial dystrophy congenital hereditary with nail hypoplasia
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D001819||bluetongue
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D001819||blue tongue
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D001819||tongue blue
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C565592||endocardial fibroelastosis and coarctation of abdominal aorta
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C565594||encephalopathy with intracranial calcification growth hormone deficiency microcephaly and retinal degeneration
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C564263||craniosynostosis with ocular abnormalities and hallucal defects
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C564262||scimitar anomaly multiple cardiac malformations and craniofacial and central nervous system abnormalities
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C564262||anomalous pulmonary venous return multiple cardiac malformations and craniofacial and central nervous system abnormalities
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D055677||refeeding syndrome
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D055677||syndrome refeeding
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C564261||lelis syndrome
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C564261||ectodermal dysplasia hypohidrotic with acanthosis nigricans
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D053018||pyonephrosis
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D053018||hydronephrosis infected
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D053018||infected hydronephrosis
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C564267||mandibulofacial dysostosis with ptosis autosomal dominant
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C564264||growth failure microcephaly mental retardation cataracts large joint contractures osteoporosis cortical dysplasia and cerebellar atrophy
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613162||spastic paraplegia 45 autosomal recessive
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613162||spg45
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C565596||encephalopathy axonal with necrotizing myopathy cardiomyopathy and cataracts
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C565597||encephalomalacia multilocular
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270400|D019082||smith lemli opitz syndrome
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270400|D019082||7 dehydrocholesterol reductase deficiencies
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270400|D019082||7 dehydrocholesterol reductase deficiency
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270400|D019082||acrodysgenital syndrome lethal
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270400|D019082||acrodysgenital syndromes lethal
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270400|D019082||deficiencies 7 dehydrocholesterol reductase
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270400|D019082||deficiency 7 dehydrocholesterol reductase
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270400|D019082||hyperotosis corticalis generalisata familiaris
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270400|D019082||lethal acrodysgenital syndrome
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270400|D019082||lethal acrodysgenital syndromes
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270400|D019082||polydactyly sex reversal renal hypoplasia and unilobar lung
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270400|D019082||reductase deficiencies 7 dehydrocholesterol
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270400|D019082||reductase deficiency 7 dehydrocholesterol
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270400|D019082||rsh slo syndrome
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270400|D019082||rsh slo syndromes
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270400|D019082||rsh syndrome
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270400|D019082||rsh syndromes
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270400|D019082||rutledge friedman harrod syndrome
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270400|D019082||rutledge lethal multiple congenital anomaly syndrome
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270400|D019082||slos
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270400|D019082||slo syndrome
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270400|D019082||slo syndromes
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270400|D019082||smith lemli opitz syndrome type 1
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270400|D019082||smith lemli opitz syndrome type 2
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270400|D019082||smith lemli opitz syndrome type i
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270400|D019082||smith lemli opitz syndrome type ii
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270400|D019082||syndrome lethal acrodysgenital
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270400|D019082||syndrome rsh
|
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270400|D019082||syndrome slo
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270400|D019082||syndromes rsh
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270400|D019082||syndromes slo
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C565598||elliptocytosis atypical
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C535421|604563||charcot marie tooth disease type 4b2
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C535421|604563||charcot marie tooth disease with focally folded myelin sheaths autosomal recessive type 4b2
|
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C535421|604563||charcot marie tooth neuropathy type 4b2
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C535421|604563||charcot marie tooth neuropathy type 4b2 charcot marie tooth disease type 4b2 with early onset glaucoma included
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C535421|604563||charcot marie tooth neuropathy type 4b2 with early onset glaucoma included
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|
C535421|604563||cmt4b2
|
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D016080||arachnoid cysts
|
|
D016080||arachnoid cyst intracranial
|
|
D016080||arachnoid cysts intracranial
|
|
D016080||arachnoid diverticula
|
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D016080||arachnoid diverticulas
|
|
D016080||cyst arachnoid
|
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D016080||cyst intracranial arachnoid
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D016080||cyst leptomeningeal
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D016080||cysts arachnoid
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D016080||cysts intracranial arachnoid
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D016080||cysts leptomeningeal
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D016080||diverticula arachnoid
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D016080||diverticulas arachnoid
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D016080||intracranial arachnoid cyst
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D016080||intracranial arachnoid cysts
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D016080||leptomeningeal cyst
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D016080||leptomeningeal cysts
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D030361||papillomavirus infections
|
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D030361||papillomavirus infection
|
|
D013801||theileriasis
|
|
D013801||coast fever east
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D013801||corridor disease
|
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D013801||disease corridor
|
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D013801||east coast fever
|
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D013801||fever east coast
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D013801||theileriases
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D013801||theilerioses
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D013801||theileriosis
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C564271||craniofacial abnormalities cataracts congenital heart disease sacral neural tube defects and growth and developmental retardation
|
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C565567||fibromatosis gingival with distinctive facies
|
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C566898||peripapillary atrophy beta type
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C566898||beta ppa
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C566898||peripapillary chorioretinal atrophy beta type
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C564233||glaucoma 1 open angle e
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C565568||myofibromatosis juvenile
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C564232||glaucoma and sleep apnea
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C|D004194||diseases
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C565569||fever familial lifelong persistent
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D016055||urinary retention
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D016055||retention urinary
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613150||muscular dystrophy dystroglycanopathy congenital with brain and eye anomalies type a 2
|
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613150||mddga2
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613150||walker warburg syndrome or muscle eye brain disease pomt2 related
|
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C565562||fraser like syndrome
|
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C565562||fused eyelids airway anomalies ovarian cysts and digital anomalies
|
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C566893||gangliosidosis generalized gm1 late infantile type
|
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613151||muscular dystrophy dystroglycanopathy congenital with mental retardation type b 3
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613151||mddgb3
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613151||muscular dystrophy congenital pomgnt1 related
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C565563||ehlers danlos syndrome vi phenotype with macrocephaly
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D017380||hypertrophy right ventricular
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D017380||hypertrophies right ventricular
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D017380||right ventricular hypertrophies
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D017380||right ventricular hypertrophy
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D017380||ventricular hypertrophies right
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D017380||ventricular hypertrophy right
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C564237||giant platelet syndrome with thrombocytopenia
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613152||muscular dystrophy dystroglycanopathy congenital without mental retardation type b 4
|
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613152||mddgb4
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613152||muscular dystrophy congenital fktn related
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C565564||fleck retina familial benign
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C566895||gangliosidosis generalized gm1 type i with cardiac involvement
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C566895||gm1 gangliosidosis type i with cardiac involvement
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613153||muscular dystrophy dystroglycanopathy congenital with brain and eye anomalies type a 5
|
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613153||mddga5
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613153||walker warburg syndrome or muscle eye brain disease fkrp related
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C566896||myopathy congenital with excess of muscle spindles
|
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C564235||glaucoma with elevated episcleral venous pressure
|
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613154||muscular dystrophy dystroglycanopathy congenital with brain and eye anomalies type a 6
|
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613154||mddga6
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613154||walker warburg syndrome or muscle eye brain disease large related
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613155||muscular dystrophy dystroglycanopathy congenital with mental retardation type b 1
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613155||mddgb1
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613155||muscular dystrophy congenital pomt1 related
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613156||muscular dystrophy dystroglycanopathy congenital with mental retardation type b 2
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613156||mddgb2
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613156||muscular dystrophy congenital pomt2 related
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613157||muscular dystrophy dystroglycanopathy limb girdle type c 3
|
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613157||lgmd2o
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613157||mddgc3
|
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613157||muscular dystrophy dystroglycanopathy limb girdle pomgnt1 related
|
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613157||muscular dystrophy limb girdle type 2o
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C564239||geographic tongue and fissured tongue
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613158||muscular dystrophy dystroglycanopathy limb girdle type c 2
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613158||lgmd2n
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613158||mddgc2
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613158||muscular dystrophy dystroglycanopathy limb girdle pomt2 related
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613158||muscular dystrophy limb girdle type 2n
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D004067||digestive system neoplasms
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D004067||cancer digestive system
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D004067||cancer of digestive system
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D004067||cancer of the digestive system
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D004067||cancers digestive system
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D004067||digestive system cancer
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D004067||digestive system cancers
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D004067||digestive system neoplasm
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D004067||neoplasm digestive system
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D004067||neoplasms digestive system
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613159||nephronophthisis like nephropathy 1
|
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613159||nphpl1
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C565114|125350||failure of tooth eruption primary
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C565114|125350||dental noneruption
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C565114|125350||pfe
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C565114|125350||posterior openbite familial
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C565114|125350||primary failure of eruption nonsyndromic
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C565114|125350||primary retention of teeth
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C565114|125350||unerupted second primary molar
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D004066||digestive system diseases
|
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D004066||digestive system disease
|
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D004066||disease digestive system
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D004066||diseases digestive system
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D004066||system disease digestive
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D004066||system diseases digestive
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C567559|612796||inflammatory bowel disease 27
|
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C567559|612796||ibd27
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D017092|263700||porphyria erythropoietic
|
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D017092|263700||cep
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D017092|263700||congenital erythropoietic porphyria
|
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D017092|263700||congenital erythropoietic porphyrias
|
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D017092|263700||deficiency of uroporphyrinogen iii synthase
|
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D017092|263700||erythropoietic porphyria
|
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D017092|263700||erythropoietic porphyria congenital
|
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D017092|263700||erythropoietic porphyrias
|
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D017092|263700||erythropoietic porphyrias congenital
|
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D017092|263700||gunther disease
|
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D017092|263700||gunther apos s disease
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D017092|263700||gunthers disease
|
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D017092|263700||porphyria congenital erythropoietic
|
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D017092|263700||porphyria erythropoietic congenital
|
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D017092|263700||porphyrias congenital erythropoietic
|
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D017092|263700||porphyrias erythropoietic
|
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D017092|263700||uroporphyrinogen iii synthase deficiency
|
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D017092|263700||uroporphyrinogen iii synthase deficiency of
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D017092|263700||uros deficiency
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C536447|604931||cortisone reductase deficiency
|
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C536447|604931||11 beta hydroxysteroid dehydrogenase type i deficiency of
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C536447|604931||cortisone reductase deficiency 1
|
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C536447|604931||cortrd1
|
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C535708||manouvrier syndrome
|
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C535708||lung agenesis heart defect thumb anomalies
|
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C535708||pulmonary aplasia and triphalangia of the thumb
|
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C563699|609558||prostate cancer hereditary 6
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C563699|609558||hpc6
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C535709||manz syndrome
|
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C535709||familial hypomagnesemia hypercalciuria
|
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D054364||solitary fibrous tumors
|
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D054364||fibrous tumor solitary
|
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D054364||fibrous tumors solitary
|
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D054364||solitary fibrous tumor
|
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D054364||tumor solitary fibrous
|
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D054364||tumors solitary fibrous
|
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C566983|611252||spastic paraplegia 32 autosomal recessive
|
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C566983|611252||spg32
|
|
D054363||solitary fibrous tumor pleural
|
|
D054363||benign fibrous mesothelioma
|
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D054363||benign fibrous mesotheliomas
|
|
D054363||fibromas submesothelial
|
|
D054363||fibroma submesothelial
|
|
D054363||fibrous mesothelioma
|
|
D054363||fibrous mesothelioma benign
|
|
D054363||fibrous mesothelioma localized
|
|
D054363||fibrous mesotheliomas
|
|
D054363||fibrous mesotheliomas benign
|
|
D054363||fibrous mesotheliomas localized
|
|
D054363||fibrous mesothelioma solitary
|
|
D054363||fibrous mesotheliomas solitary
|
|
D054363||localized fibrous mesothelioma
|
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D054363||localized fibrous mesotheliomas
|
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D054363||localized mesothelioma
|
|
D054363||localized mesotheliomas
|
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D054363||mesothelioma benign fibrous
|
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D054363||mesothelioma fibrous
|
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D054363||mesothelioma localized
|
|
D054363||mesothelioma localized fibrous
|
|
D054363||mesotheliomas benign fibrous
|
|
D054363||mesotheliomas fibrous
|
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D054363||mesotheliomas localized
|
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D054363||mesotheliomas localized fibrous
|
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D054363||mesothelioma solitary fibrous
|
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D054363||mesotheliomas solitary fibrous
|
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D054363||solitary fibrous mesothelioma
|
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D054363||solitary fibrous mesotheliomas
|
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D054363||solitary fibrous tumor of the pleura
|
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D054363||submesothelial fibroma
|
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D054363||submesothelial fibromas
|
|
C535700||malignant mesenchymal tumor
|
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C535700||malignant mesenchymoma
|
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C565572||estren dameshek variant of fanconi anemia
|
|
C565572||fanconi anemia estren dameshek variant
|
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C564241||craniosynostosis calcification of basal ganglia and facial dysmorphism
|
|
C535701||malignant teratocarcinosarcoma
|
|
C535701||paranasal sinus teratocarcinosarcoma
|
|
C535701||paranasal sinus teratocarcinosarcoma type
|
|
C535701||sinonasal teratocarcinosarcoma
|
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C535701||sinonasal teratocarcinosarcoma type
|
|
C535704||malpuech facial clefting syndrome
|
|
C535704||facial clefting syndrome gypsy type
|
|
C535704||malpuech syndrome
|
|
D017379||hypertrophy left ventricular
|
|
D017379||hypertrophies left ventricular
|
|
D017379||left ventricular hypertrophies
|
|
D017379||left ventricular hypertrophy
|
|
D017379||ventricular hypertrophies left
|
|
D017379||ventricular hypertrophy left
|
|
C535703||malouf syndrome
|
|
C535703||cardiomyopathy congestive with hypergonadotropic hypogonadism
|
|
C535703||congestive cardiomyopathy hypergonadotropic hypogonadism syndrome
|
|
C535703||congestive or dilated cardiomyopathy with hypergonadotropic hypogonadism
|
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D053039||ureterolithiasis
|
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D053039||ureterolithiases
|
|
C565577|227300||familial multiple coagulation factor deficiency i
|
|
C565577||f5f8d
|
|
C565577||factor v and factor viii combined deficiency of
|
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C565577||factor v and factor viii combined deficiency of with normal protein c and protein c inhibitor
|
|
C565577|227300||fmfd1
|
|
C565577|227300||fmfd i
|
|
C565577|227300||mcfd1
|
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C565577|227300||multiple coagulation factor deficiency i
|
|
D016063||blood loss surgical
|
|
D016063||hemorrhage surgical
|
|
D016063||surgical blood loss
|
|
D016063||surgical blood losses
|
|
D016063||surgical hemorrhage
|
|
D016063||surgical hemorrhages
|
|
C565578||faciocardiomelic dysplasia lethal
|
|
C564244||vater like defects with pulmonary hypertension laryngeal webs and growth deficiency
|
|
C565579||facial dysmorphism with multiple malformations
|
|
D016066||pleural effusion malignant
|
|
D016066||effusion malignant pleural
|
|
D016066||effusions malignant pleural
|
|
D016066||malignant pleural effusion
|
|
D016066||malignant pleural effusions
|
|
D016066||pleural effusions malignant
|
|
C565573||estren dameshek variant of fanconi pancytopenia
|
|
C564247||microcephaly primary autosomal recessive 6
|
|
C563824|608957||cd8 deficiency familial
|
|
D053040||nephrolithiasis
|
|
D030341||nidovirales infections
|
|
C535719||duker weiss siber syndrome
|
|
C535718||dubowitz syndrome
|
|
C535718||dwarfism eczema peculiar facies syndrome
|
|
C536414|259900||primary hyperoxaluria type 1
|
|
C536414|259900||alanine glyoxylate aminotransferase deficiency
|
|
C536414|259900||glycolic aciduria
|
|
C536414|259900||hepatic agt deficiency
|
|
C536414|259900||hp1
|
|
C536414|259900||hyperoxaluria primary type i
|
|
C536414|259900||oxalosis 1
|
|
C536414|259900||oxalosis i
|
|
C536414|259900||peroxisomal alanine glyoxylate aminotransferase deficiency
|
|
C536414|259900||serine pyruvate aminotransferase deficiency
|
|
C565580||facial abnormalities kyphoscoliosis and mental retardation
|
|
D019305|117100||epilepsy rolandic
|
|
D019305|117100||bcects
|
|
D019305|117100||bects
|
|
D019305|117100||benign childhood epilepsy with centro temporal spikes
|
|
D019305|117100||benign epilepsy of childhood with centrotemporal spikes
|
|
D019305|117100||benign epilepsy with centrotemporal spikes
|
|
D019305|117100||benign rolandic epilepsy
|
|
D019305|117100||benign rolandic epilepsy of childhood
|
|
D019305|117100||centralopathic epilepsies
|
|
D019305|117100||centralopathic epilepsy
|
|
D019305|117100||centrotemporal epilepsies
|
|
D019305|117100||centrotemporal epilepsy
|
|
D019305|117100||ect
|
|
D019305|117100||epilepsies centralopathic
|
|
D019305|117100||epilepsies centrotemporal
|
|
D019305|117100||epilepsies rolandic
|
|
D019305|117100||epilepsy benign rolandic
|
|
D019305|117100||epilepsy centralopathic
|
|
D019305|117100||epilepsy centrotemporal
|
|
D019305|117100||epilepsy rolands
|
|
D019305|117100||epilepsy sylvian
|
|
D019305|117100||rolandic epilepsies
|
|
D019305|117100||rolandic epilepsy
|
|
D019305|117100||rolandic epilepsy benign
|
|
D019305|117100||rolands epilepsy
|
|
D019305|117100||sylvian epilepsy
|
|
D019305|117100||temporal central focal epilepsy
|
|
C535711||maple syrup urine disease type 1b
|
|
C567710|613195||weill marchesani like syndrome
|
|
C535710||maple syrup urine disease type 1a
|
|
C535713||opitz reynolds fitzgerald syndrome
|
|
D030342||genetic diseases inborn
|
|
D030342||defect single gene
|
|
D030342||defects single gene
|
|
D030342||disease hereditary
|
|
D030342||disease inborn genetic
|
|
D030342||diseases hereditary
|
|
D030342||diseases inborn genetic
|
|
D030342||genetic disease inborn
|
|
D030342||hereditary disease
|
|
D030342||hereditary diseases
|
|
D030342||inborn genetic disease
|
|
D030342||inborn genetic diseases
|
|
D030342||single gene defect
|
|
D030342||single gene defects
|
|
C535712||maple syrup urine disease type 2
|
|
C535714||neuropathy congenital with arthrogryposis multiplex
|
|
C535714||congenital non progressive peripheral neuropathy with arthrogryposis multiplex
|
|
C565544||gsd iv neuromuscular form adult with isolated myopathy
|
|
C567045|610947||coronary artery disease autosomal dominant 2
|
|
C567045|610947||adcad2
|
|
C566876|C566875|300055||mental retardation x linked 79
|
|
C564211||granddad syndrome
|
|
C564211||growth retardation aged facies normal development decreased subcutaneous fat autosomal dominant inheritance
|
|
C566877|C566875|300055||mental retardation x linked with spasticity
|
|
C567316|612422||cardiomyopathy familial restrictive 3
|
|
C567316|612422||rcm3
|
|
C564210||granulomatous disease chronic autosomal dominant type
|
|
D013262|608579||stevens johnson syndrome
|
|
D013262|608579||drug induced stevens johnson syndrome
|
|
D013262|608579||drug induced stevens johnson syndromes
|
|
D013262|608579||epidermal necrolyses toxic
|
|
D013262|608579||epidermal necrolysis toxic
|
|
D013262|608579||hypersensitivity syndrome carbamazepine induced susceptibility to included
|
|
D013262|608579||lyell apos s syndrome
|
|
D013262|608579||lyell apos s syndromes
|
|
D013262|608579||lyell syndrome
|
|
D013262|608579||mycoplasma induced stevens johnson syndrome
|
|
D013262|608579||necrolyses toxic epidermal
|
|
D013262|608579||necrolysis toxic epidermal
|
|
D013262|608579||nonstaphylococcal scalded skin syndrome
|
|
D013262|608579||scalded skin syndrome nonstaphylococcal
|
|
D013262|608579||severe cutaneous adverse reaction susceptibility to
|
|
D013262|608579||stevens johnson syndrome drug induced
|
|
D013262|608579||stevens johnson syndrome mycoplasma induced
|
|
D013262|608579||stevens johnson syndromes drug induced
|
|
D013262|608579||stevens johnson syndrome susceptibility to included
|
|
D013262|608579||stevens johnson syndrome toxic epidermal necrolysis
|
|
D013262|608579||stevens johnson syndrome toxic epidermal necrolysis spectrum
|
|
D013262|608579||syndrome lyell apos s
|
|
D013262|608579||syndrome mycoplasma induced stevens johnson
|
|
D013262|608579||syndromes lyell apos s
|
|
D013262|608579||toxic epidermal necrolyses
|
|
D013262|608579||toxic epidermal necrolysis
|
|
D013262|608579||toxic epidermal necrolysis stevens johnson syndrome
|
|
D013262|608579||toxic epidermal necrolysis stevens johnson syndrome spectrum
|
|
D013262|608579||toxic epidermal necrolysis susceptibility to included
|
|
C565540||gsd iv nonprogressive hepatic
|
|
C565541||gsd iv neuromuscular form fatal perinatal
|
|
C566872||dilution pigmentary
|
|
C566872||albinoidism oculocutaneous autosomal dominant
|
|
C564215||glyoxalase ii deficiency
|
|
C565542||gsd iv neuromuscular form congenital
|
|
C566873||hereditary bundle branch system defect
|
|
C566873|113900||cardiac conduction defect progressive
|
|
C566873||heart block progressive familial
|
|
C566873||heart block progressive familial type 1
|
|
C566873|113900||heart block progressive familial type i
|
|
C566873|113900||lenegre lev disease
|
|
C566873|113900||pfhb1a
|
|
C566873|113900||pfhbi
|
|
C566873|113900||pfhbia
|
|
C566873|113900||progressive familial heart block type ia
|
|
C564214||goniodysgenesis mental retardation short stature syndrome
|
|
C564214||gms syndrome
|
|
C565543||gsd iv neuromuscular form childhood
|
|
C564218||glutathione reductase hemolytic anemia due to deficiency of in red cells
|
|
607677|C535416||charcot marie tooth disease type 2i
|
|
607677|C535416|608673||charcot marie tooth disease axonal autosomal dominant type 2l
|
|
607677|C535416||charcot marie tooth disease axonal type 2i
|
|
607677|C535416|608673||charcot marie tooth neuropathy axonal type 2l
|
|
607677|C535416||charcot marie tooth neuropathy type 2i
|
|
607677|C535416||cmt2i
|
|
607677|C535416||cmt 2i
|
|
607677|C535416|608673||cmt2l
|
|
C564217||glutathione peroxidase deficiency hemolytic anemia possibly due to
|
|
C565548||bernard soulier syndrome type a
|
|
C566879||xeroderma pigmentosum type g cockayne syndrome
|
|
C566879||xpg cs
|
|
C565549||bernard soulier syndrome type b
|
|
D005383||finger injuries
|
|
D005383||finger injury
|
|
D005383||injuries finger
|
|
D005383||injury finger
|
|
602481|C537246||migraine familial hemiplegic 2
|
|
602481||fhm2
|
|
602481||mhp2 migraine familial basilar included
|
|
602482|C535679||axenfeld rieger syndrome type 3
|
|
602482|C535679||anterior chamber cleavage syndrome
|
|
602482|107250|C537775||anterior segment mesenchymal dysgenesis
|
|
602482||axenfeld rieger anomaly included
|
|
602482|C535679||axenfeld rieger anomaly with or without cardiac defects and or sensorineural hearing loss
|
|
602482||rieg3
|
|
602482||rieger anomaly included
|
|
602482||rieger syndrome type 3 axenfeld anomaly included
|
|
D017359||hellp syndrome
|
|
D017359||hemolysis elevated liver enzymes lowered platelets
|
|
D017359||syndrome hellp
|
|
C566880||tachycardia hypertension microphthalmia and hyperglycinuria
|
|
C565550||bernard soulier syndrome type c
|
|
C565715|610155||diabetes mellitus insulin dependent 19
|
|
C565715|610155||iddm19
|
|
C565555||gaucher disease type iiib
|
|
C564292|608097||heterotopia periventricular autosomal recessive
|
|
C564292|608097||arphm
|
|
C564292|608097||periventricular heterotopia with microcephaly autosomal recessive
|
|
C564292|608097||periventricular nodular heterotopia 2
|
|
C564292|608097||pvnh2
|
|
C565556||gaucher disease norrbottnian type
|
|
C566888||humeroradial synostosis with craniofacial anomalies
|
|
C564221||glucocorticoid receptor deficiency
|
|
C564221||body composition beneficial
|
|
C564221||cortisol resistance from glucocorticoid receptor defect
|
|
C564221||gccr deficiency
|
|
C564221||gcr deficiency
|
|
C564221||glucocorticoid resistance
|
|
C564221||pseudohermaphroditism female with hypokalemia due to glucocorticoid resistance
|
|
C565558||fructose and galactose intolerance
|
|
C566889||glycogen storage disease iiia
|
|
C566889||gsd iiia
|
|
C566878|300673||encephalopathy neonatal severe due to mecp2 mutations
|
|
C566878|300673||mecp2 related severe neonatal encephalopathy
|
|
D013915|273800||thrombasthenia
|
|
D013915|273800||bdplt2
|
|
D013915|273800||bleeding disorder platelet type 2
|
|
D013915|273800||deficiency of gp 2b 3a complex
|
|
D013915|273800||glanzmann thrombasthenia
|
|
D013915|273800||glanzmann thrombasthenia type a
|
|
D013915|273800||glycoprotein complex iib iiia deficiency of
|
|
D013915|273800||gp iib iiia complex deficiency of
|
|
D013915|273800||gt
|
|
D013915|273800||platelet fibrinogen receptor deficiency of
|
|
D013915|273800||platelet glycoprotein 2b 3a deficiency
|
|
D013915|273800||platelet glycoprotein iib iiia deficiency
|
|
D013915|273800||thrombasthenia glanzmann
|
|
D013915|273800||thrombasthenia of glanzmann and naegeli
|
|
D013915|273800||thrombasthenias
|
|
C565239|606282||deafness autosomal dominant 24
|
|
C565239|606282||dfna24
|
|
C566884||microphthalmia with hyperopia retinal degeneration macrophakia and dental anomalies
|
|
C565554||gaucher disease type iiia
|
|
C566885||lactic acidosis fatal infantile
|
|
C564229||globulin anomaly involving beta 2a globulin
|
|
D004057||hyperostosis diffuse idiopathic skeletal
|
|
D004057||ankylosing hyperostoses vertebral
|
|
D004057||ankylosing hyperostosis vertebral
|
|
D004057||ankylosing vertebral hyperostosis with tylosis
|
|
D004057||diffuse idiopathic skeletal hyperostosis
|
|
D004057||disease forestier
|
|
D004057||disease forestier rotes
|
|
D004057||disease forestier apos s
|
|
D004057||forestier disease
|
|
D004057||forestier rotes disease
|
|
D004057||forestier apos s disease
|
|
D004057||forestiers disease
|
|
D004057||hyperostoses vertebral ankylosing
|
|
D004057||hyperostosis vertebral ankylosing
|
|
D004057||vertebral ankylosing hyperostoses
|
|
D004057||vertebral ankylosing hyperostosis
|
|
246650|C535904||lipase deficiency combined
|
|
246650|C535904||lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency
|
|
246650|C535904||lpl and hl deficiency
|
|
246650|C535904||lpl and htgl deficiency
|
|
D005393||fish diseases
|
|
D005393||disease fish
|
|
D005393||diseases fish
|
|
D005393||fish disease
|
|
C536133|249000||meckel syndrome type 1
|
|
C536133|249000||dysencephalia splachnocystica
|
|
C536133|249000||dysencephalia splanchnocystica
|
|
C536133|249000||gruber syndrome
|
|
C536133|249000||meckel gruber syndrome
|
|
C536133|249000||meckel gruber syndrome type 1
|
|
C536133|249000||meckel syndrome
|
|
C536133|249000||meckel syndrome type1
|
|
C536133|249000||mes
|
|
C536133|249000||mks
|
|
C536133|249000||mks1
|
|
C567780|114200||camptodactyly 1
|
|
C567780|114200||campd1
|
|
C567780|114200||camptodactyly and knuckle pads
|
|
C567780|114200||camptodactyly and knuckle pads streblodactyly included
|
|
D004065||digestive system abnormalities
|
|
D004065||abnormalities digestive system
|
|
D004065||abnormality digestive system
|
|
D004065||digestive system abnormality
|
|
D054391||lymphoma extranodal nk t cell
|
|
D054391||extranodal nk t cell lymphoma
|
|
D054391||extranodal nk t cell lymphoma nasal
|
|
D054391||extranodal nk t cell lymphoma nasal and nasal type
|
|
D054391||extranodal nk t cell lymphoma nasal type
|
|
D054391||extranodal nk t cell lymphomas
|
|
D054391||lymphomas extranodal nk t cell
|
|
D054391||nk t cell lymphoma extranodal
|
|
D054391||nk t cell lymphomas extranodal
|
|
208100|C536614||arthrogryposis multiplex congenita neurogenic type
|
|
208100|C536614||amcn
|
|
208100|C536614||amc neurogenic type
|
|
208100|C536614||neurogenic type of amc
|
|
C576203||alcohol fetopathy
|
|
D005391||firesetting behavior
|
|
D005391||arson
|
|
D005391||arsons
|
|
D005391||behavior firesetting
|
|
D005391||behaviors firesetting
|
|
D005391||firesetting behaviors
|
|
D005391||pyromania
|
|
D005391||pyromanias
|
|
C566890||glycogen storage disease iiib
|
|
C566890||gsd iiib
|
|
C566891||glycogen storage disease iiic
|
|
C566891||gsd iiic
|
|
C566892||glycogen storage disease iiid
|
|
C566892||gsd iiid
|
|
C564230||glioma of brain familial
|
|
C565522||hemolytic anemia with thermal sensitivity of red cells
|
|
C541598||chromosome 11p deletion syndrome
|
|
C541598||11p deletion syndrome
|
|
C563683|610329||aicardi goutieres syndrome 3
|
|
C563683|610329||ags3
|
|
C565521||hemolytic uremic syndrome typical
|
|
D050805||wandering spleen
|
|
D050805||displaced spleen
|
|
D050805||displaced spleens
|
|
D050805||drifting spleen
|
|
D050805||drifting spleens
|
|
D050805||floating spleen
|
|
D050805||floating spleens
|
|
D050805||ptoses splenic
|
|
D050805||ptosis splenic
|
|
D050805||spleen displaced
|
|
D050805||spleen drifting
|
|
D050805||spleen floating
|
|
D050805||spleens displaced
|
|
D050805||spleens drifting
|
|
D050805||spleens floating
|
|
D050805||spleens wandering
|
|
D050805||spleen wandering
|
|
D050805||splenic ptoses
|
|
D050805||splenic ptosis
|
|
D050805||splenoptoses
|
|
D050805||splenoptosis
|
|
D050805||wandering spleens
|
|
D005358||fibrous dysplasia monostotic
|
|
D005358||dysplasia monostotic fibrous
|
|
D005358||dysplasias monostotic fibrous
|
|
D005358||fibrous dysplasias monostotic
|
|
D005358||monostotic fibrous dysplasia
|
|
D005358||monostotic fibrous dysplasias
|
|
D005357||fibrous dysplasia of bone
|
|
D005357||bone fibrous dysplasia
|
|
D005357||bone fibrous dysplasias
|
|
D005357||osteitis fibrosa disseminata
|
|
D005354||fibrosarcoma
|
|
D005354||fibrosarcomas
|
|
C566858||copper overload cirrhosis
|
|
D004022||dictyocaulus infections
|
|
D004022||dictyocauliases
|
|
D004022||dictyocauliasis
|
|
D004022||dictyocaulus infection
|
|
D004022||infection dictyocaulus
|
|
D004022||infections dictyocaulus
|
|
C565528||growth retardation small and puffy hands and feet and eczema
|
|
D005356||fibromyalgia
|
|
D005356||diffuse myofascial pain syndrome
|
|
D005356||fibromyalgia fibromyositis syndrome
|
|
D005356||fibromyalgia fibromyositis syndromes
|
|
D005356||fibromyalgia primary
|
|
D005356||fibromyalgias
|
|
D005356||fibromyalgia secondary
|
|
D005356||fibromyalgias primary
|
|
D005356||fibromyalgias secondary
|
|
D005356||fibromyositis fibromyalgia syndrome
|
|
D005356||fibromyositis fibromyalgia syndromes
|
|
D005356||fibrositides
|
|
D005356||fibrositis
|
|
D005356||muscular rheumatism
|
|
D005356||myofascial pain syndrome diffuse
|
|
D005356||primary fibromyalgia
|
|
D005356||primary fibromyalgias
|
|
D005356||rheumatism muscular
|
|
D005356||secondary fibromyalgia
|
|
D005356||secondary fibromyalgias
|
|
D005356||syndrome fibromyalgia fibromyositis
|
|
D005356||syndrome fibromyositis fibromyalgia
|
|
D005356||syndromes fibromyalgia fibromyositis
|
|
D005356||syndromes fibromyositis fibromyalgia
|
|
C565529||growth factors combined defect of
|
|
C565529||insulin insulin like growth factor i and epidermal growth factor deficiency
|
|
C565529||werner like syndrome due to combined growth factor deficiency
|
|
D005355||fibrosis
|
|
D005355||cirrhosis
|
|
D005355||fibroses
|
|
C563462|600649||carnitine palmitoyltransferase ii deficiency infantile
|
|
C563462|600649||carnitine palmitoyltransferase ii deficiency hepatocardiomuscular
|
|
C563462|600649||carnitine palmitoyltransferase ii deficiency with hypoketotic hypoglycemia
|
|
C563462|600649||cpt2 deficiency infantile
|
|
C563462|600649||cpt ii deficiency hepatic
|
|
D006685||hoarseness
|
|
D006685||hoarsenesses
|
|
D006685||hoarseness neurogenic
|
|
D006685||hoarseness of voice
|
|
D006685||hoarseness voice
|
|
D006685||neurogenic hoarseness
|
|
D006685||neurogenic hoarsenesses
|
|
D006685||voice hoarseness
|
|
D004030||dientamoebiasis
|
|
D004030||dientamoebiases
|
|
C535819|177170||pseudoachondroplasia
|
|
C535819|177170||psach
|
|
C535819|177170||pseudoachondroplastic dysplasia
|
|
C535819|177170||pseudoachondroplastic spondyloepiphyseal dysplasia
|
|
C535819|177170||pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
|
|
C535819|177170||spondyloepiphyseal dysplasia pseudoachondroplastic
|
|
D006691||classical swine fever
|
|
D006691||cholera hog
|
|
D006691||hog cholera
|
|
D006691||swine fever
|
|
D006691||swine fever classical
|
|
C566864||heterotaxy visceroatrial autosomal recessive
|
|
C564201||hemangiomas of small intestine
|
|
C565534||granulomatous disease with defect in neutrophil chemotaxis
|
|
C566865||ataxia telangiectasia variant
|
|
C564200||heme oxygenase 1 deficiency
|
|
C565535||granulocytopenia with immunoglobulin abnormality
|
|
C565196|610698||macular degeneration age related 4
|
|
C565196|610698||armd4
|
|
C565536||gonadal dysgenesis xy type with associated anomalies
|
|
D050815||fractures compression
|
|
D050815||compression fracture
|
|
D050815||compression fractures
|
|
D050815||fracture compression
|
|
C565530||grouped pigmentation of the macula
|
|
C565530||grouped pigmentation of retinal pigment epithelium
|
|
C566861||cataract microcephaly arthrogryposis kyphosis syndrome
|
|
C566861||camak syndrome
|
|
C566862||polyasplenia
|
|
C566862||asplenia with cardiovascular abnormalities
|
|
C564202||progressive familial heart block type ii
|
|
C564202||pfhb2
|
|
C564202||pfhbii
|
|
C564209||graying of hair precocious
|
|
C564209||white hair premature
|
|
D005368||filariasis
|
|
D005368||elaeophoriases
|
|
D005368||elaeophoriasis
|
|
D005368||filariases
|
|
D005368||filarioidea infection
|
|
D005368||filarioidea infections
|
|
D005368||infection filarioidea
|
|
D005368||infections filarioidea
|
|
C564207||prolonged bleeding time brachydactyly and mental retardation
|
|
C564206||achromatopsia 4
|
|
C565538||glycoprotein storage disease
|
|
C565539||gsd iv classic hepatic
|
|
C564699|606545||ichthyosis lamellar 5
|
|
C564699|606545||arci3
|
|
C564699|606545|C538603|242100|D017490|242300||collodion baby self healing
|
|
C564699|606545||ichthyosis congenital autosomal recessive 3
|
|
C564699|606545||ichthyosis lamellar 5 formerly
|
|
C564699|606545||lamellar ichthyosis type 5
|
|
C564699|606545||li5 formerly
|
|
230400||galactosemia galactose 1 phosphate uridylyltransferase deficiency
|
|
230400|D005693|230200||galt deficiency
|
|
230400|D005693|230200||galactosemia classic galactosemia duarte variant
|
|
C567507|611878||cardiomyopathy dilated 1y
|
|
C567507|611878||cmd1y
|
|
C567507|611878||left ventricular noncompaction 9 included
|
|
C567507|611878||lvnc9 included
|
|
C536778|212140||systemic carnitine deficiency
|
|
C536778|212140||carnitine deficiency primary
|
|
C536778|212140||carnitine deficiency systemic due to defect in renal reabsorption of carnitine
|
|
C536778|212140||carnitine deficiency systemic primary
|
|
C536778|212140||carnitine transporter deficiency
|
|
C536778|212140||carnitine transporter plasma membrane deficiency of
|
|
C536778|212140||carnitine uptake defect
|
|
C536778|212140||carnitine uptake deficiency
|
|
C536778|212140||cdsp
|
|
C536778|212140||cud
|
|
C536778|212140||primary carnitine deficiency
|
|
C536778|212140||renal carnitine transport defect
|
|
C536778|212140||scd
|
|
D013132|248800||spinocerebellar degenerations
|
|
D013132|248800||ataxia hereditary
|
|
D013132|248800||ataxias hereditary
|
|
D013132|248800||cerebellar ataxia early onset
|
|
D013132|248800||cerebellar ataxia late onset
|
|
D013132|248800||cerebellar ataxia marie
|
|
D013132|248800||cerebellar ataxia marie apos s
|
|
D013132|248800||cerebellar degeneration primary
|
|
D013132|248800||cerebellar degenerations primary
|
|
D013132|248800||corticostriatal spinal degeneration
|
|
D013132|248800||corticostriatal spinal degenerations
|
|
D013132|248800||degeneration corticostriatal spinal
|
|
D013132|248800||degeneration familial spinocerebellar
|
|
D013132|248800||degeneration hereditary spinocerebellar
|
|
D013132|248800||degeneration inherited spinocerebellar
|
|
D013132|248800||degeneration primary cerebellar
|
|
D013132|248800||degenerations corticostriatal spinal
|
|
D013132|248800||degenerations familial spinocerebellar
|
|
D013132|248800||degenerations hereditary spinocerebellar
|
|
D013132|248800||degenerations inherited spinocerebellar
|
|
D013132|248800||degeneration spinocerebellar
|
|
D013132|248800||degeneration spino cerebellar
|
|
D013132|248800||degenerations primary cerebellar
|
|
D013132|248800||degenerations spinocerebellar
|
|
D013132|248800||degenerations spino cerebellar
|
|
D013132|248800||early onset cerebellar ataxia
|
|
D013132|248800||familial spinocerebellar degeneration
|
|
D013132|248800||familial spinocerebellar degenerations
|
|
D013132|248800||garland moorhouse syndrome
|
|
D013132|248800||hereditary ataxia
|
|
D013132|248800||hereditary ataxias
|
|
D013132|248800||hereditary oligophrenic cerebello lental degeneration
|
|
D013132|248800||hereditary spinocerebellar degeneration
|
|
D013132|248800||hereditary spinocerebellar degenerations
|
|
D013132|248800||hypogonadism marinesco sjogren syndrome hypergonadotrophic
|
|
D013132|248800||inherited spinocerebellar degeneration
|
|
D013132|248800||inherited spinocerebellar degenerations
|
|
D013132|248800||late onset cerebellar ataxia
|
|
D013132|248800||marie cerebellar ataxia
|
|
D013132|248800||marie apos s cerebellar ataxia
|
|
D013132|248800||marinesco garland syndrome
|
|
D013132|248800||marinesco sjogren garland syndrome
|
|
D013132|248800||marinesco sjogren syndrome
|
|
D013132|248800||marinesco sj 246 gren syndrome
|
|
D013132|248800||marinesco sjogren syndrome hypergonadotrophic hypogonadism
|
|
D013132|248800||marinesco sjogren syndrome myopathy
|
|
D013132|248800||mss
|
|
D013132|248800||primary cerebellar degeneration
|
|
D013132|248800||primary cerebellar degenerations
|
|
D013132|248800||spinocerebellar degeneration
|
|
D013132|248800||spino cerebellar degeneration
|
|
D013132|248800||spinocerebellar degeneration familial
|
|
D013132|248800||spinocerebellar degeneration hereditary
|
|
D013132|248800||spinocerebellar degeneration inherited
|
|
D013132|248800||spino cerebellar degenerations
|
|
D013132|248800||spinocerebellar degenerations familial
|
|
D013132|248800||spinocerebellar degenerations hereditary
|
|
D013132|248800||spinocerebellar degenerations inherited
|
|
D013132|248800||spinocerebellar disease
|
|
D013132|248800||spinocerebellar diseases
|
|
D013132|248800||syndrome garland moorhouse
|
|
D013132|248800||syndrome hypergonadotrophic hypogonadism marinesco sjogren
|
|
D013132|248800||syndrome marinesco garland
|
|
D013132|248800||syndrome marinesco sjogren
|
|
D013132|248800||syndrome marinesco sj 246 gren
|
|
D013132|248800||syndrome marinesco sjogren garland
|
|
D013132|248800||syndrome myopathy marinesco sjogren
|
|
C535695|154275||malignant hyperthermia susceptibility type 2
|
|
C535695|154275||malignant hyperpyrexia susceptibility type 2
|
|
C535695|154275||malignant hyperthermia susceptibility to 2
|
|
C535695|154275||mhs2
|
|
D018677||tooth injuries
|
|
D018677||injuries teeth
|
|
D018677||injuries tooth
|
|
D018677||injury teeth
|
|
D018677||injury tooth
|
|
D018677||teeth injuries
|
|
D018677||teeth injury
|
|
D018677||tooth injury
|
|
C565500||hyperlexia
|
|
C565500||compulsive reading
|
|
C565500||precocious reading
|
|
C566831||paragangliomas with sensorineural hearing loss
|
|
C565501||breastfeeding jaundice
|
|
C566832||papillomatosis familial cutaneous
|
|
C562903|243060||male infertility with large headed multiflagellar polyploid spermatozoa
|
|
C562903|243060||infertility associated with multi tailed spermatozoa and excessive dna
|
|
C562903|243060||spermatogenic failure 5
|
|
C562903|243060||spgf5
|
|
C565502||hydroxylysinuria
|
|
C566834||panic disorder with bladder conditions
|
|
C562924|179850||dowling degos disease
|
|
C562924|179850||dark dot disease
|
|
C562924|179850||ddd
|
|
C562924|179850||ddd1
|
|
C562924|179850||dowling degos disease 1
|
|
C562924|179850||dowling degos kitamura disease
|
|
C562924|179850||kitamura reticulate acropigmentation
|
|
C562924|179850||reticular pigment anomaly of flexures
|
|
C562924|179850||reticulate acropigmentation of kitamura
|
|
C565509||humeroradial multiple synostosis syndrome
|
|
D005335||fever of unknown origin
|
|
D005335||unknown origin fever
|
|
D005335||unknown origin fevers
|
|
606408|C536193||ehlers danlos syndrome caused by tenascin x deficiency
|
|
606408|C536193||eds due to tnx deficiency
|
|
606408|C536193||ehlers danlos like syndrome due to tenascin x deficiency
|
|
606408|C536193||tnx deficiency
|
|
167000|D010051||ovarian neoplasms
|
|
167000|D010051||cancer of ovary
|
|
167000|D010051||cancer of the ovary
|
|
167000|D010051||cancer ovarian
|
|
167000|D010051||cancer ovary
|
|
167000|D010051||cancers ovarian
|
|
167000|D010051||cancers ovary
|
|
167000|D010051||neoplasm ovarian
|
|
167000|D010051||neoplasm ovary
|
|
167000|D010051||neoplasms ovarian
|
|
167000|D010051||neoplasms ovary
|
|
167000|D010051||ovarian cancer
|
|
167000|D010051||ovarian cancer epithelial included
|
|
167000|D010051||ovarian cancers
|
|
167000|D010051||ovarian cancer susceptibility to 1
|
|
167000|D010051||ovarian neoplasm
|
|
167000|D010051||ovary cancer
|
|
167000|D010051||ovary cancers
|
|
167000|D010051||ovary neoplasm
|
|
167000|D010051||ovary neoplasms
|
|
167000|D010051||ovcas1
|
|
C566835||panic disorder with joint laxity
|
|
D016584|167870||panic disorder
|
|
D016584|167870||attack panic
|
|
D016584|167870||attacks panic
|
|
D016584|167870||disorder panic
|
|
D016584|167870||disorders panic
|
|
D016584|167870||pand1
|
|
D016584|167870||pand2
|
|
D016584|167870||pand3
|
|
D016584|167870||panic attack
|
|
D016584|167870||panic attacks
|
|
D016584|167870||panic disorder 1
|
|
D016584|167870||panic disorder 2
|
|
D016584|167870||panic disorder 3
|
|
D016584|167870||panic disorder panic disorder with bladder conditions included
|
|
D016584|167870||panic disorders
|
|
D016584|167870||panic disorder susceptibility locus chromosome 13q related
|
|
D016584|167870||panic disorder susceptibility locus chromosome 4q related
|
|
D016584|167870||panic disorder susceptibility locus chromosome 9q related
|
|
D016584|167870||panic disorder with joint laxity included
|
|
C565505||muscular dystrophy congenital plus mental retardation
|
|
C565485|240600||glycogen storage disease 0 liver
|
|
C565485|240600||gsd 0a
|
|
C565485|240600||gsd0a
|
|
C565485|240600||hypoglycemia with deficiency of glycogen synthetase in the liver
|
|
C565485|240600||liver glycogen storage disease 0
|
|
C565485|240600||liver glycogen synthase deficiency
|
|
D005331||fetomaternal transfusion
|
|
D005331||fetomaternal hemorrhage
|
|
D005331||fetomaternal hemorrhages
|
|
D005331||fetomaternal transfusions
|
|
D005331||hemorrhage fetomaternal
|
|
D005331||hemorrhages fetomaternal
|
|
D005331||transfusion fetomaternal
|
|
D005331||transfusions fetomaternal
|
|
C566836||pancytopenia and occlusive vascular disease
|
|
277730|D020915||korsakoff syndrome
|
|
277730|D020915|C538669||alcohol induced encephalopathy
|
|
277730|D020915||korsakoff psychoses
|
|
277730|D020915||korsakoff psychosis
|
|
277730|D020915||psychoses korsakoff
|
|
277730|D020915||psychosis korsakoff
|
|
277730|D020915||syndrome korsakoff
|
|
277730|D020915||syndromes wernicke korsakoff
|
|
277730|D020915||syndrome wernicke korsakoff
|
|
277730|D020915|C538669||transketolase defect
|
|
277730|D020915||wernicke korsakoff syndrome
|
|
277730|D020915||wernicke korsakoff syndromes
|
|
C565506||muscular dystrophy congenital associated with calf hypertrophy microcephaly and severe mental retardation
|
|
D005334||fever
|
|
D005334||fevers
|
|
D005334||hyperthermia
|
|
D005334||hyperthermias
|
|
D005334||pyrexia
|
|
D005334||pyrexias
|
|
C566837||pancreatitis calcific
|
|
C565507||hydranencephaly with renal aplasia dysplasia
|
|
C567371|612279||generalized epilepsy with febrile seizures plus type 6
|
|
C567371|612279||gefs 6
|
|
C567371|612279||gefsp6
|
|
C567371|612279||gefs type 6
|
|
D053099||azotemia
|
|
D019973||alcohol related disorders
|
|
D019973||alcohol related disorder
|
|
D019973||disorder alcohol related
|
|
D019973||disorders alcohol related
|
|
C565512||mthfr deficiency thermolabile type
|
|
274150|D011697||purpura thrombotic thrombocytopenic
|
|
274150|D011697||congenital thrombotic thrombocytopenic purpura
|
|
274150|D011697||disease moschcowitz
|
|
274150|D011697||disease moschkowitz
|
|
274150|D011697||familial thrombotic microangiopathy
|
|
274150|D011697||familial thrombotic thrombocytopenia purpura
|
|
274150|D011697||familial thrombotic thrombocytopenic purpura
|
|
274150|D011697|D000743||microangiopathic hemolytic anemia
|
|
274150|D011697||microangiopathic hemolytic anemia congenital
|
|
274150|D011697||microangiopathy familial thrombotic
|
|
274150|D011697||moschcowitz disease
|
|
274150|D011697||moschkowitz disease
|
|
274150|D011697||purpura thrombotic thrombopenic
|
|
274150|D011697||schulman upshaw syndrome
|
|
274150|D011697||syndrome schulman upshaw
|
|
274150|D011697||syndrome upshaw schulman
|
|
274150|D011697||thrombocytopenic purpura thrombotic
|
|
274150|D011697||thrombopenic purpura thrombotic
|
|
274150|D011697||thrombotic microangiopathy familial
|
|
274150|D011697||thrombotic thrombocytopenic purpura
|
|
274150|D011697||thrombotic thrombocytopenic purpura congenital
|
|
274150|D011697||thrombotic thrombocytopenic purpura familial
|
|
274150|D011697||thrombotic thrombopenic purpura
|
|
274150|D011697||ttp
|
|
274150|D011697||upshaw factor deficiency of
|
|
274150|D011697||upshaw schulman syndrome
|
|
274150|D011697||uss
|
|
C565513||homocystinuria pyridoxine responsive
|
|
C566844||thanatophoric dysplasia type i
|
|
C566844||lethal short limbed platyspondylic dwarfism san diego type
|
|
C566844||platyspondylic lethal skeletal dysplasia san diego type
|
|
C565514||holoprosencephaly 1
|
|
C563321|601412||deafness autosomal dominant 7
|
|
C563321|601412||dfna7
|
|
304790|C562780||immunodysregulation polyendocrinopathy and enteropathy x linked
|
|
304790|C562780||autoimmunity immunodeficiency syndrome x linked
|
|
304790|C562780||diabetes mellitus congenital insulin dependent with fatal secretory diarrhea
|
|
304790|C562780||diarrhea polyendocrinopathy fatal infection syndrome x linked
|
|
304790|C562780||dmsd
|
|
304790|C562780||enteropathy autoimmune with hemolytic anemia and polyendocrinopathy
|
|
304790|C562780||iddm secretory diarrhea syndrome
|
|
304790|C562780||immunodeficiency polyendocrinopathy and enteropathy x linked formerly islets of langerhans absence of included
|
|
304790|C562780||ipex
|
|
304790|C562780||polyendocrinopathy immune dysfunction and diarrhea x linked
|
|
304790|C562780||xlaad
|
|
304790|C562780||x linked autoimmunity allergic dysregulation syndrome
|
|
304790|C562780||xpid
|
|
107250|C537775||anterior segment ocular dysgenesis
|
|
107250|C537775||asmd
|
|
107250|C537775||asod
|
|
D020966||muscular disorders atrophic
|
|
D020966||atrophic muscular disorder
|
|
D020966||atrophic muscular disorders
|
|
D020966||atrophies disuse
|
|
D020966||atrophies spinobulbar
|
|
D020966||atrophies spinobulbar muscular
|
|
D020966||atrophies spinopontine
|
|
D020966||atrophy disuse
|
|
D020966||atrophy muscular spinobulbar
|
|
D020966||atrophy spinobulbar
|
|
D020966||atrophy spinobulbar muscular
|
|
D020966||atrophy spinopontine
|
|
D020966||disorder atrophic muscular
|
|
D020966||disorders atrophic muscular
|
|
D020966||disuse atrophies
|
|
D020966||disuse atrophy
|
|
D020966||muscular atrophies spinobulbar
|
|
D020966||muscular atrophy spinobulbar
|
|
D020966||muscular disorder atrophic
|
|
D020966|C537017|313200||spinal and bulbar muscular atrophy
|
|
D020966||spinobulbar atrophies
|
|
D020966||spinobulbar atrophy
|
|
D020966||spinobulbar muscular atrophies
|
|
D020966||spinobulbar muscular atrophy
|
|
D020966||spinopontine atrophies
|
|
D020966|D017827|109150||spinopontine atrophy
|
|
C537464|309800||microphthalmia syndromic 1
|
|
C537464|309800||lenz dysmorphogenic syndrome
|
|
C537464|309800||lenz dysplasia
|
|
C537464|309800||lenz microphthalmia syndrome
|
|
C537464|309800||lenz syndrome
|
|
C537464|309800||maa formerly
|
|
C537464|309800||mcops1
|
|
C537464|309800||microphthalmia or anophthalmos with associated anomalies
|
|
C537464|309800||microphthalmia or anophthalmos with associated anomalies formerly
|
|
D006679||hiv seropositivity
|
|
D006679||aids seroconversion
|
|
D006679||aids seroconversions
|
|
D006679||aids seropositivities
|
|
D006679||aids seropositivity
|
|
D006679||antibody positivities hiv
|
|
D006679||antibody positivity hiv
|
|
D006679||anti hiv positivities
|
|
D006679||anti hiv positivity
|
|
D006679||hiv antibody positivities
|
|
D006679||hiv antibody positivity
|
|
D006679||hiv seroconversion
|
|
D006679||hiv seroconversions
|
|
D006679||hiv seropositivities
|
|
D006679||htlv iii seroconversion
|
|
D006679||htlv iii seroconversions
|
|
D006679||htlv iii seropositivities
|
|
D006679||htlv iii seropositivity
|
|
D006679||positivities anti hiv
|
|
D006679||positivities hiv antibody
|
|
D006679||positivity anti hiv
|
|
D006679||positivity hiv antibody
|
|
D006679||seroconversion aids
|
|
D006679||seroconversion hiv
|
|
D006679||seroconversion htlv iii
|
|
D006679||seroconversions aids
|
|
D006679||seroconversions hiv
|
|
D006679||seroconversions htlv iii
|
|
D006679||seropositivities aids
|
|
D006679||seropositivities hiv
|
|
D006679||seropositivities htlv iii
|
|
D006679||seropositivity aids
|
|
D006679||seropositivity hiv
|
|
D006679||seropositivity htlv iii
|
|
D020964||embryo loss
|
|
D020964||blastocyst disintegration
|
|
D020964||death embryo
|
|
D020964||disintegration blastocyst
|
|
D020964||disintegration of blastocyst
|
|
D020964||disintegration of embryo
|
|
D020964||embryo death
|
|
D020964||embryo deaths
|
|
D020964||embryo disintegration
|
|
D020964||embryo resorption
|
|
D020964||resorption embryo
|
|
D006677||histrionic personality disorder
|
|
D006677||disorder histrionic personality
|
|
D006677||disorders histrionic personality
|
|
D006677||histrionic personality disorders
|
|
D006677||hysterical personalities
|
|
D006677||hysterical personality
|
|
D006677||personalities hysterical
|
|
D006677||personality disorder histrionic
|
|
D006677||personality disorders histrionic
|
|
D006677||personality hysterical
|
|
D005348||fibrocystic breast disease
|
|
D005348||adenoses microglandular
|
|
D005348||adenosis microglandular
|
|
D005348||adenosis of breast
|
|
D005348||breast adenosis
|
|
D005348||breast cystic disease
|
|
D005348||breast cystic diseases
|
|
D005348||breast disease cystic
|
|
D005348||breast disease fibrocystic
|
|
D005348||breast dysplasia
|
|
D005348||breast fibrocystic change
|
|
D005348||breast fibrocystic changes
|
|
D005348||breast fibrocystic disease
|
|
D005348||chronic cystic mastitis
|
|
D005348||cystic breast disease
|
|
D005348||cystic disease of breast
|
|
D005348||cystic mastitis chronic
|
|
D005348||disease cystic breast
|
|
D005348||disease fibrocystic breast
|
|
D005348||dysplasia breast
|
|
D005348||dysplasia mammary
|
|
D005348||fibrocystic changes of breast
|
|
D005348||fibrocystic disease of breast
|
|
D005348||fibrocystic mastopathy
|
|
D005348||mammary dysplasia
|
|
D005348||mastopathy fibrocystic
|
|
D005348||microglandular adenoses
|
|
D005348||microglandular adenosis
|
|
D004011||dicrocoeliasis
|
|
D004011||dicrocoeliases
|
|
C565517||hirschsprung disease with ulnar polydactyly polysyndactyly of big toes and ventricular septal defect
|
|
612782|C557826||immune dysfunction with t cell inactivation due to calcium entry defect 1
|
|
612782|C557826||imd9
|
|
612782|C557826||immunodeficiency 9
|
|
C565518||hirschsprung disease with polydactyly renal agenesis and deafness
|
|
D005350||fibroma
|
|
D005350||fibromas
|
|
D005350||fibromatoses
|
|
D005350||fibromatosis
|
|
D005350||fibromyxoma
|
|
D005350||fibromyxomas
|
|
D005350||myxofibroma
|
|
D005350||myxofibromas
|
|
C564423|305800||membranoproliferative glomerulonephritis x linked
|
|
C564423|305800||mesangiocapillary glomerulonephritis x linked
|
|
D005352||fibromuscular dysplasia
|
|
D005352||dysplasia fibromuscular
|
|
D005352||dysplasias fibromuscular
|
|
D005352||fibromuscular dysplasias
|
|
D005351||fibromatosis gingival
|
|
D005351||fibromatoses gingival
|
|
D005351||fibromatosis gingivae
|
|
D005351||gingival fibromatoses
|
|
D005351||gingival fibromatosis
|
|
D020969||disease attributes
|
|
D020969||attribute disease
|
|
D020969||attributes disease
|
|
D020969||disease attribute
|
|
D020967||myotonic disorders
|
|
D020967||congenita paramyotonia
|
|
D020967||disease eulenburg
|
|
D020967||disease eulenburg apos s
|
|
D020967||disorder myotonic
|
|
D020967||disorders myotonic
|
|
D020967||eulenburg disease
|
|
D020967||eulenburg apos s disease
|
|
D020967||eulenburgs disease
|
|
D020967||fluctuans myotonia
|
|
D020967||myopathies myotonic
|
|
D020967||myopathies proximal myotonic
|
|
D020967||myopathy myotonic
|
|
D020967||myopathy proximal myotonic
|
|
D020967|C538353|608390||myotonia fluctuans
|
|
D020967||myotonic disorder
|
|
D020967||myotonic myopathies
|
|
D020967||myotonic myopathies proximal
|
|
D020967||myotonic myopathy
|
|
D020967|602668|C538009||myotonic myopathy proximal
|
|
D020967||paramyotonia congenita
|
|
D020967||paramyotonia congenitas
|
|
D020967||promm proximal myotonic myopathy
|
|
D020967||promms proximal myotonic myopathy
|
|
D020967||proximal myotonic myopathies
|
|
D020967|602668|C538009||proximal myotonic myopathy
|
|
609981||natural killer cell and glucocorticoid deficiency with dna repair defect
|
|
609981|C566492||natural killer cell deficiency familial isolated
|
|
609981||nkcd
|
|
609981||nkgcd
|
|
C566452|610048||corneal dystrophy congenital stromal
|
|
C566452|610048||congenital hereditary stromal dystrophy of the cornea
|
|
C566452|610048||congenital stromal corneal dystrophy
|
|
C566452|610048||congenital stromal dystrophy of the cornea
|
|
C566452|610048||cscd
|
|
C566452|610048||decorin associated congenital stromal corneal dystrophy
|
|
C566452|610048||dystrophia corneae parenchymatosa congenita
|
|
D018658||ventricular septal rupture
|
|
D018658||septal ruptures ventricular
|
|
D018658||septal rupture ventricular
|
|
D018658||ventricular septal perforation
|
|
D018658||ventricular septal ruptures
|
|
C563785|609153||pseudohyperkalemia familial 2 due to red cell leak
|
|
C563785|609153||pseudohyperkalemia chiswick
|
|
C563785|609153||pseudohyperkalemia falkirk
|
|
C563785|609153||pseudohyperkalemia lille
|
|
C563785|609153||pshk2
|
|
C566810||wegener like granulomatosis
|
|
C566811||pelvis shoulder dysplasia
|
|
C566811||kosenow syndrome
|
|
C566811||scapuloiliac dysostosis
|
|
144200|D053546||keratoderma palmoplantar epidermolytic
|
|
144200|D053546||epidermolytic hyperkeratoses localized
|
|
144200|D053546||epidermolytic hyperkeratosis localized
|
|
144200|D053546||epidermolytic palmoplantar keratoderma
|
|
144200|D053546||epidermolytic palmoplantar keratodermas
|
|
144200|D053546||epidermolytic palmoplantar keratoderma vorner type
|
|
144200|D053546||epidermolytic thost unna disease
|
|
144200|D053546||epidermolytic unna thost disease
|
|
144200|D053546||eppk
|
|
144200|D053546||eppk epidermolytic palmoplantar keratoderma
|
|
144200|D053546||eppks epidermolytic palmoplantar keratoderma
|
|
144200|D053546||greither keratosis
|
|
144200|D053546||hyperkeratoses localized epidermolytic
|
|
144200|D053546||hyperkeratosis localized epidermolytic
|
|
144200|D053546||keratoderma epidermolytic palmoplantar
|
|
144200|D053546||keratodermas epidermolytic palmoplantar
|
|
144200|D053546||keratosis of greither
|
|
144200|D053546||keratosis of greither palmoplantar keratoderma epidermolytic with knuckle pads included
|
|
144200|D053546|D015776||keratosis palmaris et plantaris familiaris
|
|
144200|D053546||localized epidermolytic hyperkeratoses
|
|
144200|D053546||localized epidermolytic hyperkeratosis
|
|
144200|D053546||palmoplantar keratoderma epidermolytic
|
|
144200|D053546||palmoplantar keratodermas epidermolytic
|
|
144200|D053546|C567914||palmoplantar keratoderma vorner type
|
|
144200|D053546||thost unna disease epidermolytic
|
|
144200|D053546|C563422|600962|D015776||tylosis
|
|
144200|D053546||unna thost disease epidermolytic
|
|
D019960||elimination disorders
|
|
D019960||disorder elimination
|
|
D019960||disorders elimination
|
|
D019960||elimination disorder
|
|
C536943|186570||nog related symphalangism spectrum disorder
|
|
C536943|186570|184460||ankylosis of stapes hyperopia broad thumbs broad first toes and syndactyly
|
|
C536943|186570|611377||brachydactyly type b2
|
|
C536943|186570|186500||deafness symphalangism syndrome of herrmann
|
|
C536943|186570|186500||facioaudiosymphalangism syndrome
|
|
C536943|186570|186500||multiple synostoses syndrome 1
|
|
C536943|186570|184460||stapes ankylosis syndrome without symphalangism
|
|
C536943|186570|184460||stapes ankylosis with broad thumb and toes
|
|
C536943|186570|186500||symphalangism brachydactyly syndrome
|
|
C536943|186570|186500||synostoses multiple with brachydactyly
|
|
C536943|186570||synostosis of talus and calcaneus with short stature included
|
|
C536943|186570||tarsal carpal coalition syndrome
|
|
C536943|186570||tcc
|
|
C536943|186570|184460||teunissen cremers syndrome
|
|
C566812||pelvic lipomatosis with crossed renal ectopia
|
|
D005317||fetal growth retardation
|
|
D005317||growth retardation fetal
|
|
D005317||growth retardation intrauterine
|
|
D005317||intrauterine growth retardation
|
|
D005317||iugr
|
|
D005317||retardation fetal growth
|
|
D005317||retardation intrauterine growth
|
|
D007979||levocardia
|
|
D007979||isolated levocardia
|
|
D007979||levocardia isolated
|
|
D007979||situs inversus with levocardia
|
|
C566817||paroxysmal tonic upgaze benign childhood with ataxia
|
|
D020955||striatonigral degeneration
|
|
D020955||atrophies striatonigral
|
|
D020955||atrophy striatonigral
|
|
D020955||degeneration striatonigral
|
|
D020955||striatonigral atrophies
|
|
D020955||striatonigral atrophy
|
|
D020955||striatonigral degenerations
|
|
D006646||histiocytosis langerhans cell
|
|
D006646||aleukemic reticuloendothelioses systemic
|
|
D006646||aleukemic reticuloendotheliosis systemic
|
|
D006646||cell granulomatoses langerhans
|
|
D006646||cell granulomatosis langerhans
|
|
D006646||cell histiocytoses langerhans
|
|
D006646||cell histiocytosis langerhans
|
|
D006646||disease hand schueller christian
|
|
D006646||disease hand sch 252 ller christian
|
|
D006646||disease letterer siwe
|
|
D006646||disease schueller christian
|
|
D006646||generalized histiocytoses
|
|
D006646||generalized histiocytosis
|
|
D006646||granulomatoses langerhans cell
|
|
D006646||granulomatosis langerhans cell
|
|
D006646||hand schueller christian disease
|
|
D006646||hand schueller christian syndrome
|
|
D006646||hand sch 252 ller christian disease
|
|
D006646||hand sch 252 ller christian syndrome
|
|
D006646||hashimoto pritzger disease
|
|
D006646||histiocytoses generalized
|
|
D006646||histiocytoses langerhans cell
|
|
D006646||histiocytoses type 2
|
|
D006646||histiocytosis generalized
|
|
D006646||histiocytosis type 2
|
|
D006646||histiocytosis x
|
|
D006646||histiocytosis x pulmonary
|
|
D006646||langerhans cell granulomatoses
|
|
D006646||langerhans cell granulomatosis
|
|
D006646||langerhans cell granulomatosis pulmonary
|
|
D006646||langerhans cell histiocytoses
|
|
D006646||langerhans cell histiocytosis
|
|
D006646||letterer siwe disease
|
|
D006646||non lipid reticuloendothelioses
|
|
D006646||non lipid reticuloendotheliosis
|
|
D006646||pulmonary histiocytosis x
|
|
D006646||pulmonary langerhans cell granulomatosis
|
|
D006646||reticuloendothelioses non lipid
|
|
D006646||reticuloendothelioses systemic aleukemic
|
|
D006646||reticuloendotheliosis non lipid
|
|
D006646||reticuloendotheliosis systemic aleukemic
|
|
D006646||schueller christian disease
|
|
D006646||syndrome hand schueller christian
|
|
D006646||syndrome hand sch 252 ller christian
|
|
D006646||systemic aleukemic reticuloendothelioses
|
|
D006646||systemic aleukemic reticuloendotheliosis
|
|
D006646||type 2 histiocytoses
|
|
D006646||type 2 histiocytosis
|
|
D005313||fetal death
|
|
D005313||death fetal
|
|
D005313||fetal deaths
|
|
D005313||fetal mummification
|
|
D005313||fetal mummifications
|
|
D005313||mummification fetal
|
|
D005313||mummifications fetal
|
|
D005316||fetal distress
|
|
D005316||fetal status nonreassuring
|
|
D005316||nonreassuring fetal status
|
|
D020953||neuroaspergillosis
|
|
D020953||aspergillosis nervous system invasive
|
|
D020953||nervous system invasive aspergillosis
|
|
D020953||neuroaspergilloses
|
|
D005315||fetal diseases
|
|
D005315||disease fetal
|
|
D005315||diseases fetal
|
|
D005315||embryopathies
|
|
D005315||embryopathy
|
|
D005315||fetal disease
|
|
C538320|235800||histidinemia
|
|
C538320|235800||deficiency in histidase
|
|
C538320|235800||hal deficiency
|
|
C538320|235800||his deficiency
|
|
C538320|235800||histidase deficiency
|
|
C538320|235800||histidine ammonia lyase deficiency
|
|
C538320|235800||hyperhistidinemia
|
|
C566813|D020371|169500||leukodystrophy demyelinating adult onset autosomal dominant
|
|
C566813||multiple sclerosis like disorder
|
|
C566813||pelizaeus merzbacher disease autosomal dominant or late onset type
|
|
D007973||leukorrhea
|
|
D007973||leukorrheas
|
|
C566814||pechet factor deficiency
|
|
C566814||dynia factor deficiency
|
|
C565377|251600||microphthalmia isolated 1
|
|
C565377|251600|C566446|610093||anophthalmia clinical isolated
|
|
C565377|251600||mcop
|
|
C565377|251600||mcop1
|
|
C565377|251600||microphthalmos autosomal recessive
|
|
D007971||leukoplakia
|
|
D007971||lesion leukoplakic
|
|
D007971||lesions leukoplakic
|
|
D007971||leukokeratoses
|
|
D007971||leukokeratosis
|
|
D007971||leukoplakias
|
|
D007971||leukoplakic lesion
|
|
D007971||leukoplakic lesions
|
|
D005311||fetal hypoxia
|
|
D005311||anoxia fetal
|
|
D005311||fetal anoxia
|
|
D005311||hypoxia fetal
|
|
C566816||patella familial recurrent dislocation of
|
|
D007972||leukoplakia oral
|
|
D007972||keratosis oral
|
|
D007972||leukokeratoses oral
|
|
D007972||leukokeratosis oral
|
|
D007972||leukoplakias oral
|
|
D007972||oral leukokeratoses
|
|
D007972||oral leukokeratosis
|
|
D007972||oral leukoplakia
|
|
D007972||oral leukoplakias
|
|
D019959||feeding and eating disorders of childhood
|
|
D019959||childhood eating and feeding disorders
|
|
D019959||disorder rumination
|
|
D019959||rumination disorder
|
|
D019959||rumination disorders
|
|
D019958||attention deficit and disruptive behavior disorders
|
|
D019958||behavior disorder disruptive
|
|
D019958||defiant disorder oppositional
|
|
D019958||disruptive behavior disorder
|
|
D019958||oppositional defiant disorder
|
|
D019955||conduct disorder
|
|
D019955||conduct disorders
|
|
D019954||neurobehavioral manifestations
|
|
D019954||cognitive manifestation
|
|
D019954||cognitive manifestations
|
|
D019954||cognitive symptom
|
|
D019954||cognitive symptoms
|
|
D019954||manifestation cognitive
|
|
D019954||manifestation neurobehavioral
|
|
D019954||manifestations cognitive
|
|
D019954||manifestations neurobehavioral
|
|
D019954||neurobehavioral manifestation
|
|
D019954||neurobehavioral signs and symptoms
|
|
D019954||signs and symptoms neurobehavioral
|
|
D019954||symptom cognitive
|
|
D019954||symptoms cognitive
|
|
D019957||motor skills disorders
|
|
D019957||coordination disorder developmental
|
|
D019957||developmental coordination disorder
|
|
D019957||developmental coordination disorders
|
|
D019957||motor skills disorder
|
|
D019956||stereotypic movement disorder
|
|
D019956||body rocking
|
|
D019956||head banging
|
|
D019956||movement disorder stereotypic
|
|
D019956||stereotypic movement disorders
|
|
605841|D009290||narcolepsy
|
|
605841|D009290||gelineau apos s syndrome
|
|
605841|D009290||gelineaus syndrome
|
|
605841|D009290||gelineau apos s syndromes
|
|
605841|D009290||gelineau syndrome
|
|
605841|D009290||narcolepsy 2 susceptibility to
|
|
605841|D009290||narcolepsy 3
|
|
605841|D009290||narcolepsy 4 susceptibility to
|
|
605841|D009290||narcolepsy 5 susceptibility to
|
|
605841|D009290||narcolepsy 6 susceptibility to
|
|
605841|D009290||narcolepsy cataplexy syndrome
|
|
605841|D009290||narcolepsy cataplexy syndromes
|
|
605841|D009290||narcoleptic syndrome
|
|
605841|D009290||narcoleptic syndromes
|
|
605841|D009290||nrclp2
|
|
605841|D009290||nrclp3
|
|
605841|D009290||nrclp4
|
|
605841|D009290||nrclp5
|
|
605841|D009290||nrclp6
|
|
605841|D009290||paroxysmal sleep
|
|
605841|D009290||sleep paroxysmal
|
|
605841|D009290||syndrome gelineau
|
|
605841|D009290||syndrome gelineau apos s
|
|
605841|D009290||syndrome narcolepsy cataplexy
|
|
605841|D009290||syndrome narcoleptic
|
|
605841|D009290||syndromes gelineau apos s
|
|
605841|D009290||syndromes narcolepsy cataplexy
|
|
605841|D009290||syndromes narcoleptic
|
|
D002583|603956||uterine cervical neoplasms
|
|
D002583|603956||cancer cervix
|
|
D002583|603956||cancer of cervix
|
|
D002583|603956||cancer of the cervix
|
|
D002583|603956||cancer of the uterine cervix
|
|
D002583|603956||cancers cervix
|
|
D002583|603956||cancers uterine cervical
|
|
D002583|603956||cancer uterine cervical
|
|
D002583|603956||cervical cancer
|
|
D002583|603956||cervical cancers uterine
|
|
D002583|603956||cervical cancer uterine
|
|
D002583|603956||cervical neoplasm
|
|
D002583|603956||cervical neoplasms
|
|
D002583|603956||cervical neoplasms uterine
|
|
D002583|603956||cervical neoplasm uterine
|
|
D002583|603956||cervix cancer
|
|
D002583|603956||cervix neoplasm
|
|
D002583|603956||cervix neoplasms
|
|
D002583|603956||neoplasm cervical
|
|
D002583|603956||neoplasm cervix
|
|
D002583|603956||neoplasms cervical
|
|
D002583|603956||neoplasms cervix
|
|
D002583|603956||neoplasms uterine cervical
|
|
D002583|603956||neoplasm uterine cervical
|
|
D002583|603956||uterine cervical cancer
|
|
D002583|603956||uterine cervical cancers
|
|
D002583|603956||uterine cervical neoplasm
|
|
D019952||mental disorders diagnosed in childhood
|
|
D019952||child mental disorder
|
|
D019952||child mental disorders
|
|
D019952||disorder child mental
|
|
D019952||disorders child mental
|
|
D019952||disorders usually diagnosed in infancy childhood or adolescence
|
|
D019952||mental disorder child
|
|
D019952||mental disorders child
|
|
C566820||passovoy factor
|
|
C566821||parotidomegaly hereditary bilateral
|
|
D018640||stomatognathic system abnormalities
|
|
D018640||abnormalities stomatognathic system
|
|
D018640||abnormality stomatognathic system
|
|
D018640||stomatognathic system abnormality
|
|
C566823||parkinson disease familial type 1
|
|
C566823||atypical parkinson disease
|
|
C566823||lewy body parkinsonism
|
|
C566823||parkinson disease autosomal dominant
|
|
D019970||cocaine related disorders
|
|
D019970||abuse cocaine
|
|
D019970||addiction cocaine
|
|
D019970||cocaine abuse
|
|
D019970||cocaine addiction
|
|
D019970||cocaine dependence
|
|
D019970||cocaine related disorder
|
|
D019970||dependence cocaine
|
|
D019970||dependences cocaine
|
|
D019970||disorder cocaine related
|
|
D019970||disorders cocaine related
|
|
D005329||fetishism psychiatric
|
|
D005329||fetishisms psychiatric
|
|
607154|C567078||allergic rhinitis
|
|
607154|C567078||alrh
|
|
D020943||aids arteritis central nervous system
|
|
D020943||aids associated cerebral aneurysmal arteriopathy
|
|
D020943||central nervous system aids arteritis
|
|
D020943||cerebral aneurysmal arteriopathy aids associated
|
|
D020943||cns vasculitides hiv 1 associated
|
|
D020943||cns vasculitides hiv associated
|
|
D020943||cns vasculitis hiv 1 associated
|
|
D020943||cns vasculitis hiv associated
|
|
D020943||hiv 1 associated cns vasculitides
|
|
D020943||hiv 1 associated cns vasculitis
|
|
D020943||hiv associated cns vasculitides
|
|
D020943||hiv associated cns vasculitis
|
|
D020943||hiv associated vasculitis of the central nervous system
|
|
D020943||vasculitides hiv 1 associated cns
|
|
D020943||vasculitides hiv associated cns
|
|
D020943||vasculitis hiv 1 associated cns
|
|
D020943||vasculitis hiv associated cns
|
|
D020943||vasculitis of the central nervous system hiv associated
|
|
D005327||fetal resorption
|
|
D005327||fetal resorptions
|
|
D005327||resorption fetal
|
|
D005327||resorptions fetal
|
|
D020941||myasthenia gravis neonatal
|
|
D020941||antenatal myasthenia gravis
|
|
D020941||myasthenia gravis antenatal
|
|
D020941||myasthenia gravis neonatal persistent
|
|
D020941||myasthenia gravis neonatal transient
|
|
D020941||myasthenia gravis persistent neonatal
|
|
D020941||myasthenia gravis transient neonatal
|
|
D020941||neonatal myasthenia gravis
|
|
D020941||neonatal myasthenia gravis persistent
|
|
D020941||neonatal myasthenia gravis transient
|
|
D020941||persistent neonatal myasthenia gravis
|
|
D020941||transient neonatal myasthenia gravis
|
|
D007984||leydig cell tumor
|
|
D007984||interstitial cell tumor
|
|
D007984||interstitial cell tumors
|
|
D007984||tumor interstitial cell
|
|
D007984||tumor leydig cell
|
|
D007984||tumors interstitial cell
|
|
D005320||fetal macrosomia
|
|
D005320||fetal macrosomias
|
|
D005320||macrosomia fetal
|
|
D005320||macrosomias fetal
|
|
C538322|602782||histiocytosis with joint contractures and sensorineural deafness
|
|
C538322|602782||faisalabad histiocytosis
|
|
C538322|602782||histiocytosis and lymphadenopathy with or without cutaneous cardiac and or endocrine features joint contractures and or deafness
|
|
C538322|602782||histiocytosis lymphadenopathy plus syndrome
|
|
C538322|602782||hjcd
|
|
C538322|602782||h syndrome
|
|
C538322|602782||hyperpigmentation cutaneous with hypertrichosis hepatosplenomegaly heart anomalies and hypogonadism with or without hearing loss
|
|
C538322|602782||phid
|
|
C538322|602782||pigmented hypertrichosis with insulin dependent diabetes mellitus
|
|
C538322|602782||pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome
|
|
C538322|602782||rosai dorfman disease familial
|
|
C538322|602782||shml
|
|
C538322|602782||sinus histiocytosis and massive lymphadenopathy
|
|
D005322||fetal membranes premature rupture
|
|
D005322||membrane premature rupture pregnancy
|
|
D005322||membrane premature ruptures pregnancy
|
|
D005322||premature rupture of fetal membranes
|
|
D005322||premature rupture of membrane pregnancy
|
|
D005322||preterm premature rupture of fetal membranes
|
|
D005322||preterm prom pregnancy
|
|
D005322||prom pregnancy
|
|
D005322||prom preterm pregnancy
|
|
C566827||parietal foramina 1
|
|
D006660||histoplasmosis
|
|
D006660||histoplasmoses
|
|
C566465|609636||alzheimer disease 10
|
|
C566465|609636||ad10
|
|
C566465|609636||alzheimer disease familial 10
|
|
D005330||fetofetal transfusion
|
|
D005330||cross transfusion intrauterine
|
|
D005330||cross transfusions intrauterine
|
|
D005330||fetal transfusion syndrome
|
|
D005330||fetal transfusion syndromes
|
|
D005330||fetofetal transfusions
|
|
D005330||fetofetal transfusion syndrome
|
|
D005330||fetofetal transfusion syndromes
|
|
D005330||intrauterine cross transfusion
|
|
D005330||intrauterine cross transfusions
|
|
D005330||syndrome fetal transfusion
|
|
D005330||syndrome fetofetal transfusion
|
|
D005330||syndromes fetal transfusion
|
|
D005330||syndromes fetofetal transfusion
|
|
D005330||syndromes twin to twin transfusion
|
|
D005330||syndromes twin transfusion
|
|
D005330||syndrome twin to twin transfusion
|
|
D005330||syndrome twin transfusion
|
|
D005330||transfusion fetofetal
|
|
D005330||transfusions fetofetal
|
|
D005330||transfusions twin
|
|
D005330||transfusion syndrome fetal
|
|
D005330||transfusion syndrome fetofetal
|
|
D005330||transfusion syndromes fetal
|
|
D005330||transfusion syndromes fetofetal
|
|
D005330||transfusion syndromes twin
|
|
D005330||transfusion syndromes twin to twin
|
|
D005330||transfusion syndrome twin
|
|
D005330||transfusion syndrome twin to twin
|
|
D005330||transfusion twin
|
|
D005330||twin to twin transfusion syndrome
|
|
D005330||twin to twin transfusion syndromes
|
|
D005330||twin transfusion
|
|
D005330||twin transfusions
|
|
D005330||twin transfusion syndrome
|
|
D005330||twin transfusion syndromes
|
|
D005330||twin twin transfusion syndrome
|
|
D019969||amphetamine related disorders
|
|
D019969||abuse amphetamine
|
|
D019969||addiction amphetamine
|
|
D019969||amphetamine abuse
|
|
D019969||amphetamine addiction
|
|
D019969||amphetamine dependence
|
|
D019969||dependence amphetamine
|
|
D019969||disorder amphetamine related
|
|
D019969||disorders amphetamine related
|
|
C567134|220290||deafness autosomal recessive 1a
|
|
C567134|220290||deafness digenic gjb2 gjb3
|
|
C567134|220290||deafness digenic gjb2 gjb3 included
|
|
C567134|220290||deafness digenic gjb2 gjb6
|
|
C567134|220290||deafness digenic gjb2 gjb6 included
|
|
C567134|220290||dfnb1a
|
|
D020945||lupus vasculitis central nervous system
|
|
D020945||central nervous system lupus
|
|
D020945||central nervous system lupus vasculitis
|
|
D020945||central nervous system systemic lupus erythematosis
|
|
D020945||lupus meningoencephalitides
|
|
D020945||lupus meningoencephalitis
|
|
D020945||meningoencephalitides lupus
|
|
D020945||meningoencephalitis lupus
|
|
D020945||neuropsychiatric systemic lupus erythematosus
|
|
D020945||systemic lupus erythematosis central nervous system
|
|
D019966||substance related disorders
|
|
D019966||abuse drug
|
|
D019966||abuses substance
|
|
D019966||abuse substance
|
|
D019966||addiction drug
|
|
D019966||addiction substance
|
|
D019966||dependence drug
|
|
D019966||dependence substance
|
|
D019966||disorder drug use
|
|
D019966||disorder substance use
|
|
D019966||drug abuse
|
|
D019966||drug addiction
|
|
D019966||drug dependence
|
|
D019966||drug habituation
|
|
D019966||drug use disorder
|
|
D019966||drug use disorders
|
|
D019966||habituation drug
|
|
D019966||organic mental disorders substance induced
|
|
D019966||substance abuse
|
|
D019966||substance abuses
|
|
D019966||substance addiction
|
|
D019966||substance dependence
|
|
D019966||substance use disorder
|
|
D019966||substance use disorders
|
|
D019965||delirium dementia amnestic cognitive disorders
|
|
D019965||clerambault syndrome
|
|
D019965||disorders organic mental
|
|
D019965||kandinsky syndrome
|
|
D019965||mental disorder organic
|
|
D019965||mental disorders organic
|
|
D019965||nonpsychotic organic brain syndrome
|
|
D019965||organic brain syndrome nonpsychotic
|
|
D019965||organic mental disorder
|
|
D019965||organic mental disorders
|
|
D019965||organic mental disorders psychotic
|
|
D019965||psychoses traumatic
|
|
D019965||traumatic psychoses
|
|
D019968||sexual and gender disorders
|
|
D019967||schizophrenia and disorders with psychotic features
|
|
138110||glucose 6 phosphate dehydrogenase like
|
|
138110||g6pdl
|
|
D019962||reactive attachment disorder
|
|
D019962||attachment disorder reactive
|
|
D019962||attachment disorders reactive
|
|
D019962||disorder reactive attachment
|
|
D019962||disorders reactive attachment
|
|
D019962||reactive attachment disorders
|
|
D018630||vitreoretinopathy proliferative
|
|
D018630||inflammatories vitreoretinopathy neovascular
|
|
D018630||inflammatory vitreoretinopathy neovascular
|
|
D018630||neovascular inflammatories vitreoretinopathy
|
|
D018630||neovascular inflammatory vitreoretinopathy
|
|
D018630||proliferative vitreoretinopathies
|
|
D018630|193235||proliferative vitreoretinopathy
|
|
D018630||vitreoretinopathies proliferative
|
|
D018630||vitreoretinopathy neovascular inflammatories
|
|
D018630|193235||vitreoretinopathy neovascular inflammatory
|
|
D019964||mood disorders
|
|
D019964||affective disorder
|
|
D019964||affective disorders
|
|
D019964||disorder affective
|
|
D019964||disorder mood
|
|
D019964||disorders affective
|
|
D019964||disorders mood
|
|
D019964||mood disorder
|
|
D018633||pulmonary atresia
|
|
D018633||atresia pulmonary
|
|
D018633||atresia pulmonary valve
|
|
D018633||atresias pulmonary
|
|
D018633||atresias pulmonary valve
|
|
D018633||pulmonary atresias
|
|
D018633||pulmonary valve atresia
|
|
D018633||pulmonary valve atresias
|
|
D018633||valve atresia pulmonary
|
|
D018633||valve atresias pulmonary
|
|
136680|D052159||frasier syndrome
|
|
136680|D052159||syndrome frasier
|
|
D006628||hirsutism
|
|
C565537|233420||46 xy gonadal dysgenesis complete or partial dhh related
|
|
C565537|233420||46 xy sex reversal 7
|
|
C565537|233420||46 xy sex reversal partial or complete dhh related
|
|
C565537|233420||gdxym
|
|
C565537|233420||gonadal dysgenesis xy male limited
|
|
C565537|233420||srxy7
|
|
203200|C537730||oculocutaneous albinism type 2
|
|
203200|C537730||albinism 2
|
|
203200|C537730||albinism ii
|
|
203200|C537730||albinism ii albinism brown oculocutaneous included
|
|
203200|C537730||albinism oculocutaneous type 2
|
|
203200|C537730||albinism oculocutaneous type ii
|
|
203200|C537730||albinoidism
|
|
203200|C537730||boca included
|
|
203200|C537730||brown oculocutaneous albinism included
|
|
203200|C537730||oca2
|
|
203200|C537730||oculocutaneous albinism type ii
|
|
203200|C537730||oculocutaneous albinism tyrosinase positive
|
|
203200|C537730||tyrosinase positive oculocutaneous albinism
|
|
D007955||leukemoid reaction
|
|
D007955||leukemoid reactions
|
|
D007955||reaction leukemoid
|
|
D007955||reactions leukemoid
|
|
C537415|166700||buschke ollendorff syndrome
|
|
C537415|166700||bos
|
|
C537415|166700||dermatofibrosis disseminated with osteopoikilosis
|
|
C537415|166700||dermatofibrosis lenticularis disseminata isolated included
|
|
C537415|166700||dermatofibrosis lenticularis disseminata with osteopoikilosis
|
|
C537415|166700||dermatoosteopoikilosis
|
|
C537415|166700||osteopathia condensans disseminata
|
|
C537415|166700||osteopathia condensans disseminata osteopoikilosis isolated included
|
|
C537415|166700||osteopoikilosis with melorheostosis included
|
|
D007953||leukemia radiation induced
|
|
D007953||leukemias radiation induced
|
|
D007953||radiation induced leukemia
|
|
D007953||radiation induced leukemias
|
|
C565611|224230||dyskeratosis congenita autosomal recessive
|
|
C565611|224230||dkcb1
|
|
C565611|224230||dyskeratosis congenita autosomal recessive 1
|
|
D007951||leukemia myeloid
|
|
D007951||chronic monocytic leukemia
|
|
D007951||chronic monocytic leukemias
|
|
D007951||granulocytic leukemia
|
|
D007951||granulocytic leukemias
|
|
D007951||leukemia chronic monocytic
|
|
D007951||leukemia granulocytic
|
|
D007951||leukemia monocytic chronic
|
|
D007951||leukemia myelocytic
|
|
D007951||leukemia myelogenous
|
|
D007951||leukemias chronic monocytic
|
|
D007951||leukemias granulocytic
|
|
D007951||leukemias myelocytic
|
|
D007951||leukemias myelogenous
|
|
D007951||leukemias myeloid
|
|
D007951||monocytic leukemia chronic
|
|
D007951||monocytic leukemias chronic
|
|
D007951||myelocytic leukemia
|
|
D007951||myelocytic leukemias
|
|
D007951||myelogenous leukemia
|
|
D007951||myelogenous leukemias
|
|
D007951||myeloid leukemia
|
|
D007951||myeloid leukemias
|
|
D006620||hip fractures
|
|
D006620||fractures hip
|
|
D006620||fractures intertrochanteric
|
|
D006620||fractures subtrochanteric
|
|
D006620||fractures trochanteric
|
|
D006620||intertrochanteric fractures
|
|
D006620||subtrochanteric fractures
|
|
D006620||trochanteric fractures
|
|
D007952||leukemia plasma cell
|
|
D007952||leukemia plasmacytic
|
|
D007952||leukemias plasma cell
|
|
D007952||leukemias plasmacytic
|
|
D007952||plasma cell leukemia
|
|
D007952||plasma cell leukemias
|
|
D007952||plasmacytic leukemia
|
|
D007952||plasmacytic leukemias
|
|
D020938||epilepsy partial motor
|
|
D020938||clonic seizures focal
|
|
D020938||epilepsy focal motor
|
|
D020938||epilepsy hemimotor
|
|
D020938||epilepsy motor partial
|
|
D020938||focal clonic seizure
|
|
D020938||focal clonic seizures
|
|
D020938||focal motor epilepsy
|
|
D020938||focal tonic seizure
|
|
D020938||focal tonic seizures
|
|
D020938||hemimotor epilepsies
|
|
D020938||hemimotor epilepsy
|
|
D020938||hemimotor seizure disorder
|
|
D020938||hemimotor seizure disorders
|
|
D020938||motor epilepsy focal
|
|
D020938||motor partial seizure disorder
|
|
D020938||motor seizure disorder
|
|
D020938||motor seizure disorders
|
|
D020938||partial epilepsy motor
|
|
D020938||partial seizure disorder motor
|
|
D020938||seizure disorder hemimotor
|
|
D020938||seizure disorder motor
|
|
D020938||seizure disorder partial motor
|
|
D020938||seizure disorders hemimotor
|
|
D020938||seizure disorders motor
|
|
D020938||seizure focal clonic
|
|
D020938||seizures versive
|
|
D020938||seizure versive
|
|
D020938||tonic seizure focal
|
|
D020938||tonic seizures focal
|
|
D020938||versive seizure
|
|
D020938||versive seizures
|
|
D020937||epilepsy partial sensory
|
|
D020937||epilepsy sensory
|
|
D020937||epilepsy sensory partial
|
|
D020937||focal seizure disorder sensory
|
|
D020937||focal sensory seizure
|
|
D020937||focal sensory seizures
|
|
D020937||gustatory partial seizure
|
|
D020937||gustatory partial seizures
|
|
D020937||olfactory partial seizure
|
|
D020937||olfactory partial seizures
|
|
D020937||partial epilepsy sensory
|
|
D020937||partial seizure gustatory
|
|
D020937||partial seizure olfactory
|
|
D020937||partial seizures gustatory
|
|
D020937||partial seizures olfactory
|
|
D020937||partial seizures vertiginous
|
|
D020937||partial seizures visual
|
|
D020937||partial seizure vertiginous
|
|
D020937||partial seizure visual
|
|
D020937||partial sensory seizure
|
|
D020937||partial sensory seizures
|
|
D020937||seizure disorder partial sensory
|
|
D020937||seizure disorder sensory
|
|
D020937||seizure disorder sensory focal
|
|
D020937||seizure disorders sensory
|
|
D020937||seizure focal sensory
|
|
D020937||seizure gustatory partial
|
|
D020937||seizure olfactory partial
|
|
D020937||seizure partial sensory
|
|
D020937||seizures focal sensory
|
|
D020937||seizures olfactory partial
|
|
D020937||seizures partial sensory
|
|
D020937||seizures simple partial special sensory symptoms
|
|
D020937||seizures vertiginous partial
|
|
D020937||seizure vertiginous partial
|
|
D020937||seizure visual partial
|
|
D020937||sensory epilepsy
|
|
D020937||sensory focal seizure disorder
|
|
D020937||sensory partial epilepsy
|
|
D020937||sensory partial seizure disorder
|
|
D020937||sensory seizure disorder
|
|
D020937||sensory seizure disorders
|
|
D020937||sensory seizure focal
|
|
D020937||sensory seizure partial
|
|
D020937||sensory seizures focal
|
|
D020937||sensory seizures partial
|
|
D020937||simple partial seizures special sensory symptoms
|
|
D020937||vertiginous partial seizure
|
|
D020937||vertiginous partial seizures
|
|
D020937||visual partial seizure
|
|
D020937||visual partial seizures
|
|
C567653|613287||charcot marie tooth disease axonal type 2n
|
|
C567653|613287||charcot marie tooth disease axonal autosomal dominant type 2n
|
|
C567653|613287||charcot marie tooth neuropathy axonal type 2n
|
|
C567653|613287||cmt2n
|
|
D018602||milk sickness
|
|
D018602||sickness milk
|
|
609958||asthma related traits susceptibility to 3
|
|
609958||asrt3
|
|
D018601||king apos s evil
|
|
D018601||evil king apos s
|
|
D018601||kings evil
|
|
611102|C567010||deafness sensorineural and male infertility
|
|
611102|C567010||chromosome 15q15 3 deletion syndrome
|
|
611102|C567010||deafness infertility syndrome
|
|
611102|C567010||sensorineural deafness and male infertility
|
|
C566800||platelet aggregation spontaneous
|
|
D007968||leukoencephalopathy progressive multifocal
|
|
D007968||encephalitis jc polyomavirus
|
|
D007968||encephalopathies jc polyomavirus
|
|
D007968||encephalopathy jc polyomavirus
|
|
D007968||jc polyomavirus encephalitis
|
|
D007968||jc polyomavirus encephalopathy
|
|
D007968||leukoencephalopathies progressive multifocal
|
|
D007968||multifocal leukoencephalopathies progressive
|
|
D007968||multifocal leukoencephalopathy progressive
|
|
D007968||progressive multifocal leukoencephalopathies
|
|
D007968||progressive multifocal leukoencephalopathy
|
|
211980|D008175||lung neoplasms
|
|
211980|D008175||adenocarcinoma of lung included
|
|
211980|D008175||adenocarcinoma of lung susceptibility to
|
|
211980|D008175||alveolar cell carcinoma included
|
|
211980|D008175||cancer lung
|
|
211980|D008175||cancer of lung
|
|
211980|D008175||cancer of the lung
|
|
211980|D008175||cancer pulmonary
|
|
211980|D008175||cancers lung
|
|
211980|D008175||cancers pulmonary
|
|
211980|D008175||lncr1
|
|
211980|D008175||lncr2 included
|
|
211980|D008175||lncr3
|
|
211980|D008175||lncr4
|
|
211980|D008175||lncr5
|
|
211980|D008175||lung cancer
|
|
211980|D008175||lung cancer protection against included
|
|
211980|D008175||lung cancers
|
|
211980|D008175||lung cancer susceptibility 1
|
|
211980|D008175||lung cancer susceptibility 3
|
|
211980|D008175||lung cancer susceptibility 4
|
|
211980|D008175||lung cancer susceptibility 5
|
|
211980|D008175||lung neoplasm
|
|
211980|D008175||neoplasm lung
|
|
211980|D008175||neoplasm pulmonary
|
|
211980|D008175||neoplasms lung
|
|
211980|D008175||neoplasms pulmonary
|
|
211980|D008175||nicotine dependence susceptibility to lung cancer susceptibility 2 included
|
|
211980|D008175||nonsmall cell lung cancer included
|
|
211980|D008175||pulmonary cancer
|
|
211980|D008175||pulmonary cancers
|
|
211980|D008175||pulmonary neoplasm
|
|
211980|D008175||pulmonary neoplasms
|
|
211980|D008175||smoking as a quantitative trait locus 3
|
|
211980|D008175||sqtl3
|
|
D048550||hepatic insufficiency
|
|
D048550||insufficiency hepatic
|
|
D048550||insufficiency liver
|
|
D048550||liver insufficiency
|
|
D007969||leukomalacia periventricular
|
|
D007969||cerebral leukomalacia neonatal
|
|
D007969||cerebral leukomalacias neonatal
|
|
D007969||cystic periventricular leukomalacia
|
|
D007969||cystic periventricular leukomalacias
|
|
D007969||encephalomalacia periventricular
|
|
D007969||encephalomalacias periventricular
|
|
D007969||leucomalacia periventricular
|
|
D007969||leucomalacias periventricular
|
|
D007969||leukomalacia cystic periventricular
|
|
D007969||leukomalacia neonatal cerebral
|
|
D007969||leukomalacias cystic periventricular
|
|
D007969||leukomalacias neonatal cerebral
|
|
D007969||leukomalacias periventricular
|
|
D007969||neonatal cerebral leukomalacia
|
|
D007969||neonatal cerebral leukomalacias
|
|
D007969||periventricular encephalomalacia
|
|
D007969||periventricular encephalomalacias
|
|
D007969||periventricular leucomalacia
|
|
D007969||periventricular leucomalacias
|
|
D007969||periventricular leukomalacia
|
|
D007969||periventricular leukomalacia cystic
|
|
D007969||periventricular leukomalacias
|
|
D007969||periventricular leukomalacias cystic
|
|
C566806||phlebectasia of lips
|
|
D020922||sleep wake transition disorders
|
|
D020922||cramp nocturnal leg
|
|
D020922||cramps nocturnal leg
|
|
D020922||jactatio capitis nocturna
|
|
D020922||leg cramp nocturnal
|
|
D020922||leg cramps nocturnal
|
|
D020922||movement disorders rhythmic nocturnal
|
|
D020922||nocturna jactatio capitis
|
|
D020922||nocturnal leg cramp
|
|
D020922||nocturnal leg cramps
|
|
D020922||nocturnal sleep head banging
|
|
D020922||rhythmic movement disorders nocturnal
|
|
D020922||sleep starts
|
|
D020922||sleep talking
|
|
D020922||sleep wake transitional disorder
|
|
D020922||sleep wake transitional disorders
|
|
D020922||sleep wake transition disorder
|
|
D020922||somnolescent starts
|
|
D020922||starts sleep
|
|
D020922||starts somnolescent
|
|
D020922||talking sleep
|
|
D020922||transitional disorder sleep wake
|
|
D020922||transitional disorders sleep wake
|
|
D020922||transition disorder sleep wake
|
|
D020922||transition disorders sleep wake
|
|
253310|C537194||lethal congenital contracture syndrome 1
|
|
253310|C537194||lccs
|
|
253310|C537194||lccs1
|
|
253310|C537194||lethal autosomal recessive syndrome of multiple congenital contractures
|
|
253310|C537194||multiple contracture syndrome finnish type
|
|
C566807||pheochromocytoma islet cell tumor syndrome
|
|
D007967||leukoedema oral
|
|
D007967||leukoedemas oral
|
|
D007967||oral leukoedema
|
|
D007967||oral leukoedemas
|
|
D020921||sleep arousal disorders
|
|
D020921||arousal confusional
|
|
D020921||arousal disorder sleep
|
|
D020921||arousal disorders sleep
|
|
D020921||arousals confusional
|
|
D020921||confusional arousal
|
|
D020921||confusional arousals
|
|
D020921||sleep arousal disorder
|
|
C566808||phagocytosis plasma related defect in
|
|
D007964||leukocytosis
|
|
D007964||leukocytoses
|
|
D007964||pleocytoses
|
|
D007964||pleocytosis
|
|
D020920||dyssomnias
|
|
D020920||adjustment sleep disorder
|
|
D020920||adjustment sleep disorders
|
|
D020920||dyssomnia
|
|
D020920||eating drinking syndrome nocturnal
|
|
D020920||eating drinking syndromes nocturnal
|
|
D020920||environmental sleep disorder
|
|
D020920||environmental sleep disorders
|
|
D020920||extrinsic sleep disorder
|
|
D020920||extrinsic sleep disorders
|
|
D020920||inadequate sleep hygiene
|
|
D020920||limit setting sleep disorder
|
|
D020920||limit setting sleep disorders
|
|
D020920||nocturnal eating drinking syndrome
|
|
D020920||nocturnal eating drinking syndromes
|
|
D020920||sleep disorder adjustment
|
|
D020920||sleep disorder environmental
|
|
D020920||sleep disorder extrinsic
|
|
D020920||sleep disorder limit setting
|
|
D020920||sleep disorders adjustment
|
|
D020920||sleep disorders environmental
|
|
D020920||sleep disorders extrinsic
|
|
D020920||sleep disorders limit setting
|
|
D020920||sleep hygiene inadequate
|
|
D020920||syndrome nocturnal eating drinking
|
|
D020920||syndromes nocturnal eating drinking
|
|
C566809||normokalemic periodic paralysis potassium sensitive
|
|
270420|C562576||diarrhea 3 secretory sodium congenital
|
|
270420|C562576||diar3
|
|
270420|C562576||sodium diarrhea congenital
|
|
270420|C562576||sodium diarrhea congenital csd diarrhea 3 secretory sodium congenital syndromic included
|
|
C566803||6 phosphogluconolactonase deficiency
|
|
C566803||6pgl deficiency
|
|
D007960||leukocyte disorders
|
|
D007960||disorder leukocyte
|
|
D007960||disorders leukocyte
|
|
D007960||leukocyte disorder
|
|
159001|C535898||limb girdle muscular dystrophy type 1b
|
|
159001|C535898||lgmd1b
|
|
159001|C535898||muscular dystrophy limb girdle type 1b
|
|
159001|C535898||muscular dystrophy proximal type 1b
|
|
D007970||leukopenia
|
|
D007970||leukocytopenia
|
|
D007970||leukocytopenias
|
|
D007970||leukopenias
|
|
C537348|600383||mesomelia synostoses syndrome
|
|
C537348|600383||chromosome 8q13 deletion syndrome
|
|
C537348|600383||mesomelia synostoses
|
|
C537348|600383||mesomelic dysplasia syndromic
|
|
C537348|600383||mesomelic dysplasia with acral synostoses verloes david pfeiffer type
|
|
C537348|600383||verloes david syndrome
|
|
D062846||non filarial lymphedema
|
|
D062846||lymphedema non filarial
|
|
D062846||lymphedemas non filarial
|
|
D062846||non filarial lymphedemas
|
|
C567214|612644||deafness autosomal dominant 2b
|
|
C567214|612644||dfna2b
|
|
D020925||hypoxia ischemia brain
|
|
D020925||anoxia ischemia brain
|
|
D020925||anoxia ischemia cerebral
|
|
D020925||anoxia ischemias brain
|
|
D020925||anoxia ischemias cerebral
|
|
D020925||anoxic ischemic encephalopathies
|
|
D020925||anoxic ischemic encephalopathy
|
|
D020925||brain anoxia ischemia
|
|
D020925||brain anoxia ischemias
|
|
D020925||brain hypoxia ischemia
|
|
D020925||brain hypoxia ischemias
|
|
D020925||brain ischemia anoxia
|
|
D020925||brain ischemia anoxias
|
|
D020925||brain ischemia hypoxia
|
|
D020925||brain ischemia hypoxias
|
|
D020925||cerebral anoxia ischemia
|
|
D020925||cerebral anoxia ischemias
|
|
D020925||cerebral hypoxia ischemia
|
|
D020925||cerebral hypoxia ischemias
|
|
D020925||cerebral ischemia anoxia
|
|
D020925||cerebral ischemia anoxias
|
|
D020925||cerebral ischemia hypoxia
|
|
D020925||cerebral ischemia hypoxias
|
|
D020925||encephalopathies anoxic ischemic
|
|
D020925||encephalopathies hypoxic ischemic
|
|
D020925||encephalopathies ischemic hypoxic
|
|
D020925||encephalopathy anoxic ischemic
|
|
D020925||encephalopathy hypoxic ischemic
|
|
D020925||encephalopathy ischemic hypoxic
|
|
D020925||hypoxia ischemia cerebral
|
|
D020925||hypoxia ischemias brain
|
|
D020925||hypoxia ischemias cerebral
|
|
D020925||hypoxic ischemic encephalopathies
|
|
D020925||hypoxic ischemic encephalopathy
|
|
D020925||ischemia anoxia brain
|
|
D020925||ischemia anoxia cerebral
|
|
D020925||ischemia anoxias brain
|
|
D020925||ischemia anoxias cerebral
|
|
D020925||ischemia hypoxia brain
|
|
D020925||ischemia hypoxia cerebral
|
|
D020925||ischemia hypoxias brain
|
|
D020925||ischemia hypoxias cerebral
|
|
D020925||ischemic hypoxic encephalopathies
|
|
D020925||ischemic hypoxic encephalopathy
|
|
D020924||urological manifestations
|
|
D020924||manifestations urological
|
|
D020924||manifestation urological
|
|
D020924||urological manifestation
|
|
D020923||rem sleep parasomnias
|
|
D020923||erection sleep related painful
|
|
D020923||erections sleep related painful
|
|
D020923||painful erection sleep related
|
|
D020923||painful erections sleep related
|
|
D020923||parasomnia rem sleep
|
|
D020923||parasomnias rem sleep
|
|
D020923||rapid eye movement sleep parasomnias
|
|
D020923||rem sleep parasomnia
|
|
D020923||rem sleep related sinus arrest
|
|
D020923||sinus arrest rem sleep related
|
|
D020923||sleep related painful erection
|
|
D020923||sleep related painful erections
|
|
D020923||sleep rem parasomnias
|
|
C537365|308200||ichthyosis and male hypogonadism
|
|
C537365|308200||ichthyosis bilateral cryptorchidism hypogenitalism and mental retardation
|
|
C537365|308200||ruds included
|
|
C537365|308200||rud syndrome included
|
|
D018614||sweating sickness
|
|
D018614||english sweating sickness
|
|
D018614||sickness sweating
|
|
D018614||sudor anglicus
|
|
C537307|608768||spinocerebellar ataxia 8
|
|
C537307|608768||sca8
|
|
D007939||leukemia l1210
|
|
D007939||l 1210 leukemia
|
|
D007939||l1210 leukemia
|
|
D007939||leukemia l 1210
|
|
613194|C567712||retinitis pigmentosa 50
|
|
613194||retinitis pigmentosa concentric included
|
|
613194||rp50
|
|
D006606||hiccup
|
|
D006606||hiccough
|
|
D006606||hiccoughs
|
|
D006606||hiccups
|
|
C536560|275630||triglyceride storage disease with impaired long chain fatty acid oxidation
|
|
C536560|275630||cds
|
|
C536560|275630||chanarin dorfman disease
|
|
C536560|275630||chanarin dorfman syndrome
|
|
C536560|275630||dcs
|
|
C536560|275630||dorfman chanarin syndrome
|
|
C536560|275630||ichthyosiform erythroderma with leukocyte vacuolation
|
|
C536560|275630||ichthyotic neutral lipid storage disease
|
|
C536560|275630||neutral lipid storage disease with ichthyosis
|
|
C536560|275630||neutral lipid storage myopathy
|
|
C536560|275630||nlsdi
|
|
C536560|275630||triglyceride storage disease with ichthyosis
|
|
D007938||leukemia
|
|
D007938||leucocythaemia
|
|
D007938||leucocythaemias
|
|
D007938||leucocythemia
|
|
D007938||leucocythemias
|
|
D007938||leukemias
|
|
D006607||adenoma sweat gland
|
|
D006607||adenomas sweat gland
|
|
D006607||sweat gland adenoma
|
|
D006607||sweat gland adenomas
|
|
D006607||syringadenoma
|
|
D006607||syringadenomas
|
|
C538254|105563||anal sphincter dysplasia
|
|
C538254|105563||asdp
|
|
C563790|609129||auditory neuropathy autosomal dominant 1
|
|
C563790|609129||auditory neuropathy nonsyndromic dominant
|
|
C563790|609129||auna1
|
|
C563790|609129||nsdan
|
|
C535397|601536||athabaskan brainstem dysgenesis
|
|
C535397|601536||abds
|
|
C535397|601536||athabaskan brainstem dysgenesis syndrome
|
|
C535397|601536||bosley salih alorainy syndrome
|
|
C535397|601536||bsas included
|
|
C535397|601536||navajo brainstem syndrome
|
|
C535397|601536||navajo brainstem syndrome bosley salih alorainy syndrome included
|
|
C564616|607136||spinocerebellar ataxia 17
|
|
C564616|607136||hdl4
|
|
C564616|607136||huntington disease like 4
|
|
C564616|607136||sca17
|
|
D020919||sleep disorders intrinsic
|
|
D020919||hypersomnia posttraumatic
|
|
D020919||hypersomnia post traumatic
|
|
D020919||hypersomnias posttraumatic
|
|
D020919||hypersomnias post traumatic
|
|
D020919||intrinsic sleep disorder
|
|
D020919||intrinsic sleep disorders
|
|
D020919||posttraumatic hypersomnia
|
|
D020919||post traumatic hypersomnia
|
|
D020919||posttraumatic hypersomnias
|
|
D020919||post traumatic hypersomnias
|
|
D020919||sleep disorder intrinsic
|
|
D020919||sleep state misperception
|
|
D020919||sleep state misperceptions
|
|
D020918||complex regional pain syndromes
|
|
D020918||crps complex regional pain syndromes
|
|
D020918||pain syndromes regional complex
|
|
D005271|608805||femur head necrosis
|
|
D005271|608805||anfh
|
|
D005271|608805||aseptic necrosis of femur head
|
|
D005271|608805||avascular necrosis of femoral head primary
|
|
D005271|608805||avascular necrosis of femur head
|
|
D005271|608805||femoral head aseptic necrosis of
|
|
D005271|608805||femoral head avascular necrosis of
|
|
D005271|608805||femur head necroses
|
|
D005271|608805||head necrosis femur
|
|
D005271|608805||ischemic necrosis of femoral head
|
|
D005271|608805||necrosis aseptic of femur head
|
|
D005271|608805||necrosis avascular of femur head
|
|
D005271|608805||necrosis femur head
|
|
D005271|608805||osteonecrosis of femoral head
|
|
C564510|300471||cubitus valgus with mental retardation and unusual facies
|
|
D020914||myopathies structural congenital
|
|
D020914||aggregate myopathies tubular
|
|
D020914||aggregate myopathy tubular
|
|
D020914||autosomal dominant myotubular myopathy
|
|
D020914||autosomal recessive centronuclear myopathy
|
|
D020914||centronuclear myopathies
|
|
D020914||centronuclear myopathies x linked
|
|
D020914||centronuclear myopathy
|
|
D020914||centronuclear myopathy x linked
|
|
D020914|C580011||congenital fiber type disproportion
|
|
D020914||congenital non progressive myopathies
|
|
D020914||congenital non progressive myopathy
|
|
D020914||congenital structural myopathies
|
|
D020914||congenital structural myopathy
|
|
D020914|255310||fiber type disproportion myopathy congenital
|
|
D020914||myopathies centronuclear
|
|
D020914||myopathies congenital non progressive
|
|
D020914||myopathies congenital structural
|
|
D020914||myopathies myotubular
|
|
D020914||myopathies tubular aggregate
|
|
D020914||myopathies x linked centronuclear
|
|
D020914||myopathies x linked myotubular
|
|
D020914||myopathy 1 myotubular
|
|
D020914||myopathy 1s myotubular
|
|
D020914||myopathy centronuclear
|
|
D020914||myopathy congenital non progressive
|
|
D020914||myopathy congenital structural
|
|
D020914|255310||myopathy congenital with fiber type disproportion
|
|
D020914||myopathy myotubular
|
|
D020914||myopathy tubular aggregate
|
|
D020914||myopathy x linked centronuclear
|
|
D020914||myopathy x linked myotubular
|
|
D020914||myotubular myopathies
|
|
D020914||myotubular myopathies x linked
|
|
D020914||myotubular myopathy
|
|
D020914|310400||myotubular myopathy 1
|
|
D020914||myotubular myopathy 1s
|
|
D020914||non progressive myopathies congenital
|
|
D020914||non progressive myopathy congenital
|
|
D020914||structural myopathies congenital
|
|
D020914||structural myopathy congenital
|
|
D020914||tubular aggregate myopathies
|
|
D020914||tubular aggregate myopathy
|
|
D020914||x linked centronuclear myopathies
|
|
D020914||x linked centronuclear myopathy
|
|
D020914||x linked myotubular myopathies
|
|
D020914||x linked myotubular myopathy
|
|
D020914|310400||xlmtm
|
|
C567675|613270||corneal dystrophy fuchs endothelial 6
|
|
C567675|613270|C567674|613271|C567676|613269|C567677|613268|C535479|610158|C567678|613267||corneal dystrophy fuchs endothelial late onset
|
|
C567675|613270||fecd6
|
|
D006619||hip dysplasia canine
|
|
D006619||canine hip dysplasia
|
|
D006619||dysplasia canine hip
|
|
D012497|268800||sandhoff disease
|
|
D012497|268800||adult sandhoff disease
|
|
D012497|268800||beta hexosaminidase beta subunit deficiencies
|
|
D012497|268800||beta hexosaminidase beta subunit deficiency
|
|
D012497|268800||deficiencies beta hexosaminidase beta subunit
|
|
D012497|268800||deficiencies total hexosaminidase
|
|
D012497|268800||deficiency beta hexosaminidase beta subunit
|
|
D012497|268800||deficiency disease hexosaminidase a and b
|
|
D012497|268800||deficiency total hexosaminidase
|
|
D012497|268800||disease sandhoff jatzkewitz pilz
|
|
D012497|268800||gangliosidosis g m2 type ii
|
|
D012497|268800||gangliosidosis gm2 type ii
|
|
D012497|268800||gm2 gangliosidoses type ii
|
|
D012497|268800||gm2 gangliosidosis type 2
|
|
D012497|268800||g m2 gangliosidosis type ii
|
|
D012497|268800||gm2 gangliosidosis type ii
|
|
D012497|268800||hexosaminidase a and b deficiency disease
|
|
D012497|268800||hexosaminidase deficiencies total
|
|
D012497|268800||hexosaminidase deficiency total
|
|
D012497|268800||hexosaminidases a and b deficiency
|
|
D012497|268800||hexosaminidases a and b deficiency sandhoff disease adult type included
|
|
D012497|268800||infantile sandhoff disease
|
|
D012497|268800||juvenile sandhoff disease
|
|
D012497|268800||sandhoff disease adult
|
|
D012497|268800||sandhoff disease infantile
|
|
D012497|268800||sandhoff disease infantile type included
|
|
D012497|268800||sandhoff disease juvenile
|
|
D012497|268800||sandhoff disease juvenile type included
|
|
D012497|268800||sandhoff jatzkewitz pilz disease
|
|
D012497|268800||sandhoff apos s disease
|
|
D012497|268800||sandhoffs disease
|
|
D012497|268800||total hexosaminidase deficiencies
|
|
D012497|268800||total hexosaminidase deficiency
|
|
D012497|268800||type ii gm2 gangliosidoses
|
|
D012497|268800||type ii gm2 gangliosidosis
|
|
610906||asthma related traits susceptibility to 4
|
|
610906||asrt4
|
|
610906||asthma and allergic rhinitis susceptibility to
|
|
D007948||leukemia monocytic acute
|
|
D007948||acute monoblastic leukemia
|
|
D007948||acute monoblastic leukemias
|
|
D007948||acute monocytic leukemia
|
|
D007948||acute monocytic leukemias
|
|
D007948||leukemia acute monocytic
|
|
D007948||leukemia monoblastic acute
|
|
D007948||leukemia myeloid acute m5
|
|
D007948||leukemia myeloid schilling type
|
|
D007948||leukemias acute monoblastic
|
|
D007948||leukemias acute monocytic
|
|
D007948||leukemia schilling type myeloid
|
|
D007948||monoblastic leukemia acute
|
|
D007948||monoblastic leukemias acute
|
|
D007948||monocytic leukemia acute
|
|
D007948||monocytic leukemias acute
|
|
D007948||myeloid leukemia acute m5
|
|
D007948||myeloid leukemia schilling type
|
|
D007948||schilling type myeloid leukemia
|
|
D006617||hip dislocation
|
|
D006617||dislocation hip
|
|
D006617||dislocations hip
|
|
D006617||displacement hip
|
|
D006617||displacements hip
|
|
D006617||hip dislocations
|
|
D006617||hip displacement
|
|
D006617||hip displacements
|
|
D006617||hip dysplasia
|
|
D006618||hip dislocation congenital
|
|
D006618||congenital dysplasia of the hip
|
|
D006618||congenital hip dislocation
|
|
D006618||congenital hip dislocations
|
|
D006618||congenital hip displacement
|
|
D006618||congenital hip displacements
|
|
D006618||congenital hip dysplasia
|
|
D006618||congenital hip dysplasias
|
|
D006618||dislocation congenital hip
|
|
D006618||dislocation of hip congenital
|
|
D006618||dislocations congenital hip
|
|
D006618||displacement congenital hip
|
|
D006618||displacements congenital hip
|
|
D006618||dysplasia congenital hip
|
|
D006618||dysplasias congenital hip
|
|
D006618||hip dislocation of congenital
|
|
D006618||hip dislocations congenital
|
|
D006618||hip displacement congenital
|
|
D006618||hip displacements congenital
|
|
D006618|142700||hip dysplasia congenital
|
|
D006618||hip dysplasia congenital nonsyndromic
|
|
D006618||hip dysplasias congenital
|
|
D007946||leukemia mast cell
|
|
D007946||leukemias mast cell
|
|
D007946||mast cell leukemia
|
|
D007946||mast cell leukemias
|
|
D007947||leukemia megakaryoblastic acute
|
|
D007947||acute megakaryoblastic leukemia
|
|
D007947||acute megakaryoblastic leukemias
|
|
D007947||acute megakaryocytic leukemia
|
|
D007947||acute megakaryocytic leukemias
|
|
D007947||leukemia acute megakaryoblastic
|
|
D007947||leukemia acute megakaryocytic
|
|
D007947||leukemia megakaryocytic
|
|
D007947||leukemia megakaryocytic acute
|
|
D007947||leukemia myeloid acute m7
|
|
D007947||leukemias acute megakaryoblastic
|
|
D007947||leukemias acute megakaryocytic
|
|
D007947||leukemias megakaryocytic
|
|
D007947||megakaryoblastic leukemia acute
|
|
D007947||megakaryoblastic leukemias acute
|
|
D007947||megakaryocytic leukemia
|
|
D007947||megakaryocytic leukemia acute
|
|
D007947||megakaryocytic leukemias
|
|
D007947||megakaryocytic leukemias acute
|
|
D007947||myeloid leukemia acute m7
|
|
D006616||hip contracture
|
|
D006616||contracture hip
|
|
D006616||contractures hip
|
|
D006616||hip contractures
|
|
D007945||leukemia lymphoid
|
|
D007945||leukemia lymphocytic
|
|
D007945||leukemias lymphocytic
|
|
D007945||leukemias lymphoid
|
|
D007945||lymphocytic leukemia
|
|
D007945||lymphocytic leukemias
|
|
D007945||lymphoid leukemia
|
|
D007945||lymphoid leukemias
|
|
D007942||leukemia experimental
|
|
D007942||animal leukemia model
|
|
D007942||animal leukemia models
|
|
D007942||experimental leukemia
|
|
D007942||experimental leukemias
|
|
D007942||leukemia model animal
|
|
D007942||leukemia models animal
|
|
D007942||leukemias experimental
|
|
D007943||leukemia hairy cell
|
|
D007943||hairy cell leukemia
|
|
D007943||hairy cell leukemias
|
|
D007943||leukemias hairy cell
|
|
D007943||leukemic reticuloendothelioses
|
|
D007943||leukemic reticuloendotheliosis
|
|
D007943||reticuloendothelioses leukemic
|
|
D007943||reticuloendotheliosis leukemic
|
|
D007940||leukemia l5178
|
|
D007940||l5178 leukemia
|
|
D007940||l5178 lymphoma
|
|
D007940||lymphoma l5178
|
|
D007941||leukemia p388
|
|
D007941||p388d 1 leukemia
|
|
D007941||p388 leukemia
|
|
D006610||high pressure neurological syndrome
|
|
D006610||experimental high pressure neurological syndrome
|
|
D006610||high pressure nervous syndrome
|
|
D006610||high pressure neural syndrome
|
|
D006610||high pressure neurological syndrome experimental
|
|
D006610||hpns
|
|
D006610||hpnss
|
|
C566910|611590||renal tubular acidosis distal with hemolytic anemia
|
|
C566910|611590||rta distal autosomal recessive with hemolytic anemia
|
|
C566910|611590||rta distal autosomal recessive with hemolytic anemia renal tubular acidosis distal with normal red cell morphology included
|
|
D059226||nociceptive pain
|
|
D059226||nociceptive pains
|
|
D059226||pain nociceptive
|
|
D059226||pains nociceptive
|
|
D059226||pain somatic
|
|
D059226||pains somatic
|
|
D059226||pains tissue
|
|
D059226||pain tissue
|
|
D059226||somatic pain
|
|
D059226||somatic pains
|
|
D059226||tissue pain
|
|
D059226||tissue pains
|
|
D059228||renal nutcracker syndrome
|
|
D059228||nutcracker phenomenon renal
|
|
D059228||nutcracker phenomenons renal
|
|
D059228||nutcracker syndrome renal
|
|
D059228||nutcracker syndromes renal
|
|
D059228||phenomenon renal nutcracker
|
|
D059228||phenomenons renal nutcracker
|
|
D059228||renal nutcracker phenomenon
|
|
D059228||renal nutcracker phenomenons
|
|
D059228||renal nutcracker syndromes
|
|
D059228||renal vein entrapment syndrome
|
|
153670||bernard soulier syndrome type a2 autosomal dominant
|
|
153670||bssa2
|
|
C565299|605746||anisomastia
|
|
C567558|612813||spondyloepimetaphyseal dysplasia aggrecan type
|
|
C567558|612813||semd aggrecan type
|
|
C536333|174700||polydactyly preaxial 4
|
|
C536333|174700||cp1 included
|
|
C536333|174700||polydactyly preaxial iv
|
|
C536333|174700||polysyndactyly uncomplicated
|
|
C536333|174700||polysyndactyly uncomplicated crossed polydactyly type i included
|
|
D001606|231200||bernard soulier syndrome
|
|
D001606|231200||bdplt1
|
|
D001606|231200||bernard soulier syndrome type b included
|
|
D001606|231200||bernard soulier syndrome type c included
|
|
D001606|231200||bleeding disorder platelet type 1
|
|
D001606|231200|C536611|132700||bss
|
|
D001606|231200||deficiency of platelet glycoprotein 1b
|
|
D001606|231200||giant platelet syndrome
|
|
D001606|231200||glycoprotein ib platelet deficiency of
|
|
D001606|231200||platelet glycoprotein 1b deficiency of
|
|
D001606|231200||platelet glycoprotein ib deficiency
|
|
D001606|231200||platelet syndromes giant
|
|
D001606|231200||syndrome bernard soulier
|
|
D001606|231200||syndrome giant platelet
|
|
D001606|231200||syndromes giant platelet
|
|
D001606|231200||von willebrand factor receptor deficiency
|
|
D001606|231200||von willebrand factor receptor deficiency bernard soulier syndrome type a1 included
|
|
C536227|162800||cyclic neutropenia
|
|
C536227|162800||cyclic hematopoesis
|
|
C536227|162800||cyclic hematopoiesis
|
|
C536227|162800||cyclic leucopenia
|
|
C536227|162800||neutropenia cyclic
|
|
C536227|162800||periodic neutropenia
|
|
C538346|601214||naxos disease
|
|
C538346|601214||keratosis palmoplantaris with arrhythmogenic cardiomyopathy
|
|
C538346|601214||mal de naxos
|
|
C538346|601214||palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and woolly hair
|
|
C538346|601214||woolly hair palmoplantar keratoderma and cardiac abnormalities
|
|
D011293||premenstrual syndrome
|
|
D011293||premenstrual syndromes
|
|
D011293||premenstrual tension
|
|
D011293||premenstrual tensions
|
|
D011293||syndrome premenstrual
|
|
D011293||syndromes premenstrual
|
|
D011293||tension premenstrual
|
|
D011293||tensions premenstrual
|
|
D011297||prenatal exposure delayed effects
|
|
D011297||delayed effects prenatal exposure
|
|
D011297||late effects prenatal exposure
|
|
D006014|232800||glycogen storage disease type vii
|
|
D006014|232800||deficiencies muscle phosphofructokinase
|
|
D006014|232800||deficiencies pfkm
|
|
D006014|232800||deficiency muscle phosphofructokinase
|
|
D006014|232800||deficiency pfkm
|
|
D006014|232800||disease tarui
|
|
D006014|232800||disease tarui apos s
|
|
D006014|232800||glycogenosis 7
|
|
D006014|232800||glycogen storage disease vii
|
|
D006014|232800||gsd7
|
|
D006014|232800||gsd vii
|
|
D006014|232800||muscle phosphofructokinase deficiencies
|
|
D006014|232800||muscle phosphofructokinase deficiency
|
|
D006014|232800||pfkm deficiencies
|
|
D006014|232800||pfkm deficiency
|
|
D006014|232800||phosphofructokinase deficiencies muscle
|
|
D006014|232800||phosphofructokinase deficiency muscle
|
|
D006014|232800||tarui disease
|
|
D006014|232800||tarui apos s disease
|
|
D006014|232800||taruis disease
|
|
D020162|207800||hyperargininemia
|
|
D020162|207800||arg1 deficiencies
|
|
D020162|207800||arg1 deficiency
|
|
D020162|207800||arginase deficiencies
|
|
D020162|207800||arginase deficiency
|
|
D020162|207800||arginase deficiency disease
|
|
D020162|207800||arginase deficiency diseases
|
|
D020162|207800||argininemia
|
|
D020162|207800||deficiencies arg1
|
|
D020162|207800||deficiencies arginase
|
|
D020162|207800||deficiency arg1
|
|
D020162|207800||deficiency arginase
|
|
D020162|207800||deficiency disease arginase
|
|
D020162|207800||deficiency diseases arginase
|
|
D020162|207800||hyperargininemias
|
|
215300|D002813||chondrosarcoma
|
|
215300|D002813||chondrosarcomas
|
|
D050798||sunct syndrome
|
|
D050798||sunct syndromes
|
|
D050798||syndromes sunct
|
|
D050798||syndrome sunct
|
|
C536137|174000||medullary cystic kidney disease 1
|
|
C536137|174000||admckd1
|
|
C536137|174000||mckd
|
|
C536137|174000||mckd1
|
|
C536137|174000||medullary cystic kidney disease autosomal dominant
|
|
C536137|174000||polycystic kidneys medullary type
|
|
C536861|608220||spastic paraplegia 25 autosomal recessive
|
|
C536861|608220||disc herniation with spastic paraplegia autosomal recessive
|
|
C536861|608220||spg25
|
|
C536861|608220||spinal disc herniation with autosomal recessive spastic paraplegia
|
|
C567343|612347||jervell and lange nielsen syndrome 2
|
|
C567343|612347||jlns2
|
|
607279||systemic lupus erythematosus with hemolytic anemia susceptibility to 1
|
|
607279||sleh1
|
|
607279||systemic lupus erythematosus hemolytic anemia related
|
|
607277||asthma related traits susceptibility to 1
|
|
607277||as1
|
|
607277||asrt1
|
|
D011271||pregnancy ectopic
|
|
D011271||ectopic pregnancies
|
|
D011271||ectopic pregnancy
|
|
D011271||ovarian pregnancies
|
|
D011271||ovarian pregnancy
|
|
D011271||pregnancies ectopic
|
|
D011271||pregnancies ovarian
|
|
D011271||pregnancy ovarian
|
|
D011274||pregnancy tubal
|
|
D011274||pregnancies tubal
|
|
D011274||tubal pregnancies
|
|
D011274||tubal pregnancy
|
|
D011273||pregnancy prolonged
|
|
D011273||pregnancies prolonged
|
|
D011273||prolonged pregnancies
|
|
D011273||prolonged pregnancy
|
|
C535803|271980||succinic semialdehyde dehydrogenase deficiency
|
|
C535803|271980||4 hydroxybutyric aciduria
|
|
C535803|271980||4 hydroxybutyricaciduria
|
|
C535803|271980||gaba metabolic defect
|
|
C535803|271980||gamma hydroxybutyric acidemia
|
|
C535803|271980||gamma hydroxybutyric aciduria
|
|
C535803|271980||ssadhd
|
|
C535803|271980||ssadh deficiency
|
|
C564675|606705||deafness autosomal dominant 36
|
|
C564675|606705||dfna36
|
|
163000||capillary malformations congenital
|
|
163000|C562760||capillary malformations
|
|
163000||cmal
|
|
163000||cmc
|
|
163000|C535816||nevi flammei familial multiple
|
|
163000|D019339||port wine stain
|
|
602629|C538003||dystonia 6 torsion
|
|
602629|C538003||dyt6
|
|
602629|C538003||torsion dystonia adult onset mixed type
|
|
D062787||drug overdose
|
|
D062787||drug overdoses
|
|
D062787||overdose drug
|
|
D062787||overdoses drug
|
|
D062788||adenomyosis
|
|
D062788||adenomyoses
|
|
C566490|609994||myopia 11
|
|
C566490|609994||myopia 11 autosomal dominant
|
|
C566490|609994||myp11
|
|
605275|C548081||noonan syndrome 2
|
|
605275|C548081||noonan syndrome autosomal recessive
|
|
605275|C548081||ns2
|
|
C564300|608031||amyotrophic lateral sclerosis 7
|
|
C564300|608031||als7
|
|
D011289||preleukemia
|
|
D011289||preleukemias
|
|
612780|C557674||sesame syndrome
|
|
612780|C557674||east syndrome
|
|
612780|C557674||epilepsy ataxia sensorineural deafness and tubulopathy
|
|
612780|C557674||seizures sensorineural deafness ataxia mental retardation and electrolyte imbalance
|
|
612780|C557674||sesames
|
|
191900|607115|D056587||muckle wells syndrome
|
|
191900||caps2
|
|
191900||cryopyrin associated periodic syndrome 2
|
|
191900||mws
|
|
191900|607115|D056587||uda syndrome
|
|
191900|607115|D056587||urticaria deafness amyloidosis syndrome
|
|
C567680|613265||waardenburg syndrome type 4b
|
|
C567680|613265||waardenburg syndrome type 4b with hirschsprung disease
|
|
C567680|613265||waardenburg syndrome type ivb
|
|
C567680|613265||ws4b
|
|
D044904||mannosidase deficiency diseases
|
|
D044904||deficiency disease mannosidase
|
|
D044904||deficiency diseases mannosidase
|
|
D044904||deficiency syndrome mannosidase
|
|
D044904||deficiency syndromes mannosidase
|
|
D044904||diseases mannosidase deficiency
|
|
D044904||mannosidase deficiency disease
|
|
D044904||mannosidase deficiency syndrome
|
|
D044904||mannosidase deficiency syndromes
|
|
D044904||mannosidoses
|
|
D044904||mannosidosis
|
|
D015160|236750||hydrops fetalis
|
|
D015160|236750||edema fetal
|
|
D015160|236750||familial non immune hydrops fetalis
|
|
D015160|236750||fetal edema
|
|
D015160|236750||fetal hydrops
|
|
D015160|236750||fetali idiopathic hydrops
|
|
D015160|236750||fetalis idiopathic hydrops
|
|
D015160|236750||fetalis nonimmune hydrops
|
|
D015160|236750||fetalis nonimmunes hydrops
|
|
D015160|236750||hemoglobin h hydrops fetalis syndrome included
|
|
D015160|236750||hydrops fetal
|
|
D015160|236750||hydrops fetali idiopathic
|
|
D015160|236750||hydrops fetali nonimmune
|
|
D015160|236750||hydrops fetalis alpha thalassemia related included
|
|
D015160|236750||hydrops fetalis idiopathic
|
|
D015160|236750||hydrops fetalis immune
|
|
D015160|236750||hydrops fetalis nonimmune
|
|
D015160|236750||hydrops fetalis non immune
|
|
D015160|236750||hydrops fetalis nonimmunes
|
|
D015160|236750||idiopathic hydrops fetali
|
|
D015160|236750||idiopathic hydrops fetalis
|
|
D015160|236750||immune hydrops fetalis
|
|
D015160|236750||nihf
|
|
D015160|236750||nonimmune hydrops fetali
|
|
D015160|236750||nonimmune hydrops fetalis
|
|
D015160|236750||non immune hydrops fetalis
|
|
D015160|236750||nonimmunes hydrops fetalis
|
|
608584||asthma related traits susceptibility to 2
|
|
608584||asrt2
|
|
D044905|248510|C538599||beta mannosidosis
|
|
D044905||beta mannosidase deficiencies
|
|
D044905|248510|C538599||beta mannosidase deficiency
|
|
D044905||beta mannosidoses
|
|
D044905||deficiency beta mannosidase
|
|
D044905||lysosomal beta a mannosidosis
|
|
D044905|248510|C538599||mannosidosis beta a lysosomal
|
|
D011250||pregnancy complications hematologic
|
|
D011250||complication hematological pregnancy
|
|
D011250||complication hematologic pregnancy
|
|
D011250||complications hematological pregnancy
|
|
D011250||complications hematologic pregnancy
|
|
D011250||hematological pregnancy complication
|
|
D011250||hematological pregnancy complications
|
|
D011250||hematologic pregnancy complication
|
|
D011250||hematologic pregnancy complications
|
|
D011250||pregnancies hematologic complications
|
|
D011250||pregnancy complication hematologic
|
|
D011250||pregnancy complication hematological
|
|
D011250||pregnancy complications hematological
|
|
D011250||pregnancy hematologic complications
|
|
D011252||pregnancy complications neoplastic
|
|
D011252||complication neoplastic pregnancy
|
|
D011252||complications neoplastic pregnancy
|
|
D011252||neoplastic pregnancy complication
|
|
D011252||neoplastic pregnancy complications
|
|
D011252||pregnancies neoplastic complications
|
|
D011252||pregnancy complication neoplastic
|
|
D011252||pregnancy neoplastic complications
|
|
D011251||pregnancy complications infectious
|
|
D011251||complication infectious pregnancy
|
|
D011251||complications infectious pregnancy
|
|
D011251||infectious pregnancy complication
|
|
D011251||infectious pregnancy complications
|
|
D011251||pregnancies infectious complications
|
|
D011251||pregnancy complication infectious
|
|
D011251||pregnancy infectious complications
|
|
D011254||pregnancy in diabetics
|
|
D011254||pregnancy in diabete
|
|
D011254||pregnancy in diabetes
|
|
D011254||pregnancy in diabetic
|
|
D012585||sciatica
|
|
D012585||bilateral sciatica
|
|
D012585||bilateral sciaticas
|
|
D012585||neuralgia sciatic
|
|
D012585||neuralgias sciatic
|
|
D012585||sciatica bilateral
|
|
D012585||sciatic neuralgia
|
|
D012585||sciatic neuralgias
|
|
C564621|607131||macrocephaly with multiple epiphyseal dysplasia and distinctive facies
|
|
C564621|607131||mmedf
|
|
C537915|200700||chondrodysplasia grebe type
|
|
C537915|200700||achondrogenesis brazilian
|
|
C537915|200700||achondrogenesis type ii formerly
|
|
C537915|200700||acromesomelic dysplasia grebe type
|
|
C537915|200700||amdg
|
|
C537915|200700||brazilian achondrogenesis
|
|
C537915|200700||grebe chondrodysplasia
|
|
C537915|200700||grebe dysplasia
|
|
C537915|200700||grebe syndrome
|
|
610504|C563032||preterm premature rupture of the membranes
|
|
610504|C563032||pprom
|
|
611031|C567026||episodic kinesigenic dyskinesia 2
|
|
611031|C567026||dystonia 19
|
|
611031|C567026||dyt19
|
|
611031|C567026||ekd2
|
|
D011269||pregnancy abdominal
|
|
D011269||abdominal pregnancies
|
|
D011269||abdominal pregnancy
|
|
D011269||pregnancies abdominal
|
|
187300|D013683||telangiectasia hereditary hemorrhagic
|
|
187300|D013683||disease osler apos s
|
|
187300|D013683||hemorrhagic telangiectasia hereditary
|
|
187300|D013683||hereditary hemorrhagic telangiectasia
|
|
187300|D013683||hht
|
|
187300|D013683||hht1 included
|
|
187300|D013683||orw disease telangiectasia hereditary hemorrhagic type 1 included
|
|
187300|D013683||osler disease
|
|
187300|D013683||osler rendu disease
|
|
187300|D013683||osler rendu weber disease
|
|
187300|D013683||osler apos s disease
|
|
187300|D013683||osler weber rendu syndrome
|
|
187300|D013683||rendu osler weber
|
|
187300|D013683||telangiectasia hereditary hemorrhagic of rendu osler and weber
|
|
187300|D013683||telangiectasia hereditary hemorrhagic type 1
|
|
187300|D013683||weber osler
|
|
D012593||sclerema neonatorum
|
|
D012594||scleroderma localized
|
|
D012594||circumscribed scleroderma
|
|
D012594||dermatosclerosis
|
|
D012594||frontal linear scleroderma en coup de sabre
|
|
D012594||linear scleroderma
|
|
D012594||localized scleroderma
|
|
D012594||morphea
|
|
D012594||morpheas
|
|
D012594||scleroderma circumscribed
|
|
D012594||scleroderma linear
|
|
D012594||sclerodermas localized
|
|
D012592||scleredema adultorum
|
|
D012592||buschke scleredema
|
|
D012592||buschke scleredema adultorum
|
|
D012592||buschke scleredema diabeticorum
|
|
D012592||buschke apos s scleredema
|
|
D012592||buschkes scleredema
|
|
D012592||diabeticorum scleredema
|
|
D012592||diabeticorums scleredema
|
|
D012592||scleredema
|
|
D012592||scleredema adultorum of buschke
|
|
D012592||scleredema buschke apos s
|
|
D012592||scleredema diabeticorum
|
|
D012592||scleredema diabeticorum of buschke
|
|
D012592||scleredema diabeticorums
|
|
D012592||scleredemas
|
|
D012598||sclerosis
|
|
D012598||scleroses
|
|
D012595||scleroderma systemic
|
|
D012595||sclerosis systemic
|
|
D012595||systemic scleroderma
|
|
D012595||systemic sclerosis
|
|
C536390|222448||donnai barrow syndrome
|
|
C536390|222448||dbs foar syndrome
|
|
C536390|222448||diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia and sensorineural deafness
|
|
C536390|222448||diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia sensorineural deafness and proteinuria
|
|
C536390|222448||diaphragmatic hernia exomphalos corpus callosum agenesis
|
|
C536390|222448||diaphragmatic hernia exomphalos hypertelorism syndrome
|
|
C536390|222448||faciooculoacousticorenal syndrome
|
|
C536390|222448||facio oculo acoustico renal syndrome
|
|
C536390|222448||foar syndrome
|
|
609040|C563808||arrhythmogenic right ventricular dysplasia familial 9
|
|
609040|C563808||arrhythmogenic right ventricular cardiomyopathy 9
|
|
609040|C563808||arvc9
|
|
609040|C563808||arvd9
|
|
C566447|610092||microphthalmia isolated with coloboma 3
|
|
C566447|610092||mcopcb3
|
|
C566447|610092||microphthalmia colobomatous isolated 3
|
|
C566447|610092||microphthalmia colobomatous isolated 3 microphthalmia cataracts and iris abnormalities included
|
|
C566980|136630||mental retardation fra12a type
|
|
C565510|236270||homocystinuria megaloblastic anemia due to defect in cobalamin metabolism cble complementation type
|
|
C565510|236270||hmae
|
|
C565510|236270||homocystinuria megaloblastic anemia cble complementation type
|
|
C565510|236270||methylcobalamin deficiency cble type
|
|
C565510|236270||vitamin b12 responsive homocystinuria cble type
|
|
D013899||thoracic neoplasms
|
|
D013899||neoplasms thoracic
|
|
D013899||neoplasm thoracic
|
|
D013899||thoracic neoplasm
|
|
D011236||prediabetic state
|
|
D011236||prediabetes
|
|
D011236||prediabetic states
|
|
D011236||state prediabetic
|
|
D011236||states prediabetic
|
|
D012569||schizotypal personality disorder
|
|
D012569||borderline schizophrenia
|
|
D012569||borderline schizophrenias
|
|
D012569||disorder schizotypal personality
|
|
D012569||disorders schizotypal personality
|
|
D012569||incipient schizophrenia
|
|
D012569||incipient schizophrenias
|
|
D012569||latent schizophrenia
|
|
D012569||latent schizophrenias
|
|
D012569||personality disorder schizotypal
|
|
D012569||personality disorders schizotypal
|
|
D012569||pseudoneurotic schizophrenia
|
|
D012569||pseudoneurotic schizophrenias
|
|
D012569||pseudopsychopathic schizophrenia
|
|
D012569||pseudopsychopathic schizophrenias
|
|
D012569||schizophrenia borderline
|
|
D012569||schizophrenia incipient
|
|
D012569||schizophrenia latent
|
|
D012569||schizophrenia pseudoneurotic
|
|
D012569||schizophrenia pseudopsychopathic
|
|
D012569||schizophrenias borderline
|
|
D012569||schizophrenias incipient
|
|
D012569||schizophrenias latent
|
|
D012569||schizophrenias pseudoneurotic
|
|
D012569||schizophrenias pseudopsychopathic
|
|
D012569||schizotypal personality disorders
|
|
D013898||thoracic injuries
|
|
D013898||chest injuries
|
|
D013898||chest injury
|
|
D013898||injuries chest
|
|
D013898||injuries thoracic
|
|
D013898||injury chest
|
|
D013898||injury thoracic
|
|
D013898||thoracic injury
|
|
192600|C566005||cardiomyopathy familial hypertrophic 1
|
|
192600|C566005||ash
|
|
192600|C566005|D002312||asymmetric septal hypertrophy
|
|
192600|C566005||cmh
|
|
192600|C566005||cmh1
|
|
192600|C566005|D024741||hypertrophic subaortic stenosis idiopathic
|
|
192600|C566005|D024741||ventricular hypertrophy hereditary
|
|
C566591|133200||erythrokeratodermia progressive symmetric
|
|
C566591|133200||ekv
|
|
C566591|133200||ekvp
|
|
C566591|133200|C536154||erythrokeratodermia figurata congenital familial in plaques
|
|
C566591|133200|D056266||erythrokeratodermia variabilis
|
|
C566591|133200||erythrokeratodermia variabilis et progressiva
|
|
C566591|133200||erythrokeratodermia variabilis with erythema gyratum repens greither disease included
|
|
C566591|133200||keratosis palmoplantaris transgrediens et progrediens included
|
|
C566591|133200||psek
|
|
D007966|250100||leukodystrophy metachromatic
|
|
D007966|250100||adult metachromatic leukodystrophies
|
|
D007966|250100||adult metachromatic leukodystrophy
|
|
D007966|250100||adult type metachromatic leukodystrophies
|
|
D007966|250100||adult type metachromatic leukodystrophy
|
|
D007966|250100||arsa deficiencies
|
|
D007966|250100||arsa deficiency
|
|
D007966|250100||arylsulfatase a deficiencies
|
|
D007966|250100||arylsulfatase a deficiency
|
|
D007966|250100||arylsulfatase a deficiency disease
|
|
D007966|250100||cerebral sclerosis diffuse metachromatic form
|
|
D007966|250100||cerebroside sulfatase deficiencies
|
|
D007966|250100||cerebroside sulfatase deficiency
|
|
D007966|250100||cerebroside sulfatase deficiency pseudoarylsulfatase a deficiency included
|
|
D007966|250100||cerebroside sulphatase deficiency disease
|
|
D007966|250100||deficiencies arsa
|
|
D007966|250100||deficiencies arylsulfatase a
|
|
D007966|250100||deficiencies cerebroside sulfatase
|
|
D007966|250100||deficiency arsa
|
|
D007966|250100||deficiency arylsulfatase a
|
|
D007966|250100||deficiency cerebroside sulfatase
|
|
D007966|250100||greenfield disease
|
|
D007966|250100||greenfield apos s disease
|
|
D007966|250100||infant metachromatic leukodystrophies
|
|
D007966|250100||infant metachromatic leukodystrophy
|
|
D007966|250100||infant type metachromatic leukodystrophies
|
|
D007966|250100||infant type metachromatic leukodystrophy
|
|
D007966|250100||juvenile metachromatic leukodystrophies
|
|
D007966|250100||juvenile metachromatic leukodystrophy
|
|
D007966|250100||juvenile type metachromatic leukodystrophies
|
|
D007966|250100||juvenile type metachromatic leukodystrophy
|
|
D007966|250100||leukodystrophies adult metachromatic
|
|
D007966|250100||leukodystrophies adult type metachromatic
|
|
D007966|250100||leukodystrophies juvenile metachromatic
|
|
D007966|250100||leukodystrophies juvenile type metachromatic
|
|
D007966|250100||leukodystrophies metachromatic
|
|
D007966|250100||leukodystrophy adult metachromatic
|
|
D007966|250100||leukodystrophy adult type metachromatic
|
|
D007966|250100||leukodystrophy juvenile metachromatic
|
|
D007966|250100||leukodystrophy juvenile type metachromatic
|
|
D007966|250100||leukodystrophy metachromatic adult
|
|
D007966|250100||leukodystrophy metachromatic juvenile
|
|
D007966|250100||leukoencephalopathies metachromatic
|
|
D007966|250100||leukoencephalopathy metachromatic
|
|
D007966|250100||lipidosis sulfatide
|
|
D007966|250100||metachromatic leukodystrophies
|
|
D007966|250100||metachromatic leukodystrophies adult
|
|
D007966|250100||metachromatic leukodystrophies adult type
|
|
D007966|250100||metachromatic leukodystrophies infant
|
|
D007966|250100||metachromatic leukodystrophies infant type
|
|
D007966|250100||metachromatic leukodystrophies juvenile
|
|
D007966|250100||metachromatic leukodystrophies juvenile type
|
|
D007966|250100||metachromatic leukodystrophy
|
|
D007966|250100||metachromatic leukodystrophy adult
|
|
D007966|250100||metachromatic leukodystrophy adult included
|
|
D007966|250100||metachromatic leukodystrophy adult type
|
|
D007966|250100||metachromatic leukodystrophy infant
|
|
D007966|250100||metachromatic leukodystrophy infant type
|
|
D007966|250100||metachromatic leukodystrophy juvenile
|
|
D007966|250100||metachromatic leukodystrophy juvenile included
|
|
D007966|250100||metachromatic leukodystrophy juvenile type
|
|
D007966|250100||metachromatic leukodystrophy late infantile
|
|
D007966|250100||metachromatic leukodystrophy late infantile included
|
|
D007966|250100||metachromatic leukoencephalopathies
|
|
D007966|250100||metachromatic leukoencephalopathy
|
|
D007966|250100||mld
|
|
D007966|250100||sulfatase deficiencies cerebroside
|
|
D007966|250100||sulfatase deficiency cerebroside
|
|
D007966|250100||sulfatide lipidosis
|
|
D012561||schizophrenia childhood
|
|
D012561||childhood onset schizophrenia
|
|
D012561||childhood schizophrenia
|
|
D012561||schizophrenia childhood onset
|
|
D011230||precancerous conditions
|
|
D011230||condition precancerous
|
|
D011230||condition preneoplastic
|
|
D011230||conditions precancerous
|
|
D011230||conditions preneoplastic
|
|
D011230||precancerous condition
|
|
D011230||preneoplastic condition
|
|
D011230||preneoplastic conditions
|
|
D013896||thoracic diseases
|
|
D013896||diseases thoracic
|
|
D013896||disease thoracic
|
|
D013896||thoracic disease
|
|
D012562||schizophrenia disorganized
|
|
D012562||disorganized schizophrenia
|
|
D012562||disorganized schizophrenias
|
|
D012562||hebephrenic schizophrenia
|
|
D012562||hebephrenic schizophrenias
|
|
D012562||schizophrenia hebephrenic
|
|
D012562||schizophrenias disorganized
|
|
D012562||schizophrenias hebephrenic
|
|
D012563||schizophrenia paranoid
|
|
D012563||delusional disorder
|
|
D012563||delusional disorders
|
|
D012563||disorder delusional
|
|
D012563||disorders delusional
|
|
D012563||paranoid schizophrenia
|
|
D012563||paranoid schizophrenias
|
|
D012563||schizophrenias paranoid
|
|
C567050|610898||supranuclear palsy progressive 3
|
|
C567050|610898||psnp3
|
|
C563897|608622||hypertension diastolic resistance to
|
|
C563740|609311||charcot marie tooth disease type 4h
|
|
C563740|609311||charcot marie tooth disease autosomal recessive type 4h
|
|
C563740|609311||charcot marie tooth disease demyelinating autosomal recessive type 4h
|
|
C563740|609311||charcot marie tooth neuropathy type 4h
|
|
C563740|609311||cmt4h
|
|
C567564|612781||isolated growth hormone deficiency type ib
|
|
C567564|612781||dwarfism of sindh
|
|
C567564|612781||ighd1b
|
|
C567564|612781||ighd ib
|
|
C567419|612098||cardiomyopathy familial hypertrophic 11
|
|
C567419|612098||cmh11
|
|
D000592||amino acid metabolism inborn errors
|
|
D000592||amino acid metabolism disorders inborn
|
|
D000592||amino acid metabolism inborn error
|
|
D000592||amino acid metabolism inherited disorders
|
|
D000592||amino acidopathies congenital
|
|
D000592||amino acidopathies inborn
|
|
D000592||amino acidopathy congenital
|
|
D000592||amino acidopathy inborn
|
|
D000592||congenital amino acidopathies
|
|
D000592||congenital amino acidopathy
|
|
D000592||inborn amino acidopathies
|
|
D000592||inborn amino acidopathy
|
|
D000592||inborn errors amino acid metabolism
|
|
D000592||inherited errors of amino acid metabolism
|
|
C563906|608569||cardiomyopathy dilated 1o
|
|
C563906|608569||cardiomyopathy dilated with ventricular tachycardia
|
|
C563906|608569||cmd1o
|
|
D043604||glomus tympanicum tumor
|
|
D043604||glomus tympanicum tumors
|
|
D043604||tumor glomus tympanicum
|
|
D043604||tumors glomus tympanicum
|
|
D011249||pregnancy complications cardiovascular
|
|
D011249||cardiovascular pregnancy complication
|
|
D011249||cardiovascular pregnancy complications
|
|
D011249||complication cardiovascular pregnancy
|
|
D011249||complications cardiovascular pregnancy
|
|
D011249||pregnancies cardiovascular complications
|
|
D011249||pregnancy cardiovascular complications
|
|
D011249||pregnancy complication cardiovascular
|
|
C565195|610706||deafness congenital with inner ear agenesis microtia and microdontia
|
|
C565195|610706||deafness congenital with labyrinthine aplasia microtia and microdontia
|
|
C565195|610706|C580009||deafness with lamm
|
|
D011248||pregnancy complications
|
|
D011248||complication pregnancy
|
|
D011248||complications pregnancy
|
|
D011248||pregnancy complication
|
|
D011561|177850||pseudoxanthoma elasticum
|
|
D011561|177850||elasticum incomplete pseudoxanthoma
|
|
D011561|177850||elasticums incomplete pseudoxanthoma
|
|
D011561|177850||groenblad strandberg syndrome
|
|
D011561|177850||gronblad strandberg syndrome
|
|
D011561|177850||gronblad strandberg syndrome pseudoxanthoma elasticum modifier of severity of included
|
|
D011561|177850||incomplete pseudoxanthoma elasticum
|
|
D011561|177850||incomplete pseudoxanthoma elasticums
|
|
D011561|177850||pseudoxanthoma elasticum autosomal dominant
|
|
D011561|177850||pseudoxanthoma elasticum forme fruste
|
|
D011561|177850||pseudoxanthoma elasticum heterozygous included
|
|
D011561|177850||pseudoxanthoma elasticum incomplete
|
|
D011561|177850||pseudoxanthoma elasticums incomplete
|
|
D011561|177850||pxe
|
|
D011561|177850||pxe modifier of severity of included
|
|
D011561|177850||syndrome gronblad strandberg
|
|
D056912||binge eating disorder
|
|
D056912||binge eating disorders
|
|
D056912||disorder binge eating
|
|
D056912||disorders binge eating
|
|
C563758|609259||myopia 10
|
|
C563758|609259||myp10
|
|
D019280|113620||branchio oto renal syndrome
|
|
D019280|113620||bofs
|
|
D019280|113620||bof syndrome
|
|
D019280|113620||bor1
|
|
D019280|113620||bor2
|
|
D019280|113620||bor syndrome
|
|
D019280|113620||branchial clefts with characteristic facies growth retardation imperforate nasolacrimal duct and premature aging
|
|
D019280|113620||branchiooculofacial syndrome
|
|
D019280|113620||branchio oculo facial syndrome
|
|
D019280|113620||branchiootorenal dysplasia
|
|
D019280|113620||branchio otorenal dysplasia
|
|
D019280|113620||branchio otorenal syndrome
|
|
D019280|113620||branchiootorenal syndrome 1
|
|
D019280|113620||branchiootorenal syndrome 2
|
|
D019280|113620||dysplasia branchiootorenal
|
|
D019280|113620||hemangiomatous branchial clefts lip pseudocleft syndrome
|
|
D019280|113620||lee root fenske syndrome
|
|
D019280|113620||lip pseudocleft hemangiomatous branchial cyst syndrome
|
|
D019280|113620||melnick fraser syndrome
|
|
D019280|113620||syndrome bof
|
|
D019280|113620||syndrome bor
|
|
D019280|113620||syndrome branchiooculofacial
|
|
D019280|113620||syndrome branchio oculo facial
|
|
D019280|113620||syndrome branchio oto renal
|
|
D019280|113620||syndrome melnick fraser
|
|
214150|C562434||cerebrooculofacioskeletal syndrome 1
|
|
214150|C562434||cofs
|
|
214150|C562434||cofs1
|
|
214150|C562434||cofs syndrome
|
|
214150|C562434||pena shokeir syndrome type ii
|
|
160800|255300|D009224||myotonia congenita autosomal dominant
|
|
160800||thomsen disease thd myotonia levior included
|
|
303900||colorblindness partial protan series
|
|
303900||cbp
|
|
303900||protanopia
|
|
303900||red colorblindness protanomaly included
|
|
D000568||amenorrhea
|
|
D000568||amenorrhea postpartum
|
|
D000568||postpartum amenorrhea
|
|
D000568||postpartum amenorrheas
|
|
D001899||borrelia infections
|
|
D001899||borrelia infection
|
|
D001899||infection borrelia
|
|
D001899||infections borrelia
|
|
D000567||amelogenesis imperfecta
|
|
D000567||congenital enamel hypoplasia
|
|
C536128|216900||achromatopsia 2
|
|
C536128|216900||achm2
|
|
C536128|216900||colorblindness total
|
|
C536128|216900||rmch2
|
|
C536128|216900||rod monochromacy 2
|
|
C536128|216900||rod monochromatism 2
|
|
C536128|216900||total color blindness
|
|
C535771||dandy walker malformation postaxial polydactyly
|
|
C535771||dandy walker malformation with postaxial polydactyly
|
|
C535771||dwm with postaxial polydactyly
|
|
C564528|300355||mental retardation x linked 73
|
|
C564528|300355||mrx73
|
|
C535770||daish hardman lamont syndrome
|
|
C535770||hydrocephalus tall stature joint laxity and kyphoscoliosis
|
|
C535772||dandy walker variant
|
|
C572568|610984||complement factor i deficiency
|
|
C572568|610984||c3 inactivator deficiency
|
|
C572568|610984||cfid
|
|
C572568|610984||complement component 3 inactivator deficiency
|
|
D001890||borna disease
|
|
C536131|603194||meckel syndrome type 2
|
|
C536131|603194||meckel gruber syndrome type 2
|
|
C536131|603194||mks2
|
|
D000564||ameloblastoma
|
|
D000564||ameloblastomas
|
|
D025861||blood coagulation disorders inherited
|
|
D025861||coagulation disorder hereditary
|
|
D025861||coagulation disorder inherited
|
|
D025861||coagulation disorders hereditary
|
|
D025861||coagulation disorders inherited
|
|
D025861||hereditary blood coagulation disorders
|
|
D025861||hereditary coagulation disorder
|
|
D025861||hereditary coagulation disorders
|
|
D025861||inherited blood coagulation disorders
|
|
D025861||inherited coagulation disorder
|
|
D025861||inherited coagulation disorders
|
|
D000562||amebiasis
|
|
D000562||abscess amebic
|
|
D000562||abscesses amebic
|
|
D000562||amebiases
|
|
D000562||amebic abscess
|
|
D000562||amebic abscesses
|
|
D000562||ameboma
|
|
D000562||amebomas
|
|
D000562||amoebiases
|
|
D000562||amoebiasis
|
|
D000562||iodamoebiases
|
|
D000562||iodamoebiasis
|
|
D011213||poxviridae infections
|
|
D011213||infection poxviridae
|
|
D011213||infection poxvirus
|
|
D011213||infections poxviridae
|
|
D011213||infections poxvirus
|
|
D011213||milker nodes
|
|
D011213||milker apos s node
|
|
D011213||milker apos s nodes
|
|
D011213||milkers nodes
|
|
D011213||node milker apos s
|
|
D011213||nodes milker apos s
|
|
D011213||poxviridae infection
|
|
D011213||poxvirus infection
|
|
D011213||poxvirus infections
|
|
607174|C537443||meningioma familial
|
|
607174|C537443||familial meningioma
|
|
607174|C537443||meningioma familial susceptibility to
|
|
C537182|603829||paroxysmal ventricular fibrillation
|
|
C537182|603829||idiopathic ventricular fibrillation
|
|
C537182|603829||paroxysmal familial ventricular fibrillation
|
|
C537182|603829||ventricular fibrillation during myocardial infarction susceptibility to
|
|
C537182|603829||ventricular fibrillation paroxysmal familial
|
|
C537182|603829|C567851||ventricular fibrillation paroxysmal familial 1
|
|
C537182|603829|C567841||ventricular fibrillation paroxysmal familial 2
|
|
C537182|603829||vf1
|
|
C537182|603829||vf2
|
|
C535763||euhidrotic ectodermal dysplasia
|
|
C535763||kopysc barczyk krol syndrome
|
|
C535763||pilodental dysplasia with refractive errors
|
|
C535763||trichodental dysplasia with hyperopia
|
|
600510|C563184||glaucoma related pigment dispersion syndrome
|
|
600510|C563184||glaucoma pigment dispersion type
|
|
600510|C563184||gpds1
|
|
600510|C563184|C536648|274600||pds
|
|
600510|C563184||pigment dispersion syndrome
|
|
C535766||czech dysplasia metatarsal type
|
|
C535766||czech dysplasia
|
|
C535766||progressive pseudorheumatoid dysplasia with hypoplastic toes
|
|
C535766||pseudorheumatoid dysplasia progressive with hypoplastic toes
|
|
C535766||spondyloarthropathy with short third and fourth toes
|
|
C535396|108720||atelosteogenesis type 1
|
|
C535396|108720||ao1
|
|
C535396|108720||aoi
|
|
C535396|108720||atelosteogenesis type i
|
|
C535396|108720||giant cell chondrodysplasia
|
|
C535396|108720||spondylohumerofemoral hypoplasia
|
|
C538157|186580||synovitis granulomatous with uveitis and cranial neuropathies
|
|
C538157|186580||acug
|
|
C538157|186580||arthrocutaneouveal granulomatosis
|
|
C538157|186580||blau syndrome
|
|
C538157|186580||early onset sarcoidosis
|
|
C538157|186580||familial granulomatosis blau type
|
|
C538157|186580||familial juvenile systemic granulomatosis
|
|
C538157|186580||granulomatosis familial blau type
|
|
C538157|186580||granulomatosis familial blau type synovitis granulomatous with uveitis and cranial neuropathies included
|
|
C538157|186580||granulomatosis familial juvenile systemic
|
|
C538157|186580||granulomatous inflammatory arthritis dermatitis and uveitis familial
|
|
C538157|186580||jabs syndrome
|
|
C538157|186580||pediatric granulomatous arthritis
|
|
C535768||daentl towsend siegel syndrome
|
|
C535768||familial nephrosis hydrocephalus thin skin blue sclerae syndrome
|
|
C535768||hydrocephalus blue sclera nephropathy
|
|
C535767||d glycericacidemia
|
|
C535767||d glycerate kinase deficiency
|
|
C535767||d glyceric acidemia
|
|
C535767||glycerate kinase deficiency
|
|
C535767||non ketotic hyperglycinemia syndrome
|
|
D012541||scarlet fever
|
|
D012541||fever scarlet
|
|
D012541||fevers scarlet
|
|
D012541||scarlet fevers
|
|
C535769||dahlberg borer newcomer syndrome
|
|
C535769||hypoparathyroidism lymphedema syndrome
|
|
C535769||lymphedema hypoparathyroidism syndrome
|
|
C567400|612201||atrial fibrillation familial 6
|
|
C567400|612201||atfb6
|
|
C535782||spondyloenchondrodysplasia
|
|
C535782||spondyloenchondromatosis
|
|
C535782||spondylometaphyseal dysplasia with enchondromatous changes
|
|
C535781||spondylocostal dysostosis autosomal recessive
|
|
C535781||autosomal recessive spondylocostal dysostosis
|
|
C535781|608681||spondylocostal dysostosis 2 autosomal recessive
|
|
C535781|609813||spondylocostal dysostosis 3 autosomal recessive
|
|
C535784||spondyloepimetaphyseal dysplasia with multiple dislocations
|
|
C535784||spondyloepimetaphyseal dysplasia with multiple dislocations hall type
|
|
C535784||spondyloepimetaphyseal dysplasia with multiple dislocations leptodactylic type
|
|
C535783||spondyloepimetaphyseal dysplasia with hypotrichosis
|
|
C535783||whyte petersen mcalister syndrome
|
|
C535783||whyte syndrome
|
|
D012557||schizoid personality disorder
|
|
D012557||disorder schizoid personality
|
|
D012557||disorders schizoid personality
|
|
D012557||personalities schizoid
|
|
D012557||personality disorder schizoid
|
|
D012557||personality disorders schizoid
|
|
D012557||personality schizoid
|
|
D012557||schizoid personalities
|
|
D012557||schizoid personality
|
|
D012557||schizoid personality disorders
|
|
C565634|221820||gliosis familial progressive subcortical
|
|
C565634|221820||dementia familial neumann type
|
|
C565634|221820||gpsc
|
|
C565634|221820||hdls
|
|
C565634|221820||leukoencephalopathy diffuse hereditary with spheroids
|
|
C565634|221820||leukoencephalopathy with neuroaxonal spheroids autosomal dominant
|
|
C565634|221820||subcortical gliosis of neumann
|
|
C041229||bot heavy chain disease protein human
|
|
D011227||pre excitation mahaim type
|
|
D011227||mahaim type preexcitation
|
|
D011227||mahaim type pre excitation
|
|
D011227||mahaim type pre excitation nodofascicular
|
|
D011227||mahaim type pre excitation nodoventricular
|
|
D011227||nodofascicular mahaim type pre excitation
|
|
D011227||nodoventricular mahaim type pre excitation
|
|
D011227||preexcitation mahaim type
|
|
D011227||pre excitation nodofascicular mahaim type
|
|
D011227||pre excitation nodoventricular mahaim type
|
|
C563679|610353||epilepsy nocturnal frontal lobe type 4
|
|
C563679|610353||enfl4
|
|
C563679|610353||epilepsy familial with nocturnal wandering and ictal fear
|
|
C563679|610353||epilepsy nocturnal frontal lobe 4
|
|
D011226||pre excitation syndromes
|
|
D011226||preexcitation syndrome
|
|
D011226||pre excitation syndrome
|
|
D011226||preexcitation syndromes
|
|
C563929|608443||mental retardation autosomal recessive 3
|
|
C563929|608443||mrt3
|
|
C535775||pierre robin sequence with pectus excavatum and rib and scapular anomalies
|
|
C535775||campomelic dysplasia mild
|
|
C535774||piepkorn karp hickok syndrome
|
|
C535777||split hand foot deformity
|
|
D012553||schistosomiasis haematobia
|
|
D012553||schistosomiases urinary
|
|
D012553||schistosomiases urogenital
|
|
D012553||schistosomiasis haematobium
|
|
D012553||schistosomiasis urinary
|
|
D012553||schistosomiasis urogenital
|
|
D012553||urinary schistosomiases
|
|
D012553||urinary schistosomiasis
|
|
D012553||urogenital schistosomiases
|
|
D012553||urogenital schistosomiasis
|
|
C535779||spondylocamptodactyly
|
|
C535779||camptodactyly with cervical platyspondyly
|
|
C535779||spondylo camptodactyly syndrome
|
|
D012554||schistosomiasis japonica
|
|
D012554||schistosomiasis japonicum
|
|
D012552||schistosomiasis
|
|
D012552||bilharziases
|
|
D012552||bilharziasis
|
|
D012552||fever katayama
|
|
D012552||katayama fever
|
|
D012552||schistosomiases
|
|
133239|D004938||esophageal neoplasms
|
|
133239|D004938||aerodigestive tract cancer susceptibility to included
|
|
133239|D004938||cancer esophageal
|
|
133239|D004938||cancer esophagus
|
|
133239|D004938||cancer of esophagus
|
|
133239|D004938||cancer of the esophagus
|
|
133239|D004938||cancers esophageal
|
|
133239|D004938||cancers esophagus
|
|
133239|D004938||escc susceptibility to included
|
|
133239|D004938||esophageal cancer
|
|
133239|D004938||esophageal cancers
|
|
133239|D004938||esophageal neoplasm
|
|
133239|D004938||esophageal squamous cell carcinoma susceptibility to included
|
|
133239|D004938||esophagus cancer
|
|
133239|D004938||esophagus cancers
|
|
133239|D004938||esophagus neoplasm
|
|
133239|D004938||esophagus neoplasms
|
|
133239|D004938||gastric cardia adenocarcinoma susceptibility to included
|
|
133239|D004938||neoplasm esophageal
|
|
133239|D004938||neoplasm esophagus
|
|
133239|D004938||neoplasms esophageal
|
|
133239|D004938||neoplasms esophagus
|
|
C535791||spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
|
|
C535791||smd with bowed forearms and facial dysmorphism
|
|
C535790||spondylohypoplasia arthrogryposis and popliteal pterygium
|
|
C535793||spondylometaphyseal dysplasia apos corner fracture apos type
|
|
C535793||spondylometaphyseal dysplasia corner fracture type
|
|
C535793||spondylometaphyseal dysplasia sutcliffe type
|
|
C566541|602477||febrile convulsions familial 2
|
|
C566541|602477||convulsions familial febrile 2
|
|
C566541|602477||feb2
|
|
C566541|602477||febrile seizures familial 2
|
|
C566541|602477||seizures familial febrile 2
|
|
D003410|123450||cri du chat syndrome
|
|
D003410|123450||5p deletion syndrome
|
|
D003410|123450||5p deletion syndromes
|
|
D003410|123450||5p minus syndrome
|
|
D003410|123450||5p minus syndromes
|
|
D003410|123450||5p syndrome
|
|
D003410|123450||5p syndrome chromosome
|
|
D003410|123450||5p syndromes
|
|
D003410|123450||5p syndromes chromosome
|
|
D003410|123450||cat cry syndrome
|
|
D003410|123450||cat cry syndromes
|
|
D003410|123450||chromosome 5p deletion syndrome
|
|
D003410|123450|C537648||chromosome 5p syndrome
|
|
D003410|123450||chromosome 5p syndromes
|
|
D003410|123450||chromosome 5 short arm deletion syndrome
|
|
D003410|123450||cri du chat syndromes
|
|
D003410|123450||crying cat syndrome
|
|
D003410|123450||crying cat syndromes
|
|
D003410|123450||deletion of short arm of chromosome 5 syndrome
|
|
D003410|123450||deletion syndrome 5p
|
|
D003410|123450||deletion syndromes 5p
|
|
D003410|123450||minus syndrome 5p
|
|
D003410|123450||minus syndromes 5p
|
|
D003410|123450||syndrome 5p
|
|
D003410|123450||syndrome 5p deletion
|
|
D003410|123450||syndrome 5p minus
|
|
D003410|123450||syndrome cat cry
|
|
D003410|123450||syndrome chromosome 5p
|
|
D003410|123450||syndrome cri du chat
|
|
D003410|123450||syndrome crying cat
|
|
D003410|123450||syndromes 5p
|
|
D003410|123450||syndromes 5p deletion
|
|
D003410|123450||syndromes 5p minus
|
|
D003410|123450||syndromes cat cry
|
|
D003410|123450||syndromes chromosome 5p
|
|
D003410|123450||syndromes cri du chat
|
|
D003410|123450||syndromes crying cat
|
|
C535792||spondylometaphyseal dysplasia with dentinogenesis imperfecta
|
|
C535792||odontochondrodysplasia
|
|
C535795||spondylometaphyseal dysplasia axial
|
|
C535795||axial smd
|
|
C535795||smd axial
|
|
C535794||spondylometaphyseal dysplasia algerian type
|
|
C535794||spondylometaphyseal dysplasia schmidt type
|
|
C535794||spondylometaphyseal dysplasia with severe genu valgum
|
|
D006211|234200||pantothenate kinase associated neurodegeneration
|
|
D006211|234200||degeneration pigmentary pallidal
|
|
D006211|234200||dystrophies juvenile onset neuroaxonal
|
|
D006211|234200||dystrophy juvenile onset neuroaxonal
|
|
D006211|234200||hallervorden spatz disease
|
|
D006211|234200||hallervorden spatz syndrome
|
|
D006211|234200||juvenile onset neuroaxonal dystrophies
|
|
D006211|234200||juvenile onset neuroaxonal dystrophy
|
|
D006211|234200||nbia1
|
|
D006211|234200||neuroaxonal dystrophies juvenile onset
|
|
D006211|234200||neuroaxonal dystrophy juvenile onset
|
|
D006211|234200||neurodegeneration pantothenate kinase associated
|
|
D006211|234200||neurodegeneration with brain iron accumulation 1
|
|
D006211|234200||neurodegeneration with brain iron accumulation type 1
|
|
D006211|234200||pallidal atrophy pigmentary
|
|
D006211|234200||pigmentary pallidal atrophy
|
|
D006211|234200||pigmentary pallidal degeneration
|
|
D006211|234200||pkan
|
|
D006211|234200||pkan neuroaxonal dystrophy juvenile onset
|
|
D000542||alveolitis extrinsic allergic
|
|
D000542||allergic alveolitides extrinsic
|
|
D000542||allergic alveolitis extrinsic
|
|
D000542||alveolitides extrinsic allergic
|
|
D000542||extrinsic allergic alveolitides
|
|
D000542||extrinsic allergic alveolitis
|
|
D000542||hypersensitivity pneumonitides
|
|
D000542||hypersensitivity pneumonitis
|
|
D000542||pneumonitides hypersensitivity
|
|
D000542||pneumonitis hypersensitivity
|
|
167800|C537262||hereditary pancreatitis
|
|
167800|C537262||autosomal dominant hereditary pancreatitis
|
|
167800|C537262||familial pancreatitis
|
|
167800|C537262||hereditary chronic pancreatitis
|
|
167800|C537262||hp
|
|
167800|C537262||hpc
|
|
167800|C537262||pancreatitis calcific included
|
|
167800|C537262||pancreatitis chronic pancreatitis chronic susceptibility to included
|
|
167800|C537262||pancreatitis chronic protection against included
|
|
167800|C537262||pancreatitis hereditary
|
|
167800|C537262||pctt
|
|
D012523||sarcocystosis
|
|
D012523||sarcocystoses
|
|
D012523||sarcosporidioses
|
|
D012523||sarcosporidiosis
|
|
D055613||multiple pulmonary nodules
|
|
D055613||multiple pulmonary nodule
|
|
D055613||pulmonary nodule multiple
|
|
D055613||pulmonary nodules multiple
|
|
C535786||spondyloepimetaphyseal dysplasia sponastrime type
|
|
C535786||sponastrime dysplasia
|
|
C535786||spondylar and nasal alterations with striated metaphyses
|
|
C535785||spondyloepimetaphyseal dysplasia genevieve type
|
|
C535785||semd genevieve type
|
|
C535787||spondyloepiphyseal dysplasia tarda toledo type
|
|
C535787||brachyolmia toledo type
|
|
C535787||brachyolmia type 1 toledo type
|
|
C535787||paps chondroitin sulfate sulfotransferase deficiency
|
|
C535787||sed chondroitin sulfate type
|
|
C535787||spondyloepiphyseal dysplasia chondroitin sulfate type
|
|
C535787||toledo type brachyolmia
|
|
D013851||thinness
|
|
D013851||leanness
|
|
D013851||underweight
|
|
C535789|143095||spondyloepiphyseal dysplasia omani type
|
|
C535789|143095||chondrodysplasia with multiple dislocations
|
|
C535789||chst3 related skeletal dysplasia
|
|
C535789|143095||humerospinal dysostosis
|
|
C535789||humero spinal dysostosis
|
|
C535789||humero spinal dysostosis with congenital heart disease
|
|
C535789||kozlowski celermajer tink syndrome
|
|
C535789||omani type of spondyloepiphyseal dysplasia
|
|
C535789||sed omani type
|
|
C535789||sed with luxations chst3 type
|
|
C535789||spondyloepiphyseal dysplasia chst3 related
|
|
C535789|143095||spondyloepiphyseal dysplasia with congenital joint dislocations
|
|
D008059|607014||mucopolysaccharidosis i
|
|
D008059|607014||alpha l iduronidase deficiencies
|
|
D008059|607014||alpha l iduronidase deficiency
|
|
D008059|607014||deficiencies alpha l iduronidase
|
|
D008059|607014||deficiency alpha l iduronidase
|
|
D008059|607014||disease hurler
|
|
D008059|607014||disease hurler apos s
|
|
D008059|607014||gargoylism
|
|
D008059|607014||gargoylism hurler syndrome
|
|
D008059|607014||gargoylisms
|
|
D008059|607014||hurler disease
|
|
D008059|607014||hurler scheie syndrome
|
|
D008059|607014||hurler apos s disease
|
|
D008059|607014||hurlers disease
|
|
D008059|607014||hurler apos s syndrome
|
|
D008059|607014||hurlers syndrome
|
|
D008059|607014||hurler syndrome
|
|
D008059|607014||hurler syndrome gargoylism
|
|
D008059|607014||lipochondrodystrophies
|
|
D008059|607014||lipochondrodystrophy
|
|
D008059|607014||mps1 h
|
|
D008059|607014||mps1 hs
|
|
D008059|607014||mps1 s
|
|
D008059|607014||mps5 formerly
|
|
D008059|607014||mps v formerly
|
|
D008059|607014||mucopolysaccharidosis 1
|
|
D008059|607014||mucopolysaccharidosis 5
|
|
D008059|607014||mucopolysaccharidosis is
|
|
D008059|607014||mucopolysaccharidosis i s
|
|
D008059|607014||mucopolysaccharidosis type i
|
|
D008059|607014||mucopolysaccharidosis type ih
|
|
D008059|607014||mucopolysaccharidosis type ihs
|
|
D008059|607014||mucopolysaccharidosis type ih s
|
|
D008059|607014||mucopolysaccharidosis type ih ss
|
|
D008059|607014||mucopolysaccharidosis type is
|
|
D008059|607014||mucopolysaccharidosis type v formerly
|
|
D008059|607014||mucopolysaccharidosis v
|
|
D008059|607014||pfaundler hurler syndrome
|
|
D008059|607014||scheie apos s syndrome
|
|
D008059|607014||scheie syndrome
|
|
D008059|607014||syndrome hurler
|
|
D008059|607014||syndrome hurler apos s
|
|
D008059|607014||syndrome hurler scheie
|
|
D008059|607014||syndrome pfaundler hurler
|
|
D008059|607014||syndrome scheie
|
|
D008059|607014||syndrome scheie apos s
|
|
D008059|607014||type ih mucopolysaccharidosis
|
|
D008059|607014||type ihs mucopolysaccharidosis
|
|
D008059|607014||type ih s mucopolysaccharidosis
|
|
D008059|607014||type ih ss mucopolysaccharidosis
|
|
D001885||bordetella infections
|
|
D001885||bordetella infection
|
|
D001885||infection bordetella
|
|
D001885||infections bordetella
|
|
C538353|608390||potassium aggravated myotonia
|
|
C538353|608390||myotonia congenita acetazolamide responsive
|
|
C538353|608390||myotonia congenita atypical
|
|
C538353|608390||myotonia congenita atypical laryngospasm severe neonatal episodic included
|
|
C538353|608390||myotonia permanens
|
|
C538353|608390||myotonia potassium aggravated
|
|
C538353|608390||snel included
|
|
C538353|608390|D020513|170500||sodium channel muscle disease
|
|
C538353|608390||sodium channel myotonia
|
|
D001883||borderline personality disorder
|
|
D001883||borderline personality disorders
|
|
D001883||disorder borderline personality
|
|
D001883||disorders borderline personality
|
|
D001883||personality disorder borderline
|
|
D001883||personality disorders borderline
|
|
D001882||border disease
|
|
D001882||border diseases
|
|
D000550||amblyopia
|
|
D000550||amblyopia anisometropic
|
|
D000550||amblyopia developmental
|
|
D000550||amblyopias
|
|
D000550||amblyopias anisometropic
|
|
D000550||amblyopias developmental
|
|
D000550||amblyopias stimulus deprivation induced
|
|
D000550||amblyopias suppression
|
|
D000550||amblyopia stimulus deprivation induced
|
|
D000550||amblyopia suppression
|
|
D000550||anisometropic amblyopia
|
|
D000550||anisometropic amblyopias
|
|
D000550||deprivation induced amblyopias stimulus
|
|
D000550||deprivation induced amblyopia stimulus
|
|
D000550||developmental amblyopia
|
|
D000550||developmental amblyopias
|
|
D000550||eye lazy
|
|
D000550||eyes lazy
|
|
D000550||lazy eye
|
|
D000550||lazy eyes
|
|
D000550||stimulus deprivation induced amblyopia
|
|
D000550||stimulus deprivation induced amblyopias
|
|
D000550||suppression amblyopia
|
|
D000550||suppression amblyopias
|
|
C567733|613122||cardiomyopathy dilated 1cc
|
|
C567733|613122||cmd1cc
|
|
D012536||scalp dermatoses
|
|
D012536||dermatoses scalp
|
|
D012536||dermatosis scalp
|
|
D012536||scalp dermatosis
|
|
C565276|605909||parkinson disease 6 autosomal recessive early onset
|
|
C565276|605909||park6
|
|
C565276|605909||parkinson disease 6 early onset
|
|
C565276|605909||parkinson disease 6 early onset park6 parkinson disease 6 late onset susceptibility to included
|
|
C565276|605909||parkinson disease autosomal recessive early onset digenic pink1 dj1
|
|
C565276|605909||parkinson disease autosomal recessive early onset digenic pink1 dj1 included
|
|
146520||hypotrichosis 2
|
|
146520||htss
|
|
146520||htss1
|
|
146520||hypotrichosis simplex of the scalp 1
|
|
146520|C564143||hypotrichosis spanish type
|
|
146520||hypt2
|
|
241800|C537158||hypothalamic hamartomas
|
|
241800|C537158||chhs included
|
|
241800|C537158||congenital hypothalamic hamartoma syndrome
|
|
241800|C537158||congenital hypothalamic hamartoma syndrome included
|
|
241800|C537158||hamartoma of the hypothalamus
|
|
C535796||spondylometaphyseal dysplasia east african type
|
|
C535799||spondyloperipheral dysplasia short ulna
|
|
C535799||familial spondyloepiphyseal dysplasia
|
|
C535799|271700||spondyloperipheral dysplasia
|
|
C535799|271700||spondyloperipheral dysplasia with short ulna
|
|
C535798||spondylometaphyseal dysplasia sedaghatian type
|
|
C535798||lethal metaphyseal dysplasia
|
|
C535798||metaphyseal chondrodysplasia congenital lethal
|
|
C535798||sedaghatian chondrodysplasia
|
|
194190|D054877||wolf hirschhorn syndrome
|
|
194190|D054877||4p deletion syndrome
|
|
194190|D054877||4p syndrome
|
|
194190|D054877||4p syndrome chromosome
|
|
194190|D054877||4p syndromes chromosome
|
|
194190|D054877||chromosome 4p16 3 deletion syndrome
|
|
194190|D054877||chromosome 4p deletion syndrome
|
|
194190|D054877||chromosome 4p monosomy
|
|
194190|D054877||chromosome 4p syndrome
|
|
194190|D054877||chromosome 4p syndromes
|
|
194190|D054877||del 4p syndrome
|
|
194190|D054877||mental retardation unusual facies and intrauterine growth retardation
|
|
194190|D054877||partial monosomy 4p
|
|
194190|D054877||pitt rogers danks syndrome
|
|
194190|D054877||pitt syndrome
|
|
194190|D054877||pitt syndromes
|
|
194190|D054877||prds
|
|
194190|D054877||syndrome chromosome 4p
|
|
194190|D054877||syndrome pitt
|
|
194190|D054877||syndrome pitt rogers danks
|
|
194190|D054877||syndromes chromosome 4p
|
|
194190|D054877||syndromes pitt
|
|
194190|D054877||syndrome wolf
|
|
194190|D054877||syndrome wolf hirchhorn
|
|
194190|D054877||syndrome wolf hirschhorn
|
|
194190|D054877||whs
|
|
194190|D054877||wolf hirchhorn syndrome
|
|
194190|D054877||wolf syndrome
|
|
D012532||scabies
|
|
D012532||mange sarcoptic
|
|
D012532||sarcoptic mange
|
|
D055622||orbital myositis
|
|
D055622||myositides orbital
|
|
D055622||myositis orbital
|
|
D055622||orbital myositides
|
|
D011201||poultry diseases
|
|
D011201||disease poultry
|
|
D011201||diseases poultry
|
|
D011201||poultry disease
|
|
D055623||keratosis actinic
|
|
D055623||actinic keratoses
|
|
D055623||actinic keratosis
|
|
D055623||keratoses actinic
|
|
D001855||bone marrow diseases
|
|
D001855||bone marrow disease
|
|
D001855||disease bone marrow
|
|
D001855||diseases bone marrow
|
|
D001855||marrow disease bone
|
|
D001855||marrow diseases bone
|
|
C564298||bile and pancreatic ducts complete absence of
|
|
D001859||bone neoplasms
|
|
D001859||bone cancer
|
|
D001859||bone neoplasm
|
|
D001859||cancer of bone
|
|
D001859||cancer of the bone
|
|
D001859||neoplasm bone
|
|
D001859||neoplasms bone
|
|
D012509||sarcoma
|
|
D012509||epithelioid sarcoma
|
|
D012509||epithelioid sarcomas
|
|
D012509||sarcoma epithelioid
|
|
D012509||sarcomas
|
|
D012509||sarcomas epithelioid
|
|
D012509||sarcoma soft tissue
|
|
D012509||sarcoma spindle cell
|
|
D012509||sarcomas soft tissue
|
|
D012509||sarcomas spindle cell
|
|
D012509||soft tissue sarcoma
|
|
D012509||soft tissue sarcomas
|
|
D012509||spindle cell sarcoma
|
|
D012509||spindle cell sarcomas
|
|
D001851||bone diseases metabolic
|
|
D001851||bone disease metabolic
|
|
D001851||disease metabolic bone
|
|
D001851||diseases metabolic bone
|
|
D001851||metabolic bone disease
|
|
D001851||metabolic bone diseases
|
|
D001851||osteopenia
|
|
D001851||osteopenias
|
|
D001850||bone diseases infectious
|
|
D001850||bone disease infectious
|
|
D001850||disease infectious bone
|
|
D001850||diseases infectious bone
|
|
D001850||infectious bone disease
|
|
D001850||infectious bone diseases
|
|
C535728||dysautonomia like disorder
|
|
D037801||hammer toe syndrome
|
|
D037801||clawtoe
|
|
D037801||claw toe
|
|
D037801||clawtoes
|
|
D037801||claw toes
|
|
D037801||hammer toe
|
|
D037801||hammer toes
|
|
D037801||hammertoe syndrome
|
|
D037801||hammertoe syndromes
|
|
D037801||mallet toe
|
|
D037801||mallet toes
|
|
D037801||syndrome hammertoe
|
|
D037801||syndrome hammer toe
|
|
D037801||syndromes hammertoe
|
|
D037801||toe claw
|
|
D037801||toe hammer
|
|
D037801||toe mallet
|
|
D037801||toes claw
|
|
D037801||toes hammer
|
|
D037801||toes mallet
|
|
C535727||dykes markes harper syndrome
|
|
C535727||ichthyosis hepatosplenomegaly and cerebellar degeneration
|
|
C535727||ichthyosis hepatosplenomegaly cerebellar degeneration
|
|
D013832||thiamine deficiency
|
|
D013832||deficiencies thiamine
|
|
D013832||deficiency thiamine
|
|
D013832||thiamine deficiencies
|
|
131760|D016110||epidermolysis bullosa simplex
|
|
131760|D016110||acral form ebs
|
|
131760|D016110||acral form ebss
|
|
131760|D016110||bullosa simplices epidermolysis
|
|
131760|D016110||ebs acral form
|
|
131760|D016110||ebs dm
|
|
131760|D016110||ebs generalized
|
|
131760|D016110||ebss acral form
|
|
131760|D016110||ebss generalized
|
|
131760|D016110||epidermolysis bullosa herpetiformis dowling meara
|
|
131760|D016110||epidermolysis bullosa herpetiformis dowling meara type
|
|
131760|D016110||epidermolysis bullosa of hands and feet
|
|
131760|D016110||epidermolysis bullosa simplex cockayne touraine type
|
|
131760|D016110||epidermolysis bullosa simplex dowling meara type
|
|
131760|D016110||epidermolysis bullosa simplex generalized
|
|
131760|D016110||epidermolysis bullosa simplex kobner
|
|
131760|D016110||epidermolysis bullosa simplex koebner type
|
|
131760|D016110||epidermolysis bullosa simplex localized
|
|
131760|D016110||epidermolysis bullosa simplex weber cockayne type
|
|
131760|D016110||epidermolysis bullosa simplices
|
|
131760|D016110||generalized ebs
|
|
131760|D016110||generalized ebss
|
|
131760|D016110||weber cockayne syndrome
|
|
131760|D016110||weber cockayne type epidermolysis bullosa simplex
|
|
193000|D014718||vesico ureteral reflux
|
|
193000|D014718||reflux vesicoureteral
|
|
193000|D014718||reflux vesico ureteral
|
|
193000|D014718||vesicoureteral reflux
|
|
193000|D014718||vesicoureteral reflux 1
|
|
193000|D014718||vur
|
|
193000|D014718||vur1
|
|
C535720||familial duodenal atresia
|
|
C535720||duodenal atresia
|
|
C535720||duodenal stenosis
|
|
C535395|256050||atelosteogenesis type 2
|
|
C535395|256050||ao2
|
|
C535395|256050||aoii
|
|
C535395|256050||atelosteogenesis de la chapelle type
|
|
C535395|256050||atelosteogenesis type ii
|
|
C535395|256050||de la chapelle dysplasia
|
|
C535395|256050||dlcd included
|
|
C535395|256050||mcalister dysplasia
|
|
C535395|256050||neonatal osseous dysplasia 1
|
|
C535395|256050||neonatal osseous dysplasia i
|
|
C535395|256050||neonatal osseous dysplasia i de la chapelle dysplasia included
|
|
C535722||duodenojejunal atresia with volvulus absent dorsal mesentery and absent superior mesenteric artery
|
|
C535722||duodenojejunal atresia volvulus absent dorsal mesentery and absent superior mesenteric artery
|
|
C535721||duodenal ulcer due to antral g cell hyperfunction
|
|
C535721||hypergastrinemic hyperpepsinogenemic duodenal ulcer
|
|
C535724||dwarfism stiff joint ocular abnormalities
|
|
C535724||dwarfism with stiff joints and ocular abnormalities
|
|
C535724||moore federman syndrome
|
|
607626|C564365||ichthyosis leukocyte vacuoles alopecia and sclerosing cholangitis
|
|
607626|C564365||ichthyosis sclerosing cholangitis syndrome
|
|
607626|C564365||ilvasc
|
|
607626|C564365||neonatal ichthyosis sclerosing cholangitis syndrome
|
|
607626|C564365||nisch syndrome
|
|
C535723||subungual exostoses
|
|
C535723||dupuytren subungual exostosis
|
|
C535723||exostosis dupuytren subungual
|
|
602400||ichthyosis congenital autosomal recessive 11
|
|
602400||arci11
|
|
602400||arih
|
|
602400||ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis
|
|
602400|C536273||ichthyosis with hypotrichosis autosomal recessive
|
|
602400||ifah
|
|
C538263|607941||atrial septal defect 2
|
|
C538263|607941||asd2
|
|
C535725||dwarfism tall vertebrae
|
|
C535725||dwarfism with disproportionately high vertebral bodies
|
|
C535725||dwarfism with tall vertebrae
|
|
C535725||short stature and tall vertebrae
|
|
607225|C537217||hereditary spastic paralysis infantile onset ascending
|
|
607225|C537217||iahsp
|
|
607225|C537217||infantile onset ascending hereditary spastic paralysis
|
|
607225|C537217||spastic paralysis infantile onset ascending
|
|
C567339|607728|612353||porokeratosis disseminated superficial actinic 4
|
|
C567339|607728||dsap2
|
|
C567339|607728||porok4
|
|
C567339|607728||porokeratosis 4 disseminated superficial actinic type
|
|
C567339|607728|D017499||porokeratosis disseminated superficial actinic 2
|
|
C567838|612964||premature ovarian failure 7
|
|
C567838|612964||pof7
|
|
C565337|605362||cardiomyopathy dilated 1j
|
|
C565337|605362||cardiomyopathy dilated with sensorineural hearing loss autosomal dominant
|
|
C565337|605362||cmd1j
|
|
D000532||altitude sickness
|
|
D000532||altitude sicknesses
|
|
D000532||mountain sickness
|
|
D000532||mountain sicknesses
|
|
D000532||sickness altitude
|
|
D000532||sicknesses altitude
|
|
D000532||sicknesses mountain
|
|
D000532||sickness mountain
|
|
D054319||marchiafava bignami disease
|
|
D054319||marchiafava bignami syndrome
|
|
C538380|238970||hhh syndrome
|
|
C538380|238970||hhh
|
|
C538380|238970||hhhs
|
|
C538380|238970||hyperornithinemia hyperammonemia homocitrullinemia syndrome
|
|
C538380|238970||hyperornithinemia hyperammonemia homocitrullinuria
|
|
C538380|238970||hyperornithinemia hyperammonemia homocitrullinuria syndrome
|
|
C538380|238970||ornithine translocase deficiency
|
|
C538380|238970||triple h syndrome
|
|
D001862||bone resorption
|
|
D001862||bone losses osteoclastic
|
|
D001862||bone loss osteoclastic
|
|
D001862||bone resorptions
|
|
D001862||losses osteoclastic bone
|
|
D001862||loss osteoclastic bone
|
|
D001862||osteoclastic bone loss
|
|
D001862||osteoclastic bone losses
|
|
D001862||resorption bone
|
|
D001862||resorptions bone
|
|
D012513||sarcoma experimental
|
|
D012513||ehs tumor
|
|
D012513||engelbreth holm swarm sarcoma
|
|
D012513||experimental sarcoma
|
|
D012513||experimental sarcomas
|
|
D012513||jensen sarcoma
|
|
D012513||sarcoma engelbreth holm swarm
|
|
D012513||sarcoma jensen
|
|
D012513||sarcomas experimental
|
|
D012513||tumor ehs
|
|
C535738||erythrokeratodermia with ataxia
|
|
C535738||erythrokeratodermia ataxia
|
|
C535738||giroux barbeau syndrome
|
|
D012511||sarcoma 37
|
|
D009477|256800||hereditary sensory and autonomic neuropathies
|
|
D009477|256800||acroosteolyses neurogenic
|
|
D009477|256800|201300||acroosteolysis giaccai type
|
|
D009477|256800|201300||acroosteolysis neurogenic
|
|
D009477|256800||cipa
|
|
D009477|256800||congenital insensitivity to pain with anhidrosis
|
|
D009477|256800||congenital sensory neuropathies
|
|
D009477|256800||congenital sensory neuropathy
|
|
D009477|256800||familial dysautonomia type 2
|
|
D009477|256800||familial dysautonomia type ii
|
|
D009477|256800||giaccai type acroosteolysis
|
|
D009477|256800||hereditary sensory and autonomic neuropathy 4
|
|
D009477|256800||hereditary sensory and autonomic neuropathy iv
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type 1
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type 2
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type 4
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type 5
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type i
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type ii
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type iv
|
|
D009477|256800||hereditary sensory and autonomic neuropathy type v
|
|
D009477|256800||hereditary sensory autonomic neuropathy type 1
|
|
D009477|256800||hereditary sensory autonomic neuropathy type 2
|
|
D009477|256800||hereditary sensory autonomic neuropathy type 4
|
|
D009477|256800||hereditary sensory autonomic neuropathy type 5
|
|
D009477|256800||hereditary sensory neuropathies
|
|
D009477|256800||hereditary sensory neuropathy
|
|
D009477|256800||hereditary sensory neuropathy type 1
|
|
D009477|256800||hereditary sensory neuropathy type i
|
|
D009477|256800||hereditary sensory neuropathy type ia
|
|
D009477|256800||hereditary sensory radicular neuropathy
|
|
D009477|256800||hereditary sensory radicular neuropathy recessive form
|
|
D009477|256800||hsan
|
|
D009477|256800||hsan 1
|
|
D009477|256800||hsan2
|
|
D009477|256800||hsan4
|
|
D009477|256800||hsan 4
|
|
D009477|256800||hsan5
|
|
D009477|256800||hsan 5
|
|
D009477|256800||hsan hereditary sensory autonomic neuropathy
|
|
D009477|256800||hsan i
|
|
D009477|256800||hsanii
|
|
D009477|256800||hsan iv
|
|
D009477|256800||hsans hereditary sensory autonomic neuropathy
|
|
D009477|256800||hsan type i
|
|
D009477|256800||hsan type ii
|
|
D009477|256800||hsan type iv
|
|
D009477|256800||hsan type v
|
|
D009477|256800||hsan v
|
|
D009477|256800||hsn type i
|
|
D009477|256800||hsn type ii
|
|
D009477|256800||hsn type iis
|
|
D009477|256800|D000699||insensitivity to pain congenital
|
|
D009477|256800||insensitivity to pain congenital with anhidrosis
|
|
D009477|256800||insensitivity to pain with anhidrosis congenital
|
|
D009477|256800||neurogenic acroosteolyses
|
|
D009477|256800||neurogenic acroosteolysis
|
|
D009477|256800||neuropathies congenital sensory
|
|
D009477|256800||neuropathies hereditary sensory
|
|
D009477|256800||neuropathies hereditary sensory and autonomic
|
|
D009477|256800|201300||neuropathy congenital sensory
|
|
D009477|256800||neuropathy congenital sensory with anhidrosis
|
|
D009477|256800||neuropathy hereditary sensory
|
|
D009477|256800||neuropathy hereditary sensory and autonomic type 1
|
|
D009477|256800||neuropathy hereditary sensory and autonomic type i
|
|
D009477|256800||neuropathy hereditary sensory and autonomic type v
|
|
D009477|256800||neuropathy hereditary sensory radicular autosomal dominant
|
|
D009477|256800|201300||neuropathy hereditary sensory radicular autosomal recessive
|
|
D009477|256800||neuropathy hereditary sensory type i
|
|
D009477|256800|201300||neuropathy progressive sensory of children
|
|
D009477|256800||pain insensitivity with anhidrosis congenital
|
|
D009477|256800||sensory and autonomic neuropathies hereditary
|
|
D009477|256800||sensory neuropathies congenital
|
|
D009477|256800||sensory neuropathies hereditary
|
|
D009477|256800||sensory neuropathy congenital
|
|
D009477|256800||sensory neuropathy hereditary
|
|
D009477|256800||type i hsan
|
|
D009477|256800||type i hsn
|
|
D009477|256800||type iv hsan
|
|
D012517||sarcoma yoshida
|
|
D012517||reticulum cell like sarcoma yoshida
|
|
D012517||yoshida sarcoma
|
|
D012515||mast cell sarcoma
|
|
D012515||malignant mastocytoma
|
|
D012515||malignant mastocytomas
|
|
D012515||mast cell sarcomas
|
|
D012515||mastocytoma malignant
|
|
D012515||mastocytomas malignant
|
|
D012515||sarcoma mast cell
|
|
D012515||sarcomas mast cell
|
|
C535730||dyschromatosis universalis hereditaria
|
|
C535735||congenital lobar emphysema
|
|
C535735||emphysema congenital lobar
|
|
D054318||no reflow phenomenon
|
|
D054318||phenomenon slow flow
|
|
D054318||slow flow phenomenon
|
|
D012510||sarcoma 180
|
|
D012510||crocker sarcoma 180
|
|
D012510||sarcoma 180 crocker
|
|
C535734||muscular dystrophy tardive emery dreifuss type with contractures
|
|
C535736||encephalocraniocutaneous lipomatosis
|
|
C535736||fishman syndrome
|
|
C564277||immunodeficiency with hyper igm type 4
|
|
C564277||hyper igm syndrome 4
|
|
D016097||simian acquired immunodeficiency syndrome
|
|
D016097||aids simian
|
|
D016097||aidss simian
|
|
D016097||saids
|
|
D016097||simian acquired immune deficiency syndrome
|
|
D016097||simian acquired immuno deficiency syndrome
|
|
D016097||simian aids
|
|
D016097||simian aidss
|
|
D001832||body temperature changes
|
|
D001832||body temperature change
|
|
D001832||change body temperature
|
|
D001832||changes body temperature
|
|
D001832||temperature change body
|
|
D001832||temperature changes body
|
|
D007340|606960||insulinoma
|
|
D007340|606960||adenoma beta cell
|
|
D007340|606960||adenomas beta cell
|
|
D007340|606960||beta cell adenoma
|
|
D007340|606960||beta cell adenomas
|
|
D007340|606960||beta cell tumor
|
|
D007340|606960||beta cell tumors
|
|
D007340|606960||insulinomas
|
|
D007340|606960||insulinoma tumor suppressor gene locus
|
|
D007340|606960||insuloma
|
|
D007340|606960||insulomas
|
|
D007340|606960||tumor beta cell
|
|
D007340|606960||tumors beta cell
|
|
D000506||alopecia areata
|
|
D000506||alopecia circumscripta
|
|
C563875|608691||major depressive disorder 2
|
|
C563875|608691||mdd2
|
|
C563875|608691||unipolar depression 2
|
|
D001836||body weight changes
|
|
D001836||body weight change
|
|
D001836||change body weight
|
|
D001836||changes body weight
|
|
D001836||weight change body
|
|
D001836||weight changes body
|
|
C535751||congenital disorder of glycosylation type 1x
|
|
D001835||body weight
|
|
D001835||body weights
|
|
D001835||weight body
|
|
D001835||weights body
|
|
C563534|161400||narcolepsy 1
|
|
C563534|161400||narcoleptic syndrome 1
|
|
C563534|161400||narcoleptic syndrome 1 cataplexy included
|
|
C563534|161400||nrclp1
|
|
C536603|608553||amaurosis congenita of leber type 9
|
|
C536603|608553||lca9
|
|
C536603|608553||leber congenital amaurosis 9
|
|
C536603|608553||leber congenital amaurosis type 9
|
|
D055652||gray platelet syndrome
|
|
D055652||alpha granule deficiencies platelet
|
|
D055652||alpha granule deficiency platelet
|
|
D055652||gray platelet syndromes
|
|
D055652||grey platelet syndrome
|
|
D055652||grey platelet syndromes
|
|
D055652||platelet alpha granule deficiencies
|
|
D055652||platelet alpha granule deficiency
|
|
D055652||platelet syndromes grey
|
|
D055652||syndrome gray platelet
|
|
D055652||syndrome grey platelet
|
|
D055652||syndromes gray platelet
|
|
C565785|604364||epilepsy partial with variable foci
|
|
C565785|604364||epilepsy familial focal with variable foci
|
|
C565785|604364||ffevf
|
|
C565785|604364||fpevf
|
|
D056988||anterior wall myocardial infarction
|
|
D056988||acute anterior wall myocardial infarction
|
|
D056988||anterolateral myocardial infarction
|
|
D056988||anterolateral myocardial infarctions
|
|
D056988||anteroseptal myocardial infarction
|
|
D056988||anteroseptal myocardial infarctions
|
|
D056988||infarction anterolateral myocardial
|
|
D056988||infarction anteroseptal myocardial
|
|
D056988||infarctions anterolateral myocardial
|
|
D056988||infarctions anteroseptal myocardial
|
|
D056988||myocardial infarction anterior wall
|
|
D056988||myocardial infarction anterolateral
|
|
D056988||myocardial infarction anteroseptal
|
|
D056988||myocardial infarctions anterolateral
|
|
D056988||myocardial infarctions anteroseptal
|
|
D056989||inferior wall myocardial infarction
|
|
D056989||acute inferior myocardial infarction
|
|
D056989||diaphragmatic myocardial infarction
|
|
D056989||diaphragmatic myocardial infarctions
|
|
D056989||infarction diaphragmatic myocardial
|
|
D056989||infarction inferior myocardial
|
|
D056989||infarctions diaphragmatic myocardial
|
|
D056989||infarctions inferior myocardial
|
|
D056989||inferior myocardial infarction
|
|
D056989||inferior myocardial infarctions
|
|
D056989||myocardial infarction diaphragmatic
|
|
D056989||myocardial infarction inferior
|
|
D056989||myocardial infarction inferior wall
|
|
D056989||myocardial infarctions diaphragmatic
|
|
D056989||myocardial infarctions inferior
|
|
C535683|602771||rigid spine syndrome
|
|
C535683|602771||desmin related myopathies with mallory bodies
|
|
C535683|602771||desmin related myopathy with mallory bodies
|
|
C535683|602771||mdrs1
|
|
C535683|602771||minicore myopathy severe classic form
|
|
C535683|602771||multicore myopathy severe classic form
|
|
C535683|602771||multiminicore disease severe classic form
|
|
C535683|602771||muscular dystrophy congenital eichsfeld type
|
|
C535683|602771||muscular dystrophy congenital merosin positive with early spine rigidity
|
|
C535683|602771||myopathy sepn1 related
|
|
C535683|602771||rigid spine muscular dystrophy 1
|
|
C535683|602771||rsmd1
|
|
C535683|602771|D056730|180860||rss
|
|
D000507||mucinosis follicular
|
|
D000507||alopecia mucinosa
|
|
D000507||follicular mucinoses
|
|
D000507||follicular mucinosis
|
|
D000507||mucinoses follicular
|
|
C564285||pseudoxanthoma elasticum modifier of severity of
|
|
D056986||euglenozoa infections
|
|
D056986||euglenozoa infection
|
|
D056986||infection euglenozoa
|
|
D056986||infections euglenozoa
|
|
C564283||lipodystrophy generalized with mental retardation deafness short stature and slender bones
|
|
D056987||vasoplegia
|
|
D056987||post operative vasoplegic syndrome
|
|
D056987||postoperative vasoplegic syndrome
|
|
D056987||post operative vasoplegic syndromes
|
|
D056987||syndrome post operative vasoplegic
|
|
D056987||syndromes post operative vasoplegic
|
|
D056987||vasoplegias
|
|
D056987||vasoplegic syndrome
|
|
D056987||vasoplegic syndrome post operative
|
|
D056987||vasoplegic syndromes post operative
|
|
C564282||campomelic dysplasia with autosomal sex reversal
|
|
C564288|612126||dystonia 18
|
|
C564288||paroxysmal exercise induced dystonia
|
|
C564288||paroxysmal exertion induced dyskinesia
|
|
C563903|608988||atrial fibrillation familial 2
|
|
C563903|608988||atfb2
|
|
C564286||zinc deficiency neonatal due to low breast milk zinc
|
|
261630|D010661|261600||hyperphenylalaninemia bh4 deficient c
|
|
261630|D010661|261600||dhpr deficiency
|
|
261630|D010661|261600||dihydropteridine reductase deficiency
|
|
261630|D010661|261600||hpabh4c
|
|
261630|D010661|261600||hyperphenylalaninemia tetrahydrobiopterin deficient due to dhpr deficiency
|
|
261630|D010661|261600||qdpr deficiency
|
|
261630|D010661|261600||quinoid dihydropteridine reductase deficiency
|
|
D001848||bone diseases developmental
|
|
D001848||bone disease developmental
|
|
D001848||bone dysplasia
|
|
D001848||bone dysplasias
|
|
D001848||developmental bone disease
|
|
D001848||developmental bone diseases
|
|
D001848||dysplasia bone
|
|
D001848||dysplasias bone
|
|
C538246|609924||aminoacylase 1 deficiency
|
|
C538246|609924||acy1d
|
|
C538246|609924||deficiency of the aminoacylase 1 enzyme
|
|
D001847||bone diseases
|
|
D001847||bone disease
|
|
D001847||disease bone
|
|
D001847||diseases bone
|
|
183900|C535788||spondyloepiphyseal dysplasia congenita
|
|
183900|C535788||sedc
|
|
183900|C535788||sed congenita
|
|
183900|C535788||sed congenital type
|
|
183900|C535788||spondyloepiphyseal dysplasia congenital type
|
|
C535762||congenital pseudoarthrosis
|
|
D001845||bone cysts
|
|
D001845||bone cyst
|
|
D001845||cyst bone
|
|
D001845||cysts bone
|
|
D001845||cyst solitary
|
|
D001845||cysts solitary
|
|
D001845||cysts subchondral
|
|
D001845||cyst subchondral
|
|
D001845||ganglia intraosseous
|
|
D001845||ganglia intra osseous
|
|
D001845||ganglias intraosseous
|
|
D001845||ganglias intra osseous
|
|
D001845||ganglion intraosseous
|
|
D001845||ganglion intra osseous
|
|
D001845||ganglions intra osseous
|
|
D001845||intraosseous ganglia
|
|
D001845||intra osseous ganglia
|
|
D001845||intraosseous ganglias
|
|
D001845||intra osseous ganglias
|
|
D001845||intraosseous ganglion
|
|
D001845||intra osseous ganglion
|
|
D001845||intraosseous ganglions
|
|
D001845||intra osseous ganglions
|
|
D001845||solitary cyst
|
|
D001845||solitary cysts
|
|
D001845||subchondral cyst
|
|
D001845||subchondral cysts
|
|
C536163|607654||keratosis palmoplantaris striata 3
|
|
C536163|607654||keratoderma palmoplantar striate form 3
|
|
C536163|607654||keratoderma palmoplantar striate form iii
|
|
C536163|607654||keratosis palmoplantaris striata iii
|
|
C536163|607654||kpps3
|
|
C536163|607654||ppks3
|
|
C536163|607654||sppk3
|
|
C536163|607654||striate palmoplantar keratoderma 3
|
|
C536163|607654||striate palmoplantar keratoderma iii
|
|
C537521|254090||scleroatonic muscular dystrophy
|
|
C537521|254090||late onset scleroatonic familial myopathy
|
|
C537521|254090||muscular dystrophy scleroatonic
|
|
C537521|254090||ucmd
|
|
C537521|254090||ullrich congenital muscular dystrophy
|
|
C537521|254090||ullrich disease
|
|
C537521|254090||ullrich scleroatonic muscular dystrophy
|
|
D015212|266600||inflammatory bowel diseases
|
|
D015212|266600||bowel diseases inflammatory
|
|
D015212|266600||crohn disease associated growth failure susceptibility to included
|
|
D015212|266600||crohn disease included
|
|
D015212|266600||ibd1
|
|
D015212|266600||inflammatory bowel disease
|
|
D015212|266600|D003424||inflammatory bowel disease 1
|
|
D015212|266600||regional enteritis included
|
|
D015212|266600||ulcerative colitis included
|
|
121201||seizures benign familial neonatal 2
|
|
121201||bfnc2
|
|
121201||bfns2
|
|
121201|C535466||convulsions benign familial neonatal 2
|
|
C536277|604288||idiopathic dilation cardiomyopathy
|
|
C536277|604288||cardiomyopathy dilated 1h
|
|
C536277|604288||cardiomyopathy dilated with conduction defect
|
|
C536277|604288||cmd1h
|
|
C536277|604288||dilated cardiomyopathy with conduction defect
|
|
121200||seizures benign familial neonatal 1
|
|
121200||bfns1
|
|
121200||epilepsy benign neonatal 1 and or myokymia included
|
|
121200||seizures benign familial neonatal 1 and or myokymia included
|
|
D019871|305000||dyskeratosis congenita
|
|
D019871|305000||cerebellar hypoplasia with pancytopenia included
|
|
D019871|305000||congenita x linked dyskeratosis
|
|
D019871|305000||dkcx
|
|
D019871|305000||dyskeratosis congenita x linked
|
|
D019871|305000||growth retardation prenatal with progressive pancytopenia and cerebellar hypoplasia included
|
|
D019871|305000||hhs included
|
|
D019871|305000||syndrome zinsser cole engman
|
|
D019871|305000||x linked dyskeratosis congenita
|
|
D019871|305000||x linked dyskeratosis congenitas
|
|
D019871|305000||zinsser cole engman syndrome
|
|
D019871|305000||zinsser cole engman syndrome hoyeraal hreidarsson syndrome included
|
|
D001849||bone diseases endocrine
|
|
D001849||bone disease endocrine
|
|
D001849||disease endocrine bone
|
|
D001849||diseases endocrine bone
|
|
D001849||endocrine bone disease
|
|
D001849||endocrine bone diseases
|
|
C535757||congenital ectodermal dysplasia with hearing loss
|
|
C535757||mikaelian syndrome
|
|
C537014|611775||infantile polyarteritis
|
|
C537014|611775|D009080||kawasaki disease
|
|
C537014|611775|C537017|313200||kd
|
|
C537014|611775|D009080||mucocutaneous lymph node syndrome
|
|
D055665||purpura fulminans
|
|
D055665||fulminans purpura
|
|
C536645|169610||pemphigus vulgaris familial
|
|
C536645|169610||familial pemphigus vulgaris
|
|
C535758||congenital heart block
|
|
C535758||congenital complete heart block
|
|
C535758||familial congenital heart block
|
|
C535758||heart block congenital
|
|
C566798||platelet factor 3 deficiency
|
|
C564135||immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine 1 antagonist
|
|
224690|C538012||meier gorlin syndrome
|
|
224690|C538012||ear patella short stature syndrome
|
|
224690|C538012||eps
|
|
224690|C538012||meier gorlin syndrome 1
|
|
224690|C538012||meier gorlin syndrome 2
|
|
224690|C538012||meier gorlin syndrome 3
|
|
224690|C538012||meier gorlin syndrome 4
|
|
224690|C538012||meier gorlin syndrome 5
|
|
224690|C538012||mgors1
|
|
224690|C538012||mgors2
|
|
224690|C538012||mgors3
|
|
224690|C538012||mgors4
|
|
224690|C538012||mgors5
|
|
224690|C538012||microtia absent patellae micrognathia syndrome
|
|
D001932||brain neoplasms
|
|
D001932||benign brain neoplasm
|
|
D001932||benign brain neoplasms
|
|
D001932||benign neoplasm brain
|
|
D001932||benign neoplasms brain
|
|
D001932||brain benign neoplasm
|
|
D001932||brain benign neoplasms
|
|
D001932||brain cancer
|
|
D001932||brain cancers
|
|
D001932||brain malignant neoplasm
|
|
D001932||brain malignant neoplasms
|
|
D001932||brain neoplasm
|
|
D001932||brain neoplasm benign
|
|
D001932||brain neoplasm malignant
|
|
D001932||brain neoplasm primary
|
|
D001932||brain neoplasms benign
|
|
D001932||brain neoplasms malignant
|
|
D001932||brain neoplasms malignant primary
|
|
D001932||brain neoplasms primary
|
|
D001932||brain neoplasms primary malignant
|
|
D001932||brain tumor
|
|
D001932||brain tumor primary
|
|
D001932||brain tumor recurrent
|
|
D001932||brain tumors
|
|
D001932||brain tumors primary
|
|
D001932||brain tumors recurrent
|
|
D001932||cancer brain
|
|
D001932||cancer of brain
|
|
D001932||cancer of the brain
|
|
D001932||cancers brain
|
|
D001932||intracranial neoplasm
|
|
D001932||intracranial neoplasms
|
|
D001932||malignant brain neoplasm
|
|
D001932||malignant brain neoplasms
|
|
D001932||malignant neoplasm brain
|
|
D001932||malignant neoplasms brain
|
|
D001932||malignant primary brain neoplasms
|
|
D001932||malignant primary brain tumors
|
|
D001932||neoplasm brain
|
|
D001932||neoplasm intracranial
|
|
D001932||neoplasms brain
|
|
D001932||neoplasms brain benign
|
|
D001932||neoplasms brain malignant
|
|
D001932||neoplasms brain primary
|
|
D001932||neoplasms intracranial
|
|
D001932||primary brain neoplasm
|
|
D001932||primary brain neoplasms
|
|
D001932||primary brain tumor
|
|
D001932||primary brain tumors
|
|
D001932||primary malignant brain neoplasms
|
|
D001932||primary malignant brain tumors
|
|
D001932||recurrent brain tumor
|
|
D001932||recurrent brain tumors
|
|
D001932||tumor brain
|
|
D001932||tumors brain
|
|
C536866|600363||spastic paraplegia 6 autosomal dominant
|
|
C536866|600363||familial spastic paraplegia autosomal dominant 3
|
|
C536866|600363||fsp3
|
|
C536866|600363||spg6
|
|
C565468||immunodeficiency partial combined with absence of hla determinants and beta 2 microglobulin from lymphocytes
|
|
C566799||platelet disorder undefined
|
|
614380|C565167||complement component 4a deficiency
|
|
614380||c4ad
|
|
614380||c4a deficiency
|
|
C565469||immune deficiency disease
|
|
D001930||brain injuries
|
|
D001930||acute brain injuries
|
|
D001930||acute brain injury
|
|
D001930||brain contusion
|
|
D001930||brain contusions
|
|
D001930||brain injuries acute
|
|
D001930||brain injuries diffuse
|
|
D001930||brain injuries focal
|
|
D001930||brain injuries traumatic
|
|
D001930||brain injury
|
|
D001930||brain injury acute
|
|
D001930||brain injury diffuse
|
|
D001930||brain injury focal
|
|
D001930||brain injury traumatic
|
|
D001930||brain laceration
|
|
D001930||brain lacerations
|
|
D001930||brain trauma
|
|
D001930||brain traumas
|
|
D001930||contusion brain
|
|
D001930||contusion cortical
|
|
D001930||contusions brain
|
|
D001930||contusions cortical
|
|
D001930||cortical contusion
|
|
D001930||cortical contusions
|
|
D001930||diffuse brain injuries
|
|
D001930||diffuse brain injury
|
|
D001930||encephalopathies post concussive
|
|
D001930||encephalopathies post traumatic
|
|
D001930||encephalopathies traumatic
|
|
D001930||encephalopathy post concussive
|
|
D001930||encephalopathy post traumatic
|
|
D001930||encephalopathy traumatic
|
|
D001930||focal brain injuries
|
|
D001930||focal brain injury
|
|
D001930||injuries acute brain
|
|
D001930||injuries brain
|
|
D001930||injuries diffuse brain
|
|
D001930||injuries focal brain
|
|
D001930||injuries traumatic brain
|
|
D001930||injury acute brain
|
|
D001930||injury brain
|
|
D001930||injury brain traumatic
|
|
D001930||injury brain traumatic mild
|
|
D001930||injury diffuse brain
|
|
D001930||injury focal brain
|
|
D001930||injury traumatic brain
|
|
D001930||laceration brain
|
|
D001930||lacerations brain
|
|
D001930||mild traumatic brain injury
|
|
D001930||post concussive encephalopathies
|
|
D001930||post concussive encephalopathy
|
|
D001930||post traumatic encephalopathies
|
|
D001930||post traumatic encephalopathy
|
|
D001930||tbis traumatic brain injury
|
|
D001930||tbi traumatic brain injury
|
|
D001930||trauma brain
|
|
D001930||traumas brain
|
|
D001930||traumatic brain injuries
|
|
D001930||traumatic brain injury
|
|
D001930||traumatic encephalopathies
|
|
D001930||traumatic encephalopathy
|
|
C566954|611407||cardiomyopathy dilated 1w
|
|
C566954|611407||cmd1w
|
|
C566794||platelet alpha delta storage pool deficiency
|
|
D001935||branchioma
|
|
D001935||branchial cleft cyst
|
|
D001935||branchial cleft cysts
|
|
D001935||branchial cyst
|
|
D001935||branchial cysts
|
|
D001935||branchiomas
|
|
D001935||cleft cyst branchial
|
|
D001935||cleft cysts branchial
|
|
D001935||cyst branchial
|
|
D001935||cyst branchial cleft
|
|
D001935||cysts branchial
|
|
D001935||cysts branchial cleft
|
|
C565465||inosine phosphorylase deficiency immune defect due to
|
|
C566796||platelet signal processing defect
|
|
C565466||indolylacroyl glycinuria with mental retardation
|
|
C564136||immune deficiency familial variable
|
|
D013919||thromboangiitis obliterans
|
|
D013919||buerger disease
|
|
D013919||buerger apos s disease
|
|
D013919||buergers disease
|
|
D013919||disease buerger
|
|
D013919||disease buerger apos s
|
|
D013919||thromboangitis obliterans
|
|
D001249|600807||asthma
|
|
D001249|600807||asthma bronchial
|
|
D001249|600807||asthma diminished response to antileukotriene treatment in included
|
|
D001249|600807||asthma related traits susceptibility to asthma protection against included
|
|
D001249|600807||asthmas
|
|
D001249|600807||asthma susceptibility to
|
|
D001249|600807||bronchial asthma
|
|
605027|D008228||lymphoma non hodgkin
|
|
605027|D008228||diffuse lymphoma
|
|
605027|D008228||diffuse lymphomas
|
|
605027|D008228||diffuse mixed cell lymphoma
|
|
605027|D008228||diffuse mixed cell lymphomas
|
|
605027|D008228||diffuse mixed small and large cell lymphoma
|
|
605027|D008228||diffuse small cleaved cell lymphoma
|
|
605027|D008228||diffuse undifferentiated lymphoma
|
|
605027|D008228||diffuse undifferentiated lymphomas
|
|
605027|D008228||high grade lymphoma
|
|
605027|D008228||high grade lymphomas
|
|
605027|D008228||intermediate grade lymphoma
|
|
605027|D008228||intermediate grade lymphomas
|
|
605027|D008228||low grade lymphoma
|
|
605027|D008228||low grade lymphomas
|
|
605027|D008228||lymphatic sarcoma
|
|
605027|D008228||lymphatic sarcomas
|
|
605027|D008228||lymphocytic histiocytic lymphoma mixed
|
|
605027|D008228||lymphocytic histiocytic lymphomas mixed
|
|
605027|D008228||lymphoma atypical diffuse small lymphoid
|
|
605027|D008228||lymphoma diffuse
|
|
605027|D008228||lymphoma diffuse mixed cell
|
|
605027|D008228||lymphoma diffuse mixed lymphocytic histiocytic
|
|
605027|D008228||lymphoma diffuse undifferentiated
|
|
605027|D008228||lymphoma high grade
|
|
605027|D008228||lymphoma intermediate grade
|
|
605027|D008228||lymphoma low grade
|
|
605027|D008228||lymphoma mixed
|
|
605027|D008228||lymphoma mixed cell
|
|
605027|D008228||lymphoma mixed cell diffuse
|
|
605027|D008228||lymphoma mixed lymphocytic histiocytic
|
|
605027|D008228||lymphoma mixed small and large cell diffuse
|
|
605027|D008228||lymphoma nonhodgkin
|
|
605027|D008228||lymphoma non hodgkin familial
|
|
605027|D008228||lymphoma nonhodgkins
|
|
605027|D008228||lymphoma nonhodgkin apos s
|
|
605027|D008228||lymphoma non hodgkins
|
|
605027|D008228||lymphoma non hodgkin apos s
|
|
605027|D008228||lymphoma pleomorphic
|
|
605027|D008228||lymphomas diffuse
|
|
605027|D008228||lymphomas diffuse mixed cell
|
|
605027|D008228||lymphomas diffuse undifferentiated
|
|
605027|D008228||lymphomas high grade
|
|
605027|D008228||lymphomas intermediate grade
|
|
605027|D008228||lymphomas low grade
|
|
605027|D008228||lymphoma small and large cleaved cell diffuse
|
|
605027|D008228||lymphoma small cleaved cell diffuse
|
|
605027|D008228||lymphoma small noncleaved cell
|
|
605027|D008228||lymphoma small non cleaved cell
|
|
605027|D008228||lymphomas mixed
|
|
605027|D008228||lymphomas mixed cell
|
|
605027|D008228||lymphomas mixed lymphocytic histiocytic
|
|
605027|D008228||lymphomas pleomorphic
|
|
605027|D008228||lymphomas small noncleaved cell
|
|
605027|D008228||lymphomas small non cleaved cell
|
|
605027|D008228||lymphomas undifferentiated
|
|
605027|D008228||lymphoma undifferentiated
|
|
605027|D008228||lymphoma undifferentiated diffuse
|
|
605027|D008228||lymphosarcoma
|
|
605027|D008228||lymphosarcomas
|
|
605027|D008228||mixed cell lymphoma
|
|
605027|D008228||mixed cell lymphoma diffuse
|
|
605027|D008228||mixed cell lymphomas
|
|
605027|D008228||mixed cell lymphomas diffuse
|
|
605027|D008228||mixed lymphocytic histiocytic lymphoma
|
|
605027|D008228||mixed lymphocytic histiocytic lymphomas
|
|
605027|D008228||mixed lymphoma
|
|
605027|D008228||mixed lymphomas
|
|
605027|D008228||mixed small and large cell lymphoma diffuse
|
|
605027|D008228||nhl
|
|
605027|D008228||noncleaved cell lymphoma small
|
|
605027|D008228||non cleaved cell lymphoma small
|
|
605027|D008228||noncleaved cell lymphomas small
|
|
605027|D008228||non cleaved cell lymphomas small
|
|
605027|D008228||non hodgkin lymphoma
|
|
605027|D008228||nonhodgkin apos s lymphoma
|
|
605027|D008228||nonhodgkins lymphoma
|
|
605027|D008228||non hodgkin apos s lymphoma
|
|
605027|D008228||non hodgkins lymphoma
|
|
605027|D008228||pleomorphic lymphoma
|
|
605027|D008228||pleomorphic lymphomas
|
|
605027|D008228||reticulosarcoma
|
|
605027|D008228||reticulosarcomas
|
|
605027|D008228||reticulum cell sarcoma
|
|
605027|D008228||reticulum cell sarcomas
|
|
605027|D008228||sarcoma lymphatic
|
|
605027|D008228||sarcoma reticulum cell
|
|
605027|D008228||sarcomas lymphatic
|
|
605027|D008228||sarcomas reticulum cell
|
|
605027|D008228||small cleaved cell lymphoma diffuse
|
|
605027|D008228||small noncleaved cell lymphoma
|
|
605027|D008228||small non cleaved cell lymphoma
|
|
605027|D008228||small noncleaved cell lymphomas
|
|
605027|D008228||small non cleaved cell lymphomas
|
|
605027|D008228||undifferentiated lymphoma
|
|
605027|D008228||undifferentiated lymphoma diffuse
|
|
605027|D008228||undifferentiated lymphomas
|
|
605027|D008228||undifferentiated lymphomas diffuse
|
|
D056733|160980||carney complex
|
|
D056733|160980||car
|
|
D056733|160980||carney complex type 1
|
|
D056733|160980||carney complex type 2
|
|
D056733|160980||carney complex type i
|
|
D056733|160980||carney complex type ii
|
|
D056733|160980||carney myxoma endocrine complex
|
|
D056733|160980||carney myxoma endocrine complex type 2
|
|
D056733|160980||carney myxoma endocrine complex type ii
|
|
D056733|160980||carney syndrome
|
|
D056733|160980||cnc1
|
|
D056733|160980||cnc2
|
|
D056733|160980||complex carney
|
|
D056733|160980||complex carney myxoma endocrine
|
|
D056733|160980||lamb lentigines atrial myxoma mucocutaneous myoma blue nevus syndrome
|
|
D056733|160980||lamb syndrome
|
|
D056733|160980||lamb syndromes
|
|
D056733|160980||myxoma endocrine complex carney
|
|
D056733|160980||myxoma spotty pigmentation and endocrine overactivity
|
|
D056733|160980||name syndrome
|
|
D056733|160980||name syndromes
|
|
D056733|160980||nevi atrial myxoma skin myxoma ephelides syndrome
|
|
D056733|160980||syndrome carney
|
|
D056733|160980||syndrome lamb
|
|
D056733|160980||syndromes lamb
|
|
C562602|606824||glucose galactose malabsorption
|
|
C562602|606824||carbohydrate intolerance
|
|
C562602|606824||complex carbohydrate intolerance
|
|
C562602|606824||ggm
|
|
C562602|606824||gm
|
|
C562602|606824||monosaccharide malabsorption
|
|
601072||deafness autosomal recessive 8
|
|
601072|C565341||deafness autosomal recessive 10
|
|
601072|C563395||deafness childhood onset neurosensory autosomal recessive 8
|
|
601072|C565341||dfnb10
|
|
601072||dfnb8
|
|
601072|C563395||neurosensory nonsyndromic recessive deafness 8
|
|
601072||nsrd8
|
|
C565471||ichthyosis split hairs and amino aciduria
|
|
D000608||renal aminoacidurias
|
|
D000608||aminoaciduria renal
|
|
D000608||aminoacidurias renal
|
|
D000608||renal aminoaciduria
|
|
C567063|300676||mental retardation x linked syndromic 14
|
|
C567063|300676||mrxs14
|
|
C565473||self healing collodion baby
|
|
154500|D008342||mandibulofacial dysostosis
|
|
154500|D008342||collins syndrome treacher
|
|
154500|D008342||dysostoses mandibulofacial
|
|
154500|D008342||dysostosis mandibulofacial
|
|
154500|D008342||franceschetti zwahlen klein syndrome
|
|
154500|D008342||mandibulofacial dysostoses
|
|
154500|D008342||mandibulofacial dysostosis mfd1
|
|
154500|D008342||mfd1
|
|
154500|D008342||syndrome treacher collins
|
|
154500|D008342||tcof
|
|
154500|D008342||tcs
|
|
154500|D008342||tcs1
|
|
154500|D008342||treacher collins franceschetti syndrome
|
|
154500|D008342||treacher collins syndrome
|
|
154500|D008342||treacher collins syndrome 1
|
|
C537834|217800||macular dystrophy corneal type 1
|
|
C537834|217800||corneal dystrophy macular type
|
|
C537834|217800||groenouw type ii corneal dystrophy
|
|
C537834|217800||macular corneal dystrophy type 1
|
|
C537834|217800||macular corneal dystrophy type i
|
|
C537834|217800||macular corneal dystrophy type i macular corneal dystrophy type ii included
|
|
C537834|217800||macular dystrophy corneal 1
|
|
C537834|217800||mcd
|
|
C537834|217800||mcdc1
|
|
C564140||leber congenital amaurosis 11
|
|
C565478||hypophosphatemia renal with intracerebral calcifications
|
|
C564146||odontohypophosphatasia
|
|
D041441|312700||retinoschisis
|
|
D041441|312700||congenital x linked retinoschisis
|
|
D041441|312700||degenerative retinoschises
|
|
D041441|312700||degenerative retinoschisis
|
|
D041441|312700||juvenile retinoschises
|
|
D041441|312700||juvenile retinoschises x linked
|
|
D041441|312700||juvenile retinoschisis
|
|
D041441|312700||juvenile retinoschisis x linked
|
|
D041441|312700||juveniles retinoschisis x linked
|
|
D041441|312700||retinoschises
|
|
D041441|312700||retinoschises degenerative
|
|
D041441|312700||retinoschises juvenile
|
|
D041441|312700||retinoschises x linked
|
|
D041441|312700||retinoschises x linked juvenile
|
|
D041441|312700||retinoschisis 1 x linked juvenile
|
|
D041441|312700||retinoschisis degenerative
|
|
D041441|312700||retinoschisis juvenile
|
|
D041441|312700||retinoschisis juvenile x chromosome linked
|
|
D041441|312700||retinoschisis juvenile x linked
|
|
D041441|312700||retinoschisis x linked
|
|
D041441|312700||retinoschisis x linked juvenile
|
|
D041441|312700||retinoschisis x linked juveniles
|
|
D041441|312700||rs
|
|
D041441|312700||rs1
|
|
D041441|312700||x linked juvenile retinoschises
|
|
D041441|312700||x linked juvenile retinoschisis
|
|
D041441|312700||x linked juveniles retinoschisis
|
|
D041441|312700||x linked retinoschises
|
|
D041441|312700||x linked retinoschisis
|
|
D041441|312700||xlrs1
|
|
C564144||hypoplasia of teeth roots
|
|
D001941||breast diseases
|
|
D001941||breast disease
|
|
D001941||breast disease endocrine
|
|
D001941||breast diseases endocrine
|
|
D001941||disease breast
|
|
D001941||disease endocrine breast
|
|
D001941||diseases breast
|
|
D001941||diseases endocrine breast
|
|
D001941||endocrine breast disease
|
|
D001941||endocrine breast diseases
|
|
C564143||hypotrichosis simplex of scalp
|
|
C565475||hypouricemia hypercalcinuria and decreased bone density
|
|
D001946||breech presentation
|
|
D001946||breech complete
|
|
D001946||breech fetal presentation
|
|
D001946||breech incomplete
|
|
D001946||breech labor presentation
|
|
D001946||breech presentation frank
|
|
D001946||complete breech
|
|
D001946||fetal presentation breech
|
|
D001946||frank breech presentation
|
|
D001946||incomplete breech
|
|
D001946||labor presentation breech
|
|
D001946||presentation breech
|
|
D001946||presentation breech fetal
|
|
D001946||presentation breech labor
|
|
D001946||presentation frank breech
|
|
C564148||hypoparathyroidism autosomal recessive
|
|
C565477||hypopituitarism congenital with central diabetes insipidus
|
|
D013927||thrombosis
|
|
D013927||thromboses
|
|
D013927||thrombus
|
|
614379||complement component 4b deficiency
|
|
614379||c4bd
|
|
614379||c4b deficiency
|
|
D013921||thrombocytopenia
|
|
D013921||thrombocytopenias
|
|
D013921||thrombopenia
|
|
D013921||thrombopenias
|
|
D013922||thrombocytosis
|
|
D013922||thrombocythemia
|
|
D013922||thrombocythemias
|
|
D013922||thrombocytoses
|
|
C536907||thymic renal anal lung dysplasia
|
|
C536904||thumb deformity alopecia pigmentation anomaly
|
|
C536904||congenital deformity of the thumb and congenital alopecia
|
|
C536904||hypotrichosis associated with congenital hypoplasia of the thumb
|
|
C536905||thymic epithelial tumor
|
|
C536905||epithelial tumor of thymus
|
|
C536905||thymoma adult
|
|
D013923||thromboembolism
|
|
D013923||thromboembolisms
|
|
C536908||thyrocerebral retinal syndrome
|
|
C536908||thyrocerebroretinal syndrome
|
|
D013924||thrombophlebitis
|
|
D013924||dolens phlegmasia alba
|
|
D013924||phlegmasia alba dolens
|
|
D013924||thrombophlebitides
|
|
C536909||thyroglossal tract cyst
|
|
C536909||familial thyroglossal duct cyst
|
|
C536909||hereditary thyroglossal duct cysts
|
|
C536909||thyroglossal duct cyst familial
|
|
C536909||thyroglossal duct cysts familial
|
|
C565481||hypohidrosis aith abnormal palmar dermal ridges
|
|
C565481||sweat gland hypoplasia
|
|
C565482||hypogonadism with low grade mental deficiency and microcephaly
|
|
C565484||hypoglycemia neonatal simulating foetopathia diabetica
|
|
D001948||brenner tumor
|
|
D001948||benign brenner tumor
|
|
D001948||brenner tumor benign
|
|
D001948||brenner tumor malignant
|
|
D001948||brenner tumor of ovary
|
|
D001948||brenner tumor proliferative
|
|
D001948||malignant brenner tumor
|
|
D001948||ovarian brenner tumor
|
|
D001948||ovary brenner tumor
|
|
D001948||proliferative brenner tumor
|
|
C536903||thumb deformity
|
|
C536903||thumb absent or hypoplastic
|
|
C536903||thumb hypoplastic
|
|
C564152||hypertrophia musculorum vera
|
|
C536900||thrombomodulin anomalies familial
|
|
C564151||hypocalciuric hypercalcemia acquired
|
|
C536901||thrombotic thrombocytopenic purpura acquired
|
|
C536901||idiopathic thrombotic thrombocytopenic purpura
|
|
C536901||moschowitz syndrome
|
|
611283|C535541||isobutyryl coa dehydrogenase deficiency
|
|
611283|C535541||acad8 deficiency
|
|
611283|C535541||acyl coa dehydrogenase family member 8 deficiency of
|
|
611283|C535541||ibd deficiency
|
|
611283|C535541||isobutyryl coenzyme a dehydrogenase deficiency
|
|
C566776||polyposis intestinal with multiple exostoses
|
|
C565446||lactic aciduria due to d lactic acid
|
|
C564112||leukemia acute x linked
|
|
C566778||adenomatous polyposis coli attenuated
|
|
C566778||brain tumor polyposis syndrome 2
|
|
260350||pancreatic cancer pancreatic carcinoma
|
|
260350|D010190|260350|C562463||pancreatic acinar carcinoma
|
|
C564110||macular dystrophy x linked
|
|
C565441||leukemia acute myelocytic with polyposis coli and colon cancer
|
|
C565442||leg absence deformity of with congenital cataract
|
|
C566773||polysyndactyly crossed
|
|
D016170||accelerated idioventricular rhythm
|
|
D016170||accelerated idioventricular rhythms
|
|
D016170||aivr
|
|
D016170||idioventricular rhythm accelerated
|
|
D016170||idioventricular rhythms accelerated
|
|
D016170||slow ventricular tachycardia
|
|
D016170||slow ventricular tachycardias
|
|
D016170||ventricular tachycardia slow
|
|
D016170||ventricular tachycardias slow
|
|
D001913||bowen apos s disease
|
|
D001913||bowen disease
|
|
D001913||bowens disease
|
|
D001913||disease bowen
|
|
D001913||disease bowen apos s
|
|
C566774||polyps multiple and recurrent inflammatory fibroid gastrointestinal
|
|
D016171||torsades de pointes
|
|
D016171||de pointes torsade
|
|
D016171||de pointes torsades
|
|
D016171||pointes torsade de
|
|
D016171||pointes torsades de
|
|
D016171||torsade de pointes
|
|
D001912||bovine virus diarrhea mucosal disease
|
|
D001912||mucosal disease bovine viral diarrhea
|
|
C566775||polyposis of gastric fundus without polyposis coli
|
|
C566775||fundic gland polyposis
|
|
C564118||jaundice familial obstructive of infancy
|
|
C562490|115080||cardiac conduction defect
|
|
C562490|115080||familial sudden death included
|
|
C562490|115080||scd included
|
|
C562490|115080||sudden cardiac death included
|
|
D004195||disease models animal
|
|
D004195||animal disease model
|
|
D004195||animal disease models
|
|
D004195||disease model animal
|
|
C536918||tibia absent polydactyly arachnoid cyst
|
|
C567652|613291||bile acid malabsorption primary
|
|
C567652|613291||pbam
|
|
D004194||disease
|
|
C536916||thyroid hormone plasma membrane transport defect
|
|
C536916||hyperthyroxinemia eumetabolic due to t4 plasma membrane transport
|
|
C536916||thyroid hormone resistance due to t4 plasma membrane transport defect
|
|
D053159||dysuria
|
|
C536910||thyroid cancer anaplastic
|
|
C536910||anaplastic thyroid cancer
|
|
C536910||anaplastic thyroid carcinoma
|
|
C536910||thyroid carcinoma anaplastic
|
|
C566780||actinic prurigo
|
|
C566780||polymorphic light eruption hereditary
|
|
D053158||nocturia
|
|
D053158||nycturia
|
|
C566781||juvenile spring eruption of ears
|
|
D017497||hidradenitis suppurativa
|
|
D017497||acne inversa
|
|
D017497||acne inversas
|
|
D017497||hidradenitides suppurative
|
|
D017497||hidradenitis suppurative
|
|
D017497||inversa acne
|
|
D017497||inversas acne
|
|
D017497||suppurative hidradenitides
|
|
D017497||suppurative hidradenitis
|
|
C564120||immunodeficiency x linked with deficiency of 115 000 dalton surface glycoprotein
|
|
C564120||gpl115 deficiency
|
|
C536914||thyroid cancer medullary
|
|
C536914||medullary thyroid cancer mtc
|
|
C536914||thyroid carcinoma medullary
|
|
D017499||porokeratosis
|
|
D017499||disseminated superficial actinic porokeratosis
|
|
D017499||keratoderma palmoplantar punctate type 2
|
|
D017499||linear porokeratosis
|
|
D017499||mibelli porokeratosis
|
|
D017499||palmoplantar porokeratosis
|
|
D017499||porokeratosis disseminated superficial actinic
|
|
D017499||porokeratosis linear
|
|
D017499||porokeratosis mibelli
|
|
D017499||porokeratosis of mibelli
|
|
D017499|C536338|175850||porokeratosis palmaris et plantaris disseminata
|
|
D017499|C536338|175850||porokeratosis palmar plantar and disseminated 1
|
|
D017499||porokeratosis palmoplantar
|
|
D017499|C536338|175850||porokeratosis plantaris palmaris et disseminata
|
|
D017499||porokeratosis punctate
|
|
D017499||punctate porokeratosis
|
|
D017499||type 2 punctate ppk
|
|
D001919||bradycardia
|
|
D001919||bradyarrhythmia
|
|
D001919||bradyarrhythmias
|
|
D001919||bradycardias
|
|
C565456||keratoconus and congenital hip dysplasia
|
|
C564122||hyperthyroxinemia due to decreased peripheral conversion of t4
|
|
C564122||5 prime deiodinase deficiency generalized causing euthyroid hyperthyroxinemia
|
|
C565452||kniest like dysplasia with pursed lips and ectopia lentis
|
|
C565452||burton syndrome
|
|
C566783||crossed polydactyly type i
|
|
C564128||indifference to pain congenital autosomal dominant
|
|
C564128||congenital analgesia autosomal dominant
|
|
D016180||lentivirus infections
|
|
D016180||infection lentivirus
|
|
D016180||infections lentivirus
|
|
D016180||lentivirus infection
|
|
D001925||brain damage chronic
|
|
D001925||chronic brain damage
|
|
D001925||chronic encephalopathy
|
|
D001925||encephalopathy chronic
|
|
C565453||ketoadipicaciduria
|
|
C566784||polydactyly preaxial iii
|
|
C566784||index finger polydactyly
|
|
C564127||inosine triphosphatase deficiency
|
|
D016181||feline acquired immunodeficiency syndrome
|
|
D016181||aids feline
|
|
D016181||faids
|
|
D016181||feline acquired immune deficiency syndrome
|
|
D016181||feline acquired immuno deficiency syndrome
|
|
D016181||feline aids
|
|
D001924||brain concussion
|
|
D001924||brain concussions
|
|
D001924||cerebral concussion
|
|
D001924||cerebral concussions
|
|
D001924||commotio cerebri
|
|
D001924||concussion brain
|
|
D001924||concussion cerebral
|
|
D001924||concussion intermediate
|
|
D001924||concussion mild
|
|
D001924||concussion severe
|
|
D001924||intermediate concussion
|
|
D001924||intermediate concussions
|
|
D001924||mild concussion
|
|
D001924||mild concussions
|
|
D001924||severe concussion
|
|
D001924||severe concussions
|
|
C565454||keratoderma palmoplantar norrbotten recessive type
|
|
D016182||visna
|
|
D016182||encephalomyelitides ovine
|
|
D016182||encephalomyelitis ovine
|
|
D016182||ovine encephalomyelitides
|
|
D016182||ovine encephalomyelitis
|
|
D016182||visnas
|
|
C565455||keratoconus posticus circumscriptus with associated malformations
|
|
C565455||kpc with associated malformations
|
|
C564125||internal carotid artery spontaneous dissection of
|
|
D016183||murine acquired immunodeficiency syndrome
|
|
D016183||aids murine
|
|
D016183||aidss murine
|
|
D016183||maids
|
|
D016183||murine acquired immune deficiency syndrome
|
|
D016183||murine acquired immuno deficiency syndrome
|
|
D016183||murine aids
|
|
D016183||murine aidss
|
|
D001922||brain abscess
|
|
D001922||abscess brain
|
|
D001922||abscess cerebral
|
|
D001922||abscess child brain
|
|
D001922||abscesses cerebral
|
|
D001922||abscesses multiple brain
|
|
D001922||abscess multiple brain
|
|
D001922||abscess pyogenic brain
|
|
D001922||brain abscess child
|
|
D001922||brain abscesses
|
|
D001922||brain abscesses multiple
|
|
D001922||brain abscesses pyogenic
|
|
D001922||brain abscesses sterile
|
|
D001922||brain abscess multiple
|
|
D001922||brain abscess pyogenic
|
|
D001922||brain abscess sterile
|
|
D001922||cerebral abscess
|
|
D001922||cerebral abscesses
|
|
D001922||child brain abscess
|
|
D001922||multiple brain abscess
|
|
D001922||multiple brain abscesses
|
|
D001922||pyogenic brain abscess
|
|
D001922||pyogenic brain abscesses
|
|
D001922||sterile brain abscess
|
|
D001922||sterile brain abscesses
|
|
D004198||disease susceptibility
|
|
D004198||diatheses
|
|
D004198||diathesis
|
|
D004198||disease susceptibilities
|
|
D004198||susceptibilities disease
|
|
D004198||susceptibility disease
|
|
C563869|608728||spondyloepimetaphyseal dysplasia matrilin 3 related
|
|
C563869|608728||semd matn3 related
|
|
D029481||bronchitis chronic
|
|
D029481||chronic bronchitis
|
|
C536927||tunglang savage bellman syndrome
|
|
C536927||hearing loss and familial salivary gland insensitivity to aldosterone
|
|
C536927||hearing loss insensitivity to aldosterone
|
|
D013901||thoracic outlet syndrome
|
|
D013901||aperture syndrome thoracic outlet
|
|
D013901||arterial thoracic outlet syndrome
|
|
D013901||costoclavicular syndrome
|
|
D013901||costoclavicular syndromes
|
|
D013901||nerve compression syndrome thoracic outlet
|
|
D013901||neurogenic thoracic outlet syndrome
|
|
D013901||neurologic syndrome thoracic outlet
|
|
D013901||neurovascular syndrome thoracic outlet
|
|
D013901||outlet syndromes thoracic
|
|
D013901||outlet syndrome thoracic
|
|
D013901||scalenus anticus syndrome
|
|
D013901||superior thoracic aperture syndrome
|
|
D013901||syndrome costoclavicular
|
|
D013901||syndrome scalenus anticus
|
|
D013901||syndromes costoclavicular
|
|
D013901||syndromes thoracic outlet
|
|
D013901||syndrome thoracic outlet
|
|
D013901||thoracic outlet nerve compression syndrome
|
|
D013901||thoracic outlet neurologic syndrome
|
|
D013901||thoracic outlet neurovascular syndrome
|
|
D013901||thoracic outlet syndrome neurogenic
|
|
D013901||thoracic outlet syndromes
|
|
D013901||venous thoracic outlet syndrome
|
|
C563786|609152||hyperthyroidism nonautoimmune
|
|
C563786|609152||hyperthyroidism congenital nonautoimmune
|
|
C563786|609152||hyperthyroidism nonautoimmune autosomal dominant
|
|
C563786|609152||toxic thyroid hyperplasia autosomal dominant
|
|
D001929||brain edema
|
|
D001929||brain edema cytotoxic
|
|
D001929||brain edema vasogenic
|
|
D001929||brain swelling
|
|
D001929||brain swellings
|
|
D001929||cerebral edema
|
|
D001929||cerebral edema cytotoxic
|
|
D001929||cerebral edemas vasogenic
|
|
D001929||cerebral edema vasogenic
|
|
D001929||cytotoxic brain edema
|
|
D001929||cytotoxic cerebral edema
|
|
D001929||edema brain
|
|
D001929||edema cerebral
|
|
D001929||edema cytotoxic brain
|
|
D001929||edema cytotoxic cerebral
|
|
D001929||edema intracranial
|
|
D001929||edema vasogenic brain
|
|
D001929||edema vasogenic cerebral
|
|
D001929||intracranial edema
|
|
D001929||swelling brain
|
|
D001929||vasogenic brain edema
|
|
D001929||vasogenic cerebral edema
|
|
C536921||tiglic acidemia
|
|
C536921||disorder of isoleucine metabolism
|
|
C565460||jejunal atresia with microcephaly and ocular anomalies
|
|
C565460||apple peel syndrome with microcephaly and ocular anomalies
|
|
C565460||stromme syndrome
|
|
D001928||brain diseases metabolic
|
|
D001928||acquired metabolic diseases brain
|
|
D001928||acquired metabolic diseases nervous system
|
|
D001928||acquired metabolic encephalopathies
|
|
D001928||acquired metabolic encephalopathy
|
|
D001928||brain disease metabolic
|
|
D001928||brain diseases metabolic acquired
|
|
D001928||brain disorder metabolic
|
|
D001928||brain disorders metabolic
|
|
D001928||brain disorders metabolic acquired
|
|
D001928||brain metabolic disorder
|
|
D001928||brain metabolic disorders
|
|
D001928||brain syndrome metabolic
|
|
D001928||brain syndrome metabolic acquired
|
|
D001928||central nervous system metabolic disorders
|
|
D001928||cns metabolic disorder
|
|
D001928||cns metabolic disorders
|
|
D001928||cns metabolic disorders acquired
|
|
D001928||encephalopathies acquired metabolic
|
|
D001928||encephalopathies metabolic
|
|
D001928||encephalopathy acquired metabolic
|
|
D001928||encephalopathy metabolic
|
|
D001928||encephalopathy metabolic acquired
|
|
D001928||metabolic brain disease
|
|
D001928||metabolic brain diseases
|
|
D001928||metabolic brain diseases acquired
|
|
D001928||metabolic brain disorder
|
|
D001928||metabolic brain disorders
|
|
D001928||metabolic brain syndrome
|
|
D001928||metabolic brain syndrome acquired
|
|
D001928||metabolic brain syndromes
|
|
D001928||metabolic brain syndromes acquired
|
|
D001928||metabolic diseases acquired nervous system
|
|
D001928||metabolic disorder brain
|
|
D001928||metabolic disorder central nervous system acquired
|
|
D001928||metabolic disorder cns
|
|
D001928||metabolic disorders brain
|
|
D001928||metabolic disorders central nervous system
|
|
D001928||metabolic disorders cns
|
|
D001928||metabolic disorders cns acquired
|
|
D001928||metabolic encephalopathies
|
|
D001928||metabolic encephalopathies acquired
|
|
D001928||metabolic encephalopathy
|
|
D001928||metabolic encephalopathy acquired
|
|
D001928||nervous system acquired metabolic diseases
|
|
C565461||intrinsic factor and r binder combined congenital deficiency of
|
|
C566792||potter type iii polycystic kidney disease
|
|
D001927||brain diseases
|
|
D001927||brain disease
|
|
D001927||brain disorder
|
|
D001927||brain disorders
|
|
D001927||brain pathology
|
|
D001927||central nervous system disorders intracranial
|
|
D001927||central nervous system intracranial disorders
|
|
D001927||cns disorder intracranial
|
|
D001927||cns disorders intracranial
|
|
D001927||encephalon disease
|
|
D001927||encephalon diseases
|
|
D001927||intracranial central nervous system disorders
|
|
D001927||intracranial cns disorder
|
|
D001927||intracranial cns disorders
|
|
D001927||pathology brain
|
|
C565462||iris coloboma with ptosis hypertelorism and mental retardation
|
|
C566793||pectoralis muscle absence of
|
|
C535556|300262||abidi x linked mental retardation syndrome
|
|
C535556|300262||mental retardation x linked abidi type
|
|
C535556|300262||mental retardation x linked syndromic abidi type
|
|
C535556|300262||mrxsab
|
|
C535556|300262||short stature small head circumference sloping forehead hearing loss cupped ears and small testes
|
|
D001926||brain death
|
|
D001926||brain dead
|
|
D001926||brain deads
|
|
D001926||coma depasse
|
|
D001926||coma irreversible
|
|
D001926||death brain
|
|
D001926||irreversible coma
|
|
C536924||tufted angioma
|
|
C536924||angioma tufted
|
|
C564131||kappa chain deficiency
|
|
604715|D054971||orthostatic intolerance
|
|
604715|D054971||intolerance orthostatic
|
|
604715|D054971|C531763||irritable heart
|
|
604715|D054971|D008945||mitral valve prolapse syndrome
|
|
604715|D054971|D009449||neurocirculatory asthenia
|
|
604715|D054971|C531763||soldiers heart
|
|
C536922||tubulointerstitial nephritis and uveitis
|
|
C536922||tubulointerstitial nephritis with uveitis
|
|
C536923||tucker syndrome
|
|
C536923||congenital bilateral recurrent nerve paralysis and ptosis
|
|
C536923||ptosis vocal cord paralysis
|
|
C536923||vocal cord paralysis and ptosis
|
|
C566754||pruritus hereditary localized
|
|
C566755||hyperprothrombinemia
|
|
C566755||prothrombin g20210a thrombophilia
|
|
C566755||prothrombin thrombophilia
|
|
C565021|134610||familial mediterranean fever autosomal dominant
|
|
C565021|134610||fmf autosomal dominant
|
|
C565425||macrosomia adiposa congenita
|
|
D017484||dermatitis phototoxic
|
|
D017484||contact dermatitides phototoxic
|
|
D017484||contact dermatitis phototoxic
|
|
D017484||dermatitides phototoxic
|
|
D017484||dermatitides phototoxic contact
|
|
D017484||dermatitis contact phototoxic
|
|
D017484||dermatitis phototoxic contact
|
|
D017484||phototoxic contact dermatitides
|
|
D017484||phototoxic contact dermatitis
|
|
D017484||phototoxic dermatitides
|
|
D017484||phototoxic dermatitis
|
|
D017484||phototoxicity
|
|
C566757||pronation supination of the forearm impairment of
|
|
D016154||digestive system fistula
|
|
D016154||digestive system fistulas
|
|
D016154||fistula digestive system
|
|
D016154||fistulas digestive system
|
|
C566750||acholinesterasemia
|
|
C565420||mandibulofacial dysostosis with mental deficiency
|
|
C566751||butyrylcholinesterase deficiency fluoride resistant japanese type
|
|
C566751||hypocholinesterasemia fluoride resistant japanese type
|
|
C565421||malocclusion and short stature
|
|
C566753||pseudoarthrogryposis
|
|
C566753||ankylosis at elbow and knee
|
|
C566753||hereditary congenital rigidity of elbows and knees
|
|
D004169||diphyllobothriasis
|
|
D004169||diphyllobothriases
|
|
116600||cataract 6 multiple types
|
|
116600|C567814||arcc2
|
|
116600|C567814||cataract age related cortical 2
|
|
116600|C535339||cataract posterior polar 1
|
|
116600||ctpp1
|
|
116600||ctrct6
|
|
160900|C538008||dystrophia myotonica 1
|
|
160900|C538008||dm
|
|
160900|C538008||dm1
|
|
160900|C538008|D009223||dystrophia myotonica
|
|
160900|C538008||myotonic dystrophy 1
|
|
160900|C538008|D009223||steinert disease
|
|
160900|C538008||steinert myotonic dystrophy
|
|
D005497||follicular cyst
|
|
D005497||cyst follicular
|
|
D005497||cysts follicular
|
|
D005497||follicular cysts
|
|
C565427||lymphopenic hypergammaglobulinemia antibody deficiency autoimmune hemolytic anemia and glomerulonephritis
|
|
D049914||dna repair deficiency disorders
|
|
D049914||chromosome instability syndrome
|
|
D049914||chromosome instability syndromes
|
|
D049914||deficient dna repair
|
|
D049914||deficient dna repairs
|
|
D049914||disorder dna repair deficiency
|
|
D049914||disorders dna repair deficiency
|
|
D049914||dna repair deficiencies
|
|
D049914||dna repair deficiency
|
|
D049914||dna repair deficiency disorder
|
|
D049914||dna repair deficient
|
|
D049914||dna repairs deficient
|
|
D049914||repair deficient dna
|
|
D049914||repairs deficient dna
|
|
D049914||syndrome chromosome instability
|
|
D049914||syndromes chromosome instability
|
|
C565428||lymphokine deficiency
|
|
D004165||diphtheria
|
|
D004165||diphtherias
|
|
C566759||primary release disorder of platelets
|
|
D005499||folliculitis
|
|
D005499||folliculitides
|
|
D005499||sycoses
|
|
D005499||sycosis
|
|
256850|D056768||giant axonal neuropathy
|
|
256850|D056768||axonal neuropathy giant
|
|
256850|D056768||axonal neuropathy giant gan
|
|
256850|D056768||gan
|
|
256850|D056768||gan1
|
|
256850|D056768||giant axonal neuropathy 1
|
|
256850|D056768||giant axonal neuropathy 1 autosomal recessive
|
|
256850|D056768||giant axonal neuropathy 1 gan1
|
|
256850|D056768||giant axonal neuropathy gan
|
|
256850|D056768||neuropathy giant axonal
|
|
256850|D056768||neuropathy giant axonal autosomal recessive
|
|
256850|D056768||neuropathy giant axonal gan
|
|
D004172||diplopia
|
|
D004172||cortical diplopia
|
|
D004172||cortical diplopias
|
|
D004172||diplopia cortical
|
|
D004172||diplopia horizontal
|
|
D004172||diplopia intermittent
|
|
D004172||diplopia monocular
|
|
D004172||diplopia refractive
|
|
D004172||diplopias
|
|
D004172||diplopias cortical
|
|
D004172||diplopias horizontal
|
|
D004172||diplopias intermittent
|
|
D004172||diplopias monocular
|
|
D004172||diplopias refractive
|
|
D004172||diplopias unilateral
|
|
D004172||diplopias vertical
|
|
D004172||diplopia unilateral
|
|
D004172||diplopia vertical
|
|
D004172||double vision
|
|
D004172||horizontal diplopia
|
|
D004172||horizontal diplopias
|
|
D004172||intermittent diplopia
|
|
D004172||intermittent diplopias
|
|
D004172||monocular diplopia
|
|
D004172||monocular diplopias
|
|
D004172||polyopsia
|
|
D004172||polyopsias
|
|
D004172||refractive diplopia
|
|
D004172||refractive diplopias
|
|
D004172||unilateral diplopia
|
|
D004172||unilateral diplopias
|
|
D004172||vertical diplopia
|
|
D004172||vertical diplopias
|
|
D004172||vision double
|
|
C535407|613163||gamma aminobutyric acid transaminase deficiency
|
|
C535407|613163||4 alpha aminobutyrate transaminase deficiency
|
|
C535407|613163||gaba transaminase deficiency
|
|
C535407|613163||gamma aminobutyrate transaminase deficiency
|
|
C536465|600193||waardenburg syndrome type 2b
|
|
C536465|600193||waardenburg syndrome type iib
|
|
C536465|600193||ws2b
|
|
C566765||long qt syndrome 2 5
|
|
C565436||fibular aplasia tibial campomelia and oligosyndactyly syndrome
|
|
C565436||fatco syndrome
|
|
C566767||postaxial oligodactyly tetramelic
|
|
D017495||hyperpigmentation
|
|
D017495||hypermelanoses
|
|
D017495||hypermelanosis
|
|
C564100|309630||metacarpal 4 5 fusion
|
|
C565437|246560||limb deficiencies distal with micrognathia
|
|
C565437|246560||split hand foot malformation 3
|
|
C566768||porphyria cutanea tarda type i
|
|
C566768||pct sporadic type
|
|
C566768||pct type i
|
|
D017496||hypopigmentation
|
|
D017496||hypomelanoses
|
|
D017496||hypomelanosis
|
|
C565430||lymphoid system deterioration progressive
|
|
C565431||lymphoblastic transformation intrinsic defect in
|
|
C566762||sacral agenesis syndrome
|
|
C566762||sacral agenesis hereditary with presacral mass anterior meningocele and or teratoma and anorectal malformation
|
|
D018192|606690||lymphangioleiomyomatosis
|
|
D018192|606690||lam
|
|
D018192|606690||lymphangioleiomyomatoses
|
|
D018192|606690||lymphangiomyomatoses
|
|
D018192|606690||lymphangiomyomatosis
|
|
C565432||lymphedema congenital recessive
|
|
C565433||lymphoblastic transformation inhibition of
|
|
C566764||prader willi like syndrome associated with chromosome 6
|
|
613000|C538682||palmoplantar keratoderma nonepidermolytic focal
|
|
613000|C538682||fneppk
|
|
613000|C538682||focal nonepidermolytic palmoplantar keratoderma
|
|
613000|C538682||keratoderma focal nonepidermolytic palmoplantar
|
|
607115|D056587||cryopyrin associated periodic syndromes
|
|
607115|D056587||caps3
|
|
607115|D056587||chronic infantile neurological cutaneous and articular syndrome
|
|
607115|D056587||chronic infantile neurological cutaneous articular syndrome
|
|
607115|D056587||chronic infantile neurologic cutaneous and articular syndrome
|
|
607115|D056587||chronic neurologic cutaneous and articular syndrome
|
|
607115|D056587||cinca
|
|
607115|D056587||cinca syndrome
|
|
607115|D056587|120100||cold induced autoinflammatory syndrome familial
|
|
607115|D056587|120100||cold urticaria familial
|
|
607115|D056587||cold urticarias familial
|
|
607115|D056587||cryopyrin associated periodic syndrome
|
|
607115|D056587||cryopyrin associated periodic syndrome 3
|
|
607115|D056587||cryopyrinopathies
|
|
607115|D056587||cryopyrinopathy
|
|
607115|D056587||familial cold autoinflammatory syndrome
|
|
607115|D056587|120100||familial cold autoinflammatory syndrome 1
|
|
607115|D056587||familial cold induced autoinflammatory syndrome
|
|
607115|D056587||familial cold urticaria
|
|
607115|D056587||familial cold urticarias
|
|
607115|D056587|120100||fcas1
|
|
607115|D056587||infantile onset multisystem inflammatory disease
|
|
607115|D056587||iomid
|
|
607115|D056587||iomid syndrome
|
|
607115|D056587||iomid syndromes
|
|
607115|D056587||multisystem inflammatory disease neonatal onset
|
|
607115|D056587||neonatal onset multisystem inflammatory disease
|
|
607115|D056587||nomid
|
|
607115|D056587||periodic syndrome cryopyrin associated
|
|
607115|D056587||periodic syndromes cryopyrin associated
|
|
607115|D056587||prieur griscelli syndrome
|
|
607115|D056587||prieur griscelli syndromes
|
|
607115|D056587||syndrome cryopyrin associated periodic
|
|
607115|D056587||syndrome iomid
|
|
607115|D056587||syndrome muckle wells
|
|
607115|D056587||syndrome prieur griscelli
|
|
607115|D056587||syndromes cryopyrin associated periodic
|
|
607115|D056587||syndromes iomid
|
|
607115|D056587||syndromes prieur griscelli
|
|
607115|D056587||syndromes uda
|
|
607115|D056587||syndromes urticaria deafness amyloidosis
|
|
607115|D056587||syndrome uda
|
|
607115|D056587||syndrome urticaria deafness amyloidosis
|
|
607115|D056587||uda syndromes
|
|
607115|D056587||urticaria deafness amyloidosis syndromes
|
|
607115|D056587||urticaria deafness and amyloidosis
|
|
607115|D056587||urticaria familial cold
|
|
607115|D056587||urticarias familial cold
|
|
C564109||male pseudohermaphroditism due to deficiency of testicular 17 20 desmolase
|
|
C567389|612240||atrial fibrillation familial 7
|
|
C567389|612240||atfb7
|
|
C564107||mental retardation associated with psoriasis
|
|
C567273|127500||dyschromatosis universalis hereditaria 1
|
|
C567273|127500||duh1
|
|
C565438||limb defects distal transverse with mental retardation and spasticity
|
|
C566769||porphyria acute intermittent nonerythroid variant
|
|
C565439||leukotriene c4 synthase deficiency
|
|
C565439||ltc4 synthase deficiency
|
|
C567315|612437||epilepsy progressive myoclonic 1b
|
|
C567315|612437|C580388||epm1b
|
|
D004184||dirofilariasis
|
|
D004184||dirofilariases
|
|
D004184||disease heartworm
|
|
D004184||heartworm disease
|
|
D010214|245000||papillon lefevre disease
|
|
D010214|245000||haim monk syndrome
|
|
D010214|245000||keratosis palmoplantaris with periodontopathia
|
|
D010214|245000||keratosis palmoplantar periodontopathies
|
|
D010214|245000||keratosis palmoplantar periodontopathy
|
|
D010214|245000||palmoplantar periodontopathies keratosis
|
|
D010214|245000||pals
|
|
D010214|245000||papillon lefevre syndrome
|
|
D010214|245000||pls
|
|
D001907||boutonneuse fever
|
|
D001907||boutonneuse fevers
|
|
D001907||fever boutonneuse
|
|
D001907||fever mediterranean spotted
|
|
D001907||fevers boutonneuse
|
|
D001907||mediterranean spotted fever
|
|
D001907||spotted fever mediterranean
|
|
D001906||botulism
|
|
D001906||botulism foodborne
|
|
D001906||botulism infant
|
|
D001906||botulism infantile
|
|
D001906||botulisms foodborne
|
|
D001906||botulisms infant
|
|
D001906||botulisms wound
|
|
D001906||botulism toxico infectious
|
|
D001906||botulism wound
|
|
D001906||foodborne botulism
|
|
D001906||foodborne botulisms
|
|
D001906||infant botulism
|
|
D001906||infant botulisms
|
|
D001906||infantile botulism
|
|
D001906||toxico infectious botulism
|
|
D001906||wound botulism
|
|
D001906||wound botulisms
|
|
C565440||leukomelanoderma infantilism mental retardation hypodontia hypotrichosis
|
|
D017486||acneiform eruptions
|
|
D017486||acneiform eruption
|
|
D017486||eruption acneiform
|
|
D017486||eruptions acneiform
|
|
D016155||oral fistula
|
|
D016155||fistula oral
|
|
D016155||fistulas oral
|
|
D016155||oral fistulas
|
|
D016156||respiratory tract fistula
|
|
D016156||fistula respiratory tract
|
|
D016156||fistulas respiratory tract
|
|
D016156||respiratory tract fistulas
|
|
C567465|300750||spastic paraplegia 34 x linked
|
|
C567465|300750||spg34
|
|
184900|C566112||stiff skin syndrome
|
|
184900|C566112||ssks
|
|
611431|C548032||legius syndrome
|
|
611431|C548032||neurofibromatosis type 1 like syndrome
|
|
611431|C548032||nfls
|
|
D016157||vascular fistula
|
|
D016157||fistulas vascular
|
|
D016157||fistula vascular
|
|
D016157||vascular fistulas
|
|
603688||prostate cancer brain cancer susceptibility
|
|
603688||capb
|
|
603688||pcbc
|
|
D018792||encephalitis viral
|
|
D018792||encephalomyelitis infectious viral
|
|
D018792||encephalomyelitis viral infectious
|
|
D018792||infectious encephalomyelitis viral
|
|
D018792||viral encephalitis
|
|
D018792||viral infectious encephalomyelitis
|
|
C566733||ciuffo syndrome
|
|
C566733||pulmonic stenosis atrial septal defect and unique electrocardiographic abnormalities
|
|
C565403||pseudoarylsulfatase a deficiency
|
|
C565404||mesomelic limb shortening and bowing
|
|
C566961|611369||lethal congenital contractural syndrome 3
|
|
C566961|611369||lccs3
|
|
C566961|611369||lethal congenital contracture syndrome 3
|
|
C566961|611369||multiple contractural syndrome israeli bedouin type b
|
|
C566961|611369||multiple contracture syndrome israeli bedouin type b
|
|
C566735||pubic bone dysplasia
|
|
312080|D020371|169500||pelizaeus merzbacher disease
|
|
312080||pmd leukodystrophy hypomyelinating 1
|
|
312080|D020371|169500||hld1
|
|
C566730|179010||pyloric stenosis infantile hypertrophic 1
|
|
C566730|179010||pyloric stenosis infantile
|
|
C566730|179010||pyloric stenosis infantile hypertrophic
|
|
607458|C537197||sensorimotor neuropathy with ataxia autosomal dominant
|
|
607458|C537197||sca18
|
|
607458|C537197||smna
|
|
607458|C537197||spinocerebellar ataxia 18
|
|
C565400||metaphyseal chondrodysplasia kaitila type
|
|
C566731||pupil egg shaped
|
|
C536687|277590||weaver syndrome
|
|
C536687|277590||weaver smith syndrome
|
|
C536687|277590||weaver smith syndrome wss weaver like syndrome included
|
|
C536687|277590||wvs
|
|
C565405||mesangial sclerosis diffuse renal with ocular abnormalities
|
|
C564505|300491||epilepsy x linked with variable learning disabilities and behavior disorders
|
|
C566736||ptosis strabismus and ectopic pupils
|
|
C566738||pterygium antecubital
|
|
C565408||megalencephaly with dysmyelination
|
|
C565408||megalencephaly with diffuse white matter hypodensity
|
|
C566739||multiple pterygium syndrome autosomal dominant
|
|
C566739||arthrogryposis distal type 8
|
|
C566739||pterygium syndrome multiple autosomal dominant
|
|
D005483||flushing
|
|
D005483||flushings
|
|
D016127||heart valve prolapse
|
|
D016127||heart valve prolapses
|
|
D016127||prolapse heart valve
|
|
D016127||prolapses heart valve
|
|
D016127||valve prolapse heart
|
|
D016127||valve prolapses heart
|
|
D011087|263300||polycythemia vera
|
|
D011087|263300||disease osler vaquez
|
|
D011087|263300||erythremia
|
|
D011087|263300||erythremias
|
|
D011087|263300||osler vaquez disease
|
|
D011087|263300||polycythemia ruba vera
|
|
D011087|263300||polycythemia rubra vera
|
|
D011087|263300||polycythemia rubra veras
|
|
D011087|263300||primary polycythemia
|
|
D011087|263300||prv
|
|
D011087|263300||pv
|
|
D011087|263300||vera polycythemia rubra
|
|
D011087|263300||veras polycythemia rubra
|
|
600059|C564008||retinitis pigmentosa 13
|
|
600059|C564008||rp13
|
|
D017453||dermatitis irritant
|
|
D017453||dermatitides irritant
|
|
D017453||dermatitides primary irritant
|
|
D017453||dermatitis primary irritant
|
|
D017453||irritant dermatitides
|
|
D017453||irritant dermatitides primary
|
|
D017453||irritant dermatitis
|
|
D017453||irritant dermatitis primary
|
|
D017453||primary irritant dermatitides
|
|
D017453||primary irritant dermatitis
|
|
D017454||dermatitis photoallergic
|
|
D017454||contact dermatitides photoallergic
|
|
D017454||contact dermatitides photosensitive
|
|
D017454||contact dermatitis photoallergic
|
|
D017454||contact dermatitis photosensitive
|
|
D017454||dermatitides photoallergic
|
|
D017454||dermatitides photoallergic contact
|
|
D017454||dermatitides photocontact
|
|
D017454||dermatitides photosensitive contact
|
|
D017454||dermatitis contact photoallergic
|
|
D017454||dermatitis contact photosensitive
|
|
D017454||dermatitis photoallergic contact
|
|
D017454||dermatitis photocontact
|
|
D017454||dermatitis photosensitive contact
|
|
D017454||photoallergic contact dermatitides
|
|
D017454||photoallergic contact dermatitis
|
|
D017454||photoallergic dermatitides
|
|
D017454||photoallergic dermatitis
|
|
D017454||photoallergies
|
|
D017454||photoallergy
|
|
D017454||photocontact dermatitides
|
|
D017454||photocontact dermatitis
|
|
D017454||photosensitive contact dermatitides
|
|
D017454||photosensitive contact dermatitis
|
|
D018784||abdominal abscess
|
|
D018784||abdominal abscesses
|
|
D018784||abscess abdominal
|
|
D018784||abscesses abdominal
|
|
D018784||abscesses intra abdominal
|
|
D018784||abscess intra abdominal
|
|
D018784||intra abdominal abscess
|
|
D018784||intra abdominal abscesses
|
|
C565412||maple syrup urine disease e3 deficient with lactic acidosis
|
|
C563410|600994||deafness autosomal dominant 5
|
|
C563410|600994||dfna5
|
|
C565413||maple syrup urine disease type ia
|
|
C565413||msud1a
|
|
C566744||pseudoxanthoma elasticum heterozygous
|
|
C565414||maple syrup urine disease type ib
|
|
C565414||msud1b
|
|
612518|C567287||ciliary dyskinesia primary 10
|
|
612518|C567287||cild10
|
|
C565415||maple syrup urine disease type ii
|
|
C565948|206900||microphthalmia syndromic 3
|
|
C565948|206900||aeg syndrome
|
|
C565948|206900||aeg syndrome optic nerve hypoplasia and abnormalities of the central nervous system included
|
|
C565948|206900||anophthalmia clinical with associated anomalies
|
|
C565948|206900||anophthalmia esophageal genital syndrome
|
|
C565948|206900||mcops3
|
|
C565948|206900||microphthalmia and esophageal atresia syndrome
|
|
C565948|206900||sox2 anophthalmia syndrome
|
|
C565948|206900||sox2 related eye disorders
|
|
C565948|206900||syndromic microphthalmia 3
|
|
607598|C564369||lethal congenital contracture syndrome 2
|
|
607598|C564369||lccs2
|
|
607598|C564369||multiple contracture syndrome israeli bedouin type a
|
|
C565336|605365||breast cancer 3
|
|
C565336|605365||brca3
|
|
C565336|605365||brcax
|
|
C565410||marfanoid mental retardation syndrome autosomal
|
|
C566741||pterygium colli isolated
|
|
D044542|151100||leopard syndrome
|
|
D044542|151100||cardio cutaneous syndrome
|
|
D044542|151100||cardio cutaneous syndromes
|
|
D044542|151100||cardiomyopathic lentiginoses
|
|
D044542|151100||cardiomyopathic lentiginoses progressive
|
|
D044542|151100||cardiomyopathic lentiginosis
|
|
D044542|151100||cardiomyopathic lentiginosis progressive
|
|
D044542|151100||cardiomyopathics lentiginosis
|
|
D044542|151100||lentigines syndrome multiple
|
|
D044542|151100||lentigines syndromes multiple
|
|
D044542|151100||lentiginoses cardiomyopathic
|
|
D044542|151100||lentiginoses progressive cardiomyopathic
|
|
D044542|151100||lentiginosis cardiomyopathic
|
|
D044542|151100||lentiginosis cardiomyopathics
|
|
D044542|151100||lentiginosis progressive cardiomyopathic
|
|
D044542|151100||leopard syndrome 1
|
|
D044542|151100||leopard syndrome 1s
|
|
D044542|151100||leopard syndromes
|
|
D044542|151100||leopard syndromes 1
|
|
D044542|151100||multiple lentigines syndrome
|
|
D044542|151100||multiple lentigines syndromes
|
|
D044542|151100||noonan syndrome with multiple lentigines
|
|
D044542|151100||progressive cardiomyopathic lentiginoses
|
|
D044542|151100||progressive cardiomyopathic lentiginosis
|
|
D044542|151100||syndrome cardio cutaneous
|
|
D044542|151100||syndrome leopard
|
|
D044542|151100||syndrome multiple lentigines
|
|
D044542|151100||syndromes 1 leopard
|
|
D044542|151100||syndromes cardio cutaneous
|
|
D044542|151100||syndromes leopard
|
|
D044542|151100||syndromes multiple lentigines
|
|
C565411||marfanoid habitus with microcephaly and glomerulonephritis
|
|
D006527|277900||hepatolenticular degeneration
|
|
D006527|277900||cerebral pseudoscleroses
|
|
D006527|277900||cerebral pseudosclerosis
|
|
D006527|277900||copper storage disease
|
|
D006527|277900||degeneration hepatocerebral
|
|
D006527|277900||degeneration hepatolenticular
|
|
D006527|277900||degeneration neurohepatic
|
|
D006527|277900||degeneration progressive lenticular
|
|
D006527|277900||degenerations hepatocerebral
|
|
D006527|277900||degenerations neurohepatic
|
|
D006527|277900||diseases hepato neurologic wilson
|
|
D006527|277900||diseases kinnier wilson
|
|
D006527|277900||hepatic form of wilson disease
|
|
D006527|277900||hepatocerebral degeneration
|
|
D006527|277900||hepatocerebral degenerations
|
|
D006527|277900||hepatolenticular degeneration syndrome
|
|
D006527|277900||hepato neurologic wilson disease
|
|
D006527|277900||hepato neurologic wilson diseases
|
|
D006527|277900||kinnier wilson disease
|
|
D006527|277900||kinnier wilson diseases
|
|
D006527|277900||lenticular degeneration progressive
|
|
D006527|277900||neurohepatic degeneration
|
|
D006527|277900||neurohepatic degenerations
|
|
D006527|277900||progressive lenticular degeneration
|
|
D006527|277900||pseudoscleroses cerebral
|
|
D006527|277900||pseudosclerosis
|
|
D006527|277900||pseudosclerosis cerebral
|
|
D006527|277900||wd
|
|
D006527|277900||westphal strumpell syndrome
|
|
D006527|277900||westphal strumpell syndromes
|
|
D006527|277900||wilson disease
|
|
D006527|277900||wilson disease hepatic form
|
|
D006527|277900||wilson disease hepato neurologic
|
|
D006527|277900||wilson diseases hepato neurologic
|
|
D006527|277900||wilson apos s disease
|
|
D006527|277900||wilsons disease
|
|
D006527|277900||wnd
|
|
C535278|608644||primary ciliary dyskinesia 3
|
|
C535278|608644||cild3
|
|
C535278|608644||ciliary dyskinesia primary 3
|
|
C535278|608644||ciliary dyskinesia primary 3 with or without situs inversus
|
|
D004154||dipetalonema infections
|
|
D004154||dipetalonema infection
|
|
D004154||dipetalonemiases
|
|
D004154||dipetalonemiasis
|
|
D004154||infection dipetalonema
|
|
D004154||infections dipetalonema
|
|
C566748||pseudoglaucoma
|
|
C565418||alpha mannosidosis type ii
|
|
C566467|610505||combined oxidative phosphorylation deficiency 3
|
|
C566467|610505||concentric cardiomyopathy hypotonia and lactic acidosis
|
|
C566467|610505||coxpd3
|
|
C566467|610505||encephalomyopathy respiratory failure and lactic acidosis
|
|
255800|239100|D010009||schwartz jampel syndrome type 1
|
|
255800||sjs1 schwartz jampel syndrome
|
|
255800|239100|D010009||sjs
|
|
255800|239100|D010009||myotonic myopathy dwarfism chondrodystrophy and ocular and facial abnormalities
|
|
255800|239100|D010009||schwartz jampel aberfeld syndrome
|
|
255800|239100|D010009||sja syndrome
|
|
255800|239100|D010009||chondrodystrophic myotonia
|
|
D005494||folic acid deficiency
|
|
D005494||acid deficiencies folic
|
|
D005494||acid deficiency folic
|
|
D005494||deficiencies folic acid
|
|
D005494||deficiency folic acid
|
|
D005494||folic acid deficiencies
|
|
D005491||focal infection dental
|
|
D005491||dental focal infection
|
|
D005491||dental focal infections
|
|
D005491||focal infections dental
|
|
D005491||infection dental focal
|
|
D005491||infections dental focal
|
|
D005490||focal infection
|
|
D005490||focal infections
|
|
D005490||infection focal
|
|
D005490||infections focal
|
|
603663||mental health wellness 1
|
|
603663||mhw1
|
|
D016137||spina bifida cystica
|
|
D016137||open spina bifida
|
|
D016137||spina bifida aperta
|
|
D016137||spina bifida manifesta
|
|
D016137||spina bifida open
|
|
603664||mental health wellness 2
|
|
603664||mhw2
|
|
C536708|309585||wilson turner x linked mental retardation syndrome
|
|
C536708|309585||mental retardation x linked syndromic 6
|
|
C536708|309585||mental retardation x linked with gynecomastia and obesity
|
|
C536708|309585||mrxs6
|
|
C536708|309585||wilson turner mental retardation syndrome
|
|
C536708|309585||wts
|
|
D016135||spinal dysraphism
|
|
D016135||bifida spina
|
|
D016135||cleft spine
|
|
D016135||dysraphia spinal
|
|
D016135||dysraphias spinal
|
|
D016135||dysraphicus status
|
|
D016135||dysraphism spinal
|
|
D016135||dysraphisms spinal
|
|
D016135||open spine
|
|
D016135||rachischises
|
|
D016135||rachischisis
|
|
D016135||schistorrhachis
|
|
D016135||spina bifida
|
|
D016135||spina bifidas
|
|
D016135||spinal dysraphia
|
|
D016135||spinal dysraphias
|
|
D016135||spinal dysraphisms
|
|
D016135||status dysraphicus
|
|
D018798||anemia iron deficiency
|
|
D018798||anemias iron deficiency
|
|
D018798||iron deficiency anemia
|
|
D018798||iron deficiency anemias
|
|
D016136||spina bifida occulta
|
|
D016136||closed spinal bifida
|
|
D016136||dermal sinus
|
|
D016136||occult spina bifida
|
|
D016136||sinus dermal
|
|
D016136||spina bifida occult
|
|
D016136||spinal bifida closed
|
|
C566711||retinol binding protein deficiency
|
|
C566711||familial hypo rbp
|
|
C566713||retinopathy pericentral pigmentary dominant
|
|
D017441||necrobiotic disorders
|
|
D017441||disorder necrobiotic
|
|
D017441||disorders necrobiotic
|
|
D017441||necrobioses
|
|
D017441||necrobiosis
|
|
D017441||necrobiotic disorder
|
|
D018771||arthralgia
|
|
D018771||arthralgias
|
|
D018771||joint pain
|
|
D018771||joint pains
|
|
D018771||pain joint
|
|
D018771||pains joint
|
|
D018771||polyarthralgia
|
|
D018771||polyarthralgias
|
|
D049950||hyperparathyroidism primary
|
|
D049950||hyperparathyroidisms primary
|
|
D049950||primary hyperparathyroidism
|
|
D049950||primary hyperparathyroidisms
|
|
C537047|300523||allan herndon dudley syndrome
|
|
C537047|300523||ahds
|
|
C537047|300523||allan herndon syndrome
|
|
C537047|300523||mct8 slc16a2 specific thyroid hormone cell transporter deficiency
|
|
C537047|300523||mental retardation and muscular atrophy
|
|
C537047|300523||mental retardation x linked with hypotonia
|
|
C537047|300523||monocarboxylate transporter 8 deficiency
|
|
C537047|300523||monocarboxylate transporter 8 mct8 deficiency
|
|
C537047|300523||t3 resistance
|
|
C537047|300523||triiodothyronine resistance
|
|
C537047|300523||x linked mental retardation with hypotonia
|
|
C566718||retinitis pigmentosa 20
|
|
D048629||micronuclei chromosome defective
|
|
D048629||chromosome defective micronuclei
|
|
D048629||chromosome defective micronucleus
|
|
D048629||genotoxicant induced micronuclei
|
|
D048629||genotoxicant induced micronucleus
|
|
D048629||micronuclei genotoxicant induced
|
|
D048629||micronucleus chromosome defective
|
|
D048629||micronucleus genotoxicant induced
|
|
D005458||fluoride poisoning
|
|
D005458||fluoride poisonings
|
|
D005458||poisoning fluoride
|
|
D005458||poisonings fluoride
|
|
C567935|609893||hypothyroidism congenital nongoitrous 3
|
|
C567935|609893||chng3
|
|
C567935|609893||congenital hypothyroidism nongoitrous 3
|
|
C567935|609893|218700|C566852||resistance to thyrotropin
|
|
C567935|609893|218700|C566852||rtsh
|
|
C567935|609893|218700|C566852||thyrotropin resistance
|
|
C566714||osteosarcoma retinoblastoma related
|
|
612521|C567285||diabetes mellitus insulin dependent 21
|
|
612521|C567285||iddm21
|
|
C566717||retinal nonattachment and falciform detachment
|
|
C564511|300454||mental retardation x linked 77
|
|
C564511|300454||mrx77
|
|
D017439||cicatrix hypertrophic
|
|
D017439||cicatrices hypertrophic
|
|
D017439||hypertrophic cicatrices
|
|
D017439||hypertrophic cicatrix
|
|
D017439||hypertrophic scar
|
|
D017439||hypertrophic scars
|
|
D017439||scar hypertrophic
|
|
D017439||scars hypertrophic
|
|
300082||cognitive function 1 social
|
|
300082||cgf1
|
|
300082||social cognition
|
|
D016104||oligohydramnios
|
|
D017437||skin and connective tissue diseases
|
|
D016107||epidermolysis bullosa acquisita
|
|
D016107||acquired epidermolysis bullosa
|
|
D016107||acquired form of epidermolysis bullosa
|
|
D016107||epidermolysis bullosa acquired
|
|
D016103||spinal fractures
|
|
D016103||fracture spinal
|
|
D016103||fractures spinal
|
|
D016103||spinal fracture
|
|
C566721||reticular dystrophy of retinal pigment epithelium
|
|
D018781||tension type headache
|
|
D018781||headache idiopathic
|
|
D018781||headache psychogenic
|
|
D018781||headaches idiopathic
|
|
D018781||headaches psychogenic
|
|
D018781||headaches stress
|
|
D018781||headaches tension
|
|
D018781||headaches tension type
|
|
D018781||headaches tension vascular
|
|
D018781||headache stress
|
|
D018781||headache tension
|
|
D018781||headache tension type
|
|
D018781||headache tension vascular
|
|
D018781||idiopathic headache
|
|
D018781||idiopathic headaches
|
|
D018781||psychogenic headache
|
|
D018781||psychogenic headaches
|
|
D018781||stress headache
|
|
D018781||stress headaches
|
|
D018781||tension headache
|
|
D018781||tension headaches
|
|
D018781||tension type headaches
|
|
D018781||tension vascular headache
|
|
D018781||tension vascular headaches
|
|
D018783||impotence vasculogenic
|
|
D018783||arteriogenic impotence
|
|
D018783||impotence arteriogenic
|
|
D018783||impotence venogenic
|
|
D018783||leakage penile venous
|
|
D018783||penile venous leakage
|
|
D018783||vasculogenic impotence
|
|
D018783||venogenic impotence
|
|
D018783||venous leakage penile
|
|
C566724||raindrop hypopigmentation
|
|
C566720||retinal aplasia
|
|
C566720||amaurosis congenita
|
|
C566729||pyruvate dehydrogenase e1 beta deficiency
|
|
C566728||radial heads posterior dislocation of
|
|
C566728||congenital posterior dislocation of the radial head
|
|
146550|C535912||marie unna congenital hypotrichosis
|
|
146550|C535912|C567718||hypotrichosis 4
|
|
146550|C535912||hypotrichosis marie unna type
|
|
146550|C535912|C567718||hypotrichosis marie unna type 1
|
|
146550|C535912||hypt4
|
|
146550|C535912||marie unna hereditary hypotrichosis
|
|
146550|C535912|C567718||marie unna hereditary hypotrichosis 1
|
|
146550|C535912||muhh1
|
|
115310|C565335|605373||paragangliomas 4
|
|
115310|C565335|605373||carotid body tumors and multiple extraadrenal pheochromocytomas
|
|
115310|C565335|605373||paraganglioma familial malignant
|
|
115310|C565335|605373||paragangliomas hereditary extraadrenal
|
|
115310||pgl4
|
|
115310|C565335|605373||pheochromocytoma extraadrenal and cervical paraganglioma
|
|
115310|C565335|605373||pheochromocytoma familial extraadrenal
|
|
D016115||albinism oculocutaneous
|
|
D016115||albinism tyrosinase negative
|
|
D016115||albinism tyrosinase positive
|
|
D016115||albinism yellow mutant
|
|
D016115||mutant albinisms yellow
|
|
D016115||mutant albinism yellow
|
|
D016115||oculocutaneous albinism
|
|
D016115||tyrosinase negative albinism
|
|
D016115||tyrosinase positive albinism
|
|
D016115||yellow mutant albinism
|
|
D018778||hantavirus infections
|
|
D018778||hantavirus infection
|
|
D018778||infections hantavirus
|
|
D018777||multiple chemical sensitivity
|
|
D018777||chemical sensitivities multiple
|
|
D018777||chemical sensitivity multiple
|
|
D018777||environmental intolerance idiopathic
|
|
D018777||environmental intolerances idiopathic
|
|
D018777||idiopathic environmental intolerance
|
|
D018777||idiopathic environmental intolerances
|
|
D018777||intolerance idiopathic environmental
|
|
D018777||intolerances idiopathic environmental
|
|
D018777||multiple chemical sensitivities
|
|
D018777||multiple chemical sensitivity syndrome
|
|
D018777||sensitivities multiple chemical
|
|
D018777||sensitivity multiple chemical
|
|
D016117||albinism ocular
|
|
D016117||ocular albinism
|
|
C567674|613271||corneal dystrophy fuchs endothelial 7
|
|
C567674|613271||fcd4 locus
|
|
C567674|613271||fecd7
|
|
D017449||dermatitis allergic contact
|
|
D017449||allergic contact dermatitides
|
|
D017449||allergic contact dermatitis
|
|
D017449||allergic eczematous dermatitides
|
|
D017449||allergic eczematous dermatitis
|
|
D017449||contact dermatitides allergic
|
|
D017449||contact dermatitis allergic
|
|
D017449||dermatitides allergic contact
|
|
D017449||dermatitides allergic eczematous
|
|
D017449||dermatitis allergic eczematous
|
|
D017449||dermatitis contact allergic
|
|
D017449||eczematous dermatitides allergic
|
|
D017449||eczematous dermatitis allergic
|
|
D017443||skin diseases eczematous
|
|
D017443||disease eczematous skin
|
|
D017443||diseases eczematous skin
|
|
D017443||disorder eczematous
|
|
D017443||disorders eczematous
|
|
D017443||eczematous disorder
|
|
D017443||eczematous disorders
|
|
D017443||eczematous skin disease
|
|
D017443||eczematous skin diseases
|
|
D017443||skin disease eczematous
|
|
D017444||skin diseases papulosquamous
|
|
D017444||disease papulosquamous skin
|
|
D017444||diseases papulosquamous skin
|
|
D017444||disorder papulosquamous
|
|
D017444||disorders papulosquamous
|
|
D017444||papulosquamous disorder
|
|
D017444||papulosquamous disorders
|
|
D017444||papulosquamous skin disease
|
|
D017444||papulosquamous skin diseases
|
|
D017444||skin disease papulosquamous
|
|
D016113||ichthyosiform erythroderma congenital
|
|
D016113||congenital ichthyosiform erythroderma
|
|
D016113||congenital ichthyosiform erythroderma dry type
|
|
D016113||congenital ichthyosiform erythrodermas
|
|
D016113||congenital ichthyosiform erythroderma wet type
|
|
D016113||erythroderma congenital ichthyosiform
|
|
D016113||erythrodermas congenital ichthyosiform
|
|
D016113||ichthyosiform erythrodermas congenital
|
|
D017445||skin diseases vascular
|
|
D017445||diseases vascular skin
|
|
D017445||disease vascular skin
|
|
D017445||skin disease vascular
|
|
D017445||vascular skin disease
|
|
D017445||vascular skin diseases
|
|
D004108||dilatation pathologic
|
|
D004108||dilatation pathological
|
|
D004108||dilatations pathologic
|
|
D004108||dilatations pathological
|
|
D004108||ectasia
|
|
D004108||pathological dilatation
|
|
D004108||pathological dilatations
|
|
D004108||pathologic dilatation
|
|
D004108||pathologic dilatations
|
|
D049970||graves ophthalmopathy
|
|
D049970||congestive ophthalmopathies
|
|
D049970||congestive ophthalmopathy
|
|
D049970||dysthyroid ophthalmopathies
|
|
D049970||dysthyroid ophthalmopathy
|
|
D049970||edematous ophthalmopathies
|
|
D049970||edematous ophthalmopathy
|
|
D049970||infiltrative ophthalmopathies
|
|
D049970||infiltrative ophthalmopathy
|
|
D049970||myopathic ophthalmopathies
|
|
D049970||myopathic ophthalmopathy
|
|
D049970||ophthalmopathies congestive
|
|
D049970||ophthalmopathies dysthyroid
|
|
D049970||ophthalmopathies edematous
|
|
D049970||ophthalmopathies infiltrative
|
|
D049970||ophthalmopathies myopathic
|
|
D049970||ophthalmopathies thyroid associated
|
|
D049970||ophthalmopathy congestive
|
|
D049970||ophthalmopathy dysthyroid
|
|
D049970||ophthalmopathy edematous
|
|
D049970||ophthalmopathy graves
|
|
D049970||ophthalmopathy infiltrative
|
|
D049970||ophthalmopathy myopathic
|
|
D049970||ophthalmopathy thyroid associated
|
|
D049970||thyroid associated ophthalmopathies
|
|
D049970||thyroid associated ophthalmopathy
|
|
C536091|601462||myasthenic syndrome congenital postsynaptic slow channel
|
|
C536091|601462||cms2a
|
|
C536091|601462||cms iia
|
|
C536091|601462|D020294||myasthenic syndrome congenital slow channel
|
|
C536091|601462||myasthenic syndrome congenital type iia
|
|
C536091|601462||sccms
|
|
603471|C538053||adult onset citrullinemia type 2
|
|
603471|C538053||autosomal dominant retinoschisis
|
|
603471|C538053||citrin deficiency
|
|
603471|C538053||citrullinemia type ii adult onset
|
|
603471|C538053||ctln2
|
|
603471|C538053||retinoschisis autosomal dominant
|
|
300310|C538057||agammaglobulinemia x linked type 2
|
|
300310|C538057||agmx2
|
|
300310|C538057||xla2
|
|
D004314|190685||down syndrome
|
|
D004314|190685||47 xx 21
|
|
D004314|190685||47 xy 21
|
|
D004314|190685||dcr included
|
|
D004314|190685||down apos s syndrome
|
|
D004314|190685||downs syndrome
|
|
D004314|190685||down syndrome chromosome region included
|
|
D004314|190685||down syndrome critical region included
|
|
D004314|190685||down syndrome partial trisomy 21
|
|
D004314|190685||dscr included
|
|
D004314|190685||leukemia megakaryoblastic of down syndrome included
|
|
D004314|190685||mongolism
|
|
D004314|190685||partial trisomy 21 down syndrome
|
|
D004314|190685||syndrome down
|
|
D004314|190685||syndrome down apos s
|
|
D004314|190685||transient myeloproliferative disorder of down syndrome included
|
|
D004314|190685||trisomy 21
|
|
D004314|190685||trisomy 21 included
|
|
D004314|190685||trisomy 21 meiotic nondisjunction
|
|
D004314|190685||trisomy 21 mitotic nondisjunction
|
|
D004314|190685||trisomy g
|
|
C567423|612089||hypophosphatemic rickets and hyperparathyroidism
|
|
C567449|611955||prostate cancer hereditary 11
|
|
C567449|611955||hpc11
|
|
C562746|608051||macular dystrophy retinal 2
|
|
C562746|608051||mcdr2
|
|
D018746||systemic inflammatory response syndrome
|
|
D018746||inflammatory response syndrome systemic
|
|
D018746||sepsis syndrome
|
|
D018746||sepsis syndromes
|
|
D018746||syndrome sepsis
|
|
D018746||syndromes sepsis
|
|
C566700||hypermethioninemia with deficiency of s adenosylhomocysteine hydrolase
|
|
C566702||parotid aplasia or hypoplasia
|
|
C566708||rhiny
|
|
C566709||rhabdomyosarcoma embryonal 2
|
|
C566703||lacrimal puncta absence of
|
|
C564590|607324||polydactyly postaxial type a3
|
|
C564590|607324||papa3
|
|
C564590|607324||postaxial polydactyly type a3
|
|
D017436|147950||kallmann syndrome
|
|
D017436|147950||anosmic hypogonadism
|
|
D017436|147950||anosmic hypogonadisms
|
|
D017436|147950||anosmic idiopathic hypogonadotropic hypogonadism
|
|
D017436|147950||autosomal dominant form of kallmann syndrome
|
|
D017436|147950||autosomal recessive form of kallmann syndrome
|
|
D017436|147950||dysplasia olfactogenitalis of de morsier
|
|
D017436|147950||hh1
|
|
D017436|147950||hh2
|
|
D017436|147950||hh3
|
|
D017436|147950||hh4
|
|
D017436|147950||hh5
|
|
D017436|147950||hh6
|
|
D017436|147950||hha
|
|
D017436|147950||hypogonadism anosmic
|
|
D017436|147950||hypogonadisms anosmic
|
|
D017436|147950||hypogonadotropic hypogonadism 1 with or without anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism 2 with or without anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism 3 with or without anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism 4 with or without anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism 5 with or without anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism 6 with or without anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism and anosmia
|
|
D017436|147950||hypogonadotropic hypogonadism anosmia and midline cranial anomalies cleft lip cleft palate and imperfect fusion
|
|
D017436|147950||hypogonadotropic hypogonadism anosmia syndrome
|
|
D017436|147950||kal1
|
|
D017436|147950||kal2
|
|
D017436|147950||kallmann apos s syndrome
|
|
D017436|147950||kallmanns syndrome
|
|
D017436|147950||kallmann syndrome 1
|
|
D017436|147950||kallmann syndrome 2
|
|
D017436|147950||kallmann syndrome 3
|
|
D017436|147950||kallmann syndrome type 1 x linked
|
|
D017436|147950||kallmann syndrome type 3 recessive
|
|
D017436|147950|C537705|147920||kms
|
|
D017436|147950||syndrome kallmann
|
|
D017436|147950||syndrome kallmann apos s
|
|
C565342|605309||macrocephaly autism syndrome
|
|
300071|C536122||night blindness congenital stationary type 2a
|
|
300071|C536122||csnb2
|
|
300071|C536122||csnb2a
|
|
300071|C536122||csnb incomplete x linked
|
|
300071|C536122||night blindness congenital stationary type 2
|
|
D054198|613065||precursor cell lymphoblastic leukemia lymphoma
|
|
D054198|613065||acute lymphoblastic leukemia
|
|
D054198|613065||acute lymphocytic leukemia
|
|
D054198|613065||acute lymphoid leukemia
|
|
D054198|613065||all
|
|
D054198|613065||all1 included
|
|
D054198|613065||all2
|
|
D054198|613065||all childhood
|
|
D054198|613065||childhood all
|
|
D054198|613065||l1 lymphocytic leukemia
|
|
D054198|613065||l2 lymphocytic leukemia
|
|
D054198|613065||leukemia acute lymphoblastic
|
|
D054198|613065||leukemia acute lymphoblastic b hyperdiploid susceptibility to included
|
|
D054198|613065||leukemia acute lymphoblastic susceptibility to 1 included
|
|
D054198|613065||leukemia acute lymphoblastic susceptibility to 2
|
|
D054198|613065||leukemia acute lymphocytic
|
|
D054198|613065||leukemia acute lymphocytic susceptibility to 1 included
|
|
D054198|613065||leukemia acute lymphocytic susceptibility to 2
|
|
D054198|613065||leukemia acute lymphoid
|
|
D054198|613065||leukemia b cell acute lymphoblastic susceptibility to included
|
|
D054198|613065||leukemia l1 lymphocytic
|
|
D054198|613065||leukemia l2 lymphocytic
|
|
D054198|613065||leukemia lymphoblastic
|
|
D054198|613065||leukemia lymphoblastic acute
|
|
D054198|613065||leukemia lymphoblastic acute l1
|
|
D054198|613065||leukemia lymphoblastic acute l2
|
|
D054198|613065||leukemia lymphoblastic acute philadelphia positive
|
|
D054198|613065||leukemia lymphocytic acute
|
|
D054198|613065||leukemia lymphocytic acute l1
|
|
D054198|613065||leukemia lymphocytic acute l2
|
|
D054198|613065||leukemia lymphoid acute
|
|
D054198|613065||leukemia t cell acute lymphoblastic susceptibility to included
|
|
D054198|613065||lymphoblastic leukemia
|
|
D054198|613065||lymphoblastic leukemia acute
|
|
D054198|613065||lymphoblastic leukemia acute adult
|
|
D054198|613065||lymphoblastic leukemia acute childhood
|
|
D054198|613065||lymphoblastic leukemia acute l1
|
|
D054198|613065||lymphoblastic leukemia acute l2
|
|
D054198|613065||lymphoblastic lymphoma
|
|
D054198|613065||lymphocytic leukemia acute
|
|
D054198|613065||lymphocytic leukemia l1
|
|
D054198|613065||lymphocytic leukemia l2
|
|
D054198|613065||lymphoid leukemia acute
|
|
D054198|613065||lymphoma lymphoblastic
|
|
C563763|609254||senior loken syndrome 5
|
|
C563763|609254||slsn5
|
|
D018754||ventricular dysfunction
|
|
D018754||dysfunctions ventricular
|
|
D018754||dysfunction ventricular
|
|
D018754||ventricular dysfunctions
|
|
613091||short rib thoracic dysplasia 3 with or without polydactyly
|
|
613091|C567761||asphyxiating thoracic dystrophy 3
|
|
613091||atd3
|
|
613091|D012779|263520||polydactyly with neonatal chondrodystrophy type i
|
|
613091|C537602||polydactyly with neonatal chondrodystrophy type iii
|
|
613091|D012779|263520||saldino noonan syndrome
|
|
613091|D012779|263520||short rib polydactyly syndrome type i
|
|
613091||short rib polydactyly syndrome type iib
|
|
613091|C537602||short rib polydactyly syndrome type iii
|
|
613091||srps1
|
|
613091||srps2b
|
|
613091||srps3
|
|
613091||srtd3
|
|
613091|C537602||verma naumoff syndrome
|
|
613092|C567760||hyperuricemic nephropathy familial juvenile 2
|
|
613092|C567760||early onset hyperuricemia anemia and progressive kidney failure
|
|
613092|C567760||hnfj2
|
|
604168|C565822||congenital cataracts facial dysmorphism and neuropathy
|
|
604168|C565822||cataract congenital with facial dysmorphism and neuropathy
|
|
604168|C565822||ccfdn
|
|
613099||melanoma cutaneous malignant susceptibility to 5
|
|
613099||cmm5
|
|
D005413||flatfoot
|
|
D005413||feet flat
|
|
D005413||flatfeet
|
|
D005413||flat feet
|
|
D005413||flat foot
|
|
D005413||foot flat
|
|
D005413||pes planus
|
|
313350|C564056||split hand foot malformation 2
|
|
313350||shfd2
|
|
313350||shfm2
|
|
313350||shsf2
|
|
313350|C564056||split hand foot deformity 2
|
|
313350|C564056||split hand split foot anomaly x linked
|
|
214100|D015211||zellweger syndrome
|
|
214100|D015211||cerebrohepatorenal syndrome
|
|
214100|D015211||cerebro hepato renal syndrome
|
|
214100|D015211||cerebrohepatorenal syndrome chr peroxisome biogenesis disorder complementation group 1 included
|
|
214100|D015211||cg1 included
|
|
214100|D015211||cge included
|
|
214100|D015211||pbd1a
|
|
214100|D015211||pbd zss
|
|
214100|D015211||peroxisome biogenesis disorder 1a zellweger
|
|
214100|D015211||peroxisome biogenesis disorder complementation group e included
|
|
214100|D015211||peroxisome biogenesis disorders zellweger syndrome spectrum
|
|
214100|D015211||spectrum zellweger
|
|
214100|D015211||zellweger disease
|
|
214100|D015211||zellweger like syndrome
|
|
214100|D015211||zellweger spectrum
|
|
214100|D015211||zellweger apos s syndrome
|
|
214100|D015211||zellweger syndrome spectrum
|
|
214100|D015211||zs
|
|
214100|D015211||zws
|
|
D005414||flatulence
|
|
D005414||flatus
|
|
D017827|109150||machado joseph disease
|
|
D017827|109150||3 spinocerebellar ataxia
|
|
D017827|109150||3s spinocerebellar ataxia
|
|
D017827|109150||ataxia 3 spinocerebellar
|
|
D017827|109150||ataxia 3s spinocerebellar
|
|
D017827|109150||atrophy iii spinocerebellar
|
|
D017827|109150||atrophy iiis spinocerebellar
|
|
D017827|109150||autosomal dominant striatonigral degeneration
|
|
D017827|109150||azorean ataxia
|
|
D017827|109150||azorean disease
|
|
D017827|109150||azorean disease machado joseph
|
|
D017827|109150||azorean disease nervous system
|
|
D017827|109150||azorean neurologic disease
|
|
D017827|109150||degeneration nigrospinodentatal
|
|
D017827|109150||degenerations nigrospinodentatal
|
|
D017827|109150||disease azorean
|
|
D017827|109150||disease azorean machado joseph
|
|
D017827|109150||disease azorean neurologic
|
|
D017827|109150||disease joseph
|
|
D017827|109150||disease joseph azorean
|
|
D017827|109150||disease machado joseph
|
|
D017827|109150||disease machado joseph azorean
|
|
D017827|109150||iii spinocerebellar atrophy
|
|
D017827|109150||iiis spinocerebellar atrophy
|
|
D017827|109150||joseph azorean disease
|
|
D017827|109150||joseph disease
|
|
D017827|109150||machado joseph azorean disease
|
|
D017827|109150||machado joseph disease type i
|
|
D017827|109150||machado joseph disease type ii
|
|
D017827|109150||machado joseph disease type iii
|
|
D017827|109150||machado joseph disease type iv
|
|
D017827|109150||mjd
|
|
D017827|109150||nervous system azorean disease
|
|
D017827|109150||neurologic disease azorean
|
|
D017827|109150||nigrospinodentatal degeneration
|
|
D017827|109150||nigrospinodentatal degenerations
|
|
D017827|109150||sca3
|
|
D017827|109150||spinocerebellar ataxia 3
|
|
D017827|109150||spinocerebellar ataxia 3s
|
|
D017827|109150||spinocerebellar ataxia type 3
|
|
D017827|109150||spinocerebellar atrophy iii
|
|
D017827|109150||spinocerebellar atrophy iiis
|
|
D017827|109150||spinocerebellar atrophy type 3
|
|
D017827|109150||striatonigral degeneration autosomal dominant
|
|
D017827|109150||type 3 spinocerebellar ataxia
|
|
D017827|109150||type iii machado joseph disease
|
|
D017827|109150||type ii machado joseph disease
|
|
D017827|109150||type i machado joseph disease
|
|
D017827|109150||type iv machado joseph disease
|
|
C565207|610265||deafness autosomal recessive 67
|
|
C565207|610265||dfnb67
|
|
C567338|612354||inflammatory bowel disease 21
|
|
C567338|612354||ibd21
|
|
C537758|602722||renal tubular acidosis distal autosomal recessive
|
|
C537758|602722||autosomal recessive distal renal tubular acidosis
|
|
C537758|602722||renal tubular acidosis autosomal recessive with preserved hearing
|
|
C537758|602722||renal tubular acidosis autosomal recessive with preserved hearing renal tubular acidosis distal autosomal recessive with late onset sensorineural hearing loss included
|
|
C537758|602722||rta distal autosomal recessive
|
|
C537758|602722||rtadr
|
|
142669|C564185||hip dysplasia beukes type
|
|
142669|C564185||beukes familial hip dysplasia
|
|
142669|C564185||bfhd
|
|
142669|C564185|135150|D058249||bhd
|
|
142669|C564185||osteoarthropathy premature degenerative of hip
|
|
C562625|130060||ehlers danlos syndrome type vii autosomal dominant
|
|
C562625|130060||arthrochalasis multiplex congenita
|
|
C562625|130060||eds7a
|
|
C562625|130060||eds7b included
|
|
C562625|130060||eds viia
|
|
C562625|130060||eds vii mutant procollagen type
|
|
C562625|130060||eds vii mutant procollagen type eds viib included
|
|
C562625|130060||ehlers danlos syndrome arthrochalasia type
|
|
610253|C563043||kleefstra syndrome
|
|
610253|C563043||9q34 3 deletion syndrome
|
|
610253|C563043||9q34 3 microdeletion syndrome
|
|
610253|C563043||9q subtelomeric deletion syndrome
|
|
610253|C563043||9q syndrome
|
|
610253|C563043||chromosome 9q34 3 deletion syndrome
|
|
300049|D054091||heterotopia periventricular x linked dominant
|
|
300049||bpnh heterotopia periventricular nodular with frontometaphyseal dysplasia included
|
|
300049|D054091||heterotopia familial nodular
|
|
300049||nhbp
|
|
300049|D054091||nodular heterotopia bilateral periventricular
|
|
300049|D054091||periventricular nodular heterotopia 1
|
|
300049||pvnh1
|
|
C566932|611494||atrial fibrillation familial 5
|
|
C566932|611494||atfb5
|
|
613085||glaucoma 3 primary congenital c
|
|
613085||glc3c
|
|
300510|C564499||ovarian dysgenesis 2
|
|
300510|C564499||odg2
|
|
300510|C564499||ovarian dysgenesis hypergonadotropic x linked
|
|
300510|C564499||ovarian failure hypergonadotropic due to ovarian dysgenesis
|
|
300510|C564499||ovarian failure hypergonadotropic due to ovarian dysgenesis premature ovarian failure 4 included
|
|
300510|C564499||pof4 included
|
|
300510|C564499||premature ovarian failure 4
|
|
C566593|602014||hypomagnesemia 1 intestinal
|
|
C566593|602014||homg
|
|
C566593|602014||homg1
|
|
C566593|602014||hsh
|
|
C566593|602014||hypomagnesemia intestinal with secondary hypocalcemia
|
|
C566593|602014||hypomagnesemia with secondary hypocalcemia
|
|
C566593|602014||hypomagnesemic tetany
|
|
C565386|251120||methylmalonyl coa epimerase deficiency
|
|
C565386|251120||methylmalonic aciduria iii formerly methylmalonyl coa epimerase deficiency with sepiapterin reductase deficiency included
|
|
C565386|251120||methylmalonyl coa racemase deficiency
|
|
C563757|609260||charcot marie tooth disease axonal type 2a2
|
|
C563757|609260||charcot marie tooth disease axonal autosomal dominant type 2a2
|
|
C563757|609260||charcot marie tooth disease neuronal type 2a2
|
|
C563757|609260||charcot marie tooth neuropathy type 2a2
|
|
C563757|609260||cmt2a2
|
|
C563757|609260||hereditary motor and sensory neuropathy iia2
|
|
C563757|609260||hmsn2a2
|
|
C563757|609260||hmsniia2
|
|
C563757|609260||hmsn iia2
|
|
D001506|130650||beckwith wiedemann syndrome
|
|
D001506|130650||bwcr included
|
|
D001506|130650||bws
|
|
D001506|130650||emg syndrome
|
|
D001506|130650||emg syndromes
|
|
D001506|130650||exomphalos macroglossia gigantism syndrome
|
|
D001506|130650||syndrome beckwith wiedemann
|
|
D001506|130650||syndrome emg
|
|
D001506|130650||syndromes emg
|
|
D001506|130650||syndromes wiedemann beckwith wbs
|
|
D001506|130650||syndrome wiedemann beckwith
|
|
D001506|130650||syndrome wiedemann beckwith wbs
|
|
D001506|130650||wiedemann beckwith syndrome
|
|
D001506|130650||wiedemann beckwith syndromes wbs
|
|
D001506|130650||wiedemann beckwith syndrome wbs
|
|
D001506|130650||wiedemann beckwith syndrome wbs beckwith wiedemann syndrome chromosome region included
|
|
C535697|600467||malignant hyperthermia susceptibility type 4
|
|
C535697|600467||malignant hyperpyrexia susceptibility type 4
|
|
C535697|600467||malignant hyperthermia susceptibility to 4
|
|
C535697|600467||mhs4
|
|
D059325||intra abdominal hypertension
|
|
D059325||abdominal compartment syndrome
|
|
D059325||abdominal compartment syndromes
|
|
D059325||compartment syndrome abdominal
|
|
D059325||compartment syndromes abdominal
|
|
D059325||hypertension intraabdominal
|
|
D059325||hypertension intra abdominal
|
|
D059325||hypertensions intraabdominal
|
|
D059325||hypertensions intra abdominal
|
|
D059325||intraabdominal hypertension
|
|
D059325||intraabdominal hypertensions
|
|
D059325||intra abdominal hypertensions
|
|
D059325||syndrome abdominal compartment
|
|
D059325||syndromes abdominal compartment
|
|
C567508|611876||brugada syndrome 4
|
|
C567508|611876||brgda4
|
|
D056889|302060||barth syndrome
|
|
D056889|302060||3 methylglutaconicaciduria type 2
|
|
D056889|302060||3 methylglutaconicaciduria type 2s
|
|
D056889|302060||3 methylglutaconicaciduria type ii
|
|
D056889|302060||3 methylglutaconic aciduria type ii
|
|
D056889|302060||3 methylglutaconicaciduria type iis
|
|
D056889|302060||bths
|
|
D056889|302060||cardioskeletal myopathy with neutropenia and abnormal mitochondria
|
|
D056889|302060||mga2
|
|
D056889|302060||mga type 2
|
|
D056889|302060||mga type 2s
|
|
D056889|302060||mga type ii
|
|
D056889|302060||mga type iis
|
|
D056889|302060||mgca2
|
|
D056889|302060||syndrome barth
|
|
D056889|302060||type 2 3 methylglutaconicaciduria
|
|
D056889|302060||type 2 mga
|
|
D056889|302060||type 2s mga
|
|
D056889|302060||type ii mga
|
|
D056889|302060||type iis mga
|
|
612526|C567282||lipodystrophy congenital generalized type 3
|
|
612526|C567282||berardinelli seip congenital lipodystrophy type 3
|
|
612526|C567282||bscl3
|
|
612526|C567282||cgl3
|
|
612526|C567282||lipodystrophy berardinelli seip congenital type 3
|
|
609821||bleeding disorder platelet type 8
|
|
609821||bdplt8
|
|
609821||bleeding disorder due to p2ry12 defect bleeding disorder due to p2rx1 defect somatic included
|
|
D059327||brachydactyly
|
|
D059327||brachydactylia
|
|
D059327||brachydactylias
|
|
D059327||brachydactylies
|
|
D059327||brachydactylism
|
|
D059327||brachydactylisms
|
|
613070||liver failure infantile transient
|
|
613070||lfit
|
|
D000141|179800||acidosis renal tubular
|
|
D000141|179800||acidosis renal tubular type i
|
|
D000141|179800||acidosis renal tubular type ii
|
|
D000141|179800||autosomal dominant distal renal tubular acidosis
|
|
D000141|179800||classic distal renal tubular acidosis
|
|
D000141|179800||classic type rta
|
|
D000141|179800||classic type rtas
|
|
D000141|179800||distal renal tubular acidosis
|
|
D000141|179800||gradient type rta
|
|
D000141|179800||gradient type rtas
|
|
D000141|179800||proximal renal tubular acidosis
|
|
D000141|179800||proximal type rta
|
|
D000141|179800||proximal type rtas
|
|
D000141|179800||renal tubular acidosis
|
|
D000141|179800||renal tubular acidosis 1
|
|
D000141|179800||renal tubular acidosis distal autosomal dominant
|
|
D000141|179800||renal tubular acidosis i
|
|
D000141|179800||renal tubular acidosis ii
|
|
D000141|179800||renal tubular acidosis proximal
|
|
D000141|179800||renal tubular acidosis proximal with ocular abnormalities
|
|
D000141|179800||renal tubular acidosis type i
|
|
D000141|179800||renal tubular acidosis type ii
|
|
D000141|179800||rta classic type
|
|
D000141|179800||rta distal type autosomal dominant
|
|
D000141|179800||rta gradient type
|
|
D000141|179800||rta proximal type
|
|
D000141|179800||rtas classic type
|
|
D000141|179800||rtas gradient type
|
|
D000141|179800||rtas proximal type
|
|
D000141|179800||type ii renal tubular acidosis
|
|
D000141|179800||type i renal tubular acidosis
|
|
613074||deafness autosomal dominant 50
|
|
613074||dfna50
|
|
D006725||hookworm infections
|
|
D006725||bunostomiases
|
|
D006725||bunostomiasis
|
|
D006725||hookworm infection
|
|
D006725||infection hookworm
|
|
D006725||infections hookworm
|
|
D006726||hordeolum
|
|
D006726||stye
|
|
D006726||styes
|
|
270600|C537481||spastic diplegia infantile type
|
|
270600|C537481||hereditary spastic diplegia with mental retardation
|
|
C565206|610282||retinitis pigmentosa 35
|
|
C565206|610282||rp35
|
|
C564652|606854||polymicrogyria bilateral frontoparietal
|
|
C564652|606854||bfpp
|
|
C564652|606854||cerebellar ataxia with neuronal migration defect
|
|
C536648|274600||pendred syndrome
|
|
C536648|274600||autosomal recessive sensorineural hearing impairment and goiter
|
|
C536648|274600||deafness with goiter
|
|
C536648|274600||goiter deafness syndrome
|
|
C536648|274600||hypothyroidism congenital due to dyshormonogenesis 2b
|
|
C536648|274600||pendred apos s syndrome
|
|
C536648|274600||tdh2b
|
|
C536648|274600||thyroid dyshormonogenesis 2b
|
|
C536648|274600||thyroid hormonogenesis genetic defect in 2b
|
|
C567208|612653||spherocytosis type 4
|
|
C567208|612653||hs4
|
|
C567208|612653||sph4
|
|
C567208|612653||spherocytosis hereditary 4
|
|
D018701||mononegavirales infections
|
|
D018701||infection mononegavirales
|
|
D018701||infections mononegavirales
|
|
D018701||mononegavirales infection
|
|
162100|D020968||brachial plexus neuritis
|
|
162100|D020968||amyotrophic neuralgia
|
|
162100|D020968||amyotrophic neuralgias
|
|
162100|D020968||amyotrophies hereditary neuralgic
|
|
162100|D020968||amyotrophies neuralgic
|
|
162100|D020968||amyotrophy hereditary neuralgic
|
|
162100|D020968||amyotrophy hereditary neuralgic with predilection for brachial plexus
|
|
162100|D020968||amyotrophy neuralgic
|
|
162100|D020968||brachial neuralgia
|
|
162100|D020968||brachial neuralgias
|
|
162100|D020968||brachial neuritides
|
|
162100|D020968||brachial neuritis
|
|
162100|D020968||brachial plexus neuritides
|
|
162100|D020968||brachial plexus neuropathy hereditary
|
|
162100|D020968||cervicobrachial neuralgia
|
|
162100|D020968||cervico brachial neuralgia
|
|
162100|D020968||cervicobrachial neuralgias
|
|
162100|D020968||cervico brachial neuralgias
|
|
162100|D020968||familial brachial plexus neuritis
|
|
162100|D020968||girdle neuropathies shoulder
|
|
162100|D020968||girdle neuropathy shoulder
|
|
162100|D020968||hereditary brachial plexus neuropathy
|
|
162100|D020968||hereditary neuralgic amyotrophies
|
|
162100|D020968||hereditary neuralgic amyotrophy
|
|
162100|D020968||heredofamilial neuritis with brachial plexus predilection
|
|
162100|D020968||hna
|
|
162100|D020968||napb
|
|
162100|D020968||neuralgia amyotrophic
|
|
162100|D020968||neuralgia brachial
|
|
162100|D020968||neuralgia cervicobrachial
|
|
162100|D020968||neuralgia cervico brachial
|
|
162100|D020968||neuralgias amyotrophic
|
|
162100|D020968||neuralgias brachial
|
|
162100|D020968||neuralgias cervicobrachial
|
|
162100|D020968||neuralgias cervico brachial
|
|
162100|D020968||neuralgic amyotrophies
|
|
162100|D020968||neuralgic amyotrophies hereditary
|
|
162100|D020968||neuralgic amyotrophy
|
|
162100|D020968||neuralgic amyotrophy hereditary
|
|
162100|D020968||neuritides brachial
|
|
162100|D020968||neuritides brachial plexus
|
|
162100|D020968||neuritis brachial
|
|
162100|D020968||neuritis brachial plexus
|
|
162100|D020968||neuritis with brachial predilection
|
|
162100|D020968||neuropathies shoulder girdle
|
|
162100|D020968||neuropathy shoulder girdle
|
|
162100|D020968||parsonage aldren turner syndrome
|
|
162100|D020968||parsonage turner syndrome
|
|
162100|D020968||shoulder girdle neuropathies
|
|
162100|D020968||shoulder girdle neuropathy
|
|
162100|D020968||syndrome parsonage aldren turner
|
|
162100|D020968||syndrome parsonage turner
|
|
D018702||filoviridae infections
|
|
D018702||filoviridae infection
|
|
D018702||infection filoviridae
|
|
D018702||infections filoviridae
|
|
609813||scdo3
|
|
D005409||flail chest
|
|
D005409||chest flail
|
|
D005409||chest stove in
|
|
D005409||stove in chest
|
|
D005402||fistula
|
|
D005402||fistulas
|
|
D006734||horse diseases
|
|
D006734||disease equine
|
|
D006734||disease horse
|
|
D006734||diseases equine
|
|
D006734||diseases horse
|
|
D006734||equine disease
|
|
D006734||equine diseases
|
|
D006734||horse disease
|
|
D005401||fissure in ano
|
|
D005401||anal fissure
|
|
D005401||anal ulcer
|
|
D005401||anal ulcers
|
|
D005401||fissure anal
|
|
D005401||ulcer anal
|
|
D005401||ulcers anal
|
|
D006732||horner syndrome
|
|
D006732||acquired horner syndrome
|
|
D006732||bernard apos s syndrome
|
|
D006732||bernards syndrome
|
|
D006732||bernard syndrome
|
|
D006732||bernard syndromes
|
|
D006732||central horner syndrome
|
|
D006732||claude bernard horner syndrome
|
|
D006732||horner apos s syndrome
|
|
D006732||horners syndrome
|
|
D006732||horner apos s syndrome pupil
|
|
D006732||horners syndrome pupil
|
|
D006732||horner syndrome acquired
|
|
D006732||horner syndrome central
|
|
D006732||horner syndrome pupil
|
|
D006732||miosis innervational defect
|
|
D006732||ocular ophthalmoplegias sympathetic
|
|
D006732||ocular ophthalmoplegia sympathetic
|
|
D006732||oculosympathetic syndrome
|
|
D006732||oculosympathetic syndromes
|
|
D006732||ophthalmoplegias sympathetic ocular
|
|
D006732||ophthalmoplegia sympathetic ocular
|
|
D006732||ptosis sympathetic
|
|
D006732||pupil horner apos s syndrome
|
|
D006732||sympathetic ocular ophthalmoplegia
|
|
D006732||sympathetic ocular ophthalmoplegias
|
|
D006732||syndrome acquired horner
|
|
D006732||syndrome bernard
|
|
D006732||syndrome bernard apos s
|
|
D006732||syndrome central horner
|
|
D006732||syndrome claude bernard horner
|
|
D006732||syndrome horner
|
|
D006732||syndrome horner apos s
|
|
D006732||syndrome oculosympathetic
|
|
D006732||syndrome pupil horner apos s
|
|
D006732||syndromes bernard
|
|
D006732||syndromes oculosympathetic
|
|
D059350||chronic pain
|
|
D059350||chronic pains
|
|
D059350||chronic pains widespread
|
|
D059350||chronic pain widespread
|
|
D059350||pain chronic
|
|
D059350||pains chronic
|
|
D059350||pains widespread chronic
|
|
D059350||pain widespread chronic
|
|
D059350||widespread chronic pain
|
|
D059350||widespread chronic pains
|
|
D059345||cerebral small vessel diseases
|
|
D059345||cerebral microangiopathies
|
|
D059345||cerebral microangiopathy
|
|
D059345||cerebral small vessel disease
|
|
D059345||microangiopathies cerebral
|
|
D059345||microangiopathy cerebral
|
|
D059348||peripheral nerve injuries
|
|
D059348||injuries peripheral nerve
|
|
D059348||injury peripheral nerve
|
|
D059348||nerve injuries peripheral
|
|
D059348||nerve injury peripheral
|
|
D059348||peripheral nerve injury
|
|
D059347||cardio renal syndrome
|
|
D059347||cardiorenal syndrome
|
|
D059347||cardiorenal syndromes
|
|
D059347||cardio renal syndromes
|
|
D059347||renocardiac syndrome
|
|
D059347||reno cardiac syndrome
|
|
D059347||renocardiac syndromes
|
|
D059347||reno cardiac syndromes
|
|
D059347||syndrome cardiorenal
|
|
D059347||syndrome cardio renal
|
|
D059347||syndrome renocardiac
|
|
D059347||syndrome reno cardiac
|
|
D059347||syndromes cardiorenal
|
|
D059347||syndromes cardio renal
|
|
D059347||syndromes renocardiac
|
|
D059347||syndromes reno cardiac
|
|
D056728|613554||von willebrand disease type 2
|
|
D056728|613554||type 2a von willebrand disease
|
|
D056728|613554||type 2b von willebrand disease
|
|
D056728|613554||type 2m von willebrand disease
|
|
D056728|613554||type 2n von willebrand disease
|
|
D056728|613554||type 2 von willebrand disease
|
|
D056728|613554||type iia von willebrand disease
|
|
D056728|613554||type iib von willebrand disease
|
|
D056728|613554||type iim von willebrand disease
|
|
D056728|613554||type iin von willebrand disease
|
|
D056728|613554||type ii von willebrand disease
|
|
D056728|613554||von willebrand disease type 2a
|
|
D056728|613554||von willebrand disease type 2b
|
|
D056728|613554||von willebrand disease type 2b included
|
|
D056728|613554||von willebrand disease type 2m
|
|
D056728|613554||von willebrand disease type 2m included
|
|
D056728|613554||von willebrand disease type 2n
|
|
D056728|613554||von willebrand disease type 2n included
|
|
D056728|613554||von willebrand disease type ii
|
|
D056728|613554||von willebrand disease type iia
|
|
D056728|613554||von willebrand disease type iib
|
|
D056728|613554||von willebrand disease type iim
|
|
D056728|613554||von willebrand disease type iin
|
|
D056728|613554||vwd2
|
|
D056728|613554||vwd2a included
|
|
D056728|613554||vwd2b included
|
|
D056728|613554||vwd2m included
|
|
D056728|613554||vwd2n included
|
|
D056728|613554||vwd type 2 von willebrand disease type 2a included
|
|
209880|C536209||congenital central hypoventilation syndrome
|
|
209880|C536209||autonomic control congenital failure of
|
|
209880|C536209||cchs
|
|
209880|C536209||cchs with hirschsprung disease
|
|
209880|C536209||cchs with hirschsprung disease included
|
|
209880|C536209||central hypoventilation syndrome congenital
|
|
209880|C536209||congenital failure of autonomic control
|
|
209880|C536209||congenital ondine curse
|
|
209880|C536209||haddad syndrome
|
|
209880|C536209||haddad syndrome included
|
|
209880|C536209||idiopathic congenital central alveolar hypoventilation
|
|
209880|C536209||ohd included
|
|
209880|C536209||ondine curse congenital
|
|
209880|C536209||ondine curse congenital ondine hirschsprung disease included
|
|
209880|C536209||ondine hirschsprung disease
|
|
209880|C536209||primary alveolar hypoventilation
|
|
300114||mental retardation x linked 49
|
|
300114||mrx49
|
|
C537333|300263||siderius x linked mental retardation syndrome
|
|
C537333|300263||mental retardation x linked siderius type
|
|
C537333|300263||mental retardation x linked syndromic siderius type
|
|
C537333|300263||mrxssd
|
|
C537333|300263||siderius hamel syndrome
|
|
C536398|605814||neonatal onset citrullinemia type 2
|
|
C536398|605814||cholestasis neonatal intrahepatic caused by citrin deficiency
|
|
C536398|605814||citrullinemia type ii neonatal onset
|
|
C536398|605814||neonatal intrahepatic cholestasis caused by citrin deficiency
|
|
C536398|605814||neonatal onset citrullinemia type ii
|
|
C536398|605814||niccd
|
|
C564258|608320||coronary artery disease autosomal dominant 1
|
|
C564258|608320||adcad1
|
|
C564258|608320||coronary artery disease with myocardial infarction
|
|
248510|C538599||lysosomal beta mannosidase deficiency
|
|
248510|C538599||mansb
|
|
C536253|604416||pyogenic arthritis pyoderma gangrenosum and acne
|
|
C536253|604416||familial recurrent arthritis
|
|
C536253|604416||fra
|
|
C536253|604416||papas
|
|
C536253|604416||papa syndrome
|
|
C536253|604416||pyogenic arthritis pyoderma gangrenosum and severe cystic acne
|
|
C536253|604416||pyogenic sterile arthritis pyoderma gangrenosum and acne
|
|
D018804||hantavirus pulmonary syndrome
|
|
D018804||hantavirus associated respiratory distress syndrome
|
|
D018804||hantavirus pulmonary syndromes
|
|
D018804||hards
|
|
C567372|612278||inflammatory bowel disease 19
|
|
C567372|612278||ibd19
|
|
D018805||sepsis
|
|
D018805||blood poisoning
|
|
D018805||blood poisonings
|
|
D018805||poisoning blood
|
|
D018805||poisonings blood
|
|
D018805||pyaemia
|
|
D018805||pyaemias
|
|
D018805||pyemia
|
|
D018805||pyemias
|
|
D018805||pyohemia
|
|
D018805||pyohemias
|
|
D018805||sepsis severe
|
|
D018805||septicemia
|
|
D018805||septicemias
|
|
D018805||severe sepsis
|
|
D017889|177650||exfoliation syndrome
|
|
D017889|177650||exfoliation glaucoma
|
|
D017889|177650||exfoliation syndromes
|
|
D017889|177650||exfoliative syndrome
|
|
D017889|177650||exfoliative syndromes
|
|
D017889|177650||glaucoma capsulare
|
|
D017889|177650||pexg
|
|
D017889|177650||pexs
|
|
D017889|177650||pseudoexfoliation glaucoma
|
|
D017889|177650||pseudoexfoliation of the lens
|
|
D017889|177650||pseudoexfoliation syndrome
|
|
D017889|177650||pseudo exfoliation syndrome
|
|
D017889|177650||pseudoexfoliation syndromes
|
|
D017889|177650||pseudo exfoliation syndromes
|
|
D017889|177650||syndrome exfoliation
|
|
D017889|177650||syndrome exfoliative
|
|
D017889|177650||syndrome pseudoexfoliation
|
|
D017889|177650||syndrome pseudo exfoliation
|
|
D017889|177650||syndromes exfoliation
|
|
D017889|177650||syndromes exfoliative
|
|
D017889|177650||syndromes pseudoexfoliation
|
|
D017889|177650||syndromes pseudo exfoliation
|
|
D017889|177650||xfg
|
|
D017889|177650||xfs
|
|
C536088|146590||ichthyosis hystrix curth macklin type
|
|
C536088|146590||curth macklin type ichthyosis hystrix
|
|
C536088|146590||ihcm
|
|
D047268||lingual goiter
|
|
D047268||goiter lingual
|
|
D047268||goiters lingual
|
|
D047268||lingual goiters
|
|
300125||migraine familial typical susceptibility to 2
|
|
300125||mfts
|
|
300125||mgr2
|
|
D006837||hydroa vacciniforme
|
|
D006833||hydrarthrosis
|
|
D006833||hydrarthroses
|
|
D006831||polyhydramnios
|
|
D006831||hydramnios
|
|
D006832||hydranencephaly
|
|
D006832||absence of cerebral hemispheres congenital
|
|
D006832||cerebral hemispheres absence congenital
|
|
D006832||congenital absence of cerebral hemispheres
|
|
D006832||hemihydranencephalies
|
|
D006832||hemihydranencephaly
|
|
D006832||hydranencephalies
|
|
D006832||hydranencephaly with proliferative vasculopathy
|
|
C567728|613148||inflammatory bowel disease 28 autosomal recessive
|
|
C567728|613148||ibd28
|
|
C567728|613148|612567|C567251||inflammatory bowel disease early onset autosomal recessive
|
|
253290|C537377|265000||multiple pterygium syndrome lethal type
|
|
253290||lmps
|
|
253290|C537377|265000||pterygium syndrome multiple lethal type
|
|
C565312|605635||hyperaldosteronism familial type ii
|
|
C565312|605635||fh ii
|
|
C564715|300088||epilepsy female restricted with mental retardation
|
|
C564715|300088||convulsive disorder and mental retardation
|
|
C564715|300088||efmr
|
|
C564715|300088||eiee9
|
|
C564715|300088||epileptic encephalopathy early infantile 9
|
|
C564715|300088||juberg hellman syndrome
|
|
D059246||tachypnea
|
|
D059246||tachypneas
|
|
D059249||otomycosis
|
|
D059249||otomycoses
|
|
C563144|300046||mental retardation x linked 23
|
|
C563144|300046||mrx23
|
|
D029461|269920||sialic acid storage disease
|
|
D029461|269920||finnish type sialuria
|
|
D029461|269920||finnish type sialurias
|
|
D029461|269920||french type sialuria
|
|
D029461|269920||infantile form sialuria
|
|
D029461|269920||infantile form sialurias
|
|
D029461|269920||infantile sialic acid storage disease
|
|
D029461|269920||infantile sialic acid storage disorder
|
|
D029461|269920||infantile sialic acid storage disorder issd
|
|
D029461|269920||issd
|
|
D029461|269920|C535525||n acetylneuraminic acid storage disease
|
|
D029461|269920|C535525||nana storage disease
|
|
D029461|269920||nsd
|
|
D029461|269920||salla disease
|
|
D029461|269920||sd
|
|
D029461|269920||sialic acid storage disease finnish type
|
|
D029461|269920||sialic acid storage disease infantile form
|
|
D029461|269920||sialuria
|
|
D029461|269920||sialuria finnish type
|
|
D029461|269920|C537332||sialuria french type
|
|
D029461|269920||sialuria infantile form
|
|
D029461|269920||sialurias
|
|
D029461|269920||sialurias finnish type
|
|
D029461|269920||sialurias infantile form
|
|
D059245||transient tachypnea of the newborn
|
|
D059245||newborn transient tachypnea
|
|
D059245||newborn transient tachypneas
|
|
D059245||transient tachypnea of newborn
|
|
C566451|610069||polyposis syndrome hereditary mixed 2
|
|
C566451|610069||hmps2
|
|
C566337|603776||hypercholesterolemia autosomal dominant 3
|
|
C566337|603776||fh3
|
|
C566337|603776||fh3 low density lipoprotein cholesterol level quantitative trait locus 1 included
|
|
C566337|603776||hchola3
|
|
C566337|603776||ldlcq1 included
|
|
D006800||deltaretrovirus infections
|
|
D006800||blv infection
|
|
D006800||blv infections
|
|
D006800||deltaretrovirus infection
|
|
D006800||htlv blv infection
|
|
D006800||htlv blv infections
|
|
D006800||htlv infection
|
|
D006800||htlv infections
|
|
D006800||infection deltaretrovirus
|
|
D006800||infections deltaretrovirus
|
|
C535740|602579||congenital disorder of glycosylation type 1b
|
|
C535740|602579||carbohydrate deficient glycoprotein syndrome type 1b
|
|
C535740|602579||cdg1b
|
|
C535740|602579||cdg gastrointestinal type
|
|
C535740|602579||cdgib
|
|
C535740|602579||cdg ib
|
|
C535740|602579||congenital disorder of glycosylation type ib
|
|
C535740|602579||mannosephosphate isomerase deficiency
|
|
C535740|602579||mpi deficiency
|
|
C535740|602579||protein losing enteropathy hepatic fibrosis syndrome
|
|
C535740|602579||saguenay lac saint jean syndrome
|
|
C535740|602579||slsj syndrome
|
|
C536917|275100||hypothyroidism congenital nongoitrous 4
|
|
C536917|275100||chng4
|
|
C536917|275100||congenital nongoitrous hypothyroidism 4
|
|
C536917|275100||pituitary cretinism
|
|
C536917|275100||pituitary cretinism thyrotropin biologically inactive included
|
|
C536917|275100||thyroid stimulating hormone deficiency
|
|
C536917|275100||thyroid stimulating hormone deficiency of
|
|
C536917|275100||thyrotropin deficiency isolated
|
|
C536917|275100||tsh deficiency
|
|
C565876|212550||microphthalmia isolated with cataract 2
|
|
C565876|212550||mcopct2
|
|
C565876|212550||microphthalmia and cataract 2
|
|
C565876|212550||microphthalmia cataract and nystagmus
|
|
C562889|161900||renal failure progressive with hypertension
|
|
C562889|161900||aorf
|
|
C562889|161900||nephritis familial without deafness or ocular defect
|
|
C562889|161900||nephropathy familial
|
|
C562889|161900||renal failure adult onset
|
|
C562889|161900||rfh1
|
|
607155||muscular dystrophy dystroglycanopathy limb girdle type c 5
|
|
607155|C564612||lgmd2i
|
|
607155||mddgc5
|
|
607155||muscular dystrophy dystroglycanopathy limb girdle frkp related
|
|
607155|C564612||muscular dystrophy limb girdle type 2i
|
|
D009083||mucopolysaccharidoses
|
|
D009083||mucopolysaccharidosis
|
|
D009080||kawasaki syndrome
|
|
D009080||lymph node syndrome mucocutaneous
|
|
D006819||hyaline membrane disease
|
|
D006819||disease hyaline membrane
|
|
D006819||diseases hyaline membrane
|
|
D006819||hyaline membrane diseases
|
|
606812|C538191||fumaric aciduria
|
|
606812|C538191||fumarase deficiency
|
|
606812|C538191||fumarate hydratase deficiency
|
|
606812|C538191||fumaricaciduria
|
|
C562649|226200||enterokinase deficiency
|
|
C562649|226200||enteropeptidase deficiency
|
|
C567388|612241||inflammatory bowel disease 12
|
|
C567388|612241||ibd12
|
|
C566946|608526||periodontitis aggressive 2
|
|
C563320|601414||retinitis pigmentosa 18
|
|
C563320|601414||rp18
|
|
126200|D009103||multiple sclerosis
|
|
126200|D009103||disseminated sclerosis
|
|
126200|D009103||disseminated sclerosis multiple sclerosis susceptibility to 1 included
|
|
126200|D009103||ms
|
|
126200|D009103||ms1 included
|
|
126200|D009103||ms2
|
|
126200|D009103||ms3
|
|
126200|D009103||ms4
|
|
126200|D009103||ms multiple sclerosis
|
|
126200|D009103||multiple sclerosis acute fulminating
|
|
126200|D009103||multiple sclerosis susceptibility to
|
|
126200|D009103||multiple sclerosis susceptibility to 2
|
|
126200|D009103||multiple sclerosis susceptibility to 3
|
|
126200|D009103||multiple sclerosis susceptibility to 4
|
|
126200|D009103||sclerosis disseminated
|
|
126200|D009103||sclerosis multiple
|
|
C564533|300324||mental retardation x linked 53
|
|
C564533|300324||mrx53
|
|
D006810||humeral fractures
|
|
D006810||fracture humeral
|
|
D006810||fractures humeral
|
|
D006810||humeral fracture
|
|
D059270||petrositis
|
|
D059270||apicitides petrous
|
|
D059270||apicitis petrous
|
|
D059270||gradenigo lannois syndrome
|
|
D059270||gradenigo apos s syndrome
|
|
D059270||gradenigos syndrome
|
|
D059270||gradenigo syndrome
|
|
D059270||petrositides
|
|
D059270||petrous apicitides
|
|
D059270||petrous apicitis
|
|
D059270||syndrome gradenigo
|
|
D059270||syndrome gradenigo lannois
|
|
D059270||syndrome gradenigo apos s
|
|
D059269||chilaiditi syndrome
|
|
D059269||anomaly chilaiditi
|
|
D059269||anomaly chilaiditi apos s
|
|
D059269||chilaiditi anomaly
|
|
D059269||chilaiditi apos s anomaly
|
|
D059269||chilaiditis anomaly
|
|
D059269||chilaiditi apos s syndrome
|
|
D059269||chilaiditis syndrome
|
|
D059269||syndrome chilaiditi
|
|
D059269||syndrome chilaiditi apos s
|
|
D010004|119900||osteoarthropathy primary hypertrophic
|
|
D010004|119900||acropachies hereditary
|
|
D010004|119900||acropachy hereditary
|
|
D010004|119900||autosomal dominant pachydermoperiostoses
|
|
D010004|119900||autosomal dominant pachydermoperiostosis
|
|
D010004|119900||autosomal recessive pachydermoperiostosis
|
|
D010004|119900||clubbing of digits
|
|
D010004|119900||cranioosteoarthropathies
|
|
D010004|119900||cranioosteoarthropathy
|
|
D010004|119900||currarino idiopathic osteoarthropathy
|
|
D010004|119900||digital clubbing isolated congenital
|
|
D010004|119900||familial idiopathic osteoarthropathy of childhood
|
|
D010004|119900||hereditary acropachies
|
|
D010004|119900||hereditary acropachy
|
|
D010004|119900||hypertrophic osteoarthropathy idiopathic
|
|
D010004|119900||hypertrophic osteoarthropathy primary
|
|
D010004|119900||hypertrophic osteoarthropathy primary autosomal dominant
|
|
D010004|119900||hypertrophic osteoarthropathy primary autosomal recessive
|
|
D010004|119900||idiopathic hypertrophic osteoarthropathy
|
|
D010004|119900||osteoarthropathy currarino idiopathic
|
|
D010004|119900||osteoarthropathy idiopathic hypertrophic
|
|
D010004|119900||pachydermoperiostoses autosomal dominant
|
|
D010004|119900||pachydermoperiostosis
|
|
D010004|119900||pachydermoperiostosis autosomal dominant
|
|
D010004|119900|259100||pachydermoperiostosis autosomal recessive
|
|
D010004|119900||primary hypertrophic osteoarthropathy
|
|
D010004|119900||primary hypertrophic osteoarthropathy autosomal dominant
|
|
D010004|119900||recessive pachydermoperiostosis autosomal
|
|
D010004|119900||touraine solente gole syndrome
|
|
D059268||atrophic vaginitis
|
|
D059268||atrophic vaginitides
|
|
D059268||vaginitides atrophic
|
|
D059268||vaginitis atrophic
|
|
D059265||visceral pain
|
|
D059265||pains visceral
|
|
D059265||pain visceral
|
|
D059265||visceral pains
|
|
D059266||bisphosphonate associated osteonecrosis of the jaw
|
|
D059266||bisphosphonate associated osteonecroses
|
|
D059266||bisphosphonate associated osteonecrosis
|
|
D059266||bisphosphonate associated osteonecrosis of the jaws
|
|
D059266||bisphosphonate induced osteonecrosis of the jaw
|
|
D059266||bisphosphonate induced osteonecrosis of the jaws
|
|
D059266||bisphosphonate osteonecroses
|
|
D059266||bisphosphonate osteonecrosis
|
|
D059266||bisphosphonate related osteonecrosis of the jaw
|
|
D059266||osteonecroses bisphosphonate
|
|
D059266||osteonecroses bisphosphonate associated
|
|
D059266||osteonecrosis bisphosphonate
|
|
D059266||osteonecrosis bisphosphonate associated
|
|
D059266||osteonecrosis of the jaw bisphosphonate associated
|
|
D059266||osteonecrosis of the jaw bisphosphonate induced
|
|
D059266||osteonecrosis of the jaw bisphosphonate related
|
|
D059266||osteonecrosis of the jaws bisphosphonate associated
|
|
D059266||osteonecrosis of the jaws bisphosphonate induced
|
|
D059266||osteonecrosis of the jaws bisphosphonate related
|
|
D009091||mucormycosis
|
|
D009091||mucormycoses
|
|
C535690||long chain acyl coa dehydrogenase deficiency
|
|
C535690||acyl coa dehydrogenase long chain deficiency of
|
|
C565267|606012||deafness autosomal dominant 18
|
|
C565267|606012||dfna18
|
|
C535692||male pseudohermaphroditism due to defective lh molecule
|
|
C535693||male pseudohermaphroditism mental retardation syndrome verloes type
|
|
C535693||verloes syndrome
|
|
C567859|612934||glycogen storage disease xiv
|
|
C567859|612934||gsd14
|
|
C567859|612934||gsd xiv
|
|
C567859|612934||moved to 614921
|
|
C567859|612934||pgm1 deficiency
|
|
C567859|612934||phosphoglucomutase 1 deficiency
|
|
D010048||ovarian cysts
|
|
D010048||corpus luteum cyst
|
|
D010048||corpus luteum cysts
|
|
D010048||cyst corpus luteum
|
|
D010048||cyst ovarian
|
|
D010048||cysts corpus luteum
|
|
D010048||cysts ovarian
|
|
D010048||ovarian cyst
|
|
D009069||movement disorders
|
|
D009069||dyskinesia lingual facial buccal
|
|
D009069||dyskinesia linguofacial
|
|
D009069||dyskinesia oral
|
|
D009069||dyskinesia oral facial
|
|
D009069||dyskinesia orofacial
|
|
D009069||dyskinesias lingual facial buccal
|
|
D009069||dyskinesias linguofacial
|
|
D009069||dyskinesias oral
|
|
D009069||dyskinesias oral facial
|
|
D009069||dyskinesias orofacial
|
|
D009069||dyskinesias tardive
|
|
D009069||dyskinesia syndrome
|
|
D009069||dyskinesia syndromes
|
|
D009069||dyskinesia tardive
|
|
D009069||dystonias tardive
|
|
D009069||dystonia tardive
|
|
D009069||etat marbre
|
|
D009069||lingual facial buccal dyskinesia
|
|
D009069||lingual facial buccal dyskinesias
|
|
D009069||linguofacial dyskinesia
|
|
D009069||linguofacial dyskinesias
|
|
D009069||movement disorder
|
|
D009069||movement disorder syndrome
|
|
D009069||movement disorder syndromes
|
|
D009069||oral dyskinesia
|
|
D009069||oral dyskinesias
|
|
D009069||oral facial dyskinesia
|
|
D009069||oral facial dyskinesias
|
|
D009069||orofacial dyskinesia
|
|
D009069||orofacial dyskinesias
|
|
D009069||status marmoratus
|
|
D009069||tardive dyskinesia
|
|
D009069||tardive dyskinesias
|
|
D009069||tardive dystonia
|
|
D009069||tardive dystonias
|
|
D009069||tardive oral dyskinesia
|
|
D009069||tardive oral dyskinesias
|
|
D011378||prognathism
|
|
D011378||prognathisms
|
|
D010049||ovarian diseases
|
|
D010049||disease ovarian
|
|
D010049||diseases ovarian
|
|
D010049||ovarian disease
|
|
D009066||mouth edentulous
|
|
D009066||edentulous mouth
|
|
D009066||edentulous mouths
|
|
D009066||mouth toothless
|
|
D009066||toothless mouth
|
|
607134||specific language impairment 3
|
|
607134||sli3
|
|
607134||specific language impairment quantitative trait locus on chromosome 13
|
|
D009062||mouth neoplasms
|
|
D009062||cancer mouth
|
|
D009062||cancer of mouth
|
|
D009062||cancer of the mouth
|
|
D009062||cancer oral
|
|
D009062||cancers mouth
|
|
D009062||cancers oral
|
|
D009062||mouth cancer
|
|
D009062||mouth cancers
|
|
D009062||mouth neoplasm
|
|
D009062||neoplasm mouth
|
|
D009062||neoplasm oral
|
|
D009062||neoplasms mouth
|
|
D009062||neoplasms oral
|
|
D009062||oral cancer
|
|
D009062||oral cancers
|
|
D009062||oral neoplasm
|
|
D009062||oral neoplasms
|
|
C535688||robin sequence and oligodactyly
|
|
C535688||pierre robin syndrome and oligodactyly
|
|
C483996||for heavy chain disease protein human
|
|
C483996||gamma 1 heavy chain disease protein for human
|
|
C483997||wis heavy chain disease protein human
|
|
C483997||gamma 3 heavy chain disease protein wis human
|
|
C483997||myeloma protein wis human
|
|
C483997||protein wis human
|
|
241520|C562792||hypophosphatemic rickets autosomal recessive 1
|
|
241520|C562792||arhp
|
|
241520|C562792||arhr
|
|
241520|C562792||arhr1
|
|
241520|C562792||hypophosphatemia autosomal recessive
|
|
D011391||prolapse
|
|
D011391||prolapses
|
|
C483999||cha heavy chain disease protein human
|
|
C483999||gamma heavy chain disease protein cha human
|
|
C566955|611391||cataract cortical juvenile onset
|
|
C566955|611391||cataract 33
|
|
C566955|611391||cataract 33 cortical
|
|
C566955|611391||ctrct33
|
|
D009078||mucocele
|
|
D009078||mucoceles
|
|
609782|C565229||aortic aneurysm familial abdominal 2
|
|
609782||aaa2
|
|
C536353|201475||vlcad deficiency
|
|
C536353|201475||acadvl
|
|
C536353|201475||acadvld
|
|
C536353|201475||acyl coa dehydrogenase very long chain deficiency
|
|
C536353|201475||acyl coa dehydrogenase very long chain deficiency of
|
|
C536353|201475||pearson marrow pancreas syndrome
|
|
C536353|201475||pearson apos s marrow pancreas syndrome
|
|
C536353|201475||sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction
|
|
C536353|201475||very long chain acyl coa dehydrogenase deficiency
|
|
C536353|201475||very long chain acyl coenzyme a dehydrogenase deficiency
|
|
C536353|201475||vlcad c
|
|
C536353|201475||vlcad h
|
|
D009072|C536991|252350||moyamoya disease
|
|
D009072||cerebrovascular moyamoya disease
|
|
D009072||classic moyamoya disease
|
|
D009072||disease classic moyamoya
|
|
D009072||disease moya moya
|
|
D009072||disease primary moyamoya
|
|
D009072||moya moya disease
|
|
D009072||moyamoya disease classic
|
|
D009072||moyamoya disease primary
|
|
D009072||moyamoya disease secondary
|
|
D009072||moyamoya diseases primary
|
|
D009072||moyamoya syndrome
|
|
D009072||primary moyamoya disease
|
|
D009072||primary moyamoya diseases
|
|
D009072||progressive intracranial occlusive arteropathy moyamoya
|
|
D009072||secondary moyamoya disease
|
|
217080|C536604||amaurosis hypertrichosis
|
|
217080|C536604||amaurosis congenita cone rod type with congenital hypertrichosis
|
|
217080|C536604||cone rod congenital amaurosis associated with congenital hypertrichosis
|
|
217080|C536604||cone rod dystrophy and amelogenesis imperfecta
|
|
217080|C536604||congenital amaurosis cone rod type with congenital hypertrichosis
|
|
217080|C536604||jalili syndrome
|
|
149000|D007715||klippel trenaunay weber syndrome
|
|
149000|D007715||angioosteohypertrophy syndrome
|
|
149000|D007715||angio osteohypertrophy syndrome
|
|
149000|D007715||angioosteohypertrophy syndromes
|
|
149000|D007715||angio osteohypertrophy syndromes
|
|
149000|D007715||angiopathies congenital dysplastic
|
|
149000|D007715||angiopathy congenital dysplastic
|
|
149000|D007715||congenital dysplastic angiopathies
|
|
149000|D007715||congenital dysplastic angiopathy
|
|
149000|D007715||disease klippel trenaunay
|
|
149000|D007715||dysplastic angiopathies congenital
|
|
149000|D007715||dysplastic angiopathy congenital
|
|
149000|D007715||klippel trenaunay disease
|
|
149000|D007715||klippel trenaunay syndrome
|
|
149000|D007715||klippel trenaunay syndromes
|
|
149000|D007715||klippel tr 233 naunay weber syndrome
|
|
149000|D007715||kts
|
|
149000|D007715||ktw syndrome
|
|
149000|D007715||ktw syndromes
|
|
149000|D007715||syndrome angioosteohypertrophy
|
|
149000|D007715||syndrome angio osteohypertrophy
|
|
149000|D007715||syndrome klippel trenaunay
|
|
149000|D007715||syndrome klippel trenaunay weber
|
|
149000|D007715||syndrome klippel tr 233 naunay weber
|
|
149000|D007715||syndrome ktw
|
|
149000|D007715||syndromes angioosteohypertrophy
|
|
149000|D007715||syndromes angio osteohypertrophy
|
|
149000|D007715||syndromes klippel trenaunay
|
|
149000|D007715||syndromes ktw
|
|
C536015|200600||achondrogenesis type 1a
|
|
C536015|200600||acg1a
|
|
C536015|200600||achondrogenesis houston harris type
|
|
C536015|200600||achondrogenesis type ia
|
|
C536015|200600||houston harris achondrogenesis
|
|
D020158|605899||hyperglycinemia nonketotic
|
|
D020158|605899||encephalopathies glycine
|
|
D020158|605899||encephalopathy glycine
|
|
D020158|605899||gce
|
|
D020158|605899||glycine encephalopathies
|
|
D020158|605899||glycine encephalopathy
|
|
D020158|605899||hyperglycinemia non ketotic
|
|
D020158|605899||hyperglycinemia nonketotic nkh hyperglycinemia transient neonatal included
|
|
D020158|605899||hyperglycinemia nonketotic type i
|
|
D020158|605899||hyperglycinemia nonketotic type ii
|
|
D020158|605899||hyperglycinemia nonketotic type iii
|
|
D020158|605899||hyperglycinemias nonketotic
|
|
D020158|605899||hyperglycinemias non ketotic
|
|
D020158|605899||non ketotic hyperglycinemia
|
|
D020158|605899||nonketotic hyperglycinemia
|
|
D020158|605899||non ketotic hyperglycinemias
|
|
D020158|605899||nonketotic hyperglycinemias
|
|
D020158|605899||nonketotic hyperglycinemia type i
|
|
D020158|605899||nonketotic hyperglycinemia type ii
|
|
D020158|605899||nonketotic hyperglycinemia type iii
|
|
D020158|605899||tnh included
|
|
D020158|605899||type iii nonketotic hyperglycinemia
|
|
D020158|605899||type ii nonketotic hyperglycinemia
|
|
D020158|605899||type i nonketotic hyperglycinemia
|
|
C567499|611895||amyotrophic lateral sclerosis 9
|
|
C567499|611895||als9
|
|
D011038|268400||rothmund thomson syndrome
|
|
D011038|268400||congenitale poikiloderma
|
|
D011038|268400||congenitales poikiloderma
|
|
D011038|268400||congenital poikiloderma
|
|
D011038|268400||poikiloderma atrophicans and cataract
|
|
D011038|268400||poikiloderma congenitale
|
|
D011038|268400||poikiloderma congenitale of rothmund thomson
|
|
D011038|268400||poikiloderma congenitales
|
|
D011038|268400||poikiloderma of rothmund thomson
|
|
D011038|268400||rothmund thomson poikiloderma
|
|
D011038|268400||rothmund thomson poikilodermas
|
|
D011038|268400|D015518|312750||rts
|
|
D011038|268400||syndrome rothmund thomson
|
|
D023341||chills
|
|
610762||high density lipoprotein cholesterol level quantitative trait locus 6
|
|
610762||hdlcq6
|
|
D010026||osteosclerosis
|
|
D010026||osteoscleroses
|
|
D010025||osteoradionecrosis
|
|
D010025||osteoradionecroses
|
|
D006938|144010|143890||hyperlipoproteinemia type ii
|
|
D006938|144010||apolipoprotein b 100 familial defective
|
|
D006938|144010||apolipoprotein b 100 familial ligand defective
|
|
D006938|144010||autosomal dominant hypercholesterolemia
|
|
D006938|144010||autosomal dominant hypercholesterolemias
|
|
D006938|144010||combined hyperlipoproteinemia familial
|
|
D006938|144010||combined hyperlipoproteinemias familial
|
|
D006938|144010||density lipoproteinemia hyper low
|
|
D006938|144010||density lipoproteinemias hyper low
|
|
D006938|144010||disorder ldl receptor
|
|
D006938|144010||disorders ldl receptor
|
|
D006938|144010||dominant hypercholesterolemia autosomal
|
|
D006938|144010||dominant hypercholesterolemias autosomal
|
|
D006938|144010||essential hypercholesterolemia
|
|
D006938|144010||essential hypercholesterolemias
|
|
D006938|144010||familial combined hyperlipoproteinemia
|
|
D006938|144010||familial combined hyperlipoproteinemias
|
|
D006938|144010||familial hypercholesterolemia
|
|
D006938|144010||familial hypercholesterolemias
|
|
D006938|144010||familial hypercholesterolemic xanthomatoses
|
|
D006938|144010||familial hypercholesterolemic xanthomatosis
|
|
D006938|144010||hyperbetalipoproteinemia
|
|
D006938|144010||hyper beta lipoproteinemia
|
|
D006938|144010||hyperbetalipoproteinemias
|
|
D006938|144010||hyper beta lipoproteinemias
|
|
D006938|144010||hypercholesterolemia autosomal dominant
|
|
D006938|144010||hypercholesterolemia autosomal dominant type b
|
|
D006938|144010||hypercholesterolemia essential
|
|
D006938|144010|143890||hypercholesterolemia familial
|
|
D006938|144010|C536083||hypercholesterolemia familial due to ligand defective apolipoprotein b
|
|
D006938|144010||hypercholesterolemias autosomal dominant
|
|
D006938|144010||hypercholesterolemias essential
|
|
D006938|144010||hypercholesterolemias familial
|
|
D006938|144010||hypercholesterolemic xanthomatoses familial
|
|
D006938|144010|143890||hypercholesterolemic xanthomatosis familial
|
|
D006938|144010||hyperlipoproteinemia familial combined
|
|
D006938|144010||hyperlipoproteinemias familial combined
|
|
D006938|144010||hyperlipoproteinemias type ii
|
|
D006938|144010||hyperlipoproteinemias type iia
|
|
D006938|144010||hyperlipoproteinemia type 2
|
|
D006938|144010||hyperlipoproteinemia type 2s
|
|
D006938|144010|143890||hyperlipoproteinemia type iia
|
|
D006938|144010||hyperlipoproteinemia type iias
|
|
D006938|144010||hyperlipoproteinemia type iib
|
|
D006938|144010||hyperlipoproteinemia type iibs
|
|
D006938|144010||hyperlipoproteinemia type iis
|
|
D006938|144010|143890||hyper low density lipoproteinemia
|
|
D006938|144010||hyper low density lipoproteinemias
|
|
D006938|144010||ldl receptor disorder
|
|
D006938|144010||ldl receptor disorders
|
|
D006938|144010||lipoproteinemia hyper low density
|
|
D006938|144010||lipoproteinemias hyper low density
|
|
D006938|144010||receptor disorder ldl
|
|
D006938|144010||receptor disorders ldl
|
|
D006938|144010||type 2 hyperlipoproteinemia
|
|
D006938|144010||type iia hyperlipoproteinemia
|
|
D006938|144010||type iia hyperlipoproteinemias
|
|
D006938|144010||type ii hyperlipoproteinemia
|
|
D006938|144010||type ii hyperlipoproteinemias
|
|
D006938|144010||xanthomatoses familial hypercholesterolemic
|
|
D006938|144010||xanthomatosis familial hypercholesterolemic
|
|
610761||high density lipoprotein cholesterol level quantitative trait locus 5
|
|
610761||hdlcq5
|
|
D010029||ostertagiasis
|
|
D010029||ostertagiases
|
|
611092|C567017||mental retardation autosomal recessive 6
|
|
611092|C567017||mrt6
|
|
D009041||motion sickness
|
|
D009041||airsickness
|
|
D009041||air sickness
|
|
D009041||carsickness
|
|
D009041||car sickness
|
|
D009041||seasickness
|
|
D009041||sea sickness
|
|
D009041||sickness air
|
|
D009041||sickness car
|
|
D009041||sickness motion
|
|
D009041||sickness sea
|
|
D010020||osteonecrosis
|
|
D010020||aseptic necrosis of bone
|
|
D010020||avascular necrosis of bone
|
|
D010020||bone aseptic necrosis
|
|
D010020||bone avascular necrosis
|
|
D010020||kienbock disease
|
|
D010020||kienbock apos s disease
|
|
D010020||kienboeck disease
|
|
D010020||kienboeck apos s disease
|
|
D010020||kienboecks disease
|
|
D010020||necrosis aseptic of bone
|
|
D010020||necrosis avascular of bone
|
|
D010020||osteonecroses
|
|
D011350||proctocolitis
|
|
D011350||hemorrhagic proctocolitis
|
|
D011350||hemorrhagic rectocolitis
|
|
D011350||proctocolitides ulcerative
|
|
D011350||proctocolitis hemorrhagic
|
|
D011350||proctocolitis ulcerative
|
|
D011350||proctosigmoiditis
|
|
D011350||rectocolitides ulcerative
|
|
D011350||rectocolitis
|
|
D011350||rectocolitis hemorrhagic
|
|
D011350||rectocolitis ulcerative
|
|
D011350||rectosigmoiditis
|
|
D011350||ulcerative proctocolitides
|
|
D011350||ulcerative proctocolitis
|
|
D011350||ulcerative rectocolitides
|
|
D011350||ulcerative rectocolitis
|
|
608447||carotid intimal medial thickness 2
|
|
608447||carotid intimal medial thickness quantitative trait locus on chromosome 12
|
|
608447||cimt2
|
|
214400|C535419||charcot marie tooth disease type 4a
|
|
214400|C535419||charcot marie tooth disease demyelinating autosomal recessive
|
|
214400|C535419||charcot marie tooth neuropathy type 4a
|
|
214400|C535419||cmt4a
|
|
D010023||osteopoikilosis
|
|
D010023||osteopoikiloses
|
|
264700|C562688||vitamin d hydroxylation deficient rickets type 1a
|
|
264700|C562688||1 alpha 25 hydroxyvitamin d3 deficiency selective
|
|
264700|C562688||1 alpha hydroxylase deficiency
|
|
264700|C562688||25 hydroxycholecalciferol 1 hydroxylase deficiency
|
|
264700|C562688||pddr1a
|
|
264700|C562688||pddr ia
|
|
264700|C562688||pseudovitamin d deficiency rickets type ia
|
|
264700|C562688||vdd1
|
|
264700|C562688||vddr1a
|
|
264700|C562688||vitamin d dependency type 1
|
|
264700|C562688||vitamin d dependent rickets type 1a
|
|
256500|D056770||netherton syndrome
|
|
256500|D056770||disease netherton
|
|
256500|D056770||erythroderma ichthyosiform with hypotrichosis and hyper ige
|
|
256500|D056770||neth
|
|
256500|D056770||netherton disease
|
|
256500|D056770||ns
|
|
256500|D056770||syndrome netherton
|
|
C535306|236792||2 hydroxyglutaricaciduria
|
|
C535306|236792||2 hga
|
|
C535306|236792||2 hydroxyglutaric aciduria
|
|
C535306|236792||combined d 2 and l 2 hydroxyglutaric aciduria
|
|
C535306|236792||d2hga
|
|
C535306|236792||d2hga1
|
|
C535306|236792||d2hga2
|
|
C535306|236792||d 2 hydroxyglutaric aciduria
|
|
C535306|236792||d 2 hydroxyglutaric aciduria 1
|
|
C535306|236792||d 2 hydroxyglutaric aciduria 2
|
|
C535306|236792||l 2 hydroxyglutaric acidemia
|
|
C535306|236792||l 2 hydroxyglutaric aciduria
|
|
D009059||mouth diseases
|
|
D009059||disease mouth
|
|
D009059||diseases mouth
|
|
D009059||mouth disease
|
|
D009058||mouth breathing
|
|
D009058||breathing mouth
|
|
D009058||breathings mouth
|
|
D009058||mouth breathings
|
|
D010039||otorhinolaryngologic neoplasms
|
|
D010039||cancer otorhinolaryngeal
|
|
D010039||cancers otorhinolaryngeal
|
|
D010039||neoplasm ootorhinolaryngeal
|
|
D010039||neoplasm otorhinolaryngologic
|
|
D010039||neoplasm otorhinolaryngological
|
|
D010039||neoplasms ootorhinolaryngeal
|
|
D010039||neoplasms otorhinolaryngologic
|
|
D010039||neoplasms otorhinolaryngological
|
|
D010039||ootorhinolaryngeal neoplasm
|
|
D010039||ootorhinolaryngeal neoplasms
|
|
D010039||otorhinolaryngeal cancer
|
|
D010039||otorhinolaryngeal cancers
|
|
D010039||otorhinolaryngological neoplasm
|
|
D010039||otorhinolaryngological neoplasms
|
|
D010039||otorhinolaryngologic neoplasm
|
|
D009057||stomatognathic diseases
|
|
D009057||dental disease
|
|
D009057||dental diseases
|
|
D009057||disease dental
|
|
D009057||diseases dental
|
|
D009057||diseases stomatognathic
|
|
D009057||disease stomatognathic
|
|
D009057||mouth and tooth diseases
|
|
D009057||stomatognathic disease
|
|
D010038||otorhinolaryngologic diseases
|
|
D010038||disease ent
|
|
D010038||disease otolaryngologic
|
|
D010038||disease otolaryngological
|
|
D010038||disease otorhinolaryngologic
|
|
D010038||disease otorhinolaryngological
|
|
D010038||diseases ent
|
|
D010038||diseases otolaryngologic
|
|
D010038||diseases otolaryngological
|
|
D010038||diseases otorhinolaryngologic
|
|
D010038||diseases otorhinolaryngological
|
|
D010038||ent disease
|
|
D010038||ent diseases
|
|
D010038||otolaryngological disease
|
|
D010038||otolaryngological diseases
|
|
D010038||otolaryngologic disease
|
|
D010038||otolaryngologic diseases
|
|
D010038||otorhinolaryngological disease
|
|
D010038||otorhinolaryngological diseases
|
|
D010038||otorhinolaryngologic disease
|
|
D009056||mouth abnormalities
|
|
D009056||abnormalities mouth
|
|
D009056||abnormality mouth
|
|
D009056||mouth abnormality
|
|
150600|D007873||legg calve perthes disease
|
|
150600|D007873||coxa plana
|
|
150600|D007873||disease legg calve perthes
|
|
150600|D007873||disease legg calv 233 perthes
|
|
150600|D007873||disease legg perthes
|
|
150600|D007873||disease perthes
|
|
150600|D007873||lcp
|
|
150600|D007873||lcpd
|
|
150600|D007873||legg calv 233 perthes disease
|
|
150600|D007873||legg calve perthes syndrome
|
|
150600|D007873||legg calv 233 perthes syndrome
|
|
150600|D007873||legg perthes disease
|
|
150600|D007873||osteochondritis deforman
|
|
150600|D007873||osteochondritis deformans
|
|
150600|D007873||perthes disease
|
|
150600|D007873||syndrome legg calve perthes
|
|
150600|D007873||syndrome legg calv 233 perthes
|
|
C536266|606190||radiation induced meningioma
|
|
C536266|606190||meningioma radiation induced
|
|
C536266|606190||mnri
|
|
D001008|607834||anxiety disorders
|
|
D001008|607834||anxiety
|
|
D001008|607834||anxiety disorder
|
|
D001008|607834||anxiety neuroses
|
|
D001008|607834||anxiety state neurotic
|
|
D001008|607834||anxiety states neurotic
|
|
D001008|607834||disorder anxiety
|
|
D001008|607834||disorders anxiety
|
|
D001008|607834||harm avoidance included
|
|
D001008|607834||neuroses anxiety
|
|
D001008|607834||neurotic anxiety state
|
|
D001008|607834||neurotic anxiety states
|
|
D001008|607834||state neurotic anxiety
|
|
D001008|607834||states neurotic anxiety
|
|
D009050||fluorosis dental
|
|
D009050||dental fluoroses
|
|
D009050||dental fluorosis
|
|
D009050||enamel mottled
|
|
D009050||enamels mottled
|
|
D009050||fluoroses dental
|
|
D009050||mottled enamel
|
|
D009050||mottled enamels
|
|
D010031||otitis
|
|
D010031||ear inflammation
|
|
D010031||ear inflammations
|
|
D010031||inflammation ear
|
|
D010031||inflammations ear
|
|
D010031||otitides
|
|
C535538|308500||iris hypoplasia and glaucoma
|
|
C535538|308500||ihg
|
|
C535538|308500||iris hypoplasia with glaucoma
|
|
D010032||otitis externa
|
|
D010032||external otitides
|
|
D010032||external otitis
|
|
D010032||externa otitis
|
|
D010032||otitides external
|
|
D010032||otitis external
|
|
D010035||otitis media suppurative
|
|
D010035||otitis media purulent
|
|
D010035||purulent otitis media
|
|
D010035||suppurative otitis media
|
|
C564766|274400||thyroid dyshormonogenesis 1
|
|
C564766|274400||hypothyroidism congenital due to dyshormonogenesis 1
|
|
C564766|274400||iodine accumulation transport or trapping defect
|
|
C564766|274400||tdh1
|
|
C564766|274400||thyroid hormonogenesis genetic defect in 1
|
|
D010034||otitis media with effusion
|
|
D010034||ear effusion middle
|
|
D010034||ear effusions middle
|
|
D010034||effusion middle ear
|
|
D010034||effusions middle ear
|
|
D010034||middle ear effusion
|
|
D010034||middle ear effusions
|
|
D010034||otitis media secretory
|
|
D010034||otitis media serous
|
|
D010034||secretory otitis media
|
|
D010034||serous otitis media
|
|
D000686||amyloidosis
|
|
D000686||amyloidoses
|
|
C535650||gastro enteropancreatic neuroendocrine tumor
|
|
C536983||morillo cucci passarge syndrome
|
|
C565343|605293||optic atrophy 4
|
|
C565343|605293||opa4
|
|
C535652||bellini chiumello rimoldi syndrome
|
|
C535651||gastrocutaneous syndrome
|
|
C563371|601208||diabetes mellitus insulin dependent 11
|
|
C563371|601208||iddm11
|
|
C563371|601208||insulin dependent diabetes mellitus 11
|
|
C535924|610448||chilblain lupus
|
|
C535924|610448||chbl1
|
|
C535924|610448||chilblain lupus 1
|
|
D025981||hip injuries
|
|
D025981||injuries hip
|
|
D010005||osteoarthropathy secondary hypertrophic
|
|
D010005||clubbed finger
|
|
D010005||clubbed fingers
|
|
D010005||disease marie bamberger
|
|
D010005||finger clubbed
|
|
D010005||fingers clubbed
|
|
D010005||hypertrophic osteoarthropathies secondary
|
|
D010005||hypertrophic osteoarthropathy secondary
|
|
D010005||marie bamberger disease
|
|
D010005||osteoarthropathies secondary hypertrophic
|
|
D010005||secondary hypertrophic osteoarthropathies
|
|
D010005||secondary hypertrophic osteoarthropathy
|
|
D010008||osteochondritis dissecans
|
|
D010008||dissecans osteochondritis
|
|
D010007||osteochondritis
|
|
D010007||osteochondritides
|
|
D009021||morphine dependence
|
|
D009021||abuse morphine
|
|
D009021||addiction morphine
|
|
D009021||dependence morphine
|
|
D009021||morphine abuse
|
|
D009021||morphine addiction
|
|
C536975||tracheal agenesis
|
|
C536975||congenital tracheal agenesis
|
|
C536975||congenital tracheal stenosis
|
|
C535643||gardner morrisson abbot syndrome
|
|
C535643||thrombocytopenia multiple congenital anomaly
|
|
C536976||tracheal agenesis without tracheoesophageal fistula
|
|
C536976||type 2 tracheal agenesis
|
|
D013991||tietze apos s syndrome
|
|
D013991||chondritides costal
|
|
D013991||chondritis costal
|
|
D013991||costal chondritides
|
|
D013991||costal chondritis
|
|
D013991||syndrome tietze apos s
|
|
D013991||tietzes syndrome
|
|
D013991||tietze syndrome
|
|
C535642||growth retardation alopecia pseudoanodontia and optic atrophy
|
|
C535642||gapo syndrome
|
|
C535642||odontotrichomelic syndrome
|
|
C535642||tetramelic deficiencies ectodermal dysplasia deformed ears and other abnormalities
|
|
C536973||total hypotrichosis mari type
|
|
C536973||alopecia universalis congenita mari type
|
|
C536973|278150|D007039||hypotrichosis autosomal recessive
|
|
C536973|278150|D007039||hypotrichosis localized autosomal recessive 2
|
|
C536973||hypotrichosis total mari type
|
|
C536973||mari type alopecia universalis congenita
|
|
C535645||gardner diamond syndrome
|
|
C535645||autoerythrocyte sensitization
|
|
C535645||psychogenic purpura
|
|
C536210|214700||congenital chloride diarrhea
|
|
C536210|214700||chloride diarrhea congenital finnish type
|
|
C536210|214700||chloridorrhea congenital
|
|
C536210|214700||congenital chloridorrhea
|
|
C536210|214700||darrow gamble disease
|
|
C536210|214700||diar1
|
|
C536210|214700||diarrhea 1 secretory chloride congenital
|
|
C535644||intestinal polyposis osteomas sebaceous cysts
|
|
C535644||polyposis coli and multiple hard and soft tissue tumors
|
|
D010000||osteitis
|
|
D010000||bone inflammation
|
|
D010000||inflammation bone
|
|
C535647||gas bloat syndrome
|
|
C535647||post fundoplication syndrome
|
|
185800|C536223||cushing apos s symphalangism
|
|
185800|C536223||cushing symphalangism
|
|
185800|C536223||hereditary absence of proximal interphalangeal joints
|
|
185800|C536223||hereditary absence of the proximal interphalangeal joints
|
|
185800|C536223||strasburger hawkins eldridge hargrave mckusick syndrome
|
|
185800|C536223||strasburger hawkins eldridge syndrome
|
|
185800|C536223||sym1
|
|
185800|C536223||sym1a
|
|
185800|C536223||symphalangism proximal
|
|
185800|C536223||symphalangism proximal 1a
|
|
185800|C536223||vessel apos s syndrome
|
|
C566706|613731||retinitis pigmentosa 4
|
|
C566706|613731||retinitis pigmentosa rhodopsin related
|
|
C566706|613731||rp4
|
|
C535646||garret tripp syndrome
|
|
C535646||mental retardation with postaxial polydactyly congenital absence of hair severe seborrhoeic dermatitis and perthes apos disease of the hip
|
|
C536977||tracheobronchopathia osteoplastica
|
|
C536977||cartilaginous or bony projections into the tracheobronchial lumen
|
|
C536977||tracheobronchopathia osteochondroplastica
|
|
C536977||tracheopathia osteoplastica
|
|
D010002||osteitis fibrosa cystica
|
|
D010002||recklinghausen disease bone
|
|
D010002||recklinghausen disease of bone
|
|
D010002||recklinghausens disease bone
|
|
D010002||recklinghausen apos s disease of bone
|
|
C536978||tranebjaerg svejgaard syndrome
|
|
C536978||mental retardation x linked tranebjaerg type seizures and psoriasis
|
|
C536978||x linked mental retardation associated with psoriasis
|
|
C535648||familial primary gastric lymphoma
|
|
C535648||gastric lymphoma
|
|
C535648||gastric lymphoma primary
|
|
C535648||primary gastric lymphoma
|
|
C535852|610140||heart hand syndrome slovenian type
|
|
D000699||pain insensitivity congenital
|
|
D000699||analgesia congenital
|
|
D000699||channelopathy associated insensitivity to pain
|
|
D000699||congenital analgesia
|
|
D000699||congenital indifference to pain
|
|
D000699||congenital insensitivity to pain
|
|
D000699||congenital pain indifference
|
|
D000699||congenital pain indifferences
|
|
D000699||congenital pain insensitivity
|
|
D000699||insensitivity congenital pain
|
|
D000699||pain indifference congenital
|
|
C537996|202650||dysgnathia complex
|
|
C537996|202650||agnathia holoprosencephaly
|
|
C537996|202650||agnathia otocephaly complex
|
|
C537996|202650||agotc
|
|
C537996|202650||dysgnathia complex agnathia holoprosencephaly
|
|
C537996|202650||holoprosencephaly agnathia
|
|
C537996|202650|C562503||otocephaly
|
|
C535663||acroosteolysis dominant type
|
|
C535662||acromicric dysplasia
|
|
C535662||acromicric skeletal dysplasia
|
|
C535662||geleophysic dwarfism
|
|
C535662||geleophysic dysplasia
|
|
D000690||amyotrophic lateral sclerosis
|
|
D000690||als amyotrophic lateral sclerosis
|
|
D000690||amyotrophic lateral sclerosis guam form
|
|
D000690|105500||amyotrophic lateral sclerosis parkinsonism dementia complex 1
|
|
D000690|105500||amyotrophic lateral sclerosis parkinsonism dementia complex of guam
|
|
D000690||amyotrophic lateral sclerosis with dementia
|
|
D000690||charcot disease
|
|
D000690||dementia with amyotrophic lateral sclerosis
|
|
D000690||disease guam
|
|
D000690||disease lou gehrigs
|
|
D000690||gehrig disease
|
|
D000690||gehrig apos s disease
|
|
D000690||gehrigs disease
|
|
D000690|105500||guam disease
|
|
D000690||guam form of amyotrophic lateral sclerosis
|
|
D000690||lou gehrig disease
|
|
D000690||lou gehrig apos s disease
|
|
D000690||lou gehrigs disease
|
|
D000690||motor neuron disease amyotrophic lateral sclerosis
|
|
D000690||sclerosis amyotrophic lateral
|
|
C535661|602875||acromesomelic dysplasia maroteaux type
|
|
C535661|602875||amdm
|
|
C535661|602875||st helena dysplasia included
|
|
C565133|604307||cataract coppock like
|
|
C565133|604307||cataract 2 multiple types
|
|
C565133|604307||cataract 2 multiple types with or without microcornea
|
|
C565133|604307||cataract embryonic nuclear
|
|
C565133|604307||ccl
|
|
C565133|604307||ctrct2
|
|
C535540|147891||ischiopatellar dysplasia
|
|
C535540|147891||coxopodopatellar syndrome
|
|
C535540|147891||scott taor syndrome
|
|
C535540|147891||small patella syndrome
|
|
C535540|147891|184850|D016750||sps
|
|
D000694||anal gland neoplasms
|
|
D000694||anal gland neoplasm
|
|
D000694||circumanal gland neoplasm
|
|
D000694||circumanal gland neoplasms
|
|
D000694||neoplasm anal gland
|
|
D000694||neoplasm circumanal gland
|
|
D000694||neoplasm perianal gland
|
|
D000694||neoplasms anal gland
|
|
D000694||neoplasms circumanal gland
|
|
D000694||neoplasms perianal gland
|
|
D000694||perianal gland neoplasm
|
|
D000694||perianal gland neoplasms
|
|
D012678||sensation disorders
|
|
D012678||sensation disorder
|
|
D012678||senses disorder special
|
|
D012678||senses disorders special
|
|
D012678||sensory disorder
|
|
D012678||sensory disorders
|
|
D012678||special senses disorder
|
|
D012678||special senses disorders
|
|
D010015||osteolysis essential
|
|
D010015||bone disease disappearing
|
|
D010015||cystic angiomatosis of bone diffuse
|
|
D010015||disappearing bone disease
|
|
D010015||essential osteolyses
|
|
D010015||essential osteolysis
|
|
D010015||gorham disease
|
|
D010015||gorham stout disease
|
|
D010015||idiopathic multicentric osteolyses
|
|
D010015||idiopathic multicentric osteolysis
|
|
D010015||massive osteolyses
|
|
D010015||massive osteolysis
|
|
D010015||multicentric osteolyses idiopathic
|
|
D010015||multicentric osteolysis idiopathic
|
|
D010015||osteolyses essential
|
|
D010015||osteolyses idiopathic multicentric
|
|
D010015||osteolyses massive
|
|
D010015||osteolysis idiopathic multicentric
|
|
D010015||osteolysis massive
|
|
D010014||osteolysis
|
|
D010014||osteolyses
|
|
D010017||osteoma osteoid
|
|
D010017||osteoid osteoma
|
|
D010017||osteoid osteomas
|
|
D010017||osteomas osteoid
|
|
D010016||osteoma
|
|
D010016||osteomas
|
|
D010019||osteomyelitis
|
|
D010019||osteomyelitides
|
|
D010018||osteomalacia
|
|
D010018||adult rickets
|
|
D010018||rickets adult
|
|
D011349||proctitis
|
|
D011349||proctitides
|
|
C535654||rosenthal kloepfer syndrome
|
|
C535654||acromegaloid changes cutis verticis gyrata and corneal leukoma
|
|
C535653||acrokeratoelastoidosis of costa
|
|
C535653||collagenous plaques of hand and feet
|
|
C535653||collagenous plaques of hands and feet
|
|
C535653||palmoplantar keratoderma punctate type 3
|
|
C535655||acromegaloid facial appearance syndrome
|
|
C535655||thick lips and oral mucosa
|
|
C535658||acromesomelic dysplasia
|
|
C535658|201250||acromesomelic dwarfism
|
|
C535658||acromesomelic dwarfism maroteux type
|
|
C535658|201250||acromesomelic dysplasia hunter thompson type
|
|
C535658||st helena dysplasia
|
|
C566984|611228||charcot marie tooth disease type 4j
|
|
C566984|611228||charcot marie tooth disease autosomal recessive type 4j
|
|
C566984|611228||cmt4j
|
|
C535657||acromelic frontonasal dysplasia
|
|
C536988||motor neuropathy peripheral with dysautonomia
|
|
C536988||lisker garcia ramos syndrome
|
|
C536988||peripheral motor neuropathy associated with autonomic dysfunction
|
|
C566883|259720||osteopetrosis autosomal recessive 5
|
|
C566883|259720||optb5
|
|
C566883|259720||osteopetrosis infantile malignant 3
|
|
C536989||mousa al din al nassar syndrome
|
|
C536989||bedouin spastic ataxia syndrome
|
|
C535659||acromesomelic dysplasia campailla martinelli type
|
|
C535659||mesomelic dwarfism campailla martinelli type
|
|
D001998||bronchopulmonary sequestration
|
|
D001998||bronchopulmonary sequestrations
|
|
D001998||pulmonary sequestration
|
|
D001998||pulmonary sequestrations
|
|
D001998||sequestration bronchopulmonary
|
|
D001998||sequestration pulmonary
|
|
D001998||sequestrations bronchopulmonary
|
|
D001998||sequestrations pulmonary
|
|
D001997||bronchopulmonary dysplasia
|
|
D001997||dysplasia bronchopulmonary
|
|
C564199||hemifacial hyperplasia with strabismus
|
|
C564199||bencze syndrome
|
|
C535670||accutane embryopathy
|
|
C535670||accutane exposed pregnancies
|
|
C535670||isotretinoin embryopathy
|
|
C535670||isotretinoin roaccutane embryopathy
|
|
D001996||bronchopneumonia
|
|
D001996||bronchial pneumonia
|
|
D001996||bronchial pneumonias
|
|
D001996||bronchopneumonias
|
|
D001996||pneumonia bronchial
|
|
D001996||pneumonias bronchial
|
|
C564198||hemifacial spasm familial
|
|
C535338|302200||cataract congenital with microcornea or slight microphthalmia
|
|
C535338|302200||cataract 40
|
|
C535338|302200||cataract 40 with or without microcornea
|
|
C535338|302200||cataract congenital total
|
|
C535338|302200||cataract congenital total with posterior sutural opacities in heterozygotes
|
|
C535338|302200||cataract congenital x linked
|
|
C535338|302200||cataract total congenital
|
|
C535338|302200||cataract total congenital with posterior sutural opacities in heterozygotes
|
|
C535338|302200||cct
|
|
C535338|302200||ctrct40
|
|
C535338|302200||cxn
|
|
C535672||acute cholinergic dysautonomia
|
|
C535674||richards rundle syndrome
|
|
C535674||ataxia deafness retardation syndrome with ketoaciduria
|
|
C535674||familial ataxia hypogonadism syndrome
|
|
C535674||ketoaciduria mental deficiency syndrome
|
|
C535674||ketoaciduria with mental deficiency and other features
|
|
C535673||acute erythroleukemia
|
|
C535673||acute erythroleukemia m6a subtype
|
|
C535673||acute erythroleukemia m6b subtype
|
|
C535673||acute myeloid leukemia fab m6
|
|
D001990||bronchiolitis viral
|
|
D001990||bronchiolitides viral
|
|
D001990||viral bronchiolitides
|
|
D001990||viral bronchiolitis
|
|
D001994||bronchogenic cyst
|
|
D001994||bronchial cyst
|
|
D001994||bronchial cysts
|
|
D001994||bronchogenic cysts
|
|
D001994||cyst bronchial
|
|
D001994||cyst bronchogenic
|
|
D001994||cysts bronchial
|
|
D001994||cysts bronchogenic
|
|
216550|C536438||cohen syndrome
|
|
216550|C536438||chs1 formerly
|
|
216550|C536438||coh
|
|
216550|C536438||coh1
|
|
216550|C536438||hypotonia obesity and prominent incisors
|
|
216550|C536438||norio syndrome
|
|
216550|C536438||obesity hypotonia syndrome
|
|
216550|C536438||pepper syndrome
|
|
216550|C536438||prominent incisors obesity hypotonia syndrome
|
|
D025962||septo optic dysplasia
|
|
D025962||de morsier syndrome
|
|
D025962||dysplasia septooptic
|
|
D025962||dysplasias septooptic
|
|
D025962||morsier syndrome de
|
|
D025962|182230|C531815||septooptic dysplasia
|
|
D025962||septooptic dysplasias
|
|
D025962||septo optic dysplasia with growth hormone deficiency
|
|
D025962||syndrome de morsier
|
|
D001991||bronchitis
|
|
D001991||bronchitides
|
|
C567784|605911||3 hydroxy 3 methylglutaryl coa synthase 2 deficiency
|
|
C567784|605911||hmgcs2 deficiency
|
|
C567784|605911||mitochondrial hmg coa synthase deficiency
|
|
D011317||priapism
|
|
D011317||priapisms
|
|
D013978||tibial fractures
|
|
D013978||fractures tibial
|
|
D013978||fracture tibial
|
|
D013978||tibial fracture
|
|
C536997||le marec bracq picaud syndrome
|
|
C536997||complex malformation syndrome with brachymesomelia
|
|
C536231|600884||familial dilated cardiomyopathy
|
|
C536231|600884||cardiomyopathy dilated 1b
|
|
C536231|600884||cardiomyopathy familial dilated
|
|
C536231|600884||cardiomyopathy familial dilated 1
|
|
C536231|600884||cmd1b
|
|
C536231|600884|D055036|114290||cmpd1
|
|
C536231|600884||dilated cardiomyopathy familial
|
|
C536231|600884||fdc
|
|
C536231|600884||hypokinetic dilated cardiomyopathy familial
|
|
C535665||acrorenal mandibular syndrome
|
|
C535665||acro renal uterine mandibular syndrome
|
|
C535665||acrorenal uterine mandibular syndrome
|
|
C535665||split hand and split foot with mandibular hypoplasia
|
|
C536998||leber congenital amaurosis type 3
|
|
C536998||amaurosis congenita of leber 3
|
|
C535666||acrorenal syndrome recessive
|
|
C535666||acrorenal syndrome autosomal recessive
|
|
C535666||curran syndrome
|
|
C563898|608615||oligodontia colorectal cancer syndrome
|
|
C563898|608615||odcrcs
|
|
C563898|608615||tooth agenesis colorectal cancer syndrome
|
|
C535669||actinic cheilitis
|
|
C535669||actinic cheilosis
|
|
C535668|C562707|201400||adrenocorticotropic hormone deficiency
|
|
D055732||pulmonary aspergillosis
|
|
D055732||aspergillose bronchopulmonary
|
|
D055732||aspergilloses bronchopulmonary
|
|
D055732||aspergilloses lung
|
|
D055732||aspergillosis bronchopulmonary
|
|
D055732||aspergillosis lung
|
|
D055732||aspergillosis pulmonary
|
|
D055732||bronchopulmonary aspergillose
|
|
D055732||bronchopulmonary aspergilloses
|
|
D055732||bronchopulmonary aspergillosis
|
|
D055732||lung aspergillosis
|
|
D055732||pulmonary aspergilloses
|
|
C536999||leber congenital amaurosis type 4
|
|
C536999||amaurosis congenita of leber 4
|
|
C563172|262600||pituitary hormone deficiency combined 2
|
|
C563172|262600||ateliotic dwarfism with hypogonadism
|
|
C563172|262600||cphd2
|
|
C563172|262600||hanhart dwarfism
|
|
C563172|262600|C580003||panhypopituitarism
|
|
C563172|262600||pituitary dwarfism iii
|
|
D012640||seizures
|
|
D012640||auditory seizure
|
|
D012640||auditory seizures
|
|
D012640||clonic seizure
|
|
D012640||clonic seizures
|
|
D012640||convulsion
|
|
D012640||convulsion non epileptic
|
|
D012640||convulsions
|
|
D012640||convulsions non epileptic
|
|
D012640||convulsive seizure
|
|
D012640||convulsive seizures
|
|
D012640||focal seizure
|
|
D012640||focal seizures
|
|
D012640||generalized seizure
|
|
D012640||generalized seizures
|
|
D012640||gustatory seizure
|
|
D012640||gustatory seizures
|
|
D012640||jacksonian seizure
|
|
D012640||motor seizure
|
|
D012640||motor seizures
|
|
D012640||non epileptic convulsion
|
|
D012640||non epileptic convulsions
|
|
D012640||olfactory seizure
|
|
D012640||olfactory seizures
|
|
D012640||seizure
|
|
D012640||seizure auditory
|
|
D012640||seizure clonic
|
|
D012640||seizure convulsive
|
|
D012640||seizure focal
|
|
D012640||seizure generalized
|
|
D012640||seizure gustatory
|
|
D012640||seizure jacksonian
|
|
D012640||seizure motor
|
|
D012640||seizure olfactory
|
|
D012640||seizures auditory
|
|
D012640||seizures clonic
|
|
D012640||seizures convulsive
|
|
D012640||seizure sensory
|
|
D012640||seizures focal
|
|
D012640||seizures generalized
|
|
D012640||seizures gustatory
|
|
D012640||seizures motor
|
|
D012640||seizures olfactory
|
|
D012640||seizure somatosensory
|
|
D012640||seizures sensory
|
|
D012640||seizures somatosensory
|
|
D012640||seizures tonic
|
|
D012640||seizures tonic clonic
|
|
D012640||seizures vertiginous
|
|
D012640||seizures vestibular
|
|
D012640||seizures visual
|
|
D012640||seizure tonic
|
|
D012640||seizure tonic clonic
|
|
D012640||seizure vertiginous
|
|
D012640||seizure vestibular
|
|
D012640||seizure visual
|
|
D012640||sensory seizure
|
|
D012640||sensory seizures
|
|
D012640||somatosensory seizure
|
|
D012640||somatosensory seizures
|
|
D012640||tonic clonic seizure
|
|
D012640||tonic clonic seizures
|
|
D012640||tonic seizure
|
|
D012640||tonic seizures
|
|
D012640||vertiginous seizure
|
|
D012640||vertiginous seizures
|
|
D012640||vestibular seizure
|
|
D012640||vestibular seizures
|
|
D012640||visual seizure
|
|
D012640||visual seizures
|
|
D013971|D006111|275000||thyrotoxicosis
|
|
D013971||thyrotoxicoses
|
|
D054403||leukemia prolymphocytic b cell
|
|
D054403||b cell prolymphocytic leukemia
|
|
D054403||b cell prolymphocytic leukemias
|
|
D054403||leukemia b cell prolymphocytic
|
|
D054403||leukemias b cell prolymphocytic
|
|
D054403||prolymphocytic leukemia b cell
|
|
D054403||prolymphocytic leukemias b cell
|
|
C538333|605779||nail dysplasia isolated congenital
|
|
C538333|605779||congenital isolated nail dysplasia
|
|
C538333|605779||isolated congenital nail dysplasia
|
|
C538333|605779||nail disorder nonsyndromic congenital 7
|
|
C538333|605779||ndnc7
|
|
C538333|605779||onychodysplasia isolated congenital
|
|
C536678|309583||snyder robinson syndrome
|
|
C536678|309583||mental retardation x linked snyder robinson type
|
|
C536678|309583||mental retardation x linked syndromic snyder robinson type
|
|
C536678|309583||mrxssr
|
|
C536678|309583||snyder robinson mental retardation syndrome
|
|
C536678|309583|D056730|180860||srs
|
|
C536678|309583||x linked mental retardation snyder robinson type
|
|
C535681||familial anomalous origin of right pulmonary artery
|
|
C535681||arpa familial
|
|
C535681||right pulmonary artery anomalous origin of familial
|
|
C535680||rieger syndrome 2
|
|
C535680|601499||axenfeld rieger syndrome type 2
|
|
C535680|601499||rieger syndrome type 2
|
|
C535682||right ventricle hypoplasia
|
|
C535682||hypoplasia of the right ventricle
|
|
C535682||isolated hypoplasia of the right ventricle
|
|
C535682||isolated right ventricular hypoplasia
|
|
C535682||right ventricular hypoplasia
|
|
C535682||right ventricular hypoplasia isolated
|
|
D009008||abnormalities severe teratoid
|
|
D009008||abnormality severe teratoid
|
|
D009008||severe teratoid abnormalities
|
|
D009008||severe teratoid abnormality
|
|
D009008||teratoid abnormalities severe
|
|
D009008||teratoid abnormality severe
|
|
D000673||amputation traumatic
|
|
D000673||amputations traumatic
|
|
D000673||traumatic amputation
|
|
D000673||traumatic amputations
|
|
D009006||monosomy
|
|
D009006||monosomies
|
|
D013985||tick paralysis
|
|
D013985||paralyses tick
|
|
D013985||paralysis tick
|
|
D013985||tick paralyses
|
|
D013986||tick toxicoses
|
|
D013986||toxicoses tick
|
|
123700||cutis laxa autosomal dominant 1
|
|
123700||adcl1
|
|
D009011||monteggia apos s fracture
|
|
D009011||fracture monteggia apos s
|
|
D009011||monteggia fracture
|
|
D009011||monteggias fracture
|
|
C535676||richieri costa guion almeida syndrome
|
|
C535676||acrofacial dysostosis richieri costa guion almeida type
|
|
C535676||richieri costa guion almeida cohen syndrome
|
|
C535676||richieri costa guion almeida dwarfism
|
|
C535675||richieri costa da silva syndrome
|
|
C535675||tibial hemimelia split hand foot syndrome
|
|
C535677||richieri costa pereira syndrome
|
|
C535677||richieri costa and pereira form of acrofacial dysostosis
|
|
C535677||robin sequence with cleft mandible and limb anomalies
|
|
D012652||self mutilation
|
|
D012652||mutilation self
|
|
C535568|168860||absent patella
|
|
C535568|168860||familial absence of the patella
|
|
C535568|168860||familial aplasia of the patella
|
|
C535568|168860||patella aplasia hypoplasia
|
|
C535568|168860||ptlah
|
|
D013984||tick infestations
|
|
D013984||infestations tick
|
|
D013984||infestation tick
|
|
D013984||tick infestation
|
|
C535679||axenfeld rieger syndrome
|
|
C535679||axenfeld anomaly
|
|
C535679||axenfeld rieger anomaly
|
|
C535679|180500||axenfeld rieger syndrome type 1
|
|
C535679||axenfeld syndrome
|
|
C535679||iridogoniodysgenesis with somatic anomalies
|
|
C535679||rieger syndrome
|
|
C535679|180500||rieger syndrome type 1
|
|
C535679||rieger syndrome type 3
|
|
D013981||tic disorders
|
|
D013981||childhood tic disorder
|
|
D013981||childhood tic disorders
|
|
D013981||chronic motor or vocal tic disorder
|
|
D013981||motor or vocal tic disorder chronic
|
|
D013981||motor tic disorder
|
|
D013981||motor tic disorders
|
|
D013981||post traumatic tic disorder
|
|
D013981||post traumatic tic disorders
|
|
D013981||tic disorder
|
|
D013981||tic disorder childhood
|
|
D013981||tic disorder chronic motor or vocal
|
|
D013981||tic disorder motor
|
|
D013981||tic disorder post traumatic
|
|
D013981||tic disorders childhood
|
|
D013981||tic disorders motor
|
|
D013981||tic disorders post traumatic
|
|
D013981||tic disorders transient
|
|
D013981||tic disorders vocal
|
|
D013981||tic disorder transient
|
|
D013981||tic disorder vocal
|
|
D013981||transient tic disorder
|
|
D013981||transient tic disorders
|
|
D013981||vocal tic disorder
|
|
D013981||vocal tic disorders
|
|
D055744||invasive pulmonary aspergillosis
|
|
D055744||allergic bronchopulmonary mycoses
|
|
D055744||allergic bronchopulmonary mycosis
|
|
D055744||aspergillosis invasive pulmonary
|
|
D055744||bronchopulmonary mycoses allergic
|
|
D055744||bronchopulmonary mycosis allergic
|
|
D055744||chronic necrotizing pulmonary aspergillosis
|
|
D055744||mycoses allergic bronchopulmonary
|
|
D055744||mycosis allergic bronchopulmonary
|
|
D055744||pulmonary aspergilloses invasive
|
|
D055744||pulmonary aspergillosis invasive
|
|
C564179||charcot marie tooth disease foot deformity of
|
|
C564178||horner syndrome congenital
|
|
607088|C564626||spinal muscular atrophy distal autosomal recessive 3
|
|
607088|C564626||dhmn3
|
|
607088|C564626||dhmn4
|
|
607088|C564626||dsma3
|
|
607088|C564626||hmn3
|
|
607088|C564626||hmn4
|
|
607088|C564626||hmn iii
|
|
607088|C564626||hmn iv
|
|
607088|C564626||neuronopathy distal hereditary motor type iii
|
|
607088|C564626||neuronopathy distal hereditary motor type iv
|
|
607088|C564626||neuropathy distal hereditary motor type iv
|
|
D000648||amnesia retrograde
|
|
D000648||amnesia pre ictal
|
|
D000648||amnesias pre ictal
|
|
D000648||amnesias retrograde
|
|
D000648||memory losses pre ictal
|
|
D000648||memory losses retrograde
|
|
D000648||memory loss pre ictal
|
|
D000648||memory loss retrograde
|
|
D000648||pre ictal amnesia
|
|
D000648||pre ictal amnesias
|
|
D000648||pre ictal memory loss
|
|
D000648||pre ictal memory losses
|
|
D000648||retrograde amnesia
|
|
D000648||retrograde amnesias
|
|
D000648||retrograde memory loss
|
|
D000648||retrograde memory losses
|
|
D000647||amnesia
|
|
D000647||amnesia dissociative
|
|
D000647||amnesia global
|
|
D000647||amnesia hysterical
|
|
D000647||amnesia memory loss
|
|
D000647||amnesia memory losses
|
|
D000647||amnesias
|
|
D000647||amnesias dissociative
|
|
D000647||amnesias global
|
|
D000647||amnesias hysterical
|
|
D000647||amnesias tactile
|
|
D000647||amnesias temporary
|
|
D000647||amnesia tactile
|
|
D000647||amnesia temporary
|
|
D000647||amnestic state
|
|
D000647||amnestic states
|
|
D000647||dissociative amnesia
|
|
D000647||dissociative amnesias
|
|
D000647||global amnesia
|
|
D000647||global amnesias
|
|
D000647||hysterical amnesia
|
|
D000647||hysterical amnesias
|
|
D000647||state amnestic
|
|
D000647||states amnestic
|
|
D000647||tactile amnesia
|
|
D000647||tactile amnesias
|
|
D000647||temporary amnesia
|
|
D000647||temporary amnesias
|
|
C536391|158900||facioscapulohumeral muscular dystrophy 1a
|
|
C536391|158900||facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles
|
|
C536391|158900||facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles included
|
|
C536391|158900|D020391||facioscapulohumeral muscular dystrophy
|
|
C536391|158900||facioscapulohumeral muscular dystrophy 1
|
|
C536391|158900||facioscapulohumeral muscular dystrophy infantile
|
|
C536391|158900|C538064|305620||fmd
|
|
C536391|158900||fshd
|
|
C536391|158900||fshd1
|
|
C536391|158900||fshd1a
|
|
C536391|158900||fshmd1a
|
|
C536391|158900||landouzy dejerine muscular dystrophy
|
|
C536391|158900||landouzy dejerine muscular dystrophy facioscapulohumeral muscular dystrophy infantile included
|
|
C536391|158900||muscular dystrophy facioscapulohumeral type 1
|
|
C536391|158900||muscular dystrophy facioscapulohumeral type 1a
|
|
C536939||uncombable hair syndrome
|
|
C536939||cheveux incoiffables
|
|
C536939||pili trianguli et canaliculi
|
|
C536939||unmanageable hair syndrome
|
|
D013955||thyroglossal cyst
|
|
D013955||cysts thyroglossal
|
|
D013955||cysts thyroglossal duct
|
|
D013955||cysts thyrolingual
|
|
D013955||cyst thyroglossal
|
|
D013955||cyst thyroglossal duct
|
|
D013955||cyst thyrolingual
|
|
D013955||thyroglossal cysts
|
|
D013955||thyroglossal duct cyst
|
|
D013955||thyroglossal duct cysts
|
|
D013955||thyrolingual cyst
|
|
D013955||thyrolingual cysts
|
|
D013952||thymus hyperplasia
|
|
D013952||gland hyperplasias thymus
|
|
D013952||gland hyperplasia thymus
|
|
D013952||hyperplasia of thymus gland
|
|
D013952||hyperplasias thymic
|
|
D013952||hyperplasia thymic
|
|
D013952||hyperplasia thymus
|
|
D013952||thymic hyperplasia
|
|
D013952||thymic hyperplasias
|
|
D013952||thymus gland hyperplasia
|
|
D013952||thymus gland hyperplasias
|
|
C535609||akaba hayasaka syndrome
|
|
C536938||umbilical cord ulceration and intestinal atresia
|
|
C536938||umbilical cord ulcer with intestinal atresia
|
|
C536938||umbilical ulceration and intestinal atresia
|
|
D013953||thymus neoplasms
|
|
D013953||cancer of the thymus
|
|
D013953||cancer of thymus
|
|
D013953||cancers thymic
|
|
D013953||cancers thymus
|
|
D013953||cancer thymic
|
|
D013953||cancer thymus
|
|
D013953||neoplasms thymic
|
|
D013953||neoplasms thymus
|
|
D013953||neoplasm thymic
|
|
D013953||neoplasm thymus
|
|
D013953||thymic cancer
|
|
D013953||thymic cancers
|
|
D013953||thymic neoplasm
|
|
D013953||thymic neoplasms
|
|
D013953||thymic tumor
|
|
D013953||thymic tumors
|
|
D013953||thymus cancer
|
|
D013953||thymus cancers
|
|
D013953||thymus neoplasm
|
|
D013953||thymus tumor
|
|
D013953||thymus tumors
|
|
D013953||tumors thymic
|
|
D013953||tumors thymus
|
|
D013953||tumor thymic
|
|
D013953||tumor thymus
|
|
607644|C564361||candidiasis familial 3
|
|
607644|C564361||candf3
|
|
607644|C564361||candidiasis familial chronic nail with icam1 deficiency
|
|
607644|C564361||candn1
|
|
607644|C564361||fcnc
|
|
D013958||thyroid crisis
|
|
D013958||crisis thyroid
|
|
D013958||crisis thyrotoxic
|
|
D013958||storm thyroid
|
|
D013958||storm thyrotoxic
|
|
D013958||thyroid storm
|
|
D013958||thyrotoxic crisis
|
|
D013958||thyrotoxic storm
|
|
D012628||dermatitis seborrheic
|
|
D012628||dermatitides seborrheic
|
|
D012628||dermatitis seborrheica
|
|
D012628||seborrhea
|
|
D012628||seborrheic dermatitides
|
|
D012628||seborrheic dermatitis
|
|
D013959||thyroid diseases
|
|
D013959||diseases thyroid
|
|
D013959||disease thyroid
|
|
D013959||thyroid disease
|
|
D012625||sebaceous gland diseases
|
|
D012625||disease sebaceous gland
|
|
D012625||diseases sebaceous gland
|
|
D012625||gland disease sebaceous
|
|
D012625||gland diseases sebaceous
|
|
D012625||sebaceous gland disease
|
|
D012626||sebaceous gland neoplasms
|
|
D012626||neoplasm sebaceous gland
|
|
D012626||neoplasms sebaceous gland
|
|
D012626||sebaceous gland neoplasm
|
|
D055756||meningeal carcinomatosis
|
|
D055756||carcinomatoses leptomeningeal
|
|
D055756||carcinomatoses meningeal
|
|
D055756||carcinomatosis leptomeningeal
|
|
D055756||carcinomatosis meningeal
|
|
D055756||carcinomatous meningitides
|
|
D055756||carcinomatous meningitis
|
|
D055756||leptomeningeal carcinomatoses
|
|
D055756||leptomeningeal carcinomatosis
|
|
D055756||meningeal carcinomatoses
|
|
D055756||meningitides carcinomatous
|
|
D055756||meningitis carcinomatous
|
|
C536932||uhl anomaly
|
|
C536932||parchment right ventricle
|
|
C536932||uhl apos s anomaly
|
|
D055752||small cell lung carcinoma
|
|
D055752||carcinoma small cell lung
|
|
D055752||oat cell carcinoma of lung
|
|
D055752||oat cell lung cancer
|
|
D055752|D018288|182280||small cell cancer of the lung
|
|
D055752||small cell lung cancer
|
|
C536935||ulna metaphyseal dysplasia syndrome
|
|
C536935||hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna
|
|
C536935||metaphyseal chondrodysplasia rosenberg type
|
|
C536935||metaphyseal chondroplasia rosenberg type
|
|
C536935||rosenberg lohr syndrome
|
|
C564186||histiocytosis progressive mucinous
|
|
C535603||drachtman weinblatt sitarz syndrome
|
|
C535603||marrow hypoplasia associated with congenital neurologic anomalies
|
|
C536936||ulnar hypoplasia lobster claw deformity of feet
|
|
C536936||familial ulnar aplasia and lobster claw syndrome
|
|
C536936||severe ulnar aplasia and lobster claw feet
|
|
C536936||ulnar hypoplasia with lobster claw deformity of feet
|
|
C536936||van den berghe dequeker syndrome
|
|
C536934||ulna hypoplasia with mental retardation
|
|
C536934||bilateral ulnar hypoplasia and mental retardation
|
|
C536934||mesomelia of the upper limbs absent nails clubfeet and mental retardation
|
|
C564183||histiocytic dermatoarthritis
|
|
D001987||bronchiectasis
|
|
D001987||bronchiectases
|
|
C564189||diaphragm complete agenesis of
|
|
D001986||bronchial spasm
|
|
D001986||bronchial spasms
|
|
D001986||bronchospasm
|
|
D001986||bronchospasms
|
|
D001986||spasm bronchial
|
|
D001986||spasms bronchial
|
|
C564188||diaphragmatic hernia 1
|
|
D001984||bronchial neoplasms
|
|
D001984||bronchial neoplasm
|
|
D001984||neoplasm bronchial
|
|
D001984||neoplasms bronchial
|
|
D055036|114290||campomelic dysplasia
|
|
D055036|114290||acampomelic campomelic dysplasia
|
|
D055036|114290||acampomelic campomelic dysplasia included
|
|
D055036|114290||acampomelic campomelic dysplasias
|
|
D055036|114290||acampomelic campomelic dysplasia with autosomal sex reversal included
|
|
D055036|114290||campomelic dwarfism
|
|
D055036|114290||campomelic dysplasia acampomelic
|
|
D055036|114290||campomelic dysplasias
|
|
D055036|114290||campomelic dysplasias acampomelic
|
|
D055036|114290||campomelic syndrome
|
|
D055036|114290||camptomelic dysplasia
|
|
D055036|114290||camptomelic dysplasia included
|
|
D055036|114290||camptomelic dysplasias
|
|
D055036|114290||cmd1
|
|
D055036|114290||cmpd
|
|
D055036|114290||cmpd1 sra1
|
|
D055036|114290||cmpd1 sra1 campomelic dysplasia with autosomal sex reversal included
|
|
D055036|114290||dysplasia acampomelic campomelic
|
|
D055036|114290||dysplasia campomelic
|
|
D055036|114290||dysplasia camptomelic
|
|
D055036|114290||dysplasias acampomelic campomelic
|
|
D055036|114290||dysplasias campomelic
|
|
D055036|114290||dysplasias camptomelic
|
|
C536950||teebi shaltout syndrome
|
|
C536950||craniofacial anomalies abnormal hair camptodactyly and caudal appendage
|
|
D001989||bronchiolitis obliterans
|
|
D001989||bronchiolitides constrictive
|
|
D001989||bronchiolitides exudative
|
|
D001989||bronchiolitides proliferative
|
|
D001989||bronchiolitis constrictive
|
|
D001989||bronchiolitis exudative
|
|
D001989||bronchiolitis proliferative
|
|
D001989||constrictive bronchiolitides
|
|
D001989||constrictive bronchiolitis
|
|
D001989||exudative bronchiolitides
|
|
D001989||exudative bronchiolitis
|
|
D001989||proliferative bronchiolitides
|
|
D001989||proliferative bronchiolitis
|
|
D001988||bronchiolitis
|
|
D001988||bronchiolitides
|
|
D000652||amniotic band syndrome
|
|
D000652||amniotic band
|
|
D000652||amniotic bands
|
|
D000652||amputation intrauterine
|
|
D000652||amputations intrauterine
|
|
D000652||annular groove
|
|
D000652||annular grooves
|
|
D000652||band amniotic
|
|
D000652||bands amniotic
|
|
D000652||constriction intrauterine ring
|
|
D000652||constrictions intrauterine ring
|
|
D000652||groove annular
|
|
D000652||grooves annular
|
|
D000652||intrauterine amputation
|
|
D000652||intrauterine amputations
|
|
D000652||intrauterine ring constriction
|
|
D000652||intrauterine ring constrictions
|
|
D000652||ring constriction intrauterine
|
|
D000652||ring constrictions intrauterine
|
|
D000652||streeter syndrome
|
|
D000652||syndrome amniotic band
|
|
D000652||syndrome streeter
|
|
D001983||bronchial fistula
|
|
D001983||bronchial fistulas
|
|
D001983||fistula bronchial
|
|
D001983||fistulas bronchial
|
|
D001982||bronchial diseases
|
|
D001982||bronchial disease
|
|
D001982||disease bronchial
|
|
D001982||diseases bronchial
|
|
C563907|608567||sick sinus syndrome 1 autosomal recessive
|
|
C563907|608567||sick sinus syndrome congenital
|
|
C563907|608567||sinus bradycardia syndrome familial
|
|
C563907|608567||sinus node disease familial autosomal recessive
|
|
C563907|608567||sinus rhythm congenital absence of
|
|
C563907|608567||sss1
|
|
C535618||hairy elbows
|
|
C535618||hypertrichosis cubiti
|
|
C535618||hypertrichosis cubiti short stature
|
|
C535618||macdermot patton williams syndrome
|
|
D013966||thyroiditis
|
|
D013966||thyroiditides
|
|
C535617||al gazali sabrinathan nair syndrome
|
|
D055761||reticuloendotheliosis avian
|
|
D055761||avian reticuloendothelioses
|
|
D055761||avian reticuloendotheliosis
|
|
D055761||reticuloendothelioses avian
|
|
C536948||teebi kaurah syndrome
|
|
C535934|601847||cholestasis progressive familial intrahepatic 2
|
|
C535934|601847||benign recurrent intrahepatic cholestasis 2 bric2
|
|
C535934|601847|605479||cholestasis benign recurrent intrahepatic 2
|
|
C535934|601847||pfic2
|
|
C535934|601847||progressive familial intrahepatic cholestasis 2
|
|
D011304||presbycusis
|
|
D011304||presbycuses
|
|
C536949||teebi naguib al awadi syndrome
|
|
C536949||al awadi teebi farag syndrome
|
|
C536949||profound limb deficiency thoracic dystrophy unusual facies and normal intelligence
|
|
D013964||thyroid neoplasms
|
|
D013964||adenoma thyroid
|
|
D013964||cancer of the thyroid
|
|
D013964||cancer of thyroid
|
|
D013964||cancer thyroid
|
|
D013964||carcinoma thyroid
|
|
D013964||neoplasms thyroid
|
|
D013964||neoplasm thyroid
|
|
D013964||thyroid adenoma
|
|
D013964||thyroid cancer
|
|
D013964||thyroid carcinoma
|
|
D013964||thyroid neoplasm
|
|
C535619||hairy nose tip
|
|
D013969||thyroiditis suppurative
|
|
D013969||acute infectious thyroiditides
|
|
D013969||acute infectious thyroiditis
|
|
D013969||acute suppurative thyroiditides
|
|
D013969||acute suppurative thyroiditis
|
|
D013969||infectious thyroiditides
|
|
D013969||infectious thyroiditides acute
|
|
D013969||infectious thyroiditis
|
|
D013969||infectious thyroiditis acute
|
|
D013969||suppurative thyroiditides
|
|
D013969||suppurative thyroiditides acute
|
|
D013969||suppurative thyroiditis
|
|
D013969||suppurative thyroiditis acute
|
|
D013969||thyroiditides acute infectious
|
|
D013969||thyroiditides acute suppurative
|
|
D013969||thyroiditides infectious
|
|
D013969||thyroiditides suppurative
|
|
D013969||thyroiditis acute infectious
|
|
D013969||thyroiditis acute suppurative
|
|
D013969||thyroiditis infectious
|
|
C566393|603285||cerebral cavernous malformations 3
|
|
C566393|603285||ccm3
|
|
D011305||presbyopia
|
|
D011305||presbyopias
|
|
D013968||thyroiditis subacute
|
|
D013968||cell thyroiditides giant
|
|
D013968||cell thyroiditis giant
|
|
D013968||de quervain thyroiditis
|
|
D013968||giant cell thyroiditides
|
|
D013968||giant cell thyroiditis
|
|
D013968||granulomatous thyroiditides
|
|
D013968||granulomatous thyroiditis
|
|
D013968||nonsuppurative thyroiditides subacute
|
|
D013968||nonsuppurative thyroiditis subacute
|
|
D013968||painful thyroiditides subacute
|
|
D013968||painful thyroiditis subacute
|
|
D013968||subacute nonsuppurative thyroiditides
|
|
D013968||subacute nonsuppurative thyroiditis
|
|
D013968||subacute painful thyroiditides
|
|
D013968||subacute painful thyroiditis
|
|
D013968||subacute thyroiditides
|
|
D013968||subacute thyroiditis
|
|
D013968||thyroiditides giant cell
|
|
D013968||thyroiditides granulomatous
|
|
D013968||thyroiditides subacute
|
|
D013968||thyroiditides subacute nonsuppurative
|
|
D013968||thyroiditides subacute painful
|
|
D013968||thyroiditis de quervain
|
|
D013968||thyroiditis giant cell
|
|
D013968||thyroiditis granulomatous
|
|
D013968||thyroiditis subacute nonsuppurative
|
|
D013968||thyroiditis subacute painful
|
|
304500|C564433||deafness x linked 1
|
|
304500|C564433||deafness x linked 2 sensorineural congenital
|
|
304500|C564433||dfn2
|
|
304500|C564433||dfnx1
|
|
C564193||erythremia beta globin type
|
|
611209|C535756||congenital disorder of glycosylation type 2g
|
|
611209|C535756||cdg2g
|
|
611209|C535756||cdgii cog1 cerebrocostomandibular like syndrome
|
|
611209|C535756||cdgiig
|
|
611209|C535756||cdg iig
|
|
611209|C535756||congenital disorder of glycosylation type iig
|
|
C535610||akesson syndrome
|
|
C535610||cutis verticis gyrata thyroaplasia and mental deficiency syndrome
|
|
C535610||cutis verticis gyrata thyroid aplasia and mental retardation
|
|
C535610||cutis verticis gyrata thyroid aplasia mental retardation syndrome
|
|
C564192||methemoglobinemia beta globin type
|
|
C535611||aksu von stockhausen syndrome
|
|
C535611||hereditary branchial arch defects
|
|
C536946||taurodontism
|
|
C536946||bull teeth
|
|
C536946||large pulp chambers in the molars
|
|
C564197||hemolytic poikilocytic anemia due to reduced ankyrin binding sites
|
|
C536947||taurodontism microdontia and dens invaginatus
|
|
C537436|139300||aromatase deficiency
|
|
C537436|139300||aexs
|
|
C537436|139300||aromatase activity increased
|
|
C537436|139300||aromatase activity increased gynecomastia familial due to increased aromatase activity included
|
|
C537436|139300||aromatase excess syndrome
|
|
C537436|139300||familial gynecomastia due to increased aromatase activity
|
|
C537436|139300||gynecomastia familial due to increased aromatase activity
|
|
C537436|139300||gynecomastia hereditary
|
|
C537436|139300||gynecomastia hereditary included
|
|
C537436|139300||increased aromatase activity
|
|
C537436|139300||pseudohermaphroditism female due to placental aromatase deficiency
|
|
D054438||leukemia myeloid chronic atypical bcr abl negative
|
|
D054438||atypical chronic myeloid leukemia
|
|
D054438||chronic myeloid leukemia atypical
|
|
D054438||leukemia myelogenous ph1 negative
|
|
D054438||leukemia myeloid chronic atypical
|
|
D054438||leukemia myeloid ph1 negative
|
|
D054438||leukemia myeloid philadelphia negative
|
|
D054438||leukemia ph1 negative myelogenous
|
|
D054438||leukemia ph1 negative myeloid
|
|
D054438||leukemia philadelphia negative myeloid
|
|
D054438||leukemias ph1 negative myelogenous
|
|
D054438||leukemias ph1 negative myeloid
|
|
D054438||leukemias philadelphia negative myeloid
|
|
D054438||myelogenous leukemia ph1 negative
|
|
D054438||myelogenous leukemias ph1 negative
|
|
D054438||myeloid leukemia ph1 negative
|
|
D054438||myeloid leukemia philadelphia negative
|
|
D054438||myeloid leukemias ph1 negative
|
|
D054438||myeloid leukemias philadelphia negative
|
|
D054438||ph1 negative myelogenous leukemia
|
|
D054438||ph1 negative myelogenous leukemias
|
|
D054438||ph1 negative myeloid leukemia
|
|
D054438||ph1 negative myeloid leukemias
|
|
D054438||philadelphia negative myeloid leukemia
|
|
D054438||philadelphia negative myeloid leukemias
|
|
C535613||al gazali aziz salem syndrome
|
|
C536944||thrombocytopenia absent ulnar syndrome
|
|
C564195||erythremia alpha globin type
|
|
D054437||myelodysplastic myeloproliferative diseases
|
|
D054437||disease myelodysplastic myeloproliferative
|
|
D054437||disease myeloproliferative myelodisplastic
|
|
D054437||diseases myelodysplastic myeloproliferative
|
|
D054437||diseases myeloproliferative myelodisplastic
|
|
D054437||myelodysplastic myeloproliferative disease
|
|
D054437||myeloproliferative myelodisplastic disease
|
|
D054437||myeloproliferative myelodisplastic diseases
|
|
C535616||al gazali khidr prem chandran syndrome
|
|
C535616||cherubism optic atrophy and short stature
|
|
C536945||taurodontia absent teeth sparse hair
|
|
C536945||taurodontia absent teeth and sparse hair
|
|
C536945||teeth congenital absence of with taurodontia and sparse hair
|
|
C564194||methemoglobinemia alpha globin type
|
|
C535615||al gazali hirschsprung syndrome
|
|
C535615||al gazali donnai mueller syndrome
|
|
C535615||hirschsprung disease with hypoplastic nails and dysmorphic facial features
|
|
C535615||hirschsprung apos s disease hypoplastic nails and dysmorphic facial features
|
|
C535615||hirschsprung apos s disease hypoplastic nails and minor dysmorphic features
|
|
C565489||hyperuricemia infantile with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase
|
|
C564157||hypertaurinuric cardiomyopathy
|
|
270685|C536644||spastic paraplegia 17
|
|
270685|C536644||silver spastic paraplegia syndrome
|
|
270685|C536644||silver syndrome
|
|
270685|C536644||spastic paraplegia 17 autosomal dominant
|
|
270685|C536644||spastic paraplegia with amyotrophy of hands and feet
|
|
270685|C536644||spg17
|
|
C564156||hyperthermia cutaneous with headaches and nausea
|
|
C564156||farmer syndrome
|
|
C536960||hapnes boman skeie syndrome
|
|
C564681|606674||inflammatory bowel disease 6
|
|
C564681|606674||ibd6
|
|
C565486||l gulonolactone oxidase nonfunctional
|
|
C565486||gulo nonfunctional
|
|
C564159||hyperproglucagonemia
|
|
C564159||glucagon large molecular weight species of
|
|
C535630||hantavirosis
|
|
C535630||hantavirus fever
|
|
D012607||scotoma
|
|
D012607||altitudinal scotoma
|
|
D012607||altitudinal scotomas
|
|
D012607||arcuate scotoma
|
|
D012607||arcuate scotomas
|
|
D012607||bjerrum scotoma
|
|
D012607||bjerrum scotomas
|
|
D012607||central scotoma
|
|
D012607||central scotomas
|
|
D012607||centrocecal scotoma
|
|
D012607||centrocecal scotomas
|
|
D012607||paracecal scotoma
|
|
D012607||paracecal scotomas
|
|
D012607||paracentral scotoma
|
|
D012607||paracentral scotomas
|
|
D012607||peripheral scotoma
|
|
D012607||peripheral scotomas
|
|
D012607||ring scotoma
|
|
D012607||ring scotomas
|
|
D012607||scintillating scotoma
|
|
D012607||scintillating scotomas
|
|
D012607||scotoma altitudinal
|
|
D012607||scotoma arcuate
|
|
D012607||scotoma bjerrum
|
|
D012607||scotoma central
|
|
D012607||scotoma centrocecal
|
|
D012607||scotoma paracecal
|
|
D012607||scotoma paracentral
|
|
D012607||scotoma peripheral
|
|
D012607||scotoma ring
|
|
D012607||scotomas
|
|
D012607||scotomas altitudinal
|
|
D012607||scotomas arcuate
|
|
D012607||scotomas bjerrum
|
|
D012607||scotomas central
|
|
D012607||scotomas centrocecal
|
|
D012607||scotoma scintillating
|
|
D012607||scotoma sector
|
|
D012607||scotomas paracecal
|
|
D012607||scotomas paracentral
|
|
D012607||scotomas peripheral
|
|
D012607||scotomas ring
|
|
D012607||scotomas scintillating
|
|
D012607||scotomas sector
|
|
D012607||sector scotoma
|
|
D012607||sector scotomas
|
|
108120||arthrogryposis distal type 1a
|
|
108120|C535378||amcd1
|
|
108120|C535378||arthrogryposis distal type 1
|
|
108120|C535378||arthrogryposis multiplex congenita distal type i
|
|
108120||da1
|
|
108120||da1a
|
|
212750|D002446||celiac disease
|
|
212750|D002446||ais5 included
|
|
212750|D002446|153480|D006223||cd
|
|
212750|D002446||celiac10
|
|
212750|D002446||celiac11
|
|
212750|D002446||celiac12
|
|
212750|D002446||celiac13
|
|
212750|D002446||celiac1 included
|
|
212750|D002446||celiac2
|
|
212750|D002446||celiac3
|
|
212750|D002446||celiac4
|
|
212750|D002446||celiac5
|
|
212750|D002446||celiac6
|
|
212750|D002446||celiac7
|
|
212750|D002446||celiac8
|
|
212750|D002446||celiac9
|
|
212750|D002446||celiac disease susceptibility to 10
|
|
212750|D002446||celiac disease susceptibility to 11
|
|
212750|D002446||celiac disease susceptibility to 12
|
|
212750|D002446||celiac disease susceptibility to 13
|
|
212750|D002446||celiac disease susceptibility to 2
|
|
212750|D002446||celiac disease susceptibility to 3
|
|
212750|D002446||celiac disease susceptibility to 4
|
|
212750|D002446||celiac disease susceptibility to 5
|
|
212750|D002446||celiac disease susceptibility to 6
|
|
212750|D002446||celiac disease susceptibility to 7
|
|
212750|D002446||celiac disease susceptibility to 8
|
|
212750|D002446||celiac disease susceptibility to 9
|
|
212750|D002446||celiac sprue
|
|
212750|D002446||disease celiac
|
|
212750|D002446||enteropathies gluten
|
|
212750|D002446||enteropathies gluten sensitive
|
|
212750|D002446||enteropathy gluten
|
|
212750|D002446||enteropathy gluten sensitive
|
|
212750|D002446||gluten enteropathies
|
|
212750|D002446||gluten enteropathy
|
|
212750|D002446||gluten sensitive enteropathies
|
|
212750|D002446||gluten sensitive enteropathy
|
|
212750|D002446||gluten sensitive enteropathy gse celiac disease susceptibility to 1 included
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 10
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 11
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 12
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 13
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 2
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 3
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 4
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 5
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 6 autoimmune disease susceptibility to 5 included
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 7
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 8
|
|
212750|D002446||gluten sensitive enteropathy susceptibility to 9
|
|
212750|D002446||gses
|
|
212750|D002446||nontropical sprue
|
|
212750|D002446||sprue
|
|
212750|D002446||sprue celiac
|
|
212750|D002446||sprue nontropical
|
|
D012608||scrapie
|
|
D012608||rida
|
|
D004410|127700||dyslexia
|
|
D004410|127700||alexia
|
|
D004410|127700||alexias
|
|
D004410|127700||blindnesses word
|
|
D004410|127700||blindness word
|
|
D004410|127700||developmental dyslexia
|
|
D004410|127700||developmental dyslexias
|
|
D004410|127700||developmental reading disabilities
|
|
D004410|127700||developmental reading disability
|
|
D004410|127700||developmental reading disorder
|
|
D004410|127700||developmental reading disorders
|
|
D004410|127700||disabilities developmental reading
|
|
D004410|127700||disability developmental reading
|
|
D004410|127700||disorder developmental reading
|
|
D004410|127700||disorder reading
|
|
D004410|127700||disorders developmental reading
|
|
D004410|127700||disorders reading
|
|
D004410|127700||dyslexia developmental
|
|
D004410|127700||dyslexias
|
|
D004410|127700||dyslexias developmental
|
|
D004410|127700||dyslexia susceptibility to 1
|
|
D004410|127700||dyslexia susceptibility to 2
|
|
D004410|127700||dyslexia susceptibility to 3
|
|
D004410|127700||dyslexia susceptibility to 5
|
|
D004410|127700||dyslexia susceptibility to 6
|
|
D004410|127700||dyslexia susceptibility to 7 included
|
|
D004410|127700||dyslexia susceptibility to 8
|
|
D004410|127700||dyslexia susceptibility to 9
|
|
D004410|127700||dyx1
|
|
D004410|127700||dyx2
|
|
D004410|127700||dyx3
|
|
D004410|127700||dyx4 included
|
|
D004410|127700||dyx5
|
|
D004410|127700||dyx6
|
|
D004410|127700||dyx7 included
|
|
D004410|127700||dyx8
|
|
D004410|127700||dyx9
|
|
D004410|127700||reading disabilities developmental
|
|
D004410|127700||reading disability developmental
|
|
D004410|127700||reading disability specific 1 dyslexia susceptibility to 4 included
|
|
D004410|127700||reading disability specific 2
|
|
D004410|127700||reading disorder
|
|
D004410|127700||reading disorder developmental
|
|
D004410|127700||reading disorders
|
|
D004410|127700||reading disorders developmental
|
|
D004410|127700||word blindness
|
|
D004410|127700||word blindness congenital
|
|
D004410|127700||word blindnesses
|
|
C535629||hanhart syndrome
|
|
C535629||oromandibular limb hypogenesis complex
|
|
C536959||temtamy syndrome
|
|
C536959||craniofacial dysmorphism with ocular coloboma absent corpus callosum and aortic dilatation
|
|
C536959||dysmorphism corpus callosum agenesis and colobomas
|
|
D012600||scoliosis
|
|
D012600||scolioses
|
|
C536953||tel hashomer camptodactyly syndrome
|
|
C565492||hypertrichosis congenital anterior cervical with peripheral sensory and motor neuropathy
|
|
C564160|D011546|145260||pseudohypoaldosteronism type iia
|
|
D054446||lymphoma primary cutaneous anaplastic large cell
|
|
D054446||primary cutaneous anaplastic large cell lymphoma
|
|
D054446||primary cutaneous cd30 positive large t cell lymphoma
|
|
C535621||halal setton wang syndrome
|
|
C535621||hidrotic ectodermal dysplasia halal type
|
|
C536954||telencephalic leukoencephalopathy
|
|
C535620||hairy palms and soles
|
|
C535620||circumscribed hairy dysembryoplasia of palms
|
|
C535620||hairy cutaneous malformations of palms and soles
|
|
C535620||thickened hair bearing skin on the palms of both hands
|
|
C536951||teebi syndrome
|
|
C565494||hyperphosphatemia polyuria and seizures
|
|
C535623||hall riggs mental retardation syndrome
|
|
C536952||teeth noneruption of with maxillary hypoplasia and genu valgum
|
|
C565495||hyperphosphatasia with mental retardation
|
|
C535622||halal syndrome
|
|
C535622||microcephaly cleft palate autosomal dominant
|
|
C536957||temporomandibular ankylosis
|
|
C536957||ankylosis of the temporomandibular joint tmj
|
|
C564164||hyperpigmentation of fuldauer and kuijpers
|
|
C535625||hamano tsukamoto syndrome
|
|
C536958||temtamy preaxial brachydactyly syndrome
|
|
C536958||preaxial brachydactyly syndrome temtamy type
|
|
C564163||hyperpigmentation familial progressive
|
|
C535624||hamanishi ueba tsuji syndrome
|
|
C535624||congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy
|
|
C536955||telfer sugar jaeger syndrome
|
|
C536955||piebald trait neurologic defects
|
|
C536955||white forelock and leukoderma with neurological impairment
|
|
C565490||hypertrophic neuropathy and cataract
|
|
C564162||pseudohypoaldosteronism type iic
|
|
C536956||temporal epilepsy familial
|
|
C536956||epilepsy familial temporal lobe
|
|
C536956||familial temporal lobe epilepsy
|
|
C564161||pseudohypoaldosteronism type iib
|
|
C535626||hand and foot deformity with flat facies
|
|
C564168||hyperostosis cranialis interna
|
|
241500|C562646||hypophosphatasia infantile
|
|
241500|C562646||hops
|
|
241500|C562646||phosphoethanolaminuria
|
|
241500|C562646||phosphoethanolaminuria hypophosphatasia perinatal lethal included
|
|
C564165||parathyroid adenomatosis familial cystic
|
|
C564291|608098||heterotopia periventricular associated with chromosome 5p anomalies
|
|
C564291|608098||periventricular nodular heterotopia 3
|
|
C564291|608098||pvnh3
|
|
C565496||hyperparathyroidism neonatal self limited primary with hypercalciuria
|
|
C536972||torulopsis
|
|
C536972||neonatal torulopsis glabrata fungemia
|
|
C565497||hyperopia high
|
|
C565498||hypermetabolism due to defect in mitochondria
|
|
C565499||hyperlysinemia due to defect in lysine transport into mitochondria
|
|
C565831|603965||focal segmental glomerulosclerosis 2
|
|
C565831|603965||fsgs2
|
|
C565831|603965||glomerulosclerosis focal segmental 2
|
|
C564169||hereditary renal cancer associated 1
|
|
C564169||renal carcinoma familial associated 1
|
|
C535640||fried goldberg mundel syndrome
|
|
C565280|605844||dermatitis atopic 5
|
|
C565280|605844||atod5
|
|
D012612||scrub typhus
|
|
D012612||diseases tsutsugamushi
|
|
D012612||disease tsutsugamushi
|
|
D012612||fevers tsutsugamushi
|
|
D012612||fever tsutsugamushi
|
|
D012612||tsutsugamushi disease
|
|
D012612||tsutsugamushi diseases
|
|
D012612||tsutsugamushi fever
|
|
D012612||tsutsugamushi fevers
|
|
D012612||typhus scrub
|
|
C535639||frias syndrome
|
|
C535639||growth deficiency facial anomalies and brachydactyly
|
|
D012610||screw worm infection
|
|
D012610||infection screw worm
|
|
D012610||infections screw worm
|
|
D012610||screw worm infections
|
|
D013945||thymoma
|
|
D013945||carcinomas thymic
|
|
D013945||carcinoma thymic
|
|
D013945||thymic carcinoma
|
|
D013945||thymic carcinomas
|
|
D013945||thymomas
|
|
D053120||respiratory aspiration
|
|
D053120||aspiration respiratory
|
|
D018813|171400||multiple endocrine neoplasia type 2a
|
|
D018813|171400||mea 2a
|
|
D018813|171400||mea ii
|
|
D018813|171400||mea iia
|
|
D018813|171400||men 2
|
|
D018813|171400||men2a
|
|
D018813|171400||men 2a
|
|
D018813|171400||men 2a syndrome
|
|
D018813|171400||men 2a syndromes
|
|
D018813|171400||men ii
|
|
D018813|171400||men iia
|
|
D018813|171400||multiple endocrine neoplasia type 2
|
|
D018813|171400||multiple endocrine neoplasia type iia
|
|
D018813|171400||multiple endocrine neoplasms type 2a
|
|
D018813|171400||neoplasia multiple endocrine type 2a
|
|
D018813|171400||neoplasms multiple endocrine type 2a
|
|
D018813|171400||pheochromocytoma and amyloid producing medullary thyroid carcinoma
|
|
D018813|171400||ptc syndrome
|
|
D018813|171400||sipple syndrome
|
|
D018813|171400||sipple syndrome thyroid carcinoma familial medullary included
|
|
607250|C537313||spinocerebellar ataxia autosomal recessive with axonal neuropathy
|
|
607250|C537313||scan1
|
|
C536964||tollner horst manzke syndrome
|
|
C536964||heptacarpo octatarso dactyly combined with multiple malformation
|
|
C564171||palmoplantar keratoderma epidermolytic with knuckle pads
|
|
C535632||hardikar syndrome
|
|
C535632||cholestasis pigmentary retinopathy cleft palate syndrome
|
|
C564170||hyperlipoproteinemia type ii and deafness
|
|
C535631||cod cerebroocular dysgenesis
|
|
C535634||harlequin syndrome
|
|
C535634||sudden onset of unilateral flushing and sweating
|
|
C535634||unilateral loss of facial flushing and sweating with contralateral anhidrosis
|
|
C535633||harding ataxia
|
|
C535633||ataxia harding type
|
|
C535633||cerebellar ataxia early onset with retained tendon reflex
|
|
C535633||cerebellar ataxia early onset with retained tendon reflexes
|
|
C535636||freiberg apos s disease
|
|
C535636||freiberg kohler syndrome
|
|
C535636||freiberg apos s infraction
|
|
C535636||kohler apos s second disease
|
|
C535636||second metatarsal osteochondrosis
|
|
C536969||torsion dystonia with onset in infancy
|
|
C536969||autosomal dominant torsion dystonia with onset in infancy
|
|
C535635||harrod doman keele syndrome
|
|
C535635||craniofacial digital genital anomalies
|
|
C535635||harrod syndrome
|
|
C535638||frenkel russe syndrome
|
|
C535638||retinal telangiectasia and hypogammaglobulinemia
|
|
C535638||retinal telangiectasia associated with hypogammaglobulinemia
|
|
C536967||tonoki syndrome
|
|
C536967||short stature brachydactyly nail dysplasia and mental retardation
|
|
C563250|181030||salivary gland adenoma pleomorphic
|
|
C563250|181030||psa
|
|
C563250|181030||sgpa
|
|
C564172||hyperkeratosis hyperpigmentation syndrome
|
|
C535637||freire maia odontotrichomelic syndrome
|
|
C535637||odontotrichomelic hypohidrotic dysplasia
|
|
C563167||exostoses of heel
|
|
C563164||hernia double inguinal
|
|
D000724||ancylostomiasis
|
|
D000724||ancylostomiases
|
|
C563168||askin tumor
|
|
D039141|164300||muscular dystrophy oculopharyngeal
|
|
D039141|164300||dystrophies oculopharyngeal muscular
|
|
D039141|164300||dystrophy oculopharyngeal muscular
|
|
D039141|164300||muscular dystrophies oculopharyngeal
|
|
D039141|164300||oculopharyngeal dystrophy
|
|
D039141|164300||oculopharyngeal muscular dystrophies
|
|
D039141|164300||oculopharyngeal muscular dystrophy
|
|
D039141|164300||opmd
|
|
D039141|164300||progressive muscular dystrophy oculopharyngeal type
|
|
C566403|603174||homocysteinemia
|
|
C566403|603174|D020138||hyperhomocysteinemia
|
|
D012707||sertoli cell tumor
|
|
D012707||tumor sertoli cell
|
|
D056684|153300||yellow nail syndrome
|
|
D056684|153300||lymphedema and yellow nails
|
|
D056684|153300||nail syndromes yellow
|
|
D056684|153300||nail syndrome yellow
|
|
D056684|153300||syndromes yellow nail
|
|
D056684|153300||syndrome yellow nail
|
|
D056684|153300||yellow nail syndromes
|
|
D056684|153300||yns
|
|
D012700||serositis
|
|
D012700||serositides
|
|
605280|C537485||spastic paraplegia 13 autosomal dominant
|
|
605280|C537485||spg13
|
|
C535926||chitayat meunier hodgkinson syndrome
|
|
C535926||robin sequence with facial and digital anomalies
|
|
C536030|604308||mass syndrome
|
|
C536030|604308||mass phenotype
|
|
C536030|604308||octd
|
|
C536030|604308||overlap connective tissue disease
|
|
C535928||chitty hall baraitser syndrome
|
|
C535928||deafness femoral epiphyseal dysplasia short stature and developmental delay
|
|
C535928||growth retardation deafness femoral epiphyseal dysplasia and lacrimal duct obstruction
|
|
C535927||chitayat moore del bigio syndrome
|
|
C535929||chitty hall webb syndrome
|
|
103600||albumin
|
|
103600||alb dysalbuminemic hyperthyroxinemia included
|
|
103600||hyperthyroxinemia dysalbuminemic included
|
|
103600||analbuminemia included
|
|
103600||bisalbuminemia included
|
|
C535922||chemke oliver mallek syndrome
|
|
C535922||multiple ophthalmic anomalies and digital hypoplasia
|
|
C536479|276880||urocanase deficiency
|
|
C535921||cheilitis glandularis
|
|
C563171||methemoglobin reductase deficiency
|
|
C563171||nadph dependent methemoglobin reductase deficiency
|
|
C563171||tpnh methemoglobin reductase deficiency
|
|
C535923||chikungunya virus infection
|
|
C535923||arbovirus a chikungunya type
|
|
C535923||chikungunya
|
|
C535923||chikungunya fever
|
|
C563178|109730||aortic valve disease
|
|
D012719||setariasis
|
|
D012719||setariases
|
|
612528|C567280||diamond blackfan anemia 5
|
|
612528|C567280||dba5
|
|
C535937||cholesterol pneumonia
|
|
C535937||familiaere cholesterin pneumonie
|
|
122100|D053559||corneal dystrophy juvenile epithelial of meesmann
|
|
122100|D053559||corneal dystrophies meesmann
|
|
122100|D053559||corneal dystrophy meesmann
|
|
122100|D053559||corneal dystrophy meesmann epithelial
|
|
122100|D053559||dystrophies meesmann corneal
|
|
122100|D053559||juvenile hereditary epithelial dystrophy
|
|
122100|D053559||mecd
|
|
122100|D053559||meesmann corneal dystrophies
|
|
122100|D053559||meesmann corneal dystrophy
|
|
122100|D053559||meesmann corneal epithelial dystrophy
|
|
122100|D053559||meesmann epithelial corneal dystrophy
|
|
607476|C564391||newfoundland rod cone dystrophy
|
|
607476|C564391||nfrcd
|
|
C567453|611943||riddle syndrome
|
|
C567453|611943||radiosensitivity immunodeficiency dysmorphic features and learning difficulties
|
|
C535939||chondrocalcinosis due to apatite crystal deposition
|
|
C535939||familial apatite disease
|
|
C563764|609253||febrile convulsions familial 6
|
|
C563764|609253||convulsions familial febrile 6
|
|
C563764|609253||feb6
|
|
C563764|609253||febrile seizures familial 6
|
|
C563764|609253||seizures familial febrile 6
|
|
D012713||serum sickness
|
|
D012713||serum sicknesses
|
|
D012713||sicknesses serum
|
|
D012713||sickness serum
|
|
C563142|300047||mental retardation x linked 20
|
|
C563142|300047||mrx20
|
|
C563185||hyperhidrosis palmaris et plantaris
|
|
C564527|300360||mental retardation x linked with short stature
|
|
C564527|300360||mrss
|
|
121820|C535477||corneal dystrophy epithelial basement membrane
|
|
121820|C535477||cogan corneal dystrophy
|
|
121820|C535477||corneal dystrophy anterior basement membrane
|
|
121820|C535477||corneal dystrophy cogan type
|
|
121820|C535477||corneal dystrophy map dot fingerprint type
|
|
121820|C535477||corneal dystrophy microcystic
|
|
121820|C535477||ebmd
|
|
121820|C535477||map dot fingerprint dystrophy of cornea
|
|
121820|C535477||microcystic dystrophy of the cornea
|
|
D010244|211500||bulbar palsy progressive
|
|
D010244|211500||bulbar palsies
|
|
D010244|211500||bulbar palsies progressive
|
|
D010244|211500||bulbar palsy
|
|
D010244|211500||bulbar palsy progressive of childhood
|
|
D010244|211500||bulbar paralyses
|
|
D010244|211500||bulbar paralysis
|
|
D010244|211500||childhood progressive bulbar palsy
|
|
D010244|211500||fazio londe disease
|
|
D010244|211500||fazio londe syndrome
|
|
D010244|211500||palsies bulbar
|
|
D010244|211500||palsies progressive bulbar
|
|
D010244|211500||palsy bulbar
|
|
D010244|211500||palsy progressive bulbar
|
|
D010244|211500||paralysis bulbar
|
|
D010244|211500||progressive bulbar palsies
|
|
D010244|211500||progressive bulbar palsy
|
|
D010244|211500||progressive bulbar palsy of childhood
|
|
D010244|211500||syndrome fazio londe
|
|
C537975|610474||catshl syndrome
|
|
C537975|610474||camptodactyly tall stature and hearing loss syndrome
|
|
C563148|300143||mental retardation x linked 34
|
|
C563147|300705|C563140||mental retardation x linked 31
|
|
C564478||nystagmus 5 infantile periodic alternating
|
|
C564478||nystagmus infantile periodic alternating x linked
|
|
C566449|610090||pyridoxamine 5 prime phosphate oxidase deficiency
|
|
C566449|610090||epileptic encephalopathy neonatal pnpo related
|
|
C566449|610090||pnpo deficiency
|
|
C566449|610090||pnpo related neonatal epileptic encephalopathy
|
|
C566449|610090||pyridoxal 5 apos phosphate dependent epilepsy
|
|
C566449|610090||pyridoxine 5 apos phosphate oxidase deficiency
|
|
C566449|610090||seizures pyridoxine resistant plp sensitive
|
|
C535947||devriendt syndrome
|
|
D000544|104300||alzheimer disease
|
|
D000544|104300||acute confusional senile dementia
|
|
D000544|104300||ad
|
|
D000544|104300||ad1 included
|
|
D000544|104300||alzheimer dementia ad
|
|
D000544|104300||alzheimer disease early onset
|
|
D000544|104300||alzheimer disease early onset with cerebral amyloid angiopathy included
|
|
D000544|104300||alzheimer disease late onset
|
|
D000544|104300||alzheimer disease protection against included
|
|
D000544|104300||alzheimer sclerosis
|
|
D000544|104300||alzheimer apos s disease
|
|
D000544|104300||alzheimer apos s disease focal onset
|
|
D000544|104300||alzheimer syndrome
|
|
D000544|104300||alzheimer type dementia
|
|
D000544|104300||alzheimer type dementia atd
|
|
D000544|104300||alzheimer type senile dementia
|
|
D000544|104300||dementia alzheimer ad
|
|
D000544|104300||dementia alzheimer type
|
|
D000544|104300||dementia alzheimer type atd
|
|
D000544|104300||dementia presenile
|
|
D000544|104300||dementia primary senile degenerative
|
|
D000544|104300||dementia senile
|
|
D000544|104300||disease alzheimer
|
|
D000544|104300||disease alzheimer apos s
|
|
D000544|104300||early onset alzheimer disease
|
|
D000544|104300||familial alzheimer disease fad
|
|
D000544|104300||focal onset alzheimer apos s disease
|
|
D000544|104300||late onset alzheimer disease
|
|
D000544|104300||presenile alzheimer dementia
|
|
D000544|104300||presenile and senile dementia alzheimer disease familial 1 included
|
|
D000544|104300||presenile dementia
|
|
D000544|104300||primary senile degenerative dementia
|
|
D000544|104300||sclerosis alzheimer
|
|
D000544|104300||senile dementia
|
|
D000544|104300||senile dementia acute confusional
|
|
D000544|104300||senile dementia alzheimer type
|
|
D000544|104300||syndrome alzheimer
|
|
C535949||schofer beetz bohl syndrome
|
|
D000708||anaplasia
|
|
D000708||anaplasias
|
|
C536862|609195||spastic paraplegia 26 autosomal recessive
|
|
C536862|609195||spg26
|
|
D000707||anaphylaxis
|
|
D000707||anaphylactic reaction
|
|
D000707||anaphylactic reactions
|
|
D000707||anaphylactic shock
|
|
D000707||reaction anaphylactic
|
|
D000707||reactions anaphylactic
|
|
D000707||shock anaphylactic
|
|
C564483||mental retardation x linked 92
|
|
C563705|609533||deafness autosomal recessive 23
|
|
C563705|609533||dfnb23
|
|
C563151|300558|C563146||mental retardation x linked 47
|
|
C563151|300558|C563146||mrx47
|
|
C535945||desmoplastic cerebral astrocytoma of infancy
|
|
C566303|104000||alopecia areata 1
|
|
C566303|104000||aa1 alopecia universalis included
|
|
C566303|104000||au included
|
|
D000711||anaplasmataceae infections
|
|
D000711||anaplasmataceae infection
|
|
D000711||haemobartonelloses
|
|
D000711||haemobartonellosis
|
|
D000711||infection anaplasmataceae
|
|
D000711||infections anaplasmataceae
|
|
C563154||brooks wisniewski brown syndrome
|
|
C564484||holoprosencephaly ectrodactyly and bilateral cleft lip palate
|
|
C564484||hartsfield syndrome
|
|
C563159||acrorenal syndrome
|
|
C567562|612789||deafness autosomal recessive 71
|
|
C567562|612789||dfnb71
|
|
614230||chromosome 8q21 11 deletion syndrome
|
|
D000712||anaplasmosis
|
|
D000712||anaplasmoses
|
|
C535958||epidermolysis bullosa inversa dystrophica
|
|
C535958||junctional epidermolysis bullosa inversa
|
|
C564490||mental retardation x linked nonsyndromic
|
|
C535950||dianzani autoimmune lymphoproliferative syndrome
|
|
C535950||autoimmune lymphoproliferative disease without fas mutations
|
|
C535950||autoimmune lymphoproliferative syndrome without fas mutations
|
|
C535950||dianzani autoimmune lymphoproliferative disease
|
|
C535950||dianzani form of autoimmune lymphoproliferative disease
|
|
C535953||eosinophilic pustular folliculitis
|
|
C535953||eosinophilic folliculitis pustular
|
|
C535953||ofuji disease
|
|
C535953||ofuji apos s disease
|
|
C535952||eosinophilic enteropathy
|
|
C535952||eosinophilic enteritis
|
|
C535952||eosinophilic gastritis
|
|
C535952||eosinophilic gastroenteritis
|
|
C535952||eosinophilic gastroenteropathy
|
|
C563163||stridor congenital
|
|
C535954||eosinophilic synovitis
|
|
C535954||idiopathic eosinophilic synovitis
|
|
C535954||shulman syndrome
|
|
C567839|612961||multiple synostoses syndrome 3
|
|
C567839|612961||syns3
|
|
C565786||myoclonic epilepsy congenital deafness macular dystrophy and psychiatric disorders
|
|
C537265|604777||lamellar ichthyosis type 3
|
|
C537265|604777||arci5
|
|
C537265|604777||ichthyosis congenita 3
|
|
C537265|604777||ichthyosis congenita iii
|
|
C537265|604777||ichthyosis congenital autosomal recessive 5
|
|
C537265|604777||ichthyosis lamellar 3
|
|
C537265|604777||ichthyosis lamellar 3 formerly
|
|
C537265|604777|C565749||ichthyosis nonlamellar and nonerythrodermic congenital autosomal recessive
|
|
C537265|604777||li3 formerly
|
|
C537265|604777||nnci
|
|
C537265|604777||type 3 lamellar ichthyosis
|
|
C538165||achromatopsia incomplete x linked
|
|
C538165||incomplete achromatopsia x linked
|
|
C538165||x linked achromatopsia incomplete
|
|
C564452||microphthalmia isolated with cataract 3
|
|
C564452||cataract congenital with microcornea and microphthalmia
|
|
C564452||mcopct3
|
|
C564452||microphthalmia and cataract 3
|
|
C538164||bowen syndrome
|
|
C538164||bowen syndrome of multiple malformations
|
|
C565782||patent ductus arteriosus and bicuspid aortic valve with hand anomalies
|
|
C563127||corpus callosum agenesis of with facial anomalies and robin sequence
|
|
C563127||toriello carey syndrome
|
|
C565783||ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia
|
|
C538169||acitretin embryopathy
|
|
C538169||acitretine embryofetopathy
|
|
C563124||spondylometaphyseal dysplasia x linked
|
|
C563124||spondylometaphyseal dysplasia richmond type
|
|
C567212|612649||ciliary dyskinesia primary 11
|
|
C567212|612649||cild11
|
|
C567212|612649||ciliary dyskinesia primary 11 without situs inversus
|
|
C563129||van den bosch syndrome
|
|
C536198|225400||ehlers danlos syndrome type 6
|
|
C536198|225400||eds6
|
|
C536198|225400||eds6a formerly
|
|
C536198|225400||eds vi
|
|
C536198|225400||ehlers danlos syndrome kyphoscoliotic type
|
|
C536198|225400||ehlers danlos syndrome ocular scoliotic type
|
|
C536198|225400||ehlers danlos syndrome oculoscoliotic type
|
|
C536198|225400||ehlers danlos syndrome type 6 a
|
|
C536198|225400||ehlers danlos syndrome type vi
|
|
C536198|225400||ehlers danlos syndrome type via
|
|
C536198|225400||ehlers danlos syndrome type via formerly
|
|
C536198|225400|C536113||nevo syndrome
|
|
C564459||spina bifida x linked
|
|
614227||hyperuricemic nephropathy familial juvenile 3
|
|
614227||hnfj3
|
|
C538161||mcpherson robertson cammarano syndrome
|
|
C538161||dominantly inherited ptosis strabismus and ectopic pupils
|
|
C538160||mcpherson clemens syndrome
|
|
C538160||cleft lip cleft palate characteristic facies intestinal malrotation and lethal congenital heart disease
|
|
C538160||cleft lip palate with characteristic facies intestinal malrotation and lethal congenital heart disease
|
|
C537314|302600||spinocerebellar ataxia x linked 2
|
|
C537314|302600||cerebellar ataxia with extrapyramidal involvement early onset
|
|
C537314|302600||scax2
|
|
170400||hypokalemic periodic paralysis type 1
|
|
170400|D020514||hokpp
|
|
170400||hokpp1
|
|
170400|D020514||hypokalemic periodic paralysis
|
|
C567337|612359||cowden like syndrome
|
|
C567337|612359||cowden syndrome 2
|
|
C567337|612359||cws2
|
|
D016269||milk hypersensitivity
|
|
D016269||allergies milk
|
|
D016269||allergy milk
|
|
D016269||hypersensitivities milk
|
|
D016269||hypersensitivity milk
|
|
D016269||milk allergies
|
|
D016269||milk allergy
|
|
D016269||milk hypersensitivities
|
|
241530|C562793||hypophosphatemic rickets with hypercalciuria hereditary
|
|
241530|C562793||hhrh
|
|
241530|C562793||hypercalciuric rickets
|
|
C562901|310468||nephrolithiasis x linked recessive with renal failure
|
|
C562901|310468||nephrolithiasis 1
|
|
C562901|310468||nephrolithiasis x linked recessive type 1
|
|
C562901|310468||nphl1
|
|
C562901|310468||urolithiasis x linked recessive type 1
|
|
C562901|310468||xrn
|
|
C565791||acne adult
|
|
C565792||microcephaly primary autosomal recessive 4
|
|
D017118|176000||porphyria acute intermittent
|
|
D017118|176000||acute intermittent porphyria
|
|
D017118|176000||acute intermittent porphyrias
|
|
D017118|176000||acute porphyria
|
|
D017118|176000||acute porphyrias
|
|
D017118|176000||aip
|
|
D017118|176000||deaminase deficiencies porphobilinogen
|
|
D017118|176000||deaminase deficiency porphobilinogen
|
|
D017118|176000||deficiencies hydroxymethylbilane synthase
|
|
D017118|176000||deficiencies pbgd
|
|
D017118|176000||deficiencies porphobilinogen deaminase
|
|
D017118|176000||deficiencies ups
|
|
D017118|176000||deficiencies uroporphyrinogen synthase
|
|
D017118|176000||deficiency hydroxymethylbilane synthase
|
|
D017118|176000||deficiency pbgd
|
|
D017118|176000||deficiency porphobilinogen deaminase
|
|
D017118|176000||deficiency ups
|
|
D017118|176000||deficiency uroporphyrinogen synthase
|
|
D017118|176000||hydroxymethylbilane synthase deficiencies
|
|
D017118|176000||hydroxymethylbilane synthase deficiency
|
|
D017118|176000||intermittent porphyria acute
|
|
D017118|176000||intermittent porphyrias acute
|
|
D017118|176000||pbgd deficiencies
|
|
D017118|176000||pbgd deficiency
|
|
D017118|176000||porc included
|
|
D017118|176000||porphobilinogen deaminase deficiencies
|
|
D017118|176000||porphobilinogen deaminase deficiency
|
|
D017118|176000||porphyria acute
|
|
D017118|176000||porphyria chester type included
|
|
D017118|176000||porphyrias acute
|
|
D017118|176000||porphyrias acute intermittent
|
|
D017118|176000||porphyrias swedish type
|
|
D017118|176000||porphyria swedish type
|
|
D017118|176000||swedish type porphyria
|
|
D017118|176000||swedish type porphyrias
|
|
D017118|176000||synthase deficiencies hydroxymethylbilane
|
|
D017118|176000||synthase deficiencies uroporphyrinogen
|
|
D017118|176000||synthase deficiency hydroxymethylbilane
|
|
D017118|176000||synthase deficiency uroporphyrinogen
|
|
D017118|176000||type porphyrias swedish
|
|
D017118|176000||type porphyria swedish
|
|
D017118|176000||ups deficiencies
|
|
D017118|176000||ups deficiency
|
|
D017118|176000||ups deficiency porphyria acute intermittent nonerythroid variant included
|
|
D017118|176000||uroporphyrinogen synthase deficiencies
|
|
D017118|176000||uroporphyrinogen synthase deficiency
|
|
D017599||neuroectodermal tumors
|
|
D017599||neuroectodermal tumor
|
|
D017599||tumor neuroectodermal
|
|
D017599||tumors neuroectodermal
|
|
C565797||blepharophimosis with facial and genital anomalies and mental retardation
|
|
C538177||acrocallosal syndrome schinzel type
|
|
C538177||schinzel acrocallosal syndrome
|
|
C538177||schinzel syndrome 1
|
|
C538176||acquired pure megakaryocytic aplasia
|
|
C564463|C538243|301200||amelogenesis imperfecta hypomaturation type with snow capped teeth
|
|
C538175||acquired ichthyosis
|
|
C538175||fish scale disease acquired
|
|
C538175||ichthyosis acquisita
|
|
C567126|611719||combined oxidative phosphorylation deficiency 5
|
|
C567126|611719||coxpd5
|
|
C565794||microcephaly primary autosomal recessive 2
|
|
C538179||acrodysostosis
|
|
C538179||acrodysplasia
|
|
C538179||arkless graham syndrome
|
|
C538179||maroteaux malamut syndrome
|
|
C538179||nasal hypoplasia peripheral dysostosis mental retardation syndrome
|
|
C538179||peripheral dysostosis
|
|
C538179||peripheral dysostosis nasal hypoplasia mental retardation pnm syndrome
|
|
C565796||anemia congenital hypoplastic with multiple congenital anomalies mental retardation syndrome
|
|
C538170||ackerman syndrome
|
|
C538170||glaucoma juvenile with unusual upper lip and dental roots
|
|
C538170||juvenile glaucoma with unusual upper lip and dental roots
|
|
C538170||molar roots pyramidal with juvenile glaucoma and unusual upper lip
|
|
C538170||pyramidal molars glaucoma abnormal upper lip
|
|
614211||deafness autosomal dominant 33
|
|
614211||dfna33
|
|
151623|C538639||sarcoma family syndrome of li and fraumeni
|
|
151623|C538639||lfl included
|
|
151623|C538639||lfs1
|
|
151623|C538639||li fraumeni syndrome 1
|
|
151623|C538639||sarcoma breast leukemia and adrenal gland sbla syndrome
|
|
151623|C538639||sbla syndrome li fraumeni like syndrome included
|
|
C563139|C566875|300055||mental retardation x linked 16
|
|
C538174||acquired hypoprothrombinemia
|
|
C538174||hypoprothrombinemia acquired
|
|
C538173||acquired angioedema
|
|
600060|C564007||deafness autosomal recessive 2
|
|
600060|C564007||dfnb2
|
|
600060|C564007||neurosensory nonsyndromic recessive deafness 2
|
|
600060|C564007||nsrd2
|
|
C538172||acquired amegakaryocytic thrombocytopenia
|
|
C538171||acquired agranulocytosis
|
|
C538171||agranulocytic angina
|
|
C538171||granulocytopenia primary
|
|
C538171||neutropenia malignant
|
|
614207||hyperphosphatasia with mental retardation syndrome 3
|
|
614207||hpmrs3
|
|
614207||mental retardation autosomal recessive 17
|
|
614207||mental retardation autosomal recessive 21
|
|
614207||mrt17
|
|
614207||mrt21
|
|
614208||mental retardation autosomal recessive 16
|
|
614208||mrt16
|
|
C567753|613100||glaucoma 1 open angle o
|
|
C567753|613100||glc1o
|
|
C567753|613100||primary open angle glaucoma 1o
|
|
C536857|312920||spastic paraplegia 2 x linked
|
|
C536857|312920||spg2
|
|
C536857|312920||sppx2
|
|
D058490|612965||46 xy disorders of sex development
|
|
D058490|612965||46 xy dsd
|
|
D058490|612965||46 xy dsds
|
|
D058490|612965||46 xy gonadal dysgenesis complete or partial with or without adrenal failure
|
|
D058490|612965||46 xy sex reversal 3
|
|
D058490|612965||46 xy sex reversal partial or complete nr5a1 related
|
|
D058490|612965||disorder of sex development 46 xy
|
|
D058490|612965||dsd 46 xy
|
|
D058490|612965||dsds 46 xy
|
|
D058490|612965||male pseudohermaphroditism
|
|
D058490|612965||male pseudohermaphroditisms
|
|
D058490|612965||pseudohermaphroditism male
|
|
D058490|612965||pseudohermaphroditisms male
|
|
D058490|612965||sex reversal xy with or without adrenal failure
|
|
D058490|612965||srxy3
|
|
C563141||mental retardation x linked 19
|
|
C564470|300630||mental retardation x linked 59
|
|
C567064|300661||phosphoribosylpyrophosphate synthetase superactivity
|
|
C567064|300661||gout prps related
|
|
C567064|300661||prps1 superactivity gout prps related included
|
|
C564432||deafness high frequency sensorineural x linked
|
|
C565765||hypoglobulinemia and absent b cells
|
|
C538187||acrogeria gottron type
|
|
C538187||acrometageria
|
|
C538187||metageria
|
|
C565766|D006950|144250||hyperlipidemia combined 2
|
|
C565766|D006950|144250||fchl2
|
|
C565766|D006950|144250||hyperlipidemia familial combined 2
|
|
C565766|D006950|144250||hyplip2
|
|
C564430||epidermodysplasia verruciformis x linked
|
|
C538186||acrofrontofacionasal dysostosis syndrome
|
|
C538186||acro fronto facio nasal dysostosis
|
|
C538186||acrofrontofacionasal dysostosis 1
|
|
C538186||cleft lip palate with frontonasal dysostosis and postaxial polysyndactyly
|
|
C538186||polysyndactyly postaxial frontonasal dysostosis and cleft lip palate
|
|
C565767||vdac deficiency
|
|
C566468|610498||combined oxidative phosphorylation deficiency 2
|
|
C566468|610498||corpus callosum agenesis of with dysmorphism and fatal lactic acidosis
|
|
C566468|610498||coxpd2
|
|
C565761||charcot marie tooth neuropathy type 4b2 with early onset glaucoma
|
|
C563104||orofaciodigital syndrome vii
|
|
C563104||ofd7
|
|
C563104||ofds vii
|
|
C563104||oral facial digital syndrome type vii
|
|
C563104||whelan syndrome
|
|
C564435||deafness hypogonadism syndrome
|
|
162200|D009456||neurofibromatosis 1
|
|
162200|D009456|193520||cafe au lait spots with pulmonic stenosis
|
|
162200|D009456||i neurofibromatosis type
|
|
162200|D009456||molluscum fibrosum
|
|
162200|D009456||neurofibromatoses peripheral
|
|
162200|D009456||neurofibromatoses type i
|
|
162200|D009456||neurofibromatosis i
|
|
162200|D009456||neurofibromatosis peripheral
|
|
162200|D009456||neurofibromatosis peripheral nf1
|
|
162200|D009456||neurofibromatosis peripheral nf 1
|
|
162200|D009456||neurofibromatosis peripheral type
|
|
162200|D009456||neurofibromatosis type 1
|
|
162200|D009456||neurofibromatosis type i
|
|
162200|D009456||nf1
|
|
162200|D009456||nf1 neurofibromatosis 1
|
|
162200|D009456||peripheral neurofibromatoses
|
|
162200|D009456||peripheral neurofibromatosis
|
|
162200|D009456|193520||pulmonic stenosis with cafe au lait spots
|
|
162200|D009456||recklinghausen disease nerve
|
|
162200|D009456||recklinghausen disease of nerve
|
|
162200|D009456||recklinghausen apos s disease of nerve
|
|
162200|D009456||recklinghausens disease of nerve
|
|
162200|D009456||syndrome watson
|
|
162200|D009456||type 1 neurofibromatosis
|
|
162200|D009456||type i neurofibromatoses
|
|
162200|D009456||type i neurofibromatosis
|
|
162200|D009456||von recklinghausen disease
|
|
162200|D009456||von recklinghausen apos s disease
|
|
162200|D009456||von recklinghausens disease
|
|
162200|D009456|193520||watson syndrome
|
|
C535726|223800||dyggve melchior clausen syndrome
|
|
C535726|223800||dmc
|
|
C535726|223800||dyggve melchior clausen disease
|
|
C535726|223800||dyggve melchior clausen syndrome x linked
|
|
C535726|223800||x linked dyggve melchior clausen syndrome
|
|
C538181||acrodysplasia with ossification abnormalities short stature and fibular hypoplasia
|
|
C538180||acrodysplasia scoliosis
|
|
D005599||fractures ununited
|
|
D005599||fracture ununited
|
|
D005599||ununited fracture
|
|
D005599||ununited fractures
|
|
C564439||cone dystrophy x linked 1
|
|
C564438||cone rod dystrophy x linked type 1
|
|
C564438|304020||cordx1
|
|
C538185||acrofacial dysostosis palagonia type
|
|
C538185||palagonia type of acrofacial dysostosis
|
|
C565768||alpha methylacyl coa racemase deficiency
|
|
D005596||fractures closed
|
|
D005596||closed fracture
|
|
D005596||closed fractures
|
|
D005596||fracture closed
|
|
D005596||fracture occult
|
|
D005596||fractures occult
|
|
D005596||occult fracture
|
|
D005596||occult fractures
|
|
C538183||acrofacial dysostosis rodriguez type
|
|
C538183||acrofacial dysostosis syndrome of rodriguez
|
|
C538183||rodriguez lethal acrofacial dysostosis syndrome
|
|
C567936|274300||thyroid hormone resistance generalized autosomal recessive
|
|
C567936|274300|C567934|188570||grth
|
|
C567936|274300|C567934|188570||gthr
|
|
C567936|274300|D018382||refetoff syndrome
|
|
C567936|274300|C567934|188570||thyroid hormone unresponsiveness
|
|
D005598||fractures spontaneous
|
|
D005598||fracture pathologic
|
|
D005598||fracture pathological
|
|
D005598||fractures pathologic
|
|
D005598||fractures pathological
|
|
D005598||fracture spontaneous
|
|
D005598||pathological fracture
|
|
D005598||pathological fractures
|
|
D005598||pathologic fracture
|
|
D005598||pathologic fractures
|
|
D005598||spontaneous fracture
|
|
D005598||spontaneous fractures
|
|
C538182||acrofacial dysostosis catania form
|
|
C538182||acrofacial dysostosis catania type
|
|
C538182||opitz mollica sorge syndrome
|
|
D004266||dna virus infections
|
|
D004266||dna virus infection
|
|
D004266||infection dna virus
|
|
D004266||infections dna virus
|
|
D004266||virus infection dna
|
|
D004266||virus infections dna
|
|
D005597||fractures open
|
|
D005597||compound fracture
|
|
D005597||compound fractures
|
|
D005597||fracture compound
|
|
D005597||fracture open
|
|
D005597||fractures compound
|
|
D005597||open fracture
|
|
D005597||open fractures
|
|
C536498|273395||tetra amelia autosomal recessive
|
|
C536498|273395||autosomal recessive tetra amelia
|
|
C536498|273395||tetra amelia
|
|
C536498|273395||tetraamelia autosomal recessive
|
|
C536498|273395||tetra amelia syndrome
|
|
C535905||lipoatrophy with diabetes hepatic steatosis cardiomyopathy and leukomelanodermic papules
|
|
C535908||marcus gunn phenomenon
|
|
C535908||familial marcus gunn phenomenon
|
|
C535908||jaw winking
|
|
C535908||maxillopalpebral synkinesis
|
|
C535909||marden walker like syndrome
|
|
C535909||blepharophimosis arachnodactyly and congenital contractures
|
|
C535909||marden walker like syndrome without psychomotor retardation
|
|
C535909||van den ende gupta syndrome
|
|
C535909||vdegs
|
|
C536801|606232||telomeric 22q13 monosomy syndrome
|
|
C536801|606232||22q13 3 deletion syndrome
|
|
C536801|606232||22q13 deletion syndrome
|
|
C536801|606232||chromosome 22q13 3 deletion syndrome
|
|
C536801|606232||deletion 22q13 3 syndrome
|
|
C536801|606232||deletion 22q13 syndrome
|
|
C536801|606232||monosomy 22q13
|
|
C536801|606232||phelan mcdermid syndrome
|
|
D017574||parasystole
|
|
D017574||parasystoles
|
|
D017577||cutaneous fistula
|
|
D017577||cutaneous fistulas
|
|
D017577||external fistula
|
|
D017577||external fistulas
|
|
D017577||fistula cutaneous
|
|
D017577||fistula external
|
|
D017577||fistulas cutaneous
|
|
D017577||fistulas external
|
|
D017577||fistula skin
|
|
D017577||fistulas skin
|
|
D017577||skin fistula
|
|
D017577||skin fistulas
|
|
115200|D002311|C580047||cardiomyopathy dilated
|
|
115200|D002311|C580047||1a dilated cardiomyopathy
|
|
115200|D002311|C580047||1as dilated cardiomyopathy
|
|
115200|D002311|C580047||cardiomyopathies congestive
|
|
115200|D002311|C580047||cardiomyopathies dilated
|
|
115200|D002311|C580047||cardiomyopathies familial idiopathic
|
|
115200|D002311|C580047||cardiomyopathies idiopathic dilated
|
|
115200|D002311|C580047||cardiomyopathy 1a dilated
|
|
115200|D002311|C580047||cardiomyopathy 1as dilated
|
|
115200|D002311|C580047||cardiomyopathy congestive
|
|
115200|D002311|C580047||cardiomyopathy dilated 1a
|
|
115200|D002311|C580047||cardiomyopathy dilated 1gg
|
|
115200|D002311|C580047||cardiomyopathy dilated 1r
|
|
115200|D002311|C580047|C567505|611880||cardiomyopathy dilated autosomal recessive
|
|
115200|D002311|C580047||cardiomyopathy dilated cmd1a
|
|
115200|D002311|C580047||cardiomyopathy dilated lmna
|
|
115200|D002311|C580047||cardiomyopathy dilated with conduction defect 1
|
|
115200|D002311|C580047||cardiomyopathy dilated with conduction deffect1
|
|
115200|D002311|C580047||cardiomyopathy familial idiopathic
|
|
115200|D002311|C580047||cardiomyopathy idiopathic dilated
|
|
115200|D002311|C580047||cdcd1
|
|
115200|D002311|C580047||cmd1a
|
|
115200|D002311|C580047||cmd1gg
|
|
115200|D002311|C580047||cmd1r
|
|
115200|D002311|C580047||congestive cardiomyopathies
|
|
115200|D002311|C580047||congestive cardiomyopathy
|
|
115200|D002311|C580047||dilated cardiomyopathies
|
|
115200|D002311|C580047||dilated cardiomyopathies idiopathic
|
|
115200|D002311|C580047||dilated cardiomyopathy
|
|
115200|D002311|C580047||dilated cardiomyopathy 1a
|
|
115200|D002311|C580047||dilated cardiomyopathy 1as
|
|
115200|D002311|C580047||dilated cardiomyopathy idiopathic
|
|
115200|D002311|C580047||familial idiopathic cardiomyopathies
|
|
115200|D002311|C580047||familial idiopathic cardiomyopathy
|
|
115200|D002311|C580047||idiopathic cardiomyopathies familial
|
|
115200|D002311|C580047||idiopathic cardiomyopathy familial
|
|
115200|D002311|C580047||idiopathic dilated cardiomyopathies
|
|
115200|D002311|C580047||idiopathic dilated cardiomyopathy
|
|
115200|D002311|C580047||left ventricular noncompaction 4 included
|
|
115200|D002311|C580047||lvnc4 included
|
|
115200|D002311|C580047||dmd associated dilated cardiomyopathy
|
|
115200|D002311|C580047|302045||cmd3b
|
|
115200|D002311|C580047||dilated cardiomyopathy 3b
|
|
115200|D002311|C580047||dmd related dilated cardiomyopathy
|
|
115200|D002311|C580047||x linked dilated cardiomyopathy
|
|
C538199||deafness autosomal dominant nonsyndromic sensorineural 24
|
|
C563111||absent eyebrows and eyelashes with mental retardation
|
|
C563111||pseudoprogeria syndrome
|
|
D016262||postpoliomyelitis syndrome
|
|
D016262||muscular atrophies postpoliomyelitis
|
|
D016262||muscular atrophies post poliomyelitis
|
|
D016262||muscular atrophy postpoliomyelitis
|
|
D016262||muscular atrophy post poliomyelitis
|
|
D016262||postpoliomyelitis muscular atrophies
|
|
D016262||post poliomyelitis muscular atrophies
|
|
D016262||postpoliomyelitis muscular atrophy
|
|
D016262||post poliomyelitis muscular atrophy
|
|
D016262||post poliomyelitis syndrome
|
|
D016262||post polio syndrome
|
|
D016262||post polio syndromes
|
|
D017593||kleine levin syndrome
|
|
D017593||familial hibernation kleine levin syndrome
|
|
D017593||familial kleine levin syndrome
|
|
D017593||hibernation syndrome kleine levin
|
|
D017593||hypersomnia periodic
|
|
D017593||kleine levin critchley syndrome
|
|
D017593||kleine levin hibernation syndrome
|
|
D017593||kleine levin syndrome familial
|
|
D017593||periodic hypersomnia
|
|
D017593||periodic hypersomnias
|
|
D017593||syndrome familial kleine levin
|
|
D017593||syndrome kleine levin
|
|
D017593||syndrome kleine levin critchley
|
|
D017593||syndrome kleine levin hibernation
|
|
C564442||cleft palate with ankyloglossia
|
|
C538198||deafness autosomal dominant nonsyndromic sensorineural 23
|
|
C565777||colorectal cancer hereditary nonpolyposis type 7
|
|
C565777||hnpcc7
|
|
D016263||aids associated nephropathy
|
|
D016263||aids associated nephropathies
|
|
D016263||aids nephropathies
|
|
D016263||aids nephropathy
|
|
D016263||hiv associated nephropathies
|
|
D016263||hiv associated nephropathy
|
|
D016263||hiv related nephropathies
|
|
D016263||hiv related nephropathy
|
|
D016263||human immunodeficiency virus associated nephropathy
|
|
D016263||nephropathies aids
|
|
D016263||nephropathies aids associated
|
|
D016263||nephropathies hiv associated
|
|
D016263||nephropathies hiv related
|
|
D016263||nephropathy aids
|
|
D016263||nephropathy aids associated
|
|
D016263||nephropathy hiv associated
|
|
D016263||nephropathy hiv related
|
|
C538197||deafness autosomal dominant nonsyndromic sensorineural 22
|
|
C538197||deafness autosomal dominant 22
|
|
C538197||dfna22
|
|
C538197||dfna 22
|
|
C564440||colorblindness partial tritanomaly
|
|
C564440||tritanomalous colorblindness
|
|
C565771||human herpesvirus type 6 integrated
|
|
C564446||charcot marie tooth peroneal muscular atrophy and friedreich ataxia combined
|
|
C565773||polyneuropathy lethal neonatal axonal sensorimotor autosomal recessive
|
|
D017590||myelinolysis central pontine
|
|
D017590||central pontine myelinoclasis
|
|
D017590||central pontine myelinolysis
|
|
D017590||extrapontine myelinoclases
|
|
D017590||extrapontine myelinoclasis
|
|
D017590||extrapontine myelinolyses
|
|
D017590||extrapontine myelinolysis
|
|
D017590||myelinoclases extrapontine
|
|
D017590||myelinoclasis central pontine
|
|
D017590||myelinoclasis extrapontine
|
|
D017590||myelinolyses extrapontine
|
|
D017590||myelinolysis extrapontine
|
|
D017590||pontine myelinolysis central
|
|
C538192|D055947|609192||furlong syndrome
|
|
C538192||marfanoid disorder with craniosynostosis type 2
|
|
C563119||sao paulo mca mr syndrome
|
|
C538190||muscular dystrophy congenital with central nervous system involvement
|
|
C538190||muscular dystrophy congenital progressive with mental retardation
|
|
C564449||cerebral sclerosis diffuse scholz type
|
|
C538196||atlanto axial fusion
|
|
C538196||atlantoaxial fusion
|
|
C538196||atlantoaxial joint fusion
|
|
C565779|604391||ataxia telangiectasia like disorder
|
|
C538195||atkin syndrome
|
|
C538195||atkin flaitz patil smith syndrome
|
|
C538195||atkin flaitz syndrome
|
|
C538195|300143||mental retardation x linked 21
|
|
C538195||mental retardation x linked atkin type
|
|
C538195||mental retardation x linked nonspecific
|
|
C538195||mental retardation x linked nonspecific type 1
|
|
C538195|300143||mrx21
|
|
C538195||x linked mental retardation syndrome atkin type
|
|
C538194||furunculous myiasis
|
|
C538194||furuncular myiasis
|
|
D028227||amyloid neuropathies familial
|
|
D028227||amyloid neuropathy familial
|
|
D028227||amyloid neuropathy type 1
|
|
D028227||amyloidoses hereditary neuropathic
|
|
D028227||amyloidoses portuguese polyneuritic
|
|
D028227||amyloidosis hereditary neuropathic
|
|
D028227||amyloidosis portuguese polyneuritic
|
|
D028227||amyloid polyneuropathies familial
|
|
D028227||amyloid polyneuropathy british type
|
|
D028227||amyloid polyneuropathy familial
|
|
D028227||amyloid polyneuropathy iowa type
|
|
D028227||amyloid polyneuropathy swiss type
|
|
D028227||amyloid syndrome neuropathic
|
|
D028227||amyloid syndromes neuropathic
|
|
D028227||appalachian type familial amyloid polyneuropathy
|
|
D028227||british type amyloid polyneuropathy
|
|
D028227||familial amyloid neuropathies
|
|
D028227||familial amyloid neuropathy
|
|
D028227||familial amyloid neuropathy andrade type
|
|
D028227||familial amyloid neuropathy finnish type
|
|
D028227||familial amyloid neuropathy portuguese type
|
|
D028227||familial amyloid polyneuropathies
|
|
D028227||familial amyloid polyneuropathy
|
|
D028227||familial amyloid polyneuropathy appalachian type
|
|
D028227||familial amyloid polyneuropathy jewish type
|
|
D028227||familial amyloid polyneuropathy type i
|
|
D028227||familial amyloid polyneuropathy type ii
|
|
D028227||familial amyloid polyneuropathy type iii
|
|
D028227|105120|C537459||familial amyloid polyneuropathy type iv
|
|
D028227||familial amyloid polyneuropathy type v
|
|
D028227||familial amyloid polyneuropathy type vi
|
|
D028227||familial portuguese polyneuritic amyloidosis
|
|
D028227||finnish type familial amyloid neuropathy
|
|
D028227||hereditary neuropathic amyloidoses
|
|
D028227||hereditary neuropathic amyloidosis
|
|
D028227||iowa type amyloid polyneuropathy
|
|
D028227||jewish type familial amyloid polyneuropathy
|
|
D028227||neuropathic amyloidoses hereditary
|
|
D028227||neuropathic amyloidosis hereditary
|
|
D028227||neuropathic amyloid syndrome
|
|
D028227||neuropathic amyloid syndromes
|
|
D028227||neuropathies familial amyloid
|
|
D028227||neuropathy familial amyloid
|
|
D028227||polyneuritic amyloidoses portuguese
|
|
D028227||polyneuritic amyloidosis portuguese
|
|
D028227||polyneuropathies familial amyloid
|
|
D028227||polyneuropathy familial amyloid
|
|
D028227||portuguese polyneuritic amyloidoses
|
|
D028227||portuguese polyneuritic amyloidosis
|
|
D028227||portuguese type familial amyloid neuropathy
|
|
D028227||swiss type amyloid polyneuropathy
|
|
D028227||syndrome neuropathic amyloid
|
|
D028227||syndromes neuropathic amyloid
|
|
D028227||syndrome wohlwill andrade
|
|
D028227||syndrome wohlwill corino andrade
|
|
D028227||type i familial amyloid polyneuropathy
|
|
D028227||type ii familial amyloid polyneuropathy
|
|
D028227||type iii familial amyloid polyneuropathy
|
|
D028227||type iv familial amyloid polyneuropathy
|
|
D028227||type v familial amyloid polyneuropathy
|
|
D028227||type vi familial amyloid polyneuropathy
|
|
D028227||wohlwill andrade syndrome
|
|
D028227||wohlwill corino andrade syndrome
|
|
C538193||furukawa takagi nakao syndrome
|
|
D028226||amyloidosis familial
|
|
D028226||amyloidoses familial
|
|
D028226||amyloidoses hereditary
|
|
D028226||amyloidosis hereditaries
|
|
D028226||amyloidosis hereditary
|
|
D028226||familial amyloidoses
|
|
D028226||familial amyloidosis
|
|
D028226||hereditary amyloidoses
|
|
D028226||hereditary amyloidosis
|
|
D004283||dog diseases
|
|
D004283||canine disease
|
|
D004283||canine diseases
|
|
D004283||disease canine
|
|
D004283||disease dog
|
|
D004283||diseases canine
|
|
D004283||diseases dog
|
|
D004283||dog disease
|
|
C535915||cartilage hair hypoplasia like syndrome
|
|
C535914||mononen karnes senac syndrome
|
|
C535917||cartwright nelson fryns syndrome
|
|
C565781||lissencephaly familial with cleft palate and cerebellar hypoplasia
|
|
C535911||marfan syndrome type 2
|
|
C535911||marfan like connective tissue disorder
|
|
C535910||marden walker syndrome
|
|
C535910||blepharophimosis micrognathia immobile facies kyphoscoliosis limb contractures pigeon breast and arachnodactyly
|
|
C535910||connective tissue disorder marden walker type
|
|
C535910||generalized connective tissue syndrome
|
|
C535913||marinesco sjogren like syndrome msls
|
|
D017588||hyperandrogenism
|
|
C565742||hyaluronan metabolism defect in
|
|
C538121||hirschsprung disease type 3
|
|
C565744||mandibulofacial dysostosis syndrome bauru type
|
|
C538120||hirschsprung disease polydactyly heart disease
|
|
D017562||postcholecystectomy syndrome
|
|
D017562||post cholecystectomy syndrome
|
|
D017562||postcholecystectomy syndromes
|
|
D017562||post cholecystectomy syndromes
|
|
D017562||postcholedochoduodenostomy syndrome
|
|
D017562||post choledochoduodenostomy syndrome
|
|
D017562||postcholedochoduodenostomy syndromes
|
|
D017562||post choledochoduodenostomy syndromes
|
|
D017562||postcholedochojejunostomy syndrome
|
|
D017562||post choledochojejunostomy syndrome
|
|
D017562||postcholedochojejunostomy syndromes
|
|
D017562||post choledochojejunostomy syndromes
|
|
D017562||postcholedochostomy syndrome
|
|
D017562||post choledochostomy syndrome
|
|
D017562||postcholedochostomy syndromes
|
|
D017562||post choledochostomy syndromes
|
|
D017562||sump syndrome
|
|
D017562||sump syndromes
|
|
D017562||syndrome postcholecystectomy
|
|
D017562||syndrome post cholecystectomy
|
|
D017562||syndrome postcholedochoduodenostomy
|
|
D017562||syndrome post choledochoduodenostomy
|
|
D017562||syndrome postcholedochojejunostomy
|
|
D017562||syndrome post choledochojejunostomy
|
|
D017562||syndrome postcholedochostomy
|
|
D017562||syndrome post choledochostomy
|
|
D017562||syndromes postcholecystectomy
|
|
D017562||syndromes post cholecystectomy
|
|
D017562||syndromes postcholedochoduodenostomy
|
|
D017562||syndromes post choledochoduodenostomy
|
|
D017562||syndromes postcholedochojejunostomy
|
|
D017562||syndromes post choledochojejunostomy
|
|
D017562||syndromes postcholedochostomy
|
|
D017562||syndromes post choledochostomy
|
|
D017562||syndromes sump
|
|
D017562||syndrome sump
|
|
C538126||kuster syndrome
|
|
C564413||hernia anterior diaphragmatic
|
|
C538125||kuster majewski hammerstein syndrome
|
|
C538125||alopecia macular degeneration and growth retardation
|
|
C538125||alopecia macular degeneration growth retardation
|
|
129750|C536185||ectopia pupillae
|
|
129750|C536185||familial ectopic pupil
|
|
C538124||kuskokwim disease
|
|
C538124||arthrogryposis like disorder
|
|
C565741||retinal dystrophy early onset severe
|
|
C564411||hhhh syndrome
|
|
C564411||hereditary hemihypotrophy hemiparesis hemiathetosis syndrome
|
|
C563256|121850||corneal dystrophy fleck
|
|
C563256|121850||cfd
|
|
C563256|121850||corneal dystrophy francois neetens speckled or flecked
|
|
C563256|121850||fcd
|
|
C563256|121850||fleck corneal dystrophy
|
|
C564416||gynecomastia familial
|
|
C564415||hemophilia a with vascular abnormality
|
|
C565746||microcephaly primary autosomal recessive 3
|
|
C566589|603511||muscular dystrophy limb girdle type 1e
|
|
C566589|603511||lgmd1d formerly
|
|
C566589|603511||lgmd1e
|
|
C566589|603511||muscular dystrophy limb girdle type 1d formerly
|
|
D004244||dizziness
|
|
D004244||dizzyness
|
|
D004244||lightheadedness
|
|
D004244||light headedness
|
|
D004244||orthostasis
|
|
D011504|226300||protein losing enteropathies
|
|
D011504|226300||enteropathies exudative
|
|
D011504|226300||enteropathies protein losing
|
|
D011504|226300||enteropathy exudative
|
|
D011504|226300||enteropathy protein losing
|
|
D011504|226300||exudative enteropathies
|
|
D011504|226300||exudative enteropathy
|
|
D011504|226300||hypercatabolic hypoproteinemia idiopathic
|
|
D011504|226300||hypercatabolic hypoproteinemias idiopathic
|
|
D011504|226300||hypoproteinemia idiopathic hypercatabolic
|
|
D011504|226300||hypoproteinemias idiopathic hypercatabolic
|
|
D011504|226300||idiopathic hypercatabolic hypoproteinemia
|
|
D011504|226300||idiopathic hypercatabolic hypoproteinemias
|
|
D011504|226300||protein losing enteropathy
|
|
301050|D009394||alport syndrome x linked
|
|
301050|208050|C565942|D050030|170390||ats
|
|
301050||nephropathy and deafness x linked
|
|
D018888||aphasia primary progressive
|
|
D018888||aphasias primary progressive
|
|
D018888||mesulam apos s syndrome
|
|
D018888||mesulam syndrome
|
|
D018888||primary progressive aphasia
|
|
D018888||primary progressive aphasias
|
|
D018888||progressive aphasia primary
|
|
D018888||progressive aphasias primary
|
|
D018888||syndrome mesulam
|
|
D018888||syndrome mesulam apos s
|
|
C538119||hirschsprung disease ganglioneuroblastoma
|
|
C538119||neuroblastoma with hirschsprung disease
|
|
D018887||landau kleffner syndrome
|
|
D018887||acquired aphasia with convulsive disorder
|
|
D018887||acquired childhoood aphasia with convulsive disorder
|
|
D018887||acquired epileptic aphasia
|
|
D018887||acquired epileptic aphasias
|
|
D018887||acquired epileptiform aphasia
|
|
D018887||acquired epileptiform aphasias
|
|
D018887||aphasia acquired epileptic
|
|
D018887||aphasia acquired with convulsive disorder
|
|
D018887||aphasia epileptic acquired
|
|
D018887||epileptic aphasia acquired
|
|
D018887||epileptic aphasias acquired
|
|
D018887||epileptiform aphasia acquired
|
|
D018887||epileptiform aphasias acquired
|
|
D018887||landau kleffner acquired epileptiform aphasia
|
|
D018887||syndrome landau kleffner
|
|
C538117||human herpesvirus 6 encephalitis
|
|
231550|C536008||achalasia addisonianism alacrimia syndrome
|
|
231550|C536008||aaas
|
|
231550|C536008||aaa syndrome
|
|
231550|C536008||achalasia addisonianism alacrima syndrome
|
|
231550|C536008||achalasia addisonian syndrome
|
|
231550|C536008||achalasia alacrima syndrome
|
|
231550|C536008||achalasia alacrimia syndrome
|
|
231550|C536008||acth resistant adrenal insufficiency achalasia and alacrima
|
|
231550|C536008||acth resistant adrenal insufficiency achalasia and alacrima achalasia alacrima syndrome included
|
|
231550|C536008||addisonian achalasia syndrome
|
|
231550|C536008||alacrima achalasia addisonianism
|
|
231550|C536008||alacrima achalasia adrenal insufficiency neurologic disorder
|
|
231550|C536008||allgrove syndrome
|
|
231550|C536008||glucocorticoid deficiency and achalasia
|
|
231550|C536008||hypoadrenalism with achalasia
|
|
231550|C536008||infantile achalasia with alacrima
|
|
231550|C536008||triple a syndrome
|
|
D018883||heat stroke
|
|
D018883||heatstroke
|
|
D018883||heatstrokes
|
|
D018883||heat strokes
|
|
D018883||stroke heat
|
|
D018883||strokes heat
|
|
D018886||aphasia conduction
|
|
D018886||aphasia associative
|
|
D018886||aphasias associative
|
|
D018886||aphasias conduction
|
|
D018886||associative aphasia
|
|
D018886||associative aphasias
|
|
D018886||associative dysphasia
|
|
D018886||associative dysphasias
|
|
D018886||conduction aphasia
|
|
D018886||conduction aphasias
|
|
D018886||conduction dysphasia
|
|
D018886||conduction dysphasias
|
|
D018886||dysphasia associative
|
|
D018886||dysphasia conduction
|
|
D018886||dysphasias associative
|
|
D018886||dysphasias conduction
|
|
C538134||lactic acidosis congenital infantile
|
|
C564421||liver glycogenosis x linked type ii
|
|
C535664|605967||acropectoral syndrome
|
|
C535664|605967||acrps
|
|
C535664|605967||acrp syndrome
|
|
C535664|605967||syndactyly preaxial polydactyly and sternal deformity
|
|
C565755||growth and developmental retardation ocular ptosis cardiac defect and anal atresia
|
|
C565755||roca syndrome
|
|
C565755||roca weidemann syndrome
|
|
C538131||lachiewicz sibley syndrome
|
|
C538131||hereditary renal disease and preauricular pits
|
|
D017573||focal epithelial hyperplasia
|
|
D017573||disease heck
|
|
D017573||disease heck apos s
|
|
D017573||epithelial hyperplasia focal
|
|
D017573||epithelial hyperplasias focal
|
|
D017573||focal epithelial hyperplasia oral
|
|
D017573||focal epithelial hyperplasias
|
|
D017573||heck disease
|
|
D017573||heck apos s disease
|
|
D017573||hecks disease
|
|
D017573||hyperplasia focal epithelial
|
|
D017573||hyperplasias focal epithelial
|
|
C564425||fingerprint body myopathy
|
|
C564424||genitourinary tract anomalies
|
|
190900||tritanopia
|
|
190900||blue colorblindness
|
|
190900||cbt
|
|
190900||colorblindness tritan
|
|
190900||colorblindness tritanopic
|
|
C538135||ladda zonana ramer syndrome
|
|
C538135|C535465||arthrogryposis ectodermal dysplasia cleft lip palate and developmental delay
|
|
C538135||congenital contractures ectodermal dysplasia cleft lip palate and developmental impairment
|
|
C564422||glutamyl ribose 5 phosphate storage disease
|
|
C564422||adp ribose protein hydrolase deficiency
|
|
C564429||anemia x linked without thrombocytopenia
|
|
D005588||fox fordyce disease
|
|
D005588||apocrine miliaria
|
|
D005588||disease fox fordyce
|
|
D005588||fox fordyce syndrome
|
|
D005588||miliaria apocrine
|
|
D005588||syndrome fox fordyce
|
|
C564428||exudative vitreoretinopathy familial x linked recessive
|
|
C564428|305390||exudative vitreoretinopathy familial 2
|
|
C564428|305390||fevr x linked
|
|
C564427||faciogenital dysplasia with attention deficit hyperactivity disorder
|
|
610725|C535761|256300||nephrotic syndrome type 3
|
|
610725|C535761|256300||nephrotic syndrome early onset type 3
|
|
610725|C535761|256300||nphs3
|
|
C538130||kyrle disease
|
|
C538130||hyperkeratosis follicularis et parafollicularis in cutem penetrans
|
|
C538130||kyrle apos s disease
|
|
D005585||influenza in birds
|
|
D005585||avian flu
|
|
D005585||avian influenza
|
|
D005585||avian influenzas
|
|
D005585||flu avian
|
|
D005585||fowl plague
|
|
D005585||influenza avian
|
|
D005585||influenza in bird
|
|
D005585||influenzas avian
|
|
D005585||plague fowl
|
|
C565758||aortic aneurysm giant congenital
|
|
D005586||fowlpox
|
|
D005586||birdpox
|
|
D005586||bird pox
|
|
D005586||diphtheria fowl
|
|
D005586||diphtherias fowl
|
|
D005586||epithelioma contagiosum
|
|
D005586||fowl diphtheria
|
|
D005586||fowl diphtherias
|
|
D005586||fowl pox
|
|
D005586||pox bird
|
|
D005586||pox fowl
|
|
D005586||variola avium
|
|
608410||body mass index quantitative trait locus 7
|
|
608410||bmiq7
|
|
608410|602025|603188|612362|607514|607447|300306||obesity susceptibility to
|
|
C537201|610245||spinocerebellar ataxia 23
|
|
C537201|610245||sca23
|
|
C537841|250800||nadh cytochrome b5 reductase deficiency
|
|
C537841|250800||diaphorase deficiency
|
|
C537841|250800||methemoglobinemia congenital autosomal recessive
|
|
C537841|250800||methemoglobinemia congenital autosomal recessive methemoglobinemia type i included
|
|
C537841|250800||methemoglobinemia due to deficiency of methemoglobin reductase
|
|
C537841|250800||methemoglobinemia type i
|
|
C537841|250800||methemoglobinemia type ii
|
|
C537841|250800||methemoglobinemia type ii included
|
|
C537841|250800||nadh cytochrome b5 reductase deficiency type i
|
|
C537841|250800||nadh cytochrome b5 reductase deficiency type ii
|
|
C537841|250800||nadh cytochrome b5 reductase deficiency type ii included
|
|
C537841|250800||nadh cytochrome b5 reductase deficiency type i included
|
|
C537841|250800||nadh dependent methemoglobin reductase deficiency
|
|
C537841|250800||nadh diaphorase deficiency
|
|
C537841|250800||nadh methemoglobin reductase deficiency
|
|
250460|C563574||metaphyseal dysplasia without hypotrichosis
|
|
250460|C563574||cartilage hair hypoplasia like skeletal dysplasia without hypotrichosis or immunodeficiency
|
|
250460|C563574||cartilage hair hypoplasia variant skeletal manifestations only
|
|
250460|C563574||chhv
|
|
C567129|611705||myopathy early onset with fatal cardiomyopathy
|
|
C567129|611705||eomfc
|
|
D059409||stroke lacunar
|
|
D059409||infarction lacunar
|
|
D059409||infarctions lacunar
|
|
D059409||infarct lacunar
|
|
D059409||infarcts lacunar
|
|
D059409||lacunar infarct
|
|
D059409||lacunar infarction
|
|
D059409||lacunar infarctions
|
|
D059409||lacunar infarcts
|
|
D059409||lacunar stroke
|
|
D059409||lacunar strokes
|
|
D059409||lacunar syndrome
|
|
D059409||lacunar syndromes
|
|
D059409||strokes lacunar
|
|
D059409||syndrome lacunar
|
|
D059409||syndromes lacunar
|
|
C565309|605670||late onset retinal degeneration
|
|
C565309|605670||lord
|
|
C565309|605670||retinal degeneration late onset autosomal dominant
|
|
C538128||kyphomelic dysplasia
|
|
C538128||bowing congenital with short bones
|
|
D017563||lung diseases interstitial
|
|
D017563||diffuse parenchymal lung diseases
|
|
D017563||interstitial lung disease
|
|
D017563||interstitial lung diseases
|
|
D017563||interstitial pneumonia
|
|
D017563||interstitial pneumonias
|
|
D017563||interstitial pneumonitides
|
|
D017563||interstitial pneumonitis
|
|
D017563||lung disease interstitial
|
|
D017563||pneumonia interstitial
|
|
D017563||pneumonias interstitial
|
|
D017563||pneumonitides interstitial
|
|
D017563||pneumonitis interstitial
|
|
D017564||radiation pneumonitis
|
|
D017564||fibrosis radiation
|
|
D017564||pneumonia radiation
|
|
D017564||pneumonias radiation
|
|
D017564||pneumonitides radiation
|
|
D017564||pneumonitis radiation
|
|
D017564||radiation fibrosis
|
|
D017564||radiation pneumonia
|
|
D017564||radiation pneumonias
|
|
D017564||radiation pneumonitides
|
|
D059407||pinguecula
|
|
D059407||pingueculas
|
|
D017565||sarcoidosis pulmonary
|
|
D017565||pulmonary sarcoidoses
|
|
D017565||pulmonary sarcoidosis
|
|
D017565||sarcoidoses pulmonary
|
|
D017566||microvascular angina
|
|
D017566||angina microvascular
|
|
D017566||angina pectoris with normal coronary arteriogram
|
|
D017566||angina syndrome x
|
|
D017566||angina syndrome xs
|
|
D017566||angina x syndrome
|
|
D017566||angina x syndromes
|
|
D017566||cardiac syndrome x
|
|
D017566||syndrome angina x
|
|
D017566||syndrome x angina
|
|
D017566||syndrome x cardiac
|
|
D017566||syndrome xs angina
|
|
D017566||x syndrome angina
|
|
C538145||sutton disease 2
|
|
C538145||aphthous stomatitis recurrent
|
|
C538145||aphthous ulcer recurrent
|
|
C538145||major aphthous ulcer
|
|
C538145||major canker sore
|
|
C538145||recurrent scarring aphthae
|
|
C538144||supraumbilical midabdominal raphe and facial cavernous hemangiomas
|
|
C538144||hemangiomas cavernous of face and supraumbilical midline raphe
|
|
C538144||hemangiomas cavernous of face supraumbilical midline raphe
|
|
C538144||raphe supraumbilical midline with cavernous facial hemangiomas
|
|
C538144||sternal nonunion with supraumbilical raphe
|
|
C565722||encephalopathy spastic tetraparesis and hypogonadism
|
|
C538142||summitt syndrome
|
|
C538142||recessive acrocephalosyndactyly with normal intelligence
|
|
C538142||summitt apos s acrocephalosyndactyly
|
|
C538148||symphalangism distal with microdontia dental pulp stones and narrowed zygomatic arch
|
|
C538148||distal symphalangism hypoplastic carpal bones microdontia dental pulp stones and narrowing of the zygomatic arch
|
|
C566418|603010||deafness autosomal recessive 17
|
|
C566418|603010||dfnb17
|
|
C538147||symmastia
|
|
C538147||medial confluence of the breasts
|
|
612463|D011556||pseudopseudohypoparathyroidism
|
|
612463|D011556||albright hereditary osteodystrophy without multiple hormone resistance
|
|
612463|D011556||pphp
|
|
612463|D011556||pseudopseudo hypoparathyroidism
|
|
612463|D011556||pseudo pseudohypoparathyroidism
|
|
612463|D011556||pseudopseudohypoparathyroidisms
|
|
612463|D011556||pseudopseudo hypoparathyroidisms
|
|
612463|D011556||pseudo pseudohypoparathyroidisms
|
|
C565728||alzheimer disease familial early onset with coexisting amyloid and prion pathology
|
|
C565729||clavicular hypoplasia zygomatic arch hypoplasia and micrognathia
|
|
250790|C567102||methemoglobinemia type iv
|
|
250790|C567102||methemoglobinemia due to deficiency of cytochrome b5
|
|
D059411||lower urinary tract symptoms
|
|
D059413||intraabdominal infections
|
|
D059413||infection intraabdominal
|
|
D059413||infection intra abdominal
|
|
D059413||infections intraabdominal
|
|
D059413||infections intra abdominal
|
|
D059413||intraabdominal infection
|
|
D059413||intra abdominal infection
|
|
D059413||intra abdominal infections
|
|
C567456|611928||prostate cancer hereditary 13
|
|
C567456|611928||hpc13
|
|
194470||zinc elevated plasma
|
|
194470||albumin binding of zinc elevated
|
|
194470||hyperzincemia familial dysalbuminemic hyperzincemia and hypercalprotectinemia included
|
|
D031845||hajdu cheney syndrome
|
|
D031845||acroosteolysis with osteoporosis and changes in skull and mandible
|
|
D031845||arthrodentoosteodysplasia
|
|
D031845||arthrodentoosteodysplasias
|
|
D031845||cheney syndrome
|
|
D031845||multicentric osteolyses
|
|
D031845||multicentric osteolysis
|
|
D031845||osteolyses multicentric
|
|
D031845||osteolysis multicentric
|
|
C566605|613705||orofacial cleft 10
|
|
C566605|613705||cleft lip with or without cleft palate nonsyndromic 10
|
|
C566605|613705||ofc10
|
|
C566612|601868||deafness autosomal dominant 13
|
|
C566612|601868||dfna13
|
|
C538156||synostoses tarsal carpal and digital
|
|
C538156||calcaneonavicular coalition
|
|
C565731||craniofacial anomalies empty sella turcica corneal endothelial changes and abnormal retinal and auditory bipolar cells
|
|
D018880||atrial premature complexes
|
|
D018880||atrial beat premature
|
|
D018880||atrial beats premature
|
|
D018880||atrial complex premature
|
|
D018880||atrial complices premature
|
|
D018880||atrial contraction premature
|
|
D018880||atrial contractions premature
|
|
D018880||atrial ectopic beat
|
|
D018880||atrial ectopic beats
|
|
D018880||atrial extrasystole
|
|
D018880||atrial extrasystoles
|
|
D018880||atrial premature complex
|
|
D018880||atrial premature complices
|
|
D018880||ectopic beat atrial
|
|
D018880||ectopic beats atrial
|
|
D018880||extrasystole atrial
|
|
D018880||extrasystoles atrial
|
|
D018880||premature atrial beat
|
|
D018880||premature atrial beats
|
|
D018880||premature atrial complex
|
|
D018880||premature atrial complices
|
|
D018880||premature atrial contraction
|
|
D018880||premature atrial contractions
|
|
D018880||premature complex atrial
|
|
D018880||premature complexes atrial
|
|
D018880||premature complices atrial
|
|
D018880||premature supraventricular beat
|
|
D018880||premature supraventricular beats
|
|
D018880||supraventricular beat premature
|
|
D018880||supraventricular beats premature
|
|
D000742|105600||anemia dyserythropoietic congenital
|
|
D000742|105600||anemia congenital dyserythropoietic
|
|
D000742|105600||anemia congenital dyserythropoietic type i
|
|
D000742|105600||anemia congenital dyserythropoietic type ia
|
|
D000742|105600||anemia congenital dyserythropoietic type ii
|
|
D000742|105600||anemia congenital dyserythropoietic type iii
|
|
D000742|105600||anemia congenital dyserythropoietic type iv
|
|
D000742|105600||anemia dyserythropoietic congenital type 1
|
|
D000742|105600||anemia dyserythropoietic congenital type 2
|
|
D000742|105600||anemia dyserythropoietic congenital type i
|
|
D000742|105600||anemia dyserythropoietic congenital type ii
|
|
D000742|105600||anemia dyserythropoietic congenital type iii
|
|
D000742|105600||anemias congenital dyserythropoietic
|
|
D000742|105600||anemia with multinucleated erythroblasts
|
|
D000742|105600||cda ia
|
|
D000742|105600||cda ii
|
|
D000742|105600||cda iii
|
|
D000742|105600||cdan1a
|
|
D000742|105600||cdan2
|
|
D000742|105600||cdan3
|
|
D000742|105600||cdan4
|
|
D000742|105600||cda type iv
|
|
D000742|105600||congenital dyserythropoietic anemia
|
|
D000742|105600||congenital dyserythropoietic anemias
|
|
D000742|105600||congenital dyserythropoietic anemia type 1
|
|
D000742|105600||congenital dyserythropoietic anemia type i
|
|
D000742|105600||congenital dyserythropoietic anemia type ii
|
|
D000742|105600||congenital dyserythropoietic anemia type iii
|
|
D000742|105600||dyserythropoietic anemia congenital
|
|
D000742|105600||dyserythropoietic anemia congenital type 1
|
|
D000742|105600||dyserythropoietic anemia congenital type 2
|
|
D000742|105600||dyserythropoietic anemia congenital type i
|
|
D000742|105600||dyserythropoietic anemia congenital type ia
|
|
D000742|105600||dyserythropoietic anemia congenital type ii
|
|
D000742|105600||dyserythropoietic anemia congenital type iii
|
|
D000742|105600||dyserythropoietic anemia hempas type
|
|
D000742|105600||dyserythropoietic anemias congenital
|
|
D000742|105600|C566285||erythroreticulosis hereditary benign
|
|
D000742|105600||hempas
|
|
D000742|105600||hempas anemia
|
|
D000742|105600||hempas anemias
|
|
D000742|105600||hereditary erythroblastic multinuclearity with positive acidified serum test
|
|
D000742|105600||hereditary erythroblast multinuclearity with positive acidified serum
|
|
D000742|105600||type i congenital dyserythropoietic anemia
|
|
D018882||heat stress disorders
|
|
D018882||cramp heat
|
|
D018882||cramps heat
|
|
D018882||disorder heat stress
|
|
D018882||disorders heat stress
|
|
D018882||heat cramp
|
|
D018882||heat cramps
|
|
D018882||heat stress disorder
|
|
D018882||heat stress syndrome
|
|
D018882||heat stress syndromes
|
|
D018882||stress disorder heat
|
|
D018882||stress disorders heat
|
|
D018882||stress syndrome heat
|
|
D018882||stress syndromes heat
|
|
D018882||syndrome heat stress
|
|
D018882||syndromes heat stress
|
|
C538153||syndactyly type 2
|
|
C538153||synpolydactyly
|
|
C565734||cortical defects wormian bones and dentinogenesis imperfecta
|
|
D046110||hypertension pregnancy induced
|
|
D046110||gestational hypertension
|
|
D046110||hypertension gestational
|
|
D046110||hypertension pregnancy transient
|
|
D046110||hypertensions pregnancy induced
|
|
D046110||induced hypertension pregnancy
|
|
D046110||induced hypertensions pregnancy
|
|
D046110||pregnancy induced hypertension
|
|
D046110||pregnancy transient hypertension
|
|
D046110||transient hypertension pregnancy
|
|
C564403||coenzyme q10 deficiency
|
|
C564403||coenzyme q deficiency
|
|
C564403||coq10 deficiency primary
|
|
C564403||coq deficiency
|
|
C564403||ubiquinone deficiency
|
|
D004239||diverticulitis colonic
|
|
D004239||colonic diverticulitis
|
|
C538158||mcdonough syndrome
|
|
C538158||mental retardation peculiar facies kyphoscoliosis diastasis recti cryptorchidism and congenital heart defect
|
|
C567403|612165||retinitis pigmentosa 29
|
|
C567403|612165||rp29
|
|
C565730||diabetes mellitus congenital autoimmune
|
|
C565739||asthma and nasal polyps
|
|
C564407||hydrocephalus with cerebellar agenesis
|
|
C564406||hypogonadism male with mental retardation and skeletal anomalies
|
|
D004238||diverticulitis
|
|
D004238||diverticulitides
|
|
C564405||hypouricemia familial renal due to tubular hypersecretion
|
|
190351|C566033||trichorhinophalangeal syndrome type iii
|
|
190351|C566033||sugio kajii syndrome
|
|
190351|C566033||trps3
|
|
C538152||filippi syndrome
|
|
C538152||syndactyly type i with microcephaly and mental retardation
|
|
C565735||becker nevus syndrome
|
|
C565736||hydronephrosis congenital with cleft palate characteristic facies hypotonia and mental retardation
|
|
C565736||okamoto syndrome
|
|
C536159|308800||keratosis follicularis spinulosa decalvans x linked
|
|
C536159|308800||keratosis follicularis spinulosa decalvans
|
|
C536159|308800||keratosis follicularis spinulosa decalvans cum ophiasi
|
|
C536159|308800||kfsdx
|
|
C566284|105800||aneurysm intracranial berry 1
|
|
C566284|105800||aneurysmal subarachnoid hemorrhage familial
|
|
C566284|105800||anib1
|
|
C564409||holoprosencephaly with fetal akinesia hypokinesia sequence
|
|
C565738||bardet biedl syndrome 6
|
|
C564408||hydrocephalus x linked with congenital idiopathic intestinal pseudoobstruction
|
|
256810||mitochondrial dna depletion syndrome 6 hepatocerebral type
|
|
256810|C538344||mtdps6
|
|
256810|C538344||navajo neurohepatopathy
|
|
256810||navajo neuropathy nn navajo familial neurogenic arthropathy included
|
|
256810||nnh
|
|
D004241||diverticulum colon
|
|
D004241||colon diverticula
|
|
D004241||colon diverticulum
|
|
D004241||colonic diverticula
|
|
D004241||colonic diverticulum
|
|
D004241||diverticula colon
|
|
D004241||diverticula colonic
|
|
D004241||diverticulum colonic
|
|
D004240||diverticulum
|
|
D004240||diverticula
|
|
D004240||diverticulosis
|
|
115650||cataract 32 multiple types
|
|
115650||cap
|
|
115650|C538282||cataract anterior polar
|
|
115650|C538282||cataract anterior polar 1
|
|
115650|C535340||cataract posterior polar 5
|
|
115650||ctaa1
|
|
115650||ctpp5
|
|
115650||ctrct32
|
|
D017545||aortic aneurysm thoracic
|
|
D017545||aneurysms thoracoabdominal aortic
|
|
D017545||aneurysm thoracic aortic
|
|
D017545||aneurysm thoracoabdominal aortic
|
|
D017545||aortic aneurysms thoracic
|
|
D017545||aortic aneurysms thoracoabdominal
|
|
D017545||aortic aneurysm thoracoabdominal
|
|
D017545||thoracic aortic aneurysm
|
|
D017545||thoracic aortic aneurysms
|
|
D017545||thoracoabdominal aortic aneurysm
|
|
D017545||thoracoabdominal aortic aneurysms
|
|
D018877||sick building syndrome
|
|
D018877||syndrome sick building
|
|
C535739|212065||congenital disorder of glycosylation type 1a
|
|
C535739|212065||carbohydrate deficient glycoprotein syndrome type 1a
|
|
C535739|212065||carbohydrate deficient glycoprotein syndrome type ia
|
|
C535739|212065||carbohydrate deficient glycoprotein syndrome type ia formerly
|
|
C535739|212065||cdg1a
|
|
C535739|212065||cdgia
|
|
C535739|212065||cdg ia
|
|
C535739|212065||congenital disorder of glycosylation type ia
|
|
C535739|212065||jaeken syndrome
|
|
C535739|212065||phosphomannomutase 2 deficiency
|
|
D018876||environmental illness
|
|
D018876||environmental hypersensitivities
|
|
D018876||environmental hypersensitivity
|
|
D018876||environmental illnesses
|
|
D018876||hypersensitivities environmental
|
|
D018876||hypersensitivity environmental
|
|
D018876||illness environmental
|
|
D018876||illnesses environmental
|
|
D018879||ventricular premature complexes
|
|
D018879||ectopic beats ventricular
|
|
D018879||ectopic beat ventricular
|
|
D018879||extrasystole ventricular
|
|
D018879||premature ventricular beat
|
|
D018879||premature ventricular beats
|
|
D018879||premature ventricular complex
|
|
D018879||premature ventricular contraction
|
|
D018879||premature ventricular contractions
|
|
D018879||ventricular beat premature
|
|
D018879||ventricular beats premature
|
|
D018879||ventricular complex premature
|
|
D018879||ventricular contraction premature
|
|
D018879||ventricular contractions premature
|
|
D018879||ventricular ectopic beat
|
|
D018879||ventricular ectopic beats
|
|
D018879||ventricular extrasystole
|
|
D018879||ventricular extrasystoles
|
|
D018879||ventricular premature complex
|
|
D017541||aneurysm false
|
|
D017541||aneurysms false
|
|
D017541||false aneurysm
|
|
D017541||false aneurysms
|
|
D017541||pseudoaneurysm
|
|
D017541||pseudoaneurysms
|
|
D017542||aneurysm ruptured
|
|
D017542||aneurysms ruptured
|
|
D017542||ruptured aneurysm
|
|
D017542||ruptured aneurysms
|
|
D017543||iliac aneurysm
|
|
D017543||aneurysm iliac
|
|
D017543||aneurysms iliac
|
|
D017543||iliac aneurysms
|
|
D017544||aortic aneurysm abdominal
|
|
D017544|100070||abdominal aortic aneurysm
|
|
D017544||abdominal aortic aneurysms
|
|
D017544|100070||aneurysm abdominal aortic
|
|
D017544||aneurysms abdominal aortic
|
|
D017544||aortic aneurysms abdominal
|
|
C536457|124500||vohwinkel syndrome
|
|
C536457|124500||congenital deafness with keratopachydermia and constrictions of fingers and toes
|
|
C536457|124500||deafness congenital with keratopachydermia and constrictions of fingers and toes
|
|
C536457|124500||keratoderma hereditarium mutilans
|
|
C536457|124500||khm
|
|
C536457|124500||mutilating keratoderma
|
|
C536457|124500||palmoplantar keratoderma mutilans
|
|
C536457|124500||palmoplantar keratoderma mutilans vohwinkel
|
|
C536457|124500||ppk mutilans vohwinkel
|
|
C535380|301830||arthrogryposis multiplex congenita distal x linked
|
|
C535380|301830||amc distal x linked
|
|
C535380|301830||amcx1
|
|
C535380|301830||arthrogryposis x linked type i
|
|
C535380|301830||smax2
|
|
C535380|301830||spinal muscular atrophy infantile x linked
|
|
C535380|301830||spinal muscular atrophy x linked 2
|
|
C535380|301830||spinal muscular atrophy x linked lethal infantile
|
|
C535380|301830||xlsma
|
|
D006869||hydronephrosis
|
|
D006869||hydronephroses
|
|
D005534||foot diseases
|
|
D005534||disease foot
|
|
D005534||diseases foot
|
|
D005534||foot disease
|
|
D005533||foot dermatoses
|
|
D005533||dermatoses foot
|
|
D005533||dermatosis foot
|
|
D005533||foot dermatosis
|
|
D005536||foot and mouth disease
|
|
D005536||disease foot and mouth
|
|
D005536||diseases foot and mouth
|
|
D005536||foot and mouth diseases
|
|
D004204||dislocations
|
|
D004204||dislocation
|
|
217300|C565677||cornea plana 2
|
|
217300|C565677||cna2
|
|
D005535||foot rot
|
|
D005535||foot rots
|
|
D005535||rot foot
|
|
D005535||rots foot
|
|
D005530||foot deformities
|
|
D005530||cavus deformities
|
|
D005530||cavus deformity
|
|
D005530||deformities cavus
|
|
D005530||deformities foot
|
|
D005530||deformities metatarsal
|
|
D005530||deformity cavus
|
|
D005530||deformity foot
|
|
D005530||deformity metatarsal
|
|
D005530||foot deformity
|
|
D005530||metatarsal deformities
|
|
D005530||metatarsal deformity
|
|
D005530||pes cavus
|
|
D005530||talipes cavus
|
|
D060426||anti n methyl d aspartate receptor encephalitis
|
|
D060426||anti nmda receptor encephalitides
|
|
D060426||anti nmda receptor encephalitis
|
|
D060426||anti nmdar encephalitides
|
|
D060426||anti nmdar encephalitides non paraneoplastic
|
|
D060426||anti nmdar encephalitides paraneoplastic
|
|
D060426||anti nmdar encephalitis
|
|
D060426||anti nmdar encephalitis non paraneoplastic
|
|
D060426||anti nmdar encephalitis paraneoplastic
|
|
D060426||anti n methyl d aspartate receptor encephalitides
|
|
D060426||encephalitides anti nmdar
|
|
D060426||encephalitides anti nmda receptor
|
|
D060426||encephalitides anti n methyl d aspartate receptor
|
|
D060426||encephalitides non paraneoplastic anti nmdar
|
|
D060426||encephalitides paraneoplastic anti nmdar
|
|
D060426||encephalitis anti nmdar
|
|
D060426||encephalitis anti nmda receptor
|
|
D060426||encephalitis anti n methyl d aspartate receptor
|
|
D060426||encephalitis non paraneoplastic anti nmdar
|
|
D060426||encephalitis paraneoplastic anti nmdar
|
|
D060426||non paraneoplastic anti nmda receptor encephalitis
|
|
D060426||non paraneoplastic anti nmdar encephalitides
|
|
D060426||non paraneoplastic anti nmdar encephalitis
|
|
D060426||non paraneoplastic anti n methyl d aspartate receptor encephalitis
|
|
D060426||paraneoplastic anti nmda receptor encephalitis
|
|
D060426||paraneoplastic anti nmdar encephalitides
|
|
D060426||paraneoplastic anti nmdar encephalitis
|
|
D060426||paraneoplastic anti n methyl d aspartate receptor encephalitis
|
|
D060426||receptor encephalitides anti nmda
|
|
D060426||receptor encephalitis anti nmda
|
|
D005532||foot deformities congenital
|
|
D005532||congenital foot deformities
|
|
D005532||congenital foot deformity
|
|
D005532||deformities congenital foot
|
|
D005532||deformity congenital foot
|
|
D005532||foot deformity congenital
|
|
D060425||cerebral phaeohyphomycosis
|
|
D060425||central nervous system phaeohyphomycosis
|
|
D060425||central nervous system phaeohyphomycosis primary
|
|
D060425||cerebral phaeohyphomycoses
|
|
D060425||phaeohyphomycoses cerebral
|
|
D060425||phaeohyphomycosis central nervous system
|
|
D060425||phaeohyphomycosis central nervous system primary
|
|
D060425||phaeohyphomycosis cerebral
|
|
D060425||primary central nervous system phaeohyphomycosis
|
|
D004200||diseases in twins
|
|
D004200||diseases in twin
|
|
D004200||in twin diseases
|
|
D004200||in twins diseases
|
|
D004200||twin diseases in
|
|
D004200||twins diseases in
|
|
D005531||foot deformities acquired
|
|
D005531||acquired foot deformities
|
|
D005531||acquired foot deformity
|
|
D005531||deformities acquired foot
|
|
D005531||deformity acquired foot
|
|
D005531||foot deformity acquired
|
|
D029502|D029503|105650||anemia hypoplastic congenital
|
|
D029502||anemia congenital hypoplastic
|
|
D029502||anemias congenital hypoplastic
|
|
D029502||congenital hypoplastic anemia
|
|
D029502||congenital hypoplastic anemias
|
|
D029502||hypoplastic anemia congenital
|
|
D029502||hypoplastic anemias congenital
|
|
C563538|613426||cardiomyopathy dilated 1s
|
|
C563538|613426||cmd1s
|
|
C563538|613426||left ventricular noncompaction 5 included
|
|
C563538|613426||lvnc5 included
|
|
D017512||lichenoid eruptions
|
|
D017512||eruption licheniform
|
|
D017512||eruption lichenoid
|
|
D017512||eruptions licheniform
|
|
D017512||eruptions lichenoid
|
|
D017512||licheniform eruption
|
|
D017512||licheniform eruptions
|
|
D017512||lichenoid eruption
|
|
D017513||lichen nitidus
|
|
D017514||pityriasis lichenoides
|
|
D017514||acute pityriasis lichenoides
|
|
D017514||chronic pityriasis lichenoides
|
|
D017514||disease habermann
|
|
D017514||disease habermann apos s
|
|
D017514||disease mucha habermann
|
|
D017514||habermann disease
|
|
D017514||habermann apos s disease
|
|
D017514||habermanns disease
|
|
D017514||mucha habermann disease
|
|
D017514||pityriasis lichenoides acute
|
|
D017514||pityriasis lichenoides chronic
|
|
D017514||pityriasis lichenoides chronica
|
|
D017514||pityriasis lichenoides et varioliformis acuta
|
|
172700|D020774||pick disease of the brain
|
|
172700|D020774||atrophies lobar brain
|
|
172700|D020774||atrophy lobar brain
|
|
172700|D020774||brain atrophy circumscribed lobar
|
|
172700|D020774||circumscribed lobar atrophy of the brain
|
|
172700|D020774||dementia with lobar atrophy and neuronal cytoplasmic inclusions
|
|
172700|D020774||disease pick
|
|
172700|D020774||disease pick apos s
|
|
172700|D020774||lobar atrophies brain
|
|
172700|D020774||lobar atrophy brain
|
|
172700|D020774||lobar atrophy of brain
|
|
172700|D020774||lobar atrophy of the brain
|
|
172700|D020774||pick disease
|
|
172700|D020774||pick disease of brain
|
|
172700|D020774||pick apos s disease
|
|
172700|D020774||picks disease
|
|
172700|D020774||picks disease of brain
|
|
D017515||pityriasis rosea
|
|
153600|D008258||waldenstrom macroglobulinemia
|
|
153600|D008258||familial waldenstrom macroglobulinaemia
|
|
153600|D008258||familial waldenstrom apos s macroglobulinaemia
|
|
153600|D008258||familial waldenstroms macroglobulinaemia
|
|
153600|D008258||lymphoma lymphocytic plasmacytoid
|
|
153600|D008258||lymphoma lymphoplasmacytoid
|
|
153600|D008258||lymphomas lymphoplasmacytoid
|
|
153600|D008258||lymphoplasmacytoid lymphoma
|
|
153600|D008258||lymphoplasmacytoid lymphomas
|
|
153600|D008258||macroglobulinaemia familial waldenstrom apos s
|
|
153600|D008258||macroglobulinaemia waldenstrom apos s
|
|
153600|D008258||macroglobulinemia
|
|
153600|D008258||macroglobulinemia primary
|
|
153600|D008258||macroglobulinemia waldenstrom
|
|
153600|D008258||macroglobulinemia waldenstrom apos s
|
|
153600|D008258||macroglobulinemia waldenstrom somatic included
|
|
153600|D008258||macroglobulinemia waldenstrom susceptibility to 1
|
|
153600|D008258||macroglobulinemia waldenstrom susceptibility to 2
|
|
153600|D008258||primary macroglobulinemia
|
|
153600|D008258||waldenstrom macroglobulinaemia
|
|
153600|D008258||waldenstrom apos s macroglobulinaemia
|
|
153600|D008258||waldenstroms macroglobulinaemia
|
|
153600|D008258||waldenstrom apos s macroglobulinaemia familial
|
|
153600|D008258||waldenstrom apos s macroglobulinemia
|
|
153600|D008258||waldenstroms macroglobulinemia
|
|
153600|D008258||wm1
|
|
153600|D008258||wm2
|
|
C536174|604809||diffuse panbronchiolitis
|
|
C536174|604809||dpb
|
|
C536174|604809||panbronchiolitis diffuse
|
|
C536174|604809||pblt
|
|
C563975|600209||exostoses multiple type iii
|
|
C563975|600209||ext3
|
|
D017511||pyoderma gangrenosum
|
|
251260|D049932||nijmegen breakage syndrome
|
|
251260|D049932||ataxia telangiectasia variant 1
|
|
251260|D049932||ataxia telangiectasia variant 1s
|
|
251260|D049932||ataxia telangiectasia variant v1
|
|
251260|D049932||ataxia telangiectasia variant v1s
|
|
251260|D049932||ataxia telangiectasia variant v2 included
|
|
251260|D049932||at v1
|
|
251260|D049932||at v2 included
|
|
251260|D049932||bbs included
|
|
251260|D049932||berlin breakage syndrome
|
|
251260|D049932||breakage syndrome berlin
|
|
251260|D049932||breakage syndrome nijmegen
|
|
251260|D049932||immunodeficiency microcephaly and chromosomal instability
|
|
251260|D049932||immunodeficiency microcephaly and chromosomal instability berlin breakage syndrome included
|
|
251260|D049932||microcephaly with normal intelligence immunodeficiency and lymphoreticular malignancies
|
|
251260|D049932||nbs
|
|
251260|D049932||nonsyndromal microcephaly autosomal recessive with normal intelligence
|
|
251260|D049932||seemanova syndrome 2
|
|
251260|D049932||seemanova syndrome ii
|
|
251260|D049932||syndrome berlin breakage
|
|
251260|D049932||syndrome nijmegen breakage
|
|
251260|D049932||variant 1s ataxia telangiectasia
|
|
251260|D049932||variant v1 ataxia telangiectasia
|
|
251260|D049932||variant v1s ataxia telangiectasia
|
|
D013274|137215||stomach neoplasms
|
|
D013274|137215||cancer gastric
|
|
D013274|137215||cancer of stomach
|
|
D013274|137215||cancer of the stomach
|
|
D013274|137215||cancers gastric
|
|
D013274|137215||cancers stomach
|
|
D013274|137215||cancer stomach
|
|
D013274|137215||gastric cancer
|
|
D013274|137215||gastric cancer familial diffuse
|
|
D013274|137215||gastric cancer familial diffuse and cleft lip with or without cleft palate included
|
|
D013274|137215||gastric cancer familial diffuse breast cancer lobular included
|
|
D013274|137215||gastric cancer hereditary diffuse
|
|
D013274|137215||gastric cancer intestinal included
|
|
D013274|137215||gastric cancers
|
|
D013274|137215||gastric neoplasm
|
|
D013274|137215||gastric neoplasms
|
|
D013274|137215||hdgc
|
|
D013274|137215||lbc included
|
|
D013274|137215||neoplasm gastric
|
|
D013274|137215||neoplasms gastric
|
|
D013274|137215||neoplasms stomach
|
|
D013274|137215||neoplasm stomach
|
|
D013274|137215||stomach cancer
|
|
D013274|137215||stomach cancers
|
|
D013274|137215||stomach neoplasm
|
|
D018860||sneddon syndrome
|
|
D018860||livedo reticularis and cerebrovascular accidents
|
|
D018860||livedo reticularis systemic involvement
|
|
D018860||sneddon champion syndrome
|
|
D018860||syndrome sneddon
|
|
D018860||syndrome sneddon champion
|
|
D005549||foreign body reaction
|
|
D005549||reaction foreign body
|
|
D005548||foreign body migration
|
|
D005548||foreign body migrations
|
|
D005548||migration foreign body
|
|
D005548||migrations foreign body
|
|
C537627|245010||keratosis palmoplantaris with periodontopathia and onychogryposis
|
|
C537627|245010||cochin jewish disorder
|
|
C537627|245010||haim munk syndrome
|
|
C537627|245010||hms
|
|
D004213||dissociative disorders
|
|
D004213||disorder dissociative
|
|
D004213||disorders dissociative
|
|
D004213||dissociation
|
|
D004213||dissociative disorder
|
|
D004213||dissociative hysteria
|
|
D004213||dissociative reaction
|
|
D004213||dissociative reactions
|
|
D004213||fugue
|
|
D004213||hysteria dissociative
|
|
D004213||hysterias dissociative
|
|
D004213||reaction dissociative
|
|
D004213||reactions dissociative
|
|
D004216||distemper
|
|
D004216||canine distemper
|
|
D004216||canine distempers
|
|
D004216||distemper canine
|
|
D004216||distempers
|
|
D004216||distempers canine
|
|
D005547||foreign bodies
|
|
D005547||bodies foreign
|
|
D005547||body foreign
|
|
D005547||foreign body
|
|
313000||spatial visualization aptitude for
|
|
313000||visuospatial perceptual abilities vspa turner syndrome associated neurocognitive phenotype included
|
|
D006876||hydrothorax
|
|
D060437||artificial lens implant migration
|
|
D060437||artificial intra ocular implant dislocation
|
|
D060437||artificial lens implant dislocation
|
|
607731|C535415||charcot marie tooth disease type 2h
|
|
607731|C535415||charcot marie tooth disease axonal type 2h
|
|
607731|C535415||charcot marie tooth disease axonal with pyramidal features autosomal recessive
|
|
607731|C535415||charcot marie tooth neuropathy axonal with pyramidal features autosomal recessive
|
|
607731|C535415||cmt2h
|
|
D005543||forearm injuries
|
|
D005543||forearm injury
|
|
D005543||injuries forearm
|
|
D005543||injury forearm
|
|
D006871||hydrophthalmos
|
|
D006871||buphthalmos
|
|
D004211||disseminated intravascular coagulation
|
|
D004211||coagulation disseminated intravascular
|
|
D004211||coagulation intravascular disseminated
|
|
D004211||coagulations disseminated intravascular
|
|
D004211||coagulations intravascular disseminated
|
|
D004211||coagulopathies consumption
|
|
D004211||coagulopathy consumption
|
|
D004211||consumption coagulopathies
|
|
D004211||consumption coagulopathy
|
|
D004211||disseminated coagulation intravascular
|
|
D004211||disseminated coagulations intravascular
|
|
D004211||disseminated intravascular coagulations
|
|
D004211||intravascular coagulation disseminated
|
|
D004211||intravascular coagulations disseminated
|
|
D004211||intravascular disseminated coagulation
|
|
D004211||intravascular disseminated coagulations
|
|
D006872||hydropneumothorax
|
|
D059445||anhedonia
|
|
D059445||anhedonia physical
|
|
D059445||anhedonias
|
|
D059445||anhedonia social
|
|
D059445||anhedonias physical
|
|
D059445||anhedonias social
|
|
D059445||physical anhedonia
|
|
D059445||physical anhedonias
|
|
D059445||social anhedonia
|
|
D059445||social anhedonias
|
|
144120|C564173||hyperimmunoglobulin g1 a1 syndrome
|
|
144120|C564173||ighr
|
|
144120|C564173||immunoglobulin heavy chain regulator included
|
|
D018856||cystitis interstitial
|
|
D018856||chronic interstitial cystitides
|
|
D018856||chronic interstitial cystitis
|
|
D018856||cystitides chronic interstitial
|
|
D018856||cystitides interstitial
|
|
D018856||cystitis chronic interstitial
|
|
D018856||interstitial cystitides
|
|
D018856||interstitial cystitides chronic
|
|
D018856||interstitial cystitis
|
|
D018856||interstitial cystitis chronic
|
|
D018856||painful bladder syndrome
|
|
D017520||mucinoses
|
|
D017520||mucinosis
|
|
C538100||pagon stephan syndrome
|
|
C538100||septo optic dysplasia with digital anomalies
|
|
C538105||pallister killian syndrome
|
|
C538105||hexasomy 12p mosaic
|
|
C538105||isochromosome 12p syndrome
|
|
C538105||pallister killian mosaic syndrome
|
|
C538105||teschler nicola killian syndrome
|
|
C538105||tetrasomy 12p mosaic
|
|
D006848||testicular hydrocele
|
|
D006848||hydrocele scrotal
|
|
D006848||hydroceles scrotal
|
|
D006848||hydroceles testicular
|
|
D006848||hydroceles vaginal
|
|
D006848||hydrocele testicular
|
|
D006848||hydrocele vaginal
|
|
D006848||scrotal hydrocele
|
|
D006848||scrotal hydroceles
|
|
D006848||testicular hydroceles
|
|
D006848||vaginal hydrocele
|
|
D006848||vaginal hydroceles
|
|
C538103||palindromic rheumatism
|
|
C538103||palindromic rheumatism syndrome
|
|
C538102||palant cleft palate syndrome
|
|
C538102||unusual facies cleft palate mental retardation and limb abnormalities
|
|
D005517||foodborne diseases
|
|
D005517||disease foodborne
|
|
D005517||disease food borne
|
|
D005517||diseases foodborne
|
|
D005517||diseases food borne
|
|
D005517||food borne disease
|
|
D005517||foodborne disease
|
|
D005517||food borne diseases
|
|
D005517||food borne illnesses
|
|
D005517||foodborne illnesses
|
|
D005517||food poisoning
|
|
D005517||food poisonings
|
|
D005517||illnesses foodborne
|
|
D005517||illnesses food borne
|
|
D005517||poisoning food
|
|
D005517||poisonings food
|
|
D005512||food hypersensitivity
|
|
D005512||allergies food
|
|
D005512||allergy food
|
|
D005512||food allergies
|
|
D005512||food allergy
|
|
D005512||food hypersensitivities
|
|
D005512||hypersensitivities food
|
|
D005512||hypersensitivity food
|
|
600740|C537147||familial benign hypercalcemia type 3
|
|
600740|C537147||familial benign hypercalcemia oklahoma variant
|
|
600740|C537147||familial benign hypercalcemia type iii
|
|
600740|C537147||fbh3
|
|
600740|C537147||hhc3
|
|
600740|C537147||hypercalcemia familial benign oklahoma type
|
|
600740|C537147||hypercalcemia familial benign type 3
|
|
600740|C537147||hypercalcemia familial benign type iii
|
|
600740|C537147||hypocalciuric hypercalcemia familial type 3
|
|
600740|C537147||hypocalciuric hypercalcemia familial type iii
|
|
C566446|610093||microphthalmia isolated 2
|
|
C566446|610093||mcop2
|
|
D034081||wasting disease chronic
|
|
D034081||chronic wasting disease
|
|
D060446||phaeohyphomycosis
|
|
D060446||cutaneous phaeohyphomycoses
|
|
D060446||cutaneous phaeohyphomycosis
|
|
D060446||phaeohyphomycoses
|
|
D060446||phaeohyphomycoses cutaneous
|
|
D060446||phaeohyphomycoses subcutaneous
|
|
D060446||phaeohyphomycosis cutaneous
|
|
D060446||phaeohyphomycosis subcutaneous
|
|
D060446||subcutaneous phaeohyphomycoses
|
|
D060446||subcutaneous phaeohyphomycosis
|
|
C537686|601349||microcephaly microphthalmia ectrodactyly of lower limbs and prognathism
|
|
C537686|601349||mcops8
|
|
C537686|601349||microphthalmia syndromic 8
|
|
C537686|601349||mmep
|
|
C537111|211530||brown vialetto van laere syndrome
|
|
C537111|211530||brown vialetto van laere syndrome 1
|
|
C537111|211530||bulbar palsy progressive with sensorineural deafness
|
|
C537111|211530||bvvls1
|
|
C537111|211530||pontobulbar palsy and neurosensory deafness
|
|
C537111|211530||pontobulbar palsy with deafness
|
|
C537111|211530||progressive bulbar palsy with sensorineural deafness
|
|
C564622|607116||alzheimer disease 8
|
|
C564622|607116||ad8
|
|
C564622|607116||alzheimer disease familial 8
|
|
D018827||carcinoma lewis lung
|
|
D018827||lewis lung carcinoma
|
|
D018827||lung carcinoma lewis
|
|
611107|C567008||mental retardation autosomal recessive 4
|
|
611107|C567008||mrt4
|
|
D046151||lingual thyroid
|
|
D046151||lingual thyroids
|
|
D046151||thyroid lingual
|
|
D046151||thyroids lingual
|
|
D047489||preconception injuries
|
|
D047489||injuries preconception
|
|
D047489||injury preconception
|
|
D047489||preconception injury
|
|
C538112||hernandez aguirre negrete syndrome
|
|
C538112||ehlers danlos syndrome with progeroid facies and mild mental retardation
|
|
C538112||hern 225 ndez aguirre negrete syndrome
|
|
C538110||pancreatic adenoma
|
|
C538115||heterochromia iridis
|
|
C538115||asymmetry in the pigmentation of the irides
|
|
C538115||pigmentary abnormality of the anterior segment of the eye
|
|
C537394|243180||neuronal intestinal pseudoobstruction
|
|
C537394|243180||argyrophil myenteric plexus deficiency of
|
|
C537394|243180||intestinal pseudoobstruction due to neuronal disease
|
|
C537394|243180||neuronal intestinal dysplasia type a
|
|
C537394|243180||neuronal intestinal dysplasia type b
|
|
C537394|243180||nid a included
|
|
C537394|243180||nid b
|
|
C537394|243180||pseudoobstruction chronic idiopathic intestinal neuronal type
|
|
C537394|243180||pseudoobstruction chronic idiopathic intestinal neuronal type neuronal intestinal dysplasia type a included
|
|
C537394|243180||visceral neuropathy familial autosomal recessive
|
|
C538114||hersh podruch weisskopk syndrome
|
|
C538114||toluene embryopathy
|
|
C538113||herrmann syndrome
|
|
C538113||photomyoclonus diabetes mellitus deafness nephropathy and cerebral dysfunction
|
|
C564461|301220||pigmentary disorder reticulate with systemic manifestations
|
|
C564461|301220||amyloidosis familial cutaneous
|
|
C564461|301220||pdr
|
|
C567681|613255||cardiomyopathy familial hypertrophic 15
|
|
C567681|613255||cmh15
|
|
D059466||white coat hypertension
|
|
D059466||clinic hypertension isolated
|
|
D059466||hypertension isolated clinic
|
|
D059466||hypertension white coat
|
|
D059466||isolated clinic hypertension
|
|
D059466||syndrome white coat
|
|
D059466||white coat syndrome
|
|
C535941|302950||chondrodysplasia punctata brachytelephalangic
|
|
C535941|302950||brachytelephalangic chondrodysplasia punctata
|
|
C535941|302950|C580533||cdpx1
|
|
C535941|302950||chondrodysplasia punctata 1 x linked recessive
|
|
C535941|302950||chondrodysplasia punctata brachytelephalangic autosomal
|
|
C535941|302950||cpxr
|
|
D059468||masked hypertension
|
|
D059468||hypertension masked
|
|
D059468||hypertensions masked
|
|
D059468||masked hypertensions
|
|
C538109||pancreas agenesis dorsal
|
|
C538109||agenesis of the dorsal pancreas
|
|
C538109||pancreas dorsal agenesis of
|
|
C538107||palmer pagon syndrome
|
|
C536690|604454||welander distal myopathy swedish type
|
|
C536690|604454||distal myopathy swedish type
|
|
C536690|604454|D049310|160500||muscular dystrophy distal late onset autosomal dominant
|
|
C536690|604454|D049310|160500||myopathy distal swedish
|
|
C536690|604454||wdm
|
|
C536690|604454|D049310|160500||welander distal myopathy
|
|
C538106||pallister w syndrome
|
|
C538106||median cleft upper lip mental retardation and pugilistic facies
|
|
C538106||w syndrome
|
|
D006949||hyperlipidemias
|
|
D006949||hyperlipemia
|
|
D006949||hyperlipemias
|
|
D006949||hyperlipidemia
|
|
D006949||lipemia
|
|
D006949||lipemias
|
|
D006949||lipidemia
|
|
D006949||lipidemias
|
|
D006947||hyperkalemia
|
|
D006947||hyperkalemias
|
|
D006947||hyperpotassemia
|
|
D006947||hyperpotassemias
|
|
D006948||hyperkinesis
|
|
D006948||generalized hyperkinesia
|
|
D006948||generalized hyperkinesias
|
|
D006948||hyperactivity motor
|
|
D006948||hyperkinesia
|
|
D006948||hyperkinesia generalized
|
|
D006948||hyperkinesias generalized
|
|
D006948||hyperkinetic movement
|
|
D006948||hyperkinetic movements
|
|
D006948||motor hyperactivity
|
|
D006948||movement hyperkinetic
|
|
D006948||movements hyperkinetic
|
|
D031901|D006828|231090||gestational trophoblastic disease
|
|
D031901||disease gestational trophoblastic
|
|
D031901||diseases gestational trophoblastic
|
|
D031901||gestational trophoblastic diseases
|
|
D031901||gestational trophoblastic neoplasia
|
|
D031901||gestational trophoblastic neoplasm
|
|
D031901||gestational trophoblastic neoplasms
|
|
D031901||neoplasia gestational trophoblastic
|
|
D031901||neoplasm gestational trophoblastic
|
|
D031901||neoplasms gestational trophoblastic
|
|
D031901||trophoblastic disease gestational
|
|
D031901||trophoblastic diseases gestational
|
|
D031901||trophoblastic neoplasia gestational
|
|
D031901||trophoblastic neoplasm gestational
|
|
D031901||trophoblastic neoplasms gestational
|
|
D006945||hyperhidrosis
|
|
D006946||hyperinsulinism
|
|
D006946||compensatory hyperinsulinemia
|
|
D006946||endogenous hyperinsulinism
|
|
D006946||exogenous hyperinsulinism
|
|
D006946||hyperinsulinemia
|
|
D006946||hyperinsulinemia compensatory
|
|
D006946||hyperinsulinism endogenous
|
|
D006946||hyperinsulinism exogenous
|
|
C570377||benign pseudohypertrophic muscular dystrophy
|
|
D005611||freemartinism
|
|
D006943||hyperglycemia
|
|
D006943||hyperglycemia postprandial
|
|
D006943||hyperglycemias
|
|
D006943||hyperglycemias postprandial
|
|
D006943||postprandial hyperglycemia
|
|
D006943||postprandial hyperglycemias
|
|
D006944||hyperglycemic hyperosmolar nonketotic coma
|
|
D006944||coma hyperglycemic hyperosmolar nonketotic
|
|
D006944||coma nonketotic hyperglycemic
|
|
D006944||hyperglycemic coma nonketotic
|
|
D006944||hyperosmolar hyperglycemic nonketotic coma
|
|
D006944||nonketotic hyperglycemic coma
|
|
D006941||hyperesthesia
|
|
D006941||hyperesthesias
|
|
D006941||hyperesthesias tactile
|
|
D006941||hyperesthesias thermal
|
|
D006941||hyperesthesia tactile
|
|
D006941||hyperesthesia thermal
|
|
D006941||hyperesthetic sensation
|
|
D006941||hyperesthetic sensations
|
|
D006941||oxyesthesia
|
|
D006941||oxyesthesias
|
|
D006941||sensation hyperesthetic
|
|
D006941||sensations hyperesthetic
|
|
D006941||tactile hyperesthesia
|
|
D006941||tactile hyperesthesias
|
|
D006941||thermal hyperesthesia
|
|
D006941||thermal hyperesthesias
|
|
C562787|176400||precocious puberty central
|
|
C562787|176400||cppb1
|
|
C562787|176400||precocious puberty central 1
|
|
D006942||hypergammaglobulinemia
|
|
D006942||hypergammaglobulinemias
|
|
D006942||hyperimmunoglobulinemia
|
|
D006942||hyperimmunoglobulinemias
|
|
C537168|120330||papillorenal syndrome
|
|
C537168|120330||cakut with ocular abnormalities
|
|
C537168|120330||coloboma of optic nerve with renal disease
|
|
C537168|120330||coloboma ureteral renal syndrome
|
|
C537168|120330||congenital anomalies of the kidney and urinary tract with ocular abnormalities
|
|
C537168|120330||optic coloboma vesicoureteral reflux and renal anomalies
|
|
C537168|120330||optic nerve coloboma renal syndrome
|
|
C537168|120330||optic nerve coloboma with renal disease
|
|
C537168|120330||paprs
|
|
C537168|120330||renal coloboma syndrome
|
|
C537168|120330||renal coloboma syndrome with macular abnormalities
|
|
C537168|120330||renal hypoplasia isolated
|
|
D006940||hyperemia
|
|
D006940||active hyperemia
|
|
D006940||arterial hyperemia
|
|
D006940||congestion venous
|
|
D006940||engorgement venous
|
|
D006940||hyperemia active
|
|
D006940||hyperemia arterial
|
|
D006940||hyperemia passive
|
|
D006940||hyperemia reactive
|
|
D006940||hyperemias
|
|
D006940||hyperemias reactive
|
|
D006940||passive hyperemia
|
|
D006940||reactive hyperemia
|
|
D006940||reactive hyperemias
|
|
D006940||venous congestion
|
|
D006940||venous engorgement
|
|
D061686||premature ejaculation
|
|
D061686||ejaculation premature
|
|
D061686||ejaculations premature
|
|
D061686||ejaculatio praecox
|
|
D061686||ejaculatio praecoxs
|
|
D061686||praecox ejaculatio
|
|
D061686||praecoxs ejaculatio
|
|
D061686||premature ejaculations
|
|
C567470|300716||mental retardation x linked 95
|
|
C567470|300716||mrx95
|
|
607053||high density lipoprotein cholesterol level quantitative trait locus 2
|
|
607053||hdlcq2
|
|
D014897|158600||spinal muscular atrophies of childhood
|
|
D014897|158600||atrophies infantile muscular
|
|
D014897|158600||atrophies juvenile muscular
|
|
D014897|158600||atrophy infantile muscular
|
|
D014897|158600||atrophy juvenile muscular
|
|
D014897|158600||hmn hereditary motor neuropathy proximal type i
|
|
D014897|158600||hoffman diseases werdnig
|
|
D014897|158600||hoffman disease werdnig
|
|
D014897|158600||infantile muscular atrophies
|
|
D014897|158600||infantile muscular atrophy
|
|
D014897|158600||infantile spinal muscular atrophy
|
|
D014897|158600||juvenile muscular atrophies
|
|
D014897|158600||juvenile muscular atrophy
|
|
D014897|158600||juvenile spinal muscular atrophy
|
|
D014897|158600||kugelberg welander disease
|
|
D014897|158600||kugelberg welander syndrome
|
|
D014897|158600|C563560||kugelberg welander syndrome autosomal dominant
|
|
D014897|158600||kugelberg welander syndromes
|
|
D014897|158600||kws
|
|
D014897|158600||muscular atrophies juvenile
|
|
D014897|158600||muscular atrophy infantile
|
|
D014897|158600||muscular atrophy juvenile
|
|
D014897|158600||muscular atrophy spinal infantile
|
|
D014897|158600|C536879||muscular atrophy spinal infantile chronic form
|
|
D014897|158600|C536879||muscular atrophy spinal intermediate type
|
|
D014897|158600||muscular atrophy spinal type i
|
|
D014897|158600||muscular atrophy spinal type ii
|
|
D014897|158600||muscular atrophy spinal type iii
|
|
D014897|158600||proximal hereditary motor neuropathy type i
|
|
D014897|158600||sma1
|
|
D014897|158600||sma2
|
|
D014897|158600||sma3
|
|
D014897|158600||sma i
|
|
D014897|158600||sma ii
|
|
D014897|158600||sma iii
|
|
D014897|158600||sma infantile acute form
|
|
D014897|158600||sma led
|
|
D014897|158600||smaled1
|
|
D014897|158600||spinal muscular atrophy 1
|
|
D014897|158600|C563560||spinal muscular atrophy childhood proximal autosomal dominant
|
|
D014897|158600||spinal muscular atrophy infantile
|
|
D014897|158600||spinal muscular atrophy juvenile
|
|
D014897|158600|C563560||spinal muscular atrophy juvenile proximal autosomal dominant
|
|
D014897|158600||spinal muscular atrophy lower extremity predominant 1 autosomal dominant
|
|
D014897|158600||spinal muscular atrophy mild childhood and adolescent form
|
|
D014897|158600||spinal muscular atrophy type 2
|
|
D014897|158600||spinal muscular atrophy type 3
|
|
D014897|158600||spinal muscular atrophy type i
|
|
D014897|158600||spinal muscular atrophy type ii
|
|
D014897|158600||spinal muscular atrophy type iii
|
|
D014897|158600||type iii spinal muscular atrophy
|
|
D014897|158600||type ii spinal muscular atrophy
|
|
D014897|158600||type i spinal muscular atrophy
|
|
D014897|158600||werdnig hoffman disease
|
|
D014897|158600||werdnig hoffman diseases
|
|
D014897|158600||werdnig hoffmann disease
|
|
D006828|231090||hydatidiform mole
|
|
D006828|231090|303100|D015794||chm
|
|
D006828|231090||complete hydatidiform mole
|
|
D006828|231090||complete hydatidiform moles
|
|
D006828|231090||hydatidiform mole complete
|
|
D006828|231090||hydatidiform mole partial
|
|
D006828|231090||hydatidiform mole recurrent 1
|
|
D006828|231090||hydatidiform moles
|
|
D006828|231090||hydatidiform moles complete
|
|
D006828|231090||hydatidiform moles partial
|
|
D006828|231090||hydatid mole
|
|
D006828|231090||hydatid moles
|
|
D006828|231090||hydm
|
|
D006828|231090||hydm1
|
|
D006828|231090||molar pregnancies
|
|
D006828|231090||molar pregnancy
|
|
D006828|231090||mole complete hydatidiform
|
|
D006828|231090||mole hydatid
|
|
D006828|231090||mole hydatidiform
|
|
D006828|231090||mole partial hydatidiform
|
|
D006828|231090||moles complete hydatidiform
|
|
D006828|231090||moles hydatid
|
|
D006828|231090||moles hydatidiform
|
|
D006828|231090||moles partial hydatidiform
|
|
D006828|231090||partial hydatidiform mole
|
|
D006828|231090||partial hydatidiform moles
|
|
D006828|231090||pregnancies molar
|
|
D006828|231090||pregnancy molar
|
|
D006210|234100||hallermann apos s syndrome
|
|
D006210|234100||dyscephalic syndrome francois
|
|
D006210|234100||dyscephalic syndromes francois
|
|
D006210|234100||francois dyscephalic syndrome
|
|
D006210|234100||francois dyscephalic syndromes
|
|
D006210|234100||hallermanns syndrome
|
|
D006210|234100||hallermann streiff francois syndrome
|
|
D006210|234100||hallermann streiff syndrome
|
|
D006210|234100||hallermann syndrome
|
|
D006210|234100||hss
|
|
D006210|234100||syndrome francois dyscephalic
|
|
D006210|234100||syndrome hallermann apos s
|
|
D006210|234100||syndrome hallermann streiff
|
|
D006210|234100||syndromes francois dyscephalic
|
|
D059352||musculoskeletal pain
|
|
D059352||musculoskeletal pains
|
|
D059352||pain musculoskeletal
|
|
D059352||pains musculoskeletal
|
|
178300|C566737||ptosis hereditary congenital 1
|
|
178300|C566737||ptos1
|
|
D018921||leukostasis
|
|
D018921||leukostases
|
|
D018921||leukostasis syndrome
|
|
D018921||leukostasis syndromes
|
|
D018921||syndrome leukostasis
|
|
D018921||syndromes leukostasis
|
|
C566429|602685||mental retardation severe with spasticity and pigmentary tapetoretinal degeneration
|
|
C566429|602685||mrst
|
|
D018923||persian gulf syndrome
|
|
D018923||gulf war syndrome
|
|
D018923||syndrome gulf war
|
|
D018923||syndrome persian gulf
|
|
C535414|608591||charcot marie tooth disease type 2g
|
|
C535414|608591||charcot marie tooth disease axonal type 2g
|
|
C535414|608591|607706||charcot marie tooth disease axonal with vocal cord paresis autosomal recessive
|
|
C535414|608591||charcot marie tooth neuropathy type 2g
|
|
C535414|608591||cmt2g
|
|
C535414|608591||cmt 2g
|
|
C564706|606451||deafness autosomal dominant 30
|
|
C564706|606451||dfna30
|
|
D006959||hyperoxaluria
|
|
D006959||oxalosis
|
|
D006959||oxaluria
|
|
D006956||hyperopia
|
|
D006956||farsightedness
|
|
D006956||hypermetropia
|
|
D005627||frostbite
|
|
D005627||frostbites
|
|
D006957||hyperostosis frontalis interna
|
|
D006957||leontiasis ossium
|
|
D006957||morgagni stewart morel syndrome
|
|
D006957||syndrome morgagni stewart morel
|
|
D005621||friedreich ataxia
|
|
D005621||ataxia friedreich
|
|
D005621||ataxia friedreich familial
|
|
D005621||ataxia friedreich hereditary
|
|
D005621||ataxia friedreich apos s
|
|
D005621||ataxia friedreich apos s familial
|
|
D005621||ataxia friedreich apos s hereditary
|
|
D005621||ataxia friedreich spinocerebellar
|
|
D005621||ataxias friedreich
|
|
D005621||ataxias friedreich apos s hereditary
|
|
D005621||disease friedreich
|
|
D005621||disease friedreich apos s
|
|
D005621||familial ataxia friedreich
|
|
D005621||familial ataxia friedreich apos s
|
|
D005621||friedreich ataxias
|
|
D005621||friedreich disease
|
|
D005621||friedreich familial ataxia
|
|
D005621||friedreich hereditary ataxia
|
|
D005621||friedreich hereditary spinal ataxia
|
|
D005621||friedreich apos s ataxia
|
|
D005621||friedreich apos s disease
|
|
D005621||friedreich apos s familial ataxia
|
|
D005621||friedreichs familial ataxia
|
|
D005621||friedreich apos s hereditary ataxia
|
|
D005621||friedreichs hereditary ataxia
|
|
D005621||friedreich apos s hereditary ataxias
|
|
D005621||friedreich apos s hereditary spinal ataxia
|
|
D005621||friedreich spinocerebellar ataxia
|
|
D005621||hereditary ataxia friedreich
|
|
D005621||hereditary ataxia friedreich apos s
|
|
D005621||hereditary ataxias friedreich apos s
|
|
D005621||hereditary spinal ataxia friedreich
|
|
D005621||hereditary spinal ataxia friedreich apos s
|
|
D005621||hereditary spinal scleroses
|
|
D005621||hereditary spinal sclerosis
|
|
D005621||scleroses hereditary spinal
|
|
D005621||sclerosis hereditary spinal
|
|
D005621||spinal scleroses hereditary
|
|
D005621||spinal sclerosis hereditary
|
|
D005621||spinocerebellar ataxia friedreich
|
|
D006955||hypernatremia
|
|
D006955||hypernatremias
|
|
D059373||mastodynia
|
|
D059373||breast pain
|
|
D059373||breast pains
|
|
D059373||mammalgia
|
|
D059373||mammalgias
|
|
D059373||mastalgia
|
|
D059373||mastalgias
|
|
D059373||mastodynias
|
|
D059373||pain breast
|
|
D059373||pains breast
|
|
D006952||hyperlipoproteinemia type iii
|
|
D006952||broad beta disease
|
|
D006952||broad beta hyperlipoproteinemia
|
|
D006952||dysbetalipoproteinemia
|
|
D006952||dysbetalipoproteinemia familial
|
|
D006952||familial dysbetalipoproteinemia
|
|
D006952||familial hypercholesterolemia with hyperlipemia
|
|
D006952||hyperlipoproteinemia broad beta
|
|
D006952||hyperlipoproteinemias type iii
|
|
D006952||type iii hyperlipoproteinemia
|
|
D006952||type iii hyperlipoproteinemias
|
|
C566470|610478||retinal cone dystrophy 4
|
|
C566470|610478||rcd4
|
|
D006951||hyperlipoproteinemias
|
|
D006951||hyperlipoproteinemia
|
|
C563881|608664||seckel syndrome 3
|
|
C563881|608664||sckl3
|
|
D059369||pott puffy tumor
|
|
D059369||pott apos s puffy tumor
|
|
D059369||potts puffy tumor
|
|
D059369||puffy tumor pott
|
|
D059369||puffy tumor pott apos s
|
|
D059369||tumor pott puffy
|
|
D059369||tumor pott apos s puffy
|
|
D059366||asthma occupational
|
|
D059366||asthmas occupational
|
|
D059366||occupational asthma
|
|
D059366||occupational asthmas
|
|
C565344|605289||split hand foot malformation 4
|
|
C565344|605289||shfm4
|
|
D017600||neuroectodermal tumor melanotic
|
|
D017600||anlage tumor retinal
|
|
D017600||anlage tumors retinal
|
|
D017600||melanoameloblastoma
|
|
D017600||melanoameloblastomas
|
|
D017600||melanotic neuroectodermal tumor
|
|
D017600||melanotic neuroectodermal tumors
|
|
D017600||melanotic progonoma
|
|
D017600||melanotic progonomas
|
|
D017600||neuroectodermal tumors melanotic
|
|
D017600||progonoma melanotic
|
|
D017600||progonomas melanotic
|
|
D017600||retinal anlage tumor
|
|
D017600||retinal anlage tumors
|
|
D017600||tumor melanotic neuroectodermal
|
|
D017600||tumor retinal anlage
|
|
D017600||tumors melanotic neuroectodermal
|
|
D017600||tumors retinal anlage
|
|
D018934||fournier gangrene
|
|
D018934||fournier disease
|
|
D018934||fournier apos s disease
|
|
D018934||fourniers disease
|
|
D018934||fournier apos s gangrene
|
|
D018934||fourniers gangrene
|
|
D018934||gangrene fournier
|
|
D018934||gangrene fournier apos s
|
|
D006929||hyperaldosteronism
|
|
D006929||aldosteronism
|
|
D006929||conn apos s syndrome
|
|
D006929||conns syndrome
|
|
D006929||conn syndrome
|
|
D006929||hyperaldosteronism primary
|
|
D006929||primary hyperaldosteronism
|
|
D006929||syndrome conn
|
|
D006929||syndrome conn apos s
|
|
C538329|600737||inclusion body myopathy autosomal recessive
|
|
C538329|600737|C536816|605820||ibm2
|
|
C538329|600737||inclusion body myopathy 2 autosomal recessive
|
|
C538329|600737||inclusion body myopathy quadriceps sparing
|
|
C538329|600737||qsm
|
|
D006925||hymenolepiasis
|
|
D006925||hymenolepiases
|
|
D006925||hymenolepis infection
|
|
D006925||hymenolepis infections
|
|
D006925||infection hymenolepis
|
|
D006925||infections hymenolepis
|
|
D010192||pancreatic pseudocyst
|
|
D010192||pancreatic pseudocysts
|
|
D010192||pseudocyst pancreatic
|
|
D010192||pseudocysts pancreatic
|
|
D034161||pelvic infection
|
|
D034161||infection pelvic
|
|
D034161||infections pelvic
|
|
D034161||pelvic infections
|
|
C567505|611880||cardiomyopathy dilated 2a
|
|
C567505|611880||cardiomyopathy congestive autosomal recessive
|
|
C567505|611880||cmd2a
|
|
C565223|609815||zygodactyly 1
|
|
C565223|609815||zd1
|
|
D060368||lobomycosis
|
|
D060368||blastomycoses keloidal
|
|
D060368||blastomycosis keloidal
|
|
D060368||disease jorge lobo
|
|
D060368||disease jorge lobo apos s
|
|
D060368||jorge lobo disease
|
|
D060368||jorge lobo apos s disease
|
|
D060368||jorge lobos disease
|
|
D060368||keloidal blastomycoses
|
|
D060368||keloidal blastomycosis
|
|
D060368||lacazioses
|
|
D060368||lacaziosis
|
|
D060368||lobomycoses
|
|
D018908||muscle weakness
|
|
D018908||muscle weaknesses
|
|
D018908||muscular weakness
|
|
D018908||muscular weaknesses
|
|
D018908||weaknesses muscle
|
|
D018908||weaknesses muscular
|
|
D018908||weakness muscle
|
|
D018908||weakness muscular
|
|
300537|C564492||heterotopia periventricular ehlers danlos variant
|
|
300537|C564492||periventricular nodular heterotopia 4
|
|
300537|C564492||pvnh4
|
|
D018902||chondrodysplasia punctata rhizomelic
|
|
D018902|215100|C531651||chondrodysplasia punctata rhizomelic form
|
|
D018902||chondrodysplasia punctatas rhizomelic
|
|
D018902||punctata rhizomelic chondrodysplasia
|
|
D018902||punctatas rhizomelic chondrodysplasia
|
|
D018902||rhizomelic chondrodysplasia punctata
|
|
D018902||rhizomelic chondrodysplasia punctatas
|
|
D010182||pancreatic diseases
|
|
D010182||disease pancreatic
|
|
D010182||diseases pancreatic
|
|
D010182||pancreatic disease
|
|
D018901||peroxisomal disorders
|
|
D018901||acidemia hyperpipecolic
|
|
D018901||acidemias hyperpipecolic
|
|
D018901||adrenoleukodystrophies neonatal
|
|
D018901||adrenoleukodystrophy autosomal neonatal form
|
|
D018901||adrenoleukodystrophy neonatal
|
|
D018901||dysfunction general peroxisomal
|
|
D018901||dysfunction multiple peroxisomal
|
|
D018901||dysfunctions general peroxisomal
|
|
D018901||dysfunction single peroxisomal
|
|
D018901||dysfunctions multiple peroxisomal
|
|
D018901||dysfunctions single peroxisomal
|
|
D018901||general peroxisomal dysfunction
|
|
D018901||general peroxisomal dysfunctions
|
|
D018901||hyperpipecolatemia
|
|
D018901||hyperpipecolic acidemia
|
|
D018901||hyperpipecolic acidemias
|
|
D018901||multiple peroxisomal dysfunction
|
|
D018901||multiple peroxisomal dysfunctions
|
|
D018901||neonatal adrenoleukodystrophies
|
|
D018901||neonatal adrenoleukodystrophy
|
|
D018901||peroxisomal disorder
|
|
D018901||peroxisomal dysfunction general
|
|
D018901||peroxisomal dysfunction multiple
|
|
D018901||peroxisomal dysfunctions general
|
|
D018901||peroxisomal dysfunction single
|
|
D018901||peroxisomal dysfunctions multiple
|
|
D018901||peroxisomal dysfunctions single
|
|
D018901||single peroxisomal dysfunction
|
|
D018901||single peroxisomal dysfunctions
|
|
D010185||pancreatic fistula
|
|
D010185||fistula pancreatic
|
|
D010185||fistulas pancreatic
|
|
D010185||pancreatic fistulas
|
|
300581|C564480||fg syndrome 5
|
|
300581|C564480||fgs5
|
|
D010188||exocrine pancreatic insufficiency
|
|
D010188||exocrine pancreatic insufficiencies
|
|
D010188||insufficiencies exocrine pancreatic
|
|
D010188||insufficiencies pancreatic
|
|
D010188||insufficiency exocrine pancreatic
|
|
D010188||insufficiency pancreatic
|
|
D010188||pancreatic insufficiencies
|
|
D010188||pancreatic insufficiencies exocrine
|
|
D010188||pancreatic insufficiency
|
|
D010188||pancreatic insufficiency exocrine
|
|
167200|D053549||pachyonychia congenita
|
|
167200|D053549||congenital pachyonychia
|
|
167200|D053549||congenital pachyonychias
|
|
167200|D053549||congenita pachyonychia
|
|
167200|D053549||congenita syndrome pachyonychia
|
|
167200|D053549||congenita syndromes pachyonychia
|
|
167200|D053549||jackson lawler syndrome pc 2
|
|
167200|D053549||jackson lawler type pachyonychia congenita
|
|
167200|D053549||jadassohn lewandowski syndrome pc 1
|
|
167200|D053549||jadassohn lewandowsky syndrome
|
|
167200|D053549||jadassohn lewandowsky syndrome formerly
|
|
167200|D053549||pachyonychia congenita 1
|
|
167200|D053549||pachyonychia congenita 2
|
|
167200|D053549||pachyonychia congenita jackson lawler type
|
|
167200|D053549||pachyonychia congenita jackson lawler type formerly
|
|
167200|D053549||pachyonychia congenita jadassohn lewandowsky type
|
|
167200|D053549||pachyonychia congenita jadassohn lewandowsky type formerly
|
|
167200|D053549||pachyonychia congenital
|
|
167200|D053549||pachyonychia congenita syndrome
|
|
167200|D053549||pachyonychia congenita syndromes
|
|
167200|D053549||pachyonychia congenita tarda type 1
|
|
167200|D053549||pachyonychia congenita type 1
|
|
167200|D053549||pachyonychia congenita type 2
|
|
167200|D053549||pachyonychias congenital
|
|
167200|D053549||pc1
|
|
167200|D053549||pc2
|
|
167200|D053549||syndrome pachyonychia congenita
|
|
167200|D053549||syndromes pachyonychia congenita
|
|
167200|D053549||type 1 pachyonychia congenita
|
|
167200|D053549||type 2 pachyonychia congenita
|
|
D006939||hyperemesis gravidarum
|
|
D006939||pernicious vomiting of pregnancy
|
|
D006939||pregnancy pernicious vomiting
|
|
D006936||hypercementosis
|
|
D006936||hypercementoses
|
|
D006937||hypercholesterolemia
|
|
D006937||elevated cholesterol
|
|
D006937||hypercholesteremia
|
|
D006937||hypercholesteremias
|
|
D006937||hypercholesterolemias
|
|
D006934||hypercalcemia
|
|
D006934||hypercalcemias
|
|
D006934||milk alkali syndrome
|
|
D006934||syndrome milk alkali
|
|
D006935||hypercapnia
|
|
D006932||hyperbilirubinemia
|
|
D006932||bilirubinemia
|
|
D006932||bilirubinemias
|
|
D006932||hyperbilirubinemias
|
|
D006933||hyperbilirubinemia hereditary
|
|
D006933||hereditary hyperbilirubinemia
|
|
D006933||hereditary hyperbilirubinemias
|
|
D006933||hyperbilirubinemia rotor type
|
|
D006933||hyperbilirubinemias hereditary
|
|
D006933||rotor syndrome
|
|
D006933||rotor type hyperbilirubinemia
|
|
D006933||syndrome rotor
|
|
D006930||hyperalgesia
|
|
D006930||allodynia
|
|
D006930||allodynia mechanical
|
|
D006930||allodynias mechanical
|
|
D006930||allodynias tactile
|
|
D006930||allodynias thermal
|
|
D006930||allodynia tactile
|
|
D006930||allodynia thermal
|
|
D006930||hyperalgesia mechanical
|
|
D006930||hyperalgesia primary
|
|
D006930||hyperalgesias
|
|
D006930||hyperalgesia secondary
|
|
D006930||hyperalgesias mechanical
|
|
D006930||hyperalgesias primary
|
|
D006930||hyperalgesias secondary
|
|
D006930||hyperalgesias tactile
|
|
D006930||hyperalgesias thermal
|
|
D006930||hyperalgesia tactile
|
|
D006930||hyperalgesia thermal
|
|
D006930||hyperalgesic sensations
|
|
D006930||mechanical allodynia
|
|
D006930||mechanical hyperalgesia
|
|
D006930||tactile allodynia
|
|
D006930||thermal allodynia
|
|
D006930||thermal hyperalgesia
|
|
D059390||breakthrough pain
|
|
D059390||breakthrough pains
|
|
D059390||pain breakthrough
|
|
D059390||pains breakthrough
|
|
D018917||optic neuropathy ischemic
|
|
D018917||anterior ischemic optic neuropathy
|
|
D018917||ischemia optic nerve
|
|
D018917||ischemias optic nerve
|
|
D018917||ischemic optic neuropathies
|
|
D018917||ischemic optic neuropathy
|
|
D018917||nerve ischemia optic
|
|
D018917||nerve ischemias optic
|
|
D018917||neuropathies ischemic optic
|
|
D018917||neuropathy ischemic optic
|
|
D018917||optic nerve ischemia
|
|
D018917||optic nerve ischemias
|
|
D018917||optic neuropathies ischemic
|
|
D018917||optic neuropathy anterior ischemic
|
|
D018917||optic neuropathy posterior ischemic
|
|
D018917||posterior ischemic optic neuropathy
|
|
201750||antley bixler syndrome with genital anomalies and disordered steroidogenesis
|
|
201750||abs1
|
|
234050|D054463||trichothiodystrophy syndromes
|
|
234050|D054463||abhs
|
|
234050|D054463||amish brittle hair brain syndrome
|
|
234050|D054463||amish brittle hair syndrome
|
|
234050|D054463||bids syndrome
|
|
234050|D054463||bids syndromes
|
|
234050|D054463||brittle hair intellectual impairment decreased fertility short stature syndrome
|
|
234050|D054463||hair brain syndrome
|
|
234050|D054463||hair brain syndromes
|
|
234050|D054463||ibids syndrome
|
|
234050|D054463||ibids syndromes
|
|
234050|D054463||ichthyosiform erythroderma with hair abnormality and mental and growth retardation
|
|
234050|D054463||ichthyosis brittle hair intellectual impairment decreased fertility and short stature
|
|
234050|D054463||nonphotosensitive 1 trichothiodystrophies
|
|
234050|D054463||nonphotosensitive 1 trichothiodystrophy
|
|
234050|D054463||photosensitive trichothiodystrophies
|
|
234050|D054463||photosensitive trichothiodystrophy
|
|
234050|D054463||pibids syndrome
|
|
234050|D054463||pibids syndromes
|
|
234050|D054463||tay syndrome
|
|
234050|D054463||trichothiodystrophies
|
|
234050|D054463||trichothiodystrophies nonphotosensitive 1
|
|
234050|D054463||trichothiodystrophies photosensitive
|
|
234050|D054463||trichothiodystrophy
|
|
234050|D054463||trichothiodystrophy nonphotosensitive 1
|
|
234050|D054463||trichothiodystrophy photosensitive
|
|
234050|D054463||trichothiodystrophy syndrome
|
|
234050|D054463||trichothiodystrophy with congenital ichtyosis
|
|
234050|D054463||ttdn1
|
|
D034141||hypoalbuminemia
|
|
D059388||pelvic girdle pain
|
|
D059388||dysfunctions symphysis pubis
|
|
D059388||dysfunction symphysis pubis
|
|
D059388||girdle pain pelvic
|
|
D059388||girdle pains pelvic
|
|
D059388||pain pelvic girdle
|
|
D059388||pains pelvic girdle
|
|
D059388||pelvic girdle pains
|
|
D059388||pubis dysfunctions symphysis
|
|
D059388||pubis dysfunction symphysis
|
|
D059388||symphysis pubis dysfunction
|
|
D059388||symphysis pubis dysfunctions
|
|
C563461|255110||carnitine palmitoyltransferase ii deficiency late onset
|
|
C563461|255110||carnitine palmitoyltransferase ii deficiency adult onset
|
|
C563461|255110||carnitine palmitoyltransferase ii deficiency myopathic
|
|
C563461|255110||cpt2 deficiency late onset
|
|
C563461|255110||cpt ii deficiency myopathic
|
|
D010195||pancreatitis
|
|
D010195||pancreatitides
|
|
D010198||pancytopenia
|
|
D010198||pancytopenias
|
|
C535461|603523||chylothorax congenital
|
|
C535461|603523||hydrothorax congenital
|
|
C536409|601634||neural tube defect folate sensitive
|
|
C536409|601634||neural tube defects folate sensitive
|
|
C536409|601634||ntd folate sensitive spina bifida folate sensitive included
|
|
D046088||hearing loss unilateral
|
|
D046088||unilateral hearing loss
|
|
609060|C563797||combined oxidative phosphorylation deficiency 1
|
|
609060|C563797||coxpd1
|
|
609060|C563797||hepatoencephalopathy early fatal progressive
|
|
D046089||hearing loss mixed conductive sensorineural
|
|
D046089||hearing loss mixed
|
|
D046089||losses mixed hearing
|
|
D046089||loss mixed hearing
|
|
D046089||mixed hearing loss
|
|
108420||spermatogenic failure 2
|
|
108420||asg
|
|
108420||aspermiogenesis factor
|
|
108420||spgf2
|
|
D058070||asymptomatic diseases
|
|
D058070||asymptomatic condition
|
|
D058070||asymptomatic conditions
|
|
D058070||asymptomatic disease
|
|
D058070||asymptomatic state
|
|
D058070||asymptomatic states
|
|
D058070||condition asymptomatic
|
|
D058070||conditions asymptomatic
|
|
D058070||disease asymptomatic
|
|
D058070||disease presymptomatic
|
|
D058070||disease pre symptomatic
|
|
D058070||diseases asymptomatic
|
|
D058070||diseases presymptomatic
|
|
D058070||diseases pre symptomatic
|
|
D058070||presymptomatic disease
|
|
D058070||pre symptomatic disease
|
|
D058070||presymptomatic diseases
|
|
D058070||pre symptomatic diseases
|
|
D058069||neglected diseases
|
|
D058069||disease neglected
|
|
D058069||diseases neglected
|
|
D058069||neglected disease
|
|
142945|C564181||holoprosencephaly 3
|
|
142945|C564181||hlp3
|
|
142945|C564181||hpe3
|
|
D009188||myelitis transverse
|
|
D009188||acute transverse myelitis
|
|
D009188||demyelinative myelitis
|
|
D009188||myelitides subacute transverse
|
|
D009188||myelitis acute transverse
|
|
D009188||myelitis demyelinative
|
|
D009188||myelitis necrotizing
|
|
D009188||myelitis paraneoplastic
|
|
D009188||myelitis postinfectious
|
|
D009188||myelitis postvaccinal
|
|
D009188||myelitis subacute transverse
|
|
D009188||necrotizing myelitis
|
|
D009188||paraneoplastic myelitis
|
|
D009188||postinfectious myelitis
|
|
D009188||postvaccinal myelitis
|
|
D009188||subacute transverse myelitis
|
|
D009188||transverse myelitis
|
|
D009188||transverse myelitis acute
|
|
D009188||transverse myelitis subacute
|
|
D009188||transverse myelopathy syndrome
|
|
D009188||transverse myelopathy syndromes
|
|
D058066||digital dermatitis
|
|
D058066||bovine digital dermatitides
|
|
D058066||bovine digital dermatitis
|
|
D058066||bovine foot wart
|
|
D058066||bovine foot warts
|
|
D058066||bovine hairy footwart
|
|
D058066||bovine hairy footwarts
|
|
D058066||dermatitides bovine digital
|
|
D058066||dermatitides digital
|
|
D058066||dermatitis bovine digital
|
|
D058066||dermatitis digital
|
|
D058066||digital dermatitides
|
|
D058066||digital dermatitides bovine
|
|
D058066||digital dermatitides ovine
|
|
D058066||digital dermatitides papillomatous
|
|
D058066||digital dermatitis bovine
|
|
D058066||digital dermatitis ovine
|
|
D058066||digital dermatitis papillomatous
|
|
D058066||digital papillomatoses
|
|
D058066||digital papillomatosis
|
|
D058066||foot wart bovine
|
|
D058066||footwart bovine hairy
|
|
D058066||foot warts bovine
|
|
D058066||footwarts bovine hairy
|
|
D058066||hairy footwart bovine
|
|
D058066||hairy footwarts bovine
|
|
D058066||ovine digital dermatitides
|
|
D058066||ovine digital dermatitis
|
|
D058066||papillomatoses digital
|
|
D058066||papillomatosis digital
|
|
D058066||papillomatous digital dermatitides
|
|
D058066||papillomatous digital dermatitis
|
|
D058066||wart bovine foot
|
|
D058066||warts bovine foot
|
|
D009187||myelitis
|
|
D009187||infectious myelitis
|
|
D009187||inflammation spinal cord
|
|
D009187||inflammations spinal cord
|
|
D009187||inflammatory myelopathies
|
|
D009187||inflammatory myelopathy
|
|
D009187||myelitides
|
|
D009187||myelitis infectious
|
|
D009187||myelitis subacute necrotising
|
|
D009187||myelopathies inflammatory
|
|
D009187||myelopathy inflammatory
|
|
D009187||necrotising myelitis subacute
|
|
D009187||spinal cord inflammation
|
|
D009187||spinal cord inflammations
|
|
D009187||subacute necrotising myelitis
|
|
D058065||diabetic cardiomyopathies
|
|
D058065||cardiomyopathies diabetic
|
|
D058065||cardiomyopathy diabetic
|
|
D058065||diabetic cardiomyopathy
|
|
D009182||mycosis fungoides
|
|
D009181||mycoses
|
|
D009181||disease fungus
|
|
D009181||diseases fungus
|
|
D009181||fungus disease
|
|
D009181||fungus diseases
|
|
D009180||mycoplasmatales infections
|
|
D009180||infection mycoplasmatales
|
|
D009180||infections mycoplasmatales
|
|
D009180||mycoplasmatales infection
|
|
D010167||pallor
|
|
D010167||pallors
|
|
C565832|603964||deafness autosomal dominant 16
|
|
C565832|603964||dfna16
|
|
D010181||pancreatic cyst
|
|
D010181||cyst pancreatic
|
|
D010181||cysts pancreatic
|
|
D010181||pancreatic cysts
|
|
610644||palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46 xx sex reversal
|
|
610644||palmoplantar hyperkeratosis and true hermaphroditism included
|
|
267010|C537756||renal hepatic pancreatic dysplasia dandy walker cyst
|
|
267010|C537756||goldston syndrome
|
|
267010|C537756||meckel like syndrome
|
|
267010|C537756||meckel syndrome type 7
|
|
267010|C537756||mks7
|
|
267010|C537756||renal hepatic pancreatic dysplasia with dandy walker cyst
|
|
D009198||myiasis
|
|
D009198||infestation maggot
|
|
D009198||infestations maggot
|
|
D009198||maggot infestation
|
|
D009198||maggot infestations
|
|
D009198||myiases
|
|
D009196||myeloproliferative disorders
|
|
D009196||disorder myeloproliferative
|
|
D009196||disorders myeloproliferative
|
|
D009196||myeloproliferative disorder
|
|
D009190||myelodysplastic syndromes
|
|
D009190||dysmyelopoietic syndrome
|
|
D009190||dysmyelopoietic syndromes
|
|
D009190||hematopoetic myelodysplasia
|
|
D009190||hematopoetic myelodysplasias
|
|
D009190||myelodysplasia hematopoetic
|
|
D009190||myelodysplasias hematopoetic
|
|
D009190||myelodysplastic syndrome
|
|
D009190||syndrome dysmyelopoietic
|
|
D009190||syndrome myelodysplastic
|
|
D009190||syndromes dysmyelopoietic
|
|
D009190||syndromes myelodysplastic
|
|
C536841|604218||familial encephalopathy with neuroserpin inclusion bodies
|
|
C536841|604218||encephalopathy familial with collins bodies
|
|
C536841|604218||encephalopathy familial with neuroserpin inclusion bodies
|
|
C536841|604218||familial dementia with neuroserpin inclusion bodies
|
|
C536841|604218||fenib
|
|
D010178||pancoast syndrome
|
|
D010178||pancoast apos s syndrome
|
|
D010178||pancoasts syndrome
|
|
D010178||pancoast tumor
|
|
D010178||syndrome pancoast
|
|
D010178||syndrome pancoast apos s
|
|
D010178||tumor pancoast
|
|
600634|D015175||prolactinoma
|
|
600634|D015175||adenoma lactotroph
|
|
600634|D015175||adenoma prolactin secreting pituitary
|
|
600634|D015175||adenomas lactotroph
|
|
600634|D015175||lactotroph adenoma
|
|
600634|D015175||lactotroph adenomas
|
|
600634|D015175||macroprolactinoma
|
|
600634|D015175||macroprolactinomas
|
|
600634|D015175||microprolactinoma
|
|
600634|D015175||microprolactinomas
|
|
600634|D015175||pituitary adenoma prl secreting
|
|
600634|D015175||pituitary adenoma prolactin producing
|
|
600634|D015175||pituitary adenoma prolactin secreting
|
|
600634|D015175||pituitary adenomas prl secreting
|
|
600634|D015175||pituitary adenomas prolactin producing
|
|
600634|D015175||pituitary adenomas prolactin secreting
|
|
600634|D015175||prl secreting pituitary adenoma
|
|
600634|D015175||prl secreting pituitary adenomas
|
|
600634|D015175||prolactinoma familial
|
|
600634|D015175||prolactinomas
|
|
600634|D015175||prolactin producing pituitary adenoma
|
|
600634|D015175||prolactin producing pituitary adenomas
|
|
600634|D015175||prolactin secreting pituitary adenoma
|
|
600634|D015175||prolactin secreting pituitary adenomas
|
|
109730||aortic valve disease 1
|
|
109730|C562942||aortic stenosis calcific
|
|
109730|C562388||aortic valve bicuspid
|
|
109730|C562942||aortic valve calcification of
|
|
109730||aovd1
|
|
109730||bav
|
|
109730|C562388||bicuspid aortic valve
|
|
608415|C564243||prolonged electroretinal response suppression
|
|
608415|C564243||bradyopsia
|
|
608415|C564243||perrs
|
|
C567932|300000||opitz gbbb syndrome x linked
|
|
C567932|300000||bbbg1
|
|
C567932|300000||gggb1
|
|
C567932|300000|C538387|145410||hypertelorism hypospadias syndrome
|
|
C567932|300000|C538387|145410||hypertelorism with esophageal abnormality and hypospadias
|
|
C567932|300000||ogs1
|
|
C567932|300000||opitz bbbg syndrome type i
|
|
C567932|300000||opitz gbbb syndrome type i
|
|
C567932|300000||opitz g syndrome type i
|
|
C567932|300000||opitz syndrome
|
|
C567932|300000||opitz syndrome x linked
|
|
C567932|300000||os
|
|
C567932|300000||osx
|
|
C567932|300000|C538387|145410||telecanthus hypospadias syndrome
|
|
C567932|300000||x linked opitz syndrome xlos
|
|
D010146||pain
|
|
D010146||ache
|
|
D010146||aches
|
|
D010146||burning pain
|
|
D010146||burning pains
|
|
D010146||crushing pain
|
|
D010146||crushing pains
|
|
D010146||migratory pain
|
|
D010146||migratory pains
|
|
D010146||pain burning
|
|
D010146||pain crushing
|
|
D010146||pain migratory
|
|
D010146||pain radiating
|
|
D010146||pains burning
|
|
D010146||pains crushing
|
|
D010146||pains migratory
|
|
D010146||pain splitting
|
|
D010146||pains radiating
|
|
D010146||pains splitting
|
|
D010146||physical suffering
|
|
D010146||physical sufferings
|
|
D010146||radiating pain
|
|
D010146||radiating pains
|
|
D010146||splitting pain
|
|
D010146||splitting pains
|
|
D010146||suffering physical
|
|
D010146||sufferings physical
|
|
D010149||pain postoperative
|
|
D010149||postoperative pain
|
|
D010149||postoperative pains
|
|
C567448|611958||prostate cancer hereditary 14
|
|
C567448|611958||hpc14
|
|
D010148||pain intractable
|
|
D010148||intractable pain
|
|
D010148||intractable pains
|
|
D010148||pain refractory
|
|
D010148||pains intractable
|
|
D010148||pains refractory
|
|
D010148||refractory pain
|
|
D010148||refractory pains
|
|
D009164||mycobacterium infections
|
|
D009164||infection mycobacterium
|
|
D009164||infections mycobacterium
|
|
D009164||mycobacterium infection
|
|
D011470||prostatic hyperplasia
|
|
D011470||adenoma prostatic
|
|
D011470||adenomas prostatic
|
|
D011470||benign prostatic hyperplasia
|
|
D011470||benign prostatic hypertrophy
|
|
D011470||hyperplasia prostatic
|
|
D011470||hypertrophy benign prostatic
|
|
D011470||prostatic adenoma
|
|
D011470||prostatic adenomas
|
|
D011470||prostatic hyperplasia benign
|
|
D011470||prostatic hypertrophy
|
|
D011470||prostatic hypertrophy benign
|
|
C537592|610738||neutropenia severe congenital autosomal recessive 3
|
|
C537592|610738||agranulocytosis infantile
|
|
C537592|610738||agranulocytosis infantile genetic
|
|
C537592|610738||autosomal dominant or sporadic congenital neutropenia
|
|
C537592|610738||congenital agranulocytosis
|
|
C537592|610738||congenital neutropenia
|
|
C537592|610738||infantile genetic agranulocytosis
|
|
C537592|610738||kostmann disease
|
|
C537592|610738||kostmann apos s agranulocytosis
|
|
C537592|610738||kostmann apos s syndrome
|
|
C537592|610738||kostmann syndrome
|
|
C537592|610738||neutropenia severe congenital 3 autosomal recessive
|
|
C537592|610738||scn3
|
|
C537592|610738||severe congenital neutropenia
|
|
C537592|610738||severe infantile genetic neutropenia
|
|
D011472||prostatitis
|
|
D011472||acute bacterial prostatitides
|
|
D011472||acute bacterial prostatitis
|
|
D011472||asymptomatic inflammatory prostatitides
|
|
D011472||asymptomatic inflammatory prostatitis
|
|
D011472||bacterial prostatitides acute
|
|
D011472||bacterial prostatitides chronic
|
|
D011472||bacterial prostatitis acute
|
|
D011472||bacterial prostatitis chronic
|
|
D011472||chronic bacterial prostatitides
|
|
D011472||chronic bacterial prostatitis
|
|
D011472||chronic prostatitis with chronic pelvic pain syndrome
|
|
D011472||inflammatory prostatitis asymptomatic
|
|
D011472||prostatitides
|
|
D011472||prostatitides chronic bacterial
|
|
D010145||paget disease extramammary
|
|
D010145||extramammary paget disease
|
|
D010145||extra mammary paget disease
|
|
D010145||extramammary paget apos s disease
|
|
D010145||extramammary pagets disease
|
|
D010145||extra mammary paget apos s disease
|
|
D010145||extra mammary pagets disease
|
|
D010145||paget disease extra mammary
|
|
D010145||paget apos s disease extramammary
|
|
D010145||pagets disease extramammary
|
|
D010145||paget apos s disease extra mammary
|
|
D010145||pagets disease extra mammary
|
|
D011475||prosthesis failure
|
|
D011475||durabilities prosthesis
|
|
D011475||durability prosthesis
|
|
D011475||failure prosthesis
|
|
D011475||failures prosthesis
|
|
D011475||loosening prosthesis
|
|
D011475||loosenings prosthesis
|
|
D011475||migration prosthesis
|
|
D011475||migrations prosthesis
|
|
D011475||prosthesis durabilities
|
|
D011475||prosthesis durability
|
|
D011475||prosthesis failures
|
|
D011475||prosthesis loosening
|
|
D011475||prosthesis loosenings
|
|
D011475||prosthesis migration
|
|
D011475||prosthesis migrations
|
|
D011475||prosthesis survival
|
|
D011475||prosthesis survivals
|
|
D011475||survival prosthesis
|
|
D011475||survivals prosthesis
|
|
D010144||paget apos s disease mammary
|
|
D010144||disease mammary paget
|
|
D010144||disease mammary paget apos s
|
|
D010144||mammary paget disease
|
|
D010144||mammary paget apos s disease
|
|
D010144||mammary pagets disease
|
|
D010144||paget disease breast
|
|
D010144||paget disease mammary
|
|
D010144||paget disease of breast
|
|
D010144||pagets disease breast
|
|
D010144||pagets disease mammary
|
|
D010144||paget apos s disease of breast
|
|
D010144||paget apos s disease of the breast
|
|
D010144||paget apos s disease of the nipple
|
|
D010144||paget apos s disease of the nipple and areola
|
|
D022125||lacerations
|
|
D022125||laceration
|
|
607483|C537658||basal ganglia disease biotin responsive
|
|
607483|C537658||bbgd
|
|
607483|C537658||biotin responsive basal ganglia disease
|
|
607483|C537658||encephalopathy thiamine responsive
|
|
607483|C537658||thiamine metabolism dysfunction syndrome 2 biotin or thiamine responsive type
|
|
607483|C537658||thmd2
|
|
C563761|609256||myopia 7
|
|
C563761|609256||myp7
|
|
612587|C567237||aneurysm intracranial berry 10
|
|
612587|C567237||anib10
|
|
D006850|236690||hydrocephalus normal pressure
|
|
D006850|236690||hakim apos s syndrome
|
|
D006850|236690||hakims syndrome
|
|
D006850|236690||hakim apos s syndromes
|
|
D006850|236690||hakim syndrome
|
|
D006850|236690||hakim syndromes
|
|
D006850|236690||normal pressure hydrocephalus
|
|
D006850|236690||nph normal pressure hydrocephalus
|
|
D006850|236690||nphs normal pressure hydrocephalus
|
|
D006850|236690||syndrome hakim
|
|
D006850|236690||syndrome hakim apos s
|
|
D006850|236690||syndromes hakim
|
|
D006850|236690||syndromes hakim apos s
|
|
D022124||hyperammonemia
|
|
D011488||protein deficiency
|
|
D011488||deficiencies protein
|
|
D011488||deficiency protein
|
|
D011488||protein deficiencies
|
|
D010157||palatal neoplasms
|
|
D010157||neoplasm palatal
|
|
D010157||neoplasms palatal
|
|
D010157||palatal neoplasm
|
|
611960||asthma related traits susceptibility to 7
|
|
611960||asrt7
|
|
D009175||mycoplasma infections
|
|
D009175||eperythrozoonoses
|
|
D009175||eperythrozoonosis
|
|
D009175||infection mycoplasma
|
|
D009175||infections mycoplasma
|
|
D009175||mycoplasma infection
|
|
607778|C564334||acrocapitofemoral dysplasia
|
|
607778|C564334||acfd
|
|
C536850|175780||familial porencephaly
|
|
C536850|175780||adt1p
|
|
C536850|175780||autosomal dominant porencephaly type 1
|
|
C536850|175780||familial porencephalic white matter disease
|
|
C536850|175780||hemiplegia infantile with porencephaly
|
|
C536850|175780||hemiplegia infantile with porencephaly porencephaly type 1
|
|
C536850|175780||infantile hemiplegia with porencephaly
|
|
C536850|175780||poren1
|
|
C536850|175780||porencephaly 1
|
|
C536850|175780||porencephaly familial
|
|
C536850|175780||porencephaly type 1
|
|
C536850|175780||porencephaly type 1 autosomal dominant
|
|
C536850|175780||t1p
|
|
C548084|613224||noonan syndrome 6
|
|
C548084|613224||ns6
|
|
C567215|612643||deafness autosomal dominant 3b
|
|
C567215|612643||dfna3b
|
|
D054508||acute radiation syndrome
|
|
D054508||acute radiation syndromes
|
|
D054508||radiation syndrome acute
|
|
D054508||radiation syndromes acute
|
|
D054506||chloracne
|
|
D054506||acne chlorine
|
|
D054506||acnes chlorine
|
|
D054506||chloracnes
|
|
D054506||chlorine acne
|
|
D054506||chlorine acnes
|
|
C565359|605115||hypertension early onset autosomal dominant with severe exacerbation in pregnancy
|
|
D009139||musculoskeletal abnormalities
|
|
D009139||abnormalities musculoskeletal
|
|
D009139||abnormality musculoskeletal
|
|
D009139||musculoskeletal abnormality
|
|
129500|D004476||ectodermal dysplasia
|
|
129500|D004476||anhidrotic ectodermal dysplasia
|
|
129500|D004476||anhidrotic ectodermal dysplasias
|
|
129500|D004476||anhidrotics ectodermal dysplasia
|
|
129500|D004476||anhydrotic ectodermal dysplasia
|
|
129500|D004476||anhydrotic ectodermal dysplasias
|
|
129500|D004476||aplasia cutis congenita
|
|
129500|D004476||aplasia cutis congenita nonsyndromic
|
|
129500|D004476||autosomal dominant hidrotic ectodermal dysplasia
|
|
129500|D004476||clouston hidrotic ectodermal dysplasia
|
|
129500|D004476||clouston apos s hidrotic ectodermal dysplasia
|
|
129500|D004476||clouston apos s syndrome
|
|
129500|D004476||cloustons syndrome
|
|
129500|D004476||clouston syndrome
|
|
129500|D004476||congenital ectodermal defect
|
|
129500|D004476||congenital ectodermal defects
|
|
129500|D004476||defect congenital ectodermal
|
|
129500|D004476||defects congenital ectodermal
|
|
129500|D004476||dysplasia anhidrotic ectodermal
|
|
129500|D004476||dysplasia anhidrotics ectodermal
|
|
129500|D004476||dysplasia anhydrotic ectodermal
|
|
129500|D004476||dysplasia ectodermal
|
|
129500|D004476||dysplasia hidrotic ectodermal
|
|
129500|D004476||dysplasia hydrotic ectodermal
|
|
129500|D004476||dysplasias anhidrotic ectodermal
|
|
129500|D004476||dysplasias anhydrotic ectodermal
|
|
129500|D004476||dysplasias ectodermal
|
|
129500|D004476||dysplasias hidrotic ectodermal
|
|
129500|D004476||dysplasias hydrotic ectodermal
|
|
129500|D004476||ectd2
|
|
129500|D004476||ectodermal defect congenital
|
|
129500|D004476||ectodermal defects congenital
|
|
129500|D004476||ectodermal dysplasia 2 clouston type
|
|
129500|D004476||ectodermal dysplasia 2 hidrotic
|
|
129500|D004476|224900|D053360||ectodermal dysplasia anhidrotic
|
|
129500|D004476||ectodermal dysplasia anhydrotic
|
|
129500|D004476||ectodermal dysplasia hidrotic
|
|
129500|D004476||ectodermal dysplasia hidrotic 2 formerly
|
|
129500|D004476||ectodermal dysplasia hidrotic autosomal dominant
|
|
129500|D004476||ectodermal dysplasia hydrotic
|
|
129500|D004476||ectodermal dysplasias
|
|
129500|D004476||ectodermal dysplasias anhidrotic
|
|
129500|D004476||ectodermal dysplasias anhydrotic
|
|
129500|D004476||ectodermal dysplasias hydrotic
|
|
129500|D004476||hed2 formerly
|
|
129500|D004476||hidrotic ectodermal dysplasia
|
|
129500|D004476||hidrotic ectodermal dysplasia autosomal dominant
|
|
129500|D004476||hidrotic ectodermal dysplasias
|
|
129500|D004476||hydrotic ectodermal dysplasia
|
|
129500|D004476||hydrotic ectodermal dysplasias
|
|
129500|D004476||syndrome clouston
|
|
129500|D004476||syndrome clouston apos s
|
|
D009137||muscular dystrophy animal
|
|
D009137||animal muscular dystrophies
|
|
D009137||animal muscular dystrophy
|
|
D009137||dystrophies animal muscular
|
|
D009137||dystrophy animal muscular
|
|
D009137||muscular dystrophies animal
|
|
D009145||mushroom poisoning
|
|
D009145||mushroom poisonings
|
|
D009145||poisoning mushroom
|
|
D009145||poisonings mushroom
|
|
C567373|612274||ciliary dyskinesia primary 8
|
|
C567373|612274||cild8
|
|
C567373|612274||ciliary dyskinesia primary 8 with or without situs inversus
|
|
D055653|158320||muir torre syndrome
|
|
D055653|158320||cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas
|
|
D055653|158320||mrtes
|
|
D055653|158320||syndrome muir torre
|
|
120100||caps1
|
|
120100|C569627||cold hypersensitivity
|
|
120100||cryopyrin associated periodic syndrome 1
|
|
120100||fcas
|
|
120100||fcu
|
|
D009140||musculoskeletal diseases
|
|
D009140||disease musculoskeletal
|
|
D009140||diseases musculoskeletal
|
|
D009140||musculoskeletal disease
|
|
C535699|601888||malignant hyperthermia susceptibility type 6
|
|
C535699|601888||malignant hyperpyrexia susceptibility type 6
|
|
C535699|601888||malignant hyperthermia susceptibility to 6
|
|
C535699|601888||mhs6
|
|
252150|C535811||molybdenum cofactor deficiency
|
|
252150|C535811||mocoda
|
|
252150|C535811|C565372||molybdenum cofactor deficiency complementation group a
|
|
252150|C535811||sulfite oxidase xanthine dehydrogenase and aldehyde oxidase combined deficiency of
|
|
D012784||shoulder fractures
|
|
D012784||fracture proximal humeral
|
|
D012784||fracture shoulder
|
|
D012784||fractures proximal humeral
|
|
D012784||fractures shoulder
|
|
D012784||humeral fracture proximal
|
|
D012784||humeral fractures proximal
|
|
D012784||proximal humeral fracture
|
|
D012784||proximal humeral fractures
|
|
D012784||shoulder fracture
|
|
D010123||oxyuriasis
|
|
D010123||aspiculariases
|
|
D010123||aspiculariasis
|
|
D010123||oxyuriases
|
|
D012783||shoulder dislocation
|
|
D012783||dislocation glenohumeral
|
|
D012783||dislocations glenohumeral
|
|
D012783||dislocation shoulder
|
|
D012783||dislocations shoulder
|
|
D012783||glenohumeral dislocation
|
|
D012783||glenohumeral dislocations
|
|
D012783||glenohumeral subluxation
|
|
D012783||glenohumeral subluxations
|
|
D012783||shoulder dislocations
|
|
D012783||subluxation glenohumeral
|
|
D012783||subluxations glenohumeral
|
|
239500|C538384||hyperprolinemia
|
|
239500|C538384||hpi
|
|
239500|C538384||hyperprolinemia type 1
|
|
239500|C538384||hyperprolinemia type i
|
|
239500|C538384||proline hydrogenase deficiency
|
|
239500|C538384||prolinemia
|
|
239500|C538384||proline oxidase deficiency
|
|
239500|C538384||pyrroline 5 carboxylate dehydrogenase deficiency
|
|
239500|C538384||pyrroline carboxylate dehydrogenase deficiency
|
|
132100||photoparoxysmal response 1
|
|
132100|D020195||epilepsy photogenic
|
|
132100||photoconvulsive reaction
|
|
132100||photosensitivity
|
|
132100||ppr
|
|
132100||ppr1
|
|
D054517||orbital cellulitis
|
|
D054517||cellulitides orbital
|
|
D054517||cellulitis orbital
|
|
D054517||orbital cellulitides
|
|
225753|C536716||pontocerebellar hypoplasia type 4
|
|
225753|C536716||encephalopathy fatal infantile with olivopontocerebellar hypoplasia
|
|
225753||pch4
|
|
C563677|610357||spastic paraplegia 30 autosomal recessive
|
|
C563677|610357||spg30
|
|
D009157||myasthenia gravis
|
|
D009157||generalized myasthenia gravis
|
|
D009157||myasthenia gravis generalized
|
|
D009157||myasthenia gravis ocular
|
|
D009157||ocular myasthenia gravis
|
|
D012797||sialometaplasia necrotizing
|
|
D012797||necrotizing sialometaplasia
|
|
D012797||necrotizing sialometaplasias
|
|
D012797||sialometaplasias necrotizing
|
|
C537449|300218||mental retardation x linked syndromic 7
|
|
C537449|300218||ahmad x linked mental retardation syndrome
|
|
C537449|300218||mrxs7
|
|
D011469||prostatic diseases
|
|
D011469||disease prostatic
|
|
D011469||diseases prostatic
|
|
D011469||prostatic disease
|
|
C565274|605934||holoprosencephaly 6
|
|
C565274|605934||hpe6
|
|
D012798||sialorrhea
|
|
D012798||drooling
|
|
D012798||hypersalivation
|
|
D009155||mutism
|
|
D009155||aphasia kussmaul
|
|
D009155||aphasia kussmaul apos s
|
|
D009155||conversion mutism
|
|
D009155||conversion mutisms
|
|
D009155||elective mutism
|
|
D009155||elective mutisms
|
|
D009155||kussmaul aphasia
|
|
D009155||kussmaul apos s aphasia
|
|
D009155||kussmauls aphasia
|
|
D009155||mutism conversion
|
|
D009155||mutism elective
|
|
D009155||mutism organic
|
|
D009155||mutisms
|
|
D009155||mutisms conversion
|
|
D009155||mutisms elective
|
|
D009155||mutism selective
|
|
D009155||mutisms organic
|
|
D009155||mutisms voluntary
|
|
D009155||mutism voluntary
|
|
D009155||organic mutism
|
|
D009155||organic mutisms
|
|
D009155||selective mutism
|
|
D009155||voluntary mutism
|
|
D009155||voluntary mutisms
|
|
D005199|227650||fanconi anemia
|
|
D005199|227650||anemia fanconi
|
|
D005199|227650||anemia fanconi apos s
|
|
D005199|227650||anemias fanconi
|
|
D005199|227650||estren dameshek variant of fanconi anemia included
|
|
D005199|227650||estren dameshek variant of fanconi pancytopenia included
|
|
D005199|227650||fanca
|
|
D005199|227650||fanconi anemia complementation group a
|
|
D005199|227650||fanconi anemia fa fanconi anemia estren dameshek variant included
|
|
D005199|227650||fanconi anemias
|
|
D005199|227650||fanconi hypoplastic anemia
|
|
D005199|227650||fanconi pancytopenia
|
|
D005199|227650||fanconi panmyelopathy
|
|
D005199|227650||fanconi apos s anemia
|
|
D012791||shy drager syndrome
|
|
D012791||autonomic failure progressive
|
|
D012791||autonomic failures progressive
|
|
D012791||dysautonomia orthostatic hypotension syndrome
|
|
D012791||dysautonomia orthostatic hypotension syndromes
|
|
D012791||dysautonomic orthostatic hypotension
|
|
D012791||dysautonomic orthostatic hypotensions
|
|
D012791||failure progressive autonomic
|
|
D012791||failures progressive autonomic
|
|
D012791||hypotension dysautonomic orthostatic
|
|
D012791||hypotensions dysautonomic orthostatic
|
|
D012791||hypotension syndrome dysautonomia orthostatic
|
|
D012791||hypotension syndromes dysautonomia orthostatic
|
|
D012791||idiopathic orthostatic hypotension shy drager type
|
|
D012791||orthostatic hypotension dysautonomic
|
|
D012791||orthostatic hypotensions dysautonomic
|
|
D012791||progressive autonomic failure
|
|
D012791||progressive autonomic failures
|
|
D012791||syndrome dysautonomia orthostatic hypotension
|
|
D012791||syndromes dysautonomia orthostatic hypotension
|
|
D012791||syndrome shy drager
|
|
605389|C537160||hypotrichosis simplex
|
|
605389|C537160||hereditary hypotrichosis simplex
|
|
605389|C537160|C566870|211900|D058747|214800||hhs
|
|
605389|C537160||hts
|
|
605389|C537160||hypotrichosis 1
|
|
605389|C537160||hypotrichosis simplex generalized hereditary
|
|
605389|C537160||hypt1
|
|
D012790||shwartzman phenomenon
|
|
D012790||phenomenon schwartzman
|
|
D012790||phenomenon shwartzman
|
|
D012790||schwartzman phenomenon
|
|
D012790||schwartzman reaction
|
|
D012790||schwartzman reactions
|
|
D012790||shwartzman reaction
|
|
D054515||vulvar vestibulitis
|
|
D054515||vestibulitides vulvar
|
|
D054515||vestibulitis vulvar
|
|
D054515||vulvar vestibulitides
|
|
D054515||vulvar vestibulitis syndrome
|
|
D012793||sialadenitis
|
|
D012793||adenitides salivary gland
|
|
D012793||adenitis salivary gland
|
|
D012793||chronic sialadenitides
|
|
D012793||chronic sialadenitis
|
|
D012793||inflammation salivary gland
|
|
D012793||inflammations salivary gland
|
|
D012793||irradiation induced sialadenitides
|
|
D012793||irradiation induced sialadenitis
|
|
D012793||salivary gland adenitides
|
|
D012793||salivary gland adenitis
|
|
D012793||salivary gland inflammation
|
|
D012793||salivary gland inflammations
|
|
D012793||sialadenitides
|
|
D012793||sialadenitides chronic
|
|
D012793||sialadenitides irradiation induced
|
|
D012793||sialadenitis chronic
|
|
D012793||sialadenitis irradiation induced
|
|
D012793||sialitides
|
|
D012793||sialitis
|
|
D012793||sialoadenitides
|
|
D012793||sialoadenitis
|
|
D054514||persistent hyperplastic primary vitreous
|
|
D054514||persistent fetal vasculature syndrome
|
|
D054514||persistent hyaloid arteries
|
|
D054514||persistent hyaloid artery
|
|
D054514||persistent hyaloid vasculature
|
|
D054514||persistent hyaloid vasculatures
|
|
C537839|609628||majeed syndrome
|
|
C537839|609628||chronic recurrent multifocal osteomyelitis congenital
|
|
C537839|609628||chronic recurrent multifocal osteomyelitis congenital dyserythropoietic anemia and neutrophilic dermatosis
|
|
C537839|609628||congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis
|
|
C537839|609628||dyserythropoietic anemia and neutrophilic dermatosis
|
|
D000788||angina pectoris variant
|
|
D000788||angina prinzmetal
|
|
D000788||angina prinzmetal apos s
|
|
D000788||prinzmetal angina
|
|
D000788||prinzmetal apos s angina
|
|
D000788||prinzmetals angina
|
|
D000788||variant angina pectoris
|
|
C536833|231670||glutaric aciduria 1
|
|
C536833|231670||ga i
|
|
C536833|231670||glutaric acidemia 1
|
|
C536833|231670||glutaric acidemia i
|
|
C536833|231670||glutaric acidemia type 1
|
|
C536833|231670||glutaric acidemia type i
|
|
C536833|231670||glutaric aciduria i
|
|
C536833|231670||glutaryl coa dehydrogenase deficiency
|
|
D000787||angina pectoris
|
|
D000787||angor pectoris
|
|
D000787||stenocardia
|
|
D000787||stenocardias
|
|
C564563|300215||lissencephaly x linked 2
|
|
C564563|300215||hydranencephaly and abnormal genitalia
|
|
C564563|300215||lissencephaly x linked with ambiguous genitalia
|
|
C564563|300215||lisx2
|
|
C564563|300215||xlag
|
|
C564563|300215||xlisg hydranencephaly and abnormal genitalia included
|
|
C541083|613282||non alcoholic fatty liver disease
|
|
C541083|613282||fatty liver disease nonalcoholic susceptibility to 1
|
|
C541083|613282||fatty liver disease nonalcoholic susceptibility to 2
|
|
C541083|613282||fatty liver nonalcoholic
|
|
C541083|613282||liver disease alcoholic susceptibility to 1 included
|
|
C541083|613282||nafld
|
|
C541083|613282||nafld1
|
|
C541083|613282||nafld2
|
|
C541083|613282||nonalcoholic fatty liver disease
|
|
D000785||aneurysm infected
|
|
D000785||aneurysm bacterial
|
|
D000785||aneurysm fungal
|
|
D000785||aneurysm mycotic
|
|
D000785||aneurysms bacterial
|
|
D000785||aneurysms fungal
|
|
D000785||aneurysms infected
|
|
D000785||aneurysms mycotic
|
|
D000785||bacterial aneurysm
|
|
D000785||bacterial aneurysms
|
|
D000785||fungal aneurysm
|
|
D000785||fungal aneurysms
|
|
D000785||infected aneurysm
|
|
D000785||infected aneurysms
|
|
D000785||mycotic aneurysm
|
|
D000785||mycotic aneurysms
|
|
D000789||angina unstable
|
|
D000789||angina at rest
|
|
D000789||angina pectoris unstable
|
|
D000789||angina pectori unstable
|
|
D000789||angina preinfarction
|
|
D000789||anginas preinfarction
|
|
D000789||anginas unstable
|
|
D000789||myocardial preinfarction syndrome
|
|
D000789||myocardial preinfarction syndromes
|
|
D000789||preinfarction angina
|
|
D000789||preinfarction anginas
|
|
D000789||preinfarction syndrome myocardial
|
|
D000789||preinfarction syndromes myocardial
|
|
D000789||syndrome myocardial preinfarction
|
|
D000789||syndromes myocardial preinfarction
|
|
D000789||unstable angina
|
|
D000789||unstable angina pectori
|
|
D000789||unstable angina pectoris
|
|
D000789||unstable anginas
|
|
C563278|160120||episodic ataxia type 1
|
|
C563278|160120||aem
|
|
C563278|160120||aemk
|
|
C563278|160120||ataxia episodic with myokymia
|
|
C563278|160120||continuous muscle fiber activity hereditary included
|
|
C563278|160120||ea1
|
|
C563278|160120||eam
|
|
C563278|160120||episodic ataxia with myokymia
|
|
C563278|160120||isaacs mertens syndrome included
|
|
C563278|160120||myokymia 1 with or without hypomagnesemia
|
|
C563278|160120||myokymia 1 with or without hypomagnesemia included
|
|
C563278|160120||myokymia with periodic ataxia
|
|
C563278|160120||myokymia with periodic ataxia myokymia 1 included
|
|
C563278|160120||paroxysmal ataxia with neuromyotonia hereditary
|
|
D000784||aneurysm dissecting
|
|
D000784||aneurysms dissecting
|
|
D000784||dissecting aneurysm
|
|
D000784||dissecting aneurysms
|
|
D000783||aneurysm
|
|
D000783||aneurysm fusiform
|
|
D000783||aneurysms
|
|
D000783||aneurysms fusiform
|
|
D000783||fusiform aneurysm
|
|
D000783||fusiform aneurysms
|
|
D000783||saccular aneurysm
|
|
D000782||aneuploidy
|
|
D000782||aneuploid
|
|
D000782||aneuploid cell
|
|
D000782||aneuploid cells
|
|
D000782||aneuploidies
|
|
D000782||aneuploids
|
|
D000782||cell aneuploid
|
|
D000782||cells aneuploid
|
|
C566450|610071||hyperparathyroidism 3
|
|
C566450|610071||hrpt3
|
|
C566450|610071||hyperparathyroidism familial isolated
|
|
D012766||pasteurellosis pneumonic
|
|
D012766||fever shipping
|
|
D012766||pneumonic pasteurellosis
|
|
D012766||shipping fever
|
|
D012614|240400||scurvy
|
|
D012614|240400||gulo nonfunctional included
|
|
D012614|240400||gulop included
|
|
D012614|240400||hypoascorbemia
|
|
D012614|240400||hypoascorbemias
|
|
D012614|240400||l gulonolactone oxidase nonfunctional included
|
|
D012614|240400||scorbutus
|
|
D012614|240400||scurvies
|
|
D012614|240400||vitamin c inability to synthesize l gulonolactone oxidase pseudogene included
|
|
D009123||muscle hypotonia
|
|
D009123||decreased muscle tone
|
|
D009123||flaccidity muscle
|
|
D009123||flaccidity muscular
|
|
D009123||flaccid muscle tone
|
|
D009123||floppy muscle
|
|
D009123||floppy muscles
|
|
D009123||hypomyotonia
|
|
D009123||hypotonia
|
|
D009123||hypotonia muscle
|
|
D009123||hypotonia muscular
|
|
D009123||hypotonia neonatal
|
|
D009123||hypotonias neonatal
|
|
D009123||hypotonias unilateral
|
|
D009123||hypotonia unilateral
|
|
D009123||hypotony muscle
|
|
D009123||muscle flaccidity
|
|
D009123||muscle floppy
|
|
D009123||muscle hypotony
|
|
D009123||muscles floppy
|
|
D009123||muscle tone atonic
|
|
D009123||muscle tone atonics
|
|
D009123||muscle tone decreased
|
|
D009123||muscle tone flaccid
|
|
D009123||muscle tone poor
|
|
D009123||muscular flaccidities
|
|
D009123||muscular flaccidity
|
|
D009123||muscular hypotonia
|
|
D009123||neonatal hypotonia
|
|
D009123||neonatal hypotonias
|
|
D009123||tone atonic muscle
|
|
D009123||tone poor muscle
|
|
D009123||unilateral hypotonia
|
|
D009122||muscle hypertonia
|
|
D009122||detrusor muscle hypertonia
|
|
D009122||detrusor muscle hypertonias
|
|
D009122||hypermyotonia
|
|
D009122||hypermyotonias
|
|
D009122||hypertonia detrusor muscle
|
|
D009122||hypertonia infantile
|
|
D009122||hypertonia muscle
|
|
D009122||hypertonia neonatal
|
|
D009122||hypertonias detrusor muscle
|
|
D009122||hypertonias infantile
|
|
D009122||hypertonias muscle
|
|
D009122||hypertonias neonatal
|
|
D009122||hypertonia sphincter
|
|
D009122||hypertonias sphincter
|
|
D009122||hypertonias transient
|
|
D009122||hypertonia transient
|
|
D009122||hypertonicities muscular
|
|
D009122||hypertonicity muscular
|
|
D009122||increased muscle tone
|
|
D009122||infantile hypertonia
|
|
D009122||infantile hypertonias
|
|
D009122||muscle hypertonia detrusor
|
|
D009122||muscle hypertonias
|
|
D009122||muscle hypertonias detrusor
|
|
D009122||muscle tone increased
|
|
D009122||muscular hypertonicities
|
|
D009122||muscular hypertonicity
|
|
D009122||neonatal hypertonia
|
|
D009122||neonatal hypertonias
|
|
D009122||sphincter hypertonia
|
|
D009122||sphincter hypertonias
|
|
D009122||tone increased muscle
|
|
D009122||transient hypertonia
|
|
D009122||transient hypertonias
|
|
D009120||muscle cramp
|
|
D009120||cramp
|
|
D009120||cramp limb
|
|
D009120||cramp muscle
|
|
D009120||cramp muscular
|
|
D009120||cramps
|
|
D009120||cramps limb
|
|
D009120||cramps muscle
|
|
D009120||cramps muscular
|
|
D009120||limb cramp
|
|
D009120||limb cramps
|
|
D009120||muscle cramps
|
|
D009120||muscular cramp
|
|
D009120||muscular cramps
|
|
D012769||shock
|
|
D012769||circulatory collapse
|
|
D012769||circulatory failure
|
|
D012769||collapse circulatory
|
|
D012769||failure circulatory
|
|
D012769||hypovolemic shock
|
|
D012769||shock hypovolemic
|
|
145900|D015417||hereditary sensory and motor neuropathy
|
|
145900|D015417||alpha methylacyl coa racemase
|
|
145900|D015417||amacr
|
|
145900|D015417||charcot marie tooth disease demyelinating type 4f
|
|
145900|D015417||charcot marie tooth disease type 3
|
|
145900|D015417||cmt3
|
|
145900|D015417||cmt4f
|
|
145900|D015417||dejerine sottas disease
|
|
145900|D015417||dejerine sottas hypertrophic neuropathy
|
|
145900|D015417||dejerine sottas neuropathy
|
|
145900|D015417|C538392||dejerine sottas syndrome
|
|
145900|D015417||disease dejerine sottas
|
|
145900|D015417||dsn
|
|
145900|D015417|C535601|300018||dss
|
|
145900|D015417||herditary sensory and motor neuropathy
|
|
145900|D015417||hereditary motor and sensory neuropathies
|
|
145900|D015417||hereditary motor and sensory neuropathy
|
|
145900|D015417||hereditary motor and sensory neuropathy 3
|
|
145900|D015417||hereditary motor and sensory neuropathy type iii
|
|
145900|D015417||hereditary type iii motor and sensory neuropathy
|
|
145900|D015417||hereditary type vii motor and sensory neuropathy
|
|
145900|D015417||hmsn
|
|
145900|D015417||hmsn3
|
|
145900|D015417||hmsn type iii
|
|
145900|D015417||hmsn type iiis
|
|
145900|D015417||hmsn type vii
|
|
145900|D015417||hmsn type viis
|
|
145900|D015417||hypertrophic neuropathy of dejerine sottas
|
|
145900|D015417||neuropathies hereditary motor and sensory
|
|
145900|D015417||neuropathy dejerine sottas
|
|
145900|D015417||syndrome dejerine sottas
|
|
145900|D015417||type vii hmsn
|
|
608219|C564273||deafness autosomal recessive 38
|
|
608219|C564273||dfnb38
|
|
D000799||angioedema
|
|
D000799||angioedemas
|
|
D000799||angioneurotic edema
|
|
D000799||angioneurotic edemas
|
|
D000799||edema angioneurotic
|
|
D000799||edema quincke apos s
|
|
D000799||edemas angioneurotic
|
|
D000799||giant urticaria
|
|
D000799||giant urticarias
|
|
D000799||quincke edema
|
|
D000799||quincke apos s edema
|
|
D000799||quinckes edema
|
|
D000799||urticaria giant
|
|
D000799||urticarias giant
|
|
D000798||angiomatosis
|
|
D000798||angiomatoses
|
|
D054882|613571||antley bixler syndrome phenotype
|
|
D054882|613571||adrenal hyperplasia congenital due to cytochrome p450 oxidoreductase deficiency
|
|
D054882|613571||antley bixler syndrome
|
|
D054882|613571||antley bixler syndrome autosomal dominant
|
|
D054882|613571||antley bixler syndrome like phenotype with disordered steroidogenesis
|
|
D054882|613571||antley bixler syndrome with disordered steroidogenesis
|
|
D054882|613571||combined partial deficiency of 17 hydroxylase and 21 hydroxylase
|
|
D054882|613571||congenital adrenal hyperplasia due to apparent combined p450c17 and p450c21 deficiency
|
|
D054882|613571||cytochrome p450 oxidoreductase deficiency
|
|
D054882|613571||disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency
|
|
D054882|613571||disordered steroidogenesis due to por deficiency
|
|
D054882|613571||multisynostotic osteodysgenesis
|
|
D054882|613571|207410||multisynostotic osteodysgenesis with long bone fractures
|
|
D054882|613571||osteodysgenesis multisynostotic
|
|
D054882|613571|207410||osteodysgenesis multisynostotic with fractures
|
|
D054882|613571||phenotype antley bixler syndrome
|
|
D054882|613571||por deficiency
|
|
D054882|613571||syndrome antley bixler
|
|
D054882|613571||syndrome phenotype antley bixler
|
|
D054882|613571||syndromes trapezoidocephaly synostosis
|
|
D054882|613571||syndrome trapezoidocephaly synostosis
|
|
D054882|613571|207410||trapezoidocephaly synostosis syndrome
|
|
D054882|613571||trapezoidocephaly synostosis syndromes
|
|
C566603|601941||diabetes mellitus insulin dependent 6
|
|
C566603|601941||aitd5 included
|
|
C566603|601941||iddm6
|
|
C566603|601941||insulin dependent diabetes mellitus 6
|
|
C566603|601941||insulin dependent diabetes mellitus 6 autoimmune thyroid disease susceptibility to 5 included
|
|
C565311|605637||inclusion body myopathy 3 autosomal dominant
|
|
C565311|605637||ibm3
|
|
C565311|605637||myopathy with congenital joint contractures ophthalmoplegia and rimmed vacuoles
|
|
D000796||angiolymphoid hyperplasia with eosinophilia
|
|
D000796||disease kimura
|
|
D000796||eosinophilic granuloma of soft tissue
|
|
D000796||eosinophilic hyperplastic lymphogranuloma
|
|
D000796||eosinophilic hyperplastic lymphogranulomas
|
|
D000796||eosinophilic lymphofollicular granuloma
|
|
D000796||eosinophilic lymphofollicular granulomas
|
|
D000796||eosinophilic lymphofolliculoses
|
|
D000796||eosinophilic lymphofolliculosis
|
|
D000796||granuloma eosinophilic lymphofollicular
|
|
D000796||granuloma pseudopyogenic
|
|
D000796||granulomas eosinophilic lymphofollicular
|
|
D000796||granulomas pseudopyogenic
|
|
D000796||hyperplastic lymphogranuloma eosinophilic
|
|
D000796||hyperplastic lymphogranulomas eosinophilic
|
|
D000796||kimura disease
|
|
D000796||lymphofollicular granuloma eosinophilic
|
|
D000796||lymphofollicular granulomas eosinophilic
|
|
D000796||lymphofolliculoses eosinophilic
|
|
D000796||lymphofolliculosis eosinophilic
|
|
D000796||lymphogranuloma eosinophilic hyperplastic
|
|
D000796||lymphogranulomas eosinophilic hyperplastic
|
|
D000796||pseudopyogenic granuloma
|
|
D000796||pseudopyogenic granulomas
|
|
C537706|259690||kaler garrity stern syndrome
|
|
C537706|259690||osteopenia and sparse hair
|
|
C537706|259690||osteopenia mental retardation sparse hair
|
|
D009128||muscle spasticity
|
|
D009128||clasp knife spasticity
|
|
D009128||spastic
|
|
D009128||spasticity clasp knife
|
|
D009128||spasticity muscle
|
|
D000794||angiokeratoma
|
|
D000794||angiokeratomas
|
|
D009127||muscle rigidity
|
|
D009127||catatonic rigidity
|
|
D009127||cogwheel rigidities
|
|
D009127||cogwheel rigidity
|
|
D009127||extensor rigidity
|
|
D009127||extrapyramidal rigidity
|
|
D009127||gegenhalten
|
|
D009127||gegenhaltens
|
|
D009127||muscular rigidity
|
|
D009127||nuchal rigidity
|
|
D009127||rigidities cogwheel
|
|
D009127||rigidity catatonic
|
|
D009127||rigidity cogwheel
|
|
D009127||rigidity extensor
|
|
D009127||rigidity extrapyramidal
|
|
D009127||rigidity muscle
|
|
D009127||rigidity muscular
|
|
D009127||rigidity nuchal
|
|
D000793||angioid streaks
|
|
D000793||angioid streak
|
|
D000793||streak angioid
|
|
D000793||streaks angioid
|
|
D024741||cardiomyopathy hypertrophic familial
|
|
D024741||asymmetric septal hypertrophy familial
|
|
D024741||cardiomyopathies familial hypertrophic
|
|
D024741||cardiomyopathy familial hypertrophic
|
|
D024741||familial hypertrophic cardiomyopathies
|
|
D024741||familial hypertrophic cardiomyopathy
|
|
D024741||familial ventricular hypertrophies
|
|
D024741||familial ventricular hypertrophy
|
|
D024741||hereditary ventricular hypertrophies
|
|
D024741||hereditary ventricular hypertrophy
|
|
D024741||hypertrophic cardiomyopathies familial
|
|
D024741||hypertrophic cardiomyopathy familial
|
|
D024741||hypertrophies hereditary ventricular
|
|
D024741||hypertrophy familial ventricular
|
|
D024741||hypertrophy hereditary ventricular
|
|
D024741||obstructive asymmetric septal hypertrophy
|
|
D024741||ventricular hypertrophies familial
|
|
D024741||ventricular hypertrophies hereditary
|
|
D024741||ventricular hypertrophy familial
|
|
D009136||muscular dystrophies
|
|
D009136||dystrophies muscular
|
|
D009136||dystrophy muscular
|
|
D009136||muscular dystrophy
|
|
D009136||myodystrophica
|
|
D009136||myodystrophicas
|
|
D009136||myodystrophies
|
|
D009136||myodystrophy
|
|
D012778||short bowel syndrome
|
|
D012778||bowel syndrome short
|
|
D012778||bowel syndromes short
|
|
D012778||short bowel syndromes
|
|
D012778||syndrome short bowel
|
|
D012778||syndromes short bowel
|
|
D009135||muscular diseases
|
|
D009135||muscle disorder
|
|
D009135||muscle disorders
|
|
D009135||muscular disease
|
|
D009135||myopathic condition
|
|
D009135||myopathic conditions
|
|
D009135||myopathies
|
|
D009135||myopathy
|
|
D009134||muscular atrophy spinal
|
|
D009134||adult onset spinal muscular atrophy
|
|
D009134||adult spinal muscular atrophy
|
|
D009134||amyotrophies spinal
|
|
D009134|181405||amyotrophy neurogenic scapuloperoneal new england type
|
|
D009134||amyotrophy spinal
|
|
D009134||atrophies progressive muscular
|
|
D009134||atrophy myelopathic muscular
|
|
D009134||atrophy progressive muscular
|
|
D009134||atrophy spinal muscular
|
|
D009134||bulbospinal neuronopathies
|
|
D009134||bulbospinal neuronopathy
|
|
D009134||distal spinal muscular atrophy
|
|
D009134||hereditary motor neuronopathies
|
|
D009134||hereditary motor neuronopathy
|
|
D009134||motor neuronopathies hereditary
|
|
D009134||motor neuronopathy hereditary
|
|
D009134||muscular atrophies progressive
|
|
D009134||muscular atrophy adult spinal
|
|
D009134||muscular atrophy myelopathic
|
|
D009134||muscular atrophy progressive
|
|
D009134||myelopathic muscular atrophy
|
|
D009134||myelopathic muscular atrophy progressive
|
|
D009134||neuronopathies bulbospinal
|
|
D009134||neuronopathies hereditary motor
|
|
D009134||neuronopathy bulbospinal
|
|
D009134||neuronopathy hereditary motor
|
|
D009134||oculopharyngeal spinal muscular atrophy
|
|
D009134||progressive muscular atrophies
|
|
D009134||progressive muscular atrophy
|
|
D009134||progressive myelopathic muscular atrophy
|
|
D009134||progressive proximal myelopathic muscular atrophy
|
|
D009134||proximal myelopathic muscular atrophy progressive
|
|
D009134||scapuloperoneal form of spinal muscular atrophy
|
|
D009134|181405||scapuloperoneal spinal muscular atrophy
|
|
D009134||spinal amyotrophies
|
|
D009134||spinal amyotrophy
|
|
D009134||spinal muscular atrophy
|
|
D009134||spinal muscular atrophy distal
|
|
D009134||spinal muscular atrophy oculopharyngeal
|
|
D009134||spinal muscular atrophy scapuloperoneal
|
|
D009134||spinal muscular atrophy scapuloperoneal form
|
|
D009133||muscular atrophy
|
|
D009133||atrophies muscle
|
|
D009133||atrophies muscular
|
|
D009133||atrophies neurogenic muscular
|
|
D009133||atrophies neurotrophic muscular
|
|
D009133||atrophy muscle
|
|
D009133||atrophy muscular
|
|
D009133||atrophy neurogenic muscular
|
|
D009133||atrophy neurotrophic muscular
|
|
D009133||muscle atrophies
|
|
D009133||muscle atrophy
|
|
D009133||muscular atrophies
|
|
D009133||muscular atrophies neurogenic
|
|
D009133||muscular atrophies neurotrophic
|
|
D009133||muscular atrophy neurogenic
|
|
D009133||muscular atrophy neurotrophic
|
|
D009133||neurogenic muscular atrophies
|
|
D009133||neurogenic muscular atrophy
|
|
D009133||neurotrophic muscular atrophies
|
|
D009133||neurotrophic muscular atrophy
|
|
246200|D056731||donohue syndrome
|
|
246200|D056731||leprechaunism
|
|
246200|D056731||leprechaunism insulin receptor defect in included
|
|
246200|D056731||leprechaunisms
|
|
246200|D056731||mendenhall syndrome
|
|
246200|D056731||pineal hyperplasia insulin resistant diabetes mellitus and somatic abnormalities
|
|
246200|D056731||rabson mendenhall syndrome
|
|
246200|D056731||syndrome donohue
|
|
246200|D056731||syndrome mendenhall
|
|
246200|D056731||syndrome rabson mendenhall
|
|
D012770||shock cardiogenic
|
|
D012770||cardiogenic shock
|
|
D053202||urinary incontinence urge
|
|
D053202||incontinence urge
|
|
D053202||incontinence urinary reflex
|
|
D053202||urge incontinence
|
|
D053202||urinary reflex incontinence
|
|
D053202||urinary urge incontinence
|
|
D053201||urinary bladder overactive
|
|
D053201||bladder overactive
|
|
D053201||detrusor function overactive
|
|
D053201||detrusor overactive
|
|
D053201||overactive bladder
|
|
D053201||overactive detrusor
|
|
D053201||overactive detrusor function
|
|
D053201||overactive urinary bladder
|
|
D012773||shock surgical
|
|
D012773||surgical shock
|
|
D012773||surgical shocks
|
|
D053207||diurnal enuresis
|
|
D053207||daytime urinary incontinence
|
|
D053207||daytime wetting
|
|
D053207||enuresis diurnal
|
|
D053207||incontinence daytime urinary
|
|
D053207||urinary incontinence daytime
|
|
D053207||wetting daytime
|
|
D012774||shock traumatic
|
|
D012774||traumatic shock
|
|
D054537||atrioventricular block
|
|
D054537||atrioventricular blocks
|
|
D054537||atrioventricular conduction block
|
|
D054537||atrioventricular conduction blocks
|
|
D054537||av block
|
|
D054537||av blocks
|
|
D054537||block av
|
|
D054537||blocks av
|
|
D054537||conduction block atrioventricular
|
|
D054537||conduction blocks atrioventricular
|
|
D012771||shock hemorrhagic
|
|
D012771||hemorrhagic shock
|
|
D008527|155255||medulloblastoma
|
|
D008527|155255||adult medulloblastoma
|
|
D008527|155255||adult medulloblastomas
|
|
D008527|155255||arachnoidal cerebellar sarcoma circumscribed
|
|
D008527|155255||childhood medulloblastoma
|
|
D008527|155255||childhood medulloblastomas
|
|
D008527|155255||desmoplastic medulloblastoma
|
|
D008527|155255||desmoplastic medulloblastomas
|
|
D008527|155255||mben included
|
|
D008527|155255||mdb
|
|
D008527|155255||medulloblastoma adult
|
|
D008527|155255||medulloblastoma childhood
|
|
D008527|155255||medulloblastoma desmoplastic
|
|
D008527|155255||medulloblastoma desmoplastic included
|
|
D008527|155255||medulloblastoma melanocytic
|
|
D008527|155255||medulloblastomas
|
|
D008527|155255||medulloblastomas adult
|
|
D008527|155255||medulloblastomas childhood
|
|
D008527|155255||medulloblastomas desmoplastic
|
|
D008527|155255||medulloblastomas melanocytic
|
|
D008527|155255||medulloblastoma with extensive nodularity included
|
|
D008527|155255||medullomyoblastoma
|
|
D008527|155255||medullomyoblastomas
|
|
D008527|155255||melanocytic medulloblastoma
|
|
D008527|155255||melanocytic medulloblastomas
|
|
D008527|155255||sarcoma cerebellar circumscribed arachnoidal
|
|
D012772||shock septic
|
|
D012772||endotoxic shock
|
|
D012772||septic shock
|
|
D012772||shock endotoxic
|
|
D012772||shock syndromes toxic
|
|
D012772||shock syndrome toxic
|
|
D012772||shock toxic
|
|
D012772||syndromes toxic shock
|
|
D012772||syndrome toxic shock
|
|
D012772||toxic shock
|
|
D012772||toxic shock syndrome
|
|
D012772||toxic shock syndromes
|
|
C538215|125400||dentin dysplasia type 1
|
|
C538215|125400||dentin dysplasia shields type i
|
|
C538215|125400||dentin dysplasia type i
|
|
C538215|125400||dtdp1
|
|
C538215|125400||radicular dentin dysplasia
|
|
C538215|125400||radicular dentin dysplasia dentin dysplasia type i with extreme microdontia and misshapen teeth included
|
|
C538215|125400||rootless teeth
|
|
D046150|262500||laron syndrome
|
|
D046150|262500||dwarfism ii pituitary
|
|
D046150|262500||dwarfism iis pituitary
|
|
D046150|262500||dwarfism laron
|
|
D046150|262500||gh resistance primary
|
|
D046150|262500||growth hormone insensitivity syndrome
|
|
D046150|262500||growth hormone receptor defect
|
|
D046150|262500||growth hormone receptor deficiency
|
|
D046150|262500||laron dwarfism
|
|
D046150|262500||laron type dwarfism i
|
|
D046150|262500||pituitary dwarfism ii
|
|
D046150|262500||pituitary dwarfism iis
|
|
D046150|262500||primary gh resistance
|
|
D046150|262500||primary growth hormone resistance
|
|
D046150|262500||severe gh insensitivity
|
|
D046150|262500||syndrome laron
|
|
D013661|272800||tay sachs disease
|
|
D013661|272800||amaurotic familial idiocy
|
|
D013661|272800||amaurotic idiocy familial
|
|
D013661|272800||b variant gm2 gangliosidoses
|
|
D013661|272800||b variant gm2 gangliosidosis
|
|
D013661|272800||deficiency disease hexosaminidase a
|
|
D013661|272800||deficiency hexosaminidase a
|
|
D013661|272800||deficiency hexosaminidase alpha subunit variant b
|
|
D013661|272800||familial amaurotic idiocy
|
|
D013661|272800||gangliosidosis gm2 b variant
|
|
D013661|272800||gangliosidosis gm2 type 1
|
|
D013661|272800||gangliosidosis g m2 type i
|
|
D013661|272800||gangliosidosis gm2 type i
|
|
D013661|272800||gm2 gangliosidosis adult chronic type included
|
|
D013661|272800||gm2 gangliosidosis b variant
|
|
D013661|272800||gm2 gangliosidosis type 1
|
|
D013661|272800||g m2 gangliosidosis type i
|
|
D013661|272800||gm2 gangliosidosis type i
|
|
D013661|272800||gm2 gangliosidosis variant b1 included
|
|
D013661|272800||hexa deficiency
|
|
D013661|272800||hexa deficiency tay sachs disease juvenile included
|
|
D013661|272800||hexosaminidase a deficiency
|
|
D013661|272800||hexosaminidase a deficiency adult type included
|
|
D013661|272800||hexosaminidase a deficiency disease
|
|
D013661|272800||hexosaminidase alpha subunit deficiency variant b
|
|
D013661|272800||sphingolipidosis tay sachs
|
|
D013661|272800||tay sachs disease b variant
|
|
D013661|272800||tay sachs disease pseudo ab variant included
|
|
D013661|272800||tay sachs disease variant b1 included
|
|
D013661|272800||tay sachs sphingolipidosis
|
|
D013661|272800||tsd
|
|
D013661|272800||type i gm2 gangliosidosis
|
|
226700|D016109||epidermolysis bullosa junctional
|
|
226700|D016109||bullosa herlitz pearson type epidermolysis
|
|
226700|D016109||bullosa letali epidermolysis
|
|
226700|D016109||bullosa letalis epidermolysis
|
|
226700|D016109||disease herlitz
|
|
226700|D016109||disease herlitz apos s
|
|
226700|D016109||epidermolysis bullosa generalized atrophic benign
|
|
226700|D016109||epidermolysis bullosa herlitz pearson type
|
|
226700|D016109||epidermolysis bullosa junctional herlitz pearson type
|
|
226700|D016109||epidermolysis bullosa junctional herlitz type
|
|
226700|D016109|226650|C562639||epidermolysis bullosa junctionalis disentis type
|
|
226700|D016109||epidermolysis bullosa junctionalis herlitz type
|
|
226700|D016109|226650|C562639||epidermolysis bullosa junctionalis progressive
|
|
226700|D016109|226650|C562639||epidermolysis bullosa junctionalis severe nonlethal
|
|
226700|D016109||epidermolysis bullosa letali
|
|
226700|D016109||epidermolysis bullosa letalis
|
|
226700|D016109||epidermolysis bullosa progressiva
|
|
226700|D016109||herlitz disease
|
|
226700|D016109||herlitz pearson type epidermolysis bullosa
|
|
226700|D016109||herlitz apos s disease
|
|
226700|D016109||herlitzs disease
|
|
226700|D016109||jeb herlitz type
|
|
226700|D016109||junctional epidermolysis bullosa
|
|
226700|D016109||letali epidermolysis bullosa
|
|
226700|D016109||letalis epidermolysis bullosa
|
|
226700|D016109||lethal junctional epidermolysis bullosa
|
|
C535971||coloboma cleft lip palate and mental retardation syndrome
|
|
C535971||coloboma microphthalmos syndrome
|
|
C535971||coloboma microphthalmos syndrome associated with sensorineural hearing loss hematuria and cleft lip palate
|
|
C535971||uveal coloboma cleft lip palate mental retardation syndrome
|
|
C536093|600080||myelocytic leukemia like syndrome familial chronic
|
|
C536093|600080||cml like syndrome familial
|
|
259100||hypertrophic osteoarthropathy primary autosomal recessive 1
|
|
259100||cio included
|
|
259100||coa included
|
|
259100||currarino idiopathic osteoarthropathy included
|
|
259100||familial idiopathic osteoarthropathy of childhood included
|
|
259100||pdp autosomal recessive
|
|
259100||phoar1
|
|
259100||pho autosomal recessive
|
|
259100||touraine solente gole syndrome cranioosteoarthropathy included
|
|
188580||thyrotoxic periodic paralysis susceptibility to 1
|
|
188580||ttpp1
|
|
D009102||multiple organ failure
|
|
D009102||failure multiple organ
|
|
D009102||mods
|
|
D009102||multiple organ dysfunction syndrome
|
|
D009102||multiple organ failures
|
|
D009102||organ dysfunction syndrome multiple
|
|
D009102||organ failure multiple
|
|
C535969||coloboma of macula type b brachydactyly
|
|
C535969||coloboma of macula with type b brachydactyly
|
|
C535969||sorsby syndrome
|
|
D009100||multiple carboxylase deficiency
|
|
D009100||carboxylase deficiencies combined
|
|
D009100||carboxylase deficiencies multiple
|
|
D009100||carboxylase deficiency combined
|
|
D009100||carboxylase deficiency multiple
|
|
D009100||combined carboxylase deficiencies
|
|
D009100||combined carboxylase deficiency
|
|
D009100||deficiencies combined carboxylase
|
|
D009100||deficiencies multiple carboxylase
|
|
D009100||deficiency combined carboxylase
|
|
D009100||deficiency multiple carboxylase
|
|
D009100||multiple carboxylase deficiencies
|
|
D010022|166600||osteopetrosis
|
|
D010022|166600||albers schoenberg disease
|
|
D010022|166600||albers schonberg disease
|
|
D010022|166600||albers sch 246 nberg disease
|
|
D010022|166600||albers schonberg disease autosomal dominant
|
|
D010022|166600||autosomal dominant osteopetrosis type 2
|
|
D010022|166600||congenital osteopetrosis
|
|
D010022|166600||disease albers schoenberg
|
|
D010022|166600||disease albers schonberg
|
|
D010022|166600||disease albers sch 246 nberg
|
|
D010022|166600||disease marble bone
|
|
D010022|166600||marble bone disease
|
|
D010022|166600||marble bones autosomal dominant
|
|
D010022|166600||opta2
|
|
D010022|166600||osteopetroses
|
|
D010022|166600||osteopetrosis autosomal dominant 2
|
|
D010022|166600||osteopetrosis autosomal dominant type 2
|
|
D010022|166600||osteopetrosis autosomal dominant type ii
|
|
D010022|166600||osteosclerosis fragilis
|
|
D010022|166600||osteosclerosis fragilis generalisata
|
|
D010022|166600||osteosclerosis fragilis generalisatas
|
|
D012749||sexually transmitted diseases
|
|
D012749||disease sexually transmitted
|
|
D012749||diseases sexually transmitted
|
|
D012749||diseases venereal
|
|
D012749||disease venereal
|
|
D012749||sexually transmitted disease
|
|
D012749||stds
|
|
D012749||venereal disease
|
|
D012749||venereal diseases
|
|
C537472|309605||miles carpenter x linked mental retardation syndrome
|
|
C537472|309605||mcs
|
|
C537472|309605||mental retardation x linked syndromic 4
|
|
C537472|309605||mental retardation x linked with congenital contractures and low fingertip arches
|
|
C537472|309605||mrxs4
|
|
C564507|300476||cone rod dystrophy x linked 3
|
|
C564507|300476||cordx3
|
|
C535964||collagenopathy type 2 alpha 1
|
|
C535964||cartilage collagen
|
|
C535963||cole carpenter syndrome
|
|
C535966||colloid cysts of third ventricle
|
|
C535966||neuroepithelial cysts of third ventricle
|
|
D054549||takotsubo cardiomyopathy
|
|
D054549||apical ballooning syndrome
|
|
D054549||broken heart syndrome
|
|
D054549||cardiomyopathy stress
|
|
D054549||cardiomyopathy takotsubo
|
|
D054549||cardiomyopathy tako tsubo
|
|
D054549||left ventricular apical ballooning syndrome
|
|
D054549||stress cardiomyopathy
|
|
D054549||syndrome apical ballooning
|
|
D054549||syndrome broken heart
|
|
D054549||syndromes broken heart
|
|
D054549||syndromes tako tsubo
|
|
D054549||syndrome tako tsubo
|
|
D054549||tako tsubo cardiomyopathy
|
|
D054549||tako tsubo syndrome
|
|
D054549||takotsubo syndrome
|
|
D054549||tako tsubo syndromes
|
|
D054549||transient apical ballooning syndrome
|
|
C535968||hereditary macular coloboma
|
|
C535968||agenesis of macula
|
|
C535968||coloboma of macula
|
|
C535968||macular coloboma
|
|
C535967||coloboma of alar nasal cartilages with telecanthus
|
|
C535967||alar nasal cartilages coloboma of with telecanthus
|
|
C535967||frontonasal dysplasia with alar clefts
|
|
C566501|609633||major affective disorder 3
|
|
C566501|609633||bipolar affective disorder early onset
|
|
C566501|609633||bpeo
|
|
C566501|609633||mafd3
|
|
604804||microcephaly 3 primary autosomal recessive
|
|
604804||mcph3
|
|
C536534|192350||vater association
|
|
C536534|192350||vacterl association included
|
|
C536534|192350||vertebral defects anal atresia tracheoesophageal fistula with esophageal atresia and radial dysplasia
|
|
277180|C535984||congenital bilateral aplasia of vas deferens
|
|
277180|C535984||absence of vas deferens
|
|
277180|C535984||absent vasa
|
|
277180|C535984||cavd
|
|
277180|C535984||cbavd
|
|
277180|C535984||congenital absence of vas deferens
|
|
277180|C535984||congenital aplasia of vas deferens
|
|
277180|C535984||congenital bilateral absence of the vas deferens
|
|
277180|C535984||congenital bilateral absence of vas deferens
|
|
277180|C535984||vas deferens congenital bilateral aplasia of
|
|
C535981||congenital alopecia x linked
|
|
C535981||alopecia congenital
|
|
C535981||congenital alopecia
|
|
606764|D046152||gastrointestinal stromal tumors
|
|
606764|D046152||gastrointestinal stromal neoplasm
|
|
606764|D046152||gastrointestinal stromal neoplasms
|
|
606764|D046152||gastrointestinal stromal sarcoma
|
|
606764|D046152||gastrointestinal stromal tumor
|
|
606764|D046152|C564650|606864||gist
|
|
606764|D046152||neoplasm gastrointestinal stromal
|
|
606764|D046152||neoplasms gastrointestinal stromal
|
|
606764|D046152||stromal neoplasm gastrointestinal
|
|
606764|D046152||stromal neoplasms gastrointestinal
|
|
606764|D046152||stromal tumor gastrointestinal
|
|
606764|D046152||stromal tumors gastrointestinal
|
|
606764|D046152||tumor gastrointestinal stromal
|
|
606764|D046152||tumors gastrointestinal stromal
|
|
D009107||mumps
|
|
D009107||epidemic parotitides
|
|
D009107||epidemic parotitis
|
|
D009107||parotitides epidemic
|
|
D009107||parotitis epidemic
|
|
C565504|236680||hydrolethalus syndrome 1
|
|
C565504|236680||hls1
|
|
D009105||multiple personality disorder
|
|
D009105||disorder dissociative identity
|
|
D009105||disorder multiple identity
|
|
D009105||disorder multiple personality
|
|
D009105||dissociative identity disorder
|
|
D009105||dual personality
|
|
D009105||identity disorder dissociative
|
|
D009105||identity disorder multiple
|
|
D009105||multiple identity disorder
|
|
D009105||multiple identity disorders
|
|
D009105||multiple personalities
|
|
D009105||multiple personality
|
|
D009105||multiple personality disorders
|
|
D009105||personalities dual
|
|
D009105||personalities multiple
|
|
D009105||personality disorder multiple
|
|
D009105||personality disorders multiple
|
|
D009105||personality dual
|
|
D009105||personality multiple
|
|
D009104||multiple trauma
|
|
D009104||injuries multiple
|
|
D009104||injury multiple
|
|
D009104||multiple injuries
|
|
D009104||multiple injury
|
|
D009104||multiple traumas
|
|
D009104||multiple wound
|
|
D009104||multiple wounds
|
|
D009104||polytrauma
|
|
D009104||polytraumas
|
|
D009104||trauma multiple
|
|
D009104||traumas multiple
|
|
D009104||wound multiple
|
|
D009104||wounds multiple
|
|
D055882||nevus halo
|
|
D055882||halo nevi
|
|
D055882||halo nevus
|
|
D055882||leukoderma acquisitum centrifugum of sutton
|
|
D055882||nevi halo
|
|
D012753||shared paranoid disorder
|
|
D012753||disorder shared paranoid
|
|
D012753||disorder shared psychotic
|
|
D012753||disorders shared paranoid
|
|
D012753||disorders shared psychotic
|
|
D012753||folie a deux
|
|
D012753||folie a trois
|
|
D012753||paranoid disorder shared
|
|
D012753||paranoid disorders shared
|
|
D012753||psychotic disorder shared
|
|
D012753||psychotic disorders shared
|
|
D012753||shared paranoid disorders
|
|
D012753||shared psychotic disorder
|
|
D012753||shared psychotic disorders
|
|
249420|C537274||ter haar syndrome
|
|
249420|C537274||frank ter haar syndrome
|
|
249420|C537274||fths
|
|
249420|C537274||megalocornea multiple skeletal anomalies and developmental delay
|
|
249420|C537274||melnick needles syndrome autosomal recessive formerly
|
|
D009110||munchausen syndrome
|
|
D009110||hospital addiction syndrome
|
|
D009110||hospital addiction syndromes
|
|
D009110||munchhausen syndrome
|
|
D009110||syndrome hospital addiction
|
|
D009110||syndrome munchausen
|
|
D009110||syndrome munchhausen
|
|
D009110||syndromes hospital addiction
|
|
D012757||sheep diseases
|
|
D012757||disease ovine
|
|
D012757||disease sheep
|
|
D012757||diseases ovine
|
|
D012757||diseases sheep
|
|
D012757||ovine disease
|
|
D012757||ovine diseases
|
|
D012757||sheep disease
|
|
C562465|608251||phobia specific
|
|
C562465|608251||phobia simple
|
|
208530|D059446||heterotaxy syndrome
|
|
208530|D059446||ambiguus situs
|
|
208530|D059446||ambiguus viscerum situs
|
|
208530|D059446||ambiguus viscerums situs
|
|
208530|D059446||asplenia syndrome
|
|
208530|D059446||asplenia syndromes
|
|
208530|D059446||asplenia with cardiovascular anomalies
|
|
208530|D059446||atrial isomerism left
|
|
208530|D059446||atrial isomerism right
|
|
208530|D059446||atrial isomerisms left
|
|
208530|D059446||atrial isomerisms right
|
|
208530|D059446||heterotaxies visceral
|
|
208530|D059446||heterotaxy syndromes
|
|
208530|D059446||heterotaxy visceral
|
|
208530|D059446||heterotaxy visceroatrial autosomal recessive included
|
|
208530|D059446||isomerism left atrial
|
|
208530|D059446||isomerism right atrial
|
|
208530|D059446||isomerisms left atrial
|
|
208530|D059446||isomerisms right atrial
|
|
208530|D059446||ivemark syndrome
|
|
208530|D059446||ivemark syndrome polysplenia syndrome included
|
|
208530|D059446||left atrial isomerism
|
|
208530|D059446||left atrial isomerisms
|
|
208530|D059446||left atrial isomerism with polysplenia
|
|
208530|D059446||polyasplenia included
|
|
208530|D059446||polysplenia syndrome
|
|
208530|D059446||polysplenia syndromes
|
|
208530|D059446||rai
|
|
208530|D059446||right atrial isomerism
|
|
208530|D059446||right atrial isomerisms
|
|
208530|D059446||right atrial isomerism with asplenia
|
|
208530|D059446||situs ambiguus
|
|
208530|D059446||situs ambiguus viscerum
|
|
208530|D059446||situs ambiguus viscerums
|
|
208530|D059446||situs ambiguus with asplenia
|
|
208530|D059446||situs ambiguus with polysplenia
|
|
208530|D059446||syndrome asplenia
|
|
208530|D059446||syndrome heterotaxy
|
|
208530|D059446||syndrome ivemark
|
|
208530|D059446||syndrome polysplenia
|
|
208530|D059446||syndromes asplenia
|
|
208530|D059446||syndromes heterotaxy
|
|
208530|D059446||syndromes polysplenia
|
|
208530|D059446||vah autosomal recessive included
|
|
208530|D059446||visceral heterotaxies
|
|
208530|D059446||visceral heterotaxy
|
|
208530|D059446||viscerum situs ambiguus
|
|
208530|D059446||viscerums situs ambiguus
|
|
215100|C531651||rhizomelic chondrodysplasia punctata type 1
|
|
215100|C531651||cdpr
|
|
215100|C531651||chondrodystrophia calcificans punctata
|
|
215100|C531651||pbd9
|
|
215100|C531651||peroxisome biogenesis disorder 9
|
|
215100|C531651||rcdp1
|
|
C535973||colpocephaly
|
|
D054556||venous thromboembolism
|
|
D054556||thromboembolism venous
|
|
C535972|120435|C537261||colorectal cancer hereditary nonpolyposis type 1
|
|
C535972|120435|C537261||colon cancer familial nonpolyposis type 1
|
|
C535975||cone dystrophy x linked with tapetal like sheen
|
|
C535974||complete atrioventricular septal defect
|
|
C535974||common atrioventricular canal
|
|
C535974||complete atrioventricular canal
|
|
D012751||sezary syndrome
|
|
D012751||erythroderma sezary
|
|
D012751||lymphoma sezary apos s
|
|
D012751||sezary erythroderma
|
|
D012751||sezary lymphoma
|
|
D012751||sezary apos s lymphoma
|
|
D012751||sezarys lymphoma
|
|
D012751||syndrome sezary
|
|
C535977||congenital absence of the sternocleidomastoid muscle
|
|
C535976||cone rod dystrophy amelogenesis imperfecta
|
|
D054559||hyperphosphatemia
|
|
D054559||hyperphosphatemias
|
|
D000743||anemia hemolytic
|
|
D000743||acquired hemolytic anemia
|
|
D000743||anemia acquired hemolytic
|
|
D000743||anemia hemolytic acquired
|
|
D000743||anemia microangiopathic
|
|
D000743||hemolytic anemia
|
|
D000743||hemolytic anemia acquired
|
|
D000743||microangiopathic anemia
|
|
C535991||de hauwere leroy adriaenssens syndrome
|
|
C535991||iris dysplasia orbital hypertelorism and psychomotor retardation
|
|
D000748||anemia macrocytic
|
|
D000748||anemias macrocytic
|
|
D000748||macrocytic anemia
|
|
D000748||macrocytic anemias
|
|
C535990||de barsy syndrome
|
|
C535990||corneal clouding cutis laxa mental retardation
|
|
C535990||cutis laxa corneal clouding and mental retardation
|
|
C535990||de barsy moens diercks syndrome
|
|
C535990||progeroid syndrome of de barsy
|
|
D000747|C536761|300751||anemia hypochromic
|
|
D000747||anemias hypochromic
|
|
D000747||chloroses
|
|
D000747||chlorosis
|
|
D000747||hypochromic anemia
|
|
D000747||hypochromic anemias
|
|
C535993||deafness conductive ptosis skeletal anomalies
|
|
C535993||deafness conductive with ptosis and skeletal anomalies
|
|
C535993||jackson barr syndrome
|
|
D000746||anemia hemolytic congenital nonspherocytic
|
|
D000746||anemia congenital nonspherocytic hemolytic
|
|
D000746||congenital nonspherocytic hemolytic anemia
|
|
D000746||hemolytic anemia congenital nonspherocytic
|
|
D000745||anemia hemolytic congenital
|
|
D000745||anemia congenital hemolytic
|
|
D000745||anemia hemolytic hereditary
|
|
D000745||anemia hereditary hemolytic
|
|
D000745||anemias congenital hemolytic
|
|
D000745||anemias hereditary hemolytic
|
|
D000745||congenital hemolytic anemia
|
|
D000745||congenital hemolytic anemias
|
|
D000745||hemolytic anemia congenital
|
|
D000745||hemolytic anemia hereditary
|
|
D000745||hemolytic anemias congenital
|
|
D000745||hemolytic anemias hereditary
|
|
D000745||hereditary hemolytic anemia
|
|
D000745||hereditary hemolytic anemias
|
|
D012729||sex chromosome aberrations
|
|
D012729||aberration sex chromosome
|
|
D012729||aberrations sex chromosome
|
|
D012729||abnormalities sex chromosome
|
|
D012729||abnormality sex chromosome
|
|
D012729||chromosome aberration sex
|
|
D012729||chromosome aberrations sex
|
|
D012729||chromosome abnormalities sex
|
|
D012729||chromosome abnormality sex
|
|
D012729||sex chromosome aberration
|
|
D012729||sex chromosome abnormalities
|
|
D012729||sex chromosome abnormality
|
|
C562479|153800||macular degeneration age related 2
|
|
C562479|153800||armd2
|
|
C562479|153800||macular degeneration senile
|
|
C562479|153800||maculopathy age related 2
|
|
D000740||anemia
|
|
D000740||anemias
|
|
C565697|610612||leber congenital amaurosis 12
|
|
C565697|610612||lca12
|
|
C535986||daneman davy mancer syndrome
|
|
C535986||goiter multinodular cystic renal disease and digital anomalies
|
|
C535986||multinodular goiter cystic renal disease and digital anomalies
|
|
C535986||multinodular goiter cystic renal disease digital anomalies
|
|
C566925|611528||arrhythmogenic right ventricular dysplasia familial 12
|
|
C566925|611528||arrhythmogenic right ventricular cardiomyopathy 12
|
|
C566925|611528||arvc12
|
|
C566925|611528||arvd12
|
|
C535985||dandy walker malformation with mental retardation macrocephaly myopia and brachytelephalangy
|
|
C535985||facial dysmorphism macrocephaly myopia and dandy walker malformation
|
|
D000749||anemia megaloblastic
|
|
D000749||anemias megaloblastic
|
|
D000749||megaloblastic anemia
|
|
D000749||megaloblastic anemias
|
|
C535988||davenport donlan syndrome
|
|
C535988||dominant hearing loss white hair contractures hyperkeratotic papillomata and depressed chemotaxis
|
|
D006013|232700||glycogen storage disease type vi
|
|
D006013|232700||disease hers
|
|
D006013|232700||disease hers apos
|
|
D006013|232700||glycogenosis 6
|
|
D006013|232700||glycogenosis type vi
|
|
D006013|232700||glycogenosis vi
|
|
D006013|232700||glycogen storage disease vi
|
|
D006013|232700||gsd6
|
|
D006013|232700||gsd vi
|
|
D006013|232700||hepatic glycogen phosphorylase deficiency
|
|
D006013|232700||her disease
|
|
D006013|232700||hers disease
|
|
D006013|232700||hers apos disease
|
|
D006013|232700||liver phosphorylase deficiency syndrome
|
|
D006013|232700||phosphorylase deficiency glycogen storage disease of liver
|
|
D006013|232700||type vi glycogenosis
|
|
C535989||davis lafer syndrome
|
|
C535989||lafer davis syndrome
|
|
C535989||mental retardation unusual facies davis lafer type
|
|
D000754||anemia refractory with excess of blasts
|
|
D000754||leukemia smoldering
|
|
D000754||leukemia smouldering
|
|
D000754||leukemias smoldering
|
|
D000754||raeb
|
|
D000754||raem
|
|
D000754||refractory anemia with excess of blasts
|
|
D000754||smoldering leukemia
|
|
D000754||smoldering leukemias
|
|
D000754||smouldering leukemia
|
|
C564832|268200||myoglobinuria acute recurrent autosomal recessive
|
|
C564832|268200||myoglobinuria familial paroxysmal paralytic
|
|
C564832|268200||rhabdomyolysis acute recurrent
|
|
D000753||anemia refractory
|
|
D000753||anemias refractory
|
|
D000753||refractory anemia
|
|
D000753||refractory anemias
|
|
D000752||anemia pernicious
|
|
D000752||addison anemia
|
|
D000752||addison apos s anemia
|
|
D000752||addisons anemia
|
|
D000752||anemia addison
|
|
D000752||anemia addisons
|
|
D000752||anemia addison apos s
|
|
D000752||pernicious anemia
|
|
D000756||anemia sideroblastic
|
|
D000756||anemias sideroblastic
|
|
D000756||sideroblastic anemia
|
|
D000756||sideroblastic anemias
|
|
C537027|201710||lipoid congenital adrenal hyperplasia
|
|
C537027|201710||adrenal hyperplasia 1
|
|
C537027|201710||adrenal hyperplasia i
|
|
C537027|201710||lcah
|
|
C537027|201710||lipoid hyperplasia congenital of adrenal cortex with male pseudohermaphroditism
|
|
608391||autoimmune disease susceptibility to 2
|
|
608391||ais2
|
|
608391||autoimmune disease susceptibility locus chromosome 7 related
|
|
608391||vamas3
|
|
608391||vitiligo associated multiple autoimmune disease susceptibility 3
|
|
608392||autoimmune disease susceptibility to 3
|
|
608392||ais3
|
|
608392||autoimmune disease susceptibility locus chromosome 8 related
|
|
608392||vamas4
|
|
608392||vitiligo associated multiple autoimmune disease susceptibility 4
|
|
608393||microcephaly 6 primary autosomal recessive
|
|
608393||mcph6
|
|
C537580|266900||senior loken syndrome
|
|
C537580|266900||juvenile nephronophthisis with leber amaurosis
|
|
C537580|266900||loken senior syndrome
|
|
C537580|266900||renal dysplasia and retinal aplasia
|
|
C537580|266900||renal dysplasia retinal aplasia
|
|
C537580|266900||renal retinal syndrome
|
|
C537580|266900||senior l 248 ken syndrome
|
|
C537580|266900||senior loken syndrome 1
|
|
C537580|266900||slsn1
|
|
D000751||anemia neonatal
|
|
D000751||anemia neonatorum
|
|
D000751||anemias neonatal
|
|
D000751||neonatal anemia
|
|
D000751||neonatal anemias
|
|
D000750||anemia myelophthisic
|
|
D000750||anemia leukoerythroblastic
|
|
D000750||anemias leukoerythroblastic
|
|
D000750||anemias myelophthisic
|
|
D000750||leukoerythroblastic anemia
|
|
D000750||leukoerythroblastic anemias
|
|
D000750||myelophthisic anemia
|
|
D000750||myelophthisic anemias
|
|
607060||parkinson disease 8 autosomal dominant
|
|
607060||park8
|
|
C536643|300266||spastic paraplegia 16 x linked
|
|
C536643|300266||spg16
|
|
D012734||disorders of sex development
|
|
D012734||ambiguities genital
|
|
D012734||ambiguity genital
|
|
D012734||ambiguous genitalia
|
|
D012734||condition intersex
|
|
D012734||conditions intersex
|
|
D012734||differentiation disorder sex
|
|
D012734||differentiation disorder sexual
|
|
D012734||differentiation disorders sex
|
|
D012734||differentiation disorders sexual
|
|
D012734||disorder sex differentiation
|
|
D012734||disorder sexual differentiation
|
|
D012734||disorders of sexual development
|
|
D012734||disorders sex differentiation
|
|
D012734||disorders sexual differentiation
|
|
D012734||genital ambiguities
|
|
D012734||genital ambiguity
|
|
D012734||genitalia ambiguous
|
|
D012734||hermaphroditism
|
|
D012734||intersex condition
|
|
D012734||intersex conditions
|
|
D012734||intersexualities
|
|
D012734||intersexuality
|
|
D012734||pseudohermaphroditism
|
|
D012734||sex development disorder
|
|
D012734||sex development disorders
|
|
D012734||sex differentiation disorder
|
|
D012734||sex differentiation disorders
|
|
D012734||sexual development disorder
|
|
D012734||sexual development disorders
|
|
D012734||sexual differentiation disorder
|
|
D012734||sexual differentiation disorders
|
|
D012735||sexual dysfunction physiological
|
|
D012735||physiological sexual disorder
|
|
D012735||physiological sexual disorders
|
|
D012735||physiological sexual dysfunction
|
|
D012735||physiological sexual dysfunctions
|
|
D012735||sex disorders
|
|
D012735||sexual disorder physiological
|
|
D012735||sexual disorders physiological
|
|
D012735||sexual dysfunctions physiological
|
|
606369|C535500||epileptic encephalopathy lennox gastaut type
|
|
606369|C535500||childhood epileptic encephalopathy with diffuse slow spikes and waves
|
|
606369|C535500||encephalopathy of childhood
|
|
606369|C535500||lennox gastaut syndrome
|
|
606369|C535500||macrocephaly and epileptic encephalopathy
|
|
C535995||deafness hyperuricemia neurologic ataxia
|
|
C535994||deafness enamel hypoplasia nail defects
|
|
C535994||bilateral sensorineural hearing loss enamel hypoplasia and nail defects
|
|
C535994||hearing loss sensorineural with enamel hypoplasia and nail defects
|
|
C535994||heimler syndrome
|
|
C535994||sensorineural hearing loss enamel hypoplasia and nail abnormalities
|
|
C535996||deafness nephritis ano rectal malformation
|
|
C535996||dominant ano rectal malformation nephritis and nerve deafness
|
|
C535998||galactocele
|
|
C535998||galactocoele
|
|
C535998||galactocoele of childhood
|
|
C535998||lacteal cyst
|
|
C535998||lactocele
|
|
C564377||myopathy distal with early respiratory failure autosomal dominant
|
|
C538209|117300||dementia familial danish
|
|
C538209|117300||cerebellar ataxia cataract deafness and dementia or psychosis
|
|
C538209|117300||cerebral amyloid angiopathy itm2b related 2
|
|
C538209|117300||familial danish dementia
|
|
C538209|117300||fdd
|
|
C538209|117300||heredopathia ophthalmootoencephalica
|
|
C538209|117300||hooe
|
|
C538088||oculocerebrocutaneous syndrome
|
|
C538088||delleman syndrome
|
|
C538088||oculo cerebro cutaneous syndrome
|
|
C538088||orbital cyst with cerebral and focal dermal malformations
|
|
C564375|C536860|607584||spastic paraplegia 24 autosomal recessive
|
|
C538087||distal trisomy 10q syndrome
|
|
C538087||chromosome 10 distal trisomy 10q
|
|
C538087||chromosome 10 partial trisomy 10q24 qter
|
|
C538087||chromosome 10 trisomy 10q2
|
|
C538087||distal duplication 10q
|
|
C563047||cleft palate lateral synechia syndrome
|
|
C563047||cpls syndrome
|
|
C564378||spastic paraplegia ataxia and mental retardation
|
|
D000844||ankylosis
|
|
D000844||ankyloses
|
|
D012829||silicosis
|
|
D012829||silicoses
|
|
C538082||chromosome 1 q42 11 q42 12 duplication
|
|
C538082||duplication 1q42 11 q42 12
|
|
C538082||trisomy 1q42 11 q42 12
|
|
C564717|300085||cone rod dystrophy x linked 2
|
|
C564717|300085||cod2
|
|
C564717|300085||cone dystrophy 2 x linked
|
|
C564717|300085||cone dystrophy x linked 2
|
|
C564717|300085||cordx2
|
|
C538081||congenital dislocation of the patella
|
|
C538081||congenital patellar dislocation
|
|
D016518|101000||neurofibromatosis 2
|
|
D016518|101000||2 neurofibromatosis type
|
|
D016518|101000||acn
|
|
D016518|101000||acoustic neurinoma bilateral
|
|
D016518|101000||acoustic neurinomas bilateral
|
|
D016518|101000||acoustic neurofibromatoses bilateral
|
|
D016518|101000||acoustic neurofibromatosis bilateral
|
|
D016518|101000||acoustic neuroma familial
|
|
D016518|101000||acoustic neuromas familial
|
|
D016518|101000||acoustic schwannoma bilateral
|
|
D016518|101000||acoustic schwannomas bilateral
|
|
D016518|101000||banf
|
|
D016518|101000||bilateral acoustic neurinoma
|
|
D016518|101000||bilateral acoustic neurinomas
|
|
D016518|101000||bilateral acoustic neurofibromatoses
|
|
D016518|101000||bilateral acoustic neurofibromatosis
|
|
D016518|101000||bilateral acoustic schwannoma
|
|
D016518|101000||bilateral acoustic schwannomas
|
|
D016518|101000||central neurofibromatoses
|
|
D016518|101000||central neurofibromatosis
|
|
D016518|101000||central nf2 neurofibromatoses
|
|
D016518|101000||central nf2 neurofibromatosis
|
|
D016518|101000||familial acoustic neuroma
|
|
D016518|101000||familial acoustic neuromas
|
|
D016518|101000||neurinoma bilateral acoustic
|
|
D016518|101000||neurinomas bilateral acoustic
|
|
D016518|101000||neurofibromatoses bilateral acoustic
|
|
D016518|101000||neurofibromatoses central
|
|
D016518|101000||neurofibromatoses central nf2
|
|
D016518|101000||neurofibromatoses type 2
|
|
D016518|101000||neurofibromatoses type ii
|
|
D016518|101000||neurofibromatosis acoustic bilateral
|
|
D016518|101000||neurofibromatosis bilateral acoustic
|
|
D016518|101000||neurofibromatosis central
|
|
D016518|101000||neurofibromatosis central nf2
|
|
D016518|101000||neurofibromatosis central nf 2
|
|
D016518|101000||neurofibromatosis central type
|
|
D016518|101000||neurofibromatosis ii
|
|
D016518|101000||neurofibromatosis iis
|
|
D016518|101000||neurofibromatosis type 2
|
|
D016518|101000||neurofibromatosis type ii
|
|
D016518|101000||neuroma acoustic bilateral
|
|
D016518|101000||neuroma familial acoustic
|
|
D016518|101000||neuromas familial acoustic
|
|
D016518|101000||nf2
|
|
D016518|101000||nf2 neurofibromatosis 2
|
|
D016518|101000||nf2s neurofibromatosis 2
|
|
D016518|101000||schwannoma acoustic bilateral
|
|
D016518|101000||schwannoma bilateral acoustic
|
|
D016518|101000||schwannomas bilateral acoustic
|
|
D016518|101000||type 2 neurofibromatoses
|
|
D016518|101000||type 2 neurofibromatosis
|
|
D016518|101000||type ii neurofibromatoses
|
|
D016518|101000||type ii neurofibromatosis
|
|
C538086||chromosome 10 ring
|
|
C538086||ring chromosome 10
|
|
614149||nail disorder nonsyndromic congenital 9
|
|
614149||anonychia onycholysis isolated
|
|
614149||nail dysplasia
|
|
614149||ndnc9
|
|
614149||onychodystrophy
|
|
C538085||chromosome 1 uniparental disomy 1q12 q21
|
|
C538085||mosaic trisomy 1q12 q21
|
|
C538085||uniparental disomy 1q12 q21
|
|
C538084||chromosome 1 trisomy 1q42 qter
|
|
C538084||duplication 1q42 qter
|
|
C538084||trisomy 1q42 qter
|
|
C538083||chromosome 1 trisomy 1q32 qter
|
|
C538083||duplication 1q32 qter
|
|
C538083||trisomy 1q32 qter
|
|
C564597|610283||cone rod dystrophy 10
|
|
C564597|610283||cord10
|
|
C535806||moebius axonal neuropathy hypogonadism
|
|
C535809||mollica pavone antener syndrome
|
|
C535809||dwarfism mental retardation and eye abnormality
|
|
C535809||mollica syndrome
|
|
C535809||short stature mental retardation and ocular alterations
|
|
D000849||anomia
|
|
D000849||amnesic aphasia
|
|
D000849||anomia color
|
|
D000849||anomias color
|
|
D000849||anomic aphasia
|
|
D000849||anomic dysphasia
|
|
D000849||anomic dysphasias
|
|
D000849||aphasia amnesic
|
|
D000849||aphasia anomic
|
|
D000849||aphasia nominal
|
|
D000849||color anomia
|
|
D000849||color anomias
|
|
D000849||dysnomia
|
|
D000849||dysnomias
|
|
D000849||dysphasia anomic
|
|
D000849||dysphasia nominal
|
|
D000849||dysphasias anomic
|
|
D000849||dysphasias nominal
|
|
D000849||nominal aphasia
|
|
D000849||nominal dysphasia
|
|
D000849||nominal dysphasias
|
|
C563655|610840||mitral valve prolapse myxomatous 3
|
|
C563655|610840||mmvp3
|
|
C563655|610840||myxomatous mitral valve prolapse 3
|
|
125853|D003924||diabetes mellitus type 2
|
|
125853|D003924||adult onset diabetes mellitus
|
|
125853|D003924||diabetes mellitus adult onset
|
|
125853|D003924||diabetes mellitus ketosis resistant
|
|
125853|D003924||diabetes mellitus maturity onset
|
|
125853|D003924||diabetes mellitus noninsulin dependent
|
|
125853|D003924||diabetes mellitus non insulin dependent
|
|
125853|D003924||diabetes mellitus slow onset
|
|
125853|D003924||diabetes mellitus stable
|
|
125853|D003924||diabetes mellitus type ii
|
|
125853|D003924||ketosis resistant diabetes mellitus
|
|
125853|D003924||maturity onset diabetes
|
|
125853|D003924||maturity onset diabetes insulin resistance susceptibility to included
|
|
125853|D003924||maturity onset diabetes mellitus
|
|
125853|D003924|606391|C562772||mody
|
|
125853|D003924||niddm
|
|
125853|D003924||noninsulin dependent diabetes mellitus
|
|
125853|D003924||non insulin dependent diabetes mellitus
|
|
125853|D003924||slow onset diabetes mellitus
|
|
125853|D003924||stable diabetes mellitus
|
|
125853|D003924||t2d
|
|
125853|D003924||type 2 diabetes mellitus
|
|
C535801||spranger schinzel myers syndrome
|
|
C535801||arthromyodysplasia dyscephaly sacral agenesis and hypoplastic digits
|
|
C535801||cerebroarthrodigital syndrome
|
|
C563052||digitorenocerebral syndrome
|
|
C563052||brachydactyly due to absence of distal phalanges
|
|
C563052||deafness onychodystrophy osteodystrophy and mental retardation syndrome
|
|
C563052||door syndrome
|
|
C563052||eronen syndrome
|
|
C564383||camptosynpolydactyly complex
|
|
C564383||camptopolydactyly disorganization type
|
|
C535800|137440|D016098||amyloidosis cerebral with spongiform encephalopathy
|
|
C535800|137440|D016098||cerebellar ataxia progressive dementia and amyloid deposits in cns
|
|
C535800||prion dementia
|
|
C563051||edinburgh malformation syndrome
|
|
C564382||secretory diarrhea myopathy and deafness
|
|
C535802||sprengel deformity
|
|
C535802||high scapula
|
|
C535802||maladie de sprengel familiale
|
|
C535802||sprengel apos s shoulder
|
|
C562718|611881||glycogen storage disease xii
|
|
C562718|611881||aldoa deficiency
|
|
C562718|611881||aldolase a deficiency
|
|
C562718|611881||aldolase deficiency red cell
|
|
C562718|611881||gsd12
|
|
C562718|611881||gsd xii
|
|
C562718|611881||red cell aldolase deficiency
|
|
D000853||anophthalmos
|
|
D000853||anophthalmia
|
|
D000853||anophthalmias
|
|
D024801||tauopathies
|
|
D024801||tauopathy
|
|
C538098||familial paget apos s disease of bone
|
|
C538098||paget disease of bone type 1
|
|
C564385||migraine familial hemiplegic 4
|
|
D000858||anovulation
|
|
D000858||anovulations
|
|
D000857||olfaction disorders
|
|
D000857||anosmia
|
|
D000857||cacosmia
|
|
D000857||cacosmias
|
|
D000857||dysosmia
|
|
D000857||dysosmias
|
|
D000857||olfaction disorder
|
|
D000857||paraosmia
|
|
D000857||paraosmias
|
|
D000857||smell disorder
|
|
D000857||smell disorders
|
|
C564560|300220||mental retardation x linked syndromic 10
|
|
C564560|300220||camr
|
|
C564560|300220||chorioathetosis with mental retardation and abnormal behavior
|
|
C564560|300220||mental retardation with chorioathetosis and abnormal behavior
|
|
C564560|300220||mrxs10
|
|
D000855||anorexia
|
|
D000855||anorexias
|
|
C538092||pachygyria frontotemporal
|
|
C538092||autosomal recessive frontotemporal pachygyria
|
|
D011507||proteinuria
|
|
D011507||proteinurias
|
|
C538091||kuzniecky syndrome
|
|
C538091||pachygyria mental retardation and epilepsy
|
|
C538091|600176||pachygyria with mental retardation and seizures
|
|
C536089|254300||congenital myasthenic syndrome ib
|
|
C536089|254300||cms1b
|
|
C536089|254300||cms ib
|
|
C536089|254300||congenital myasthenic syndrome type ib
|
|
C536089|254300||lgm
|
|
C536089|254300||myasthenia familial limb girdle
|
|
C536089|254300||myasthenia limb girdle familial
|
|
C536089|254300||myasthenic myopathy formerly
|
|
C538090||ovarian epithelial cancer
|
|
C538090||epithelial ovarian cancer
|
|
C538090||ovarian cancer epithelial
|
|
C538095||pacman dysplasia
|
|
C538095||epiphyseal stippling with osteoclastic hyperplasia
|
|
C538095||pacman syndrome
|
|
C538094||pachyonychia congenita recessive
|
|
C538094||autosomal recessive pachyonychia congenita
|
|
D012832||silo filler apos s disease
|
|
D012832||disease silo filler
|
|
D012832||disease silo fillers
|
|
D012832||disease silo filler apos s
|
|
D012832||disease silo fillers apos
|
|
D012832||silo filler disease
|
|
D012832||silo fillers disease
|
|
D012832||silo fillers apos disease
|
|
C535816||port wine stain familial multiple
|
|
C566902|611631||epilepsy familial temporal lobe 4
|
|
C566902|611631||epilepsy occipitotemporal lobe and migraine with aura
|
|
C566902|611631||epolm
|
|
C566902|611631||etl4
|
|
C535815||neutropenia severe chronic
|
|
C535815||leukopenia benign familial
|
|
C535815||neutropenia chronic familial
|
|
D012830||silicotuberculosis
|
|
D012830||silicotuberculoses
|
|
D011502||protein energy malnutrition
|
|
D011502||malnutrition protein calorie
|
|
D011502||malnutrition protein energy
|
|
D011502||malnutritions protein energy
|
|
D011502||marasmus
|
|
D011502||protein calorie malnutrition
|
|
C535818||pseudo zellweger syndrome
|
|
C535818||pseudo zellweger syndrome leukodystrophy
|
|
C535817||pruritic urticarial papules plaques of pregnancy
|
|
C535817||polymorphic eruption of pregnancy
|
|
C535817||pruritic urticarial papules and plaques of pregnancy
|
|
C535817||pruritic urticarial papules and plaques of pregnancy familial
|
|
182290|D058496||smith magenis syndrome
|
|
182290|D058496||17p11 2 monosomy
|
|
182290|D058496||chromosome 17p11 2 deletion syndrome
|
|
182290|D058496||chromosome 17p11 2 deletion syndrome smith magenis chromosome region included
|
|
182290|D058496||smcr included
|
|
182290|D058496||sms
|
|
182290|D058496||syndrome smith magenis
|
|
612371|C567529||major affective disorder 7
|
|
612371|C567529|C565111|125480|C567530|612357|C567074|611535|612372|C567531|611247|C567073|309200|C564108|C567075|611536||bipolar affective disorder
|
|
612371|C567529||mafd7
|
|
C564650|606864||carney stratakis syndrome
|
|
C564650|606864||paraganglioma and gastric stromal sarcoma
|
|
C564650|606864||paraganglioma and gastrointestinal stromal tumor
|
|
C566342|603694||diabetes mellitus noninsulin dependent 3
|
|
C566342|603694||niddm3
|
|
C566342|603694||noninsulin dependent diabetes mellitus 3
|
|
C535810||moloney syndrome
|
|
C535810||choroidal atrophy alopecia
|
|
C535810||regional choroidal atrophy and alopecia
|
|
C564395||spinocerebellar ataxia with epilepsy
|
|
C564395||myoclonic epilepsy myopathy sensory ataxia
|
|
C535812||macrosomia obesity macrocephaly ocular abnormalities
|
|
C535812||macrocrania obesity ocular abnormalities retinal coloboma and nystagmus
|
|
C535812||macrosomia obesity macrocephaly and ocular abnormalities
|
|
C535812||momo syndrome
|
|
194300||woolly hair autosomal dominant
|
|
194300||adwh
|
|
C564393||vitamin k dependent clotting factors combined deficiency of type 2
|
|
C564393|607473||vkcfd2
|
|
C538202|609941||deafness autosomal recessive 51
|
|
C538202|609941||dfnb51
|
|
C535814||neurosarcoidosis
|
|
C535814||nervous system sarcoidosis
|
|
202010|C535978||congenital adrenal hyperplasia due to 11 beta hydroxylase deficiency
|
|
202010|C535978||11 beta hydroxylase deficiency
|
|
202010|C535978||11b hydroxylase deficiency
|
|
202010|C535978||adrenal hyperplasia 4
|
|
202010|C535978||adrenal hyperplasia congenital due to 11 beta hydroxylase deficiency
|
|
202010|C535978||adrenal hyperplasia congenital due to steroid 11 beta hydroxylase deficiency
|
|
202010|C535978||adrenal hyperplasia hypertensive form
|
|
202010|C535978||adrenal hyperplasia iv
|
|
202010|C535978||congenital adrenal hyperplasia type 4
|
|
202010|C535978||hypertensive form of adrenal hyperplasia
|
|
202010|C535978||p450c11b1 deficiency
|
|
202010|C535978||steroid 11 beta hydroxylase deficiency
|
|
C565687||collagenosis familial reactive perforating
|
|
C563024||spastic pseudosclerosis
|
|
C563024||corticopallidodegeneration
|
|
C563024||disseminated encephalomyelopathy
|
|
D000820||animal diseases
|
|
D000820||diseases animal
|
|
C564353||cataract congenital with mental impairment and dentate gyrus atrophy
|
|
C565279|605845||dermatitis atopic 6
|
|
C565279|605845||atod6
|
|
C563028||splenic hypoplasia
|
|
C563028||asplenia familial
|
|
C563028||hyposplenia isolated congenital
|
|
C565684||combined inflammatory and immunologic defect
|
|
C564357||hypotrichosis osteolysis periodontitis palmoplantar keratoderma syndrome
|
|
C565686||coloboma of macula and skeletal anomalies
|
|
C564356||acute tubulointerstitial nephritis
|
|
120050||coxsackievirus b3 susceptibility
|
|
120050||cb3s
|
|
120050||cxb3s
|
|
D012805||sickle cell trait
|
|
D012805||cell trait sickle
|
|
D012805||cell traits sickle
|
|
D012805||sickle cell traits
|
|
D012805||trait sickle cell
|
|
D012805||traits sickle cell
|
|
D012806||siderosis
|
|
D012806||sideroses
|
|
611094|C567015||mental retardation autosomal recessive 8
|
|
611094|C567015||mrt8
|
|
C564256|608340||charcot marie tooth disease recessive intermediate a
|
|
C564256|608340||charcot marie tooth neuropathy recessive intermediate a
|
|
C564256|608340||cmtria
|
|
C564256|608340||ri cmta
|
|
614129||perrault syndrome 3
|
|
614129||deafness autosomal recessive 81 formerly
|
|
614129||dfnb81 formerly
|
|
614129||prlts3
|
|
D051359|267700||lymphohistiocytosis hemophagocytic
|
|
D051359|267700||erythrophagocytic lymphohistiocytoses familial
|
|
D051359|267700||erythrophagocytic lymphohistiocytosis familial
|
|
D051359|267700||familial erythrophagocytic lymphohistiocytoses
|
|
D051359|267700||familial erythrophagocytic lymphohistiocytosis
|
|
D051359|267700||familial hemophagocytic histiocytoses
|
|
D051359|267700||familial hemophagocytic histiocytosis
|
|
D051359|267700||familial hemophagocytic lymphocytoses
|
|
D051359|267700||familial hemophagocytic lymphocytosis
|
|
D051359|267700||familial hemophagocytic lymphohistiocytoses
|
|
D051359|267700||familial hemophagocytic lymphohistiocytosis
|
|
D051359|267700||familial hemophagocytic reticuloses
|
|
D051359|267700||familial hemophagocytic reticulosis
|
|
D051359|267700||familial histiocytic reticuloses
|
|
D051359|267700||familial histiocytic reticulosis
|
|
D051359|267700||fel
|
|
D051359|267700||fhl
|
|
D051359|267700||fhl1
|
|
D051359|267700||fhlh
|
|
D051359|267700||hemophagocytic histiocytoses familial
|
|
D051359|267700||hemophagocytic histiocytosis familial
|
|
D051359|267700||hemophagocytic hymphohistiocytoses primary
|
|
D051359|267700||hemophagocytic hymphohistiocytosis primary
|
|
D051359|267700||hemophagocytic lymphocytoses familial
|
|
D051359|267700||hemophagocytic lymphocytosis familial
|
|
D051359|267700||hemophagocytic lymphohistiocytoses
|
|
D051359|267700||hemophagocytic lymphohistiocytoses familial
|
|
D051359|267700||hemophagocytic lymphohistiocytoses primary
|
|
D051359|267700||hemophagocytic lymphohistiocytosis
|
|
D051359|267700||hemophagocytic lymphohistiocytosis familial
|
|
D051359|267700||hemophagocytic lymphohistiocytosis familial 1
|
|
D051359|267700||hemophagocytic lymphohistiocytosis primary
|
|
D051359|267700||hemophagocytic reticuloses familial
|
|
D051359|267700||hemophagocytic reticulosis familial
|
|
D051359|267700||hemophagocytic syndrome
|
|
D051359|267700||hemophagocytic syndrome infection associated
|
|
D051359|267700||hemophagocytic syndrome reactive
|
|
D051359|267700||hemophagocytic syndromes
|
|
D051359|267700||histiocytic reticuloses familial
|
|
D051359|267700||histiocytic reticulosis familial
|
|
D051359|267700||histiocytoses familial hemophagocytic
|
|
D051359|267700||histiocytosis familial hemophagocytic
|
|
D051359|267700||hlh1
|
|
D051359|267700||hplh
|
|
D051359|267700||hplh1
|
|
D051359|267700||hymphohistiocytoses primary hemophagocytic
|
|
D051359|267700||hymphohistiocytosis primary hemophagocytic
|
|
D051359|267700||infection associated hemophagocytic syndrome
|
|
D051359|267700||lymphocytoses familial hemophagocytic
|
|
D051359|267700||lymphocytosis familial hemophagocytic
|
|
D051359|267700||lymphohistiocytoses familial erythrophagocytic
|
|
D051359|267700||lymphohistiocytoses familial hemophagocytic
|
|
D051359|267700||lymphohistiocytoses hemophagocytic
|
|
D051359|267700||lymphohistiocytoses primary hemophagocytic
|
|
D051359|267700||lymphohistiocytosis familial erythrophagocytic
|
|
D051359|267700||lymphohistiocytosis familial hemophagocytic
|
|
D051359|267700||lymphohistiocytosis primary hemophagocytic
|
|
D051359|267700||primary hemophagocytic hymphohistiocytoses
|
|
D051359|267700||primary hemophagocytic hymphohistiocytosis
|
|
D051359|267700||primary hemophagocytic lymphohistiocytoses
|
|
D051359|267700||primary hemophagocytic lymphohistiocytosis
|
|
D051359|267700||reactive hemophagocytic syndrome
|
|
D051359|267700||reticuloses familial hemophagocytic
|
|
D051359|267700||reticuloses familial histiocytic
|
|
D051359|267700||reticulosis familial hemophagocytic
|
|
D051359|267700||reticulosis familial histiocytic
|
|
C535827||pseudohyperkalemia cardiff
|
|
C535827||cryohydrocytosis
|
|
C535827||stomatocytosis cold sensitive
|
|
C535826||pseudodiastrophic dysplasia
|
|
C535826||pseudodiastrophic dwarfism
|
|
C535829||pseudotrisomy 13 syndrome
|
|
C535829||holoprosencephaly polydactyly syndrome
|
|
C535829||pseudo trisomy 13 syndrome
|
|
C566472|610475||pigmented nodular adrenocortical disease primary 2
|
|
C566472|610475||cushing syndrome adrenal due to ppnad2
|
|
C566472|610475||pigmented micronodular adrenocortical disease primary 2
|
|
C566472|610475||ppnad2
|
|
C535828||pseudoinflammatory fundus dystrophy finnish type
|
|
C535828||fundus dystrophy pseudoinflammatory recessive form
|
|
C535828||pseudoinflammatory fundus dystrophy
|
|
C535828||pseudoinflammatory fundus dystrophy lavia type
|
|
D052065||vaginismus
|
|
D012804||sick sinus syndrome
|
|
D012804||dysfunction sinus node
|
|
D012804||dysfunctions sinus node
|
|
D012804||sick sinus node syndrome
|
|
D012804||sinus node disease
|
|
D012804||sinus node diseases
|
|
D012804||sinus node dysfunction
|
|
D012804||syndrome sick sinus
|
|
146350|C564145||hypophosphatemic bone disease
|
|
146350|C564145||hbd
|
|
C535821||pseudoainhum
|
|
C565693||palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal
|
|
C535820||pseudoachondroplastic dysplasia 2
|
|
C535820||recessive pseudoachondroplasia
|
|
C535820||spondyloepiphyseal dysplasia pseudoachondroplastic 2
|
|
C535823||pseudoaminopterin syndrome
|
|
C535823||aminopterin syndrome sine aminopterin
|
|
C566928|611521||tyrosine kinase 2 deficiency
|
|
C566928|611521||hies with atypical mycobacteriosis autosomal recessive
|
|
C566928|611521||hyper ige syndrome with atypical mycobacteriosis autosomal recessive
|
|
C566928|611521||tyk2 deficiency
|
|
C535824||pseudoangiomatous stromal hyperplasia
|
|
C535824||mammary pseudoangiomatous stromal hyperplasia
|
|
C535824||pseudoangiomatous stromal hyperplasia of the breast
|
|
C564366||niemann pick disease type f
|
|
C565699|610217||nbia2b
|
|
C565699||neuroaxonal dystrophy atypical
|
|
C565699|610217||neurodegeneration with brain iron accumulation 2b
|
|
C565699|610217||neurodegeneration with brain iron accumulation pla2g6 related
|
|
C565696||kallmann syndrome 4
|
|
C563037||arthritis sacroiliac
|
|
C564368||epidermolysis bullosa simplex superficialis
|
|
C535575|275355||carcinoma squamous cell of head and neck
|
|
C535575|275355||hnscc
|
|
C535575|275355||squamous cell carcinoma head and neck
|
|
C535575|275355||squamous cell carcinoma of the head and neck
|
|
D012818||signs and symptoms respiratory
|
|
604173|C565820||poikiloderma with neutropenia
|
|
604173|C565820||pn
|
|
604173|C565820||poikiloderma with neutropenia clericuzio type
|
|
D012816||signs and symptoms
|
|
D012816||symptoms and signs
|
|
D012817||signs and symptoms digestive
|
|
C563908|608565||deafness autosomal recessive 35
|
|
C563908|608565||dfnb35
|
|
D012810||sigmoid diseases
|
|
D012810||colon disease sigmoid
|
|
D012810||colon diseases sigmoid
|
|
D012810||disease sigmoid
|
|
D012810||disease sigmoid colon
|
|
D012810||diseases sigmoid
|
|
D012810||diseases sigmoid colon
|
|
D012810||sigmoid colon disease
|
|
D012810||sigmoid colon diseases
|
|
D012810||sigmoid disease
|
|
C535838||pancreatic islet cell tumors
|
|
C535838||islet of langerhans tumor
|
|
D012811||sigmoid neoplasms
|
|
D012811||cancer of sigmoid
|
|
D012811||cancer of the sigmoid
|
|
D012811||cancer sigmoid
|
|
D012811||cancer sigmoid colon
|
|
D012811||colon cancer sigmoid
|
|
D012811||colon neoplasms sigmoid
|
|
D012811||neoplasm sigmoid
|
|
D012811||neoplasm sigmoid colon
|
|
D012811||neoplasms sigmoid
|
|
D012811||neoplasms sigmoid colon
|
|
D012811||sigmoidal cancer
|
|
D012811||sigmoid cancer
|
|
D012811||sigmoid colon cancer
|
|
D012811||sigmoid colon neoplasm
|
|
D012811||sigmoid colon neoplasms
|
|
D012811||sigmoid neoplasm
|
|
C535837||pancreatic carcinoma familial
|
|
C535837||familial pancreatic carcinoma
|
|
C535839||pancreatic lipomatosis duodenal stenosis
|
|
C535839||pancreatic lipomatosis and duodenal atresia
|
|
D012544|181440||scheuermann disease
|
|
D012544|181440||adolescent kyphoses
|
|
D012544|181440||adolescent kyphosis
|
|
D012544|181440||juvenile kyphoses
|
|
D012544|181440||juvenile kyphoses scheuermann
|
|
D012544|181440||juvenile kyphosis
|
|
D012544|181440||juvenile kyphosis scheuermann
|
|
D012544|181440||juvenile osteochondrosis of spine
|
|
D012544|181440||kyphoses adolescent
|
|
D012544|181440||kyphoses juvenile
|
|
D012544|181440||kyphoses scheuermann
|
|
D012544|181440||kyphoses scheuermann juvenile
|
|
D012544|181440||kyphoses scheuermann apos s
|
|
D012544|181440||kyphosis adolescent
|
|
D012544|181440||kyphosis juvenile
|
|
D012544|181440||kyphosis scheuermann
|
|
D012544|181440||kyphosis scheuermann juvenile
|
|
D012544|181440||kyphosis scheuermann apos s
|
|
D012544|181440||scheuermann juvenile kyphoses
|
|
D012544|181440||scheuermann juvenile kyphosis
|
|
D012544|181440||scheuermann kyphoses
|
|
D012544|181440||scheuermann kyphosis
|
|
D012544|181440||scheuermann apos s disease
|
|
D012544|181440||scheuermanns disease
|
|
D012544|181440||scheuermann apos s kyphoses
|
|
D012544|181440||scheuermann apos s kyphosis
|
|
D012544|181440||scheuermanns kyphosis
|
|
D012544|181440|D055035||spinal osteochondrosis
|
|
D012544|181440||spine juvenile osteochondroses
|
|
D012544|181440||spine juvenile osteochondrosis
|
|
C566400|603204||epilepsy nocturnal frontal lobe type 2
|
|
C566400|603204||enfl2
|
|
C566400|603204||epilepsy nocturnal frontal lobe 2
|
|
D000839||aniseikonia
|
|
C535832||pulmonary alveolar proteinosis congenital
|
|
C535832||congenital pulmonary alveolar proteinosis
|
|
C535831||pterygium colli mental retardation digital anomalies
|
|
C535831||khalifa graham syndrome
|
|
C535831||pterygium colli and mental retardation with facial and digital anomalies
|
|
C535833||pulmonary edema of mountaineers
|
|
C535833||high altitude pulmonary hypertension
|
|
603467||fanconi anemia complementation group f
|
|
603467||fancf
|
|
C535836||pancreatic cancer adult
|
|
C564370||microphthalmia with cyst bilateral facial clefts and limb anomalies
|
|
C535835||schwartz cohen addad lambert syndrome
|
|
C535835||congenital melanocytosis with myelomeningocele and hydrocephalus
|
|
C538046||chromosome 17 ring
|
|
C538046||ring chromosome 17
|
|
C565665||craniosynostosis with fibular aplasia
|
|
C563002||opticocochleodentate degeneration
|
|
D016393||lymphoma b cell
|
|
D016393||b cell lymphoma
|
|
D016393||b cell lymphomas
|
|
D016393||lymphomas b cell
|
|
D018500|125800||diabetes insipidus nephrogenic
|
|
D018500|125800||acquired nephrogenic diabetes insipidus
|
|
D018500|125800||adh resistant diabetes insipidus
|
|
D018500|125800||congenital nephrogenic diabetes insipidus
|
|
D018500|125800||diabetes insipidus nephrogenic autosomal
|
|
D018500|125800||diabetes insipidus nephrogenic type 1
|
|
D018500|125800||diabetes insipidus nephrogenic type i
|
|
D018500|125800||diabetes insipidus nephrogenic type ii
|
|
D018500|125800||diabetes insipidus nephrogenic x linked
|
|
D018500|125800||diabetes insipidus renalis
|
|
D018500|125800||ndi
|
|
D018500|125800||nephrogenic diabetes insipidus
|
|
D018500|125800||nephrogenic diabetes insipidus type i
|
|
D018500|125800||nephrogenic diabetes insipidus type ii
|
|
D018500|125800||vasopressin resistant diabetes insipidus
|
|
C538045||chromosome 17 deletion
|
|
C538045||17p syndrome
|
|
C538045||chromosome 17p deletion syndrome
|
|
C538045||deletion 17p syndrome
|
|
C538045||interstitial deletion 17p
|
|
C538045||partial monosomy 17p
|
|
C566997||aplasia cutis congenita congenital heart defect and frontonasal cysts
|
|
C565666||craniosynostosis with anomalies of the cranial base and digits
|
|
C538044||chromosome 17 trisomy
|
|
C538044||chromosome 17 duplication
|
|
C538044||trisomy 17
|
|
C538044||trisomy 17 mosaicism
|
|
C562594|232220||glycogen storage disease ib
|
|
C562594|232220||glucose 6 phosphate transport defect
|
|
C562594|232220||gsd1b
|
|
C562594|232220||gsd ib
|
|
C565667||craniosynostosis microcephaly with chromosomal breakage and other abnormalities
|
|
C538043||chromosome 16 uniparental disomy
|
|
C538043||uniparental disomy of 16
|
|
C567857|612937||congenital disorder of glycosylation type io
|
|
C567857|612937||cdg1 dpm3
|
|
C567857|612937||cdg1o
|
|
C567857|612937||cdgio
|
|
C567857|612937||cdg io
|
|
C565661||cutis verticis gyrata and mental deficiency
|
|
C538049||deafness oligodontia syndrome
|
|
C538049||autosomal recessive sensorineural hearing impairment dizziness and hypodontia
|
|
C538049||congenital profound sensorineural deafness and oligodontia
|
|
C566993||ataxia spastic 1 autosomal dominant
|
|
C538048||chromosome 17 trisomy 17p
|
|
C538048||duplication 17p
|
|
C538048||trisomy 17p
|
|
C566994||tooth agenesis selective with orofacial cleft
|
|
C565663||craniosynostosis mental retardation clefting syndrome
|
|
C538047||chromosome 17 deletion 17q23 q24
|
|
C538047||deletion 17q23 q24
|
|
C538047||monosomy 17q23 q24
|
|
C566995||hypodontia oligodontia with orofacial cleft
|
|
C565664||craniosynostosis mental retardation syndrome of lin and gettig
|
|
C563003||pallidopontonigral degeneration
|
|
C563009|138500||glycinuria with or without oxalate urolithiasis
|
|
C563009|138500||glycinuria with or without oxalate nephrolithiasis
|
|
C563009|138500||iminoglycinuria type ii
|
|
145000|C564166||hyperparathyroidism 1
|
|
145000|C564166||familial isolated hyperparathyroidism
|
|
145000|C564166||hrpt1
|
|
145000|C564166||hyperparathyroidism familial isolated primary
|
|
145000|C564166||hyperparathyroidism familial isolated primary fihp parathyroid adenoma familial included
|
|
145000|C564166||parathyroid adenoma familial
|
|
C563007||hypochondrogenesis
|
|
263000|C562470||interstitial pneumonitis desquamative familial
|
|
263000|C562470||dip
|
|
263000|C562470||ild desquamative
|
|
263000|C562470||interstitial lung disease desquamative
|
|
263000|C562470||pneumonia desquamative interstitial familial
|
|
263000|C562470||pneumonitis desquamative interstitial familial
|
|
C538042||chromosome 16 trisomy 16q
|
|
C538042||duplication 16q
|
|
C538042||trisomy 16q
|
|
C538041||chromosome 16 trisomy
|
|
C538041||mosaic trisomy 16
|
|
C538041||trisomy 16
|
|
C538040||chromosome 15q trisomy
|
|
C538040||duplication 15q
|
|
C538040||trisomy 15q
|
|
C566815|169100||char syndrome
|
|
C566815|169100||char
|
|
C566815|169100||patent ductus arteriosus with facial dysmorphism and abnormal fifth digits
|
|
D056807|207900||argininosuccinic aciduria
|
|
D056807|207900||acidemia argininosuccinate
|
|
D056807|207900||acidemias argininosuccinate
|
|
D056807|207900||aciduria argininosuccinic
|
|
D056807|207900||acidurias argininosuccinic
|
|
D056807|207900||arginino succinase deficiencies
|
|
D056807|207900||argininosuccinase deficiency
|
|
D056807|207900||arginino succinase deficiency
|
|
D056807|207900||argininosuccinate acidemia
|
|
D056807|207900||argininosuccinate acidemias
|
|
D056807|207900||argininosuccinate lyase deficiencies
|
|
D056807|207900||argininosuccinate lyase deficiency
|
|
D056807|207900||argininosuccinic acidemia
|
|
D056807|207900||argininosuccinic acid lyase deficiency
|
|
D056807|207900||argininosuccinicaciduria
|
|
D056807|207900||argininosuccinicacidurias
|
|
D056807|207900||argininosuccinic acidurias
|
|
D056807|207900||argininosuccinyl coa lyase deficiency
|
|
D056807|207900||arginosuccinase deficiency
|
|
D056807|207900||asa deficiencies
|
|
D056807|207900||asa deficiency
|
|
D056807|207900||asauria
|
|
D056807|207900||asl deficiencies
|
|
D056807|207900||asl deficiency
|
|
D056807|207900||deficiencies arginino succinase
|
|
D056807|207900||deficiencies argininosuccinate lyase
|
|
D056807|207900||deficiencies asa
|
|
D056807|207900||deficiencies asl
|
|
D056807|207900||deficiency arginino succinase
|
|
D056807|207900||deficiency argininosuccinate lyase
|
|
D056807|207900||deficiency asa
|
|
D056807|207900||deficiency asl
|
|
D056807|207900||inborn error of urea synthesis arginino succinic type
|
|
D056807|207900||urea cycle disorder arginino succinase type
|
|
D003085||colic
|
|
D003085||abdominal cramp
|
|
D003085||abdominal cramps
|
|
D003085||colic infantile
|
|
D003085||colicky pain
|
|
D003085||cramp abdominal
|
|
D003085||cramps abdominal
|
|
D003085||infantile colic
|
|
D003085||pain colicky
|
|
C567650|613308||diamond blackfan anemia 9
|
|
C567650|613308||dba9
|
|
261800|D010855||pierre robin syndrome
|
|
261800|D010855||glossoptosis micrognathia and cleft palate
|
|
261800|D010855||pierre robin sequence
|
|
261800|D010855||pierre robin apos s sequence
|
|
261800|D010855||pierre robins sequence
|
|
261800|D010855||robin syndrome pierre
|
|
261800|D010855||sequence pierre robin
|
|
261800|D010855||sequence pierre robin apos s
|
|
261800|D010855||syndrome pierre robin
|
|
612554|C567259||myopia 16
|
|
612554|C567259||myopia 16 autosomal dominant
|
|
612554|C567259||myp16
|
|
D016388||tooth loss
|
|
D016388||loss tooth
|
|
C564683|606664||glycine n methyltransferase deficiency
|
|
C564683|606664||deficiency of methionine adenosyltransferase
|
|
C564683|606664||gnmt deficiency
|
|
C564683|606664||hepatic methionine adenosyltransferase deficiency
|
|
C564683|606664||hypermethioninemia
|
|
C564683|606664||methioninemia
|
|
C564683|606664||s adenosylhomocysteine hydrolase deficiency
|
|
C563013||membranous obstruction of inferior vena cava
|
|
C536017|200610||achondrogenesis type 2
|
|
C536017|200610||acg2
|
|
C536017|200610||achondrogenesis langer saldino type
|
|
C536017|200610||achondrogenesis type ib formerly hypochondrogenesis included
|
|
C536017|200610||achondrogenesis type ii
|
|
C536017|200610||chondrogenesis imperfecta
|
|
C536017|200610||langer saldino achondrogenesis
|
|
C564344||leukodystrophy dysmyelinating with oligodontia
|
|
C564344||dentoleukoencephalopathy
|
|
C538056||agammaglobulinemia non bruton type
|
|
C538056||agammaglobulinemia autosomal recessive
|
|
C538056||agammaglobulinemia due to early prob cell defect
|
|
C538056||agammaglobulinemia non bruton type autosomal recessive
|
|
C538055||agammaglobulinemia microcephaly and severe dermatitis
|
|
C565678||convulsive disorder familial with prenatal or early onset
|
|
C564342||noonan like syndrome with loose anagen hair
|
|
C538054||aerobic actinomyces infection
|
|
C565679||contractures congenital torticollis and malignant hyperthermia
|
|
C565672||cranial nerves recurrent paresis of
|
|
C563017||gigantiform cementoma familial
|
|
C563017||cemental dysplasia periapical
|
|
C563017||cementomas familial multiple
|
|
C565673||cranial nerves congenital paresis of
|
|
C538059||agnathia microstomia synotia
|
|
C538059||agnathia microstomia synotia and cardiac and pulmonary maldevelopment
|
|
C538059||plurimalformative syndrome
|
|
C565674||cortical blindness retardation and postaxial polydactyly
|
|
C538058||aganglionosis total intestinal
|
|
C538058||near total intestinal aganglionosis
|
|
C563014||facial hemihypertrophy
|
|
C563014||hemifacial hyperplasia
|
|
C564345||parkinson disease 11
|
|
C564345|607688||park11
|
|
D047508||massive hepatic necrosis
|
|
D047508||acute yellow atrophies
|
|
D047508||acute yellow atrophy
|
|
D047508||acute yellow atrophy of liver
|
|
D047508||hepatic necrosis massive
|
|
D047508||yellow atrophy acute
|
|
D064068||collagenous sprue
|
|
D064068||collagenous sprues
|
|
D064068||sprue collagenous
|
|
D064068||sprues collagenous
|
|
D038921|303600||coffin lowry syndrome
|
|
D038921|303600||cls
|
|
D038921|303600||coffin syndrome
|
|
D038921|303600||mental retardation with osteocartilaginous abnormalities
|
|
D038921|303600||syndrome coffin
|
|
D038921|303600||syndrome coffin lowry
|
|
D003398|123100||craniosynostoses
|
|
D003398|123100||acrocephaly
|
|
D003398|123100||anterior plagiocephalies synostotic
|
|
D003398|123100||anterior plagiocephaly synostotic
|
|
D003398|123100||brachycephalies
|
|
D003398|123100||brachycephaly
|
|
D003398|123100||coronal synostoses unilateral
|
|
D003398|123100||coronal synostosis unilateral
|
|
D003398|123100||craniostenoses
|
|
D003398|123100||craniostenosis
|
|
D003398|123100||craniosynostoses lambdoidal
|
|
D003398|123100||craniosynostosis
|
|
D003398|123100||craniosynostosis 1
|
|
D003398|123100||craniosynostosis 4
|
|
D003398|123100||craniosynostosis lambdoidal
|
|
D003398|123100||craniosynostosis plagiocephalies
|
|
D003398|123100||craniosynostosis plagiocephaly
|
|
D003398|123100||craniosynostosis type 1
|
|
D003398|123100||crs
|
|
D003398|123100||crs1
|
|
D003398|123100||crs4
|
|
D003398|123100||lambdoidal craniosynostoses
|
|
D003398|123100||lambdoidal craniosynostosis
|
|
D003398|123100||lambdoid synostoses
|
|
D003398|123100||lambdoid synostosis
|
|
D003398|123100||metopic synostoses
|
|
D003398|123100||metopic synostosis
|
|
D003398|123100||oxycephaly
|
|
D003398|123100||plagiocephalies craniosynostosis
|
|
D003398|123100||plagiocephalies synostotic
|
|
D003398|123100||plagiocephalies synostotic anterior
|
|
D003398|123100||plagiocephalies synostotic posterior
|
|
D003398|123100||plagiocephaly craniosynostosis
|
|
D003398|123100||plagiocephaly synostotic
|
|
D003398|123100||plagiocephaly synostotic anterior
|
|
D003398|123100||plagiocephaly synostotic posterior
|
|
D003398|123100||posterior plagiocephalies synostotic
|
|
D003398|123100||posterior plagiocephaly synostotic
|
|
D003398|123100||sagittal synostoses
|
|
D003398|123100||sagittal synostosis
|
|
D003398|123100||scaphocephalies
|
|
D003398|123100||scaphocephaly
|
|
D003398|123100||synostoses lambdoid
|
|
D003398|123100||synostoses metopic
|
|
D003398|123100||synostoses sagittal
|
|
D003398|123100||synostoses unilateral coronal
|
|
D003398|123100||synostosis lambdoid
|
|
D003398|123100||synostosis metopic
|
|
D003398|123100||synostosis sagittal
|
|
D003398|123100||synostosis unilateral coronal
|
|
D003398|123100||synostotic anterior plagiocephalies
|
|
D003398|123100||synostotic anterior plagiocephaly
|
|
D003398|123100||synostotic plagiocephalies
|
|
D003398|123100||synostotic plagiocephaly
|
|
D003398|123100||synostotic posterior plagiocephalies
|
|
D003398|123100||synostotic posterior plagiocephaly
|
|
D003398|123100||trigonocephalies
|
|
D003398|123100||trigonocephaly
|
|
D003398|123100||unilateral coronal synostoses
|
|
D003398|123100||unilateral coronal synostosis
|
|
C535424|176860||congenital thrombotic disease due to protein c deficiency
|
|
C535424|176860||proc deficiency
|
|
C535424|176860||proc deficiency autosomal dominant protein c deficiency acquired included
|
|
C535424|176860|C567163||protein c deficiency autosomal dominant
|
|
C535424|176860||thph3
|
|
C535424|176860||thrombophilia due to protein c deficiency autosomal dominant
|
|
C535424|176860||thrombophilia hereditary due to pc deficiency
|
|
C536771|601706||yemenite deaf blind hypopigmentation syndrome
|
|
C536771|601706||warburg thomsen syndrome
|
|
C536771|601706||yemenite warburg deaf blind hypopigmentation syndrome
|
|
C538051||adrenomyodystrophy
|
|
D003095||collagen diseases
|
|
D003095||collagen disease
|
|
D003095||disease collagen
|
|
D003095||diseases collagen
|
|
D003092||colitis
|
|
D003092||colitides
|
|
604772||ventricular tachycardia catecholaminergic polymorphic 1 with or without atrial dysfunction and or dilated cardiomyopathy
|
|
604772||cpvt1
|
|
604772|611938||ventricular tachycardia stress induced polymorphic
|
|
604772|611938||vtsip
|
|
C565681||terminal transverse defects of arm
|
|
C565682||amputation congenital
|
|
121050|C536211||congenital contractural arachnodactyly
|
|
121050|C536211||arachnodactyly contractural beals type
|
|
121050|C536211||arthrogryposis distal type 9
|
|
121050|C536211||beals hecht syndrome
|
|
121050|C536211||beals syndrome
|
|
121050|C536211||cca
|
|
121050|C536211||contractural arachnodactyly congenital
|
|
121050|C536211||contractures multiple with arachnodactyly
|
|
121050|C536211||da9
|
|
121050|C536211||ear anomalies contractures dysplasia of bone with kyphoscoliosis
|
|
C566930|611498||nephronophthisis 7
|
|
C566930|611498||nphp7
|
|
D016399||lymphoma t cell
|
|
D016399||lymphomas t cell
|
|
D016399||t cell lymphoma
|
|
D016399||t cell lymphomas
|
|
C566975||febrile convulsions familial 8
|
|
C565644||deafness conductive with malformed external ear
|
|
C565645||deafness cochlear with myopia and intellectual impairment
|
|
C566557|613313||hemochromatosis type 2b
|
|
C566557|613313||hfe2b
|
|
C563854|608807||muscular dystrophy limb girdle type 2j
|
|
C563854|608807||lgmd2j
|
|
C538065|136760||frontonasal dysplasia
|
|
C538065|136760||frontonasal malformation
|
|
C538065|136760||frontorhiny
|
|
C538065|136760||median facial cleft syndrome
|
|
C565646||deafness congenital with total albinism
|
|
D015043||zollinger ellison syndrome
|
|
D015043||syndrome zollinger ellison
|
|
C565640||deafness neural congenital moderate
|
|
C564680|606675||inflammatory bowel disease 4
|
|
C564680|606675||ibd4
|
|
C564313||epilepsy myoclonic benign adult familial type 2
|
|
C564313|607876||bafme2
|
|
C564313|607876||benign adult familial myoclonic epilepsy 2
|
|
C564313|607876||cortical myoclonus and epilepsy autosomal dominant
|
|
C564313|607876||epilepsy familial adult myoclonic 2
|
|
C564313|607876||fame2
|
|
C538069||fryns hofkens fabry syndrome
|
|
C538069||ulna hypoplasia
|
|
C538069||ulnar hypoplasia
|
|
C538069||upper limb mesomelic dysplasia
|
|
C566973||dystonia focal task specific
|
|
C566973||focal hand dystonia
|
|
C566973||focal task specific dystonia
|
|
C566973||occupational cramp
|
|
C566973||occupational dystonia
|
|
C566973||task specific dystonia
|
|
C566973||task specific focal dystonia
|
|
C565642||deafness congenital with vitiligo and achalasia
|
|
C564312|278150|D007039||hypotrichosis localized autosomal recessive 1
|
|
C564312|278150|D007039||hypotrichosis localized autosomal recessive
|
|
C564317||muscular dystrophy congenital due to partial lama2 deficiency
|
|
C566978||copd severe early onset
|
|
C538063||fronto facio nasal dysplasia
|
|
C538063||fronto facio nasal dysostosis
|
|
C538063||frontofacionasal dysostosis
|
|
C538063||frontofacionasal dysplasia
|
|
C538062||frints de smet fabry fryns syndrome
|
|
C538062||symbrachydactyly of the hand and foot
|
|
C565649||deafness congenital and familial myoclonic epilepsy
|
|
C538061||friedreich ataxia congenital glaucoma
|
|
C538061||congenital glaucoma and friedreich ataxia
|
|
C538061||friedreich ataxia and congenital glaucoma
|
|
D004393||dwarfism pituitary
|
|
D004393||dwarfism growth hormone deficiency
|
|
D004393||growth hormone deficiency dwarfism
|
|
D004393||hypophysial dwarf
|
|
D004393||hyposomatotrophic dwarfism
|
|
D004393||isolated gh deficiency
|
|
D004393||isolated growth hormone deficiency
|
|
D004393||isolated hgh deficiency
|
|
D004393||isolated human growth hormone deficiency
|
|
D004393||isolated somatotropin deficiency
|
|
D004393||isolated somatotropin deficiency disorder
|
|
D004393||nanism pituitary
|
|
D004393||pituitary dwarf
|
|
D004393||pituitary dwarfism
|
|
D004393||pituitary nanism
|
|
D004392||dwarfism
|
|
D004392||nanism
|
|
C536048|610682||osteogenesis imperfecta type 7
|
|
C536048|610682||oi2b formerly
|
|
C536048|610682|C565200||oi7
|
|
C536048|610682|C565200||oi type vii
|
|
C536048|610682||osteogenesis imperfecta type iib formerly
|
|
C536048|610682|C565200||osteogenesis imperfecta type vii
|
|
C536213|606785||crigler najjar syndrome type 2
|
|
C536213|606785||crigler najjar syndrome type ii
|
|
C536213|606785||hblrcn2
|
|
C536213|606785||hyperbilirubinemia crigler najjar type ii
|
|
D028361||mitochondrial diseases
|
|
D028361||deficiencies oxidative phosphorylation
|
|
D028361||deficiencies respiratory chain
|
|
D028361||deficiency oxidative phosphorylation
|
|
D028361||deficiency respiratory chain
|
|
D028361||disease mitochondrial
|
|
D028361||disorder mitochondrial
|
|
D028361||disorders mitochondrial
|
|
D028361||electron transport chain deficiencies mitochondrial
|
|
D028361||mitochondrial disease
|
|
D028361||mitochondrial disorder
|
|
D028361||mitochondrial disorders
|
|
D028361||mitochondrial electron transport chain deficiencies
|
|
D028361||mitochondrial respiratory chain deficiencies
|
|
D028361||oxidative phosphorylation deficiencies
|
|
D028361||oxidative phosphorylation deficiency
|
|
D028361||phosphorylation deficiencies oxidative
|
|
D028361||phosphorylation deficiency oxidative
|
|
D028361||respiratory chain deficiencies mitochondrial
|
|
D028361||respiratory chain deficiency
|
|
D017699||pelvic pain
|
|
D017699||pain pelvic
|
|
D017699||pains pelvic
|
|
D017699||pelvic pains
|
|
D016369||smear layer
|
|
D016369||layer smear
|
|
D017695||soft tissue injuries
|
|
D017695||injuries soft tissue
|
|
D017695||injury soft tissue
|
|
D017695||soft tissue injury
|
|
D017696||myopathies nemaline
|
|
D017696||adult onset nemaline myopathy
|
|
D017696||autosomal dominant nemaline myopathy
|
|
D017696||autosomal recessive nemaline myopathy
|
|
D017696||childhood onset nemaline myopathy
|
|
D017696||late onset nemaline myopathy
|
|
D017696||myopathies rod
|
|
D017696||myopathies rod body
|
|
D017696||myopathy nemaline
|
|
D017696||myopathy rod
|
|
D017696||myopathy rod body
|
|
D017696||nemaline body disease
|
|
D017696||nemaline myopathies
|
|
D017696||nemaline myopathy
|
|
D017696||nemaline myopathy adult onset
|
|
D017696||nemaline myopathy autosomal dominant
|
|
D017696||nemaline myopathy autosomal recessive
|
|
D017696||nemaline myopathy childhood onset
|
|
D017696||nemaline myopathy late onset
|
|
D017696||nemaline rod disease
|
|
D017696||rod body disease
|
|
D017696||rod body myopathies
|
|
D017696||rod body myopathy
|
|
D017696||rod myopathies
|
|
D017696||rod myopathy
|
|
C538079||charcot marie tooth disease with ptosis and parkinsonism
|
|
C566985||microphthalmia syndromic 10
|
|
C566985||mcops10
|
|
C566985||microphthalmia and brain atrophy
|
|
C538078|C566136|118300||charcot marie tooth disease and deafness
|
|
C538078||deafness with charcot marie tooth disease
|
|
C538078||neuropathy hereditary motor and sensory with deafness mental retardation and absent sensory large myelinated fibers
|
|
C565655||cystinosis infantile nephropathic
|
|
C538077||charcot marie tooth type 1 aplasia cutis congenita
|
|
C538077||charcot marie tooth peroneal muscular atrophy x linked with aplasia cutis congenita
|
|
C566988||hypertelorism severe with midface prominence myopia mental retardation and bone fragility
|
|
C565657||cystic kidney disease with ventriculomegaly
|
|
142330|C564190||hepatic adenomas familial
|
|
142330|C564190||liver cell adenomas familial
|
|
C566981||creutzfeldt jakob disease heidenhain variant
|
|
C564325||charcot marie tooth disease autosomal dominant type 2k
|
|
C565652||cystinuria type a
|
|
C565652||cystinuria type a b
|
|
C565652||cystinuria type b
|
|
D015051||zygomatic fractures
|
|
D015051||fractures zygomatic
|
|
D015051||fracture zygomatic
|
|
D015051||zygomatic fracture
|
|
C564323||neuroticism
|
|
C538071||fuchs atrophia gyrata chorioideae et retinae
|
|
C538071||fuchs gyrate atrophy
|
|
C538071||fuchs gyrate atrophy of the choroid and retina
|
|
C538070||fryns syndrome
|
|
C538070||diaphragmatic hernia abnormal face and distal limb anomalies
|
|
C538070||moerman van den berghe fryns syndrome
|
|
C564329||alzheimer disease familial 3 with spastic paraparesis and unusual plaques
|
|
C538075||chang davidson carlson syndrome
|
|
C566989||short stature mental retardation callosal agenesis heminasal hypoplasia microphthalmia and atypical clefting
|
|
C565658||cystic fibrosis with helicobacter pylori gastritis megaloblastic anemia and subnormal mentality
|
|
C538074||curly hair ankyloblepharon nail dysplasia syndrome
|
|
C538074||chands
|
|
C565659||cysteine peptiduria
|
|
182230|C531815||hypopituitarism and septooptic apos dysplasia apos
|
|
182230|C531815||cphd5 included
|
|
182230|C531815||de morsier syndrome pituitary hormone deficiency combined 5 included
|
|
182230|C531815||growth hormone deficiency with pituitary anomalies included
|
|
C538072||cervical ribs sprengel anomaly anal atresia urethral obstruction
|
|
C538072||cervical ribs sprengel anomaly anal atresia and urethral obstruction
|
|
C538072||cervical ribs sprengel anomaly preaxial polydactyly anal atresia and urethral obstruction
|
|
D003072||cognition disorders
|
|
D003072||disorder cognition
|
|
D003072||disorders cognition
|
|
D003072||overinclusion
|
|
D003074||solitary pulmonary nodule
|
|
D003074||coin lesion pulmonary
|
|
D003074||coin lesions pulmonary
|
|
D003074||lesion pulmonary coin
|
|
D003074||lesions pulmonary coin
|
|
D003074||nodule solitary pulmonary
|
|
D003074||nodules solitary pulmonary
|
|
D003074||pulmonary coin lesion
|
|
D003074||pulmonary coin lesions
|
|
D003074||pulmonary nodule solitary
|
|
D003074||pulmonary nodules solitary
|
|
D003074||solitary pulmonary nodules
|
|
C565633|221900||retinal nonattachment nonsyndromic congenital
|
|
C565633|221900||detachment of retina congenital
|
|
C565633|221900||ncrna
|
|
C565633|221900||retinal detachment congenital
|
|
C565633|221900||rnanc
|
|
D015047||zoonoses
|
|
D015047||diseases zoonotic
|
|
D015047||diseases zoonotic infectious
|
|
D015047||disease zoonotic
|
|
D015047||disease zoonotic infectious
|
|
D015047||infections zoonotic
|
|
D015047||infection zoonotic
|
|
D015047||infectious diseases zoonotic
|
|
D015047||infectious disease zoonotic
|
|
D015047||zoonotic disease
|
|
D015047||zoonotic diseases
|
|
D015047||zoonotic infection
|
|
D015047||zoonotic infections
|
|
D015047||zoonotic infectious disease
|
|
D015047||zoonotic infectious diseases
|
|
C565660||cyanosis and hepatic disease
|
|
D064090||intraocular lymphoma
|
|
D064090||intraocular lymphomas
|
|
D064090||lymphoma intraocular
|
|
D064090||lymphomas intraocular
|
|
611277|C565811||generalized epilepsy with febrile seizures plus type 3
|
|
611277|C565811||feb8 included
|
|
611277|C565811||gefsp3
|
|
611277|C565811||gefs type 3
|
|
611277|C565811||gefs type 3 gefs 3 febrile seizures familial 8 included
|
|
C567097|611722||krabbe disease atypical due to saposin a deficiency
|
|
C567097|611722||saposin a deficiency
|
|
C540322||hemorrhagic jaundice
|
|
C540322||icterohemorrhagic fever
|
|
C565621||disseminated sclerosis with narcolepsy
|
|
C538000||dystelephalangy
|
|
C538000||kirner deformity
|
|
D017682||myocardial stunning
|
|
D017682||hibernation myocardial
|
|
D017682||myocardial hibernation
|
|
D017682||myocardium stunned
|
|
D017682||stunned myocardium
|
|
D017682||stunning myocardial
|
|
C565624||2 4 dienoyl coa reductase deficiency
|
|
C538004|128101|C536698||dystonia musculorum deformans 4
|
|
C538004|128101|C536698||dystonia 4 torsion autosomal dominant
|
|
C538004||torsion dystonia 4 autosomal dominant type
|
|
C566950||hypotrichosis localized autosomal recessive 3
|
|
C565620||diverticulosis small intestinal
|
|
D004368||dry socket
|
|
D004368||alveolalgia
|
|
D004368||alveolalgias
|
|
D004368||alveolar osteitides
|
|
D004368||alveolar osteitis
|
|
D004368||alveolar periostitides
|
|
D004368||alveolar periostitis
|
|
D004368||alveolitis sicca dolorosa
|
|
D004368||dry sockets
|
|
D004368||osteitides alveolar
|
|
D004368||osteitis alveolar
|
|
D004368||periostitides alveolar
|
|
D004368||periostitis alveolar
|
|
D004368||socket dry
|
|
D004368||sockets dry
|
|
C566956||ataxia spastic 3 autosomal recessive
|
|
C566956|611390||autosomal recessive spastic ataxia with leukoencephalopathy
|
|
C565626||diastrophic dysplasia broad bone platyspondylic variant
|
|
600628|D058247||loose anagen hair syndrome
|
|
600628|D058247||anagen syndrome loose
|
|
600628|D058247||anagen syndromes loose
|
|
600628|D058247||loose anagen syndrome
|
|
600628|D058247||loose anagen syndromes
|
|
600628|D058247||syndrome loose anagen
|
|
600628|D058247||syndromes loose anagen
|
|
C565627||trichohepatoenteric syndrome
|
|
C565627||diarrhea fatal infantile with trichorrhexis nodosa
|
|
C565627||diarrhea syndromic
|
|
304400|C536424||progressive hearing loss stapes fixation
|
|
304400|C536424||deafness 3 conductive with stapes fixation
|
|
304400|C536424||deafness conductive with stapes fixation
|
|
304400|C536424||deafness mixed with perilymphatic gusher
|
|
304400|C536424||deafness x linked 2
|
|
304400|C536424||dfn3
|
|
304400|C536424||dfnx2
|
|
304400|C536424||nance deafness
|
|
304400|C536424||perilymphatic gusher deafness syndrome
|
|
304400|C536424||sensorineural deafness profound with or without a conductive component
|
|
304400|C536424||sensorineural deafness profound with or without a conductive component associated with a unique developmental abnormality of the ear
|
|
C538374|602485||hyperinsulinemic hypoglycemia familial 3
|
|
C538374|602485||hhf3
|
|
D015012||yersinia pseudotuberculosis infections
|
|
D015012||infections yersinia pseudotuberculosis
|
|
D015012||pasteurella pseudotuberculoses
|
|
D015012||pasteurella pseudotuberculosis
|
|
D015012||pseudotuberculoses pasteurella
|
|
D015012||pseudotuberculosis pasteurella
|
|
D017674||hypophosphatemia
|
|
D017674||hypophosphatemias
|
|
D017675||crest syndrome
|
|
D017675||calcinosis raynaud phenomenon sclerodactyly telangiectasia
|
|
D017675||calcinosis raynaud apos s phenomenon esophageal dismobility sclerodactyly telangiectasia syndrome
|
|
D017675||crest syndromes
|
|
D017675||crst syndrome
|
|
D017675||crst syndromes
|
|
D017675||phenomenon sclerodactyly telangiectasia calcinosis raynaud
|
|
D017675||syndrome crest
|
|
D017675||syndrome crst
|
|
D017676||lichen planus oral
|
|
D017676||oral lichen planus
|
|
103580|D011547||pseudohypoparathyroidism type ia
|
|
103580|D011547||albright hereditary osteodystrophy with multiple hormone resistance
|
|
103580||php1a
|
|
103580|D011547||php ia
|
|
C565632||diabetes insipidus nephrogenic with mental retardation and intracerebral calcification
|
|
D006502|600880||budd chiari syndrome
|
|
D006502|600880||bdchs
|
|
D006502|600880||chiari apos s syndrome
|
|
D006502|600880||chiaris syndrome
|
|
D006502|600880||chiari syndrome
|
|
D006502|600880||hepatic vein thromboses
|
|
D006502|600880||hepatic vein thrombosis
|
|
D006502|600880||hepatic venous outflow obstruction
|
|
D006502|600880||membranous obstruction of inferior vena cava included
|
|
D006502|600880||movc included
|
|
D006502|600880||thromboses hepatic vein
|
|
D006502|600880||thrombosis hepatic vein
|
|
D006502|600880||vein thromboses hepatic
|
|
D006502|600880||vein thrombosis hepatic
|
|
C538011||eales disease
|
|
C538011||idiopathic obliterative vasculopathy
|
|
C538011||idiopathic recurrent vitreal hemorrhage
|
|
C538010||eagle syndrome
|
|
C538010||eagle apos s syndrome
|
|
C538010||elongated styloid process syndrome
|
|
C538010||styloid stylohoid syndrome
|
|
C566966||persistent hyperplastic primary vitreous autosomal recessive
|
|
C566966||persistent hyperplastic primary vitreous autosomal dominant
|
|
C538016||ectodermal dysplasia alopecia preaxial polydactyly
|
|
C538016||absence of body amp scalp hair rounded nails thin dental enamel preaxial polydactyly of the feet and unusual facial appearance
|
|
C564303||thai symphalangism syndrome
|
|
C538015||ectodermal dysplasia adrenal cyst
|
|
C538015||adrenal cyst with ectodermal dysplasia
|
|
C538015||ectodermal dysplasia with adrenal cyst
|
|
C565630||diaminopentanuria
|
|
C565630||cystine lysinuria
|
|
165800|C580095||osteochondritis dissecans short stature and early onset osteoarthritis
|
|
165800||od
|
|
611938|C536334||ventricular tachycardia catecholaminergic polymorphic 2
|
|
611938|C536334||cpvt2
|
|
C565631||wolfram like syndrome autosomal dominant
|
|
D003047||coccidioidomycosis
|
|
D003047||coccidioides immitis infection
|
|
D003047||coccidioides immitis infections
|
|
D003047||coccidioidomycoses
|
|
D003047||infection coccidioides immitis
|
|
D003047||infections coccidioides immitis
|
|
D003047||san joaquin valley fever
|
|
D003047||valley fever
|
|
D003047||valley fevers
|
|
D004379||duodenal neoplasms
|
|
D004379||cancer duodenal
|
|
D004379||cancer of duodenum
|
|
D004379||cancer of the duodenum
|
|
D004379||duodenal cancer
|
|
D004379||duodenal neoplasm
|
|
D004379||duodenum cancer
|
|
D004379||neoplasm duodenal
|
|
D004379||neoplasms duodenal
|
|
D003048||coccidiosis
|
|
D003048||besnoitiases
|
|
D003048||besnoitiasis
|
|
D003048||besnoitioses
|
|
D003048||besnoitiosis
|
|
D003048||coccidioses
|
|
D004378||duodenal diseases
|
|
D004378||disease duodenal
|
|
D004378||diseases duodenal
|
|
D004378||duodenal disease
|
|
C564307||combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia
|
|
C564307||spondyloenchondrodysplasia with immune dysregulation
|
|
C564305||diaphanospondylodysostosis
|
|
C564305||vertebral ossification defect in with nephrogenic rests
|
|
D003043||cocarcinogenesis
|
|
D003043||cocarcinogeneses
|
|
C565637||deafness sensorineural autosomal mitochondrial type
|
|
D004377||dumping syndrome
|
|
D004377||dumping syndromes
|
|
D004377||syndrome dumping
|
|
D004377||syndromes dumping
|
|
C566969||ataxia spastic 2 autosomal recessive
|
|
C565111|125480||major affective disorder 1
|
|
C565111|125480|C567074|611535|611247|C567073|309200|C564108|C567075|611536||bpad
|
|
C565111|125480||mafd1
|
|
C565111|125480|D001714||manic depressive psychosis
|
|
C565111|125480||manic depressive psychosis autosomal
|
|
C565111|125480||md1
|
|
C565639||deafness neural with atypical atopic dermatitis
|
|
C563713|609469||nephropathy progressive with deafness
|
|
C563713|609469||alport focal segmental glomerulosclerosis like syndrome
|
|
C563713|609469||nede
|
|
D004382||duodenitis
|
|
D004382||duodenitis erosive
|
|
D004382||erosive duodenitis
|
|
D004381||duodenal ulcer
|
|
D004381||curling apos s ulcer
|
|
D004381||curlings ulcer
|
|
D004381||curling ulcer
|
|
D004381||duodenal ulcers
|
|
D004381||ulcer curling
|
|
D004381||ulcer duodenal
|
|
D004381||ulcers duodenal
|
|
D004383||duodenogastric reflux
|
|
D004383||duodenal reflux
|
|
D004383||duodenal refluxs
|
|
D004383||duodeno gastric reflux
|
|
D004383||reflux duodenal
|
|
D004383||reflux duodenogastric
|
|
D004383||reflux duodeno gastric
|
|
C537914|215045||chondrodysplasia blomstrand type
|
|
C537914|215045||blomstrand lethal osteochondrodysplasia
|
|
C537914|215045||blomstrand osteochondrodysplasia
|
|
C537914|215045||blomstrand syndrome
|
|
C537914|215045||bocd
|
|
C537914|215045||lethal congenital dwarfism with accelerated skeletal maturation
|
|
D004380||duodenal obstruction
|
|
D004380||duodenal obstructions
|
|
D004380||obstruction duodenal
|
|
D004380||obstructions duodenal
|
|
C535696|154276||malignant hyperthermia susceptibility type 3
|
|
C535696|154276||malignant hyperpyrexia susceptibility type 3
|
|
C535696|154276||malignant hyperthermia susceptibility to 3
|
|
C535696|154276||mhs3
|
|
D017688||cholera morbus
|
|
D017688||choleras summer
|
|
D017688||cholera summer
|
|
D017688||summer cholera
|
|
D017688||summer choleras
|
|
D017689||polydactyly
|
|
D017689||hyperdactylies
|
|
D017689||hyperdactyly
|
|
D017689||polydactylia
|
|
D017689||polydactylias
|
|
D017689||polydactylies
|
|
D017689||polydactylism
|
|
D017689||polydactylisms
|
|
C538133|612933||lactate dehydrogenase deficiency type a
|
|
C538133|612933|D005198|134600||glycogen storage disease xi
|
|
C538133|612933||gsd11
|
|
C538133|612933||gsd xi
|
|
C538133|612933||lactate dehydrogenase a deficiency
|
|
184252|C535797||spondylometaphyseal dysplasia kozlowski type
|
|
184252|C535797||smdk
|
|
184252|C535797||smd kozlowski type
|
|
D059525||supraglottitis
|
|
D059525||supraglottitides
|
|
C565740|604864||osteoarthritis with mild chondrodysplasia
|
|
C538024||chromosome 9p deletion syndrome
|
|
C538024||chromosome 9 monosomy 9p
|
|
C538024||monosomy 9p
|
|
C538024||monosomy 9p syndrome
|
|
C538023||chromosome 9 duplication 9q21
|
|
C538023||disomy 9q21
|
|
C538023||duplication 9q21
|
|
C565600||ehlers danlos syndrome with platelet dysfunction from fibronectin abnormality
|
|
C565600||ehlers danlos syndrome dysfibronectinemic type
|
|
C565600||ehlers danlos syndrome type x
|
|
C538022||chromosome 9 ring
|
|
C538022||ring 9 chromosome
|
|
C565601||ectrodactyly polydactyly
|
|
C538021||chromosome 9 inversion or duplication
|
|
C538021||trisomy 9 translocation
|
|
C566933|611490||osteopetrosis autosomal recessive 4
|
|
C566933|611490||osteopetrosis infantile malignant 2
|
|
C536987|257300||mosaic variegated aneuploidy syndrome
|
|
C536987|257300||chromosomal mosaicism due to mitotic instability
|
|
C536987|257300||instability mitotic non disjunction syndrome
|
|
C536987|257300||mixoploidy familial
|
|
C536987|257300||mosaicism chromosomal
|
|
C536987|257300||mosaic variegated aneuploidy syndrome 1
|
|
C536987|257300||mva1
|
|
C536987|257300||mva syndrome
|
|
C536987|257300||nondisjunction
|
|
C538028||chromosome 9 trisomy
|
|
C538028||duplication 9
|
|
C538028||trisomy 9
|
|
C538027||chromosome 9 tetrasomy 9p
|
|
C538027||chromosome 9 tetrasomy 9p mosaicism
|
|
C538027||mosaic tetrasomy 9p
|
|
C538027||tetrasomy 9p
|
|
C538027||tetrasomy short arm of chromosome 9
|
|
C538026||chromosome 9 partial trisomy 9p
|
|
C538026||duplication 9p partial
|
|
C538026||trisomy 9p partial
|
|
C538025||chromosome 9 partial monosomy 9p
|
|
C538025||9p partial monosomy
|
|
C538025||9p syndrome partial
|
|
C538025||deletion 9p syndrome partial
|
|
C538025||distal monosomy 9p
|
|
C538025||partial deletion of short arm of chromosome 9
|
|
C567463|300756||alzheimer disease 16
|
|
C567463|300756||ad16
|
|
C566938||mpgn ii with complement factor h deficiency
|
|
D003015||clostridium infections
|
|
D003015||clostridium infection
|
|
D003015||infection clostridium
|
|
D003015||infections clostridium
|
|
C565334|605375||epilepsy nocturnal frontal lobe type 3
|
|
C565334|605375||enfl3
|
|
C565334|605375||epilepsy nocturnal frontal lobe 3
|
|
C566939||glomerulonephritis with isolated c3 deposits and factor h deficiency
|
|
C566939||membranoproliferative glomerulonephritis type ii with complement factor h deficiency
|
|
C565608||dystonia with ringbinden
|
|
D004342||drug hypersensitivity
|
|
D004342||allergies drug
|
|
D004342||allergy drug
|
|
D004342||drug allergies
|
|
D004342||drug allergy
|
|
D004342||drug hypersensitivities
|
|
D004342||hypersensitivities drug
|
|
D004342||hypersensitivity drug
|
|
C538020||chromosome 8 trisomy 8q
|
|
C538020||duplication 8q
|
|
C538020||trisomy 8q
|
|
C566934||corticosteroid binding globulin elevated
|
|
C565603||cleft lip with or without cleft palate nonsyndromic 7
|
|
C565604||ectodermal dysplasia hypohidrotic with hypothyroidism and ciliary dyskinesia
|
|
C565605||ectodermal dysplasia hypohidrotic with hypothyroidism and agenesis of the corpus callosum
|
|
C563791|609128||arthrogryposis distal type 4
|
|
C563791|609128||arthrogryposis distal type iid
|
|
C563791|609128||arthrogryposis with severe scoliosis
|
|
C563791|609128||da4
|
|
C563791|609128||daiid
|
|
D005674||fusobacterium infections
|
|
D005674||fusobacterium infection
|
|
D005674||infection fusobacterium
|
|
D005674||infections fusobacterium
|
|
D005674||infection sphaerophorus
|
|
D005674||infections sphaerophorus
|
|
D005674||necrobacilloses
|
|
D005674||necrobacillosis
|
|
D005674||sphaerophorus infection
|
|
D005674||sphaerophorus infections
|
|
C565606||ectodermal dysplasia and neurosensory deafness
|
|
C553654||congenital deficiency of pulmonary surfactant protein b
|
|
C553654||congenital surfactant protein b deficiency
|
|
C553654||pulmonary surfactant protein b deficiency of
|
|
C553654||surfactant protein b deficiency
|
|
253600|C535895||limb girdle muscular dystrophy type 2a
|
|
253600|C535895||calpainopathy
|
|
253600|C535895||calpainopathy myositis eosinophilic included
|
|
253600|C535895||leyden moebius muscular dystrophy
|
|
253600|C535895||lgmd2
|
|
253600|C535895||lgmd2a
|
|
253600|C535895||limb girdle muscular dystrophy type 2
|
|
253600|C535895||muscular dystrophy limb girdle type 2
|
|
253600|C535895||muscular dystrophy limb girdle type 2a
|
|
253600|C535895||muscular dystrophy pelvofemoral
|
|
114480|D001943||breast neoplasms
|
|
114480|D001943||breast cancer
|
|
114480|D001943||breast cancer familial breast cancer familial male included
|
|
114480|D001943||breast carcinoma
|
|
114480|D001943||breast neoplasm
|
|
114480|D001943||breast tumor
|
|
114480|D001943||breast tumors
|
|
114480|D001943||cancer breast
|
|
114480|D001943||cancer of breast
|
|
114480|D001943||cancer of the breast
|
|
114480|D001943||carcinoma human mammary
|
|
114480|D001943||carcinomas human mammary
|
|
114480|D001943||human mammary carcinoma
|
|
114480|D001943||human mammary carcinomas
|
|
114480|D001943||human mammary neoplasm
|
|
114480|D001943||human mammary neoplasms
|
|
114480|D001943||malignant neoplasm of breast
|
|
114480|D001943||malignant tumor of breast
|
|
114480|D001943||mammary cancer
|
|
114480|D001943||mammary carcinoma human
|
|
114480|D001943||mammary carcinomas human
|
|
114480|D001943||mammary neoplasm human
|
|
114480|D001943||mammary neoplasms human
|
|
114480|D001943||neoplasm breast
|
|
114480|D001943||neoplasm human mammary
|
|
114480|D001943||neoplasms breast
|
|
114480|D001943||neoplasms human mammary
|
|
114480|D001943||tumor breast
|
|
114480|D001943||tumors breast
|
|
C566976|611276||glaucoma 1 open angle h
|
|
C566976|611276||glc1h
|
|
C562704|173100||isolated growth hormone deficiency type ii
|
|
C562704|173100||growth hormone deficiency isolated autosomal dominant
|
|
C562704|173100||ighd2
|
|
C562704|173100||ighd ii
|
|
C562704|173100||pituitary dwarfism due to isolated growth hormone deficiency autosomal dominant
|
|
C537421|114030||cafe au lait spots multiple
|
|
C537421|114030||multiple cafe au lait spots
|
|
C538019||chromosome 8 trisomy 8p
|
|
C538019||duplication 8p
|
|
C538019||trisomy 8p
|
|
C567676|613269||corneal dystrophy fuchs endothelial 5
|
|
C567676|613269||fcd3 locus
|
|
C567676|613269||fecd5
|
|
C538018||ectodermal dysplasia mental retardation syndactyly
|
|
C538018||ectodermal dysplasia with mental retardation and syndactyly
|
|
C538035||chromosome 15 ring
|
|
C538035||ring 15 chromosome
|
|
C538035||ring 15 chromosome mosaic pattern
|
|
C565610||dysmyelination with jaundice
|
|
C538034||chromosome 14q terminal duplication
|
|
C538034||duplication 14qter
|
|
C538034||trisomy 14qter
|
|
C538033||chromosome 14q terminal deletion
|
|
C538033||deletion 14qter
|
|
C538033||monosomy 14qter
|
|
C538032||chromosome 14q proximal duplication
|
|
C538032||duplication 14q proximal
|
|
C538032||trisomy 14q proximal
|
|
C538039||chromosome 15q tetrasomy
|
|
C538039||tetrasomy 15q
|
|
C538038||chromosome 15q partial deletion
|
|
C538038||deletion 15q1
|
|
C538038||deletion 15q25
|
|
C538038||monosomy 15q1
|
|
C538038||monosomy 15q25
|
|
C538037||chromosome 15 trisomy mosaicism
|
|
C538037||trisomy 15 mosaicism
|
|
C538037||uniparental disomy of 15
|
|
C538036||partial duplication 15q syndrome
|
|
C538036||chromosome 15 distal trisomy 15q
|
|
C538036||chromosome 15 trisomy 15q2
|
|
C538036||distal duplication 15q
|
|
C566949||tremor hereditary essential 3
|
|
C565618||dk phocomelia syndrome
|
|
C565618||phocomelia thrombocytopenia encephalocele urogenital malformations
|
|
C565618||von voss cherstvoy syndrome
|
|
D005687||galactorrhea
|
|
D005687||galactorrheas
|
|
C565619||diverticulosis of bowel hernia and retinal detachment
|
|
D003027||cluster headache
|
|
D003027||atypical cluster headache
|
|
D003027||atypical cluster headaches
|
|
D003027||cephalgia histamine
|
|
D003027||cephalgias histamine
|
|
D003027||chronic cluster headache
|
|
D003027||chronic cluster headaches
|
|
D003027||ciliary neuralgia
|
|
D003027||ciliary neuralgias
|
|
D003027||cluster headache atypical
|
|
D003027||cluster headache chronic
|
|
D003027||cluster headache episodic
|
|
D003027||cluster headaches
|
|
D003027||cluster headaches atypical
|
|
D003027||cluster headaches chronic
|
|
D003027||cluster headaches episodic
|
|
D003027||cluster headache syndrome
|
|
D003027||cluster headache syndromes
|
|
D003027||episodic cluster headache
|
|
D003027||episodic cluster headaches
|
|
D003027||headache atypical cluster
|
|
D003027||headache chronic cluster
|
|
D003027||headache cluster
|
|
D003027||headache episodic cluster
|
|
D003027||headaches atypical cluster
|
|
D003027||headaches chronic cluster
|
|
D003027||headaches cluster
|
|
D003027||headaches episodic cluster
|
|
D003027||headache syndrome cluster
|
|
D003027||headache syndromes cluster
|
|
D003027||histamine cephalgia
|
|
D003027||histamine cephalgias
|
|
D003027||horton apos s syndrome
|
|
D003027||hortons syndrome
|
|
D003027||horton syndrome
|
|
D003027||migraine neuralgic
|
|
D003027||migraines neuralgic
|
|
D003027||neuralgia ciliary
|
|
D003027||neuralgias ciliary
|
|
D003027||neuralgic migraine
|
|
D003027||neuralgic migraines
|
|
D003027||syndrome cluster headache
|
|
D003027||syndrome horton
|
|
D003027||syndrome horton apos s
|
|
D003027||syndromes cluster headache
|
|
C538031||chromosome 14q partial deletions
|
|
C538031||deletion 14q11
|
|
C538031||deletion 14q31
|
|
C538031||monosomy 14q11
|
|
C538031||monosomy 14q31
|
|
C565614||dwarfism proportionate with hip dislocation
|
|
C538030||chromosome 9 trisomy 9q
|
|
C538030||duplication 9q
|
|
C538030||trisomy 9q
|
|
D005683||gagging
|
|
D005683||pharyngeal reflex
|
|
D005683||reflex pharyngeal
|
|
C565615||dwarfism low birth weight type with unresponsiveness to growth hormone
|
|
C566948||kallmann syndrome 2 with selective tooth agenesis
|
|
C565617||dohle bodies and leukemia
|
|
610446|D054312||buruli ulcer
|
|
610446|D054312||buruli ulcer disease
|
|
610446|D054312||buruli ulcer diseases
|
|
610446|D054312||buruli ulcer susceptibility to
|
|
610446|D054312||disease buruli ulcer
|
|
610446|D054312||diseases buruli ulcer
|
|
610446|D054312||infection mycobacterium ulcerans
|
|
610446|D054312||infections mycobacterium ulcerans
|
|
610446|D054312||mycobacterium ulcerans infection
|
|
610446|D054312||mycobacterium ulcerans infections
|
|
610446|D054312||mycobacterium ulcerans susceptibility to
|
|
610446|D054312||ulcer buruli
|
|
610446|D054312||ulcer disease buruli
|
|
610446|D054312||ulcer diseases buruli
|
|
D015009||yersinia infections
|
|
D015009||infections yersinia
|
|
D015009||infection yersinia
|
|
D015009||yersinia infection
|
|
D059545||paraneoplastic syndromes ocular
|
|
D059545||bilateral diffuse uveal melanocytic proliferation paraneoplastic
|
|
D059545||cancer associated retinopathies
|
|
D059545||cancer associated retinopathy
|
|
D059545||disease ocular paraneoplastic
|
|
D059545||diseases ocular paraneoplastic
|
|
D059545||melanocytic proliferation paraneoplastic
|
|
D059545||melanocytic proliferations paraneoplastic
|
|
D059545||melanoma associated retinopathies
|
|
D059545||melanoma associated retinopathy
|
|
D059545||ocular paraneoplastic disease
|
|
D059545||ocular paraneoplastic diseases
|
|
D059545||ocular paraneoplastic syndrome
|
|
D059545||ocular paraneoplastic syndromes
|
|
D059545||paraneoplastic disease ocular
|
|
D059545||paraneoplastic diseases ocular
|
|
D059545||paraneoplastic melanocytic proliferation
|
|
D059545||paraneoplastic melanocytic proliferations
|
|
D059545||paraneoplastic syndrome ocular
|
|
D059545||retinopathies cancer associated
|
|
D059545||retinopathies melanoma associated
|
|
D059545||retinopathy cancer associated
|
|
D059545||retinopathy melanoma associated
|
|
D059545||syndrome ocular paraneoplastic
|
|
D059545||syndromes ocular paraneoplastic
|
|
D031954||choriocarcinoma non gestational
|
|
D031954||choriocarcinomas non gestational
|
|
D031954||non gestational choriocarcinoma
|
|
D031954||non gestational choriocarcinomas
|
|
D020165|237300||carbamoyl phosphate synthase i deficiency disease
|
|
D020165|237300||carbamoyl phosphate synthase ammonia deficiency disease
|
|
D020165|237300||carbamoyl phosphate synthase i deficiency disease ornithine carbamoyl phosphate deficiency
|
|
D020165|237300||carbamoyl phosphate synthetase i deficiency
|
|
D020165|237300||carbamoylphosphate synthetase i deficiency disease
|
|
D020165|237300||carbamoyl phosphate synthetase i deficiency disease
|
|
D020165|237300||carbamoyl phosphate synthetase i deficiency hyperammonemia due to
|
|
D020165|237300||carbamyl phosphate synthetase cps deficiency
|
|
D020165|237300||carbamyl phosphate synthetase deficiency disease
|
|
D020165|237300||carbamyl phosphate synthetase i deficiency disease
|
|
D020165|237300||cps 1 deficiencies
|
|
D020165|237300||cps 1 deficiency
|
|
D020165|237300||cps i deficiencies
|
|
D020165|237300||cps i deficiency
|
|
D020165|237300||deficiencies cps 1
|
|
D020165|237300||deficiencies cps i
|
|
D020165|237300||deficiency cps 1
|
|
D020165|237300||deficiency cps i
|
|
D020165|237300||deficiency disease carbamoyl phosphate synthase
|
|
D020165|237300||deficiency disease carbamoyl phosphate synthase ammonia
|
|
D020165|237300||deficiency disease carbamoylphosphate synthetase i
|
|
D020165|237300||deficiency disease carbamyl phosphate synthetase
|
|
D020165|237300||hyperammonemia due to carbamoyl phosphate synthetase 1 deficiency
|
|
D015001||yaws
|
|
D015001||frambesia
|
|
D015001||frambesias
|
|
D015001||frambesia tropica
|
|
D015001||frambesia tropicas
|
|
C538029||chromosome 9 trisomy 9p
|
|
D015004||yellow fever
|
|
D015004||fevers yellow
|
|
D015004||fever yellow
|
|
D015004||yellow fevers
|
|
C566911||renal tubular acidosis distal with normal red cell morphology
|
|
D006030|233100||glycosuria renal
|
|
D006030|233100||glys1
|
|
D006030|233100||renal glucosuria
|
|
D006030|233100||renal glycosuria
|
|
129490|D053359||ectodermal dysplasia 3 anhidrotic
|
|
129490|D053359||ectd10a
|
|
129490|D053359||ectodermal dysplasia 10a hypohidrotic hair nail type autosomal dominant
|
|
129490|D053359||ectodermal dysplasia hypohidrotic autosomal dominant
|
|
129490|D053359|224900|D053360||hed
|
|
C567317|612421||alopecia androgenetic 3
|
|
C567317|612421||aga3
|
|
614187||hypertelorism preauricular sinus punctal pits and deafness
|
|
614187||hppd
|
|
C563689|609913||retinitis pigmentosa 32
|
|
C563689|609913||rp32
|
|
D006987||hypesthesia
|
|
D006987||hypesthesias
|
|
D006987||hypesthesias tactile
|
|
D006987||hypesthesias thermal
|
|
D006987||hypesthesia tactile
|
|
D006987||hypesthesia thermal
|
|
D006987||hypoesthesia
|
|
D006987||hypoesthesias
|
|
D006987||impaired sensation
|
|
D006987||impaired sensations
|
|
D006987||numbness
|
|
D006987||reduced sensation
|
|
D006987||reduced sensations
|
|
D006987||sensation impaired
|
|
D006987||sensation reduced
|
|
D006987||sensations impaired
|
|
D006987||sensations reduced
|
|
D006987||tactile hypesthesia
|
|
D006987||tactile hypesthesias
|
|
D006987||thermal hypesthesia
|
|
D006987||thermal hypesthesias
|
|
C566513|602639||tooth agenesis selective 2
|
|
C566513|602639||hyd2
|
|
C566513|602639||hypodontia oligodontia 2
|
|
C566513|602639||sthag2
|
|
D006988||hyphema
|
|
D006988||hyphemas
|
|
C566918||renal tubular acidosis distal with nephrocalcinosis short stature mental retardation and distinctive facies
|
|
D006985||hyperventilation
|
|
D006985||hyperventilations
|
|
D006986||hypervitaminosis a
|
|
D004320||dracunculiasis
|
|
D004320||disease guinea worm
|
|
D004320||diseases guinea worm
|
|
D004320||dracunculiases
|
|
D004320||dracunculoses
|
|
D004320||dracunculosis
|
|
D004320||guinea worm disease
|
|
D004320||guinea worm diseases
|
|
D004320||guinea worm infection
|
|
D004320||infection guinea worm
|
|
D004320||worm disease guinea
|
|
C566912|611588||muscular dystrophy limb girdle type 2m
|
|
C566912|611588||lgmd2m
|
|
D006983||hypertrichosis
|
|
D006983||hypertrichoses
|
|
D006984||hypertrophy
|
|
D006984||hypertrophies
|
|
D046248||pyloric stenosis hypertrophic
|
|
D046248||hypertrophic pyloric stenosis
|
|
D046248||stenosis hypertrophic pyloric
|
|
D006981||hyperthyroxinemia
|
|
D006981||hyperthyroxinemias
|
|
D060545||pudendal neuralgia
|
|
D060545||entrapment pudendal nerve
|
|
D060545||entrapments pudendal nerve
|
|
D060545||nerve entrapment pudendal
|
|
D060545||nerve entrapments pudendal
|
|
D060545||neuralgia pudendal
|
|
D060545||neuralgias pudendal
|
|
D060545||neuropathies pudendal
|
|
D060545||neuropathy pudendal
|
|
D060545||pudendal canal entrapment syndrome
|
|
D060545||pudendal nerve entrapment
|
|
D060545||pudendal nerve entrapments
|
|
D060545||pudendal nerve entrapment syndrome
|
|
D060545||pudendal neuralgias
|
|
D060545||pudendal neuropathies
|
|
D060545||pudendal neuropathy
|
|
613545|D008265||macrostomia
|
|
613545|D008265||commissural cleft isolated
|
|
613545|D008265||lateral cleft isolated
|
|
613545|D008265||macrostomia isolated
|
|
613545|D008265||macrostomias
|
|
613545|D008265||transverse cleft isolated
|
|
D005660||funnel chest
|
|
D005660||chest funnel
|
|
D005660||chests funnel
|
|
D005660||excavatum pectus
|
|
D005660||funnel chests
|
|
D005660||pectus excavatum
|
|
D058226||plaque atherosclerotic
|
|
D058226||arterial fatty streak
|
|
D058226||arterial fatty streaks
|
|
D058226||atheroma
|
|
D058226||atheromas
|
|
D058226||atheromatous plaques
|
|
D058226||atherosclerotic plaque
|
|
D058226||atherosclerotic plaques
|
|
D058226||fatty streak arterial
|
|
D058226||fatty streaks arterial
|
|
D058226||fibroatheroma
|
|
D058226||fibroatheromas
|
|
D058226||fibroatheromatous plaque
|
|
D058226||fibroatheromatous plaques
|
|
D058226||plaque fibroatheromatous
|
|
D058226||plaques atherosclerotic
|
|
D058226||plaques fibroatheromatous
|
|
D058226||streak arterial fatty
|
|
D058226||streaks arterial fatty
|
|
C565532|233700||granulomatous disease chronic autosomal recessive cytochrome b positive type i
|
|
C565532|233700||cgd autosomal recessive cytochrome b positive type i
|
|
C565532|233700||granulomatous disease chronic due to ncf1 deficiency
|
|
C565532|233700||ncf1 deficiency of
|
|
C565532|233700||neutrophil cytosol factor 1 deficiency of
|
|
C565532|233700||p47 phox deficiency of
|
|
C565532|233700||soc2 deficiency of
|
|
C565532|233700||soluble oxidase component ii deficiency of
|
|
D058225||plaque amyloid
|
|
D058225||amyloid deposit
|
|
D058225||amyloid deposits
|
|
D058225||amyloid plaque
|
|
D058225||amyloid plaques
|
|
D058225||deposit amyloid
|
|
D058225||deposits amyloid
|
|
D058225||neuritic plaque
|
|
D058225||neuritic plaques
|
|
D058225||plaque neuritic
|
|
D058225||plaques amyloid
|
|
D058225||plaque senile
|
|
D058225||plaques neuritic
|
|
D058225||plaques senile
|
|
D058225||senile plaque
|
|
D058225||senile plaques
|
|
C537525|269500||sclerosteosis
|
|
C537525|269500||cortical hyperostosis with syndactyly
|
|
C537525|269500||sclerosteosis 1
|
|
C537525|269500||sost
|
|
C537525|269500||sost1
|
|
D031941||hemorrhagic septicemia viral
|
|
D031941||haemorrhagic septicaemia viral
|
|
D031941||septicaemia viral haemorrhagic
|
|
D031941||septicemia viral hemorrhagic
|
|
D031941||viral haemorrhagic septicaemia
|
|
D031941||viral hemorrhagic septicemia
|
|
C535303|302802||charcot marie tooth disease x linked recessive 3
|
|
C535303|302802||charcot marie tooth neuropathy x linked recessive 3
|
|
C535303|302802||cmtx3
|
|
D016301||alveolar bone loss
|
|
D016301||alveolar bone atrophies
|
|
D016301||alveolar bone atrophy
|
|
D016301||alveolar bone losses
|
|
D016301||alveolar process atrophies
|
|
D016301||alveolar process atrophy
|
|
D016301||alveolar resorption
|
|
D016301||alveolar resorptions
|
|
D016301||bone atrophies alveolar
|
|
D016301||bone atrophy alveolar
|
|
D016301||bone loss alveolar
|
|
D016301||bone losses periodontal
|
|
D016301||bone loss periodontal
|
|
D016301||periodontal bone loss
|
|
D016301||periodontal bone losses
|
|
D016301||periodontal resorption
|
|
D016301||periodontal resorptions
|
|
D016301||resorption alveolar
|
|
D016301||resorption periodontal
|
|
D016301||resorptions alveolar
|
|
D018981||congenital disorders of glycosylation
|
|
D018981||carbohydrate deficient glycoprotein syndrome
|
|
D018981||carbohydrate deficient glycoprotein syndromes
|
|
D018981||glycoprotein syndrome carbohydrate deficient
|
|
D018981||syndrome carbohydrate deficient glycoprotein
|
|
D018981||syndromes carbohydrate deficient glycoprotein
|
|
C564972|255125||myopathy with lactic acidosis hereditary
|
|
C564972|255125||hereditary myopathy with lactic acidosis
|
|
C564972|255125||hml
|
|
C564972|255125||iron sulfur cluster deficiency myopathy
|
|
C564972|255125||myoglobinuria due to abnormal glycolysis
|
|
C564972|255125||myopathy with deficiency of iron sulfur cluster assembly enzyme
|
|
C564972|255125||myopathy with deficiency of iscu
|
|
C564972|255125||myopathy with deficiency of succinate dehydrogenase and aconitase
|
|
C564972|255125||myopathy with exercise intolerance swedish type
|
|
304100|C564115||corpus callosum partial agenesis of x linked
|
|
D003003||clonorchiasis
|
|
D003003||clonorchiases
|
|
D006998||hypochondriasis
|
|
D006998||hypochondriacal neuroses
|
|
D006998||hypochondriacal neurosis
|
|
D006998||neurosis hypochondriacal
|
|
D006996||hypocalcemia
|
|
D006996||hypocalcemias
|
|
D005667||furunculosis
|
|
D005667||boils
|
|
D005667||furuncle
|
|
D005667||furuncles
|
|
D005667||furunculoses
|
|
D006994||hypoaldosteronism
|
|
D006994||acidosis renal tubular type iv
|
|
D006994||hypoaldosteronism hyporeninemic
|
|
D006994||hyporeninemic hypoaldosteronism
|
|
D006994||renal tubular acidosis type iv
|
|
D006994||type iv renal tubular acidosis
|
|
C563681|610333||aicardi goutieres syndrome 4
|
|
C563681|610333||ags4
|
|
D006995||hypobetalipoproteinemias
|
|
D006995||familial hypobetalipoproteinemia
|
|
D006995||hypobetalipoproteinemia
|
|
D006995||hypo beta lipoproteinemia
|
|
D006995||hypo beta lipoproteinemias
|
|
D004332||drowning
|
|
D004332||drownings
|
|
C538398|609273||nemaline myopathy 6
|
|
C538398|609273||nem6
|
|
C535579|115150||cardiofaciocutaneous syndrome
|
|
C535579|115150||cardio facio cutaneous syndrome
|
|
C535579|115150||cardiofaciocutaneous syndrome 1
|
|
C535579|115150||cfc1
|
|
C535579|115150||cfcs
|
|
C535579|115150||cfc syndrome
|
|
D005671||fused teeth
|
|
D005671||double tooth
|
|
D005671||double tooths
|
|
D005671||fused mandibular incisor
|
|
D005671||fused mandibular incisors
|
|
D005671||incisor fused mandibular
|
|
D005671||incisors fused mandibular
|
|
D005671||mandibular incisor fused
|
|
D005671||mandibular incisors fused
|
|
D005671||teeth fused
|
|
D005671||tooth double
|
|
D005671||tooths double
|
|
602197||cerebellar degeneration related autoantigen 3
|
|
602197||cdr3
|
|
C536865|182601||spastic paraplegia 4 autosomal dominant
|
|
C536865|182601||autosomal dominant spastic paraplegia 4
|
|
C536865|182601||familial spastic paraplegia autosomal dominant 2
|
|
C536865|182601||fsp2
|
|
C536865|182601||spg4
|
|
C567365|612284||meckel syndrome type 6
|
|
C567365|612284||mks6
|
|
C563457|600674||microtia anotia
|
|
C536662|264470||peroxisomal acyl coa oxidase deficiency
|
|
C536662|264470||pseudoneonatal adrenoleukodystrophy
|
|
C536662|264470||straight chain acyl coa oxidase deficiency
|
|
224900|D053360||ectodermal dysplasia hypohidrotic autosomal recessive
|
|
224900|D053360||anhidridic ectodermal dysplasia autosomal recessive
|
|
224900|D053360||anhidrotic ectodermal dysplasia autosomal recessive
|
|
224900|D053360||anhydridic ectodermal dysplasia autosomal recessive
|
|
224900|D053360||autosomal recessive anhidrotic ectodermal dysplasia
|
|
224900|D053360||autosomal recessive anhydrotic ectodermal dysplasia
|
|
224900|D053360||ectd10b
|
|
224900|D053360||ectodermal dysplasia 10b hypohidrotic hair tooth type autosomal recessive
|
|
224900|D053360||ectodermal dysplasia anhidrotic autosomal recessive
|
|
224900|D053360||ectodermal dysplasia hypohidrotic
|
|
224900|D053360||ectodermal dysplasia hypohydrotic autosomal recessive
|
|
224900|D053360|305100|D053358||eda
|
|
D006969||hypersensitivity immediate
|
|
D006969||atopic hypersensitivities
|
|
D006969||atopic hypersensitivity
|
|
D006969||hypersensitivities atopic
|
|
D006969||hypersensitivities ige mediated
|
|
D006969||hypersensitivities immediate
|
|
D006969||hypersensitivities type i
|
|
D006969||hypersensitivity atopic
|
|
D006969||hypersensitivity ige mediated
|
|
D006969||hypersensitivity type i
|
|
D006969||ige mediated hypersensitivities
|
|
D006969||ige mediated hypersensitivity
|
|
D006969||immediate hypersensitivities
|
|
D006969||immediate hypersensitivity
|
|
D006969||type i hypersensitivities
|
|
D006969||type i hypersensitivity
|
|
612562|C567254||diamond blackfan anemia 7
|
|
612562|C567254||dba7
|
|
D006967||hypersensitivity
|
|
D006967||allergic reaction
|
|
D006967||allergic reactions
|
|
D006967||allergies
|
|
D006967||allergy
|
|
D006967||hypersensitivities
|
|
D006967||reaction allergic
|
|
D006967||reactions allergic
|
|
D006968||hypersensitivity delayed
|
|
D006968||delayed hypersensitivities
|
|
D006968||delayed hypersensitivity
|
|
D006968||hypersensitivities delayed
|
|
D006968||hypersensitivities tuberculin type
|
|
D006968||hypersensitivities type iv
|
|
D006968||hypersensitivity tuberculin type
|
|
D006968||hypersensitivity type iv
|
|
D006968||tuberculin type hypersensitivities
|
|
D006968||tuberculin type hypersensitivity
|
|
D006968||type iv hypersensitivities
|
|
D006968||type iv hypersensitivity
|
|
614166||myopia 20 autosomal dominant
|
|
614166||myp20
|
|
D006965||hyperplasia
|
|
D006965||hyperplasias
|
|
D006966||hyperprolactinemia
|
|
D006966||hyperprolactinaemia
|
|
D006966||hyperprolactinemias
|
|
D006966||hypersecretion syndrome prolactin
|
|
D006966||inappropriate prolactin secretion
|
|
D006966||inappropriate prolactin secretion syndrome
|
|
D006966||inappropriate secretion prolactin
|
|
D006966||prolactin hypersecretion syndrome
|
|
D006966||prolactin inappropriate secretion
|
|
D006966||prolactin secretion inappropriate
|
|
D006966||secretion inappropriate prolactin
|
|
D006966||secretion prolactin inappropriate
|
|
D006966||syndrome prolactin hypersecretion
|
|
D006963||hyperphagia
|
|
D006963||overeating
|
|
C540309||abetalipoproteinemia neuropathy
|
|
D006964||hyperpituitarism
|
|
D006964||follicle stimulating hormone inappropriate secretion
|
|
D006964||fsh hypersecretion pituitary
|
|
D006964||hypersecretion pituitary fsh
|
|
D006964||hypersecretion pituitary lh
|
|
D006964||hypersecretion pituitary tsh
|
|
D006964||inappropriate follicle stimulating hormone secretion
|
|
D006964||inappropriate fsh secretion syndrome
|
|
D006964||inappropriate lh secretion syndrome
|
|
D006964||inappropriate luteinizing hormone secretion
|
|
D006964||inappropriate thyroid stimulating hormone secretion
|
|
D006964||inappropriate tsh secretion syndrome
|
|
D006964||lh hypersecretion pituitary
|
|
D006964||luteinizing hormone inappropriate secretion
|
|
D006964||pituitary fsh hypersecretion
|
|
D006964||pituitary lh hypersecretion
|
|
D006964||pituitary tsh hypersecretion
|
|
D006964||thyroid stimulating hormone inappropriate secretion
|
|
D006964||tsh hypersecretion pituitary
|
|
D006961||hyperparathyroidism
|
|
D006962||hyperparathyroidism secondary
|
|
D006962||hyperparathyroidisms secondary
|
|
D006962||secondary hyperparathyroidism
|
|
D006962||secondary hyperparathyroidisms
|
|
D006960||hyperoxaluria primary
|
|
D006960||hyperoxalurias primary
|
|
D006960||oxaloses primary
|
|
D006960||oxalosis primary
|
|
D006960||oxaluria primary
|
|
D006960||oxalurias primary
|
|
D006960||primary hyperoxaluria
|
|
D006960||primary hyperoxalurias
|
|
D006960||primary oxaloses
|
|
D006960||primary oxalosis
|
|
D006960||primary oxaluria
|
|
D006960||primary oxalurias
|
|
107970|C566254||arrhythmogenic right ventricular dysplasia familial 1
|
|
107970|C566254||arrhythmogenic right ventricular cardiomyopathy 1
|
|
107970|C566254||arrhythmogenic right ventricular cardiomyopathy 1 arvc1 uhl anomaly included
|
|
107970|C566254||arvd1
|
|
107970|C566254||cardiomyopathy right ventricular dilated included
|
|
D058246||prehypertension
|
|
D058246||pre hypertension
|
|
D058246||prehypertensions
|
|
D058246||pre hypertensions
|
|
C567735|613119||brugada syndrome 6
|
|
C567735|613119||brgda6
|
|
277400|C537359||methylmalonic acidemia with homocystinuria
|
|
277400|C537359||cobalamin c methylmalonic acidemia and homocystinuria
|
|
277400|C537359||methylmalonic acidemia and homocystinemia
|
|
277400|C537359||methylmalonic acidemia and homocystinuria cblc type
|
|
277400|C537359||methylmalonic aciduria and homocystinuria cblc type
|
|
277400|C537359||methylmalonic aciduria and homocystinuria vitamin b12 responsive
|
|
277400|C537359||vitamin b12 metabolic defect with combined deficiency of methylmalonyl coa mutase and homocysteine methyltetrahydrofolate methyltransferase
|
|
193400|D056725||von willebrand disease type 1
|
|
193400|D056725||type 1 von willebrand disease
|
|
193400|D056725||type i von willebrand disease
|
|
193400|D056725||von willebrand disease type i
|
|
193400|D056725||vwd1
|
|
193400|D056725||vwd type 1
|
|
C567594|300580||myopathy congenital with fiber type disproportion x linked
|
|
C567594|300580||cftdx
|
|
149400|C538136||hyperexplexia hereditary
|
|
149400|C538136|184850|D016750||congenital stiff person syndrome
|
|
149400|C538136||exagerrated startle reflex
|
|
149400|C538136||exaggerated startle reaction
|
|
149400|C538136||familial startle disease
|
|
149400|C538136||hkpx1
|
|
149400|C538136||hyperekplexia hereditary 1
|
|
149400|C538136||kok disease
|
|
149400|C538136||startle disease familial
|
|
149400|C538136||startle reaction exaggerated
|
|
149400|C538136||sthe
|
|
149400|C538136|184850|D016750||stiff baby syndrome
|
|
149400|C538136||stiff man syndrome congenital
|
|
149400|C538136||stiff person syndrome congenital
|
|
D006978||hypertension renovascular
|
|
D006978||goldblatt hypertension
|
|
D006978||goldblatt syndrome
|
|
D006978||hypertension goldblatt
|
|
D006978||renovascular hypertension
|
|
D006978||syndrome goldblatt
|
|
D004313||dourine
|
|
D004313||dourines
|
|
C566906|C563661|610805||cakut
|
|
C566906||congenital anomalies of kidney and urinary tract
|
|
D006977||hypertension renal
|
|
D006977||hypertensions renal
|
|
D006977||renal hypertension
|
|
D006977||renal hypertensions
|
|
C565788|604352||febrile convulsions familial 4
|
|
C565788|604352||convulsions familial febrile 4
|
|
C565788|604352||feb4
|
|
C565788|604352||febrile seizures familial 4
|
|
C565788|604352||seizures familial febrile 4
|
|
D006974||hypertension malignant
|
|
D006974||malignant hypertension
|
|
D006975||hypertension portal
|
|
D006975||cruveilhier baumgarten syndrome
|
|
D006975||hypertensions portal
|
|
D006975||portal hypertension
|
|
D006975||portal hypertensions
|
|
D006975||syndrome cruveilhier baumgarten
|
|
D006972||hypertelorism
|
|
D006972||hypertelorisms
|
|
D006973||hypertension
|
|
D006973||blood pressure high
|
|
D006973||blood pressures high
|
|
D006973||high blood pressure
|
|
D006973||high blood pressures
|
|
C566903|611630||epilepsy familial mesial temporal lobe
|
|
D005642||fuchs apos endothelial dystrophy
|
|
D005642||dystrophy fuch apos s endothelial
|
|
D005642||dystrophy fuchs apos endothelial
|
|
D005642||endothelial dystrophy fuch apos s
|
|
D005642||endothelial dystrophy fuchs apos
|
|
D005642||fuch endothelial dystrophy
|
|
D005642||fuchs atrophy
|
|
D005642||fuchs corneal dystrophy
|
|
D005642||fuchs dystrophy
|
|
D005642||fuchs endothelial corneal dystrophy
|
|
D005642||fuch apos s endothelial dystrophy
|
|
D005642||fuchs endothelial dystrophy
|
|
D006970||disorders of excessive somnolence
|
|
D006970||does disorders of excessive somnolence
|
|
D006970||doess disorders of excessive somnolence
|
|
D006970||excessive somnolence disorder
|
|
D006970||excessive somnolence disorders
|
|
D006970||hypersomnia
|
|
D006970||hypersomnia recurrent
|
|
D006970||hypersomnias
|
|
D006970||hypersomnias recurrent
|
|
D006970||hypersomnolence
|
|
D006970||hypersomnolence disorder
|
|
D006970||hypersomnolence disorder primary
|
|
D006970||hypersomnolence disorders
|
|
D006970||hypersomnolence disorder secondary
|
|
D006970||hypersomnolence disorders primary
|
|
D006970||hypersomnolence disorders secondary
|
|
D006970||primary hypersomnolence disorder
|
|
D006970||primary hypersomnolence disorders
|
|
D006970||recurrent hypersomnia
|
|
D006970||recurrent hypersomnias
|
|
D006970||secondary hypersomnolence disorder
|
|
D006970||secondary hypersomnolence disorders
|
|
D006970||somnolence disorder excessive
|
|
D006970||somnolence disorders excessive
|
|
D004310||double outlet right ventricle
|
|
D004310||anomaly taussig bing
|
|
D004310||double outlet right ventricle noncommitted vsd
|
|
D004310||double outlet right ventricle subaortic vsd
|
|
D004310||double outlet right ventricle subpulmonary vsd
|
|
D004310||taussig bing anomaly
|
|
C566904||preauricular tag isolated autosomal dominant 1
|
|
D006971||hypersplenism
|
|
D006971||anemia splenic
|
|
D006971||anemias splenic
|
|
D006971||splenic anemia
|
|
D006971||splenic anemias
|
|
D006980||hyperthyroidism
|
|
D006980||hyperthyroidism primary
|
|
D006980||primary hyperthyroidism
|
|
D006980||primary hyperthyroidisms
|
|
C565545|231900||glutathione synthetase deficiency of erythrocytes hemolytic anemia due to
|
|
C565545|231900||gssde
|
|
D058252||necrobiotic xanthogranuloma
|
|
D058252||necrobiotic xanthogranulomas
|
|
D058252||xanthogranuloma necrobiotic
|
|
D058252||xanthogranulomas necrobiotic
|
|
C536637|269250||schneckenbecken dysplasia
|
|
C536637|269250||chondrodysplasia lethal neonatal with snail like pelvis
|
|
D017622||periodontal attachment loss
|
|
D017622||attachment loss periodontal
|
|
D017622||loss periodontal attachment
|
|
D004409||dyskinesia drug induced
|
|
D004409||drug induced dyskinesia
|
|
D004409||drug induced dyskinesias
|
|
D004409||dyskinesia medication induced
|
|
D004409||dyskinesias drug induced
|
|
D004409||dyskinesias medication induced
|
|
D004409||medication induced dyskinesia
|
|
D004409||medication induced dyskinesias
|
|
D004408||dysgeusia
|
|
D004408||altered taste
|
|
D004408||distorted taste
|
|
D004408||dysgeusias
|
|
D004408||parageusia
|
|
D004408||parageusias
|
|
D004408||taste altered
|
|
D004408||taste distorted
|
|
D005739||gas poisoning
|
|
D005739||gas poisonings
|
|
D005739||poisoning gas
|
|
D005739||poisonings gas
|
|
D004405||dysentery bacillary
|
|
D004405||bacillary dysentery
|
|
D004405||boydii dysenteries shigella
|
|
D004405||boydii dysentery shigella
|
|
D004405||dysenteriae dysenteries shigella
|
|
D004405||dysenteriae dysentery shigella
|
|
D004405||dysenteries shigella
|
|
D004405||dysenteries shigella boydii
|
|
D004405||dysenteries shigella dysenteriae
|
|
D004405||dysenteries shigella flexneri
|
|
D004405||dysenteries shigella sonnei
|
|
D004405||dysentery shiga bacillus
|
|
D004405||dysentery shigella
|
|
D004405||dysentery shigella boydii
|
|
D004405||dysentery shigella dysenteriae
|
|
D004405||dysentery shigella dysenteriae type 1
|
|
D004405||dysentery shigella flexneri
|
|
D004405||dysentery shigella sonnei
|
|
D004405||flexneri dysenteries shigella
|
|
D004405||flexneri dysentery shigella
|
|
D004405||shiga bacillus dysentery
|
|
D004405||shigella boydii dysenteries
|
|
D004405||shigella boydii dysentery
|
|
D004405||shigella dysenteriae dysenteries
|
|
D004405||shigella dysenteriae dysentery
|
|
D004405||shigella dysenteries
|
|
D004405||shigella dysentery
|
|
D004405||shigella flexneri dysenteries
|
|
D004405||shigella flexneri dysentery
|
|
D004405||shigella sonnei dysenteries
|
|
D004405||shigella sonnei dysentery
|
|
D004405||shigellosis
|
|
D004405||sonnei dysenteries shigella
|
|
D004405||sonnei dysentery shigella
|
|
D005736||gardner syndrome
|
|
D005736||gardner apos s syndrome
|
|
D005736||gardners syndrome
|
|
D005736||gardner apos s syndromes
|
|
D005736||gardner syndromes
|
|
D005736||syndrome gardner
|
|
D005736||syndrome gardner apos s
|
|
D005736||syndromes gardner
|
|
D005736||syndromes gardner apos s
|
|
D004404||dysentery amebic
|
|
D004404||amebiases intestinal
|
|
D004404||amebiasis intestinal
|
|
D004404||amebic colitides
|
|
D004404||amebic colitis
|
|
D004404||amebic dysenteries
|
|
D004404||amebic dysentery
|
|
D004404||amoebiases intestinal
|
|
D004404||amoebiasis intestinal
|
|
D004404||amoebic colitides
|
|
D004404||amoebic colitis
|
|
D004404||amoebic dysenteries
|
|
D004404||amoebic dysentery
|
|
D004404||colitides amebic
|
|
D004404||colitides amoebic
|
|
D004404||colitis amebic
|
|
D004404||colitis amoebic
|
|
D004404||dysenteries amebic
|
|
D004404||dysenteries amoebic
|
|
D004404||dysentery amoebic
|
|
D004404||entamoebiases intestinal
|
|
D004404||entamoebiasis intestinal
|
|
D004404||intestinal amebiases
|
|
D004404||intestinal amebiasis
|
|
D004404||intestinal amoebiases
|
|
D004404||intestinal amoebiasis
|
|
D004404||intestinal entamoebiases
|
|
D004404||intestinal entamoebiasis
|
|
D004407||dysgerminoma
|
|
D004407||disgerminoma
|
|
D004407||disgerminomas
|
|
D004407||dysgerminomas
|
|
D005738||gas gangrene
|
|
D005738||gangrene gas
|
|
D005738||gangrenes gas
|
|
D005738||gas gangrenes
|
|
D004406||dysgammaglobulinemia
|
|
D004406||dysgammaglobulinemias
|
|
255300|D009224||myotonia congenita
|
|
255300|D009224||batten turner congenital myopathy
|
|
255300|D009224||becker disease
|
|
255300|D009224||becker generalized myotonia
|
|
255300|D009224||congenital myotonia
|
|
255300|D009224||disease becker
|
|
255300|D009224||disease thomsen
|
|
255300|D009224||disease thomsens
|
|
255300|D009224||disease thomsen apos s
|
|
255300|D009224||generalized myotonia
|
|
255300|D009224||generalized myotonia becker
|
|
255300|D009224||generalized myotonia of becker
|
|
255300|D009224||generalized myotonia of thomsen
|
|
255300|D009224||generalized myotonias
|
|
255300|D009224||myopathy congenital
|
|
255300|D009224||myotonia becker generalized
|
|
255300|D009224||myotonia congenita autosomal recessive
|
|
255300|D009224||myotonia generalized
|
|
255300|D009224||myotonia generalized becker
|
|
255300|D009224||myotonia levior
|
|
255300|D009224||myotonias generalized
|
|
255300|D009224||thomsen disease
|
|
255300|D009224||thomsen generalized myotonia
|
|
255300|D009224||thomsen apos s disease
|
|
255300|D009224||thomsens disease
|
|
D004401||dysarthria
|
|
D004401||dysarthoses
|
|
D004401||dysarthosis
|
|
D004401||dysarthria flaccid
|
|
D004401||dysarthria guttural
|
|
D004401||dysarthria mixed
|
|
D004401||dysarthrias
|
|
D004401||dysarthria scanning
|
|
D004401||dysarthrias flaccid
|
|
D004401||dysarthrias guttural
|
|
D004401||dysarthrias mixed
|
|
D004401||dysarthria spastic
|
|
D004401||dysarthrias scanning
|
|
D004401||dysarthrias spastic
|
|
D004401||flaccid dysarthria
|
|
D004401||flaccid dysarthrias
|
|
D004401||guttural dysarthria
|
|
D004401||guttural dysarthrias
|
|
D004401||mixed dysarthria
|
|
D004401||mixed dysarthrias
|
|
D004401||scanning dysarthria
|
|
D004401||scanning dysarthrias
|
|
D004401||spastic dysarthria
|
|
D004401||spastic dysarthrias
|
|
C565214|610244||spastic paraplegia 33 autosomal dominant
|
|
C565214|610244||spg33
|
|
D004403||dysentery
|
|
D004403||diarrheal disease infectious
|
|
D004403||infectious diarrheal disease
|
|
D004403||infectious diarrheal diseases
|
|
D005734||gangrene
|
|
D005734||gangrenes
|
|
D005733||gangliosidoses
|
|
D005733||ganglioside storage disease
|
|
D005733||ganglioside storage diseases
|
|
D005733||ganglioside storage disorder
|
|
D005733||ganglioside storage disorders
|
|
D005733||gangliosidosis
|
|
D005733||storage disease ganglioside
|
|
D005733||storage diseases ganglioside
|
|
D005733||storage disorder ganglioside
|
|
D005733||storage disorders ganglioside
|
|
D060467||disease resistance
|
|
D060467||disease resistances
|
|
D060467||resistance disease
|
|
D060467||resistances disease
|
|
D017719||diabetic foot
|
|
D017719||diabetic feet
|
|
D017719||feet diabetic
|
|
D017719||foot diabetic
|
|
D017719||foot ulcer diabetic
|
|
D017714||community acquired infections
|
|
D017714||community acquired infection
|
|
D017714||infection community acquired
|
|
D017714||infections community acquired
|
|
C545036|308990||low molecular weight proteinuria with hypercalciuria and nephrocalcinosis
|
|
C545036|308990||proteinuria low molecular weight with hypercalciuria and nephrocalcinosis
|
|
C536351|228100||visceral steatosis congenital
|
|
C536351|228100||fatal neonatal hepatic steatosis
|
|
C536351|228100||fatty liver disease congenital
|
|
C536351|228100||fatty metamorphosis of viscera
|
|
C536351|228100|D005234||steatosis of liver
|
|
C536351|228100||white liver disease
|
|
D016532|309900||mucopolysaccharidosis ii
|
|
D016532|309900||deficiency i2s
|
|
D016532|309900||deficiency iduronate 2 sulfatase
|
|
D016532|309900||deficiency iduronate sulfatase
|
|
D016532|309900||deficiency sulfoiduronate sulfatase
|
|
D016532|309900||gargoylism hunter syndrome
|
|
D016532|309900||hunter apos s syndrome
|
|
D016532|309900||hunters syndrome
|
|
D016532|309900||hunter syndrome
|
|
D016532|309900||hunter syndrome gargoylism
|
|
D016532|309900||i2s deficiency
|
|
D016532|309900||ids deficiency
|
|
D016532|309900||iduronate 2 sulfatase deficiency
|
|
D016532|309900||iduronate sulfatase deficiency
|
|
D016532|309900||mps2
|
|
D016532|309900||mps ii
|
|
D016532|309900||mucopolysaccharidosis 2
|
|
D016532|309900||mucopolysaccharidosis type 2
|
|
D016532|309900||mucopolysaccharidosis type ii
|
|
D016532|309900||sids deficiency
|
|
D016532|309900||sulfoiduronate sulfatase deficiency
|
|
D016532|309900||syndrome hunter
|
|
D016532|309900||syndrome hunter apos s
|
|
D004416||dysplastic nevus syndrome
|
|
D004416|155600||b k mole syndrome
|
|
D004416||dysplastic nevi
|
|
D004416||dysplastic nevus
|
|
D004416||familial atypical multiple mole melanoma
|
|
D004416||nevi dysplastic
|
|
D004416||nevus dysplastic
|
|
D004416||nevus syndrome dysplastic
|
|
D004416||syndrome b k mole
|
|
D004416||syndrome dysplastic nevus
|
|
D005747||gastric fistula
|
|
D005747||fistula gastric
|
|
D005747||fistula stomach
|
|
D005747||stomach fistula
|
|
D004415||dyspepsia
|
|
D004415||dyspepsias
|
|
D004415||indigestion
|
|
D004415||indigestions
|
|
D004418||dyspnea paroxysmal
|
|
D004418||asthma cardiac
|
|
D004418||dyspnea paroxysmal nocturnal
|
|
D004418||dyspneas paroxysmal
|
|
D004418||paroxysmal dyspnea
|
|
D004418||paroxysmal dyspneas
|
|
D004417||dyspnea
|
|
D004417||breath shortness
|
|
D004417||breath shortnesses
|
|
D004417||dyspneas
|
|
D004417||shortness of breath
|
|
D004412||dysmenorrhea
|
|
D004412||dysmenorrheas
|
|
D004412||menstrual pain
|
|
D004412||menstrual pains
|
|
D004412||menstruation painful
|
|
D004412||menstruations painful
|
|
D004412||painful menstruation
|
|
D004412||painful menstruations
|
|
D004412||pain menstrual
|
|
D004412||pains menstrual
|
|
D004411||dyslexia acquired
|
|
D004411||acquired alexia
|
|
D004411||acquired dyslexia
|
|
D004411||acquired global dyslexia
|
|
D004411||acquired reading disabilities
|
|
D004411||acquired reading disability
|
|
D004411||acquired spelling dyslexia
|
|
D004411||acquired word blindness
|
|
D004411||acquired word blindnesses
|
|
D004411||alexia acquired
|
|
D004411||blindness acquired word
|
|
D004411||blindnesses acquired word
|
|
D004411||disabilities acquired reading
|
|
D004411||disability acquired reading
|
|
D004411||dyslexia acquired global
|
|
D004411||dyslexia acquired spelling
|
|
D004411||global dyslexia acquired
|
|
D004411||reading disabilities acquired
|
|
D004411||reading disability acquired
|
|
D004411||spelling dyslexia acquired
|
|
D004411||word blindness acquired
|
|
D004411||word blindnesses acquired
|
|
D004414||dyspareunia
|
|
D004413||dysostoses
|
|
D004413||dysostosis
|
|
C567572|600638||fibrosis of extraocular muscles congenital 3a with or without extraocular involvement
|
|
C567572|600638||cfeom3a
|
|
C567572|600638||feom3 locus
|
|
277000|C537371||mayer rokitansky kuster hauser syndrome
|
|
277000||congenital absence of uterus and vagina cauv urogenital adysplasia included
|
|
277000|C537371||mrk anomaly
|
|
277000|C537371||mrkh anomaly
|
|
277000|C537371||mrkh syndrome
|
|
277000|C537371||mullerian aplasia dysgenesis
|
|
277000|C537371||uterus bipartitus solidus rudimentarius cum vagina solida
|
|
277000|C537371||von mayer rokitansky kuster anomaly
|
|
C536920|275210||tight skin contracture syndrome lethal
|
|
C536920|275210||fetal hypokinesia sequence due to restrictive dermopathy
|
|
C536920|275210||hyperkeratosis contracture syndrome
|
|
C536920|275210||restrictive dermopathy lethal
|
|
D005359|174800||fibrous dysplasia polyostotic
|
|
D005359|174800||albright mccune sternberg syndrome
|
|
D005359|174800||albright apos s disease
|
|
D005359|174800||albright apos s disease of bone
|
|
D005359|174800||albright apos s syndrome
|
|
D005359|174800||albright apos s syndrome with precocious puberty
|
|
D005359|174800||albright sternberg syndrome
|
|
D005359|174800||albright syndrome
|
|
D005359|174800||albright syndrome polyostotic fibrous dysplasia included
|
|
D005359|174800||dysplasia polyostotic fibrous
|
|
D005359|174800||dysplasias polyostotic fibrous
|
|
D005359|174800||fibrous dysplasias polyostotic
|
|
D005359|174800||fibrous dysplasia with pigmentary skin changes and precocious puberty
|
|
D005359|174800||mas
|
|
D005359|174800||mccune albright syndrome
|
|
D005359|174800||pfd included
|
|
D005359|174800||pofd included
|
|
D005359|174800||polyostotic fibrous dysplasia
|
|
D005359|174800||polyostotic fibrous dysplasias
|
|
D005359|174800||syndrome albright
|
|
D005359|174800||syndrome albright apos s
|
|
D005359|174800||syndrome mccune albright
|
|
C537342|147250||single upper central incisor
|
|
C537342|147250||fused incisors
|
|
C537342|147250||incisors fused
|
|
C537342|147250||single central maxillary incisor
|
|
C537342|147250||single central maxillary incisor solitary median maxillary central incisor syndrome included
|
|
C537342|147250||smmci
|
|
C537342|147250||smmci syndrome
|
|
C537342|147250||smmci syndrome included
|
|
C537342|147250||solitary median maxillary central incisor
|
|
C537342|147250||solitary median maxillary central incisor syndrome
|
|
D017726||cytomegalovirus retinitis
|
|
D017726||cytomegaloviral retinitis
|
|
D017726||retinitis cytomegaloviral
|
|
D017726||retinitis cytomegalovirus
|
|
D017728||lymphoma large cell anaplastic
|
|
D017728||anaplastic large cell lymphoma
|
|
D017728||anaplastic large cell lymphomas
|
|
D017728||cd30 anaplastic large cell lymphoma
|
|
D017728||cd30 positive anaplastic large cell lymphoma
|
|
D017728||ki 1 lymphoma
|
|
D017728||ki 1 lymphomas
|
|
D017728||large cell lymphoma anaplastic
|
|
D017728||large cell lymphomas anaplastic
|
|
D017728||lymphoma anaplastic large cell
|
|
D017728||lymphoma ki 1
|
|
D017728||lymphoma large cell ki 1
|
|
D017728||lymphomas anaplastic large cell
|
|
D017728||lymphomas ki 1
|
|
D017728||systemic anaplastic large cell lymphoma
|
|
C536835|266130||glutathione synthetase deficiency
|
|
C536835|266130||5 oxoprolinemia
|
|
C536835|266130||5 oxoprolinuria
|
|
C536835|266130||deficiency of glutathione synthase
|
|
C536835|266130||deficiency of glutathione synthetase
|
|
C536835|266130||gssd
|
|
C536835|266130||pyroglutamic acidemia
|
|
C536835|266130||pyroglutamic aciduria
|
|
D017241|540000||melas syndrome
|
|
D017241|540000||melas
|
|
D017241|540000||mitochondrial encephalomyopathy lactic acidosis and stroke like episodes
|
|
D017241|540000||mitochondrial myopathy encephalopathy lactic acidosis and stroke like episodes
|
|
D017241|540000||mitochondrial myopathy lactic acidosis stroke like episode
|
|
D017241|540000||myopathy mitochondrial encephalopathy lactic acidosis stroke
|
|
D017241|540000||syndrome melas
|
|
D005715||gambling
|
|
D005715||gambling pathologic
|
|
D005715||gambling pathological
|
|
D005715||gamblings
|
|
D005715||gamblings pathological
|
|
D005715||pathological gambling
|
|
D005715||pathological gamblings
|
|
C537724|309520||lujan fryns syndrome
|
|
C537724|309520||lujan syndrome
|
|
C537724|309520||marfanoid habitus mild general hypotonia hypernasal voice normal testicular size and distinct craniofacial anomalies
|
|
C537724|309520||mental retardation x linked with marfanoid habitus
|
|
C537724|309520||x linked intellectual deficit with marfanoid habitus
|
|
C537724|309520||x linked mental retardation with marfanoid habitus
|
|
C537724|309520||xlmr with marfanoid features
|
|
D060487||alternariosis
|
|
D060487||alternarioses
|
|
D060487||alternarioses cutaneous
|
|
D060487||alternarioses dermal
|
|
D060487||alternarioses subcutaneous
|
|
D060487||alternariosis cutaneous
|
|
D060487||alternariosis dermal
|
|
D060487||alternariosis subcutaneous
|
|
D060487||cutaneous alternarioses
|
|
D060487||cutaneous alternariosis
|
|
D060487||dermal alternarioses
|
|
D060487||dermal alternariosis
|
|
D060487||subcutaneous alternarioses
|
|
D060487||subcutaneous alternariosis
|
|
D060486||ophthalmoplegic migraine
|
|
D060486||migraine ophthalmoplegic
|
|
D060486||migraines ophthalmoplegic
|
|
D060486||migraine syndrome ophthalmoplegic
|
|
D060486||migraine syndromes ophthalmoplegic
|
|
D060486||ophthalmoplegic migraines
|
|
D060486||ophthalmoplegic migraine syndrome
|
|
D060486||ophthalmoplegic migraine syndromes
|
|
D060486||syndrome ophthalmoplegic migraine
|
|
D060486||syndromes ophthalmoplegic migraine
|
|
D058165||22q11 deletion syndrome
|
|
D058165||22q11 deletion syndromes
|
|
D058165||deletion syndrome 22q11
|
|
D058165||deletion syndromes 22q11
|
|
D058165||syndrome 22q11 deletion
|
|
D058165||syndromes 22q11 deletion
|
|
611891|C567501||aortic aneurysm familial abdominal 3
|
|
611891|C567501||aaa3
|
|
609572||photoparoxysmal response 2
|
|
609572||photoparoxysmal response with or without idiopathic generalized epilepsy
|
|
609572||ppr2
|
|
248390|C535707||mandibulofacial dysostosis treacher collins type autosomal recessive
|
|
248390|C535707||tcs3
|
|
248390|C535707||treacher collins syndrome 3
|
|
212500||cataract congenital or juvenile
|
|
212500||cataract juvenile hutterite type included
|
|
C567207|612656||episodic ataxia type 6
|
|
C567207|612656||ea6
|
|
D005729||ganglioneuroma
|
|
D005729||gangliocytoma
|
|
D005729||gangliocytomas
|
|
D005729||ganglioneuromas
|
|
C567466|300749||mental retardation and microcephaly with pontine and cerebellar hypoplasia
|
|
C567466|300749||mental retardation x linked syndromic najm type
|
|
C567466|300749||micpch
|
|
C567466|300749||micpch syndrome
|
|
C567466|300749||mrxsna
|
|
C567648|613310||exudative vitreoretinopathy 5
|
|
C567648|613310||evr5
|
|
300555|C564487||dent disease 2
|
|
D017703||retropharyngeal abscess
|
|
D017703||abscesses retropharyngeal
|
|
D017703||abscess retropharyngeal
|
|
D017703||retropharyngeal abscesses
|
|
609560||mitochondrial dna depletion syndrome 2 myopathic type
|
|
609560||mitochondrial dna depletion myopathy tk2 related
|
|
609560||mtdps2
|
|
D017700||embolism cholesterol
|
|
D017700||atheroembolism
|
|
D017700||atheroembolisms
|
|
D017700||cholesterol embolism
|
|
D017700||cholesterol embolisms
|
|
D017700||embolisms cholesterol
|
|
176430||premature chromatid separation trait
|
|
176430||pcs
|
|
176430||total premature chromatid separation trait
|
|
C538514|269160||familial schizencephaly
|
|
C538514|269160|D054220||schizencephaly
|
|
301201|C537412||amelogenesis imperfecta hypoplastic hypomaturation x linked 2
|
|
301201||aih3 formerly
|
|
301201||amelogenesis imperfecta 3 hypoplastic type formerly
|
|
301201|C538243|301200||enamel hypoplasia x linked
|
|
D010291||paresis
|
|
D010291||brachial pareses
|
|
D010291||brachial paresis
|
|
D010291||crural pareses
|
|
D010291||crural paresis
|
|
D010291||extremity pareses lower
|
|
D010291||extremity pareses upper
|
|
D010291||extremity paresis lower
|
|
D010291||extremity paresis upper
|
|
D010291||hemipareses
|
|
D010291||hemiparesis
|
|
D010291||lower extremity pareses
|
|
D010291||lower extremity paresis
|
|
D010291||monopareses
|
|
D010291||monoparesis
|
|
D010291||muscle pareses
|
|
D010291||muscle paresis
|
|
D010291||muscular pareses
|
|
D010291||muscular paresis
|
|
D010291||pareses
|
|
D010291||pareses brachial
|
|
D010291||pareses crural
|
|
D010291||pareses lower extremity
|
|
D010291||pareses muscle
|
|
D010291||pareses muscular
|
|
D010291||pareses upper extremity
|
|
D010291||paresis brachial
|
|
D010291||paresis crural
|
|
D010291||paresis lower extremity
|
|
D010291||paresis muscle
|
|
D010291||paresis muscular
|
|
D010291||paresis upper extremity
|
|
D010291||upper extremity pareses
|
|
D010291||upper extremity paresis
|
|
122600||spondylocostal dysostosis 5 autosomal dominant
|
|
122600||costovertebral segmentation anomalies polydysspondyly included
|
|
122600||scdo5
|
|
122600|C565149||spondylocostal dysplasia dominant form
|
|
122600|C565149||spondylothoracic dysostosis autosomal dominant
|
|
C537236|268900||sarcosinemia
|
|
C537236|268900||hypersarcosinemia
|
|
C537236|268900||sarcos
|
|
C537236|268900||sarcosin dehydrogenase complex deficiency of
|
|
C537236|268900||sarcosine dehydrogenase complex deficiency
|
|
C537236|268900||sarcosine dehydrogenase complex deficiency of
|
|
C537236|268900||sard deficiency
|
|
C537236|268900||sardhd
|
|
C537236|268900||sardh deficiency
|
|
D035583||rare diseases
|
|
D035583||disease orphan
|
|
D035583||disease rare
|
|
D035583||diseases orphan
|
|
D035583||diseases rare
|
|
D035583||orphan disease
|
|
D035583||orphan diseases
|
|
D035583||rare disease
|
|
D058186||acute kidney injury
|
|
D058186||acute kidney failure
|
|
D058186||acute kidney failures
|
|
D058186||acute kidney injuries
|
|
D058186||acute kidney insufficiencies
|
|
D058186||acute kidney insufficiency
|
|
D058186||acute renal failure
|
|
D058186||acute renal failures
|
|
D058186||acute renal injuries
|
|
D058186||acute renal injury
|
|
D058186||acute renal insufficiencies
|
|
D058186||acute renal insufficiency
|
|
D058186||kidney failure acute
|
|
D058186||kidney failures acute
|
|
D058186||kidney injuries acute
|
|
D058186||kidney injury acute
|
|
D058186||kidney insufficiencies acute
|
|
D058186||kidney insufficiency acute
|
|
D058186||renal failure acute
|
|
D058186||renal failures acute
|
|
D058186||renal injuries acute
|
|
D058186||renal injury acute
|
|
D058186||renal insufficiencies acute
|
|
D058186||renal insufficiency acute
|
|
D010284||paratyphoid fever
|
|
D010284||fever paratyphoid
|
|
D010284||fevers paratyphoid
|
|
D010284||paratyphoid fevers
|
|
D010283||paratuberculosis
|
|
D010283||disease johne
|
|
D010283||disease johne apos s
|
|
D010283||johne disease
|
|
D010283||johne apos s disease
|
|
D010283||johnes disease
|
|
D010283||paratuberculoses
|
|
D019294|213700||xanthomatosis cerebrotendinous
|
|
D019294|213700||bogaert scherer epstein disease van
|
|
D019294|213700||cerebral cholesterinoses
|
|
D019294|213700||cerebral cholesterinosis
|
|
D019294|213700||cerebrotendinous xanthomatoses
|
|
D019294|213700||cerebrotendinous xanthomatosis
|
|
D019294|213700||ctx
|
|
D019294|213700||disease van bogaert scherer epstein
|
|
D019294|213700||van bogaert scherer epstein disease
|
|
D019294|213700||xanthomatoses cerebrotendinous
|
|
C565790|604326||spinocerebellar ataxia 12
|
|
C565790|604326||sca12
|
|
D005706||gallbladder neoplasms
|
|
D005706||bladder cancer gall
|
|
D005706||bladder cancers gall
|
|
D005706||cancer gallbladder
|
|
D005706||cancer gall bladder
|
|
D005706||cancer of gallbladder
|
|
D005706||cancer of the gallbladder
|
|
D005706||cancers gallbladder
|
|
D005706||cancers gall bladder
|
|
D005706||gallbladder cancer
|
|
D005706||gall bladder cancer
|
|
D005706||gallbladder cancers
|
|
D005706||gall bladder cancers
|
|
D005706||gallbladder neoplasm
|
|
D005706||neoplasm gallbladder
|
|
D005706||neoplasms gallbladder
|
|
264600|C535830||pseudovaginal perineoscrotal hypospadias
|
|
264600|C535830||5 alpha reductase deficiency
|
|
264600|C535830||familial incomplete male pseudohermaphroditism type 2
|
|
264600|C535830||male pseudohermaphroditism due to 5 alpha reductase deficiency
|
|
264600|C535830||ppsh
|
|
264600|C535830||steroid 5 alpha reductase deficiency
|
|
D005705||gallbladder diseases
|
|
D005705||bladder disease gall
|
|
D005705||bladder diseases gall
|
|
D005705||disease gallbladder
|
|
D005705||disease gall bladder
|
|
D005705||diseases gallbladder
|
|
D005705||diseases gall bladder
|
|
D005705||gallbladder disease
|
|
D005705||gall bladder disease
|
|
D005705||gall bladder diseases
|
|
118200|D002607||charcot marie tooth disease
|
|
118200|D002607||areflexic dystasia hereditary
|
|
118200|D002607||areflexic dystasias hereditary
|
|
118200|D002607||atrophies peroneal muscular
|
|
118200|D002607||atrophy muscular peroneal
|
|
118200|D002607||atrophy peroneal muscular
|
|
118200|D002607||charcot marie disease
|
|
118200|D002607||charcot marie tooth disease autosomal dominant with focally folded myelin sheaths type 1a
|
|
118200|D002607||charcot marie tooth disease autosomal dominant with focally folded myelin sheaths type 1b
|
|
118200|D002607||charcot marie tooth disease demyelinating type 1a
|
|
118200|D002607||charcot marie tooth disease demyelinating type 1b
|
|
118200|D002607||charcot marie tooth disease slow nerve conduction type linked to duffy
|
|
118200|D002607||charcot marie tooth disease type 1a
|
|
118200|D002607||charcot marie tooth disease type 1b
|
|
118200|D002607||charcot marie tooth disease type i
|
|
118200|D002607||charcot marie tooth disease type ia
|
|
118200|D002607||charcot marie tooth disease type ib
|
|
118200|D002607||charcot marie tooth disease type ii
|
|
118200|D002607||charcot marie tooth hereditary neuropathy
|
|
118200|D002607||charcot marie tooth neuropathy type 1a
|
|
118200|D002607||charcot marie tooth neuropathy type 1b
|
|
118200|D002607||charcot marie tooth syndrome
|
|
118200|D002607||cmt1a
|
|
118200|D002607||cmt1b
|
|
118200|D002607||dystasia hereditary areflexic
|
|
118200|D002607||dystasias hereditary areflexic
|
|
118200|D002607||hereditary areflexic dystasia
|
|
118200|D002607||hereditary areflexic dystasias
|
|
118200|D002607||hereditary motor and sensory neuropathy 1a
|
|
118200|D002607||hereditary motor and sensory neuropathy 1b
|
|
118200|D002607||hereditary motor and sensory neuropathy i
|
|
118200|D002607||hereditary motor and sensory neuropathy ia
|
|
118200|D002607||hereditary motor and sensory neuropathy ib
|
|
118200|D002607||hereditary motor and sensory neuropathy type i
|
|
118200|D002607||hereditary motor and sensory neuropathy type ii
|
|
118200|D002607||hereditary neuropathy charcot marie tooth
|
|
118200|D002607||hereditary type i motor and sensory neuropathy
|
|
118200|D002607||hmn distal type i
|
|
118200|D002607||hmsn1
|
|
118200|D002607||hmsn1a
|
|
118200|D002607||hmsn 1a
|
|
118200|D002607||hmsn1b
|
|
118200|D002607||hmsn 1b
|
|
118200|D002607||hmsn i
|
|
118200|D002607||hmsn ia
|
|
118200|D002607||hmsn ib
|
|
118200|D002607||hmsn ii
|
|
118200|D002607||hmsn type i
|
|
118200|D002607||hmsn type ii
|
|
118200|D002607||muscular atrophies peroneal
|
|
118200|D002607||muscular atrophy peroneal
|
|
118200|D002607||neuropathy type i hereditary motor and sensory
|
|
118200|D002607||neuropathy type ii hereditary motor and sensory
|
|
118200|D002607||peroneal muscular atrophies
|
|
118200|D002607||peroneal muscular atrophy
|
|
118200|D002607||roussy levy disease
|
|
118200|D002607||roussy levy hereditary areflexic dystasia
|
|
118200|D002607||roussy levy syndrome
|
|
118200|D002607||syndrome charcot marie tooth
|
|
118200|D002607||syndrome roussy levy
|
|
211180|C537081||bowen conradi syndrome
|
|
211180|C537081||bowen conradi hutterite syndrome
|
|
211180|C537081||bowen hutterite syndrome formerly
|
|
211180|C537081||bwcns
|
|
C537199|608687||spinocerebellar ataxia 20
|
|
C537199|608687||chromosome 11q12 duplication syndrome 260 kb
|
|
C537199|608687||sca20
|
|
C537199|608687||spinocerebellar ataxia type 20
|
|
C537199|608687||spinocerebellar ataxia with dysphonia
|
|
C537199|608687||spinocerebellar ataxia with spasmodic cough
|
|
D057770|228600||hyalinosis systemic
|
|
D057770|228600||fibromatosis hyalinica multiplex juvenilis
|
|
D057770|228600||fibromatosis juvenile hyaline
|
|
D057770|228600||fibromatosis syndrome hyaline
|
|
D057770|228600||fibromatosis syndromes hyaline
|
|
D057770|228600||hfs
|
|
D057770|228600||hyaline fibromatosis juvenile
|
|
D057770|228600||hyaline fibromatosis syndrome
|
|
D057770|228600||hyaline fibromatosis syndromes
|
|
D057770|228600||hyalinoses infantile systemic
|
|
D057770|228600||hyalinoses juvenile
|
|
D057770|228600||hyalinoses systemic
|
|
D057770|228600||hyalinoses systemic juvenile
|
|
D057770|228600||hyalinosis infantile systemic
|
|
D057770|228600||hyalinosis juvenile
|
|
D057770|228600||hyalinosis systemic juvenile
|
|
D057770|228600||infantile systemic hyalinoses
|
|
D057770|228600||infantile systemic hyalinosis
|
|
D057770|228600||juvenile hyaline fibromatoses
|
|
D057770|228600||juvenile hyaline fibromatosis
|
|
D057770|228600||juvenile hyalinoses
|
|
D057770|228600||juvenile hyalinoses systemic
|
|
D057770|228600||juvenile hyalinosis
|
|
D057770|228600||juvenile hyalinosis systemic
|
|
D057770|228600||murray syndrome
|
|
D057770|228600||puretic syndrome
|
|
D057770|228600||puretic syndromes
|
|
D057770|228600||syndrome hyaline fibromatosis
|
|
D057770|228600||syndrome murray
|
|
D057770|228600||syndrome puretic
|
|
D057770|228600||syndromes hyaline fibromatosis
|
|
D057770|228600||syndromes puretic
|
|
D057770|228600||systemic hyalinoses
|
|
D057770|228600||systemic hyalinoses infantile
|
|
D057770|228600||systemic hyalinosis
|
|
D057770|228600||systemic hyalinosis infantile
|
|
D057770|228600||systemic juvenile hyalinoses
|
|
D057770|228600||systemic juvenile hyalinosis
|
|
D010292||paresthesia
|
|
D010292||distal paresthesia
|
|
D010292||distal paresthesias
|
|
D010292||dysesthesia
|
|
D010292||dysesthesias
|
|
D010292||formication
|
|
D010292||formications
|
|
D010292||painful paresthesia
|
|
D010292||painful paresthesias
|
|
D010292||paresthesia distal
|
|
D010292||paresthesia painful
|
|
D010292||paresthesias
|
|
D010292||paresthesias distal
|
|
D010292||paresthesias painful
|
|
303800||colorblindness partial deutan series
|
|
303800||cbd
|
|
303800||dcb
|
|
303800||deutan colorblindness
|
|
303800||deuteranopia
|
|
303800||green colorblindness deuteranomaly included
|
|
C567707|613206||spastic paraplegia 44 autosomal recessive
|
|
C567707|613206||spg44
|
|
C536962|601005||timothy syndrome
|
|
C536962|601005||long qt syndrome 8
|
|
C536962|601005||long qt syndrome with syndactyly
|
|
C536962|601005||lqt8
|
|
C536962|601005|D005879|137580|C565346|191100||ts
|
|
C567530|612357||major affective disorder 8
|
|
C567530|612357||mafd8
|
|
D010267||parapsoriasis
|
|
D010267||dermatoses digitate
|
|
D010267||dermatosis digitate
|
|
D010267||digitate dermatoses
|
|
D010267||digitate dermatosis
|
|
D010267||erythroderma maculopapular
|
|
D010267||erythrodermas maculopapular
|
|
D010267||maculopapular erythroderma
|
|
D010267||maculopapular erythrodermas
|
|
D010267||parakeratosis variegata
|
|
D010267||parapsoriases
|
|
D010267||parapsoriasis en plaque
|
|
D010267||parapsoriasis en plaques
|
|
C564696|606574||oculocutaneous albinism type iv
|
|
C564696|606574||albinism oculocutaneous type iv
|
|
C564696|606574||oca4
|
|
105250|C562643||amyloidosis ix
|
|
105250|C562643||amyloidosis familial cutaneous lichen
|
|
105250|C562643||amyloidosis primary cutaneous 1
|
|
105250|C562643||amyloidosis primary localized cutaneous 1
|
|
105250|C562643||lichen amyloidosis familial
|
|
105250|C562643||pca
|
|
105250|C562643||pca1
|
|
105250|C562643||plca1
|
|
C564653|606852||parkinson disease 10
|
|
C564653|606852||aaopd
|
|
C564653|606852||park10
|
|
C564653|606852||parkinson disease age at onset of
|
|
D010260||paranoid personality disorder
|
|
D010260||disorder paranoid personality
|
|
D010260||disorders paranoid personality
|
|
D010260||paranoid personalities
|
|
D010260||paranoid personality
|
|
D010260||paranoid personality disorders
|
|
D010260||personalities paranoid
|
|
D010260||personality disorder paranoid
|
|
D010260||personality disorders paranoid
|
|
D010260||personality paranoid
|
|
D010262||paraphilias
|
|
D010262||deviation sex
|
|
D010262||deviations sex
|
|
D010262||paraphilia
|
|
D010262||sex deviation
|
|
D010262||sex deviations
|
|
D011595||psychomotor agitation
|
|
D011595||agitation psychomotor
|
|
D011595||akathisia
|
|
D011595||excitement psychomotor
|
|
D011595||hyperactivity psychomotor
|
|
D011595||psychomotor excitement
|
|
D011595||psychomotor hyperactivity
|
|
D011595||psychomotor restlessness
|
|
D011595||restlessness
|
|
D011595||restlessness psychomotor
|
|
D010264||paraplegia
|
|
D010264||ataxic paraplegia
|
|
D010264||ataxic paraplegias
|
|
D010264||cerebral paraplegia
|
|
D010264||cerebral paraplegias
|
|
D010264||flaccid paraplegia
|
|
D010264||flaccid paraplegias
|
|
D010264||paralysis legs
|
|
D010264||paralysis lower extremities
|
|
D010264||paralysis lower limbs
|
|
D010264||paraplegia ataxic
|
|
D010264||paraplegia cerebral
|
|
D010264||paraplegia flaccid
|
|
D010264||paraplegias
|
|
D010264||paraplegias ataxic
|
|
D010264||paraplegias cerebral
|
|
D010264||paraplegias flaccid
|
|
D010264||paraplegia spastic
|
|
D010264||paraplegia spinal
|
|
D010264||paraplegias spastic
|
|
D010264||paraplegias spinal
|
|
D010264||spastic paraplegia
|
|
D010264||spastic paraplegias
|
|
D010264||spinal paraplegia
|
|
D010264||spinal paraplegias
|
|
C536980|227050||transient erythroblastopenia of childhood
|
|
C536980|227050||erythroblastopenia transient
|
|
C536980|227050||familial transient erythroblastopenia of childhood
|
|
C536980|227050||tec
|
|
D010263||paraphimosis
|
|
D010263||paraphimoses
|
|
D011596||psychomotor disorders
|
|
D011596||developmental psychomotor disorder
|
|
D011596||developmental psychomotor disorders
|
|
D011596||impairment psychomotor
|
|
D011596||impairments psychomotor
|
|
D011596||psychomotor disorder developmental
|
|
D011596||psychomotor disorders developmental
|
|
D011596||psychomotor impairment
|
|
D011596||psychomotor impairments
|
|
D010265||paraproteinemias
|
|
D010265||cell dyscrasia plasma
|
|
D010265||cell dyscrasias plasma
|
|
D010265||dyscrasia plasma cell
|
|
D010265||dyscrasias plasma cell
|
|
D010265||gammapathies monoclonal
|
|
D010265||gammapathy monoclonal
|
|
D010265||gammopathies monoclonal
|
|
D010265||gammopathy monoclonal
|
|
D010265||monoclonal gammapathies
|
|
D010265||monoclonal gammapathy
|
|
D010265||monoclonal gammopathies
|
|
D010265||monoclonal gammopathy
|
|
D010265||paraimmunoglobulinemia
|
|
D010265||paraimmunoglobulinemias
|
|
D010265||paraproteinemia
|
|
D010265||plasma cell dyscrasia
|
|
D010265||plasma cell dyscrasias
|
|
C535506|108500||episodic ataxia with nystagmus
|
|
C535506|108500||acetazolamide responsive episodic ataxia syndrome
|
|
C535506|108500||acetazolamide responsive hereditary paroxysmal cerebellar ataxia
|
|
C535506|108500||apca
|
|
C535506|108500||ataxia episodic with nystagmus
|
|
C535506|108500||ataxia familial paroxysmal
|
|
C535506|108500||capa
|
|
C535506|108500||cerebellar ataxia paroxysmal acetazolamide responsive
|
|
C535506|108500||cerebellopathy hereditary paroxysmal
|
|
C535506|108500||ea2
|
|
C535506|108500||episodic ataxia nystagmus associated
|
|
C535506|108500||episodic ataxia type 2
|
|
C535506|108500||nystagmus associated episodic ataxia
|
|
D055948||sarcopenia
|
|
D055948||sarcopenias
|
|
D055949||vasa previa
|
|
D055949||praevias vasa
|
|
D055949||praevia vasa
|
|
D055949||previas vasa
|
|
D055949||previa vasa
|
|
D055949||vasa praevia
|
|
D055949||vasa praevias
|
|
D055949||vasa previas
|
|
242500|C538424||harlequin type ichthyosis
|
|
242500|C538424||arci4b
|
|
242500|C538424||apos harlequin fetus apos
|
|
242500|C538424|D017490|242300||harlequin ichthyosis
|
|
242500|C538424||hi
|
|
242500|C538424||ichthyosis congenita harlequin fetus type
|
|
242500|C538424||ichthyosis congenital autosomal recessive 4b
|
|
242500|C538424||ichthyosis harlequin type
|
|
C565238|606324||parkinson disease 7 autosomal recessive early onset
|
|
C565238|606324||park7
|
|
116800|C535342||cataract zonular
|
|
116800|C535342|116860|D020786||cam
|
|
116800|C535342||cataract 5 multiple types
|
|
116800|C535342||cataract lamellar
|
|
116800|C535342||cataract marner type
|
|
116800|C535342||ctm
|
|
116800|C535342||ctrct5
|
|
116800|C535342||perinuclear cataract
|
|
D043963||diverticulosis colonic
|
|
D043963||colonic diverticulosis
|
|
C537124|125250||optic atrophy 1 and deafness
|
|
C537124|125250||doa
|
|
C537124|125250||dominant optic atrophy plus syndrome
|
|
C537124|125250||optic atrophy with or without deafness ophthalmoplegia myopathy ataxia and neuropathy
|
|
D010279||parathyroid diseases
|
|
D010279||disease parathyroid
|
|
D010279||diseases parathyroid
|
|
D010279||disorder parathyroid
|
|
D010279||disorders parathyroid
|
|
D010279||parathyroid disease
|
|
D010279||parathyroid disorder
|
|
D010279||parathyroid disorders
|
|
D009298||nasal polyps
|
|
D009298||nasal polyp
|
|
D009298||polyp nasal
|
|
D009298||polyps nasal
|
|
C563928|608445||speech sound disorder
|
|
C563928|608445||ssd
|
|
C563874|608695||glaucoma 1 open angle j
|
|
C563874|608695||glaucoma primary open angle juvenile onset 2
|
|
C563874|608695||glc1j
|
|
C563874|608695||joag2
|
|
D010273||parasitic diseases animal
|
|
D010273||animal parasitic disease
|
|
D010273||animal parasitic diseases
|
|
D010273||disease animal parasitic
|
|
D010273||diseases animal parasitic
|
|
D010273||parasitic disease animal
|
|
D010272||parasitic diseases
|
|
D010272||disease parasitic
|
|
D010272||diseases parasitic
|
|
D010272||parasitic disease
|
|
C566395|603266||diabetes mellitus insulin dependent 17
|
|
C566395|603266||iddm17
|
|
C566395|603266||insulin dependent diabetes mellitus 17
|
|
C565211|610248||deafness autosomal recessive 65
|
|
C565211|610248||dfnb65
|
|
C535890||levator syndrome
|
|
C535890||levator ani spasm syndrome
|
|
C535890||levator ani syndrome
|
|
D055958||piriformis muscle syndrome
|
|
D055958||muscle syndrome piriformis
|
|
D055958||muscle syndromes piriformis
|
|
D055958||piriformis muscle syndromes
|
|
D055958||piriformis syndrome
|
|
D055958||piriformis syndromes
|
|
D055958||syndrome piriformis
|
|
D055958||syndrome piriformis muscle
|
|
D055958||syndromes piriformis
|
|
D055958||syndromes piriformis muscle
|
|
C565753|604757||craniosynostosis type 2
|
|
C565753|604757||craniosynostosis 2
|
|
C565753|604757||craniosynostosis boston type
|
|
C565753|604757||crs2
|
|
C565753|604757|D003057|133540||csb
|
|
C535892||lichen planus follicularis
|
|
C535892||follicular lichen planus tumidus
|
|
C535892||lichen planus follicularis tumidus
|
|
C535892||lichen planus tumidus follicularis
|
|
D055959||intervertebral disc degeneration
|
|
D055959||degeneration disc
|
|
D055959||degeneration disk
|
|
D055959||degeneration intervertebral disc
|
|
D055959||degeneration intervertebral disk
|
|
D055959||degenerations disc
|
|
D055959||degenerations disk
|
|
D055959||degenerations intervertebral disc
|
|
D055959||degenerations intervertebral disk
|
|
D055959||degenerative intervertebral disc
|
|
D055959||degenerative intervertebral discs
|
|
D055959||degenerative intervertebral disk
|
|
D055959||degenerative intervertebral disks
|
|
D055959||degradation disc
|
|
D055959||degradation disk
|
|
D055959||degradations disc
|
|
D055959||degradations disk
|
|
D055959||disc degeneration
|
|
D055959||disc degeneration intervertebral
|
|
D055959||disc degenerations
|
|
D055959||disc degenerations intervertebral
|
|
D055959||disc degenerative intervertebral
|
|
D055959||disc degradation
|
|
D055959||disc degradations
|
|
D055959||discs degenerative intervertebral
|
|
D055959||disk degeneration
|
|
D055959||disk degeneration intervertebral
|
|
D055959||disk degenerations
|
|
D055959||disk degenerations intervertebral
|
|
D055959||disk degenerative intervertebral
|
|
D055959||disk degradation
|
|
D055959||disk degradations
|
|
D055959||disks degenerative intervertebral
|
|
D055959||intervertebral disc degenerations
|
|
D055959||intervertebral disc degenerative
|
|
D055959||intervertebral discs degenerative
|
|
D055959||intervertebral disk degeneration
|
|
D055959||intervertebral disk degenerations
|
|
D055959||intervertebral disk degenerative
|
|
D055959||intervertebral disks degenerative
|
|
C535891||familial popliteal pterygium syndrome
|
|
C535891||lewis pashayan syndrome
|
|
C535894||lichtenstein syndrome
|
|
C567421|612096||otosclerosis 8
|
|
C567421|612096||otsc8
|
|
607080|C567773||46 xy gonadal dysgenesis partial with minifascicular neuropathy
|
|
D010246||paralysis obstetric
|
|
D010246||obstetrical paralyses
|
|
D010246||obstetrical paralysis
|
|
D010246||obstetric paralyses
|
|
D010246||obstetric paralysis
|
|
D010246||paralyses obstetric
|
|
D010246||paralyses obstetrical
|
|
D010246||paralysis obstetrical
|
|
D010245||paralyses familial periodic
|
|
D010245||familial periodic paralyses
|
|
D010245||familial periodic paralysis
|
|
D010245||normokalemic periodic paralyses
|
|
D010245||normokalemic periodic paralysis
|
|
D010245||paralyses normokalemic periodic
|
|
D010245||paralysis familial periodic
|
|
D010245||paralysis normokalemic periodic
|
|
D010245||periodic paralyses familial
|
|
D010245||periodic paralyses normokalemic
|
|
D010245||periodic paralysis familial
|
|
D010245||periodic paralysis normokalemic
|
|
208000|C537440||arterial calcification of infancy
|
|
208000|C537440||arterial calcification generalized of infancy
|
|
208000|C537440||arterial calcification generalized of infancy 1
|
|
208000|C537440||arterial calcification idiopathic infantile
|
|
208000|C537440||arteriopathy occlusive infantile
|
|
208000|C537440||arteriopathy occlusive infantile coronary sclerosis medial of infancy included
|
|
208000|C537440||gaci
|
|
208000|C537440||gaci1
|
|
208000|C537440||generalized arterial calcification in infancy
|
|
208000|C537440||idiopathic infantile arterial calcification
|
|
208000|C537440||iiac
|
|
208000|C537440||occlusive infantile arteriopathy
|
|
D009265||nairobi sheep disease
|
|
D009265||disease nairobi sheep
|
|
D009265||sheep disease nairobi
|
|
D009264||nails malformed
|
|
D009264||abnormalities nail
|
|
D009264||abnormality nail
|
|
D009264||abnormal nail
|
|
D009264||abnormal nails
|
|
D009264||malformed nail
|
|
D009264||malformed nails
|
|
D009264||nail abnormal
|
|
D009264||nail abnormalities
|
|
D009264||nail abnormality
|
|
D009264||nail malformed
|
|
D009264||nails abnormal
|
|
D009264||pachyonychia
|
|
D009263||nails ingrown
|
|
D009263||ingrown nail
|
|
D009263||ingrown nails
|
|
D009263||nail ingrown
|
|
D010249||parametritis
|
|
D010249||cellulitides pelvic
|
|
D010249||cellulitis pelvic
|
|
D010249||parametritides
|
|
D010249||pelvic cellulitides
|
|
D010249||pelvic cellulitis
|
|
C536345|192950||vertical talus congenital
|
|
C536345|192950||cvt
|
|
C536345|192950||pes valgus congenital convex
|
|
C536345|192950||rocker bottom foot
|
|
C567758|613093||cone dystrophy 4
|
|
C567758|613093||achm5 included
|
|
C567758|613093||achromatopsia 5 included
|
|
C567758|613093||cod4
|
|
D055954||corneal endothelial cell loss
|
|
D055954||corneal endothelial cell damage
|
|
D055954||endothelial cell loss corneal
|
|
D009260||nail diseases
|
|
D009260||disease nail
|
|
D009260||diseases nail
|
|
D009260||nail disease
|
|
C535885||jones hersh yusk syndrome
|
|
C535885||aplasia cutis cleft palate epidermolysis
|
|
C535885||aplasia cutis congenita cleft palate epidermolysis bullosa and ectrodactyly
|
|
C535885||ptosis ectropion thin skin beaked nose
|
|
D055955||susac syndrome
|
|
D055955||retinocochleocerebral vasculopathies
|
|
D055955||retinocochleocerebral vasculopathy
|
|
D055955||susac apos s syndrome
|
|
D055955||susacs syndrome
|
|
D055955||syndrome susac
|
|
D055955||syndrome susac apos s
|
|
D055955||vasculopathies retinocochleocerebral
|
|
D055955||vasculopathy retinocochleocerebral
|
|
C535884||joint laxity familial
|
|
C535884||articular hypermobility syndrome
|
|
C535884||familial joint instability syndrome
|
|
C535884||joint instability syndrome
|
|
D055956||diffuse neurofibrillary tangles with calcification
|
|
D055956||disease kosaka shibayama
|
|
D055956||kosaka shibayama disease
|
|
C535886||jones syndrome
|
|
C535886||fibromatosis gingival progressive deafness
|
|
C535886||fibromatosis gingival with progressive deafness
|
|
C535886||gingival fibromatosis with progressive deafness
|
|
C535886||gingival fibromatosis with sensorineural hearing loss
|
|
C535889||leukonychia totalis
|
|
C535889||hereditary white nails
|
|
C535889||porcelain nails
|
|
D010241||parakeratosis
|
|
D010241||parakeratoses
|
|
C535888||leukoencephalopathy arthritis colitis and hypogammaglobulinemia
|
|
D055952||cogan syndrome
|
|
D055952||cogan apos s syndrome
|
|
D055952||cogans syndrome
|
|
D055952||syndrome cogan
|
|
D055952||syndrome cogans
|
|
D055952||syndrome cogan apos s
|
|
D055953||microscopic polyangiitis
|
|
D055953||microscopic polyangiitides
|
|
D055953||polyangiitides microscopic
|
|
D055953||polyangiitis microscopic
|
|
D010243||paralysis
|
|
D010243||palsies
|
|
D010243||palsy
|
|
D010243||paralyses
|
|
D010243||paralysis todd
|
|
D010243||paralysis todd apos s
|
|
D010243||plegia
|
|
D010243||plegias
|
|
D010243||todd paralysis
|
|
D010243||todd apos s paralysis
|
|
D010243||todds paralysis
|
|
193007|C535431||benign paroxysmal positional vertigo
|
|
193007|C535431||bppv
|
|
193007|C535431||brv
|
|
193007|C535431||brv1 included
|
|
193007|C535431||brv2
|
|
193007|C535431||familial benign recurrent vertigo
|
|
193007|C535431||familial vestibulopathy
|
|
193007|C535431||vertigo benign paroxysmal positional
|
|
193007|C535431|C562859||vertigo benign recurrent
|
|
193007|C535431|C567749||vertigo benign recurrent 2
|
|
193007|C535431||vestibulopathy familial
|
|
193007|C535431||vestibulopathy familial vertigo benign recurrent 1 included
|
|
C565778|604393||leber congenital amaurosis 4
|
|
C565778|604393||cone rod dystrophy aipl1 related
|
|
C565778|604393||cone rod dystrophy aipl1 related included
|
|
C565778|604393||lca4
|
|
C565778|604393||retinitis pigmentosa juvenile aipl1 related
|
|
C565778|604393||retinitis pigmentosa juvenile aipl1 related included
|
|
D010257||paraneoplastic syndromes
|
|
D010257||paraneoplastic syndrome
|
|
D010257||syndrome paraneoplastic
|
|
D010257||syndromes paraneoplastic
|
|
D010259||paranoid disorders
|
|
D010259||disorder paranoid
|
|
D010259||disorders paranoid
|
|
D010259||paranoia
|
|
D010259||paranoias
|
|
D010259||paranoid disorder
|
|
D010259||paranoid psychoses
|
|
D010259||psychoses paranoid
|
|
D010253||respirovirus infections
|
|
D010253||infections respirovirus
|
|
C537985|607678||charcot marie tooth disease type 1d
|
|
C537985|607678||charcot marie tooth disease demyelinating type 1d
|
|
C537985|607678||charcot marie tooth neuropathy type 1d
|
|
C537985|607678||cmt1d
|
|
C537985|607678||hereditary motor and sensory neuropathy 1d
|
|
C537985|607678||hmsn1d
|
|
C537985|607678||hmsn 1d
|
|
C537985|607678||hmsnid
|
|
C537985|607678||hmsn id
|
|
D055963||asthma aspirin induced
|
|
D055963||aspirin induced asthma
|
|
D055963||aspirin induced asthmas
|
|
D055963||aspirin induced asthma syndrome
|
|
D055963||aspirin induced asthma syndromes
|
|
D055963||asthma nsaid induced
|
|
D055963||asthmas aspirin induced
|
|
D055963||asthmas nsaid induced
|
|
D055963||asthma syndrome aspirin induced
|
|
D055963||asthma syndromes aspirin induced
|
|
D055963||induced asthma aspirin
|
|
D055963||induced asthmas aspirin
|
|
D055963||nsaid induced asthma
|
|
D055963||nsaid induced asthmas
|
|
D055963||syndrome aspirin induced asthma
|
|
D055963||syndromes aspirin induced asthma
|
|
D010255||paranasal sinus neoplasms
|
|
D010255||cancer of paranasal sinus
|
|
D010255||cancer paranasal sinus
|
|
D010255||cancers paranasal sinus
|
|
D010255||neoplasm paranasal sinus
|
|
D010255||neoplasms paranasal sinus
|
|
D010255||paranasal sinus cancer
|
|
D010255||paranasal sinus cancers
|
|
D010255||paranasal sinus neoplasm
|
|
D055964||alien hand syndrome
|
|
D055964||alien hand syndromes
|
|
D055964||anarchic hand syndrome
|
|
D055964||anarchic hand syndromes
|
|
D055964||hand syndrome alien
|
|
D055964||hand syndrome anarchic
|
|
D055964||hand syndromes alien
|
|
D055964||hand syndromes anarchic
|
|
D055964||syndrome alien hand
|
|
D055964||syndrome anarchic hand
|
|
D055964||syndromes alien hand
|
|
D055964||syndromes anarchic hand
|
|
C567748|613107||neutropenia severe congenital autosomal dominant 2
|
|
C567748|613107||neutropenia severe congenital 2 autosomal dominant
|
|
C567748|613107||scn2
|
|
C567748|613107||severe congenital neutropenia 2
|
|
D010254||paranasal sinus diseases
|
|
D010254||disease paranasal sinus
|
|
D010254||diseases paranasal sinus
|
|
D010254||paranasal sinus disease
|
|
D010254||sinus disease paranasal
|
|
D010254||sinus diseases paranasal
|
|
C566963|611363||atrial septal defect 4
|
|
C566963|611363||asd4
|
|
D009236||myxosarcoma
|
|
D009236||myxosarcomas
|
|
D012887||skull fractures
|
|
D012887||fracture non depressed skull
|
|
D012887||fracture skull
|
|
D012887||fractures linear skull
|
|
D012887||fractures non depressed skull
|
|
D012887||fractures skull
|
|
D012887||linear skull fracture
|
|
D012887||linear skull fractures
|
|
D012887||non depressed skull fracture
|
|
D012887||non depressed skull fractures
|
|
D012887||skull fracture
|
|
D012887||skull fracture linear
|
|
D012887||skull fracture non depressed
|
|
D012887||skull fractures linear
|
|
D012887||skull fractures non depressed
|
|
C566146|117210||spinocerebellar ataxia 31
|
|
C566146|117210||sca31
|
|
C566146|117210||spinocerebellar ataxia 16q22 linked
|
|
D012888||skull neoplasms
|
|
D012888||neoplasm skull
|
|
D012888||neoplasms skull
|
|
D012888||skull neoplasm
|
|
D011557||pseudorabies
|
|
D011557||aujeszky disease
|
|
D011557||aujeszky apos s disease
|
|
D011557||aujeszkys disease
|
|
D011559||pseudotumor cerebri
|
|
D011559||benign intracranial hypertension
|
|
D011559||hypertension benign intracranial
|
|
D011559||hypertension idiopathic intracranial
|
|
D011559||idiopathic intracranial hypertension
|
|
D011559||intracranial hypertension benign
|
|
D011559||intracranial hypertension idiopathic
|
|
C566310|102900||adenosine triphosphate elevated of erythrocytes
|
|
C566310|102900||pyruvate kinase hyperactivity
|
|
607842|C564321||aural atresia congenital
|
|
607842|C564321||caa
|
|
C566458|609649||trichilemmal cyst 1
|
|
C566458|609649|D004814||pilar cyst
|
|
C566458|609649||tricholemmal cyst
|
|
C566458|609649||tricy1
|
|
C567787|605714||cerebral amyloid angiopathy app related
|
|
C567787|605714||amyloidosis cerebroarterial app related
|
|
C567787|605714|C537944||amyloidosis hereditary with cerebral hemorrhage dutch variant
|
|
C567787|605714||cerebral amyloid angiopathy app related arctic variant
|
|
C567787|605714||cerebral amyloid angiopathy app related dutch variant
|
|
C567787|605714||cerebral amyloid angiopathy app related flemish variant
|
|
C567787|605714||cerebral amyloid angiopathy app related iowa variant
|
|
C567787|605714||cerebral amyloid angiopathy app related italian variant
|
|
C567787|605714|C537944||hchwad
|
|
D010229||paracoccidioidomycosis
|
|
D010229||blastomycosis south american
|
|
D010229||paracoccidioidomycoses
|
|
D010229||south american blastomycosis
|
|
C567512|611863||microtia with nasolacrimal duct imperforation and eye coloboma
|
|
D012883||skin ulcer
|
|
D012883||skin ulcers
|
|
D012883||ulcer skin
|
|
D012883||ulcers skin
|
|
D011553||pseudomyxoma peritonei
|
|
D011553||ascites gelatinous
|
|
D011553||gelatinous ascites
|
|
D011553||pseudomyxoma peritonei syndrome
|
|
D011553||pseudomyxoma peritonei syndromes
|
|
D011553||syndrome of pseudomyxoma peritonei
|
|
C566999|611154||alzheimer disease 14
|
|
C566999|611154||ad14
|
|
D011552||pseudomonas infections
|
|
D011552||infection pseudomonas
|
|
D011552||infections pseudomonas
|
|
D011552||pseudomonas infection
|
|
109660||beta amino acids renal transport of
|
|
109660||aabt
|
|
109660||taurine renal reabsorption
|
|
252900|D009084||mucopolysaccharidosis iii
|
|
252900|D009084||acetyl coa alpha glucosaminide n acetyltransferase deficiencies
|
|
252900|D009084||acetyl coa alpha glucosaminide n acetyltransferase deficiency
|
|
252900|D009084||deficiencies acetyl coa alpha glucosaminide n acetyltransferase
|
|
252900|D009084||deficiencies n acetyl alpha d glucosaminidase
|
|
252900|D009084||deficiencies n acetylglucosamine 6 sulfatase
|
|
252900|D009084||deficiencies n acetylglucosamine 6 sulfate sulfatase
|
|
252900|D009084||deficiencies naglu
|
|
252900|D009084||deficiencies sulfamidase
|
|
252900|D009084||deficiency acetyl coa alpha glucosaminide n acetyltransferase
|
|
252900|D009084||deficiency n acetyl alpha d glucosaminidase
|
|
252900|D009084||deficiency n acetylglucosamine 6 sulfatase
|
|
252900|D009084||deficiency n acetylglucosamine 6 sulfate sulfatase
|
|
252900|D009084||deficiency naglu
|
|
252900|D009084||deficiency sulfamidase
|
|
252900|D009084||heparan sulfate sulfatase deficiency
|
|
252900|D009084||iiibs mucopolysaccharidosis type
|
|
252900|D009084||mps3a
|
|
252900|D009084||mps 3 a
|
|
252900|D009084||mps3b
|
|
252900|D009084||mps 3 b
|
|
252900|D009084||mps3c
|
|
252900|D009084||mps 3 c
|
|
252900|D009084||mps3d
|
|
252900|D009084||mps 3 d
|
|
252900|D009084||mps iiia
|
|
252900|D009084||mps iii a
|
|
252900|D009084||mps iiib
|
|
252900|D009084||mps iii b
|
|
252900|D009084||mps iiic
|
|
252900|D009084||mps iii c
|
|
252900|D009084||mps iiid
|
|
252900|D009084||mps iii d
|
|
252900|D009084||mps iiids
|
|
252900|D009084||mucopolysaccharidosis 3
|
|
252900|D009084||mucopolysaccharidosis iiis
|
|
252900|D009084||mucopolysaccharidosis type 3 a
|
|
252900|D009084||mucopolysaccharidosis type 3 a sanfilippo syndrome
|
|
252900|D009084||mucopolysaccharidosis type 3 b
|
|
252900|D009084||mucopolysaccharidosis type 3 c
|
|
252900|D009084||mucopolysaccharidosis type 3 d
|
|
252900|D009084||mucopolysaccharidosis type iiia
|
|
252900|D009084||mucopolysaccharidosis type iiias
|
|
252900|D009084||mucopolysaccharidosis type iiib
|
|
252900|D009084||mucopolysaccharidosis type iiibs
|
|
252900|D009084||mucopolysaccharidosis type iiic
|
|
252900|D009084||mucopolysaccharidosis type iiics
|
|
252900|D009084||mucopolysaccharidosis type iiid
|
|
252900|D009084||mucopolysaccharidosis type iiids
|
|
252900|D009084||n acetyl alpha d glucosaminidase deficiencies
|
|
252900|D009084||n acetyl alpha d glucosaminidase deficiency
|
|
252900|D009084||n acetylglucosamine 6 sulfatase deficiencies
|
|
252900|D009084||n acetylglucosamine 6 sulfatase deficiency
|
|
252900|D009084||n acetylglucosamine 6 sulfate sulfatase deficiencies
|
|
252900|D009084||n acetylglucosamine 6 sulfate sulfatase deficiency
|
|
252900|D009084||n acetyltransferase deficiencies acetyl coa alpha glucosaminide
|
|
252900|D009084||n acetyltransferase deficiency acetyl coa alpha glucosaminide
|
|
252900|D009084||naglu deficiencies
|
|
252900|D009084||naglu deficiency
|
|
252900|D009084||oligophrenia polydystrophic
|
|
252900|D009084||oligophrenias polydystrophic
|
|
252900|D009084||polydystrophic oligophrenia
|
|
252900|D009084||polydystrophic oligophrenias
|
|
252900|D009084||sanfilippo apos s syndrome
|
|
252900|D009084||sanfilippos syndrome
|
|
252900|D009084||san filippo apos s syndrome
|
|
252900|D009084||san filippos syndrome
|
|
252900|D009084||sanfilippo syndrome
|
|
252900|D009084||san filippo syndrome
|
|
252900|D009084||sanfilippo syndrome a
|
|
252900|D009084||sanfilippo syndrome b
|
|
252900|D009084||sanfilippo syndrome c
|
|
252900|D009084||sanfilippo syndrome d
|
|
252900|D009084||sanfilippo syndromes
|
|
252900|D009084||sulfamidase deficiencies
|
|
252900|D009084||sulfamidase deficiency
|
|
252900|D009084||sulfatase deficiencies n acetylglucosamine 6 sulfate
|
|
252900|D009084||sulfatase deficiency n acetylglucosamine 6 sulfate
|
|
252900|D009084||syndrome sanfilippo
|
|
252900|D009084||syndrome sanfilippo apos s
|
|
252900|D009084||syndrome san filippo apos s
|
|
252900|D009084||syndromes sanfilippo
|
|
D012899||smallpox
|
|
D012899||alastrim
|
|
D012899||minors variola
|
|
D012899||minor variola
|
|
D012899||variola
|
|
D012899||variola minor
|
|
D012899||variola minors
|
|
D012899||variolas
|
|
D010237||paragonimiasis
|
|
D010237||infection paragonimus westermani
|
|
D010237||infections paragonimus westermani
|
|
D010237||paragonimiases
|
|
D010237||paragonimus westermani infection
|
|
D010237||paragonimus westermani infections
|
|
D010237||westermani infection paragonimus
|
|
D010237||westermani infections paragonimus
|
|
D012897||slow virus diseases
|
|
D012897||disease slow virus
|
|
D012897||diseases slow virus
|
|
D012897||slow virus disease
|
|
D012897||virus disease slow
|
|
D012897||virus diseases slow
|
|
D010236||paraganglioma extra adrenal
|
|
D010236||chemodectoma
|
|
D010236|D010235|168000||chemodectomas
|
|
D010236||extra adrenal paraganglioma
|
|
D010236||extra adrenal paragangliomas
|
|
D010236||nonchromaffin paraganglioma
|
|
D010236||non chromaffin paraganglioma
|
|
D010236||nonchromaffin paragangliomas
|
|
D010236||non chromaffin paragangliomas
|
|
D010236||paraganglioma nonchromaffin
|
|
D010236||paraganglioma non chromaffin
|
|
D010236||paragangliomas extra adrenal
|
|
D010236||paragangliomas familial nonchromaffin 1
|
|
D010236||paragangliomas nonchromaffin
|
|
D010236||paragangliomas non chromaffin
|
|
D017074|240500||common variable immunodeficiency
|
|
D017074|240500||acquired hypogammaglobulinemia
|
|
D017074|240500||acquired hypogammaglobulinemias
|
|
D017074|240500||antibody deficiency due to baffr defect
|
|
D017074|240500||antibody deficiency due to cd19 defect
|
|
D017074|240500||antibody deficiency due to cd20 defect
|
|
D017074|240500||antibody deficiency due to cd81 defect
|
|
D017074|240500||antibody deficiency due to icos defect immunodeficiency common variable included
|
|
D017074|240500||antibody deficiency due to taci defect
|
|
D017074|240500||common variable hypogammaglobulinemia
|
|
D017074|240500||common variable hypogammaglobulinemias
|
|
D017074|240500||common variable immune deficiency
|
|
D017074|240500||common variable immunodeficiencies
|
|
D017074|240500||cvid1
|
|
D017074|240500||cvid2
|
|
D017074|240500||cvid3
|
|
D017074|240500||cvid4
|
|
D017074|240500||cvid5
|
|
D017074|240500||cvid6
|
|
D017074|240500||cvid included
|
|
D017074|240500||deficiencies late onset immunoglobulin
|
|
D017074|240500||deficiency late onset immunoglobulin
|
|
D017074|240500||hypogammaglobulinemia acquired
|
|
D017074|240500||hypogammaglobulinemia common variable
|
|
D017074|240500||hypogammaglobulinemia due to taci deficiency
|
|
D017074|240500||hypogammaglobulinemias acquired
|
|
D017074|240500||hypogammaglobulinemias common variable
|
|
D017074|240500||immunodeficiencies common variable
|
|
D017074|240500||immunodeficiency common variable
|
|
D017074|240500||immunodeficiency common variable 1
|
|
D017074|240500||immunodeficiency common variable 2
|
|
D017074|240500||immunodeficiency common variable 3
|
|
D017074|240500||immunodeficiency common variable 4
|
|
D017074|240500||immunodeficiency common variable 5
|
|
D017074|240500||immunodeficiency common variable 6
|
|
D017074|240500||immunoglobulin deficiencies late onset
|
|
D017074|240500||immunoglobulin deficiency late onset
|
|
D017074|240500||late onset immunoglobulin deficiencies
|
|
D017074|240500||late onset immunoglobulin deficiency
|
|
D017074|240500||variable hypogammaglobulinemia common
|
|
D017074|240500||variable hypogammaglobulinemias common
|
|
D012891||sleep apnea syndromes
|
|
D012891||apnea sleep
|
|
D012891||apneas sleep
|
|
D012891||apnea syndrome sleep
|
|
D012891||apnea syndromes sleep
|
|
D012891||breathing sleep disordered
|
|
D012891||hypersomnia with periodic respiration
|
|
D012891||hypopnea sleep
|
|
D012891||hypopneas sleep
|
|
D012891||mixed central and obstructive sleep apnea
|
|
D012891||mixed sleep apnea
|
|
D012891||mixed sleep apneas
|
|
D012891||sleep apnea
|
|
D012891||sleep apnea mixed
|
|
D012891||sleep apnea mixed central and obstructive
|
|
D012891||sleep apneas
|
|
D012891||sleep apneas mixed
|
|
D012891||sleep apnea syndrome
|
|
D012891||sleep disordered breathing
|
|
D012891||sleep hypopnea
|
|
D012891||sleep hypopneas
|
|
C567587|300779||corneal dystrophy endothelial x linked
|
|
C567587|300779||endothelial corneal dystrophy x linked
|
|
C567587|300779||xecd
|
|
D012892||sleep deprivation
|
|
D012892||deprivation rem sleep
|
|
D012892||deprivation sleep
|
|
D012892||deprivations rem sleep
|
|
D012892||deprivations sleep
|
|
D012892||fragmentation sleep
|
|
D012892||fragmentations sleep
|
|
D012892||insufficient sleep syndrome
|
|
D012892||insufficient sleep syndromes
|
|
D012892||rem sleep deprivation
|
|
D012892||rem sleep deprivations
|
|
D012892||sleep deprivation rem
|
|
D012892||sleep deprivations
|
|
D012892||sleep deprivations rem
|
|
D012892||sleep fragmentation
|
|
D012892||sleep fragmentations
|
|
D012892||syndrome insufficient sleep
|
|
D012892||syndromes insufficient sleep
|
|
D055985||latent tuberculosis
|
|
D055985||infection latent tuberculosis
|
|
D055985||infections latent tuberculosis
|
|
D055985||latent tuberculoses
|
|
D055985||latent tuberculosis infection
|
|
D055985||latent tuberculosis infections
|
|
D055985||tuberculoses latent
|
|
D055985||tuberculosis infection latent
|
|
D055985||tuberculosis infections latent
|
|
D055985||tuberculosis latent
|
|
D036841||ciguatera poisoning
|
|
D036841||ciguatera
|
|
D036841||ciguatera fish poisoning
|
|
D036841||ciguatera fish poisonings
|
|
D036841||ciguatera poisonings
|
|
D036841||poisoning ciguatera
|
|
D036841||poisoning ciguatera fish
|
|
D036841||poisonings ciguatera
|
|
D036841||poisonings ciguatera fish
|
|
D012893||sleep disorders
|
|
D012893||long sleeper syndrome
|
|
D012893||long sleeper syndromes
|
|
D012893||neurogenic tachypnea sleep related
|
|
D012893||neurogenic tachypneas sleep related
|
|
D012893||phenotype short sleep
|
|
D012893||phenotypes short sleep
|
|
D012893||short sleeper syndrome
|
|
D012893||short sleeper syndromes
|
|
D012893||short sleep phenotype
|
|
D012893||short sleep phenotypes
|
|
D012893||sleep related neurogenic tachypnea
|
|
D012893||sleep related neurogenic tachypneas
|
|
D012893||subwakefullness syndrome
|
|
D012893||subwakefullness syndromes
|
|
D012893||syndrome long sleeper
|
|
D012893||syndrome short sleeper
|
|
D012893||syndromes long sleeper
|
|
D012893||syndromes short sleeper
|
|
D012893||syndromes subwakefullness
|
|
D012893||syndrome subwakefullness
|
|
D012893||tachypnea sleep related neurogenic
|
|
D012893||tachypneas sleep related neurogenic
|
|
C563087||mexican cardiomelic dysplasia
|
|
C563087||mesoaxial hexadactyly and cardiac malformation
|
|
C537931|228900||fibular hypoplasia and complex brachydactyly
|
|
C537931|228900||du pan syndrome
|
|
C535850||heart defects limb shortening
|
|
C535850||cardioskeletal syndrome kuwaiti type
|
|
C535850||congenital heart disease and skeletal malformations
|
|
C536737|300421||wittwer syndrome
|
|
C536737|300421||wtrs
|
|
607745|C564274||epilepsy benign neonatal 3
|
|
607745|C564274||bfic3
|
|
607745|C564274||bfis3
|
|
607745|C564274||bfnis
|
|
607745|C564274|601764|D020936||convulsions benign familial infantile 3
|
|
607745|C564274||convulsions benign familial neonatal 3
|
|
607745|C564274|601764|D020936||seizures benign familial infantile 3
|
|
607745|C564274|601764|D020936||seizures benign familial neonatal infantile
|
|
D009217||myosarcoma
|
|
D009217||myosarcomas
|
|
D000881||anthrax
|
|
D023521||chlamydophila infections
|
|
D023521||chlamydophila infection
|
|
D023521||infection chlamydophila
|
|
D023521||infections chlamydophila
|
|
D009214||myoma
|
|
D009214||myomas
|
|
D010202||panophthalmitis
|
|
D010202||panophthalmitides
|
|
C535849||heart defect tongue hamartoma and polysyndactyly
|
|
C535849||ostravik lindemann solberg syndrome
|
|
D009223||myotonic dystrophy
|
|
D009223||congenital myotonic dystrophies
|
|
D009223||congenital myotonic dystrophy
|
|
D009223||dystrophies congenital myotonic
|
|
D009223||dystrophies myotonic
|
|
D009223||dystrophy congenital myotonic
|
|
D009223||dystrophy myotonic
|
|
D009223||myotonia atrophica
|
|
D009223||myotonia dystrophica
|
|
D009223||myotonic dystrophies
|
|
D009223||myotonic dystrophies congenital
|
|
D009223||myotonic dystrophy congenital
|
|
D009223||steinert apos s disease
|
|
D010201||panniculitis nodular nonsuppurative
|
|
D010201||disease weber christian
|
|
D010201||nodular nonsuppurative panniculitides
|
|
D010201||nodular nonsuppurative panniculitis
|
|
D010201||nonsuppurative panniculitides nodular
|
|
D010201||nonsuppurative panniculitis nodular
|
|
D010201||panniculitides nodular nonsuppurative
|
|
D010201||weber christian disease
|
|
D009222||myotonia
|
|
D009222||myotonia percussion
|
|
D009222||myotonias
|
|
D009222||myotonias percussion
|
|
D009222||myotonic phenomenon
|
|
D009222||myotonic phenomenons
|
|
D009222||percussion myotonia
|
|
D009222||percussion myotonias
|
|
D009222||phenomenon myotonic
|
|
D009222||phenomenons myotonic
|
|
D009220||myositis
|
|
D009220||focal myositides
|
|
D009220||focal myositis
|
|
D009220||idiopathic inflammatory myopathies
|
|
D009220||idiopathic inflammatory myopathy
|
|
D009220||idiopathic inflammatory myositis
|
|
D009220||infectious myositides
|
|
D009220||infectious myositis
|
|
D009220||inflammatory muscle disease
|
|
D009220||inflammatory muscle diseases
|
|
D009220||inflammatory myopathies
|
|
D009220||inflammatory myopathies idiopathic
|
|
D009220||inflammatory myopathy
|
|
D009220||inflammatory myopathy idiopathic
|
|
D009220||muscle disease inflammatory
|
|
D009220||muscle diseases inflammatory
|
|
D009220||myopathies idiopathic inflammatory
|
|
D009220||myopathies inflammatory
|
|
D009220||myopathy idiopathic inflammatory
|
|
D009220||myopathy inflammatory
|
|
D009220||myositides
|
|
D009220||myositides focal
|
|
D009220||myositides infectious
|
|
D009220||myositides proliferative
|
|
D009220||myositis focal
|
|
D009220||myositis infectious
|
|
D009220||myositis proliferative
|
|
D009220||proliferative myositides
|
|
D009220||proliferative myositis
|
|
D011537||pruritus
|
|
D011537||itching
|
|
D011537||pruritis
|
|
D011536||prurigo
|
|
D011539||pruritus vulvae
|
|
D012868||skin abnormalities
|
|
D012868||abnormalities skin
|
|
D012868||abnormality skin
|
|
D012868||skin abnormality
|
|
D011538||pruritus ani
|
|
C537117|611554||leopard syndrome 2
|
|
D011125|175100||adenomatous polyposis coli
|
|
D011125|175100||aapc included
|
|
D011125|175100||adenomatous intestinal polyposes
|
|
D011125|175100||adenomatous intestinal polyposis
|
|
D011125|175100||adenomatous polyposes familial
|
|
D011125|175100||adenomatous polyposis coli attenuated included
|
|
D011125|175100||adenomatous polyposis coli familial
|
|
D011125|175100||adenomatous polyposis colus
|
|
D011125|175100||adenomatous polyposis familial
|
|
D011125|175100||adenomatous polyposis of the colon
|
|
D011125|175100||afap included
|
|
D011125|175100||apc
|
|
D011125|175100||brain tumor polyposis syndrome 2 included
|
|
D011125|175100||btps2 included
|
|
D011125|175100||coli adenomatous polyposis
|
|
D011125|175100||coli familial polyposis
|
|
D011125|175100||coli hereditary polyposis
|
|
D011125|175100||coli polyposis
|
|
D011125|175100||colus adenomatous polyposis
|
|
D011125|175100||colus familial polyposis
|
|
D011125|175100||colus hereditary polyposis
|
|
D011125|175100||colus polyposis
|
|
D011125|175100||familial adenomatous polyposes
|
|
D011125|175100||familial adenomatous polyposis
|
|
D011125|175100||familial adenomatous polyposis 1
|
|
D011125|175100||familial adenomatous polyposis attenuated included
|
|
D011125|175100||familial adenomatous polyposis coli
|
|
D011125|175100||familial adenomatous polyposis of the colon
|
|
D011125|175100||familial intestinal polyposes
|
|
D011125|175100||familial intestinal polyposis
|
|
D011125|175100||familial multiple polyposes
|
|
D011125|175100||familial multiple polyposi
|
|
D011125|175100||familial multiple polyposis
|
|
D011125|175100||familial multiple polyposis syndrome
|
|
D011125|175100||familial multiple polyposus
|
|
D011125|175100||familial polyposis coli
|
|
D011125|175100||familial polyposis colus
|
|
D011125|175100||familial polyposis of the colon
|
|
D011125|175100||familial polyposis syndrome
|
|
D011125|175100||familial polyposis syndromes
|
|
D011125|175100||fap1
|
|
D011125|175100||fpc
|
|
D011125|175100||gs included
|
|
D011125|175100||hereditary polyposis coli
|
|
D011125|175100||hereditary polyposis colus
|
|
D011125|175100||intestinal polyposes familial
|
|
D011125|175100||intestinal polyposis adenomatous
|
|
D011125|175100||intestinal polyposis familial
|
|
D011125|175100||multiple polyposes familial
|
|
D011125|175100||multiple polyposi familial
|
|
D011125|175100||multiple polyposis familial
|
|
D011125|175100||multiple polyposus familial
|
|
D011125|175100||myh associated polyposes
|
|
D011125|175100||myh associated polyposis
|
|
D011125|175100||polyposes familial adenomatous
|
|
D011125|175100||polyposes familial multiple
|
|
D011125|175100||polyposes myh associated
|
|
D011125|175100||polyposi familial multiple
|
|
D011125|175100||polyposis adenomatous intestinal
|
|
D011125|175100||polyposis adenomatous intestinal gardner syndrome included
|
|
D011125|175100||polyposis coli
|
|
D011125|175100||polyposis coli adenomatous
|
|
D011125|175100||polyposis coli familial
|
|
D011125|175100||polyposis coli hereditary
|
|
D011125|175100||polyposis colus
|
|
D011125|175100||polyposis colus adenomatous
|
|
D011125|175100||polyposis colus familial
|
|
D011125|175100||polyposis colus hereditary
|
|
D011125|175100||polyposis familial adenomatous
|
|
D011125|175100||polyposis familial multiple
|
|
D011125|175100||polyposis myh associated
|
|
D011125|175100||polyposis syndrome familial
|
|
D011125|175100||polyposus familial multiple
|
|
C536601|204100||amaurosis congenita of leber type 2
|
|
C536601|204100||amaurosis congenita of leber ii
|
|
C536601|204100||lca2
|
|
C536601|204100||leber congenital amaurosis 2
|
|
C536601|204100||leber congenital amaurosis type 2
|
|
C535841||hashimoto apos s encephalitis
|
|
C535841||autoimmune encephalitis
|
|
C535841||hashimoto apos s encephalopathy
|
|
C535841||steroid responsive encephalopathy associated with autoimmune thyroiditis
|
|
C535840||selig benacerraf greene syndrome
|
|
C535840||renal dysplasia megalocystis and sirenomelia
|
|
C535843||hashimoto pritzker syndrome
|
|
C535843||hashimoto pritzker disease
|
|
C535843||hashimoto pritzker histiocytosis
|
|
C535842||thyroiditis chronic
|
|
C565716|610154||deafness autosomal recessive 44
|
|
C565716|610154||dfnb44
|
|
C535844||haspeslagh fryns muelenaere syndrome
|
|
C535844||distinctive craniofacial features with pterygia and mental retardation
|
|
C535844||haspeslagh syndrome
|
|
C535844||mental retardation with pterygia shortness and distinct facial appearance
|
|
C535844||pterygia mental retardation and distinctive craniofacial features
|
|
C563095||mental retardation buenos aires type
|
|
C563095||mutchinick syndrome
|
|
C563094||mucopolysaccharidosis type viii
|
|
C563094||diferrante syndrome
|
|
C563094||glucosamine 6 sulfate sulfatase deficiency
|
|
C563094||mps viii
|
|
C535846||hay wells syndrome recessive type
|
|
C535846||ankyloblepharon ectodermal defects and cleft lip and palate and congenital adhesions between the upper and lower jaws alveolar synechiae
|
|
C537555|605013||microhydranencephaly
|
|
C537555|605013||hydranencephaly and microcephaly
|
|
C537555|605013||mhac
|
|
C535861||hemangiomatosis familial pulmonary capillary
|
|
C535861||familial pulmonary capillary hemangiomatosis
|
|
C563733|609338||carotid intimal medial thickness 1
|
|
C563733|609338||cimt1
|
|
C563733|609338||intimal medial thickness of internal carotid artery
|
|
D012876||skin diseases parasitic
|
|
D012876||disease parasitic skin
|
|
D012876||diseases parasitic skin
|
|
D012876||parasitic skin disease
|
|
D012876||parasitic skin diseases
|
|
D012876||skin disease parasitic
|
|
D036821||endometrial stromal tumors
|
|
D036821||endolymphatic stromal myoses
|
|
D036821||endolymphatic stromal myosis
|
|
D036821||endometrial stromal tumor
|
|
D036821||myoses endolymphatic stromal
|
|
D036821||myosis endolymphatic stromal
|
|
D036821||sarcoma endometrial stromal low grade
|
|
D036821||stromal myoses endolymphatic
|
|
D036821||stromal myosis endolymphatic
|
|
D036821||stromal tumor endometrial
|
|
D036821||stromal tumors endometrial
|
|
D036821||tumor endometrial stromal
|
|
D036821||tumors endometrial stromal
|
|
D012877||skin manifestations
|
|
D012877||manifestation skin
|
|
D012877||manifestations skin
|
|
D012877||skin manifestation
|
|
D009234||myxomatosis infectious
|
|
D009234||infectious myxomatoses
|
|
D009234||infectious myxomatosis
|
|
D009234||myxomatoses infectious
|
|
D010212||papilloma
|
|
D010212||papillomas
|
|
D010212||papilloma squamous cell
|
|
D010212||papillomas squamous cell
|
|
D010212||papillomatoses
|
|
D010212||papillomatosis
|
|
D010212||squamous cell papilloma
|
|
D010212||squamous cell papillomas
|
|
D012874||skin diseases infectious
|
|
D012874||disease infectious skin
|
|
D012874||diseases infectious skin
|
|
D012874||infectious skin disease
|
|
D012874||infectious skin diseases
|
|
D012874||skin disease infectious
|
|
C537255|235510||hennekam lymphangiectasia lymphedema syndrome
|
|
C537255|235510||lymphangiectasies and lymphedema hennekam type
|
|
C537255|235510||lymphatic dysplasia generalized
|
|
D012875||skin diseases metabolic
|
|
D012875||disease metabolic skin
|
|
D012875||diseases metabolic skin
|
|
D012875||metabolic skin disease
|
|
D012875||metabolic skin diseases
|
|
D012875||skin disease metabolic
|
|
C567732|613123||brugada syndrome 8
|
|
C567732|613123||brgda8
|
|
D009232||myxoma
|
|
D009232||angiomyxoma
|
|
D009232||angiomyxomas
|
|
D009232||myxomas
|
|
D010217||phlebotomus fever
|
|
D010217||pappataci fever
|
|
D010217||pappataci fevers
|
|
D010217||phlebotomus fevers
|
|
D010217||sandfly fever
|
|
D010217||sandfly fevers
|
|
C563759|609258||myopia 9
|
|
C563759|609258||myp9
|
|
D009230||myxedema
|
|
D009230||myxedemas
|
|
D011547||pseudohypoparathyroidism
|
|
D011547||phd1b
|
|
D011547||phd ib
|
|
D011547||phd ibs
|
|
D011547||pseudohypoparathyroidisms
|
|
D011547||pseudohypoparathyroidisms type ia
|
|
D011547||pseudohypoparathyroidisms type ib
|
|
D011547|D011546|145260||pseudohypoparathyroidism type ib
|
|
D011547||type ia pseudohypoparathyroidism
|
|
D011547||type ia pseudohypoparathyroidisms
|
|
D011547||type ib pseudohypoparathyroidism
|
|
D011547||type ib pseudohypoparathyroidisms
|
|
D012878||skin neoplasms
|
|
D012878||cancer of skin
|
|
D012878||cancer of the skin
|
|
D012878||cancer skin
|
|
D012878||cancers skin
|
|
D012878||neoplasm skin
|
|
D012878||neoplasms skin
|
|
D012878||skin cancer
|
|
D012878||skin cancers
|
|
D012878||skin neoplasm
|
|
C535854||heavy metal toxicity
|
|
C535854||chronic heavy metal poisoning
|
|
C535854||heavy metal poisoning
|
|
C535853||heart hand syndrome spanish type
|
|
C535853||brachydactyly and intraventricular conduction defect
|
|
C535853||upper limb malformations and congenital cardiac anomalies
|
|
D012872||skin diseases vesiculobullous
|
|
D012872||bullous dermatoses
|
|
D012872||bullous skin disease
|
|
D012872||bullous skin diseases
|
|
D012872||dermatoses bullous
|
|
D012872||dermatoses subcorneal pustular
|
|
D012872||dermatoses vesiculobullous
|
|
D012872||dermatosis subcorneal pustular
|
|
D012872||pustular dermatoses subcorneal
|
|
D012872||pustular dermatosis subcorneal
|
|
D012872||skin disease bullous
|
|
D012872||skin diseases bullous
|
|
D012872||skin diseases vesicular
|
|
D012872||skin disease vesicular
|
|
D012872||skin disease vesiculobullous
|
|
D012872||sneddon wilkinson disease
|
|
D012872||subcorneal pustular dermatoses
|
|
D012872||subcorneal pustular dermatosis
|
|
D012872||vesicular skin disease
|
|
D012872||vesicular skin diseases
|
|
D012872||vesiculobullous dermatoses
|
|
D012872||vesiculobullous skin disease
|
|
D012872||vesiculobullous skin diseases
|
|
C535856||hecht scott syndrome
|
|
C535856||limb deficiency heart malformation syndrome
|
|
D012873||skin diseases genetic
|
|
D012873||disease genetic skin
|
|
D012873||diseases genetic skin
|
|
D012873||genetic skin disease
|
|
D012873||genetic skin diseases
|
|
D012873||skin disease genetic
|
|
C535855||hydrocephalus endocardial fibroelastosis and cataracts
|
|
C535855||communicating hydrocephalus endocardial fibroelastosis efe and congenital cataracts
|
|
D052016||mucositis
|
|
D052016||mucositides
|
|
D011542||pseudarthrosis
|
|
D011542||pseudarthroses
|
|
D011542||pseudoarthroses
|
|
D011542||pseudoarthrosis
|
|
D010211||papilledema
|
|
D010211||choked disk
|
|
D010211||choked disks
|
|
D010211||decreased intraocular pressure associated papilledema
|
|
D010211||disk choked
|
|
D010211||disks choked
|
|
D010211||edema optic disk
|
|
D010211||edema optic papilla
|
|
D010211||edema retinal
|
|
D010211||edemas optic disk
|
|
D010211||edemas optic papilla
|
|
D010211||edemas retinal
|
|
D010211||increased intracranial pressure associated papilledema
|
|
D010211||nerve papillitides optic
|
|
D010211||nerve papillitis optic
|
|
D010211||optic disk edema
|
|
D010211||optic disk edemas
|
|
D010211||optic nerve papillitides
|
|
D010211||optic nerve papillitis
|
|
D010211||optic papilla edema
|
|
D010211||optic papilla edemas
|
|
D010211||optic papillitis
|
|
D010211||papilledema associated with decreased intraocular pressure
|
|
D010211||papilledema associated with increased intracranial pressure
|
|
D010211||papilledemas
|
|
D010211||papillitides
|
|
D010211||papillitides optic nerve
|
|
D010211||papillitis
|
|
D010211||papillitis optic
|
|
D010211||papillitis optic nerve
|
|
D010211||retinal edema
|
|
D010211||retinal edemas
|
|
C535858||hem dysplasia
|
|
C535858|215140||chondrodystrophy hydropic and prenatally lethal type
|
|
C535858|215140||greenberg dysplasia
|
|
C535858||greenberg skeletal dysplasia
|
|
C535858|215140||hem skeletal dysplasia
|
|
C535858|215140||hydrops ectopic calcification moth eaten skeletal dysplasia
|
|
C535858|215140||moth eaten skeletal dysplasia
|
|
D012871||skin diseases
|
|
D012871||dermatoses
|
|
D012871||dermatosis
|
|
D012871||disease skin
|
|
D012871||diseases skin
|
|
D012871||skin disease
|
|
C563067||hypospadias mental retardation syndrome
|
|
C535870||rombo syndrome
|
|
D000868||anterior compartment syndrome
|
|
D000868||anterior compartment syndromes
|
|
D000868||anterior tibial syndrome
|
|
D000868||anterior tibial syndromes
|
|
D000868||compartment syndrome anterior
|
|
D000868||compartment syndromes anterior
|
|
D000868||syndrome anterior compartment
|
|
D000868||syndrome anterior tibial
|
|
D000868||syndromes anterior compartment
|
|
D000868||syndromes anterior tibial
|
|
D000868||tibial syndrome anterior
|
|
D000868||tibial syndromes anterior
|
|
C535871||rommen mueller sybert syndrome
|
|
C535871||developmental delay growth deficiency congenital heart defect and multiple craniofacial anomalies
|
|
C535871||short stature heart defect and craniofacial anomalies
|
|
D000860||anoxia
|
|
D000860||anoxemia
|
|
D000860||anoxemias
|
|
D000860||anoxias
|
|
D000860||deficiencies oxygen
|
|
D000860||deficiency oxygen
|
|
D000860||hypoxemia
|
|
D000860||hypoxemias
|
|
D000860||hypoxia
|
|
D000860||hypoxias
|
|
D000860||oxygen deficiencies
|
|
D000860||oxygen deficiency
|
|
D009202||cardiomyopathies
|
|
D009202||cardiomyopathies primary
|
|
D009202||cardiomyopathies secondary
|
|
D009202||cardiomyopathy
|
|
D009202||cardiomyopathy primary
|
|
D009202||cardiomyopathy secondary
|
|
D009202||disease myocardial
|
|
D009202||disease primary myocardial
|
|
D009202||disease secondary myocardial
|
|
D009202||diseases myocardial
|
|
D009202||diseases primary myocardial
|
|
D009202||diseases secondary myocardial
|
|
D009202||myocardial disease
|
|
D009202||myocardial disease primary
|
|
D009202||myocardial diseases
|
|
D009202||myocardial disease secondary
|
|
D009202||myocardial diseases primary
|
|
D009202||myocardial diseases secondary
|
|
D009202||myocardiopathies
|
|
D009202||myocardiopathy
|
|
D009202||primary cardiomyopathies
|
|
D009202||primary cardiomyopathy
|
|
D009202||primary myocardial disease
|
|
D009202||primary myocardial diseases
|
|
D009202||secondary cardiomyopathies
|
|
D009202||secondary cardiomyopathy
|
|
D009202||secondary myocardial disease
|
|
D009202||secondary myocardial diseases
|
|
306000||glycogen storage disease ixa1
|
|
306000||glycogen storage disease viii formerly
|
|
306000||gsd9a1
|
|
306000||gsd9a2 included
|
|
306000||gsd ixa2 included
|
|
306000||gsd viii formerly gsd8 formerly glycogen storage disease ixa2 included
|
|
306000||liver glycogenosis x linked type i
|
|
306000||liver glycogenosis x linked type ii included
|
|
306000||xlg1
|
|
306000||xlg2 included
|
|
D011512||proteus infections
|
|
D011512||infection proteus
|
|
D011512||infections proteus
|
|
D011512||proteus infection
|
|
D012848||sinoatrial block
|
|
D012848||block sinoatrial
|
|
D012848||block sinoatrial exit
|
|
D012848||blocks sinoatrial
|
|
D012848||blocks sinoatrial exit
|
|
D012848||exit block sinoatrial
|
|
D012848||exit blocks sinoatrial
|
|
D012848||sinoatrial blocks
|
|
D012848||sinoatrial exit block
|
|
D012848||sinoatrial exit blocks
|
|
C535862||hemifacial myohyperplasia
|
|
C535862||hypertrophy and asymmetry of the facial muscles
|
|
C535865||rodrigues blindness
|
|
D054685||lymphoma primary effusion
|
|
D054685||effusion lymphoma primary
|
|
D054685||effusion lymphomas primary
|
|
D054685||lymphomas primary effusion
|
|
D054685||primary effusion lymphoma
|
|
D054685||primary effusion lymphomas
|
|
C535864||robinson miller bensimon syndrome
|
|
C535864||deafness and onychodystrophy dominant form
|
|
C535869||rokitansky aschoff sinuses of the gallbladder
|
|
C535869||intramural diverticulosis of the gallbladder
|
|
C535869||rokitansky aschoff sinuses
|
|
415000|C564030||spermatogenic failure nonobstructive y linked
|
|
415000|C564030||azf regions included
|
|
415000|C564030||azoospermia nonobstructive y linked
|
|
415000|C564030||oligospermia nonobstructive y linked
|
|
415000|C564030||oligozoospermia nonobstructive y linked
|
|
415000|C564030||spermatogenic arrest y linked
|
|
415000|C564030||spermatogenic arrest y linked azoospermia factor regions included
|
|
415000|C564030||spermatogenic failure y linked 2
|
|
415000|C564030||spgfy2
|
|
309300|C562829||megalocornea
|
|
309300|C562829||mgc1
|
|
309300|C562829||mgcn
|
|
D024821||metabolic syndrome x
|
|
D024821||cardiovascular syndrome metabolic
|
|
D024821||cardiovascular syndromes metabolic
|
|
D024821||dysmetabolic syndrome x
|
|
D024821||insulin resistance syndrome x
|
|
D024821||metabolic cardiovascular syndrome
|
|
D024821||metabolic x syndrome
|
|
D024821||reaven syndrome x
|
|
D024821||syndrome metabolic cardiovascular
|
|
D024821||syndrome metabolic x
|
|
D024821||syndrome x dysmetabolic
|
|
D024821||syndrome x insulin resistance
|
|
D024821||syndrome x metabolic
|
|
D024821||syndrome x reaven
|
|
D024821||x syndrome metabolic
|
|
D000874||anthracosilicosis
|
|
D000874||anthracosilicoses
|
|
C567867|612900||cerebral palsy spastic quadriplegic 2
|
|
C567867|612900||cpsq2
|
|
C535881||johnson munson syndrome
|
|
C535881||aphalangy of the hands and feet hemivertebrae and visceral malformations
|
|
C535881||aphalangy with hemivertebrae
|
|
C535883||johnston aarons schelley syndrome
|
|
C535883||arthrogryposis with hyperkeratosis
|
|
C535883||joint contractures hyperkeratosis and severe hypoplasia of the posterior columns
|
|
C535882||johnson neuroectodermal syndrome
|
|
C535882||aadh syndrome
|
|
C535882||alopecia anosmia deafness hypogonadism syndrome
|
|
C535882||johnson mcmillin syndrome
|
|
D009209||myofascial pain syndromes
|
|
D009209||myofascial pain syndrome
|
|
D009209||myofascial trigger point pain
|
|
D009209||pain syndrome myofascial
|
|
D009209||pain syndromes myofascial
|
|
D009209||syndrome myofascial pain
|
|
D009209||syndromes myofascial pain
|
|
D009209||trigger point pain myofascial
|
|
D011529||protozoan infections animal
|
|
D011529||animal protozoan infection
|
|
D011529||animal protozoan infections
|
|
D011529||infection animal protozoan
|
|
D011529||infections animal protozoan
|
|
D011529||protozoan infection animal
|
|
C538363|601777||retinal cone dystrophy 2
|
|
C538363|601777||cone degeneration autosomal dominant progressive
|
|
C538363|601777||cone rod dystrophy 6
|
|
C538363|601777||cord6
|
|
C538363|601777||rcd2
|
|
D009208||myoepithelioma
|
|
D009208||myoepithelial tumor
|
|
D009208||myoepithelial tumors
|
|
D009208||myoepitheliomas
|
|
D009208||tumor myoepithelial
|
|
D009208||tumors myoepithelial
|
|
D009207||myoclonus
|
|
D009207||action myoclonus
|
|
D009207||extremity myoclonus lower
|
|
D009207||extremity myoclonus upper
|
|
D009207||eyelid myoclonus
|
|
D009207||intention myoclonus
|
|
D009207||jerking myoclonic
|
|
D009207||jerk myoclonic
|
|
D009207||jerks myoclonic
|
|
D009207||lower extremity myoclonus
|
|
D009207||myoclonic jerk
|
|
D009207||myoclonic jerking
|
|
D009207||myoclonic jerks
|
|
D009207||myoclonus action
|
|
D009207||myoclonus eyelid
|
|
D009207||myoclonus intention
|
|
D009207||myoclonus lower extremity
|
|
D009207||myoclonus nocturnal
|
|
D009207||myoclonus oculopalatal
|
|
D009207||myoclonus palatal
|
|
D009207||myoclonus segmental
|
|
D009207||myoclonus simplex
|
|
D009207||myoclonus sleep
|
|
D009207||myoclonus upper extremity
|
|
D009207||nocturnal myoclonus
|
|
D009207||oculopalatal myoclonus
|
|
D009207||palatal myoclonus
|
|
D009207||polymyoclonus
|
|
D009207||segmental myoclonus
|
|
D009207||simplex myoclonus
|
|
D009207||sleep myoclonus
|
|
D009207||upper extremity myoclonus
|
|
D009205||myocarditis
|
|
D009205||carditis
|
|
D009205||myocarditides
|
|
261515||d bifunctional protein deficiency
|
|
261515||17 beta hydroxysteroid dehydrogenase iv deficiency
|
|
261515||dbp deficiency
|
|
261515||pbfe deficiency
|
|
261515|C537286||peroxisomal bifunctional enzyme deficiency
|
|
C565733|604928||wolfram syndrome 2
|
|
C565733|604928||wfs2
|
|
D009212||myoglobinuria
|
|
D009212||myoglobinurias
|
|
D012852||sinusitis
|
|
D012852||sinusitides
|
|
C566608|601885||cataract zonular pulverulent 3
|
|
C566608|601885||cae3
|
|
C566608|601885||cataract 14 multiple types
|
|
C566608|601885||ctrct14
|
|
C566608|601885||czp3
|
|
219500|C535408||gamma cystathionase deficiency
|
|
219500|C535408|C562680||cystathionase deficiency
|
|
219500|C535408||cystathioninuria
|
|
D011528||protozoan infections
|
|
D011528||histomoniases
|
|
D011528||histomoniasis
|
|
D011528||infection protozoan
|
|
D011528||infections protozoan
|
|
D011528||protozoan infection
|
|
D012857||situs inversus
|
|
D012857||inversus situs
|
|
D012857|270100||situs inversus viscerum
|
|
116860|D020786||hemangioma cavernous central nervous system
|
|
116860|D020786||angioma familial cavernous
|
|
116860|D020786||angiomas familial cavernous
|
|
116860|D020786||angiomatous malformation cavernous
|
|
116860|D020786||angiomatous malformations cavernous
|
|
116860|D020786||brain cavernous hemangioma
|
|
116860|D020786||brain cavernous hemangiomas
|
|
116860|D020786||capillary malformation cerebral
|
|
116860|D020786||capillary malformations cerebral
|
|
116860|D020786||cavernous angioma central nervous system
|
|
116860|D020786||cavernous angioma familial
|
|
116860|D020786||cavernous angiomas familial
|
|
116860|D020786||cavernous angiomatous malformation
|
|
116860|D020786||cavernous angiomatous malformations
|
|
116860|D020786||cavernous hemangioma central nervous system
|
|
116860|D020786||cavernous hemangioma cerebral
|
|
116860|D020786||cavernous hemangioma extracerebral
|
|
116860|D020786||cavernous hemangioma intracerebral
|
|
116860|D020786||cavernous hemangioma of brain
|
|
116860|D020786||cavernous hemangiomas cerebral
|
|
116860|D020786||cavernous hemangiomas extracerebral
|
|
116860|D020786||cavernous hemangiomas intracerebral
|
|
116860|D020786||cavernous malformation cerebral
|
|
116860|D020786||cavernous malformation familial
|
|
116860|D020786||cavernous malformations cerebral
|
|
116860|D020786||cavernous malformations familial
|
|
116860|D020786||cavernous malformations of cns and retina included
|
|
116860|D020786||ccm
|
|
116860|D020786||ccm1 included
|
|
116860|D020786||central nervous system cavernous hemangioma
|
|
116860|D020786||cerebral capillary malformation
|
|
116860|D020786||cerebral capillary malformations
|
|
116860|D020786||cerebral capillary malformations cerebral cavernous malformations 1 included
|
|
116860|D020786||cerebral cavernous hemangioma
|
|
116860|D020786||cerebral cavernous hemangiomas
|
|
116860|D020786||cerebral cavernous malformation
|
|
116860|D020786||cerebral cavernous malformations
|
|
116860|D020786||extracerebral cavernous hemangioma
|
|
116860|D020786||extracerebral cavernous hemangiomas
|
|
116860|D020786||familial cavernous angioma
|
|
116860|D020786||familial cavernous angiomas
|
|
116860|D020786||familial cavernous malformation
|
|
116860|D020786||familial cavernous malformations
|
|
116860|D020786||hemangioma cerebral cavernous
|
|
116860|D020786||hemangioma extracerebral cavernous
|
|
116860|D020786||hemangioma intracerebral cavernous
|
|
116860|D020786||hemangiomas cerebral cavernous
|
|
116860|D020786||hemangiomas extracerebral cavernous
|
|
116860|D020786||hemangiomas intracerebral cavernous
|
|
116860|D020786||hyperkeratotic cutaneous capillary venous malformations associated with cerebral capillary malformations included
|
|
116860|D020786||intracerebral cavernous hemangioma
|
|
116860|D020786||intracerebral cavernous hemangiomas
|
|
116860|D020786||malformation cavernous angiomatous
|
|
116860|D020786||malformation cerebral capillary
|
|
116860|D020786||malformation cerebral cavernous
|
|
116860|D020786||malformation familial cavernous
|
|
116860|D020786||malformations cavernous angiomatous
|
|
116860|D020786||malformations cerebral capillary
|
|
116860|D020786||malformations cerebral cavernous
|
|
116860|D020786||malformations familial cavernous
|
|
C535874||rowley rosenberg syndrome
|
|
C535874||growth retardation pulmonary hypertension and aminoaciduria
|
|
C535874||growth retardation pulmonary hypertension and amino aciduria
|
|
C563080||lysine malabsorption syndrome
|
|
C538416|302960||chondrodysplasia punctata 2 x linked dominant
|
|
C538416|302960||cdpx2
|
|
C538416|302960||cdpxd
|
|
C538416|302960|D002806||conradi hunermann happle syndrome
|
|
C538416|302960|D002806||conradi hunermann syndrome
|
|
C538416|302960||cpxd
|
|
C538416|302960|D002806||happle syndrome
|
|
C535876||rozin hertz goodman syndrome
|
|
C535876||camptodactyly joint contractures facial skeletal defects
|
|
C535876||camptodactyly myopia and fibrosis of the medial rectus muscle of eye
|
|
C535875||roy maroteaux kremp syndrome
|
|
C535875||metaphyseal modeling abnormality skin lesions and spastic paraplegia
|
|
C563086||ataxia microcephaly cataract syndrome
|
|
C563086||amc syndrome
|
|
C535878||rud syndrome
|
|
C535878||dwarfism ichthyosiform erythroderma mental deficiency syndrome
|
|
C535878||ichthyosis hypogonadism mental retardation epilepsy syndrome
|
|
C535878||ichthyosis male hypogonadism syndrome
|
|
C535878||ichthyosis mental retardation epilepsy hypogonadism syndrome
|
|
C535878||ichthyosis oligophrenia epilepsy syndrome
|
|
C535878||neuroichthyosis hypogonadism syndrome
|
|
C535878||rud apos s syndrome
|
|
D012851||sinus thrombosis intracranial
|
|
D012851||cranial sinus thromboses
|
|
D012851||cranial sinus thrombosis
|
|
D012851||intracranial sinus thrombophlebitides
|
|
D012851||intracranial sinus thrombophlebitis
|
|
D012851||intracranial sinus thromboses
|
|
D012851||intracranial sinus thrombosis
|
|
D012851||petrous sinus thrombophlebitides
|
|
D012851||petrous sinus thrombophlebitis
|
|
D012851||petrous sinus thromboses
|
|
D012851||petrous sinus thrombosis
|
|
D012851||sinus thrombophlebitides intracranial
|
|
D012851||sinus thrombophlebitides petrous
|
|
D012851||sinus thrombophlebitis intracranial
|
|
D012851||sinus thrombophlebitis petrous
|
|
D012851||sinus thromboses
|
|
D012851||sinus thromboses cranial
|
|
D012851||sinus thromboses intracranial
|
|
D012851||sinus thromboses petrous
|
|
D012851||sinus thrombosis
|
|
D012851||sinus thrombosis cranial
|
|
D012851||sinus thrombosis petrous
|
|
D012851||thrombophlebitides intracranial sinus
|
|
D012851||thrombophlebitides petrous sinus
|
|
D012851||thrombophlebitis intracranial sinus
|
|
D012851||thrombophlebitis petrous sinus
|
|
D012851||thromboses cranial sinus
|
|
D012851||thromboses intracranial sinus
|
|
D012851||thromboses petrous sinus
|
|
D012851||thromboses sinus
|
|
D012851||thrombosis cranial sinus
|
|
D012851||thrombosis intracranial sinus
|
|
D012851||thrombosis petrous sinus
|
|
D012851||thrombosis sinus
|
|
D012851||venous sinus thrombosis cranial
|
|
C563085||mercaptolactate cysteine disulfiduria
|
|
C563085||disulfiduria mixed
|
|
C535877||rubinstein taybi like syndrome
|
|
C535879||rudd klimek syndrome
|
|
C535879||caudal dysgenesis familial type
|
|
C535879||familial caudal dysgenesis
|
|
C563162|118600||chondrocalcinosis 2
|
|
C563162|118600||calcium gout
|
|
C563162|118600||calcium pyrophosphate arthropathy
|
|
C563162|118600||calcium pyrophosphate dihydrate deposition disease
|
|
C563162|118600||ccal2
|
|
C563162|118600||chondrocalcinosis familial articular
|
|
C563162|118600||cppdd
|
|
D040181||genetic diseases x linked
|
|
D040181||diseases x linked genetic
|
|
D040181||disease x linked genetic
|
|
D040181||genetic diseases x chromosome linked
|
|
D040181||genetic disease x linked
|
|
D040181||x linked genetic disease
|
|
D040181||x linked genetic diseases
|
|
C567763||capillary malformation of the lower lip lymphatic malformation of face and neck asymmetry of face and limbs and partial generalized overgrowth
|
|
C567763||clapo
|
|
C567763||lopez gutierrez syndrome
|
|
C566433||chromosome 16p13 3 deletion syndrome
|
|
C566433||rsts severe
|
|
C566433||rubinstein taybi syndrome severe
|
|
614021||ventricular tachycardia catecholaminergic polymorphic 3
|
|
614021||cpvt3
|
|
261100|C538556||megaloblastic anemia 1
|
|
261100|C538556||enterocyte cobalamin malabsorption
|
|
261100|C538556||enterocyte intrinsic factor receptor defect of
|
|
261100||igs
|
|
261100|C538556||imerslund grasbeck syndrome
|
|
261100|250950|C562801||mga1
|
|
261100||pernicious anemia juvenile due to selective intestinal malabsorption of vitamin b12 with proteinuria
|
|
C565103||dermoodontodysplasia
|
|
C566434||myasthenia limb girdle with tubular aggregates
|
|
C567228|612631||adenylate kinase deficiency hemolytic anemia due to
|
|
D011618||psychotic disorders
|
|
D011618||brief reactive psychoses
|
|
D011618||brief reactive psychosis
|
|
D011618||disorder psychotic
|
|
D011618||disorder schizoaffective
|
|
D011618||disorder schizophreniform
|
|
D011618||disorders psychotic
|
|
D011618||disorders schizoaffective
|
|
D011618||disorders schizophreniform
|
|
D011618||psychoses
|
|
D011618||psychoses brief reactive
|
|
D011618||psychosis
|
|
D011618||psychosis brief reactive
|
|
D011618||psychotic disorder
|
|
D011618||reactive psychoses brief
|
|
D011618||reactive psychosis brief
|
|
D011618||schizoaffective disorder
|
|
D011618||schizoaffective disorders
|
|
D011618||schizophreniform disorder
|
|
D011618||schizophreniform disorders
|
|
C565109||dermal ridges patternless
|
|
C566594|601992||friedreich ataxia 2
|
|
C566594|601992||frda2
|
|
C538141|272300||sulfite oxidase deficiency
|
|
C538141|272300||sulfocysteinuria
|
|
174900|C537702||juvenile polyposis syndrome
|
|
174900|C537702||bmpr1a related juvenile polyposis
|
|
174900|C537702||jip
|
|
174900|C537702||jps
|
|
174900|C537702||juvenile intestinal polyposis
|
|
174900|C537702||juvenile polyposis coli
|
|
174900|C537702||juvenile polyposis coli included
|
|
174900|C537702||juvenile polyposis infantile
|
|
174900|C537702||juvenile polyposis of infancy
|
|
174900|C537702||juvenile polyposis of stomach
|
|
174900|C537702||pji
|
|
174900|C537702||polyposis familial of entire gastrointestinal tract
|
|
174900|C537702||polyposis familial of entire gastrointestinal tract juvenile polyposis of stomach included
|
|
174900|C537702||polyposis juvenile intestinal
|
|
174900|C537702||smad4 related juvenile polyposis
|
|
C567074|611535||major affective disorder 5
|
|
C567074|611535||mafd5
|
|
D048909||diabetes complications
|
|
D048909||complications of diabetes mellitus
|
|
D048909||diabetes complication
|
|
D048909||diabetes mellitus complication
|
|
D048909||diabetes mellitus complications
|
|
D048909||diabetes related complication
|
|
D048909||diabetes related complications
|
|
D048909||diabetic complication
|
|
D048909||diabetic complications
|
|
C565357|605192||deafness autosomal dominant 23
|
|
C565357|605192||dfna23
|
|
C566924|611543||cavitary optic disc anomalies
|
|
C565110||dermal ridges nelson syndrome
|
|
C566436|610535||glaucoma 1 open angle m
|
|
C566436|610535||glc1m
|
|
C565115||dementia parkinsonism with non alzheimer amyloid plaques
|
|
C565117||optic atrophy deafness ophthalmoplegia and myopathy
|
|
C566448||microphthalmia cataracts and iris abnormalities
|
|
C565118||deafness craniofacial syndrome
|
|
C565112||deoxyribose 5 phosphate aldolase deficiency
|
|
C565221|609820||erythrocytosis familial 3
|
|
C565221|609820||ecyt3
|
|
C566444||giant axonal neuropathy autosomal dominant
|
|
C566445|D049310|160500||myopathy distal 3
|
|
D064146||chemotherapy induced febrile neutropenia
|
|
D064146||chemotherapy induced febrile neutropenias
|
|
D064146||drug induced febrile neutropenia
|
|
D064146||drug induced febrile neutropenias
|
|
D064146||febrile neutropenia chemotherapy induced
|
|
D064146||febrile neutropenia drug induced
|
|
D064146||febrile neutropenias chemotherapy induced
|
|
D064146||febrile neutropenias drug induced
|
|
D064146||neutropenia chemotherapy induced febrile
|
|
D064146||neutropenia drug induced febrile
|
|
D064146||neutropenias chemotherapy induced febrile
|
|
D064146||neutropenias drug induced febrile
|
|
D011629||puberty precocious
|
|
D011629||precocious puberty
|
|
D011628||puberty delayed
|
|
D011628||delayed puberty
|
|
D064147||febrile neutropenia
|
|
D064147||febrile neutropenias
|
|
D064147||neutropenia febrile
|
|
D064147||neutropenias febrile
|
|
C565119||deafness with anhidrotic ectodermal dysplasia
|
|
D009304||nasopharyngitis
|
|
D009304||nasopharyngitides
|
|
D009303||nasopharyngeal neoplasms
|
|
D009303||cancer nasopharyngeal
|
|
D009303||cancer nasopharynx
|
|
D009303||cancer of nasopharynx
|
|
D009303||cancer of the nasopharynx
|
|
D009303||cancers nasopharyngeal
|
|
D009303||cancers nasopharynx
|
|
D009303||nasopharyngeal cancer
|
|
D009303||nasopharyngeal cancers
|
|
D009303||nasopharyngeal neoplasm
|
|
D009303||nasopharynx cancer
|
|
D009303||nasopharynx cancers
|
|
D009303||nasopharynx neoplasm
|
|
D009303||nasopharynx neoplasms
|
|
D009303||neoplasm nasopharyngeal
|
|
D009303||neoplasm nasopharynx
|
|
D009303||neoplasms nasopharyngeal
|
|
D009303||neoplasms nasopharynx
|
|
D009302||nasopharyngeal diseases
|
|
D009302||disease nasopharyngeal
|
|
D009302||diseases nasopharyngeal
|
|
D009302||diseases of nasopharynx
|
|
D009302||nasopharyngeal disease
|
|
D009302||nasopharynx disease
|
|
D009302||nasopharynx diseases
|
|
D011625||pterygium
|
|
D011625||pterygiums
|
|
D029424|606963||pulmonary disease chronic obstructive
|
|
D029424|606963||airflow obstruction chronic
|
|
D029424|606963||airflow obstructions chronic
|
|
D029424|606963||chronic airflow obstruction
|
|
D029424|606963||chronic airflow obstructions
|
|
D029424|606963||chronic obstructive airway disease
|
|
D029424|606963||chronic obstructive lung disease
|
|
D029424|606963||chronic obstructive pulmonary disease
|
|
D029424|606963||coad
|
|
D029424|606963||copd
|
|
D029424|606963||copd severe early onset included
|
|
D029424|606963||pulmonary disease chronic obstructive rate of decline of lung function in included
|
|
D029424|606963||pulmonary disease chronic obstructive severe early onset included
|
|
C579754||abc disease
|
|
602032||ectodermal dysplasia 4 hair nail type
|
|
602032||ectd4
|
|
602032||ectodermal dysplasia apos pure apos hair nail type
|
|
C567781||bifid nose autosomal dominant
|
|
C535418|607831||charcot marie tooth disease type 2k
|
|
C535418|607831||charcot marie tooth disease axonal autosomal recessive type 2k
|
|
C535418|607831||charcot marie tooth disease axonal type 2k
|
|
C535418|607831||charcot marie tooth neuropathy axonal type 2k
|
|
C535418|607831||charcot marie tooth neuropathy axonal type 2k charcot marie tooth disease autosomal dominant type 2k included
|
|
C535418|607831||cmt2k
|
|
C535418|607831||cmt 2k
|
|
C565120||deafness sensorineural with peripheral neuropathy and arterial disease
|
|
D052177||kidney diseases cystic
|
|
D052177||cystic kidney
|
|
D052177||cystic kidney disease
|
|
D052177||cystic kidney diseases
|
|
D052177||cystic kidneys
|
|
D052177||cystic renal disease
|
|
D052177||cystic renal diseases
|
|
D052177||disease cystic kidney
|
|
D052177||disease cystic renal
|
|
D052177||diseases cystic kidney
|
|
D052177||diseases cystic renal
|
|
D052177||kidney cystic
|
|
D052177||kidney disease cystic
|
|
D052177||kidneys cystic
|
|
D052177||renal disease cystic
|
|
D052177||renal diseases cystic
|
|
C566574|602111||spondyloepimetaphyseal dysplasia missouri type
|
|
C566574|602111||mandp1 included
|
|
C566574|602111||semd missouri type
|
|
C566574|602111||semd missouri type metaphyseal anadysplasia 1 included
|
|
D052178||cephalopelvic disproportion
|
|
D052178||disproportion cephalopelvic
|
|
254500|D009101||multiple myeloma
|
|
254500|D009101||al amyloidosis included
|
|
254500|D009101||al included
|
|
254500|D009101||amyloidosis systemic included
|
|
254500|D009101||cell myeloma plasma
|
|
254500|D009101||cell myelomas plasma
|
|
254500|D009101||disease kahler
|
|
254500|D009101||kahler disease
|
|
254500|D009101||multiple myelomas
|
|
254500|D009101||myeloma multiple
|
|
254500|D009101||myeloma multiples
|
|
254500|D009101||myeloma plasma cell
|
|
254500|D009101||myelomas multiple
|
|
254500|D009101||myelomas plasma cell
|
|
254500|D009101||myelomatoses
|
|
254500|D009101||myelomatosis
|
|
254500|D009101||plasma cell myeloma
|
|
254500|D009101||plasma cell myelomas
|
|
D007184|308300||incontinentia pigmenti
|
|
D007184|308300||bloch siemens sulzberger syndrome
|
|
D007184|308300||bloch siemens syndrome
|
|
D007184|308300||bloch sulzberger syndrome
|
|
D007184|308300|C531716||incontinentia pigmenti familial male lethal type
|
|
D007184|308300||incontinentia pigmenti type ii formerly
|
|
D007184|308300||ip
|
|
D007184|308300||ip2 formerly
|
|
D007184|308300||syndrome bloch sulzberger
|
|
C567745||epilepsy benign neonatal 1 atypical severe
|
|
C567744||convulsions benign familial neonatal 1 and or myokymia
|
|
C567746||convulsions benign familial neonatal 1 atypical severe
|
|
C567743||epilepsy benign neonatal 1 and or myokymia
|
|
C566417||endotoxin hyporesponsiveness
|
|
C567217|612639||inflammatory bowel disease 26
|
|
C567217|612639||ibd26
|
|
145650|C564154||thyroid hormone resistance selective pituitary
|
|
145650|C564154||hyperthyroidism familial due to inappropriate thyrotropin secretion
|
|
145650|C564154||prth
|
|
602025||body mass index quantitative trait locus 9
|
|
602025||bmiq9
|
|
D018979|147421||myositis inclusion body
|
|
D018979|147421||ibm
|
|
D018979|147421||inclusion body myopathy sporadic
|
|
D018979|147421||inclusion body myositides
|
|
D018979|147421||inclusion body myositis
|
|
D018979|147421||inclusion body myositis sporadic
|
|
D018979|147421||myopathy inclusion body sporadic
|
|
D018979|147421||myositides inclusion body
|
|
D018979|147421||myositis inclusion body sporadic
|
|
D018979|147421||sporadic inclusion body myositis
|
|
C538348|609284||nemaline myopathy 1
|
|
C538348|609284||capm1 included
|
|
C538348|609284||cap myopathy 1 included
|
|
C538348|609284||cap myopathy tpm3 related
|
|
C538348|609284||nem1
|
|
C538348|609284||nemaline myopathy caused by mutation in the tropomyosin 3 gene
|
|
C567752||hemophagocytic lymphohistiocytosis familial 5
|
|
C567752||fhl5
|
|
208050|C565942||arterial tortuosity syndrome
|
|
208050|C565942||arterial tortuosity
|
|
C537688|610188||joubert syndrome 5
|
|
C537688|610188||jbts5
|
|
C566422||peroxisome biogenesis disorder complementation group 7
|
|
C566422||peroxisome biogenesis disorder complementation group b
|
|
D005166|227400||factor v deficiency
|
|
D005166|227400||deficiencies factor v
|
|
D005166|227400||deficiencies labile factor
|
|
D005166|227400||deficiency factor v
|
|
D005166|227400||deficiency labile factor
|
|
D005166|227400||disease owren
|
|
D005166|227400||disease owren apos s
|
|
D005166|227400||factor v deficiencies
|
|
D005166|227400||labile factor deficiencies
|
|
D005166|227400||labile factor deficiency
|
|
D005166|227400||owren disease
|
|
D005166|227400||owren parahemophilia
|
|
D005166|227400||owren apos s disease
|
|
D005166|227400||owrens disease
|
|
D005166|227400||parahemophilia
|
|
D005166|227400||parahemophilia owren
|
|
D005166|227400||parahemophilias
|
|
C566428||renal tubular acidosis distal autosomal recessive with late onset sensorineural hearing loss
|
|
194080|D030321||denys drash syndrome
|
|
194080|D030321|304700|C535808||dds
|
|
194080|D030321||drash syndrome
|
|
194080|D030321||nephropathy wilms tumor and genital anomalies
|
|
194080|D030321||pseudohermaphroditism nephron disorder and wilms apos tumor
|
|
194080|D030321||syndrome denys drash
|
|
194080|D030321||syndrome drash
|
|
194080|D030321||wilms tumor and pseudohermaphroditism
|
|
194080|D030321||wilms tumor and pseudo or true hermaphroditism
|
|
C567759||achromatopsia 5
|
|
D011602||psychophysiologic disorders
|
|
D011602||psychophysiological disorder
|
|
D011602||psychophysiological disorders
|
|
D011602||psychophysiologic disorder
|
|
D011602||psychosomatic disorder
|
|
D011602||psychosomatic disorders
|
|
D011605||psychoses substance induced
|
|
D011605||drug psychoses
|
|
D011605||psychoses drug
|
|
D011605||psychoses toxic
|
|
D011605||substance induced psychoses
|
|
D011605||toxic psychoses
|
|
D011604||psychoses alcoholic
|
|
D011604||alcoholic psychoses
|
|
C567683|613252||cardiomyopathy dilated 1ee
|
|
C567683|613252||cmd1ee
|
|
C564835|268100||enhanced s cone syndrome
|
|
C564835|268100||escs
|
|
C564835|268100||favre hyaloideoretinal degeneration
|
|
C564835|268100||favre hyaloideoretinal degeneration included
|
|
C564835|268100||goldmann favre syndrome
|
|
C564835|268100||goldmann favre syndrome included
|
|
C564835|268100||retinoschisis with early hemeralopia
|
|
C564835|268100||retinoschisis with early hemeralopia included
|
|
C536430|216360||coach syndrome
|
|
C536430|216360||cerebellar vermis hypo aplasia oligophrenia ataxia congenital coloboma and hepatic fibrosis
|
|
C536430|216360||cerebellar vermis hypo aplasia oligophrenia congenital ataxia ocular coloboma and hepatic fibrosis
|
|
C536430|216360||joubert syndrome with congenital hepatic fibrosis
|
|
D048949||labor pain
|
|
D048949||obstetric pain
|
|
D048949||pain labor
|
|
D048949||pain obstetric
|
|
C567727||walker warburg syndrome fktn related
|
|
C567727||muscular dystrophy due to defective glycosylation of dystroglycan 4a
|
|
C543759||juvenile onset scleroderma
|
|
C543759||juvenile scleroderma
|
|
C543758||juvenile linear scleroderma
|
|
D012909||snake bites
|
|
D012909||bite snake
|
|
D012909||bites snake
|
|
D012909||envenomation snake
|
|
D012909||envenomations snake
|
|
D012909||snakebite
|
|
D012909||snake bite
|
|
D012909||snakebites
|
|
D012909||snake envenomation
|
|
D012909||snake envenomations
|
|
C531767||edema of the optic disc
|
|
C531768||colangite esclerosante porracoccidiodomicose
|
|
605990||nephrolithiasis uric acid susceptibility to
|
|
605990||uan
|
|
605990||urolithiasis uric acid susceptibility to
|
|
C537849|310600||norrie disease
|
|
C537849|310600||anderson warburg syndrome
|
|
C537849|310600||atrophia bulborum hereditaria
|
|
C537849|310600||congenital progressive oculo acoustico cerebral degeneration
|
|
C537849|310600||episkopi blindness
|
|
C537849|310600||fetal iritis syndrome
|
|
C537849|310600||nd
|
|
C537849|310600||norrie apos s disease
|
|
C537849|310600||norrie syndrome
|
|
C537849|310600||norrie warburg syndrome
|
|
C537849|310600||oligophrenia microphthalmus
|
|
C537849|310600||pseudoglioma
|
|
C537849|310600||pseudoglioma congenita
|
|
C537849|310600||whitnall norman syndrome
|
|
144150|C538377||hyperkeratosis lenticularis perstans
|
|
144150|C538377||flegel disease
|
|
144150|C538377||flegel apos s disease
|
|
144150|C538377||hlp
|
|
144150|C538377||hyperkeratosis lenticularis perstans of flegel
|
|
C531760||oro facial gangrene
|
|
C531760||noma neonatorum
|
|
C531760||oral gangrene
|
|
C531760||oro facial noma
|
|
C531762||alkaptonuric ochronosis
|
|
C531762||exogenous ochronosis
|
|
C531762||ocular ochronosis
|
|
C531762||pseudo ochronosis
|
|
C565192|610717||neutral lipid storage disease with myopathy
|
|
C565192|610717||neutral lipid storage disease without ichthyosis
|
|
C565192|610717||nlsdm
|
|
C535302|302801||charcot marie tooth disease x linked recessive 2
|
|
C535302|302801||charcot marie tooth neuropathy x linked recessive 2
|
|
C535302|302801||cmtx2
|
|
C531766||inflammation of the whole uveal tract
|
|
C566402||methylmalonate semialdehyde dehydrogenase deficiency
|
|
C566402||mmsdh deficiency
|
|
D015192||infratentorial neoplasms
|
|
D015192||benign infratentorial neoplasm
|
|
D015192||benign infratentorial neoplasms
|
|
D015192||cancer infratentorial
|
|
D015192||cancers infratentorial
|
|
D015192||infratentorial cancer
|
|
D015192||infratentorial cancers
|
|
D015192||infratentorial neoplasm
|
|
D015192||infratentorial neoplasm benign
|
|
D015192||infratentorial neoplasm malignant
|
|
D015192||infratentorial neoplasms benign
|
|
D015192||infratentorial neoplasms malignant
|
|
D015192||infratentorial tumor
|
|
D015192||infratentorial tumors
|
|
D015192||malignant infratentorial neoplasm
|
|
D015192||malignant infratentorial neoplasms
|
|
D015192||neoplasm benign infratentorial
|
|
D015192||neoplasm infratentorial
|
|
D015192||neoplasm malignant infratentorial
|
|
D015192||neoplasm posterior fossa
|
|
D015192||neoplasms benign infratentorial
|
|
D015192||neoplasms infratentorial
|
|
D015192||neoplasms malignant infratentorial
|
|
D015192||neoplasms posterior fossa
|
|
D015192||posterior fossa neoplasm
|
|
D015192||posterior fossa neoplasms
|
|
D015192||posterior fossa tumor
|
|
D015192||posterior fossa tumors
|
|
D015192||tumor infratentorial
|
|
D015192||tumor posterior fossa
|
|
D015192||tumors infratentorial
|
|
D015192||tumors posterior fossa
|
|
C565712|610163||immunodeficiency due to defect in cd3 zeta
|
|
C566405||peroxisome biogenesis disorder complementation group 12
|
|
C536725|135500||zimmerman laband syndrome
|
|
C536725|135500||fibromatosis gingival with abnormal fingers fingernails nose and ears and splenomegaly
|
|
C536725|135500||laband syndrome
|
|
C536725|135500||zimmermann laband syndrome
|
|
C536725|135500||zls
|
|
C567731||hydrops fetalis nonimmune with gracile bones and dysmorphic features
|
|
C567340|612350||spondylocheirodysplasia ehlers danlos syndrome like
|
|
C567340|612350||scdeds
|
|
C567340|612350||scd eds
|
|
C566406||peroxisome biogenesis disorder complementation group g
|
|
C565081|127100||dwarfism levi type
|
|
C565081|127100||snub nosed type of dwarfism
|
|
C566408||dislocated elbows bowed tibias scoliosis deafness cataract microcephaly and mental retardation
|
|
C566409||spastic paraplegia optic atrophy microcephaly and xy sex reversal
|
|
255500|C567606||myopia 18 autosomal recessive
|
|
255500|C567606||myopia 18
|
|
255500|C567606||myp18
|
|
D012913||snoring
|
|
D012913||snorings
|
|
611152|C567000||alzheimer disease 13
|
|
611152|C567000||ad13
|
|
D012912||sneezing
|
|
D012912||sneezings
|
|
D059607||polydipsia psychogenic
|
|
D059607||polydipsia primary
|
|
D059607||polydipsias primary
|
|
D059607||polydipsias psychogenic
|
|
D059607||primary polydipsia
|
|
D059607||primary polydipsias
|
|
D059607||psychogenic polydipsia
|
|
D059607||psychogenic polydipsias
|
|
D059606||polydipsia
|
|
D059606||polydipsias
|
|
D059608||laryngocele
|
|
D059608||laryngoceles
|
|
C531774||familial pars planitis
|
|
C564502|300504||mental retardation x linked 52
|
|
C564502|300504||mrx52
|
|
C531777||islet cell tumor syndrome
|
|
C531777||bilateral pheochromocytoma and islet cell adenoma of the pancreas
|
|
C531777||chromaffinoma
|
|
C531777||familial islet cell tumors
|
|
C531777||familial pheochromocytoma
|
|
D015163||superinfection
|
|
D015163||microbial superinvasion
|
|
D015163||microbial superinvasions
|
|
D015163||superinfections
|
|
D015163||superinvasion microbial
|
|
D015163||superinvasions microbial
|
|
D015161||dementia multi infarct
|
|
D015161||dementia lacunar
|
|
D015161||dementia multiinfarct
|
|
D015161||dementia multi infarcts
|
|
D015161||dementias lacunar
|
|
D015161||dementias multiinfarct
|
|
D015161||dementias multi infarct
|
|
D015161||lacunar dementia
|
|
D015161||lacunar dementias
|
|
D015161||multiinfarct dementia
|
|
D015161||multi infarct dementia
|
|
D015161||multiinfarct dementias
|
|
D015161||multi infarct dementias
|
|
D015161||multi infarcts dementia
|
|
D016491||peripheral vascular diseases
|
|
D016491||angiopathies peripheral
|
|
D016491||angiopathy peripheral
|
|
D016491||disease peripheral vascular
|
|
D016491||diseases peripheral vascular
|
|
D016491||peripheral angiopathies
|
|
D016491||peripheral angiopathy
|
|
D016491||peripheral vascular disease
|
|
D016491||vascular disease peripheral
|
|
D016491||vascular diseases peripheral
|
|
D006526|609532||hepatitis c
|
|
D006526|609532||hcv resistance to included
|
|
D006526|609532||hcv susceptibility to hepatitis c virus resistance to included
|
|
D006526|609532||hepatitis c virus infection response to therapy of included
|
|
D006526|609532||hepatitis c virus susceptibility to
|
|
D006526|609532||hepatitis viral non a non b parenterally transmitted
|
|
D006526|609532||parenterally transmitted non a non b hepatitis
|
|
D006526|609532||pt nanbh
|
|
C535743|608799||congenital disorder of glycosylation type 1e
|
|
C535743|608799||cdg1e
|
|
C535743|608799||cdgie
|
|
C535743|608799||cdg ie
|
|
C535743|608799||congenital disorder of glycosylation type ie
|
|
D060605||hyalohyphomycosis
|
|
D060605||cutaneous hyalohyphomycoses
|
|
D060605||cutaneous hyalohyphomycosis
|
|
D060605||disseminated hyalohyphomycoses
|
|
D060605||disseminated hyalohyphomycosis
|
|
D060605||hyalohyphomycoses
|
|
D060605||hyalohyphomycoses cutaneous
|
|
D060605||hyalohyphomycoses disseminated
|
|
D060605||hyalohyphomycoses invasive
|
|
D060605||hyalohyphomycoses pulmonary
|
|
D060605||hyalohyphomycoses splenic
|
|
D060605||hyalohyphomycoses subcutaneous
|
|
D060605||hyalohyphomycosis cutaneous
|
|
D060605||hyalohyphomycosis disseminated
|
|
D060605||hyalohyphomycosis invasive
|
|
D060605||hyalohyphomycosis pulmonary
|
|
D060605||hyalohyphomycosis splenic
|
|
D060605||hyalohyphomycosis subcutaneous
|
|
D060605||invasive hyalohyphomycoses
|
|
D060605||invasive hyalohyphomycosis
|
|
D060605||pulmonary hyalohyphomycoses
|
|
D060605||pulmonary hyalohyphomycosis
|
|
D060605||splenic hyalohyphomycoses
|
|
D060605||splenic hyalohyphomycosis
|
|
D060605||subcutaneous hyalohyphomycoses
|
|
D060605||subcutaneous hyalohyphomycosis
|
|
D048968||morning sickness
|
|
D048968||sickness morning
|
|
C567705||chromosome 17p13 3 duplication syndrome
|
|
C567704|613216||csnb1c
|
|
C567704|613216||night blindness congenital stationary type 1c
|
|
C565158|121400||cornea plana 1
|
|
C565158|121400||cna1
|
|
C567504|611884||ciliary dyskinesia primary 7
|
|
C567504|611884||cild7
|
|
C567504|611884||ciliary dyskinesia primary 7 with or without situs inversus
|
|
136760||frontonasal dysplasia 1
|
|
136760||fnd
|
|
136760||fnd1
|
|
136760||fnm
|
|
D016489||head injuries closed
|
|
D016489||blunt head injuries
|
|
D016489||blunt head injury
|
|
D016489||closed head injuries
|
|
D016489||closed head injury
|
|
D016489||closed head trauma
|
|
D016489||closed head traumas
|
|
D016489||head injuries blunt
|
|
D016489||head injuries nonpenetrating
|
|
D016489||head injury blunt
|
|
D016489||head injury closed
|
|
D016489||head injury nonpenetrating
|
|
D016489||head trauma closed
|
|
D016489||head traumas closed
|
|
D016489||injuries closed head
|
|
D016489||nonpenetrating head injuries
|
|
D016489||nonpenetrating head injury
|
|
D016489||trauma closed head
|
|
D016489||traumas closed head
|
|
C531782||endemic treponematosis caused by treponema carateum
|
|
D015155||esophageal spasm diffuse
|
|
D015155||diffuse esophageal spasm
|
|
D015155||diffuse esophageal spasms
|
|
D015155||esophageal spasm
|
|
D015155||esophageal spasms
|
|
D015155||esophageal spasms diffuse
|
|
D015155||spasm diffuse esophageal
|
|
D015155||spasm esophageal
|
|
D015155||spasms diffuse esophageal
|
|
D015155||spasms esophageal
|
|
D014901|610379||west nile fever
|
|
D014901|610379||encephalitis west nile fever
|
|
D014901|610379||west nile fever encephalitis
|
|
D014901|610379||west nile fever meningitis
|
|
D014901|610379||west nile fever meningoencephalitis
|
|
D014901|610379||west nile fever myelitis
|
|
D014901|610379||west nile virus susceptibility to
|
|
D014901|610379||wnv susceptibility to
|
|
C531783||hip socket neuropathy
|
|
C531783||deep gluteal syndrome
|
|
C531783||pseudosciatica
|
|
C531783||wallet sciatica
|
|
D015154||esophageal motility disorders
|
|
D015154||disorder esophageal motility
|
|
D015154||disorders esophageal motility
|
|
D015154||dysmotilities esophageal
|
|
D015154||dysmotility esophageal
|
|
D015154||esophageal dysmotilities
|
|
D015154||esophageal dysmotility
|
|
D015154||esophageal motility disorder
|
|
D015154||esophagus nutcracker
|
|
D015154||motility disorder esophageal
|
|
D015154||motility disorders esophageal
|
|
D015154||nutcracker esophagus
|
|
C531784||familial pityriasis rubra pilaris
|
|
C531784||pityriasis rubra pilaris familial type
|
|
613024|D008224||lymphoma follicular
|
|
613024|D008224||brill symmers disease
|
|
613024|D008224||disease brill symmers
|
|
613024|D008224||fl1
|
|
613024|D008224||follicular large cell lymphoma
|
|
613024|D008224||follicular large cell lymphomas
|
|
613024|D008224||follicular lymphoma
|
|
613024|D008224||follicular lymphoma giant
|
|
613024|D008224||follicular lymphoma grade 1
|
|
613024|D008224||follicular lymphoma grade 2
|
|
613024|D008224||follicular lymphoma grade 3
|
|
613024|D008224||follicular lymphomas
|
|
613024|D008224||follicular lymphomas giant
|
|
613024|D008224||follicular lymphoma susceptibility to 1
|
|
613024|D008224||follicular mixed cell lymphoma
|
|
613024|D008224||follicular mixed cell lymphomas
|
|
613024|D008224||giant follicular lymphoma
|
|
613024|D008224||giant follicular lymphomas
|
|
613024|D008224||histiocytic lymphoma nodular
|
|
613024|D008224||histiocytic lymphomas nodular
|
|
613024|D008224||large cell lymphoma follicular
|
|
613024|D008224||large cell lymphomas follicular
|
|
613024|D008224||large lymphoid lymphoma nodular
|
|
613024|D008224||lymphocytic lymphoma nodular poorly differentiated
|
|
613024|D008224||lymphoma follicular grade 1
|
|
613024|D008224||lymphoma follicular grade 2
|
|
613024|D008224||lymphoma follicular grade 3
|
|
613024|D008224||lymphoma follicular large cell
|
|
613024|D008224||lymphoma follicular mixed cell
|
|
613024|D008224||lymphoma follicular mixed lymphocytic histiocytic
|
|
613024|D008224||lymphoma follicular mixed small and large lymphoid
|
|
613024|D008224||lymphoma follicular small and large cleaved cell
|
|
613024|D008224||lymphoma giant follicular
|
|
613024|D008224||lymphoma histiocytic nodular
|
|
613024|D008224||lymphoma large cell follicular
|
|
613024|D008224||lymphoma large lymphoid nodular
|
|
613024|D008224||lymphoma lymphocytic nodular poorly differentiated
|
|
613024|D008224||lymphoma mixed cell follicular
|
|
613024|D008224||lymphoma nodular
|
|
613024|D008224||lymphoma nodular histiocytic
|
|
613024|D008224||lymphoma nodular large follicular center cell
|
|
613024|D008224||lymphoma nodular mixed lymphocytic histiocytic
|
|
613024|D008224||lymphoma nodular mixed small and large cell
|
|
613024|D008224||lymphomas follicular
|
|
613024|D008224||lymphomas follicular large cell
|
|
613024|D008224||lymphomas follicular mixed cell
|
|
613024|D008224||lymphomas giant follicular
|
|
613024|D008224||lymphoma small cleaved cell follicular
|
|
613024|D008224||lymphoma small follicular center cell
|
|
613024|D008224||lymphoma small lymphoid follicular
|
|
613024|D008224||lymphomas nodular
|
|
613024|D008224||lymphomas nodular histiocytic
|
|
613024|D008224||mixed cell lymphoma follicular
|
|
613024|D008224||mixed cell lymphomas follicular
|
|
613024|D008224||nodular histiocytic lymphoma
|
|
613024|D008224||nodular histiocytic lymphomas
|
|
613024|D008224||nodular large follicular center cell lymphoma
|
|
613024|D008224||nodular lymphoma
|
|
613024|D008224||nodular lymphomas
|
|
613024|D008224||small cleaved cell lymphoma follicular
|
|
613024|D008224||small follicular center cell lymphoma
|
|
C563352|601318||diabetes mellitus insulin dependent 13
|
|
C563352|601318||iddm13
|
|
C563352|601318||insulin dependent diabetes mellitus 13
|
|
C567712||retinitis pigmentosa concentric
|
|
C535343|605387||cataract posterior polar 3
|
|
C535343|605387||cataract 31 multiple types
|
|
C535343|605387||cpp3
|
|
C535343|605387||ctpp3
|
|
C535343|605387||ctrct31
|
|
C566987|611182||congenital disorder of glycosylation type iih
|
|
C566987|611182||cdg2h
|
|
C566987|611182||cdg iih
|
|
C566987|611182||cdgiih
|
|
C566987|611182||cdg iiih
|
|
C563240|606215||atrioventricular canal defect
|
|
C563240|606215|C562831||atrioventricular septal defect
|
|
C563240|606215||avcd
|
|
C563240|606215||avc defect
|
|
C563240|606215||avsd
|
|
C563240|606215||avsd1 included
|
|
C563240|606215||endocardial cushion defect ecd atrioventricular septal defect susceptibility to 1 included
|
|
D015174||epidural neoplasms
|
|
D015174||epidural neoplasm
|
|
D015174||epidural neoplasm malignant
|
|
D015174||epidural neoplasms malignant
|
|
D015174||epidural tumor
|
|
D015174||epidural tumors
|
|
D015174||malignant epidural neoplasm
|
|
D015174||malignant epidural neoplasms
|
|
D015174||neoplasms epidural
|
|
D015173||supratentorial neoplasms
|
|
D015173||benign supratentorial neoplasm
|
|
D015173||benign supratentorial neoplasms
|
|
D015173||cancers supratentorial
|
|
D015173||cancer supratentorial
|
|
D015173||malignant supratentorial neoplasm
|
|
D015173||malignant supratentorial neoplasms
|
|
D015173||neoplasm benign supratentorial
|
|
D015173||neoplasm malignant supratentorial
|
|
D015173||neoplasm primary supratentorial
|
|
D015173||neoplasms benign supratentorial
|
|
D015173||neoplasms malignant supratentorial
|
|
D015173||neoplasms primary supratentorial
|
|
D015173||neoplasms supratentorial
|
|
D015173||neoplasm supratentorial
|
|
D015173||primary supratentorial neoplasm
|
|
D015173||primary supratentorial neoplasms
|
|
D015173||supratentorial cancer
|
|
D015173||supratentorial cancers
|
|
D015173||supratentorial neoplasm
|
|
D015173||supratentorial neoplasm benign
|
|
D015173||supratentorial neoplasm malignant
|
|
D015173||supratentorial neoplasm primary
|
|
D015173||supratentorial neoplasms benign
|
|
D015173||supratentorial neoplasms malignant
|
|
D015173||supratentorial neoplasms primary
|
|
D015173||supratentorial tumor
|
|
D015173||supratentorial tumors
|
|
D015173||tumors supratentorial
|
|
D015173||tumor supratentorial
|
|
180020|C566719||retinal cone dystrophy 1
|
|
180020|C566719||cone dystrophy autosomal dominant
|
|
180020|C566719||rcd1
|
|
180020|C566719||retinal cone degeneration
|
|
C563832|608930||myasthenic syndrome congenital fast channel
|
|
C563832|608930||fccms
|
|
C562419|110100||blepharophimosis ptosis and epicanthus inversus
|
|
C562419|110100||blepharophimosis ptosis and epicanthus inversus syndrome
|
|
C562419|110100||blepharophimosis ptosis and epicanthus inversus type i
|
|
C562419|110100||blepharophimosis ptosis and epicanthus inversus type ii
|
|
C562419|110100||blepharophimosis syndrome
|
|
C562419|110100||bpes
|
|
C562419|110100||bpes type i autosomal recessive included
|
|
C562419|110100||bpes type ii included
|
|
C562419|110100||bpes type i included
|
|
C562419|110100||bpes with duane retraction syndrome included
|
|
C562419|110100||bpes without ovarian failure included
|
|
C562419|110100||bpes with ovarian failure included
|
|
C537943|609528||cerebral dysgenesis neuropathy ichthyosis and palmoplantar keratoderma syndrome
|
|
C537943|609528||cednik syndrome
|
|
C567717||chromosome 5p13 duplication syndrome
|
|
C567815|613011||lymphoproliferative syndrome ebv associated autosomal 1
|
|
C567815|613011||lpfs1
|
|
C567815|613011||lymphoproliferative syndrome 1
|
|
D003193||compulsive personality disorder
|
|
D003193||compulsive personalities
|
|
D003193||compulsive personality
|
|
D003193||compulsive personality disorders
|
|
D003193||disorder compulsive personality
|
|
D003193||disorders compulsive personality
|
|
D003193||obsessive compulsive personalities
|
|
D003193||obsessive compulsive personality
|
|
D003193||personalities compulsive
|
|
D003193||personalities obsessive compulsive
|
|
D003193||personality compulsive
|
|
D003193||personality disorder compulsive
|
|
D003193||personality disorders compulsive
|
|
D003193||personality obsessive compulsive
|
|
D015168||lightning injuries
|
|
D015168||injuries lightning
|
|
D015168||injury lightning
|
|
D015168||lightning injury
|
|
D015168||lightning stroke
|
|
D015168||lightning strokes
|
|
D015168||stroke lightning
|
|
D015168||strokes lightning
|
|
C531795||idiopathic intracranial hypertension with papilledema
|
|
C535547|156232||kantaputra gorlin syndrome
|
|
C535547|156232||mdk
|
|
C535547|156232||mesomelic dysplasia kantaputra type
|
|
C535547|156232||mesomelic dysplasia thai type
|
|
C535547|156232||mesomelic dysplasia with ankle carpal and tarsal synostosis
|
|
C535547|156232||mmdk
|
|
600002|C564010||eiken skeletal dysplasia
|
|
600002|C564010||bone modeling defect of hands and feet
|
|
C537883|268210||rhabdomyosarcoma 1
|
|
C537883|268210||rhabdomyosarcoma chromosomal region
|
|
C537883|268210||rhabdomyosarcoma embryonal 1
|
|
C537883|268210||rms1
|
|
C537883|268210||rmscr
|
|
C537883|268210||rmse1
|
|
122000|C562745||corneal dystrophy posterior polymorphous 1
|
|
122000|C562745||corneal dystrophy hereditary polymorphous posterior
|
|
122000|C562745||posterior polymorphous corneal dystrophy
|
|
122000|C562745||ppcd
|
|
122000|C562745||ppcd1
|
|
D016470||bacteremia
|
|
D016470||bacteremias
|
|
D016472||motor neuron disease
|
|
D016472||anterior horn cell disease
|
|
D016472||familial motor neuron disease
|
|
D016472||lateral scleroses
|
|
D016472||lateral scleroses primary
|
|
D016472||lateral sclerosis
|
|
D016472||lateral sclerosis primary
|
|
D016472||lower motor neuron disease
|
|
D016472||motor neuron disease familial
|
|
D016472||motor neuron disease lower
|
|
D016472||motor neuron diseases
|
|
D016472||motor neuron disease secondary
|
|
D016472||motor neuron disease upper
|
|
D016472||motor system disease
|
|
D016472||motor system diseases
|
|
D016472||neuron disease motor
|
|
D016472||neuron diseases motor
|
|
D016472||primary lateral scleroses
|
|
D016472||primary lateral sclerosis
|
|
D016472||scleroses lateral
|
|
D016472||scleroses primary lateral
|
|
D016472||sclerosis lateral
|
|
D016472||sclerosis primary lateral
|
|
D016472||secondary motor neuron disease
|
|
D016472||upper motor neuron disease
|
|
129600||ectopia lentis 1 isolated autosomal dominant
|
|
129600||ectol1
|
|
D015140||dementia vascular
|
|
D015140||acute onset vascular dementia
|
|
D015140||arteriosclerotic dementia
|
|
D015140||arteriosclerotic dementias
|
|
D015140||arteriosclerotic encephalopathies subcortical
|
|
D015140||arteriosclerotic encephalopathy subcortical
|
|
D015140||binswanger disease
|
|
D015140||binswanger encephalopathy
|
|
D015140||binswanger apos s disease
|
|
D015140||binswangers disease
|
|
D015140||binswanger apos s encephalopathy
|
|
D015140||chronic progressive subcortical encephalopathy
|
|
D015140||dementia arteriosclerotic
|
|
D015140||dementias arteriosclerotic
|
|
D015140||dementias subcortical vascular
|
|
D015140||dementia subcortical vascular
|
|
D015140||dementias vascular
|
|
D015140||disease binswanger
|
|
D015140||disease binswanger apos s
|
|
D015140||encephalopathies subcortical arteriosclerotic
|
|
D015140||encephalopathy binswanger
|
|
D015140||encephalopathy binswangers
|
|
D015140||encephalopathy binswanger apos s
|
|
D015140||encephalopathy chronic progressive subcortical
|
|
D015140||encephalopathy subcortical arteriosclerotic
|
|
D015140||encephalopathy subcortical chronic progressive
|
|
D015140||leukoencephalopathies subcortical
|
|
D015140||leukoencephalopathy subcortical
|
|
D015140||subcortical arteriosclerotic encephalopathies
|
|
D015140||subcortical arteriosclerotic encephalopathy
|
|
D015140||subcortical encephalopathy chronic progressive
|
|
D015140||subcortical leukoencephalopathies
|
|
D015140||subcortical leukoencephalopathy
|
|
D015140||subcortical vascular dementia
|
|
D015140||subcortical vascular dementias
|
|
D015140||vascular dementia
|
|
D015140||vascular dementia acute onset
|
|
D015140||vascular dementias
|
|
D015140||vascular dementias subcortical
|
|
D015140||vascular dementia subcortical
|
|
D004489||edema cardiac
|
|
D004489||cardiac edema
|
|
D004489||cardiac edemas
|
|
D004489||edemas cardiac
|
|
D004488||edema disease of swine
|
|
D004488||swine edema disease
|
|
D004488||swine edema diseases
|
|
184450|D013342||stuttering familial persistent 1
|
|
184450|D013342||stammering
|
|
184450||stut1
|
|
D004485||eczema
|
|
D004485||dermatitides eczematous
|
|
D004485||dermatitis eczematous
|
|
D004485||eczemas
|
|
D004485||eczematous dermatitides
|
|
D004485||eczematous dermatitis
|
|
D004487||edema
|
|
D004487||anasarca
|
|
D004487||dropsy
|
|
D004487||hydrops
|
|
D003161||compartment syndromes
|
|
D003161||compartment syndrome
|
|
D003161||syndrome compartment
|
|
D003161||syndromes compartment
|
|
D050030|170390||andersen syndrome
|
|
D050030|170390||andersen cardiodysrhythmic periodic paralysis
|
|
D050030|170390||andersen cardiodysrythmic periodic paralysis
|
|
D050030|170390||andersen tawil syndrome
|
|
D050030|170390||long qt syndrome 7
|
|
D050030|170390||lqt7
|
|
D050030|170390||periodic paralysis potassium sensitive cardiodysrhythmic type
|
|
D050030|170390||potassium sensitive periodic paralysis ventricular ectopy and dysmorphic features
|
|
D050030|170390||syndrome andersen
|
|
D050030|170390||syndrome andersen tawil
|
|
C531728||canicola fever
|
|
C531728||cane cutter fever
|
|
C531728||mud fever
|
|
C531728||rice field fever
|
|
C531728||stuttgart disease
|
|
C531728||swineherd apos s disease
|
|
C531729||autoimmune limbic encephalitis
|
|
D016469||fungemia
|
|
D016469||fungemias
|
|
D016463||sweet syndrome
|
|
D016463||acute febrile neutrophilic dermatosis
|
|
D016463||dermatosis neutrophilic febrile acute
|
|
D016463||disease gomm button
|
|
D016463||gomm button disease
|
|
D016463||neutrophilic dermatosis acute febrile
|
|
D016463||sweet apos s syndrome
|
|
D016463||sweets syndrome
|
|
D016463||syndrome sweet
|
|
D016463||syndrome sweet apos s
|
|
D016464||lysosomal storage diseases
|
|
D016464||disease lysosomal storage
|
|
D016464||diseases lysosomal storage
|
|
D016464||disorder lysosomal enzyme
|
|
D016464||disorders lysosomal enzyme
|
|
D016464||enzyme disorder lysosomal
|
|
D016464||enzyme disorders lysosomal
|
|
D016464||lysosomal enzyme disorder
|
|
D016464||lysosomal enzyme disorders
|
|
D016464||lysosomal storage disease
|
|
C531720||noninflammatory corneal thinning
|
|
D016483||lymphoma aids related
|
|
D016483||aids associated lymphoma
|
|
D016483||aids associated lymphomas
|
|
D016483||aids related lymphoma
|
|
D016483||aids related lymphomas
|
|
D016483||hiv related lymphoma
|
|
D016483||hiv related lymphomas
|
|
D016483||lymphoma aids associated
|
|
D016483||lymphoma hiv related
|
|
D016483||lymphomas aids associated
|
|
D016483||lymphomas aids related
|
|
D016483||lymphomas hiv related
|
|
205700|D000744||anemia hemolytic autoimmune
|
|
205700|D000744||acquired autoimmune hemolytic anemia
|
|
205700|D000744||agglutinin disease cold
|
|
205700|D000744||agglutinin diseases cold
|
|
205700|D000744||anemia autoimmune hemolytic
|
|
205700|D000744||anemia hemolytic cold antibody
|
|
205700|D000744||anemia hemolytic idiopathic acquired
|
|
205700|D000744||anemias autoimmune hemolytic
|
|
205700|D000744||autoimmune hemolytic anemia
|
|
205700|D000744||autoimmune hemolytic anemias
|
|
205700|D000744||cold agglutinin disease
|
|
205700|D000744||cold agglutinin diseases
|
|
205700|D000744||cold antibody disease
|
|
205700|D000744||cold antibody diseases
|
|
205700|D000744||cold antibody hemolytic anemia
|
|
205700|D000744||disease cold agglutinin
|
|
205700|D000744||disease cold antibody
|
|
205700|D000744||diseases cold agglutinin
|
|
205700|D000744||diseases cold antibody
|
|
205700|D000744||hemolytic anemia autoimmune
|
|
205700|D000744||hemolytic anemias autoimmune
|
|
205700|D000744||idiopathic autoimmune hemolytic anemia
|
|
611812||46 xx sex reversal with dysgenesis of kidneys adrenals and lungs
|
|
611812|C567517||serkal
|
|
611812|C567517||serkal syndrome
|
|
116920|C535887||leukocyte adhesion deficiency type 1
|
|
116920|C535887||lad
|
|
116920|C535887||lad1
|
|
116920|C535887||leukocyte adhesion deficiency type i
|
|
116920|C535887||lfa1 immunodeficiency
|
|
116920|C535887||lymphocyte function associated antigen 1 immunodeficiency
|
|
C567713|613193||ciliary dyskinesia primary 13
|
|
C567713|613193||cild13
|
|
C567713|613193||ciliary dyskinesia primary 13 with or without situs inversus
|
|
C531735||congenital macroglossia
|
|
C531735||enlarged tongue
|
|
C531735||giant tongue
|
|
C531736||acute malaria
|
|
C531736||chronic malaria
|
|
C531737||malignant fever
|
|
C531737||fulminating hyperpyrexia
|
|
C531737||pharmacogenic myopathy
|
|
D010580|175200||peutz jeghers syndrome
|
|
D010580|175200||hamartomatous intestinal polyposes
|
|
D010580|175200||hamartomatous intestinal polyposis
|
|
D010580|175200||intestinal polyposes hamartomatous
|
|
D010580|175200||intestinal polyposis hamartomatous
|
|
D010580|175200||lentiginoses perioral
|
|
D010580|175200||lentiginosis perioral
|
|
D010580|175200||perioral lentiginoses
|
|
D010580|175200||perioral lentiginosis
|
|
D010580|175200||periorificial lentiginosis syndrome
|
|
D010580|175200||periorificial lentiginosis syndromes
|
|
D010580|175200||peutz jeghers polyposis
|
|
D010580|175200||peutz jegher apos s syndrome
|
|
D010580|175200||peutz jegher syndrome
|
|
D010580|175200||pjs
|
|
D010580|175200||polyposes hamartomatous intestinal
|
|
D010580|175200||polyposis hamartomatous intestinal
|
|
D010580|175200||polyposis peutz jeghers
|
|
D010580|175200||polyps and spots syndrome
|
|
D010580|175200||polyps and spots syndromes
|
|
D010580|175200||syndrome periorificial lentiginosis
|
|
D010580|175200||syndrome peutz jeghers
|
|
D010580|175200||syndrome peutz jegher apos s
|
|
D010580|175200||syndrome polyps and spots
|
|
D010580|175200||syndromes periorificial lentiginosis
|
|
D010580|175200||syndromes polyps and spots
|
|
C564908|260370||pancreatic agenesis congenital
|
|
C564908|260370||pagen
|
|
C564908|260370||pancreatic hypoplasia congenital
|
|
C531731||lissencephaly and agenesis of corpus callosum
|
|
C531731||subcortical laminar heterotopia x linked
|
|
C537581|606996||senior loken syndrome 4
|
|
C537581|606996||slsn4
|
|
C531732||ascending aortic aneurysm hypertelorism bifid uvula cleft palate and arterial tortuosity
|
|
D003139||common cold
|
|
D003139||acute coryza
|
|
D003139||catarrh
|
|
D003139||catarrhs
|
|
D003139||cold common
|
|
D003139||colds common
|
|
D003139||common colds
|
|
D003139||coryza acute
|
|
C567698|608194||cone rod dystrophy 13
|
|
C567698|608194||cord13
|
|
611809||bestrophinopathy autosomal recessive
|
|
611809||arb
|
|
217000||complement component 2 deficiency
|
|
217000||c2d
|
|
217000||c2 deficiency
|
|
D003137||common bile duct diseases
|
|
C566901|611634||febrile convulsions familial 9
|
|
C566901|611634||feb9
|
|
C566901|611634||febrile seizures familial 9
|
|
C538603|242100||ichthyosiform erythroderma brocq congenital nonbullous form
|
|
C538603|242100||arci2
|
|
C538603|242100||ichthyosiform erythroderma brocq congenital nonbullous form formerly
|
|
C538603|242100||ichthyosiform erythroderma congenital nonbullous 1
|
|
C538603|242100||ichthyosiform erythroderma nonbullous congenital 1 formerly
|
|
C538603|242100||ichthyosis congenital autosomal recessive 2
|
|
C538603|242100||ncie1 formerly
|
|
C538603|242100||nonbullous congenital ichthyosiform erythroderma 1
|
|
D003138||common bile duct neoplasms
|
|
C563206|274500||thyroid dyshormonogenesis 2a
|
|
C563206|274500||hypothyroidism congenital due to dyshormonogenesis 2a
|
|
C563206|274500||iodide peroxidase deficiency
|
|
C563206|274500||tdh2a
|
|
C563206|274500||thyroid hormonogenesis genetic defect in 2a
|
|
C563206|274500||thyroid peroxidase deficiency
|
|
C531747||congenital facial diplegia
|
|
C531747||facial diplegia congenital
|
|
D003141||communicable diseases
|
|
D003141||communicable disease
|
|
D003141||disease communicable
|
|
D003141||disease infectious
|
|
D003141||diseases communicable
|
|
D003141||diseases infectious
|
|
D003141||infectious disease
|
|
D003141||infectious diseases
|
|
612586|C567238||aneurysm intracranial berry 9
|
|
612586|C567238||anib9
|
|
D017772||amyloid neuropathies
|
|
D017772||amyloid neuropathies secondary
|
|
D017772||amyloid neuropathy
|
|
D017772||amyloid neuropathy secondary
|
|
D017772||amyloid polyneuropathies
|
|
D017772||amyloid polyneuropathy
|
|
D017772||neuropathies amyloid
|
|
D017772||neuropathies secondary amyloid
|
|
D017772||neuropathy amyloid
|
|
D017772||neuropathy secondary amyloid
|
|
D017772||polyneuropathies amyloid
|
|
D017772||polyneuropathy amyloid
|
|
D017772||secondary amyloid neuropathies
|
|
D017772||secondary amyloid neuropathy
|
|
D017119|176100||porphyria cutanea tarda
|
|
D017119|176100||hep included
|
|
D017119|176100||pct
|
|
D017119|176100||pct apos familial apos type
|
|
D017119|176100||pct type ii
|
|
D017119|176100||porphyria cutanea tarda type ii
|
|
D017119|176100||porphyria hepatocutaneous type
|
|
D017119|176100||urod deficiency porphyria hepatoerythropoietic included
|
|
D017119|176100||uroporphyrinogen decarboxylase deficiency
|
|
C531742||marfanoid hypermobility syndrome
|
|
C531742||contractural arachnodactyly
|
|
C531742||marfan syndrome type 1
|
|
C531743||cystic dilatation of renal collecting tubes
|
|
C536590|265380||alveolar capillary dysplasia
|
|
C536590|265380|D010547||acdmpv
|
|
C536590|265380|D010547||alveolar capillary dysplasia with misalignment of pulmonary veins
|
|
C536590|265380|D010547||alveolar capillary dysplasia with misalignment of pulmonary veins and other congenital anomalies
|
|
C536590|265380||congenital alveolar capillary dysplasia
|
|
115196|C566170||cardiomyopathy familial hypertrophic 3
|
|
115196|C566170||cmh3
|
|
D047688||breast cyst
|
|
D047688||breast cysts
|
|
D047688||cyst breast
|
|
D047688||cysts breast
|
|
D016460||granuloma annulare
|
|
203650|C565965||alopecia mental retardation syndrome 1
|
|
203650|C565965||amr syndrome
|
|
203650|C565965||apmr1
|
|
D046350||porphyria variegate
|
|
D046350||deficiencies protoporphyrinogen oxidase
|
|
D046350|C538659|176200||porphyria variegata
|
|
D046350||porphyria variegates
|
|
D046350||ppox deficiency
|
|
D046350|C538659|176200||protoporphyrinogen oxidase deficiency
|
|
D046350|C538659|176200||variegate porphyria
|
|
D046350||variegates porphyria
|
|
D004478||ectoparasitic infestations
|
|
D004478||ectoparasitic infestation
|
|
D004478||infestation ectoparasitic
|
|
D004478||infestations ectoparasitic
|
|
D003147||communication disorders
|
|
D003147||acquired communication disorder
|
|
D003147||acquired communication disorders
|
|
D003147||childhood communication disorder
|
|
D003147||childhood communication disorders
|
|
D003147||communication disabilities
|
|
D003147||communication disability
|
|
D003147||communication disorder
|
|
D003147||communication disorder acquired
|
|
D003147||communication disorder childhood
|
|
D003147||communication disorder developmental
|
|
D003147||communication disorder neurogenic
|
|
D003147||communication disorders acquired
|
|
D003147||communication disorders childhood
|
|
D003147||communication disorders developmental
|
|
D003147||communication disorders neurogenic
|
|
D003147||communicative disorder
|
|
D003147||communicative disorders
|
|
D003147||communicative dysfunction
|
|
D003147||communicative dysfunctions
|
|
D003147||developmental communication disorder
|
|
D003147||developmental communication disorders
|
|
D003147||disabilities communication
|
|
D003147||disability communication
|
|
D003147||dysfunction communicative
|
|
D003147||dysfunctions communicative
|
|
D003147||neurogenic communication disorder
|
|
D003147||neurogenic communication disorders
|
|
D004479||ectopia lentis
|
|
D004479||lentis ectopia
|
|
D004474||ecthyma contagious
|
|
D004474||contagious ecthyma
|
|
D004474||contagious pustular dermatitides
|
|
D004474||contagious pustular dermatitis
|
|
D004474||dermatitides contagious pustular
|
|
D004474||dermatitis contagious pustular
|
|
D004474||orf
|
|
D004474||pustular dermatitides contagious
|
|
D004474||pustular dermatitis contagious
|
|
D004473||ecthyma
|
|
D004473||ecthymas
|
|
D005923|603278||glomerulosclerosis focal segmental
|
|
D005923|603278||focal glomerulosclerosis
|
|
D005923|603278||focal sclerosing glomerulonephritides
|
|
D005923|603278||focal sclerosing glomerulonephritis
|
|
D005923|603278||focal segmental glomerulosclerosis
|
|
D005923|603278|C538457||focal segmental glomerulosclerosis 1
|
|
D005923|603278||focal segmental glomerulosclerosis 3 susceptibility to
|
|
D005923|603278|C538457||fsgs1
|
|
D005923|603278||fsgs3
|
|
D005923|603278||glomerular hyalinosis segmental
|
|
D005923|603278||glomerulonephritides focal sclerosing
|
|
D005923|603278||glomerulonephritis focal sclerosing
|
|
D005923|603278||glomerulosclerosis focal
|
|
D005923|603278|C538457||glomerulosclerosis focal segmental 1
|
|
D005923|603278||glomerulosclerosis focal segmental 3 susceptibility to
|
|
D005923|603278||hyalinosis segmental
|
|
D005923|603278||hyalinosis segmental glomerular
|
|
D005923|603278||sclerosing glomerulonephritides focal
|
|
D005923|603278||sclerosing glomerulonephritis focal
|
|
D005923|603278||segmental glomerular hyalinosis
|
|
D005923|603278||segmental glomerulosclerosis focal
|
|
D005923|603278||segmental hyalinosis
|
|
602092||deafness autosomal recessive 18a
|
|
602092|C566580||deafness autosomal recessive 18
|
|
602092|C566580||dfnb18
|
|
602092||dfnb18a
|
|
D004480||ectromelia
|
|
D004480||amelia
|
|
D004480||hemimelia
|
|
D004480||phocomelia
|
|
D004480||sirenomelia
|
|
D004483||ectropion
|
|
D004483||ectropions
|
|
D004482||ectromelia infectious
|
|
D004482||infectious ectromelia
|
|
D004482||mousepox
|
|
D004482||mouse pox
|
|
C566293|104510||amelogenesis imperfecta type iv
|
|
C566293|104510||ai4
|
|
C566293|104510||aihht
|
|
C566293|104510||amelogenesis imperfecta hypomaturation hypoplastic type with taurodontism
|
|
C563985|606719||melanoma pancreatic cancer syndrome
|
|
C563985|606719||familial atypical multiple mole melanoma pancreatic carcinoma syndrome
|
|
C563985|606719||fammmpc
|
|
C563985|606719||fammmpc syndrome
|
|
D017789||granuloma pyogenic
|
|
D017789||angiogranuloma
|
|
D017789||angiogranulomas
|
|
D017789||capillary hemangioma lobular
|
|
D017789||granuloma pyogenicum
|
|
D017789||granuloma telangiecticum
|
|
D017789||hemangioma lobular capillary
|
|
D017789||lobular capillary hemangioma
|
|
D017789||pyogenic granuloma
|
|
D016459||prosthesis related infections
|
|
D016459||infections prosthesis related
|
|
D016459||prosthesis related infection
|
|
C531754||ridges off the end syndrome
|
|
C531754||dermal ridges off the end
|
|
C531755||kidney disorder involving deposition of calcium and oxalate or phosphate in the renal tubules
|
|
C563627|151210||platyspondylic lethal skeletal dysplasia torrance type
|
|
C563627|151210||lethal short limbed platyspondylic dwarfism torrance type
|
|
C563627|151210||platyspondylic chondrodysplasia torrance luton type
|
|
C563627|151210||platyspondylic lethal skeletal dysplasia luton type
|
|
C563627|151210||platyspondylic skeletal dysplasia torrance type
|
|
C563627|151210||plsdl included
|
|
C563627|151210||plsdt
|
|
C563627|151210||plsd t
|
|
C563627|151210||plsd tl
|
|
C563627|151210||thanatophoric dysplasia luton variant
|
|
C563627|151210||thanatophoric dysplasia luton variant included
|
|
C563627|151210||thanatophoric dysplasia torrance variant
|
|
C563627|151210||thanatophoric dysplasia torrance variant platyspondylic lethal skeletal dysplasia luton type included
|
|
C535294||reardon hall slaney syndrome
|
|
C535293||reactive angioendotheliomatosis
|
|
C535296||recombinant chromosome 8 syndrome
|
|
C535296||rec 8 syndrome
|
|
C535296||recombinant 8 syndrome
|
|
C535296||san luis valley recombinant chromosome 8 syndrome
|
|
C535296||san luis valley syndrome
|
|
C535295||reardon wilson cavanagh syndrome
|
|
C535295||ataxia deafness retardation syndrome
|
|
C535295||ataxia hearing loss and mental retardation
|
|
C535295||familial ataxia deafness and developmental delay
|
|
D017760||bone malalignment
|
|
D017760||bone malalignments
|
|
D017760||bone malposition
|
|
D017760||bone malpositions
|
|
D017760||bone misalignment
|
|
D017760||bone misalignments
|
|
D017760||malalignment bone
|
|
D017760||malposition bone
|
|
D017760||misalignment bone
|
|
D003117||color vision defects
|
|
D003117||achromatopsia
|
|
D003117||acquired color blindness
|
|
D003117||blindness color
|
|
D003117||blue color blindness
|
|
D003117||color blindness
|
|
D003117||color blindness acquired
|
|
D003117||color blindness blue
|
|
D003117||color blindness green
|
|
D003117||color blindness inherited
|
|
D003117||color blindness red
|
|
D003117||color blindness red green
|
|
D003117||color vision defect
|
|
D003117||color vision deficiency
|
|
D003117||defect color vision
|
|
D003117||defect deutan
|
|
D003117||defects color vision
|
|
D003117||deutan defect
|
|
D003117||green color blindness
|
|
D003117||inherited color blindness
|
|
D003117||monochromatopsia
|
|
D003117||protan defect
|
|
D003117||red color blindness
|
|
D003117||red green color blindness
|
|
D003117||tritan defect
|
|
D003117||vision defect color
|
|
D003117||vision defects color
|
|
C535298||red cell phospholipid defect with hemolysis
|
|
C535298||high red cell phosphatidylcholine hemolytic anemia
|
|
C535298||leaky red cell syndrome
|
|
C535298||phosphatidylcholine red cell membrane disorder
|
|
C535297||recurrent respiratory papillomatosis
|
|
C535297||juvenile laryngeal papilloma
|
|
C535297||juvenile onset recurrent respiratory papillomatosis
|
|
C535297||laryngeal papilloma recurrent
|
|
C535297||respiratory papillomatosis
|
|
C535299||autoimmune progesterone dermatitis
|
|
D004445||echinococcosis pulmonary
|
|
D004445||cyst pulmonary hydatid
|
|
D004445||cysts pulmonary hydatid
|
|
D004445||echinococcoses pulmonary
|
|
D004445||hydatid cyst pulmonary
|
|
D004445||hydatid cysts pulmonary
|
|
D004445||hydatidoses pulmonary
|
|
D004445||hydatidosis pulmonary
|
|
D004445||pulmonary echinococcoses
|
|
D004445||pulmonary echinococcosis
|
|
D004445||pulmonary hydatid cyst
|
|
D004445||pulmonary hydatid cysts
|
|
D004445||pulmonary hydatidoses
|
|
D004445||pulmonary hydatidosis
|
|
D004444||echinococcosis hepatic
|
|
D004444||alveolar echinococcis hepatic
|
|
D004444||alveolar echinococcoses hepatic
|
|
D004444||alveolar echinococcosis hepatic
|
|
D004444||cyst hepatic hydatid
|
|
D004444||cysts hepatic hydatid
|
|
D004444||echinococcis hepatic alveolar
|
|
D004444||echinococcoses hepatic
|
|
D004444||echinococcoses hepatic alveolar
|
|
D004444||echinococcosis hepatic alveolar
|
|
D004444||hepatic alveolar echinococcis
|
|
D004444||hepatic alveolar echinococcoses
|
|
D004444||hepatic alveolar echinococcosis
|
|
D004444||hepatic echinococcoses
|
|
D004444||hepatic echinococcosis
|
|
D004444||hepatic hydatid cyst
|
|
D004444||hepatic hydatid cysts
|
|
D004444||hepatic hydatidoses
|
|
D004444||hepatic hydatidosis
|
|
D004444||hydatid cyst hepatic
|
|
D004444||hydatid cysts hepatic
|
|
D004444||hydatidoses hepatic
|
|
D004444||hydatidosis hepatic
|
|
C535290||rasmussen johnsen thomsen syndrome
|
|
C535290||inherited congenital bilateral atresia of the external auditory canal congenital bilateral vertical talus and increased interocular distance
|
|
D003110||colonic neoplasms
|
|
D003110||cancer colon
|
|
D003110||cancer colonic
|
|
D003110||cancer of colon
|
|
D003110||cancer of the colon
|
|
D003110||cancers colon
|
|
D003110||cancers colonic
|
|
D003110|114500|D015179||colon cancer
|
|
D003110||colon cancers
|
|
D003110||colonic cancer
|
|
D003110||colonic cancers
|
|
D003110||colonic neoplasm
|
|
D003110||colon neoplasm
|
|
D003110||colon neoplasms
|
|
D003110||neoplasm colon
|
|
D003110||neoplasm colonic
|
|
D003110||neoplasms colon
|
|
D003110||neoplasms colonic
|
|
D004443||echinococcosis
|
|
D004443||cyst hydatid
|
|
D004443||cysts hydatid
|
|
D004443||echinococcoses
|
|
D004443||hydatid cyst
|
|
D004443||hydatid cysts
|
|
D004443||hydatidoses
|
|
D004443||hydatidosis
|
|
D003111||colonic polyps
|
|
D003111||colonic polyp
|
|
D003111||polyp colonic
|
|
D003111||polyps colonic
|
|
C535292||ray peterson scott syndrome
|
|
C535292||pelvic dysplasia associated with arthrogrypotic changes in the lower extremities
|
|
C535292||pelvic hypoplasia and arthrogrypotic changes in the lower limbs
|
|
D003112||colonic pseudo obstruction
|
|
D003112||colonic pseudoobstruction
|
|
D003112||ogilvie disease
|
|
D003112||ogilvie apos s syndrome
|
|
D003112||ogilvie syndrome
|
|
D003112||pseudoobstruction colonic
|
|
D003112||pseudo obstruction colonic
|
|
D003112||syndrome ogilvie
|
|
C535291||rasmussen subacute encephalitis
|
|
C535291||subacute focal encephalitis of rasmussen
|
|
D058345||asymptomatic infections
|
|
D058345||asymptomatic infection
|
|
D058345||infection asymptomatic
|
|
D058345||infections asymptomatic
|
|
D058345||infections subclinical
|
|
D058345||infection subclinical
|
|
D058345||subclinical infection
|
|
D058345||subclinical infections
|
|
241600|C565476||hypoproteinemia hypercatabolic
|
|
612514|C567288||specific language impairment 4
|
|
612514|C567288||sli4
|
|
602081|D001072||speech language disorder 1
|
|
602081||cas
|
|
602081||childhood apraxia of speech
|
|
602081|D001072||developmental verbal dyspraxia
|
|
602081||dvd
|
|
602081||spch1
|
|
602081|D001072||speech and language disorder with orofacial dyspraxia
|
|
C536816|605820||distal myopathy nonaka type
|
|
C536816|605820||distal myopathy with rimmed vacuoles
|
|
C536816|605820||dmrv
|
|
C536816|605820||hereditary inclusion body myopathy
|
|
C536816|605820||inclusion body myopathy 2
|
|
C536816|605820||myopathy distal with rimmed vacuoles
|
|
C536816|605820|C563515|162820||nm
|
|
C536816|605820||nonaka distal myopathy
|
|
C536816|605820||nonaka myopathy
|
|
C536816|605820||rimmed vacuole myopathy
|
|
D017759||fractures malunited
|
|
D017759||crossunited fracture
|
|
D017759||crossunited fractures
|
|
D017759||fracture abnormal union
|
|
D017759||fracture crossunited
|
|
D017759||fracture malunited
|
|
D017759||fractures abnormal union
|
|
D017759||fractures crossunited
|
|
D017759||malunited fracture
|
|
D017759||malunited fractures
|
|
C565561|229300||friedreich ataxia 1
|
|
C565561|229300||fa friedreich ataxia with retained reflexes included
|
|
C565561|229300||farr included
|
|
C565561|229300||frda
|
|
C565561|229300||frda1
|
|
275220|C535563||absence of tibia
|
|
275220|C535563||bilateral absence of the tibia
|
|
275220|C535563||thm
|
|
275220|C535563||tibia absence of
|
|
275220|C535563||tibial hemimelia
|
|
D003128|C537423|257550||coma
|
|
D003128||comas
|
|
D003128||comatose
|
|
D003128||pseudocoma
|
|
D003128||pseudocomas
|
|
C537279|609460||goldberg shprintzen megacolon syndrome
|
|
C537279|609460||goldberg shprintzen syndrome
|
|
C537279|609460||goshs
|
|
C536029|303350||masa mental retardation aphasia shuffling gait adducted thumbs syndrome
|
|
C536029|303350||adducted thumb with mental retardation
|
|
C536029|303350||clasped thumb and mental retardation
|
|
C536029|303350||crash syndrome
|
|
C536029|303350||gareis mason syndrome
|
|
C536029|303350||genetic diseases x linkeds
|
|
C536029|303350||l1 syndrome
|
|
C536029|303350||masa syndrome
|
|
C536029|303350||mental retardation aphasia shuffling gait adducted thumbs masa
|
|
C536029|303350||mental retardation aphasia shuffling gait and adducted thumbs
|
|
C536029|303350||spastic paraplegia 1 x linked
|
|
C536029|303350||spastic paraplegia type 1
|
|
C536029|303350||spg1
|
|
C536029|303350||thumb congenital clasped with mental retardation
|
|
C536029|303350||x linked complicated hereditary spastic paraplegia type 1
|
|
C536029|303350||x linked corpus callosum agenesis
|
|
C536029|303350||x linked hydrocephalus with stenosis of the aqueduct of sylvius hsas
|
|
C536355|610629||anemia diamond blackfan 3
|
|
C536355|610629||dba3
|
|
C536355|610629||diamond blackfan anemia 3
|
|
606159|C548080||neuroferritinopathy
|
|
606159|C548080||basal ganglia disease adult onset
|
|
606159|C548080||ferritin related neurodegeneration
|
|
606159|C548080||hereditary ferritinopathy
|
|
606159|C548080||nbia3
|
|
606159|C548080||neurodegeneration with brain iron accumulation 3
|
|
D004457||echovirus infections
|
|
D004457||echovirus infection
|
|
D004457||echo virus infection
|
|
D004457||echo virus infections
|
|
D004457||infection echovirus
|
|
D004457||infection echo virus
|
|
D004457||infections echovirus
|
|
D004457||infections echo virus
|
|
D004451||echinostomiasis
|
|
D004451||echinostomiases
|
|
D003121||colorado tick fever
|
|
D003121||fever colorado tick
|
|
D003121||tick fever colorado
|
|
D004454||echolalia
|
|
D004454||echophrasia
|
|
D004454||echo reaction
|
|
D004454||echo speech
|
|
D004454||reaction echo
|
|
D004454||reactions echo
|
|
D004454||speech echo
|
|
612567|C567251||inflammatory bowel disease 25 autosomal recessive
|
|
612567|C567251||ibd25
|
|
D003123||colorectal neoplasms hereditary nonpolyposis
|
|
D003123||colon cancer familial nonpolyposis
|
|
D003123||colorectal cancer hereditary nonpolyposis
|
|
D003123||familial nonpolyposis colon cancer
|
|
D003123||hereditary nonpolyposis colon cancer
|
|
D003123||hereditary nonpolyposis colorectal cancer
|
|
D003123||hereditary nonpolyposis colorectal neoplasms
|
|
D003123||lynch cancer family syndrome i
|
|
D003123||lynch syndrome
|
|
D003123|120435|C537261||lynch syndrome i
|
|
D003123||syndrome lynch
|
|
D004461||eclampsia
|
|
D004461||eclampsias
|
|
D003130||combat disorders
|
|
D003130||combat disorder
|
|
D003130||combat neuroses
|
|
D003130||combat neurosis
|
|
D003130||combat stress disorder
|
|
D003130||combat stress disorders
|
|
D003130||disorder combat
|
|
D003130||disorder combat stress
|
|
D003130||disorders combat
|
|
D003130||disorders combat stress
|
|
D003130||neuroses combat
|
|
D003130||neuroses war
|
|
D003130||neurosis combat
|
|
D003130||neurosis war
|
|
D003130||shell shock
|
|
D003130||shell shocks
|
|
D003130||shock shell
|
|
D003130||shocks shell
|
|
D003130||stress disorder combat
|
|
D003130||stress disorders combat
|
|
D003130||war neuroses
|
|
D003130||war neurosis
|
|
D017769||ulnar nerve compression syndromes
|
|
D017769||compression ulnar nerve
|
|
D017769||entrapments ulnar nerve
|
|
D017769||entrapment syndrome ulnar nerve
|
|
D017769||entrapment ulnar nerve
|
|
D017769||external compression syndrome ulnar nerve
|
|
D017769||guyon syndrome
|
|
D017769||guyon syndromes
|
|
D017769||nerve compression ulnar
|
|
D017769||nerve entrapment ulnar
|
|
D017769||syndrome guyon
|
|
D017769||syndromes guyon
|
|
D017769||ulnar nerve compression
|
|
D017769||ulnar nerve compressions
|
|
D017769||ulnar nerve entrapment
|
|
D017769||ulnar nerve entrapment at the wrist
|
|
D017769||ulnar nerve entrapments
|
|
D017769||ulnar nerve entrapment syndrome
|
|
D017769||ulnar nerve external compression syndrome
|
|
D056732|170100||prolidase deficiency
|
|
D056732|170100||deficiencies imidodipeptidase
|
|
D056732|170100||deficiencies prolidase
|
|
D056732|170100||deficiency imidodipeptidase
|
|
D056732|170100||deficiency prolidase
|
|
D056732|170100||hyperimidodipeptiduria
|
|
D056732|170100||hyperimidodipeptidurias
|
|
D056732|170100||imidodipeptidase deficiencies
|
|
D056732|170100||imidodipeptidase deficiency
|
|
D056732|170100||prolidase deficiencies
|
|
C535805|600110||stargardt disease 3
|
|
C535805|600110||macular dystrophy autosomal dominant chromosome 6 linked
|
|
C535805|600110||macular dystrophy with flecks type 3
|
|
C535805|600110||stargardt like macular dystrophy autosomal dominant
|
|
C535805|600110||stgd3
|
|
611087|C567020||polyhydramnios megalencephaly and symptomatic epilepsy
|
|
611087|C567020||pmse
|
|
611087|C567020||pmse syndrome
|
|
C562890||alport syndrome like hereditary nephritis
|
|
D005758||gastritis hypertrophic
|
|
D005758||disease menetrier
|
|
D005758||disease menetrier apos s
|
|
D005758||gastritis familial giant hypertrophic
|
|
D005758||gastritis giant hypertrophic
|
|
D005758||giant hypertrophic gastritis
|
|
D005758||hypertrophic gastritis
|
|
D005758||hypertrophic gastritis giant
|
|
D005758||menetrier disease
|
|
D005758||menetrier apos s disease
|
|
D005758||menetriers disease
|
|
D004427||ear diseases
|
|
D004427||disease ear
|
|
D004427||disease otologic
|
|
D004427||disease otological
|
|
D004427||diseases ear
|
|
D004427||diseases otologic
|
|
D004427||diseases otological
|
|
D004427||ear disease
|
|
D004427||otological disease
|
|
D004427||otological diseases
|
|
D004427||otologic disease
|
|
D004427||otologic diseases
|
|
C562895||pulmonic stenosis and congenital nephrosis
|
|
D005757||gastritis atrophic
|
|
D005757||atrophic gastritides
|
|
D005757||atrophic gastritis
|
|
D005757||gastritides atrophic
|
|
D004426||ear deformities acquired
|
|
D004426||acquired ear deformities
|
|
D004426||acquired ear deformity
|
|
D004426||deformities acquired ear
|
|
D004426||deformity acquired ear
|
|
D004426||ear deformity acquired
|
|
D005759||gastroenteritis
|
|
D005759||gastroenteritides
|
|
D004428||ear neoplasms
|
|
D004428||auricular cancer
|
|
D004428||auricular cancers
|
|
D004428||auricular neoplasms
|
|
D004428||cancer auricular
|
|
D004428||cancer of ear
|
|
D004428||cancer of ear auricle
|
|
D004428||cancer of the ear
|
|
D004428||cancers auricular
|
|
D004428||ear auricle cancer
|
|
D004428||ear auricle cancers
|
|
D004428||ear auricle neoplasm
|
|
D004428||ear auricle neoplasms
|
|
D004428||ear cancer
|
|
D004428||ear neoplasm
|
|
D004428||neoplasm ear
|
|
D004428||neoplasms auricular
|
|
D004428||neoplasms ear
|
|
D004428||neoplasms of ear auricle
|
|
C562894||prune belly syndrome with pulmonic stenosis mental retardation and deafness
|
|
D004422||dystonia musculorum deformans
|
|
D004422||childhood torsion disease
|
|
D004422||dystonia deformans musculorum
|
|
D004422||dystonia deformans progressiva
|
|
D004422||dystonia idiopathic torsion
|
|
D004422||dystonias idiopathic torsion
|
|
D004422||dystonias torsion
|
|
D004422||idiopathic torsion dystonia
|
|
D004422||idiopathic torsion dystonias
|
|
D004422||oppenheim ziehen disease
|
|
D004422||progressive torsion spasm
|
|
D004422||spasm progressive torsion
|
|
D004422||torsion disease childhood
|
|
D004422||torsion disease of childhood
|
|
D004422||torsion dystonia
|
|
D004422||torsion dystonia idiopathic
|
|
D004422||torsion spasm progressive
|
|
D005756||gastritis
|
|
D005756||gastritides
|
|
C537607|222765||rhizomelic chondrodysplasia punctata type 2
|
|
C537607|222765||chondrodysplasia punctata rhizomelic due to dhapat deficiency
|
|
C537607|222765||chondrodysplasia punctata rhizomelic due to dihydroxyacetonephosphate acyltransferase deficiency
|
|
C537607|222765||dhapat deficiency
|
|
C537607|222765||dihydroxyacetonephosphate acyltransferase deficiency
|
|
C537607|222765||glyceronephosphate acyltransferase deficiency
|
|
C537607|222765||glyceronephosphate o acyltransferase deficiency
|
|
C537607|222765||gnpat deficiency
|
|
C537607|222765||human dihydroxyacetonephosphate acyltransferase deficiency
|
|
C537607|222765||peroxisomal dihydroxyacetonephosphate acyltransferase deficiency
|
|
C537607|222765||rcdp2
|
|
C537607|222765||type 2 rhizomelic chondrodysplasia punctata
|
|
D004420||dystocia
|
|
D004420||dystocias
|
|
612580|C567241||mental retardation autosomal dominant 3
|
|
612580|C567241||mrd3
|
|
300539|C564491||nephrogenic syndrome of inappropriate antidiuresis
|
|
300539|C564491||nsiad
|
|
256600|D019150||neurodegeneration with brain iron accumulation 2a
|
|
256600||inad
|
|
256600||inad1
|
|
256600|D019150||nbia2a
|
|
256600|D019150||neuroaxonal dystrophy infantile
|
|
256600|D019150||neurodegeneration pla2g6 associated
|
|
256600||plan
|
|
256600|D019150||seitelberger disease
|
|
D058365||candidiasis invasive
|
|
D058365||candidiases invasive
|
|
D058365||invasive candidiases
|
|
D058365||invasive candidiasis
|
|
600631|D053206||nocturnal enuresis
|
|
600631|D053206||bedwetting
|
|
600631|D053206||enur1
|
|
600631|D053206||enuresis nocturnal
|
|
600631|D053206||enuresis nocturnal 1
|
|
600631|D053206||incontinence nighttime urinary
|
|
600631|D053206||nighttime urinary incontinence
|
|
600631|D053206||urinary incontinence nighttime
|
|
D017733||leukoplakia hairy
|
|
D017733||hairy leukoplakia
|
|
D017733||hairy leukoplakia oral
|
|
D017733||hairy leukoplakias
|
|
D017733||hairy leukoplakias oral
|
|
D017733||leukoplakia hairy oral
|
|
D017733||leukoplakia oral hairy
|
|
D017733||leukoplakias hairy
|
|
D017733||leukoplakias oral hairy
|
|
D017733||oral hairy leukoplakia
|
|
D017733||oral hairy leukoplakias
|
|
C537240|260540||progressive supranuclear palsy atypical
|
|
C537240|260540||atypical psp
|
|
C537240|260540||parkinson dementia syndrome
|
|
C537240|260540||steele richardson olszewski syndrome atypical
|
|
C537240|260540||steele richardson olszewski syndrome atypical included
|
|
C537240|260540||supranuclear palsy progressive 1 atypical
|
|
C537240|260540||supranuclear palsy progressive 1 atypical included
|
|
C537240|260540||supranuclear palsy progressive atypical
|
|
D016403||lymphoma large b cell diffuse
|
|
D016403||diffuse histiocytic lymphoma
|
|
D016403||diffuse histiocytic lymphomas
|
|
D016403||diffuse large b cell lymphoma
|
|
D016403||diffuse large cell lymphoma
|
|
D016403||diffuse large cell lymphomas
|
|
D016403||histiocytic lymphoma
|
|
D016403||histiocytic lymphoma diffuse
|
|
D016403||histiocytic lymphomas
|
|
D016403||histiocytic lymphomas diffuse
|
|
D016403||large cell lymphoma diffuse
|
|
D016403||large cell lymphomas diffuse
|
|
D016403||large lymphoid lymphoma diffuse
|
|
D016403||lymphoma diffuse histiocytic
|
|
D016403||lymphoma diffuse large cell
|
|
D016403||lymphoma histiocytic
|
|
D016403||lymphoma histiocytic diffuse
|
|
D016403||lymphoma large cell diffuse
|
|
D016403||lymphoma large lymphoid diffuse
|
|
D016403||lymphomas diffuse histiocytic
|
|
D016403||lymphomas diffuse large cell
|
|
D016403||lymphomas histiocytic
|
|
107200|C535983||congenital anosmia
|
|
107200|C535983||anic
|
|
107200|C535983||anosmia congenital
|
|
107200|C535983||anosmia isolated congenital
|
|
107200|C535983||isolated congenital anosmia
|
|
D017731||lymphomatoid papulosis
|
|
D017731||lymphomatoid papuloses
|
|
D017731||papuloses lymphomatoid
|
|
D017731||papulosis lymphomatoid
|
|
D016400||lymphoma large cell immunoblastic
|
|
D016400||diffuse immunoblastic lymphosarcoma
|
|
D016400||diffuse immunoblastic lymphosarcomas
|
|
D016400||immunoblastic large cell lymphoma
|
|
D016400||immunoblastic large cell lymphomas
|
|
D016400||immunoblastic lymphoma large cell
|
|
D016400||immunoblastic lymphomas large cell
|
|
D016400||immunoblastic lymphosarcoma diffuse
|
|
D016400||immunoblastic lymphosarcomas diffuse
|
|
D016400||immunoblastic sarcoma
|
|
D016400||immunoblastic sarcomas
|
|
D016400||immunoblastoma
|
|
D016400||immunoblastomas
|
|
D016400||large cell immunoblastic lymphoma
|
|
D016400||large cell immunoblastic lymphomas
|
|
D016400||large cell lymphoma immunoblastic
|
|
D016400||large cell lymphomas immunoblastic
|
|
D016400||lymphoma immunoblastic large cell
|
|
D016400||lymphomas immunoblastic large cell
|
|
D016400||lymphomas large cell immunoblastic
|
|
D016400||lymphosarcoma diffuse immunoblastic
|
|
D016400||lymphosarcomas diffuse immunoblastic
|
|
D016400||sarcoma immunoblastic
|
|
D016400||sarcomas immunoblastic
|
|
C531700||diarrhea prodrome hemolytic uremic syndrome
|
|
C531700||diarrhea prodrome hus
|
|
D050031|140300||hashimoto disease
|
|
D050031|140300||chronic lymphocytic thyroiditides
|
|
D050031|140300||chronic lymphocytic thyroiditis
|
|
D050031|140300||disease hashimoto
|
|
D050031|140300||disease hashimoto apos s
|
|
D050031|140300||hashimoto apos s disease
|
|
D050031|140300||hashimotos disease
|
|
D050031|140300||hashimoto apos s struma
|
|
D050031|140300||hashimoto apos s syndrome
|
|
D050031|140300||hashimotos syndrome
|
|
D050031|140300||hashimoto apos s syndromes
|
|
D050031|140300||hashimoto struma
|
|
D050031|140300||hashimoto syndrome
|
|
D050031|140300||hashimoto thyroiditides
|
|
D050031|140300||hashimoto thyroiditis
|
|
D050031|140300||ht
|
|
D050031|140300||hypothyroidism autoimmune thyroid autoantibodies included
|
|
D050031|140300||lymphocytic thyroiditides chronic
|
|
D050031|140300||lymphocytic thyroiditis chronic
|
|
D050031|140300||syndrome hashimoto apos s
|
|
D050031|140300||syndromes hashimoto apos s
|
|
D050031|140300||thyroiditides chronic lymphocytic
|
|
D050031|140300||thyroiditides hashimoto
|
|
D050031|140300||thyroiditis chronic lymphocytic
|
|
D050031|140300||thyroiditis hashimoto
|
|
C535521|603786||stargardt disease 4
|
|
C535521|603786||stgd4
|
|
D004438||ecchymosis
|
|
D004438||ecchymoses
|
|
C564684|606662||waardenburg syndrome type 2c
|
|
C564684|606662||waardenburg syndrome type iic
|
|
C564684|606662||ws2c
|
|
D003108||colonic diseases
|
|
D003108||colonic disease
|
|
D003108||disease colonic
|
|
D003108||diseases colonic
|
|
D003109||colonic diseases functional
|
|
D003109||colonic disease functional
|
|
D003109||disease functional colonic
|
|
D003109||diseases functional colonic
|
|
D003109||functional colonic disease
|
|
D003109||functional colonic diseases
|
|
D004433||earache
|
|
D004433||earaches
|
|
D004433||otalgia
|
|
D004433||otalgias
|
|
D005767||gastrointestinal diseases
|
|
D005767||cholera infantum
|
|
D005767||disease gastrointestinal
|
|
D005767||diseases gastrointestinal
|
|
D005767||disorder functional gastrointestinal
|
|
D005767||disorders functional gastrointestinal
|
|
D005767||functional gastrointestinal disorder
|
|
D005767||functional gastrointestinal disorders
|
|
D005767||gastrointestinal disease
|
|
D005767||gastrointestinal disorder functional
|
|
D005767||gastrointestinal disorders functional
|
|
D005767||infantum cholera
|
|
D005761||gastroenteritis transmissible of swine
|
|
D005761||gastroenteritides porcine transmissible
|
|
D005761||gastroenteritides swine transmissible
|
|
D005761||gastroenteritides transmissible porcine
|
|
D005761||gastroenteritis porcine transmissible
|
|
D005761||gastroenteritis swine transmissible
|
|
D005761||gastroenteritis transmissible porcine
|
|
D005761||porcine gastroenteritides transmissible
|
|
D005761||porcine gastroenteritis transmissible
|
|
D005761||porcine transmissible gastroenteritides
|
|
D005761||porcine transmissible gastroenteritis
|
|
D005761||swine transmissible gastroenteritides
|
|
D005761||swine transmissible gastroenteritis
|
|
D005761||transmissible gastroenteritides porcine
|
|
D005761||transmissible gastroenteritides swine
|
|
D005761||transmissible gastroenteritis of swine
|
|
D005761||transmissible gastroenteritis porcine
|
|
D005761||transmissible gastroenteritis swine
|
|
D005761||transmissible porcine gastroenteritides
|
|
D005761||transmissible porcine gastroenteritis
|
|
D003100||colles apos fracture
|
|
D003100||colles fracture
|
|
D003100||fracture colles apos
|
|
D005770||gastrointestinal neoplasms
|
|
D005770||cancer gastrointestinal
|
|
D005770||cancer of gastrointestinal tract
|
|
D005770||cancer of the gastrointestinal tract
|
|
D005770||cancers gastrointestinal
|
|
D005770||gastrointestinal cancer
|
|
D005770||gastrointestinal cancers
|
|
D005770||gastrointestinal neoplasm
|
|
D005770||gastrointestinal tract cancer
|
|
D005770||gastrointestinal tract cancers
|
|
D005770||neoplasm gastrointestinal
|
|
D005770||neoplasms gastrointestinal
|
|
D057049||thrombotic microangiopathies
|
|
D057049||microangiopathies thrombotic
|
|
D057049||microangiopathy thrombotic
|
|
D057049||thrombotic microangiopathy
|
|
D057045||laryngopharyngeal reflux
|
|
D057045||gastric reflux supraesophageal
|
|
D057045||gastric regurgitation
|
|
D057045||reflux laryngopharyngeal
|
|
D057045||reflux supraesophageal gastric
|
|
D057045||regurgitation gastric
|
|
D057045||supraesophageal gastric reflux
|
|
C531719||keratitis sicca
|
|
C567515|611818||long qt syndrome 9
|
|
C567515|611818||long qt syndrome 2 9
|
|
C567515|611818|C563614|613688||long qt syndrome 2 9 digenic included lqt2 9 digenic included
|
|
C567515|611818||long qt syndrome 9 acquired susceptibility to included
|
|
C567515|611818||lqt9
|
|
D016410||lymphoma t cell cutaneous
|
|
D016410||cutaneous t cell lymphoma
|
|
D016410||cutaneous t cell lymphomas
|
|
D016410||granulomatous slack skin
|
|
D016410||lymphoma cutaneous t cell
|
|
D016410||lymphomas cutaneous t cell
|
|
D016410||slack skin granulomatous
|
|
D016410||t cell lymphoma cutaneous
|
|
D016410||t cell lymphomas cutaneous
|
|
D016411||lymphoma t cell peripheral
|
|
D016411||lymphoma peripheral t cell
|
|
D016411||lymphomas peripheral t cell
|
|
D016411||peripheral t cell lymphoma
|
|
D016411||peripheral t cell lymphomas
|
|
D016411||t cell lymphoma peripheral
|
|
D016411||t cell lymphomas peripheral
|
|
C535371||trisomy 20p
|
|
C535371||chromosome 20 duplication 20p
|
|
C535371||duplication 20p
|
|
C535370||chromosome 20 deletion 20p
|
|
C535370||deletion 20p
|
|
C535370||monosomy 20p
|
|
C535373||dermatoosteolysis kirghizian type
|
|
C535373||kirghizian dermatoosteolysis
|
|
C535372||chromosome 20 trisomy
|
|
C535372||chromosome 20 duplication
|
|
C535372||trisomy 20
|
|
C535372||trisomy 20 mosaicism
|
|
C535375||dermochondrocorneal dystrophy of fran 231 ois
|
|
C535375||dermochondrocorneal dystrophy
|
|
C535375||francois syndrome
|
|
C562995||hexokinase deficiency hemolytic anemia
|
|
C562992||pulmonary hypoplasia primary
|
|
C562993||book syndrome
|
|
C562993||phc syndrome
|
|
607361|C536132||meckel syndrome type 3
|
|
607361|C536132||meckel gruber syndrome type 3
|
|
607361|C536132||mks3
|
|
183086||spinocerebellar ataxia 6
|
|
183086||sca6
|
|
C562998|C562908|187260||telangiectasia generalized essential
|
|
C536710|221750||winkelman bethge pfeiffer syndrome
|
|
C536710|221750||cphd3
|
|
C536710|221750||deafness sensorineural with pituitary dwarfism
|
|
C536710|221750||pituitary hormone deficiency combined 3
|
|
C536710|221750||pituitary hormone deficiency combined with rigid cervical spine
|
|
C536710|221750||sensorineural deafness with pituitary dwarfism
|
|
C562999||hypercalcemia infantile
|
|
609470||left ventricular noncompaction 2
|
|
609470||lvnc2
|
|
143860||hyperchlorhidrosis isolated
|
|
D058267||flea infestations
|
|
D058267||flea infestation
|
|
D058267||infestation flea
|
|
D058267||infestations flea
|
|
183090||spinocerebellar ataxia 2
|
|
183090||sca2 spinocerebellar atrophy ii
|
|
183090||olivopontocerebellar atrophy holguin type
|
|
183090||olivopontocerebellar atrophy ii
|
|
183090||opca2
|
|
183090||spinocerebellar ataxia cuban type
|
|
183090||cerebellar degeneration with slow eye movements
|
|
183090||wadia swami syndrome
|
|
183090||spinocerebellar degeneration with slow eye movements
|
|
183090||sdsem amyotrophic lateral sclerosis susceptibility to 13 included
|
|
183090||als13 included
|
|
D060586||trichosporonosis
|
|
D060586||disseminated trichosporonoses
|
|
D060586||disseminated trichosporonosis
|
|
D060586||invasive trichosporonoses
|
|
D060586||invasive trichosporonosis
|
|
D060586||japanese summer type hypersensitivity pneumonitis
|
|
D060586||pneumonitides summer type hypersensitivity
|
|
D060586||pneumonitis summer type hypersensitivity
|
|
D060586||summer type hypersensitivity pneumonitides
|
|
D060586||summer type hypersensitivity pneumonitis
|
|
D060586||trichosporonoses
|
|
D060586||trichosporonoses disseminated
|
|
D060586||trichosporonoses invasive
|
|
D060586||trichosporonosis disseminated
|
|
D060586||trichosporonosis invasive
|
|
D060585||fusariosis
|
|
D060585||disseminated fusarioses
|
|
D060585||disseminated fusariosis
|
|
D060585||fusarioses
|
|
D060585||fusarioses disseminated
|
|
D060585||fusarioses invasive
|
|
D060585||fusarioses invasive pulmonary
|
|
D060585||fusarioses pulmonary
|
|
D060585||fusariosis disseminated
|
|
D060585||fusariosis invasive
|
|
D060585||fusariosis invasive pulmonary
|
|
D060585||fusariosis pulmonary
|
|
D060585||fusarium infection
|
|
D060585||fusarium infections
|
|
D060585||infection fusarium
|
|
D060585||infections fusarium
|
|
D060585||invasive fusarioses
|
|
D060585||invasive fusariosis
|
|
D060585||invasive pulmonary fusarioses
|
|
D060585||invasive pulmonary fusariosis
|
|
D060585||pulmonary fusarioses
|
|
D060585||pulmonary fusariosis
|
|
610460|C536512||thiopurine s methyltransferase deficiency
|
|
610460|C536512||thiopurines poor metabolism of
|
|
610460|C536512||tpmt deficiency
|
|
106300|D013167||spondylitis ankylosing
|
|
106300|D013167||ankylosing spondylarthritides
|
|
106300|D013167||ankylosing spondylarthritis
|
|
106300|D013167||ankylosing spondylitis
|
|
106300|D013167||ankylosing spondylitis susceptibility to
|
|
106300|D013167||ankylosing spondyloarthritides
|
|
106300|D013167||ankylosing spondyloarthritis
|
|
106300|D013167||bechterew disease
|
|
106300|D013167||bechterew apos s disease
|
|
106300|D013167||bechterews disease
|
|
106300|D013167|D025242||bechterew syndrome
|
|
106300|D013167||marie struempell disease
|
|
106300|D013167|D025242||marie strumpell spondylitis
|
|
106300|D013167||rheumatoid spondylitis
|
|
106300|D013167||spda1
|
|
106300|D013167||spondylarthritides ankylosing
|
|
106300|D013167||spondylarthritis ankylopoietica
|
|
106300|D013167||spondylarthritis ankylosing
|
|
106300|D013167||spondylitis ankylopoietica
|
|
106300|D013167||spondylitis rheumatoid
|
|
106300|D013167||spondyloarthritides ankylosing
|
|
106300|D013167||spondyloarthritis ankylopoietica
|
|
106300|D013167||spondyloarthritis ankylosing
|
|
106300|D013167||spondyloarthropathy susceptibility to 1
|
|
C535368||chromosome 2 trisomy 2q37
|
|
C535368||duplication 2q37
|
|
C535368||trisomy 2q37
|
|
C535367||chromosome 2 trisomy 2q
|
|
C535367||duplication 2q
|
|
C535367||trisomy 2q
|
|
C536699||whistling face syndrome recessive form
|
|
C535369||chromosome 20 ring
|
|
D046290||liver abscess pyogenic
|
|
D046290||abscesses pyogenic hepatic
|
|
D046290||abscesses pyogenic liver
|
|
D046290||abscess pyogenic hepatic
|
|
D046290||abscess pyogenic liver
|
|
D046290||hepatic abscesses pyogenic
|
|
D046290||hepatic abscess pyogenic
|
|
D046290||liver abscesses pyogenic
|
|
D046290||pyogenic hepatic abscess
|
|
D046290||pyogenic hepatic abscesses
|
|
D046290||pyogenic liver abscess
|
|
D046290||pyogenic liver abscesses
|
|
C535381||arthrogryposis multiplex with deafness inguinal hernias and early death
|
|
C535384||arthrogryposis distal type 2e
|
|
C535384||contractures of fingers and jaw
|
|
C535386||arthrogryposis like hand anomaly and sensorineural deafness
|
|
C535386||arthrogryposis distal type 6
|
|
C535386||familial hand abnormality and sensori neural deafness
|
|
C535385||arthrogryposis distal with hypopituitarism mental retardation and facial anomalies
|
|
C536046|610967||osteogenesis imperfecta type 5
|
|
C536046|610967|C567042||oi5
|
|
C536046|610967|C567042||oi type v
|
|
C536046|610967|C567042||osteogenesis imperfecta type v
|
|
D005862||gerstmann syndrome
|
|
D005862||acquired gerstmann apos s syndrome
|
|
D005862||acquired gerstmann syndrome
|
|
D005862||de gerstmann syndrome
|
|
D005862||developmental gerstmann apos s syndrome
|
|
D005862||developmental gerstmanns syndrome
|
|
D005862||developmental gerstmann syndrome
|
|
D005862||finger agnosia left right confusion acalculia agraphia
|
|
D005862||finger agnosia left right confusion acalculia agraphias
|
|
D005862||gerstmann badal syndrome
|
|
D005862||gerstmann apos s syndrome
|
|
D005862||gerstmann apos s syndrome acquired
|
|
D005862||gerstmann apos s syndrome developmental
|
|
D005862||gerstmann syndrome 2
|
|
D005862||gerstmann syndrome acquired
|
|
D005862||gerstmann syndrome de
|
|
D005862||gerstmann syndrome developmental
|
|
D005862||syndrome acquired gerstmann
|
|
D005862||syndrome acquired gerstmann apos s
|
|
D005862||syndrome de gerstmann
|
|
D005862||syndrome developmental gerstmann
|
|
D005862||syndrome gerstmann
|
|
D005862||syndrome gerstmann badal
|
|
C535379||arthrogryposis multiplex congenita distal type 2
|
|
C535379||congenital contractures with major involvement of the hands and feet
|
|
C535379||distal arthrogryposis type 2
|
|
270960||spermatogenic failure 4
|
|
270960|C536875||azoospermia due to perturbations of meiosis
|
|
270960|C536875||azoospermia with maturation arrest
|
|
270960||rprgl4
|
|
270960||spermatogenesis arrest pregnancy loss recurrent susceptibility to 4
|
|
270960||spgf4
|
|
D016511||severe combined immunodeficiency
|
|
D016511|209920|C537079||bare lymphocyte syndrome
|
|
D016511||bare lymphocyte syndromes
|
|
D016511||combined immunodeficiencies severe
|
|
D016511||combined immunodeficiency severe
|
|
D016511||familial reticuloendothelioses
|
|
D016511||familial reticuloendotheliosis
|
|
D016511||immunodeficiencies severe combined
|
|
D016511||immunodeficiency severe combined
|
|
D016511||immunodeficiency syndrome severe combined
|
|
D016511||immunologic deficiency severe combined
|
|
D016511||lymphocyte syndrome bare
|
|
D016511||lymphocyte syndromes bare
|
|
D016511||omenn apos s syndrome
|
|
D016511||omenns syndrome
|
|
D016511|C538564|603554||omenn syndrome
|
|
D016511||reticuloendothelioses familial
|
|
D016511||reticuloendotheliosis familial
|
|
D016511||severe combined immunodeficiencies
|
|
D016511||severe combined immunodeficiency syndrome
|
|
D016511||severe combined immunologic deficiency
|
|
D016511||syndrome bare lymphocyte
|
|
D016511||syndrome omenn
|
|
D016511||syndrome omenn apos s
|
|
D016511||syndromes bare lymphocyte
|
|
C537989|600882||charcot marie tooth disease type 2b
|
|
C537989|600882||charcot marie tooth disease autosomal dominant type 2b
|
|
C537989|600882||charcot marie tooth disease axonal type 2b
|
|
C537989|600882||charcot marie tooth disease neuronal type 2b
|
|
C537989|600882||charcot marie tooth neuropathy type 2b
|
|
C537989|600882||cmt2b
|
|
C537989|600882||cmt 2b
|
|
C537989|600882||hereditary motor and sensory neuropathy 2 b hmsn 2 b
|
|
C537989|600882||hereditary motor and sensory neuropathy iib
|
|
C537989|600882||hmsn2b
|
|
C537989|600882||hmsn iib
|
|
C537989|600882||peripheral sensory neuropathy autosomal dominant psn
|
|
C535378||arthrogryposis multiplex congenita distal type 1
|
|
C535378||distal arthrogryposis type 1
|
|
D016512||ankle injuries
|
|
D016512||ankle injury
|
|
D016512||ankle sprain
|
|
D016512||ankle sprains
|
|
D016512||injuries ankle
|
|
D016512||injuries syndesmotic
|
|
D016512||injury ankle
|
|
D016512||injury syndesmotic
|
|
D016512||sprain ankle
|
|
D016512||sprains ankle
|
|
D016512||syndesmotic injuries
|
|
D016512||syndesmotic injury
|
|
D016510||corneal neovascularization
|
|
D016510||angiogenesis corneal
|
|
D016510||corneal angiogenesis
|
|
D016510||corneal neovascularizations
|
|
D016510||neovascularization corneal
|
|
D016510||neovascularizations corneal
|
|
C535392||astley kendall syndrome
|
|
C535392||astley kendall dysplasia
|
|
C535392||short limbed dwarfism with extensive stippling
|
|
C563471|600593||craniosynostosis adelaide type
|
|
C563471|600593||crsa
|
|
D005834||genital neoplasms male
|
|
D005834||genital neoplasm male
|
|
D005834||male genital neoplasm
|
|
D005834||male genital neoplasms
|
|
D005834||neoplasm male genital
|
|
D005834||neoplasms male genital
|
|
C562973||dysosteosclerosis
|
|
C535399||charcot marie tooth disease dominant intermediate 1
|
|
D005831||genital diseases female
|
|
D005831||diseases female genital
|
|
D005831||diseases gynecologic
|
|
D005831||female genital disease
|
|
D005831||female genital diseases
|
|
D005831||genital disease female
|
|
D005831||gynecologic disease
|
|
D005831||gynecologic diseases
|
|
D005833||genital neoplasms female
|
|
D005833||female genital neoplasm
|
|
D005833||female genital neoplasms
|
|
D005833||genital neoplasm female
|
|
D005833||gynecologic neoplasm
|
|
D005833||gynecologic neoplasms
|
|
D005833||neoplasm female genital
|
|
D005833||neoplasm gynecologic
|
|
D005833||neoplasms female genital
|
|
D005833||neoplasms gynecologic
|
|
C562974||craniofacial dysostosis with diaphyseal hyperplasia
|
|
C562974||osteosclerosis stanescu type
|
|
608404|C564245||platelet glycoprotein iv deficiency
|
|
608404|C564245||bdplt10
|
|
608404|C564245||bleeding disorder platelet type 10
|
|
608404|C564245||cd36 deficiency
|
|
D005832||genital diseases male
|
|
D005832||disease male genital
|
|
D005832||diseases male genital
|
|
D005832||genital disease male
|
|
D005832||male genital disease
|
|
D005832||male genital diseases
|
|
143890||fh
|
|
143890||fhc
|
|
143890||ldlcq2 included
|
|
143890||ldl receptor disorder low density lipoprotein cholesterol level quantitative trait locus 2 included
|
|
C562978||fibromatosis congenital generalized
|
|
C562978||myofibromatosis infantile
|
|
C535391||asrar facharzt haque syndrome
|
|
C535390||aspergillus niger infection
|
|
C535390||aspergillus niger infection pulmonary
|
|
D058285||tungiasis
|
|
D058288||sister mary joseph apos s nodule
|
|
D058288||nodule sister joseph apos s
|
|
D058288||nodules sister joseph apos s
|
|
D058288||sister joseph nodule
|
|
D058288||sister joseph apos s nodule
|
|
D058288||sister josephs nodule
|
|
D058288||sister joseph apos s nodules
|
|
255310||cftd
|
|
255310|C580011||cftdm
|
|
609452||myopathy myofibrillar 4
|
|
609452||mfm4
|
|
C535337|610019||cataract autosomal recessive congenital 2
|
|
C535337|610019||cataract 18
|
|
C535337|610019||catc2
|
|
C535337|610019||ctrct18
|
|
188030|D016553||purpura thrombocytopenic idiopathic
|
|
188030|D016553||aitp
|
|
188030|D016553||autoimmune thrombocytopenia
|
|
188030|D016553||autoimmune thrombocytopenias
|
|
188030|D016553||autoimmune thrombocytopenic purpura
|
|
188030|D016553||autoimmune thrombocytopenic purpuras
|
|
188030|D016553||disease werlhof
|
|
188030|D016553||disease werlhof apos s
|
|
188030|D016553||idiopathic thrombocytopenic purpura
|
|
188030|D016553||idiopathic thrombocytopenic purpuras
|
|
188030|D016553||immune thrombocytopenic purpura
|
|
188030|D016553||itp
|
|
188030|D016553||purpura autoimmune thrombocytopenic
|
|
188030|D016553||purpura idiopathic thrombocytopenic
|
|
188030|D016553||purpuras autoimmune thrombocytopenic
|
|
188030|D016553||purpuras idiopathic thrombocytopenic
|
|
188030|D016553||purpura thrombocytopenic autoimmune
|
|
188030|D016553||thrombocytopenia autoimmune
|
|
188030|D016553||thrombocytopenias autoimmune
|
|
188030|D016553||thrombocytopenic purpura autoimmune
|
|
188030|D016553||thrombocytopenic purpura idiopathic
|
|
188030|D016553||thrombocytopenic purpuras idiopathic
|
|
188030|D016553||werlhof disease
|
|
188030|D016553||werlhof apos s disease
|
|
188030|D016553||werlhofs disease
|
|
C537136|258900||oroticaciduria 1
|
|
C537136|258900||oawa included
|
|
C537136|258900||oprt and odc deficiency
|
|
C537136|258900||orotate phosphoribosyltransferase and omp decarboxylase deficiency
|
|
C537136|258900||orotate phosphoribosyltransferase and orotidylic decarboxylase deficiency
|
|
C537136|258900||orotic aciduria
|
|
C537136|258900||orotic aciduria i
|
|
C537136|258900||orotidylic pyrophosphorylase and orotidylic decarboxylase deficiency
|
|
C537136|258900||umps deficiency orotic aciduria without megaloblastic anemia included
|
|
C537136|258900||ump synthase deficiency
|
|
C537136|258900||uridine monophosphate synthase deficiency
|
|
C537136|258900||uridine monophosphate synthetase deficiency
|
|
D000361|613500||agammaglobulinemia
|
|
D000361|613500||agammaglobulinemia 2 autosomal recessive
|
|
D000361|613500||agammaglobulinemia 3 autosomal recessive
|
|
D000361|613500||agammaglobulinemia 5 autosomal dominant
|
|
D000361|613500||agammaglobulinemia autosomal dominant due to lrrc8a defect
|
|
D000361|613500||agammaglobulinemia autosomal recessive due to cd79a defect
|
|
D000361|613500||agammaglobulinemia autosomal recessive due to igll1 defect
|
|
D000361|613500||agammaglobulinemias
|
|
D000361|613500||agm2
|
|
D000361|613500||agm3
|
|
D000361|613500||agm5
|
|
D000361|613500||hypogammaglobulinemia
|
|
D000361|613500||hypogammaglobulinemias
|
|
C535748|608093||congenital disorder of glycosylation type 1j
|
|
C535748|608093||cdg1j
|
|
C535748|608093||cdgij
|
|
C535748|608093||cdg ij
|
|
C535748|608093||congenital disorder of glycosylation type ij
|
|
D005489|305600||focal dermal hypoplasia
|
|
D005489|305600||dermal hypoplasia focal
|
|
D005489|305600||dermal hypoplasias focal
|
|
D005489|305600||dhof
|
|
D005489|305600||fdh
|
|
D005489|305600||focal dermal hypoplasias
|
|
D005489|305600||fodh
|
|
D005489|305600||goltz gorlin syndrome
|
|
D005489|305600||goltz apos s syndrome
|
|
D005489|305600||goltzs syndrome
|
|
D005489|305600||goltz syndrome
|
|
D005489|305600||gorlin syndrome goltz
|
|
D005489|305600||hypoplasia focal dermal
|
|
D005489|305600||hypoplasias focal dermal
|
|
D005489|305600||syndrome goltz
|
|
D005489|305600||syndrome goltz gorlin
|
|
D005489|305600||syndrome goltz apos s
|
|
231100|C536394||neonatal hemochromatosis
|
|
231100|C536394||alloimmune hepatitis congenital
|
|
231100|C536394||giant cell hepatitis formerly
|
|
231100|C536394||hemochromatosis neonatal
|
|
231100|C536394||idiopathic neonatal hemochromatosis
|
|
231100|C536394||neonatal hepatitis formerly
|
|
231100|C536394||nh
|
|
231100|C536394||nhc
|
|
D005847||geotrichosis
|
|
D005847||geotrichoses
|
|
C562988||pseudomonilethrix
|
|
610427|C536122||night blindness congenital stationary type 2b
|
|
610427|C536122||csnb2b
|
|
610427|C536122||csnb incomplete autosomal recessive
|
|
610427|C536122||night blindness congenital stationary incomplete autosomal recessive
|
|
217095|C535464||conotruncal heart malformations
|
|
217095||cafs included
|
|
217095||conotruncal anomaly face syndrome included
|
|
217095||cthm
|
|
217095||dorv included
|
|
217095||double outlet right ventricle included
|
|
217095||interrupted aortic arch included
|
|
217095||persistent truncus arteriosus included
|
|
217095||pta included
|
|
217095||truncus arteriosus communis included
|
|
610425||cataract 23
|
|
610425||cataract 23 lamellar
|
|
610425||ctrct23
|
|
C562989||amastia
|
|
C562989||amazia
|
|
C535687|268300||roberts syndrome
|
|
C535687|268300||appelt gerken lenz syndrome
|
|
C535687|268300||hypomelia hypotrichosis facial hemangioma syndrome
|
|
C535687|268300||long bone deficiencies associated with cleft lip palate
|
|
C535687|268300||pseudothalidomide syndrome
|
|
C535687|268300||rbs
|
|
C535687|268300||roberts sc phocomelia syndrome
|
|
C535687|268300||sc phocomelia syndrome
|
|
C535687|268300||sc pseudothalidomide syndrome
|
|
C535687|268300||sc syndrome
|
|
C535687|268300||tetraphocomelia cleft palate syndrome
|
|
181600|C537526||sclerotylosis
|
|
181600|C537526||hrz
|
|
181600|C537526||huriez syndrome
|
|
181600|C537526||scleroatrophic and keratotic dermatosis of limbs
|
|
181600|C537526||tys
|
|
179450|C566725||ragweed sensitivity
|
|
C565128|124000||mitochondrial complex iii deficiency
|
|
C565128|124000||mc3dn1
|
|
C565128|124000||mitochondrial complex iii deficiency nuclear type 1
|
|
C535780|272460||spondylocarpotarsal synostosis
|
|
C535780|272460||congenital scoliosis with unilateral unsegmented bar
|
|
C535780|272460||congenital synspondylism
|
|
C535780|272460||scoliosis congenital with unilateral unsegmented bar
|
|
C535780|272460||sct
|
|
C535780|272460||sct syndrome
|
|
C535780|272460||spondylocarpotarsal syndrome
|
|
C535780|272460||spondylocarpotarsal synostosis syndrome
|
|
C535780|272460||synspondylism congenital
|
|
C535780|272460||vertebral fusion with carpal coalition
|
|
D021081||chronobiology disorders
|
|
D021081||biological clock disturbance
|
|
D021081||biological clock disturbances
|
|
D021081||chronobiology disorder
|
|
D021081||circadian dysregulation
|
|
D021081||circadian rhythm disorder
|
|
D021081||circadian rhythm disorders
|
|
D021081||disturbance biological clock
|
|
D021081||disturbances biological clock
|
|
D021081||dysregulation circadian
|
|
D021081||inversion of circadian rhythm psychogenic
|
|
D021081||psychogenic inversion of circadian rhythm
|
|
221770|C536329||polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|
|
221770|C536329||brain bone fat disease
|
|
221770|C536329||dementia prefrontal with bone cysts
|
|
221770|C536329||dementia progressive with lipomembranous polycystic osteodysplasia
|
|
221770|C536329||nasu hakola disease
|
|
221770|C536329||nhd
|
|
221770|C536329||plo sl
|
|
221770|C536329||plosl
|
|
221770|C536329||presenile dementia with bone cysts
|
|
D017823||furcation defects
|
|
D017823||defect furcation
|
|
D017823||defects furcation
|
|
D017823||furcation defect
|
|
217090|C566897||plasminogen deficiency type i
|
|
217090|C566897||dysplasminogenemia
|
|
217090|C566897||dysplasminogenemia included
|
|
217090|C566897||ligneous conjunctivitis
|
|
217090|C566897||ligneous conjunctivitis included
|
|
C536660||perniola krajewska carnevale syndrome
|
|
C536660||congenital alopecia psychomotor retardation convulsions
|
|
C536660||neuroectodermosis with alopecia or hypotrichosis
|
|
D054705||mastocytoma skin
|
|
D054705||skin mastocytoma
|
|
D054705||solitary mastocytoma of skin
|
|
C562950||cleft soft palate
|
|
C537995||dysferlinopathy
|
|
C562951||trigonocephaly nonsyndromic
|
|
C562951|190440||craniosynostosis metopic
|
|
C537992||charcot marie tooth disease type 2c
|
|
C537992||charcot marie tooth disease axonal type 2c
|
|
C537992||hereditary motor and sensory neuropathy 2 c
|
|
C564577|607398||glucocorticoid deficiency 2
|
|
C564577|607398||familial glucocorticoid deficiency 2
|
|
C564577|607398||fgd2
|
|
C564577|607398||gccd2
|
|
220400|D029593||jervell lange nielsen syndrome
|
|
220400|D029593||cardio auditory syncope syndrome
|
|
220400|D029593||cardioauditory syndrome of jervell and lange nielsen
|
|
220400|D029593||deafness congenital and functional heart disease
|
|
220400|D029593||jervell and lange nielsen syndrome
|
|
220400|D029593||jervell and lange nielsen syndrome 1
|
|
220400|D029593||jlns1
|
|
220400|D029593||prolonged qt interval in ekg and sudden death
|
|
220400|D029593||surdo cardiac syndrome
|
|
220400|D029593||surdo cardiac syndromes
|
|
220400|D029593||syndrome jervell lange nielsen
|
|
220400|D029593||syndrome surdo cardiac
|
|
C535332||aase smith syndrome
|
|
C535332||aase smith syndrome i
|
|
C535332||hydrocephalus cleft palate joint contractures
|
|
C535332||joint contractures with other abnormalities
|
|
C563755|609265||li fraumeni syndrome 2
|
|
C563755|609265||lfs2
|
|
D034381||hearing loss
|
|
D034381||hearing impairment
|
|
D034381||hypoacuses
|
|
D034381||hypoacusis
|
|
D034381||loss hearing
|
|
C562952||cervical vertebrae agenesis of
|
|
C562958||spondyloepimetaphyseal dysplasia irapa type
|
|
C562958||semdit
|
|
C566384|603373||hyperthyroidism familial gestational
|
|
C536656||peptide growth factors deficiency
|
|
C536656||hoepffner dreyer reimers syndrome
|
|
C536656||peptidic growth factors deficiency
|
|
C537988||charcot marie tooth disease type 2a
|
|
C537988||charcot marie tooth disease axonal type 2a
|
|
C537988||charcot marie tooth disease neuronal type 2a
|
|
C537988||hereditary motor and sensory neuropathy 2 a
|
|
C537988||hmsn iia
|
|
607841|C564322||deafness autosomal dominant 48
|
|
607841|C564322||dfna48
|
|
C537986||charcot marie tooth disease type 1e
|
|
C535327||holzgreve wagner rehder syndrome
|
|
C535327||complex congenital heart defect renal agenesis and cleft lip and palate
|
|
C535327||holzgreve syndrome
|
|
C535329||hooft disease
|
|
C536670||skeletal dysplasia san diego type
|
|
C536671||sketetal dysplasia coarse facies mental retardation
|
|
C536671||spondyloepimetaphyseal dysplasia x linked with mental deterioration
|
|
C562961||chondrodysplasia punctata tibia metacarpal type
|
|
218600|C536788||craniosynostosis radial aplasia syndrome
|
|
218600|C536788||baller gerold syndrome
|
|
218600|C536788||bgs
|
|
218600|C536788||craniosynostosis with radial defects
|
|
C536672||slavotinek pike mills hurst syndrome
|
|
C536673||slti salem syndrome
|
|
C536673||hypogonadism and frontoparietal alopecia
|
|
C536673||hypogonadotropic hypogonadism alopecia
|
|
276600|D020176||tyrosinemias
|
|
276600|D020176||2 tyrosinemias type
|
|
276600|D020176||2 tyrosinemia type
|
|
276600|D020176||4 hydroxyphenol pyruvic acid oxidase deficiency disease
|
|
276600|D020176||4 hydroxyphenylpyruvate dioxygenase deficiency
|
|
276600|D020176||4 hydroxyphenylpyruvate dioxygenase deficiency disease
|
|
276600|D020176||4 hydroxyphenylpyruvic acid oxidase deficiency
|
|
276600|D020176||deficiencies 4 hydroxyphenylpyruvate dioxygenase
|
|
276600|D020176||deficiencies fumarylacetoacetase
|
|
276600|D020176||deficiencies tat
|
|
276600|D020176||deficiency 4 hydroxyphenylpyruvate dioxygenase
|
|
276600|D020176||deficiency disease 4 hydroxyphenol pyruvic acid oxidase
|
|
276600|D020176||deficiency disease fumarylacetoacetase
|
|
276600|D020176||deficiency diseases fumarylacetoacetase
|
|
276600|D020176||deficiency disease tyrosine transaminase
|
|
276600|D020176||deficiency fumarylacetoacetase
|
|
276600|D020176||deficiency tat
|
|
276600|D020176||dioxygenase deficiencies 4 hydroxyphenylpyruvate
|
|
276600|D020176||dioxygenase deficiency 4 hydroxyphenylpyruvate
|
|
276600|D020176||disease fumarylacetoacetase deficiency
|
|
276600|D020176||diseases fumarylacetoacetase deficiency
|
|
276600|D020176||fah deficiency
|
|
276600|D020176||fumarylacetoacetase deficiencies
|
|
276600|D020176||fumarylacetoacetase deficiency
|
|
276600|D020176||fumarylacetoacetase deficiency disease
|
|
276600|D020176||fumarylacetoacetase deficiency diseases
|
|
276600|D020176||hepatorenal tyrosinemia
|
|
276600|D020176||hepatorenal tyrosinemias
|
|
276600|D020176||hereditary tyrosinemia
|
|
276600|D020176||hereditary tyrosinemias
|
|
276600|D020176||hereditary tyrosinemia type i
|
|
276600|D020176||hereditary tyrosinemia type ii
|
|
276600|D020176||hereditary tyrosinemia type iii
|
|
276600|D020176||hypertyrosinemia
|
|
276600|D020176||hypertyrosinemias type i
|
|
276600|D020176||hypertyrosinemia type i
|
|
276600|D020176||keratosis palmoplantaris with corneal dystrophy
|
|
276600|D020176||oculocutaneous type tyrosinoses
|
|
276600|D020176||oculocutaneous type tyrosinosis
|
|
276600|D020176||oregon type tyrosinemia
|
|
276600|D020176||richner hanhart syndrome
|
|
276600|D020176||richner hanhart syndromes
|
|
276600|D020176||richner hanhart syndrome tyrosinosis oculocutaneous type
|
|
276600|D020176||syndrome richner hanhart
|
|
276600|D020176||syndromes richner hanhart
|
|
276600|D020176||tat deficiencies
|
|
276600|D020176||tat deficiency
|
|
276600|D020176||type 2 tyrosinemia
|
|
276600|D020176||type 2 tyrosinemias
|
|
276600|D020176||type i hypertyrosinemia
|
|
276600|D020176||type i hypertyrosinemias
|
|
276600|D020176||type iii tyrosinemia
|
|
276600|D020176||type iii tyrosinemias
|
|
276600|D020176||type ii tyrosinemia
|
|
276600|D020176||type ii tyrosinemias
|
|
276600|D020176||type i tyrosinemia
|
|
276600|D020176||type i tyrosinemias
|
|
276600|D020176||type tyrosinoses oculocutaneous
|
|
276600|D020176||type tyrosinosis oculocutaneous
|
|
276600|D020176||tyrosine aminotransferase deficiency
|
|
276600|D020176||tyrosinemia
|
|
276600|D020176||tyrosinemia hepatorenal
|
|
276600|D020176||tyrosinemia hereditary
|
|
276600|D020176||tyrosinemias hepatorenal
|
|
276600|D020176||tyrosinemias hereditary
|
|
276600|D020176||tyrosinemias type 2
|
|
276600|D020176||tyrosinemias type i
|
|
276600|D020176||tyrosinemias type ii
|
|
276600|D020176||tyrosinemias type iii
|
|
276600|D020176||tyrosinemia type 1
|
|
276600|D020176||tyrosinemia type 1s
|
|
276600|D020176||tyrosinemia type 2
|
|
276600|D020176||tyrosinemia type i
|
|
276600|D020176||tyrosinemia type ii
|
|
276600|D020176||tyrosinemia type iii
|
|
276600|D020176||tyrosine transaminase deficiency
|
|
276600|D020176||tyrosine transaminase deficiency disease
|
|
276600|D020176||tyrosinoses oculocutaneous type
|
|
276600|D020176||tyrosinosis oculocutaneous type
|
|
276600|D020176||tyrsn1
|
|
276600|D020176||tyrsn2
|
|
276600|D020176||tyrsn3
|
|
C562968||spondyloepimetaphyseal dysplasia with joint laxity
|
|
C562968||semdjl
|
|
C535325|261640||6 pyruvoyl tetrahydropterin synthase deficiency
|
|
C535325|261640||hpabh4a
|
|
C535325|261640||hyperphenylalaninemia bh4 deficient a
|
|
C535325|261640||hyperphenylalaninemia bh4 deficient type a
|
|
C535325|261640||hyperphenylalaninemia due to 6 pyruvoyltetrahydropterin synthase deficiency
|
|
C535325|261640||hyperphenylalaninemia tetrahydrobiopterin deficient due to pts deficiency
|
|
C535325|261640||pts deficiency
|
|
C535325|261640||pts deficiency hyperphenylalaninemia bh4 deficient due to partial pts deficiency included
|
|
210720|C565898||microcephalic osteodysplastic primordial dwarfism type ii
|
|
210720|C565898||majewski osteodysplastic primordial dwarfism type ii
|
|
210720|C565898||microcephalic osteodysplastic primordial dwarfism type 2
|
|
210720|C565898||microcephalic osteodysplastic primordial dwarfism with tooth abnormalities
|
|
210720|C565898||mopd2
|
|
210720|C565898||mopdii
|
|
210720|C565898||mopd ii
|
|
210720|C565898||osteodysplastic primordial dwarfism type 2
|
|
210720|C565898||osteodysplastic primordial dwarfism type ii
|
|
C535335||abderhalden kaufmann lignac syndrome
|
|
C535335||abderhalden lignac kaufmann disease
|
|
C537999||dyssegmental dysplasia rolland desbuquois type
|
|
C537999||anisospondylic camptomicromelic dwarfism rolland desbuquois type
|
|
C537999||dyssegmental dwarfism rolland desbuquois type
|
|
C536668||sjogren larsson like syndrome
|
|
C536668||ichthyosis sjogren larsson like without cns or eye involvement
|
|
C536668||sjogren larsson like ichthyosis without cns or eye involvement
|
|
C537997||dysplasia epiphysealis hemimelica
|
|
C537997||trevor disease
|
|
C536666||situs inversus totalis with cystic dysplasia of kidneys and pancreas
|
|
C535336||cataract alopecia sclerodactyly
|
|
C535336||cataract alopecia sclerodactyly syndrome
|
|
C535339||posterior polar cataract 1
|
|
C536669||sj 246 gren mikulicz syndrome
|
|
C536669||sjogren mikulicz syndrome
|
|
C536682||warburton anyane yeboa syndrome
|
|
C536682||mosaic variegated aneuplody microcephaly syndrome
|
|
C535351||capos syndrome
|
|
C535351||capos
|
|
C535351||cerebellar ataxia areflexia pes cavus optic atrophy and sensorineural hearing loss
|
|
C535351||cerebellar ataxia areflexia pes cavus optic atrophy and sensorinural hearing loss
|
|
C536680||sonoda syndrome
|
|
C535350||cerebellar ataxia ectodermal dysplasia
|
|
C535350||cerebellar ataxia and ectodermal dysplasia
|
|
C535350||ectodermal dysplasia and cerebellar ataxia
|
|
C536685||fatal pneumococcal waterhouse friderichsen syndrome
|
|
C535353||cerebellar hypoplasia with endosteal sclerosis
|
|
C535352||cerebellar degeneration subacute
|
|
C535352||subacute cerebellar degeneration
|
|
C536683||warfarin syndrome
|
|
C536683||congenital warfarin syndrome
|
|
C536683||coumarin syndrome
|
|
C536683||disala syndrome
|
|
C536683||fetal anticoagulant syndrome
|
|
C536683||warfarin embryopathy
|
|
D010390||pemphigoid benign mucous membrane
|
|
D010390||benign mucosal pemphigoid
|
|
D010390||benign mucosal pemphigoids
|
|
D010390||benign mucous membrane pemphigoid
|
|
D010390||cicatricial pemphigoid
|
|
D010390||cicatricial pemphigoid ocular
|
|
D010390||cicatricial pemphigoids ocular
|
|
D010390||mucosal pemphigoid benign
|
|
D010390||mucosal pemphigoids benign
|
|
D010390||mucous membrane pemphigoid benign
|
|
D010390||ocular cicatricial pemphigoid
|
|
D010390||ocular cicatricial pemphigoids
|
|
D010390||pemphigoid benign mucosal
|
|
D010390||pemphigoid cicatricial
|
|
D010390||pemphigoid ocular cicatricial
|
|
D010390||pemphigoids benign mucosal
|
|
D010390||pemphigoids ocular cicatricial
|
|
C535355||chorea remitting with nystagmus and cataracts
|
|
C535355||chorea remitting with nystagmus and cataract
|
|
C535355||familial remitting chorea nystagmus and cataracts
|
|
C536684||warman mulliken hayward syndrome
|
|
C535354||cerebral astrocytoma adult
|
|
C535354||adult cerebral astrocytoma
|
|
C536991|252350||moyamoya disease 1
|
|
C536991|252350||mymy
|
|
C536991|252350||mymy1
|
|
C536991|252350||spontaneous occlusion of the circle of willis
|
|
C562932||muscular dystrophy scapulohumeral
|
|
C548666||mycobacterial disease mendelian susceptibility to
|
|
C548666|209950|D009165||atypical mycobacterial infection familial disseminated
|
|
611726||epilepsy progressive myoclonic 3 with or without intracellular inclusions
|
|
611726||ceroid lipofuscinosis neuronal 14
|
|
611726||cln14
|
|
611726||epm3
|
|
C535503|600969||epiphyseal dysplasia multiple 3
|
|
C535503|600969||edm3
|
|
C535503|600969||epiphyseal dysplasia multiple 3 with myopathy included
|
|
C535503|600969||multiple epiphyseal dysplasia 3
|
|
C562934|255200||myopathy centronuclear autosomal recessive
|
|
C562934|255200||myotubular myopathy autosomal recessive
|
|
C562935||myopathy with abnormal lipid metabolism
|
|
C562935||lipid storage myopathy
|
|
C535282|259775||raine syndrome
|
|
C535282|259775||lethal osteosclerotic bone dysplasia
|
|
C535282|259775||osteosclerotic bone dysplasia lethal
|
|
C535282|259775||rns
|
|
C535346||catatrichy
|
|
C535346||forelock
|
|
C536679||sohval soffer syndrome
|
|
C536679||congenital testicular deficiency
|
|
C535345||cataracts ataxia short stature and mental retardation
|
|
C535345||casm syndrome
|
|
C535345||cataract ataxia short stature and mental retardation
|
|
D010383||pellagra
|
|
D010383||pellagras
|
|
D010382||peliosis hepatis
|
|
D010382||hepatis peliosis
|
|
C535347||catel manzke syndrome
|
|
C535347||hyperphalangy clinodactyly of index finger with pierre robin syndrome
|
|
C535347||index finger anomaly with pierre robin syndrome
|
|
C535347||palatodigital syndrome catel manzke type
|
|
C535347||pierre robin syndrome with hyperphalangy and clinodactyly
|
|
D010386||pelvic neoplasms
|
|
D010386||cancer of pelvis
|
|
D010386||cancer of the pelvis
|
|
D010386||cancer pelvic
|
|
D010386||cancer pelvis
|
|
D010386||cancers pelvic
|
|
D010386||cancers pelvis
|
|
D010386||neoplasm pelvic
|
|
D010386||neoplasm pelvis
|
|
D010386||neoplasms of pelvis
|
|
D010386||neoplasms pelvic
|
|
D010386||neoplasms pelvis
|
|
D010386||pelvic cancer
|
|
D010386||pelvic cancers
|
|
D010386||pelvic neoplasm
|
|
D010386||pelvis cancer
|
|
D010386||pelvis cancers
|
|
D010386||pelvis neoplasm
|
|
D010386||pelvis neoplasms
|
|
C536692||wells jankovic syndrome
|
|
C536692||familial spastic paraparesis and deafness
|
|
C536692||spastic paraparesis and deafness
|
|
C537149|307200||hypogammaglobulinemia and isolated growth hormone deficiency x linked
|
|
C537149|307200||agammaglobulinemia and isolated growth hormone deficiency x linked
|
|
C537149|307200||fleisher syndrome
|
|
C537149|307200||growth hormone deficiency with hypogammaglobulinemia
|
|
C537149|307200||ighd3
|
|
C537149|307200||ighd iii
|
|
C537149|307200||isolated growth hormone deficiency type 3
|
|
C537149|307200||isolated growth hormone deficiency type iii
|
|
C537149|307200||nanism due to growth hormone isolated deficiency with x linked hypogammaglobulinemia
|
|
C536693||wells syndrome
|
|
C536693||bullous cellulitis with eosinophilia
|
|
C536693||eosinophilic cellulitis
|
|
C536693||wells apos syndrome
|
|
D054739||dendritic cell sarcoma interdigitating
|
|
D054739||interdigitating cell sarcoma
|
|
D054739||interdigitating cell sarcomas
|
|
D054739||interdigitating dendritic cell sarcoma
|
|
D054739||sarcoma interdigitating cell
|
|
D054739||sarcomas interdigitating cell
|
|
C535362||chromosome 1p36 deletion syndrome
|
|
C535362||1p36 33 deletion
|
|
C535362||1p36 deletion syndrome
|
|
C535362||chromosome 1 1p36 deletion syndrome
|
|
C535362||deletion 1p36 33
|
|
C535362||monosomy 1p36 syndrome
|
|
C536691||wellesley carmen french syndrome
|
|
C536691||cataract aberrant oral frenula and growth retardation
|
|
C536691||cataracts aberrant oral frenula and growth retardation
|
|
C535361||chromosome 1 ring
|
|
C535361||ring chromosome 1
|
|
C536696||weyers ulnar ray oligodactyly syndrome
|
|
C535364||chromosome 1 duplication 1p21 p32
|
|
C535364||duplication 1p21 p32
|
|
C535364||trisomy 1p21 p32
|
|
C562940||craniodiaphyseal dysplasia
|
|
C535363||chromosome 1 deletion q21 q25
|
|
C535363||deletion 1q21 q25
|
|
C535363||monosomy 1q21 q25
|
|
C536694||westphal disease
|
|
C536694||westphal variant of huntington apos s disease
|
|
C535366||chromosome 2 trisomy 2pter p24
|
|
C535366||duplication 2pter p24
|
|
C535366||trisomy 2pter p24
|
|
C536658|300388||perisylvian syndrome
|
|
C536658|300388||bpp
|
|
C536658|300388||bppx
|
|
C536658|300388||cbps
|
|
C536658|300388||congenital bilateral perisylvian syndrome
|
|
C536658|300388||perisylvian syndrome congenital bilateral
|
|
C536658|300388||pmgx
|
|
C536658|300388||polymicrogyria bilateral perisylvian
|
|
C536658|300388||polymicrogyria bilateral perisylvian x linked
|
|
C535365||chromosome 2 trisomy 2p13 p21
|
|
C535365||duplication 2p13 p21
|
|
C535365||trisomy 2p13 p21
|
|
C562943||choroid plexus carcinoma
|
|
C562941||telecanthus
|
|
609400||autoimmune disease susceptibility to 4
|
|
609400||ais4
|
|
609400||autoimmune disease susceptibility locus chromosome 4 related
|
|
609400||vamas5
|
|
609400||vitiligo associated multiple autoimmune disease susceptibility 5
|
|
607084|C564629||deafness autosomal recessive 31
|
|
607084|C564629||dfnb31
|
|
607084|C564629||whirler mouse homolog of
|
|
C562949||adducted thumbs syndrome
|
|
C562949||thumbs congenital clasped
|
|
D008088||listeriosis
|
|
D008088||infection listeria
|
|
D008088||infections listeria
|
|
D008088||listeria infection
|
|
D008088||listeria infections
|
|
D008088||listerioses
|
|
205950|C567145||anemia sideroblastic pyridoxine refractory autosomal recessive
|
|
C537550|156600||microcoria congenital
|
|
C537550|156600||congenital microcoria
|
|
C537550|156600||congenital miosis
|
|
C537550|156600||mcor
|
|
C537550|156600||miosis congenital
|
|
C537550|156600||pinhole pupils
|
|
C566344|603678||deafness autosomal recessive 14
|
|
C566344|603678||dfnb14
|
|
D010392||pemphigus
|
|
D010392||foliaceus pemphigus
|
|
D010392||pemphigus foliaceus
|
|
D010392||pemphigus vulgaris
|
|
C535357||choroid plexus calcification with mental retardation
|
|
C535357||choroido cerebral calcification syndrome with retardation
|
|
C535357||choroid plexus calcification and mental retardation
|
|
D010391||pemphigoid bullous
|
|
D010391||bullous pemphigoid
|
|
D010391||pemphigoid
|
|
D010391||pemphigoids
|
|
D008080||liposarcoma
|
|
D008080||dedifferentiated liposarcoma
|
|
D008080||dedifferentiated liposarcomas
|
|
D008080||liposarcoma dedifferentiated
|
|
D008080||liposarcoma pleomorphic
|
|
D008080||liposarcomas
|
|
D008080||liposarcomas dedifferentiated
|
|
D008080||liposarcomas pleomorphic
|
|
D008080||pleomorphic liposarcoma
|
|
D008080||pleomorphic liposarcomas
|
|
C536688||weinstein kliman scully syndrome
|
|
C536688||cardiomyopathy hypogonadism and metabolic anomalies
|
|
C538216|125500||dentinogenesis imperfecta shields type 3
|
|
C538216|125500||brandywine type dentinogenesis imperfecta
|
|
C538216|125500||dentinogenesis imperfecta shields type iii
|
|
C538216|125500||dgi iii
|
|
209900|D020788||bardet biedl syndrome
|
|
209900|D020788||bardet biedl syndrome 10 included
|
|
209900|D020788||bardet biedl syndrome 11 included
|
|
209900|D020788||bardet biedl syndrome 12 included
|
|
209900|D020788||bardet biedl syndrome 13 included
|
|
209900|D020788||bardet biedl syndrome 14 included
|
|
209900|D020788||bardet biedl syndrome 15 included
|
|
209900|D020788||bardet biedl syndrome 17 included
|
|
209900|D020788||bardet biedl syndrome 18 included
|
|
209900|D020788||bardet biedl syndrome 1 included
|
|
209900|D020788||bardet biedl syndrome 2 included
|
|
209900|D020788||bardet biedl syndrome 3 included
|
|
209900|D020788||bardet biedl syndrome 4 included
|
|
209900|D020788||bardet biedl syndrome 5 included
|
|
209900|D020788||bardet biedl syndrome 6 included
|
|
209900|D020788||bardet biedl syndrome 7 included
|
|
209900|D020788||bardet biedl syndrome 8 included
|
|
209900|D020788||bardet biedl syndrome 9 included
|
|
209900|D020788||bbs
|
|
209900|D020788||bbs10 included
|
|
209900|D020788||bbs11 included
|
|
209900|D020788||bbs12 included
|
|
209900|D020788||bbs13 included
|
|
209900|D020788||bbs14 included
|
|
209900|D020788||bbs15 included
|
|
209900|D020788||bbs17 included
|
|
209900|D020788||bbs18 included
|
|
209900|D020788||bbs1 included
|
|
209900|D020788||bbs2 included
|
|
209900|D020788||bbs3 included
|
|
209900|D020788||bbs4 included
|
|
209900|D020788||bbs5 included
|
|
209900|D020788||bbs6 included
|
|
209900|D020788||bbs7 included
|
|
209900|D020788||bbs8 included
|
|
209900|D020788||bbs9 included
|
|
209900|D020788||laurence moon bardet biedl syndrome
|
|
209900|D020788||syndrome bardet biedl
|
|
209900|D020788||syndrome laurence moon bardet biedl
|
|
C567561|612794||atrial septal defect 5
|
|
C567561|612794||asd5
|
|
C536620||say meyer syndrome
|
|
C536620||trigonocephaly short stature and developmental delay
|
|
C536620||trigonocephaly short stature and retarded psychomotor development
|
|
C536620||trigonocephaly with short stature and developmental delay
|
|
C567452|611944||lymphedema hereditary ib
|
|
C567452|611944||lmph1b
|
|
172800|D016116||piebaldism
|
|
172800|D016116||albinism cutaneous
|
|
172800|D016116||albinism partial
|
|
172800|D016116||cutaneous albinism
|
|
172800|D016116||partial albinism
|
|
172800|D016116||pbt
|
|
172800|D016116||piebald trait
|
|
C562912||rudiger syndrome
|
|
D008048||lip neoplasms
|
|
D008048||cancer lip
|
|
D008048||cancer of lip
|
|
D008048||cancer of the lip
|
|
D008048||cancers lip
|
|
D008048||lip cancer
|
|
D008048||lip cancers
|
|
D008048||lip neoplasm
|
|
D008048||neoplasm lip
|
|
D008048||neoplasms lip
|
|
D009379||neoplasms muscle tissue
|
|
D009379||muscle tissue neoplasm
|
|
D009379||muscle tissue neoplasms
|
|
D009379||myoblastoma
|
|
D009379||myoblastomas
|
|
D009379||myofibroblastoma
|
|
D009379||myofibroblastomas
|
|
D009379||neoplasm muscle tissue
|
|
D009389||neovascularization pathologic
|
|
D009389||angiogenesis pathologic
|
|
D009389||angiogenesis pathological
|
|
D009389||neovascularization pathological
|
|
D009389||pathological angiogenesis
|
|
D009389||pathological neovascularization
|
|
D009389||pathologic angiogenesis
|
|
D009389||pathologic neovascularization
|
|
C536618||say barber miller syndrome
|
|
C536618||microcephaly hypogammaglobulinemia abnormal immunity
|
|
D057180|600274||frontotemporal dementia
|
|
D057180|600274||complex disinhibition dementia parkinsonism amyotrophy
|
|
D057180|600274||complex disinhibition dementia parkinsonism amytrophy
|
|
D057180|600274||complices disinhibition dementia parkinsonism amyotrophy
|
|
D057180|600274||complices disinhibition dementia parkinsonism amytrophy
|
|
D057180|600274||ddpac
|
|
D057180|600274||dementia frontotemporal
|
|
D057180|600274||dementia frontotemporal lobe
|
|
D057180|600274||dementia frontotemporal lobe fldem
|
|
D057180|600274||dementia frontotemporal with parkinsonism
|
|
D057180|600274||dementia grn related frontotemporal
|
|
D057180|600274||dementia hereditary dysphasic disinhibition
|
|
D057180|600274||dementia semantic
|
|
D057180|600274||dementias frontotemporal
|
|
D057180|600274||dementias frontotemporal lobe
|
|
D057180|600274||dementias frontotemporal lobe fldem
|
|
D057180|600274||dementias grn related frontotemporal
|
|
D057180|600274||dementias semantic
|
|
D057180|600274||dementias ubiquitin positive frontotemporal
|
|
D057180|600274||dementia ubiquitin positive frontotemporal
|
|
D057180|600274||disease familial pick apos s
|
|
D057180|600274||diseases familial pick apos s
|
|
D057180|600274||diseases wilhelmsen lynch
|
|
D057180|600274||disease wilhelmsen lynch
|
|
D057180|600274||disinhibition dementia parkinsonism amyotrophy complex
|
|
D057180|600274||disinhibition dementia parkinsonism amyotrophy complices
|
|
D057180|600274||disinhibition dementia parkinsonism amytrophy complex
|
|
D057180|600274||disinhibition dementia parkinsonism amytrophy complices
|
|
D057180|600274||familial pick disease
|
|
D057180|600274||familial pick apos s disease
|
|
D057180|600274||familial picks disease
|
|
D057180|600274||familial pick apos s diseases
|
|
D057180|600274||fldem
|
|
D057180|600274|C566288||frontotemporal dementia amyotrophic lateral sclerosis
|
|
D057180|600274||frontotemporal dementia grn related
|
|
D057180|600274||frontotemporal dementias
|
|
D057180|600274||frontotemporal dementias grn related
|
|
D057180|600274||frontotemporal dementias ubiquitin positive
|
|
D057180|600274|607485||frontotemporal dementia ubiquitin positive
|
|
D057180|600274||frontotemporal dementia with parkinsonism
|
|
D057180|600274||frontotemporal dementia with parkinsonism 17
|
|
D057180|600274||frontotemporal lobar degeneration with tau inclusions
|
|
D057180|600274|607485||frontotemporal lobar degeneration with ubiquitin positive inclusions
|
|
D057180|600274||frontotemporal lobe dementia
|
|
D057180|600274||frontotemporal lobe dementia fldem
|
|
D057180|600274||frontotemporal lobe dementias
|
|
D057180|600274||frontotemporal lobe dementias fldem
|
|
D057180|600274||ftd
|
|
D057180|600274||ftd als
|
|
D057180|600274||ftd grn
|
|
D057180|600274||ftdp17
|
|
D057180|600274||ftdp 17
|
|
D057180|600274||ftd pgrn
|
|
D057180|600274||ftld 17 grn
|
|
D057180|600274||ftld tdp
|
|
D057180|600274||ftld with tau inclusions
|
|
D057180|600274||ftld with tdp 43 pathology
|
|
D057180|600274||grn related frontotemporal dementia
|
|
D057180|600274||grn related frontotemporal dementias
|
|
D057180|600274||hddd1
|
|
D057180|600274||hddd2
|
|
D057180|600274||hereditary dysphasic disinhibition dementia
|
|
D057180|600274||lobe dementia frontotemporal
|
|
D057180|600274||lobe dementias frontotemporal
|
|
D057180|600274||mstd
|
|
D057180|600274||multiple system tauopathy with presenile dementia
|
|
D057180|600274||pallidopontonigral degeneration ppnd pick complex included
|
|
D057180|600274||pick apos s disease familial
|
|
D057180|600274||pick apos s diseases familial
|
|
D057180|600274||semantic dementia
|
|
D057180|600274||semantic dementias
|
|
D057180|600274||ubiquitin positive frontotemporal dementia
|
|
D057180|600274||ubiquitin positive frontotemporal dementias
|
|
D057180|600274||wilhelmsen lynch disease
|
|
D057180|600274||wilhelmsen lynch diseases
|
|
D057180|600274||wld
|
|
C536619||say field coldwell syndrome
|
|
C536619||triphalangeal thumbs and dislocation of patella
|
|
D009386||neoplastic syndromes hereditary
|
|
D009386||cancer syndrome hereditary
|
|
D009386||cancer syndromes hereditary
|
|
D009386||hereditary cancer syndrome
|
|
D009386||hereditary cancer syndromes
|
|
D009386||hereditary neoplastic syndrome
|
|
D009386||hereditary neoplastic syndromes
|
|
D009386||neoplastic syndrome hereditary
|
|
D009386||syndrome hereditary cancer
|
|
D009386||syndrome hereditary neoplastic
|
|
D009386||syndromes hereditary cancer
|
|
D009386||syndromes hereditary neoplastic
|
|
D009385||neoplastic processes
|
|
D009385||processes neoplastic
|
|
D009384||paraneoplastic endocrine syndromes
|
|
D009384||ectopic hormone syndrome
|
|
D009384||ectopic hormone syndromes
|
|
D009384||endocrine syndrome paraneoplastic
|
|
D009384||paraneoplastic endocrine syndrome
|
|
D009384||syndrome ectopic hormone
|
|
D009384||syndrome paraneoplastic endocrine
|
|
D009384||syndromes ectopic hormone
|
|
D009384||syndromes paraneoplastic endocrine
|
|
D009383||neoplasms vascular tissue
|
|
D009383||blood vessel tumor
|
|
D009383||blood vessel tumors
|
|
D009383||neoplasm vascular tissue
|
|
D009383||tumor blood vessel
|
|
D009383||tumors blood vessel
|
|
D009383||vascular tissue neoplasm
|
|
D009383||vascular tissue neoplasms
|
|
D009382||neoplasms unknown primary
|
|
D009382||neoplasm metastasis unknown primary
|
|
D009382||neoplasm occult primary
|
|
D009382||neoplasms occult primary
|
|
D009382||neoplasm unknown primary
|
|
D009382||occult primary neoplasm
|
|
D009382||occult primary neoplasms
|
|
D009382||primary neoplasm occult
|
|
D009382||primary neoplasms occult
|
|
D009382||primary neoplasms unknown
|
|
D009382||primary neoplasm unknown
|
|
D009382||primary tumors unknown
|
|
D009382||primary tumor unknown
|
|
D009382||tumors unknown primary
|
|
D009382||tumor unknown primary
|
|
D009382||unknown primary neoplasm
|
|
D009382||unknown primary neoplasm metastasis
|
|
D009382||unknown primary neoplasms
|
|
D009382||unknown primary tumor
|
|
D009382||unknown primary tumors
|
|
D008052||lipid metabolism inborn errors
|
|
D008052||lipid metabolism inborn error
|
|
C563930|600513||epilepsy nocturnal frontal lobe type 1
|
|
C563930|600513||enfl1
|
|
C563930|600513||epilepsy nocturnal frontal lobe 1
|
|
D009381||neoplasms radiation induced
|
|
D009381||cancer radiation induced
|
|
D009381||cancers radiation induced
|
|
D009381||neoplasm radiation induced
|
|
D009381||radiation induced cancer
|
|
D009381||radiation induced cancers
|
|
D009381||radiation induced neoplasm
|
|
D009381||radiation induced neoplasms
|
|
C537944||cerebral hemorrhage with amyloidosis hereditary dutch type
|
|
D009380||neoplasms nerve tissue
|
|
D009380||neoplasm nerve tissue
|
|
D009380||neoplasm nervous tissue
|
|
D009380||neoplasms nervous tissue
|
|
D009380||nerve tissue neoplasm
|
|
D009380||nerve tissue neoplasms
|
|
D009380||nervous tissue neoplasm
|
|
D009380||nervous tissue neoplasms
|
|
C537941||chromosome 8 partial trisomy
|
|
C537941||partial trisomy 8
|
|
C537941||trisomy partial 8
|
|
C536610||familial cerebral cavernous malformation
|
|
C536610||familial cavernous hemangioma
|
|
C536610||familial cerebral cavernous angioma
|
|
C537942||chromosome 8 trisomy
|
|
C537942||chromosome 8 duplication
|
|
C537942||trisomy 8
|
|
D054740||dendritic cell sarcoma follicular
|
|
D054740||follicular dendritic cell sarcoma
|
|
C537947||cerebrospinal fluid leak
|
|
C537947||spinal cerebrospinal fluid leak
|
|
C536616||satoyoshi syndrome
|
|
C536616||komuragaeri disease
|
|
C536616||muscle spasms intermittent with alopecia diarrhea and skeletal abnormalities
|
|
D054747||histiocytic sarcoma
|
|
D054747||histiocytic lymphomas true
|
|
D054747||histiocytic lymphoma true
|
|
D054747||histiocytic sarcomas
|
|
D054747||histiocytoses malignant
|
|
D054747||histiocytoses true malignant
|
|
D054747||histiocytosis malignant
|
|
D054747||histiocytosis true malignant
|
|
D054747||lymphomas true histiocytic
|
|
D054747||lymphoma true histiocytic
|
|
D054747||malignant histiocytoses
|
|
D054747||malignant histiocytoses true
|
|
D054747||malignant histiocytosis
|
|
D054747||malignant histiocytosis true
|
|
D054747||sarcoma histiocytic
|
|
D054747||sarcomas histiocytic
|
|
D054747||true histiocytic lymphoma
|
|
D054747||true histiocytic lymphomas
|
|
D054747||true malignant histiocytoses
|
|
D054747||true malignant histiocytosis
|
|
D011694||purpura hyperglobulinemic
|
|
D011694||benign hyperglobulinemic purpura of waldenstr 246 m
|
|
D011694||hypergammaglobulinemic purpura of waldenstrom
|
|
D011694||hyperglobulinemic purpura
|
|
D011694||hyperglobulinemic purpura of waldenstr 246 m
|
|
D011694||hyperglobulinemic purpuras
|
|
D011694||hyperglobulinemic purpura waldenstrom
|
|
D011694||purpuras hyperglobulinemic
|
|
D011694||purpura waldenstrom hyperglobulinemic
|
|
D011694||waldenstrom hypergammaglobulinemic purpura
|
|
D011694||waldenstrom hyperglobulinemic purpura
|
|
D011694||waldenstr 246 m hyperglobulinemic purpura
|
|
C537948||ceroid lipofuscinosis neuronal 1 infantile
|
|
C537948||infantile neuronal ceroid lipofuscinosis incl
|
|
C537948||neuronal ceroid lipofuscinosis infantile finnish type
|
|
C537948||santavuori disease
|
|
C536617||saul wilkes stevenson syndrome
|
|
D011693||purpura
|
|
D011693||petechiae
|
|
D011693||purpuras
|
|
C537945||cerebral palsy spastic diplegic
|
|
C537945||spastic diplegia cerebral palsy
|
|
D011696||purpura thrombocytopenic
|
|
D011696||purpuras thrombocytopenic
|
|
D011696||purpuras thrombopenic
|
|
D011696||purpura thrombopenic
|
|
D011696||thrombocytopenic purpura
|
|
D011696||thrombocytopenic purpuras
|
|
D011696||thrombopenic purpura
|
|
D011696||thrombopenic purpuras
|
|
D010282|608266||parathyroid neoplasms
|
|
D010282|608266||adenoma parathyroid
|
|
D010282|608266||adenomas parathyroid
|
|
D010282|608266||cancer of parathyroid
|
|
D010282|608266||cancer of the parathyroid
|
|
D010282|608266||cancer parathyroid
|
|
D010282|608266||cancers parathyroid
|
|
D010282|608266||carcinoma parathyroid
|
|
D010282|608266||carcinomas parathyroid
|
|
D010282|608266||neoplasm parathyroid
|
|
D010282|608266||neoplasms parathyroid
|
|
D010282|608266||parathyroid adenoma
|
|
D010282|608266||parathyroid adenomas
|
|
D010282|608266||parathyroid cancer
|
|
D010282|608266||parathyroid cancers
|
|
D010282|608266||parathyroid carcinoma
|
|
D010282|608266||parathyroid carcinomas
|
|
D010282|608266||parathyroid neoplasm
|
|
D010282|608266||prtc
|
|
C537946||cerebral sarcoma
|
|
C537946||familial cerebral sarcomas
|
|
D011695||purpura schoenlein henoch
|
|
D011695||allergic purpura
|
|
D011695||anaphylactoid purpura
|
|
D011695||hemorrhagica purpura
|
|
D011695||hemorrhagic vasculitis
|
|
D011695||henoch purpura
|
|
D011695||henoch schoenlein purpura
|
|
D011695||henoch schonlein purpura
|
|
D011695||henoch schonlein purpuras
|
|
D011695||nonthrombocytopenic purpura
|
|
D011695||nonthrombopenic purpura
|
|
D011695||nonthrombopenic purpuras
|
|
D011695||purpura allergic
|
|
D011695||purpura anaphylactoid
|
|
D011695||purpura hemorrhagica
|
|
D011695||purpura henoch
|
|
D011695||purpura henoch schoenlein
|
|
D011695||purpura henoch schonlein
|
|
D011695||purpura nonthrombocytopenic
|
|
D011695||purpura nonthrombopenic
|
|
D011695||purpura rheumatoid
|
|
D011695||purpura schonlein henoch
|
|
D011695||purpuras henoch schonlein
|
|
D011695||purpuras nonthrombopenic
|
|
D011695||purpuras schonlein henoch
|
|
D011695||rheumatoid purpura
|
|
D011695||schoenlein henoch purpura
|
|
D011695||schonlein henoch purpura
|
|
D011695||schonlein henoch purpuras
|
|
D011695||schonlein purpura henoch
|
|
D011695||schonlein purpuras henoch
|
|
D011695||vasculitis hemorrhagic
|
|
C537961||calcifying epithelial odontogenic tumor
|
|
C537961||pindborg tumor
|
|
C536630||schimke x linked mental retardation syndrome
|
|
C536630||childhood onset choreoathetosis with spasticity postnatal microcephaly growth and mental retardation ophthalmoplegia and deafness
|
|
C536630||choreoathetosis with mental retardation x linked
|
|
C536630||progressive basal ganglion dysfunction mental and growth retardation external ophthalmoplegia postnatal microcephaly and deafness
|
|
C537962||calloso genital dysplasia
|
|
C537962||primary amenorrhoea with coloboma and total agenesis of the corpus callosum
|
|
C535300||autosomal dominant compelling helio ophthalmic outburst syndrome
|
|
C535300||autosomal dominant compelling helioophthalmic outburst syndrome
|
|
C535300||peroutka sneeze
|
|
C535300||photic sneeze reflex
|
|
C537960||calabro syndrome
|
|
C562925||collagenoma familial cutaneous
|
|
C566556|602390||hemochromatosis type 2a
|
|
C566556|602390||hemochromatosis juvenile included
|
|
C566556|602390||hemochromatosis type 2 included
|
|
C566556|602390||hfe2a
|
|
C566556|602390||hfe2 included
|
|
C566556|602390||jh included
|
|
D012035|266500||refsum disease
|
|
D012035|266500||adult refsum disease
|
|
D012035|266500||adult refsum diseases
|
|
D012035|266500||classic refsum disease
|
|
D012035|266500||classic refsum diseases
|
|
D012035|266500||disease adult refsum
|
|
D012035|266500||disease classic refsum
|
|
D012035|266500||disease refsum
|
|
D012035|266500||disease refsum apos s
|
|
D012035|266500||diseases adult refsum
|
|
D012035|266500||diseases classic refsum
|
|
D012035|266500||hemeralopia heredoataxia polyneuritiformis
|
|
D012035|266500||hereditary motor and sensory neuropathy iv
|
|
D012035|266500||hereditary motor and sensory neuropathy type iv
|
|
D012035|266500||hereditary type iv motor and sensory neuropathy
|
|
D012035|266500||heredoataxia polyneuritiformis hemeralopia
|
|
D012035|266500||heredopathia atactica polyneuritiformis
|
|
D012035|266500||hmsn 4
|
|
D012035|266500||hmsn iv
|
|
D012035|266500||hmsn ivs
|
|
D012035|266500||hmsn type iv
|
|
D012035|266500||hsmn4
|
|
D012035|266500||neuropathy hereditary motor and sensory type iv
|
|
D012035|266500||phytanic acid oxidase deficiency
|
|
D012035|266500||phytanic acid storage disease
|
|
D012035|266500||polyneuritiformis hemeralopia heredoataxia
|
|
D012035|266500||polyneuritiformis heredopathia atactica
|
|
D012035|266500||refsum disease adult
|
|
D012035|266500|C567602||refsum disease adult 1
|
|
D012035|266500||refsum disease classic
|
|
D012035|266500||refsum disease phytanic acid oxidase deficiency
|
|
D012035|266500||refsum disease phytanoyl coa hydroxylase deficiency
|
|
D012035|266500||refsum diseases adult
|
|
D012035|266500||refsum diseases classic
|
|
D012035|266500||refsum apos s disease
|
|
D012035|266500||refsums disease
|
|
D012035|266500||refsum apos s syndrome
|
|
D012035|266500||refsums syndrome
|
|
D012035|266500||refsum syndrome
|
|
D012035|266500||refsum thiebaut syndrome
|
|
D012035|266500||refsum thiebaut syndromes
|
|
D012035|266500||syndrome refsum
|
|
D012035|266500||syndrome refsum apos s
|
|
D012035|266500||syndrome refsum thiebaut
|
|
D012035|266500||syndromes refsum thiebaut
|
|
D010378||pedophilia
|
|
D010378||pedophilias
|
|
D008068||lipomatosis
|
|
D008068||lipomatoses
|
|
D008069||lipomatosis multiple symmetrical
|
|
D008069||cephalothoracic lipodystrophies
|
|
D008069||cephalothoracic lipodystrophy
|
|
D008069||circumscribed lipomatoses nodular
|
|
D008069||circumscribed lipomatosis nodular
|
|
D008069||disease madelung
|
|
D008069||disease madelung apos s
|
|
D008069||lipodystrophies cephalothoracic
|
|
D008069||lipodystrophy cephalothoracic
|
|
D008069||lipomatoses multiple symmetric
|
|
D008069||lipomatoses multiple symmetrical
|
|
D008069||lipomatoses nodular circumscribed
|
|
D008069||lipomatosis familial benign cervical
|
|
D008069||lipomatosis multiple symmetric
|
|
D008069||lipomatosis nodular circumscribed
|
|
D008069||madelung disease
|
|
D008069||madelung neck
|
|
D008069||madelung apos s disease
|
|
D008069||madelungs disease
|
|
D008069||madelung apos s neck
|
|
D008069||madelungs neck
|
|
D008069||multiple symmetrical lipomatoses
|
|
D008069||multiple symmetrical lipomatosis
|
|
D008069||multiple symmetric lipomatoses
|
|
D008069||multiple symmetric lipomatosis
|
|
D008069||nodular circumscribed lipomatoses
|
|
D008069||nodular circumscribed lipomatosis
|
|
D008069||symmetrical lipomatoses multiple
|
|
D008069||symmetrical lipomatosis multiple
|
|
D008069||symmetric lipomatoses multiple
|
|
D008069||symmetric lipomatosis multiple
|
|
D034321||hyperamylasemia
|
|
D034321||macroamylasemia
|
|
D009397||nephrocalcinosis
|
|
D009397||nephrocalcinoses
|
|
D008067|151900||lipoma
|
|
D008067||atypical lipoma
|
|
D008067||atypical lipomas
|
|
D008067||fatty tumor
|
|
D008067||fatty tumors
|
|
D008067||hibernoma
|
|
D008067||hibernomas
|
|
D008067||lipoma atypical
|
|
D008067||lipoma pleomorphic
|
|
D008067||lipomas
|
|
D008067||lipomas atypical
|
|
D008067||lipomas pleomorphic
|
|
D008067||lipomata
|
|
D008067||lipomatas
|
|
D008067|151900||lipomatosis multiple
|
|
D008067||pleomorphic lipoma
|
|
D008067||pleomorphic lipomas
|
|
D008067||tumor fatty
|
|
D008067||tumors fatty
|
|
C538582|101600||pfeiffer type acrocephalosyndactyly
|
|
C538582|101600||acrocephalosyndactyly type 5
|
|
C538582|101600|101200|D000168||acrocephalosyndactyly type v
|
|
C538582|101600||acs5
|
|
C538582|101600||acs v
|
|
C538582|101600||noack syndrome craniofacial skeletal dermatologic dysplasia included
|
|
C538582|101600|101200|D000168||pfeiffer syndrome
|
|
D008064||lipidoses
|
|
D008064||lipidosis
|
|
D008064||lipoidosis
|
|
D009395||nephritis interstitial
|
|
D009395||interstitial nephritides
|
|
D009395||interstitial nephritis
|
|
D009395||nephritides interstitial
|
|
D009395||nephritides tubulointerstitial
|
|
D009395||nephritis tubulointerstitial
|
|
D009395||tubulointerstitial nephritides
|
|
D009395||tubulointerstitial nephritis
|
|
D014929|222300||wolfram syndrome
|
|
D014929|222300||diabetes insipidus and mellitus with optic atrophy and deafness
|
|
D014929|222300||diabetes insipidus diabetes mellitus optic atrophy and deafness
|
|
D014929|222300||didmoad
|
|
D014929|222300||didmoad syndrome
|
|
D014929|222300||didmoadud
|
|
D014929|222300||syndrome wolfram
|
|
D014929|222300||wfs
|
|
D014929|222300||wfs1
|
|
D014929|222300||wolfram syndrome 1
|
|
D004819|226400||epidermodysplasia verruciformis
|
|
D004819|226400||disease lewandowsky lutz
|
|
D004819|226400||disease lutz lewandowsky
|
|
D004819|226400||ev
|
|
D004819|226400||ever
|
|
D004819|226400||lewandowsky lutz disease
|
|
D004819|226400||lutz lewandowsky disease
|
|
D009394||nephritis hereditary
|
|
D009394||alport apos s syndrome
|
|
D009394||alport syndrome
|
|
D009394|C536586|104200||alport syndrome autosomal dominant
|
|
D009394|C536587|203780||alport syndrome autosomal recessive
|
|
D009394||congenital hereditary hematuria
|
|
D009394||familial nephritis
|
|
D009394||hematuria congenital hereditary
|
|
D009394||hematuria nephropathy deafness syndrome
|
|
D009394||hematuric hereditary nephritis
|
|
D009394||hemorrhagic familial nephritis
|
|
D009394||hemorrhagic hereditary nephritis
|
|
D009394||hereditary familial congenital hemorrhagic nephritis
|
|
D009394||hereditary hematuria syndrome
|
|
D009394||hereditary interstitial pyelonephritis
|
|
D009394||hereditary nephritis
|
|
D009394||nephritis familial
|
|
D009394||nephritis hematuric hereditary
|
|
D009394||nephritis hemorrhagic familial
|
|
D009394||nephritis hemorrhagic hereditary
|
|
D009394||pyelonephritis hereditary interstitial
|
|
D009394||syndrome alport
|
|
D009394||syndrome hematuria nephropathy deafness
|
|
D009394||x linked alport syndrome
|
|
D009393||nephritis
|
|
D009393||nephritides
|
|
C536868|601162||spastic paraplegia 9 autosomal dominant
|
|
C536868|601162||autosomal dominant spastic paraparesis
|
|
C536868|601162||bilateral cataracts gastroesophageal reflux and spastic paraparesis with amyotrophy
|
|
C536868|601162||cataracts motor neuronopathy short stature and skeletal abnormalities
|
|
C536868|601162||cataracts with motor neuronopathy short stature and skeletal abnormalities
|
|
C536868|601162||spastic paraparesis with amyopathy cataracts and gastroesophageal reflux
|
|
C536868|601162||spg9
|
|
C536623||scalp ear nipple syndrome
|
|
C536623||finlay marks syndrome
|
|
C536623||hereditary syndrome of lumpy scalp odd ears and rudimentary nipples
|
|
D008060||lipodystrophy
|
|
D008060||lipodystrophies
|
|
C536624||scapuloperoneal myopathy
|
|
C536624||myopathy scapuloperoneal
|
|
C536624|181430||scapuloperoneal syndrome myopathic type
|
|
D008061||whipple disease
|
|
D008061||disease whipple
|
|
D008061||disease whipple apos s
|
|
D008061||intestinal lipodystrophy
|
|
D008061||lipodystrophy intestinal
|
|
D008061||whipple apos s disease
|
|
D008061||whipples disease
|
|
C536621||say syndrome
|
|
C536621||cleft palate large ears small head
|
|
C536621||cleft palate microcephaly large ears and short stature
|
|
C536621||say barber hobbs syndrome
|
|
C537356|156530||metatropic dwarfism
|
|
C537356|156530||metatropic dysplasia
|
|
C537356|156530||metatropic dysplasia 1
|
|
C537356|156530||metatropic dysplasia type 1
|
|
D054752||langerhans cell sarcoma
|
|
D054752||langerhans cell sarcomas
|
|
D054752||sarcoma langerhans cell
|
|
D054752||sarcomas langerhans cell
|
|
D053421||hand arm vibration syndrome
|
|
D053421||hand arm vibration syndromes
|
|
D053421||syndrome hand arm vibration
|
|
D053421||syndromes hand arm vibration
|
|
D053421||vibration syndrome hand arm
|
|
D053421||vibration syndromes hand arm
|
|
C536622||scalp defects postaxial polydactyly
|
|
C536622||congenital scalp defects associated with postaxial polydactyly
|
|
C536622||scalp defects and postaxial polydactyly
|
|
D036981||fasciitis plantar
|
|
D036981||chronic plantar fasciitis
|
|
D036981||fasciitis chronic plantar
|
|
D036981||fasciitis plantar chronic
|
|
D036981||heel spur syndrome
|
|
D036981||plantar fasciitis
|
|
D036981||plantar fasciitis chronic
|
|
C536627||schaefer stein oshman syndrome
|
|
C536627||craniodiaphyseal dysplasia dominant
|
|
C536627||dominantly inherited craniodiaphyseal dysplasia
|
|
D036982||heel spur
|
|
D036982||calcaneal spur
|
|
D036982||calcaneal spurs
|
|
D036982||heel spurs
|
|
D036982||spur calcaneal
|
|
D036982||spur heel
|
|
D036982||spurs calcaneal
|
|
D036982||spurs heel
|
|
C537959||cahmr syndrome
|
|
C537959||cataract hypertrichosis mental retardation syndrome
|
|
D010373||lice infestations
|
|
D010373||infestation lice
|
|
D010373||infestations lice
|
|
D010373||lice infestation
|
|
D010373||pediculoses
|
|
D010373||pediculosis
|
|
C537956||cervical hypertrichosis neuropathy
|
|
C536625||scarf syndrome
|
|
C536625||skeletal abnormalities cutis laxa craniostenosis ambiguous genitalia retardation and facial abnormalities
|
|
C537957||acute fatty liver of pregnancy
|
|
C537957||acute fatty liver gestational
|
|
C536626||schaap taylor baraitser syndrome
|
|
C536626||cataracts sensorineural deafness hypogonadism hypertrichosis and short stature
|
|
C565166||c9 deficiency with dermatomyositis
|
|
C537972||camptodactyly taurinuria
|
|
C537972||camptodactyly with taurinuria
|
|
C537973||camptodactyly vertebral fusion
|
|
C537973||camptodactyly and sacral vertebral fusion
|
|
C563855|608804||leukodystrophy hypomyelinating 2
|
|
C563855|608804||hld2
|
|
C563855|608804||pelizaeus merzbacher like disease 1
|
|
C563855|608804||pmld1
|
|
C537970||camptodactyly syndrome guadalajara type 1
|
|
C537970||camptodactyly syndrome guadalajara type i
|
|
C537970||facio thoraco skeletal syndrome
|
|
C537970||faciothoracoskeletal syndrome
|
|
C537970||guadalajara camptodactyly syndrome
|
|
C537970||guadalajara camptodactyly syndrome type 1
|
|
C565169|613779||complement component 3 deficiency autosomal recessive
|
|
C565169|613779||c3 deficiency autosomal recessive
|
|
C537971||camptodactyly syndrome guadalajara type 2
|
|
C537971||guadalajara camptodactyly syndrome type 2
|
|
C535440|210370||bietti crystalline dystrophy
|
|
C535440|210370||bcd
|
|
C535440|210370||bietti crystalline corneoretinal dystrophy
|
|
C535440|210370||bietti crystalline retinopathy
|
|
C535440|210370||bietti apos s crystalline corneoretinal dystrophy
|
|
C535440|210370||bietti apos s crystalline dystrophy
|
|
C535440|210370||bietti tapetoretinal degeneration with marginal corneal dystrophy
|
|
C567319|612406||dystonia 17 torsion autosomal recessive
|
|
C567319|612406||dyt17
|
|
D009358||congenital hereditary and neonatal diseases and abnormalities
|
|
D009358||congenital disorder
|
|
D009358||congenital disorders
|
|
D009358||disorder congenital
|
|
D009358||disorders congenital
|
|
D009358||neonatal diseases and abnormalities
|
|
D009357||neonatal abstinence syndrome
|
|
D009357||abstinence syndrome neonatal
|
|
D009357||abstinence syndromes neonatal
|
|
D009357||addiction neonatal passive
|
|
D009357||addictions neonatal passive
|
|
D009357||neonatal abstinence syndromes
|
|
D009357||neonatal passive addiction
|
|
D009357||neonatal passive addictions
|
|
D009357||neonatal substance withdrawal
|
|
D009357||neonatal substance withdrawals
|
|
D009357||neonatal withdrawal syndrome
|
|
D009357||neonatal withdrawal syndromes
|
|
D009357||passive addiction neonatal
|
|
D009357||passive addictions neonatal
|
|
D009357||substance withdrawal neonatal
|
|
D009357||substance withdrawals neonatal
|
|
D009357||syndrome neonatal abstinence
|
|
D009357||syndrome neonatal withdrawal
|
|
D009357||syndromes neonatal abstinence
|
|
D009357||syndromes neonatal withdrawal
|
|
D009357||withdrawal neonatal substance
|
|
D009357||withdrawal syndrome neonatal
|
|
D009357||withdrawal syndromes neonatal
|
|
D009366||neoplasm seeding
|
|
D009366||seeding neoplasm
|
|
D009365||neoplasm regression spontaneous
|
|
D009365||neoplasm remission spontaneous
|
|
D009365||regression spontaneous neoplasm
|
|
D009365||remission spontaneous neoplasm
|
|
D009365||spontaneous neoplasm regression
|
|
D009365||spontaneous neoplasm remission
|
|
C562938|156250||metachondromatosis
|
|
C562938|156250||metcds
|
|
D009364||neoplasm recurrence local
|
|
D009364||local neoplasm recurrence
|
|
D009364||local neoplasm recurrences
|
|
D009364||locoregional neoplasm recurrence
|
|
D009364||locoregional neoplasm recurrences
|
|
D009364||neoplasm recurrence locoregional
|
|
D009364||neoplasm recurrences local
|
|
D009364||neoplasm recurrences locoregional
|
|
D009364||recurrence local neoplasm
|
|
D009364||recurrence locoregional neoplasm
|
|
D009364||recurrences local neoplasm
|
|
D009364||recurrences locoregional neoplasm
|
|
D009362||neoplasm metastasis
|
|
D009362||metastases
|
|
D009362||metastases neoplasm
|
|
D009362||metastasis
|
|
D009362||metastasis neoplasm
|
|
D009362||neoplasm metastases
|
|
D009361||neoplasm invasiveness
|
|
D009361||invasion neoplasm
|
|
D009361||invasiveness neoplasm
|
|
D009361||neoplasm invasion
|
|
C535308|210200||3 methylcrotonyl coa carboxylase 1 deficiency
|
|
C535308|210200||3 alpha methylcrotonylglycinuria 1
|
|
C535308|210200||3 mcc deficiency
|
|
C535308|210200||3 methylcrotonyl coa carboxylase deficiency
|
|
C535308|210200||3 methylcrotonyl coenzyme a carboxylase deficiency
|
|
C535308|210200||3 methylcrotonylglycinuria
|
|
C535308|210200||3 methylcrotonylglycinuria i
|
|
C535308|210200||bmcc deficiency
|
|
C535308|210200||deficiency of methylcrotonoyl coa carboxylase
|
|
C535308|210200||mcc1 deficiency
|
|
C535308|210200||mcc deficiency
|
|
C535308|210200||mccd type 1
|
|
C535308|210200||methylcrotonoyl coa carboxylase 1 deficiency
|
|
C535308|210200||methylcrotonyl coa carboxylase deficiency
|
|
C535308|210200||methylcrotonylglycinuria type i
|
|
D009360||neoplastic cells circulating
|
|
D009360||cell circulating neoplastic
|
|
D009360||cell circulating tumor
|
|
D009360||cell embolic tumor
|
|
D009360||cell neoplasm circulating
|
|
D009360||cells circulating neoplastic
|
|
D009360||cells circulating tumor
|
|
D009360||cells embolic tumor
|
|
D009360||cells neoplasm circulating
|
|
D009360||circulating cells neoplasm
|
|
D009360||circulating neoplastic cell
|
|
D009360||circulating neoplastic cells
|
|
D009360||circulating tumor cell
|
|
D009360||circulating tumor cells
|
|
D009360||embolic tumor cell
|
|
D009360||embolic tumor cells
|
|
D009360||embolisms tumor
|
|
D009360||embolism tumor
|
|
D009360||neoplasm circulating cell
|
|
D009360||neoplasm circulating cells
|
|
D009360||neoplastic cell circulating
|
|
D009360||tumor cell circulating
|
|
D009360||tumor cell embolic
|
|
D009360||tumor cells circulating
|
|
D009360||tumor cells embolic
|
|
D009360||tumor embolism
|
|
D009360||tumor embolisms
|
|
C565173||coloboma uveal with cleft lip and palate and mental retardation
|
|
C537965||camfak syndrome
|
|
C537965||cataract microcephaly failure to thrive kyphoscoliosis
|
|
C537965||cataract microcephaly failure to thrive kyphoscoliosis syndrome
|
|
C536634||schizotaxia
|
|
C537966||campomelia cumming type
|
|
C537966||cervical lymphocele with bowed long bones
|
|
C537966||cumming syndrome
|
|
C536635||schlegelberger grote syndrome
|
|
C536635||syndrome with triphalangia of thumbs thrombasthenia glanzmann and deafness of internal ear
|
|
C536635||triphalangeal thumbs thrombocytopathy deafness
|
|
C537963||calvarial hyperostosis
|
|
C537963||isolated hyperostosis of the calvarium
|
|
C537964||camera marugo cohen syndrome
|
|
C536633||schisis association
|
|
C536633||midline development field defects
|
|
C537969||camptodactyly joint contractures and facial skeletal dysplasia
|
|
C536638||scholte syndrome
|
|
C536638||early balding patella luxation acromicria and hypogonadism
|
|
C565170||complement component c1s deficiency
|
|
C565170||c1s deficiency
|
|
C536639||schrander stumpel theunissen hulsmans syndrome
|
|
C536639||vitiligo psychomotor retardation cleft palate and facial dysmorphism
|
|
C536639||vitiligo vulgaris cleft palate somatic and psychomotor retardation and facial dysmorphism
|
|
C535305||2 hydroxyethyl methacrylate sensitization
|
|
C535305||sensitization to 2 hydroxyethyl methacrylate
|
|
D011671||pulpitis
|
|
D011671||endodontic inflammation
|
|
D011671||endodontic inflammations
|
|
D011671||inflammation endodontic
|
|
D011671||inflammations endodontic
|
|
D011671||pulpitides
|
|
C537967||camptobrachydactyly
|
|
C537967||short foot brachydactyly of toes camptodactyly brachydactyly
|
|
C565172||colonic varices without portal hypertension
|
|
D018288|182280||carcinoma small cell
|
|
D018288|182280||carcinoma oat cell
|
|
D018288|182280||carcinomas oat cell
|
|
D018288|182280||carcinomas small cell
|
|
D018288|182280||oat cell carcinoma
|
|
D018288|182280||oat cell carcinomas
|
|
D018288|182280||sccl
|
|
D018288|182280||sclc
|
|
D018288|182280||sclc1
|
|
D018288|182280||small cell carcinoma
|
|
D018288|182280||small cell carcinomas
|
|
C537968||camptocormia
|
|
C537968||bent spine
|
|
C537968||bent spine syndrome
|
|
C537968||camptocormism
|
|
C535307||2 methylacetoacetyl coa thiolase deficiency
|
|
C564907|260450||pancreatic insufficiency combined exocrine
|
|
C537980||canomad syndrome
|
|
C565177||stickler syndrome autosomal recessive col9a1 related
|
|
C565178||oi eds combined syndrome
|
|
C536653||penttinen aula syndrome
|
|
C536653||premature aging syndrome penttinen type
|
|
C565179||vitreoretinopathy with phalangeal epiphyseal dysplasia
|
|
C537981||cantalamessa baldini ambrosi syndrome
|
|
C537981||primary gonadal failure short stature mitral valve prolapse and mental retardation
|
|
C536650||penoscrotal transposition
|
|
C536650||congenital transposition of the penis
|
|
C536650||prepenile scrotum
|
|
C535322||5 oxoprolinase deficiency
|
|
C535322||5 alpha oxoprolinase deficiency
|
|
C535322||oxoprolinuria due to 5 oxoprolinase deficiency
|
|
C535322||oxoprolinuria due to oxoprolinase deficiency
|
|
C535321||5 nucleotidase syndrome
|
|
C535321||5 apos nucleotidase syndrome
|
|
C536050|166250||osteoglophonic dwarfism
|
|
C536050|166250||fairbank keats syndrome
|
|
C536050|166250||ogd
|
|
C536050|166250||osteoglophonic dysplasia
|
|
C563914|608545||larsen like syndrome
|
|
C563914|608545||lrsl
|
|
C562900|C536826|137950||glomerulopathy with giant fibrillar deposits
|
|
C562900|C536826|137950||glomerulopathy with fibronectin deposits 1
|
|
C562900|C536826|137950||lobular glomerulopathy familial
|
|
D008039||linitis plastica
|
|
D009369||neoplasms
|
|
D009369||benign neoplasm
|
|
D009369||benign neoplasms
|
|
D009369||cancer
|
|
D009369||other cancers
|
|
D009369||cancers
|
|
D009369||neoplasia
|
|
D009369||neoplasm
|
|
D009369||neoplasm benign
|
|
D009369||neoplasms benign
|
|
D009369||tumor
|
|
D009369||tumors
|
|
C562902||oligosynaptic infertility
|
|
C562902||oligochiasmic infertility
|
|
C562907||twenty nail dystrophy
|
|
C562907||onychodystrophy totalis isolated
|
|
D009378||neoplasms multiple primary
|
|
D009378||multiple primary neoplasm
|
|
D009378||multiple primary neoplasms
|
|
D009378||multiple primary neoplasms synchronous
|
|
D009378||neoplasm multiple primary
|
|
D009378||neoplasms synchronous
|
|
D009378||neoplasms synchronous multiple primary
|
|
D009378||neoplasm synchronous
|
|
D009378||primary neoplasm multiple
|
|
D009378||primary neoplasms multiple
|
|
D009378||synchronous multiple primary neoplasms
|
|
D009378||synchronous neoplasm
|
|
D009378||synchronous neoplasms
|
|
D011686||purine pyrimidine metabolism inborn errors
|
|
D009377||multiple endocrine neoplasia
|
|
D009377||adenomatoses familial endocrine
|
|
D009377||adenomatoses multiple endocrine
|
|
D009377||adenomatosis familial endocrine
|
|
D009377||adenomatosis multiple endocrine
|
|
D009377||adenopathies multiple endocrine
|
|
D009377||adenopathy multiple endocrine
|
|
D009377||endocrine adenomatoses familial
|
|
D009377||endocrine adenomatoses multiple
|
|
D009377||endocrine adenomatosis familial
|
|
D009377|131100|D018761||endocrine adenomatosis multiple
|
|
D009377||endocrine adenopathies multiple
|
|
D009377||endocrine adenopathy multiple
|
|
D009377||endocrine neoplasia multiple
|
|
D009377||endocrine neoplasms multiple
|
|
D009377||familial endocrine adenomatoses
|
|
D009377||familial endocrine adenomatosis
|
|
D009377||multiple endocrine adenomatoses
|
|
D009377||multiple endocrine adenomatosis
|
|
D009377||multiple endocrine adenopathies
|
|
D009377||multiple endocrine adenopathy
|
|
D009377||multiple endocrine neoplasia syndromes
|
|
D009377||multiple endocrine neoplasms
|
|
D009377||neoplasia multiple endocrine
|
|
D009377||neoplasms multiple endocrine
|
|
D008047||lip diseases
|
|
D008047||disease lip
|
|
D008047||diseases lip
|
|
D008047||lip disease
|
|
D009376||neoplasms hormone dependent
|
|
D009376||hormone dependent neoplasm
|
|
D009376||hormone dependent neoplasms
|
|
D009376||neoplasm hormone dependent
|
|
D009375||neoplasms glandular and epithelial
|
|
D009375||epithelial neoplasm
|
|
D009375||epithelial neoplasm glandular
|
|
D009375||epithelial neoplasms
|
|
D009375||epithelial neoplasms glandular
|
|
D009375||glandular and epithelial neoplasms
|
|
D009375||glandular epithelial neoplasm
|
|
D009375||glandular epithelial neoplasms
|
|
D009375||glandular neoplasm
|
|
D009375||glandular neoplasms
|
|
D009375||neoplasm epithelial
|
|
D009375||neoplasm glandular
|
|
D009375||neoplasm glandular epithelial
|
|
D009375||neoplasms epithelial
|
|
D009375||neoplasms glandular
|
|
D009375||neoplasms glandular epithelial
|
|
D009374||neoplasms experimental
|
|
D009374||experimental neoplasm
|
|
D009374||experimental neoplasms
|
|
D009374||neoplasm experimental
|
|
D009373||neoplasms germ cell and embryonal
|
|
D009373||cancer embryonal
|
|
D009373||cancer embryonal and mixed
|
|
D009373||cancer germ cell
|
|
D009373||cancers embryonal
|
|
D009373||cancers germ cell
|
|
D009373||embryonal cancer
|
|
D009373||embryonal cancers
|
|
D009373||embryonal neoplasm
|
|
D009373||embryonal neoplasms
|
|
D009373||germ cell and embryonal neoplasms
|
|
D009373||germ cell and embryonic neoplasms
|
|
D009373||germ cell cancer
|
|
D009373||germ cell cancers
|
|
D009373||germ cell neoplasms
|
|
D009373||germ cell tumor
|
|
D009373||germ cell tumors
|
|
D009373||neoplasm embryonal
|
|
D009373||neoplasms embryonal
|
|
D009373||neoplasms embryonal and mixed
|
|
D009373||neoplasms germ cell
|
|
D009373||neoplasms germ cell and embryonic
|
|
D009373||tumor germ cell
|
|
D009373||tumors germ cell
|
|
C562909||pseudoatrophoderma colli
|
|
D009372||neoplasms connective tissue
|
|
D009372||connective tissue neoplasm
|
|
D009372||connective tissue neoplasms
|
|
D009372||neoplasm connective tissue
|
|
D009371||neoplasms by site
|
|
D009371||neoplasms by sites
|
|
D009371||neoplasm site
|
|
D009371||neoplasm sites
|
|
D009371||site neoplasm
|
|
D009371||sites neoplasm
|
|
C537976||camptodactyly ichthyosis syndrome
|
|
C535313||3c syndrome
|
|
C535313||ccc dysplasia
|
|
C535313||craniocerebellocardiac dysplasia
|
|
C535313||dandy walker like malformation with atrioventricular septal defect
|
|
C535313||ritscher schinzel syndrome
|
|
D009370||neoplasms by histologic type
|
|
D009370||histological type of neoplasm
|
|
D009370||histological types of neoplasms
|
|
D009370||neoplasm histological type
|
|
D009370||neoplasm histological types
|
|
D009370||neoplasms by histological type
|
|
D009370||neoplasms histological type
|
|
D009370||neoplasms histological types
|
|
C537977||camptomelic syndrome long limb type
|
|
C537977||campomelic syndrome long limb type
|
|
C536646||pena shokeir syndrome type 2
|
|
C535312||3 hydroxyisobutyric aciduria
|
|
612529|C567279||amelogenesis imperfecta hypomaturation type iia2
|
|
612529|C567279||ai2a2
|
|
612529|C567279||amelogenesis imperfecta pigmented hypomaturation type 2
|
|
C537974||camptodactyly fibrous tissue hyperplasia and skeletal dysplasia
|
|
C537974||camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia
|
|
C562601|223100||lactose intolerance adult type
|
|
C562601|223100||adult lactase deficiency
|
|
C562601|223100||disaccharide intolerance iii
|
|
C562601|223100||disaccharide intolerance iii lactase persistence included
|
|
C562601|223100||hypolactasia adult type
|
|
C535315||4 hydroxyphenylacetic aciduria
|
|
D011681||pupil disorders
|
|
D011681||abnormal pupillary function
|
|
D011681||abnormal pupillary functions
|
|
D011681||afferent pupillary defect
|
|
D011681||afferent pupillary defects
|
|
D011681||anomalies pupillary
|
|
D011681||anomaly pupillary
|
|
D011681||argyll robertson pupil non syphilitic
|
|
D011681||deformed pupil
|
|
D011681||deformed pupils
|
|
D011681||ectopic pupil
|
|
D011681||ectopic pupils
|
|
D011681||efferent pupillary defect
|
|
D011681||efferent pupillary defects
|
|
D011681||fixed pupil
|
|
D011681||fixed pupils
|
|
D011681||hemianopic pupil wernicke
|
|
D011681||hemianopic pupil wernicke apos s
|
|
D011681||keyhole pupil
|
|
D011681||keyhole pupils
|
|
D011681||malformation pupil
|
|
D011681||malformations pupil
|
|
D011681||marcus gunn pupil
|
|
D011681||non syphilitic argyll robertson pupil
|
|
D011681||occluded pupil
|
|
D011681||occluded pupils
|
|
D011681||occlusion pupillary
|
|
D011681||occlusions pupillary
|
|
D011681||paralyses pupillary
|
|
D011681||paralyses pupillary sector
|
|
D011681||paralysis pupillary
|
|
D011681||paralysis pupillary sector
|
|
D011681||pupil deformed
|
|
D011681||pupil disorder
|
|
D011681||pupil ectopic
|
|
D011681||pupil fixed
|
|
D011681||pupil keyhole
|
|
D011681||pupillary anomalies
|
|
D011681||pupillary anomaly
|
|
D011681||pupillary defect afferent
|
|
D011681||pupillary defect efferent
|
|
D011681||pupillary defects afferent
|
|
D011681||pupillary defects efferent
|
|
D011681||pupillary disorder
|
|
D011681||pupillary disorders
|
|
D011681||pupillary function abnormal
|
|
D011681||pupillary functions abnormal
|
|
D011681||pupillary occlusion
|
|
D011681||pupillary occlusions
|
|
D011681||pupillary paralyses
|
|
D011681||pupillary paralysis
|
|
D011681||pupillary sector paralyses
|
|
D011681||pupillary sector paralysis
|
|
D011681||pupillary sphincter rupture
|
|
D011681||pupillary sphincter ruptures
|
|
D011681||pupil malformation
|
|
D011681||pupil malformations
|
|
D011681||pupil marcus gunn
|
|
D011681||pupil non syphilitic argyll robertson
|
|
D011681||pupil occluded
|
|
D011681||pupil reaction absent
|
|
D011681||pupils deformed
|
|
D011681||pupils ectopic
|
|
D011681||pupils fixed
|
|
D011681||pupils keyhole
|
|
D011681||pupils occluded
|
|
D011681||pupil wernicke hemianopic
|
|
D011681||pupil wernicke apos s hemianopic
|
|
D011681||reaction absent pupil
|
|
D011681||reaction absents pupil
|
|
D011681||rupture pupillary sphincter
|
|
D011681||ruptures pupillary sphincter
|
|
D011681||sector paralyses pupillary
|
|
D011681||sector paralysis pupillary
|
|
D011681||sector pupil palsy
|
|
D011681||sphincter rupture pupillary
|
|
D011681||sphincter ruptures pupillary
|
|
D011681||wernicke hemianopic pupil
|
|
D011681||wernicke apos s hemianopic pupil
|
|
D011681||wernickes hemianopic pupil
|
|
189960|C531835||esophageal atresia with or without tracheoesophageal fistula
|
|
189960|C531835||ea tef
|
|
189960|C531835||esophageal atresia tracheoesophageal fistula
|
|
189960|C531835||tracheoesophageal fistula with or without esophageal atresia
|
|
C536649||penis agenesis
|
|
C536649||agenesis of the penis
|
|
C536649||micropenis
|
|
C536649||penis agenesia
|
|
C535317||47 xyy syndrome
|
|
C535317||jacob apos s syndrome
|
|
C535317||xyy syndrome
|
|
C535317||yy syndrome
|
|
C535316||46 xx gonadal dysgenesis epibulbar dermoid
|
|
D053448||prostatism
|
|
C537978||camurati engelmann disease type 2
|
|
C537978||progressive diaphyseal dysplasia with striations of the bones
|
|
C535319||49 xxxxx syndrome
|
|
C535319||chromosome x pentasomy
|
|
C535319||chromosome xxxxx syndrome
|
|
C535319||pentasomy x
|
|
C535319||pentasomy x syndrome
|
|
C535319||penta x syndrome
|
|
D053447||channelopathies
|
|
D053447||channelopathy
|
|
C535318||triple x syndrome
|
|
C535318||47 xxx
|
|
C535318||47 xxx syndrome
|
|
C535318||super female
|
|
C535318||triple x chromosome syndrome
|
|
C535318||triple x female
|
|
C535318||triplo x syndrome
|
|
C535318||trisomy x
|
|
C535318||xxx syndrome
|
|
C565148||coxoauricular syndrome
|
|
C565149||spondylocostal dysostosis 4 autosomal dominant
|
|
C565149||costovertebral segmentation anomalies
|
|
C565144||craniorhiny
|
|
C566476||chromosome 17q21 31 deletion syndrome
|
|
C566476||17q21 31 deletion syndrome
|
|
C566476||17q21 31 microdeletion syndrome
|
|
C566476||chromosome 17q21 31 microdeletion syndrome
|
|
C566476||koolen de vries syndrome
|
|
C566476||koolen syndrome
|
|
C566476||microdeletion 17q21 31 syndrome
|
|
C566476||monosomy 17q21 31
|
|
C565147||cranioacrofacial syndrome
|
|
C563732|609340||spastic paraplegia 28 autosomal recessive
|
|
C563732|609340||spg28
|
|
148350|C536152||keratoderma palmoplantar deafness
|
|
148350|C536152||diffuse palmoplantar keratoderma with deafness
|
|
148350|C536152||focal palmoplantar keratoderma with sensorineural deafness
|
|
148350|C536152||hereditary palmoplantar keratoderma with deafness
|
|
148350|C536152||keratoderma palmoplantar with deafness
|
|
148350|C536152||palmoplantar keratoderma and sensorineural deafness
|
|
609053|C563802||fanconi anemia complementation group i
|
|
609053|C563802||fanci
|
|
D009336||necrosis
|
|
D009336||necroses
|
|
D009335||necrobiosis lipoidica
|
|
D009335||diabeticorum necrobiosis lipoidica
|
|
D009335||necrobiosis lipoidica diabeticorum
|
|
D011654||pulmonary edema
|
|
D011654||edema pulmonary
|
|
D011654||edemas pulmonary
|
|
D011654||lungs wet
|
|
D011654||lung wet
|
|
D011654||pulmonary edemas
|
|
D011654||wet lung
|
|
D011654||wet lungs
|
|
D012560|605419||schizophrenia catatonic
|
|
D012560|605419||catatonia periodic
|
|
D012560|605419||catatonic schizophrenia
|
|
D012560|605419||catatonic schizophrenias
|
|
D012560|605419||schizophrenia 10
|
|
D012560|605419||schizophrenias catatonic
|
|
D012560|605419||schizophrenia susceptibility locus chromosome 15q15 related
|
|
D012560|605419||sczd10
|
|
C537908||barber say syndrome
|
|
C537908||hypertrichosis atrophic skin ectropion and macrostomia
|
|
D010322||parvoviridae infections
|
|
D010322||infection parvoviridae
|
|
D010322||infection parvovirus
|
|
D010322||infections parvoviridae
|
|
D010322||infections parvovirus
|
|
D010322||parvoviridae infection
|
|
D010322||parvovirus infection
|
|
D010322||parvovirus infections
|
|
C537905||baraitser brett piesowicz syndrome
|
|
C537905||microcephaly intracranial calcification
|
|
D011656||pulmonary emphysema
|
|
D011656||centriacinar emphysema
|
|
D011656||centriacinar emphysemas
|
|
D011656||centrilobular emphysema
|
|
D011656||centrilobular emphysemas
|
|
D011656||emphysema centriacinar
|
|
D011656||emphysema centrilobular
|
|
D011656||emphysema focal
|
|
D011656||emphysema panacinar
|
|
D011656||emphysema panlobular
|
|
D011656||emphysema pulmonary
|
|
D011656||emphysemas centriacinar
|
|
D011656||emphysemas centrilobular
|
|
D011656||emphysemas focal
|
|
D011656||emphysemas panacinar
|
|
D011656||emphysemas panlobular
|
|
D011656||emphysemas pulmonary
|
|
D011656||focal emphysema
|
|
D011656||focal emphysemas
|
|
D011656||panacinar emphysema
|
|
D011656||panacinar emphysemas
|
|
D011656||panlobular emphysema
|
|
D011656||panlobular emphysemas
|
|
D011656||pulmonary emphysemas
|
|
C537906||baraitser rodeck garner syndrome
|
|
D010324||passive aggressive personality disorder
|
|
D010324||disorder negativistic personality
|
|
D010324||disorder passive aggressive personality
|
|
D010324||disorders negativistic personality
|
|
D010324||disorders passive aggressive personality
|
|
D010324||negativistic personality disorder
|
|
D010324||negativistic personality disorders
|
|
D010324||passive aggressive personalities
|
|
D010324||passive aggressive personality
|
|
D010324||passive aggressive personality disorders
|
|
D010324||personalities passive aggressive
|
|
D010324||personality disorder negativistic
|
|
D010324||personality disorder passive aggressive
|
|
D010324||personality disorders negativistic
|
|
D010324||personality disorders passive aggressive
|
|
D010324||personality passive aggressive
|
|
D011655||pulmonary embolism
|
|
D011655||embolism pulmonary
|
|
D011655||embolisms pulmonary
|
|
D011655||pulmonary embolisms
|
|
D011655||pulmonary thromboembolism
|
|
D011655||pulmonary thromboembolisms
|
|
D011655||thromboembolism pulmonary
|
|
D011655||thromboembolisms pulmonary
|
|
D011658||pulmonary fibrosis
|
|
D011658||alveolitides fibrosing
|
|
D011658||alveolitis fibrosing
|
|
D011658||fibroses pulmonary
|
|
D011658||fibrosing alveolitides
|
|
D011658||fibrosing alveolitis
|
|
D011658||fibrosis pulmonary
|
|
D011658||hamman rich syndrome
|
|
D011658||pulmonary fibroses
|
|
D011658||syndrome hamman rich
|
|
D010326||pasteurella infections
|
|
D010326||infection pasteurella
|
|
D010326||infections pasteurella
|
|
D010326||pasteurella infection
|
|
D010326||pasteurelloses
|
|
D010326||pasteurellosis
|
|
D011657||pulmonary eosinophilia
|
|
D011657||eosinophilia pulmonary
|
|
D011657||eosinophilias pulmonary
|
|
D011657||eosinophilic pneumonia
|
|
D011657||eosinophilic pneumonias
|
|
D011657||eosinophilic pneumonias tropical
|
|
D011657||eosinophilic pneumonia tropical
|
|
D011657||loeffler syndrome
|
|
D011657||pneumonia eosinophilic
|
|
D011657||pneumonias eosinophilic
|
|
D011657||pulmonary eosinophilias
|
|
D011657||pulmonary eosinophilia simple
|
|
D011657||simple pulmonary eosinophilia
|
|
D011657||simple pulmonary eosinophilias
|
|
D011657||syndrome loeffler
|
|
D011657||tropical eosinophilic pneumonia
|
|
D011657||tropical eosinophilic pneumonias
|
|
D008010||lichen planus
|
|
D008010||lichen ruber planus
|
|
D008010||lichen rubra planus
|
|
C537909||bardet biedl syndrome 1
|
|
604091|D052456||hypoalphalipoproteinemias
|
|
604091|D052456||alpha lipoprotein deficiency disease familial
|
|
604091|D052456||alpha lipoproteinemia hypo
|
|
604091|D052456||familial alpha lipoprotein deficiency disease
|
|
604091|D052456|C538394||familial hdl deficiency
|
|
604091|D052456||familial high density lipoprotein deficiency disease
|
|
604091|D052456||familial hypoalphalipoproteinemia
|
|
604091|D052456||familial hypoalphalipoproteinemias
|
|
604091|D052456||fha
|
|
604091|D052456||fhd
|
|
604091|D052456||hdlc
|
|
604091|D052456||hdl cholesterol low serum
|
|
604091|D052456||hdld
|
|
604091|D052456||hdl lipoprotein deficiency disease
|
|
604091|D052456|C538394||high density lipoprotein deficiency
|
|
604091|D052456||high density lipoprotein deficiency disease familial
|
|
604091|D052456||hypoalphalipoproteinemia
|
|
604091|D052456||hypo alpha lipoproteinemia
|
|
604091|D052456||hypoalphalipoproteinemia familial
|
|
604091|D052456||hypoalphalipoproteinemia primary
|
|
604091|D052456||hypo alpha lipoproteinemias
|
|
604091|D052456||hypoalphalipoproteinemias familial
|
|
604091|D052456||hypoalphalipoproteinemias primary
|
|
604091|D052456||lipoprotein deficiency disease hdl familial
|
|
604091|D052456||lipoproteinemia hypo alpha
|
|
604091|D052456||lipoproteinemias hypo alpha
|
|
604091|D052456||primary hypoalphalipoproteinemias
|
|
C537900||baker winegrad disease
|
|
C537900||autosomal recessive fructose 1 6 diphosphatase deficiency
|
|
C567438|612004||thrombocytopenia 4
|
|
C567438|612004||thc4
|
|
C567438|612004||thrombocytopenia autosomal dominant 4
|
|
C565153||coronary artery dissection spontaneous
|
|
C566484||brachydactyly coloboma and anterior segment dysgenesis
|
|
C537903||banti apos s syndrome
|
|
C537903||banti apos s disease
|
|
C537903||idiopathic congestive splenomegaly
|
|
C537903||idiopathic portal hypertension
|
|
C537904||bantu siderosis
|
|
C537904||african iron overload
|
|
C537904||hereditary iron overload and african americans
|
|
C537904||iron overload in africa
|
|
D012983||soft tissue neoplasms
|
|
D012983||neoplasm soft tissue
|
|
D012983||neoplasms soft tissue
|
|
D012983||soft tissue neoplasm
|
|
C566480||microphthalmia isolated with cataract 4
|
|
C566480||mcopct4
|
|
C565150||polydysspondyly
|
|
C566481||cataract lamellar 2
|
|
C537902||bangstad syndrome
|
|
C565155||epithelial recurrent erosion dystrophy
|
|
C565155||corneal erosions recurring hereditary
|
|
C565156||corneal endothelial dystrophy 1
|
|
C565157||corneal degeneration ribbonlike with deafness
|
|
C565157||band keratopathy with deafness
|
|
128230|C538007||dystonia dopa responsive
|
|
128230|C538007||dopa responsive dystonia
|
|
128230|C538007||dopa responsive dystonia autosomal dominant
|
|
128230|C538007||drd
|
|
128230|C538007||dystonia 5
|
|
128230|C538007||dystonia dopa responsive autosomal dominant
|
|
128230|C538007||dystonia parkinsonism with diurnal fluctuation
|
|
128230|C538007||dystonia progressive with diurnal variation
|
|
128230|C538007||dyt5
|
|
128230|C538007||hereditary progressive dystonia with marked diurnal fluctuation
|
|
128230|C538007||segawa syndrome autosomal dominant
|
|
193900|D053529||leukokeratosis hereditary mucosal
|
|
193900|D053529||hereditary mucosal leukokeratoses
|
|
193900|D053529||hereditary mucosal leukokeratosis
|
|
193900|D053529||leukokeratoses hereditary mucosal
|
|
193900|D053529||mucosal leukokeratoses hereditary
|
|
193900|D053529||mucosal leukokeratosis hereditary
|
|
193900|D053529||white sponge nevus 1
|
|
193900|D053529||white sponge nevus of cannon
|
|
193900|D053529||wsn1
|
|
D009349||nematode infections
|
|
D009349||infection nematode
|
|
D009349||infections nematode
|
|
D009349||nematode infection
|
|
D009347||nelson syndrome
|
|
C537918||femur fibula ulna syndrome
|
|
D011665||pulmonary valve insufficiency
|
|
D011665||incompetence pulmonary valve
|
|
D011665||insufficiency pulmonary valve
|
|
D011665||pulmonary regurgitation
|
|
D011665||pulmonary valve incompetence
|
|
D011665||pulmonary valve regurgitation
|
|
D011665||regurgitation pulmonary
|
|
D011665||regurgitation pulmonary valve
|
|
D011665||valve incompetence pulmonary
|
|
D011665||valve insufficiency pulmonary
|
|
D011665||valve regurgitation pulmonary
|
|
C537916||femoral facial syndrome
|
|
C537916||femoral dysgenesis bilateral
|
|
C537916||femoral dysgenesis bilateral robin anomaly
|
|
C537916||femoral hypoplasia unusual facies syndrome
|
|
C537917||femur bifid with monodactylous ectrodactyly
|
|
C537917||femur unilateral bifid with monodactylous ectrodactyly
|
|
C537917||gollop wolfgang complex
|
|
D010335||pathologic processes
|
|
D010335||pathological processes
|
|
D010335||processes pathologic
|
|
D010335||processes pathological
|
|
D011666||pulmonary valve stenosis
|
|
D011666||pulmonary stenose
|
|
D011666||pulmonary stenoses
|
|
D011666||pulmonary stenosis
|
|
D011666||pulmonary valve stenoses
|
|
D011666||pulmonic stenoses
|
|
D011666||pulmonic stenoses valvular
|
|
D011666||pulmonic stenosis
|
|
D011666||pulmonic stenosis valvular
|
|
D011666||stenose pulmonary
|
|
D011666||stenoses pulmonary
|
|
D011666||stenoses pulmonary valve
|
|
D011666||stenoses pulmonic
|
|
D011666||stenosis pulmonary
|
|
D011666||stenosis pulmonary valve
|
|
D011666||stenosis pulmonic
|
|
D011666||valvular pulmonic stenoses
|
|
D011666||valvular pulmonic stenosis
|
|
D010505|249100||familial mediterranean fever
|
|
D010505|249100||benign paroxysmal peritonitides
|
|
D010505|249100||benign paroxysmal peritonitis
|
|
D010505|249100||disease periodic
|
|
D010505|249100||diseases periodic
|
|
D010505|249100||disease wolff periodic
|
|
D010505|249100||disease wolff apos s periodic
|
|
D010505|249100||familial mediterranean fever autosomal recessive
|
|
D010505|249100||familial paroxysmal polyserositides
|
|
D010505|249100||familial paroxysmal polyserositis
|
|
D010505|249100||fmf
|
|
D010505|249100||mediterranean fever familial
|
|
D010505|249100||paroxysmal peritonitides benign
|
|
D010505|249100||paroxysmal peritonitis benign
|
|
D010505|249100||paroxysmal polyserositides familial
|
|
D010505|249100||paroxysmal polyserositis familial
|
|
D010505|249100||periodic disease
|
|
D010505|249100||periodic diseases
|
|
D010505|249100||periodic disease wolff
|
|
D010505|249100||periodic disease wolffs
|
|
D010505|249100||periodic disease wolff apos s
|
|
D010505|249100||periodic peritonitides
|
|
D010505|249100||periodic peritonitis
|
|
D010505|249100||peritonitides benign paroxysmal
|
|
D010505|249100||peritonitides periodic
|
|
D010505|249100||peritonitis benign paroxysmal
|
|
D010505|249100||peritonitis periodic
|
|
D010505|249100||polyserositides familial paroxysmal
|
|
D010505|249100||polyserositides recurrent
|
|
D010505|249100||polyserositis familial paroxysmal
|
|
D010505|249100||polyserositis recurrent
|
|
D010505|249100||recurrent polyserositides
|
|
D010505|249100||recurrent polyserositis
|
|
D010505|249100||wolff periodic disease
|
|
D010505|249100||wolff apos s periodic disease
|
|
D010505|249100||wolffs periodic disease
|
|
C537910||bardet biedl syndrome 2
|
|
C537911||bardet biedl syndrome 3
|
|
C565164||epilepsy benign neonatal 1
|
|
C565164||convulsions benign familial neonatal 1
|
|
C537303|609227||griscelli syndrome type 3
|
|
C537303|609227||gs3
|
|
C537303|609227||hypomelanosis with no immunologic or neurologic manifestations
|
|
C565165|613825||c9 deficiency
|
|
C565165|613825||complement component 9 deficiency
|
|
D011660||pulmonary heart disease
|
|
D011660||cor pulmonale
|
|
D011660||disease pulmonary heart
|
|
D011660||diseases pulmonary heart
|
|
D011660||heart disease pulmonary
|
|
D011660||heart diseases pulmonary
|
|
D011660||pulmonary heart diseases
|
|
C565160||delayed cranial ossification due to cbfb haploinsufficiency
|
|
C537912||bardet biedl syndrome 4
|
|
C565161||coracoclavicular joint anomalous
|
|
D011662||pulmonary subvalvular stenosis
|
|
D011662||conus obstructive subaortic
|
|
D011662||infundibular stenoses pulmonary
|
|
D011662||infundibular stenosis pulmonary
|
|
D011662||obstructive subaortic conus
|
|
D011662||pulmonary infundibular stenoses
|
|
D011662||pulmonary infundibular stenosis
|
|
D011662||pulmonary stenoses subvalvular
|
|
D011662||pulmonary stenosis subvalvular
|
|
D011662||pulmonary subvalvular stenoses
|
|
D011662||stenoses pulmonary infundibular
|
|
D011662||stenoses pulmonary subvalvular
|
|
D011662||stenoses subvalvular pulmonary
|
|
D011662||stenosis pulmonary infundibular
|
|
D011662||stenosis pulmonary subvalvular
|
|
D011662||stenosis subvalvular pulmonary
|
|
D011662||subaortic conus obstructive
|
|
D011662||subvalvular pulmonary stenoses
|
|
D011662||subvalvular pulmonary stenosis
|
|
D011662||subvalvular stenoses pulmonary
|
|
D011662||subvalvular stenosis pulmonary
|
|
C565126||darier disease segmental
|
|
C566457||short stature and facioauriculothoracic malformations
|
|
C567789||basal cell carcinoma nonsyndromic
|
|
C565127||phenacetin o deethylase deficiency of
|
|
C563999|600105||retinitis pigmentosa 12
|
|
C563999|600105||retinitis pigmentosa with or without paraarteriolar preservation of retinal pigment epithelium
|
|
C563999|600105||rp12
|
|
C563999|600105||rp with or without pprpe
|
|
C563999|600105||rp with or without preserved paraarteriole retinal pigment epithelium
|
|
C565122||deafness mid tone neural
|
|
218400|C536570||craniometaphyseal dysplasia autosomal recessive type
|
|
218400|C536570||cmdr
|
|
218400|C536570||craniometaphyseal dysplasia autosomal recessive
|
|
C565123||deafness conductive stapedial with ear malformation and facial palsy
|
|
C565125||darier disease acral hemorrhagic type
|
|
C567786||prostaglandin endoperoxide synthase 1 deficiency platelet
|
|
C567786||pghs1 deficiency
|
|
C567786||platelet cox1 deficiency
|
|
C567786||platelet cyclooxygenase 1 deficiency
|
|
D000987||antisocial personality disorder
|
|
D000987||antisocial personalities
|
|
D000987||antisocial personality
|
|
D000987||antisocial personality disorders
|
|
D000987||behavior dyssocial
|
|
D000987||behaviors dyssocial
|
|
D000987||disorder antisocial personality
|
|
D000987||disorders antisocial personality
|
|
D000987||dyssocial behavior
|
|
D000987||dyssocial behaviors
|
|
D000987||personalities antisocial
|
|
D000987||personalities psychopathic
|
|
D000987||personalities sociopathic
|
|
D000987||personality antisocial
|
|
D000987||personality disorder antisocial
|
|
D000987||personality disorders antisocial
|
|
D000987||personality psychopathic
|
|
D000987||personality sociopathic
|
|
D000987||psychopathic personalities
|
|
D000987||psychopathic personality
|
|
D000987||sociopathic personalities
|
|
D000987||sociopathic personality
|
|
C567861|612932||glycogen storage disease xiii
|
|
C567861|612932||enolase 3 deficiency
|
|
C567861|612932||enolase beta deficiency
|
|
C567861|612932||gsd13
|
|
C567861|612932||gsd xiii
|
|
D010309||parotitis
|
|
D010309||parotiditides
|
|
D010309||parotiditis
|
|
D010309||parotitides
|
|
272750|D049290||tay sachs disease ab variant
|
|
272750|D049290||ab variant gangliosidosis gm2
|
|
272750|D049290||ab variant gm2 gangliosidoses
|
|
272750|D049290||ab variant gm2 gangliosidosis
|
|
272750|D049290||activator deficiencies gm2
|
|
272750|D049290||activator deficiencies hexosaminidase
|
|
272750|D049290||activator deficiency gm2
|
|
272750|D049290||activator deficiency gm2 gangliosidosis
|
|
272750|D049290||activator deficiency hexosaminidase
|
|
272750|D049290||activator deficient tay sachs disease
|
|
272750|D049290||activator deficient tay sachs diseases
|
|
272750|D049290||deficiencies gm2 activator
|
|
272750|D049290||deficiencies hexosaminidase activator
|
|
272750|D049290||deficiency disease gm2 protein activator
|
|
272750|D049290||deficiency gm2 activator
|
|
272750|D049290||deficiency hexosaminidase activator
|
|
272750|D049290||disease activator deficient tay sachs
|
|
272750|D049290||diseases activator deficient tay sachs
|
|
272750|D049290||gangliosidosis gm2 ab variant
|
|
272750|D049290||gangliosidosis gm2 type ab
|
|
272750|D049290||gm2 activator deficiencies
|
|
272750|D049290||gm2 activator deficiency
|
|
272750|D049290||gm2 activator deficiency disease
|
|
272750|D049290||gm2 gangliosidoses ab variant
|
|
272750|D049290||gm2 gangliosidosis ab variant
|
|
272750|D049290||gm2 gangliosidosis type ab
|
|
272750|D049290||gm2 protein activator deficiency disease
|
|
272750|D049290||hexosaminidase activator deficiencies
|
|
272750|D049290||hexosaminidase activator deficiency
|
|
272750|D049290||hexosaminidase activator protein deficiency disease
|
|
272750|D049290||tay sachs disease activator deficient
|
|
272750|D049290||tay sachs diseases activator deficient
|
|
272750|D049290||variant gm2 gangliosidoses ab
|
|
272750|D049290||variant gm2 gangliosidosis ab
|
|
C567467|300719||deafness cataract retinitis pigmentosa and sperm abnormalities
|
|
C537929||fibromuscular dysplasia of arteries
|
|
D010301||parkinson disease postencephalitic
|
|
D010301||economo type parkinsonism postencephalitic
|
|
D010301||encephalitis lethargica type parkinsonism
|
|
D010301||meningoencephalitic parkinsonism viral
|
|
D010301||parkinson disease post encephalitic
|
|
D010301||parkinsonian syndrome postencephalitis
|
|
D010301||parkinsonism postencephalitic
|
|
D010301||parkinsonism postencephalitic economo type
|
|
D010301||parkinsonisms viral meningoencephalitic
|
|
D010301||parkinsonism viral meningoencephalitic
|
|
D010301||postencephalitic economo type parkinsonism
|
|
D010301||postencephalitic parkinson disease
|
|
D010301||post encephalitic parkinson disease
|
|
D010301||postencephalitic parkinsonism
|
|
D010301||postencephalitis parkinsonian syndrome
|
|
D010301||viral meningoencephalitic parkinsonism
|
|
D010301||von economo encephalitis type parkinsonism
|
|
D010300||parkinson disease
|
|
D010300||idiopathic parkinson disease
|
|
D010300||idiopathic parkinson apos s disease
|
|
D010300||lewy body parkinson disease
|
|
D010300||lewy body parkinson apos s disease
|
|
D010300||paralysis agitans
|
|
D010300||parkinson disease idiopathic
|
|
D010300||parkinsonism primary
|
|
D010300||parkinson apos s disease
|
|
D010300||parkinson apos s disease idiopathic
|
|
D010300||parkinson apos s disease lewy body
|
|
D010300||primary parkinsonism
|
|
309630||mf4
|
|
C537927||fibrocartilaginous embolism
|
|
C537927||embolism fibrocartilaginous
|
|
D010302||parkinson disease secondary
|
|
D010302||atherosclerotic parkinsonism
|
|
D010302||parkinson disease secondary vascular
|
|
D010302||parkinson disease symptomatic
|
|
D010302||parkinsonism atherosclerotic
|
|
D010302||parkinsonism secondary
|
|
D010302||parkinsonism symptomatic
|
|
D010302||secondary parkinson disease
|
|
D010302||secondary parkinsonism
|
|
D010302||secondary vascular parkinson disease
|
|
D010302||symptomatic parkinson disease
|
|
D010302||symptomatic parkinsonism
|
|
D010305||parotid diseases
|
|
D010305||disease parotid
|
|
D010305||diseases parotid
|
|
D010305||parotid disease
|
|
D010304||paronychia
|
|
D010304||paronychias
|
|
D010307||parotid neoplasms
|
|
D010307||cancer of parotid
|
|
D010307||cancer of the parotid
|
|
D010307||cancer parotid
|
|
D010307||cancers parotid
|
|
D010307||neoplasm parotid
|
|
D010307||neoplasms parotid
|
|
D010307||parotid cancer
|
|
D010307||parotid cancers
|
|
D010307||parotid neoplasm
|
|
C538285|115665||cataract congenital volkmann type
|
|
C538285|115665||cataract 8 multiple types
|
|
C538285|115665||ccv
|
|
C538285|115665||ctrct8
|
|
C537921||fetal akinesia syndrome x linked
|
|
C537921||brain malformation growth retardation hypokinesia and polyhydramnios
|
|
C537921||holmes benacerraf syndrome
|
|
C537921||x linked form of fetal akinesia syndrome
|
|
C565130||cataract progressive polymorphic cortical
|
|
C537922||fetal hydantoin syndrome
|
|
C537922||dilantin embryopathy
|
|
C537922||phenytoin embryopathy
|
|
C565131|115700||cataract punctate progressive juvenile onset
|
|
C565132||cataract variable zonular pulverulent
|
|
C536858|275900||spastic paraplegia 20 autosomal recessive
|
|
C536858|275900||cross mckusick syndrome
|
|
C536858|275900||spastic paraparesis childhood onset with distal muscle wasting
|
|
C536858|275900||spastic paraplegia autosomal recessive troyer type
|
|
C536858|275900||spastic paraplegia with distal muscle wasting
|
|
C536858|275900||spg20
|
|
C536858|275900||troyer syndrome
|
|
C565137||cataract autosomal dominant nuclear
|
|
241850|C537901||bamforth syndrome
|
|
241850|C537901||bamforth lazarus syndrome
|
|
241850|C537901||bamforth lazarus syndrome hypothyroidism thyroidal with spiky hair and cleft palate included
|
|
241850|C537901||hypothyroidism athyroidal with spiky hair and cleft palate
|
|
241850|C537901||hypothyroidism cleft palate
|
|
241850|C537901||hypothyroidism thyroidal with spiky hair and cleft palate
|
|
C565138||cryptophthalmos unilateral or bilateral isolated
|
|
C565138||ankyloblepharon simple
|
|
C565138||cryptophthalmos with microphthalmia and peters anomaly
|
|
C565134||cataract posterior polar 2
|
|
C537940||chromosome 8 mosaic trisomy
|
|
C537940||trisomy 8 mosaicism
|
|
C537940||uniparental disomy of 8
|
|
C565135||cataract zonular central nuclear
|
|
C565136|604219|C565815||cataract autosomal recessive congenital 1
|
|
C566483|610024||retinal cone dystrophy 3a
|
|
C566483|610024||achm6 included
|
|
C566483|610024||cone dystrophy with night blindness and supernormal rod responses pde6h related
|
|
C566483|610024||cone dystrophy with night blindness and supernormal rod responses pde6h related achromatopsia 6 included
|
|
C566483|610024||rcd3a
|
|
D010319||parturient paresis
|
|
D010319||animal milk fever
|
|
D010319||fever animal milk
|
|
D010319||milk fever animal
|
|
D010319||pareses parturient
|
|
D010319||paresis parturient
|
|
D010319||parturient pareses
|
|
D064128||nodding syndrome
|
|
D064128||nodding syndromes
|
|
D064128||syndrome nodding
|
|
D064128||syndromes nodding
|
|
D009325||nausea
|
|
D064129||prostatic neoplasms castration resistant
|
|
D064129||androgen independent prostatic cancer
|
|
D064129||androgen independent prostatic cancers
|
|
D064129||androgen independent prostatic neoplasm
|
|
D064129||androgen independent prostatic neoplasms
|
|
D064129||androgen insensitive prostatic cancer
|
|
D064129||androgen insensitive prostatic cancers
|
|
D064129||androgen insensitive prostatic neoplasm
|
|
D064129||androgen insensitive prostatic neoplasms
|
|
D064129||androgen resistant prostatic cancer
|
|
D064129||androgen resistant prostatic cancers
|
|
D064129||androgen resistant prostatic neoplasm
|
|
D064129||androgen resistant prostatic neoplasms
|
|
D064129||cancer androgen independent prostatic
|
|
D064129||cancer androgen insensitive prostatic
|
|
D064129||cancer androgen resistant prostatic
|
|
D064129||cancer castration resistant prostatic
|
|
D064129||cancers androgen independent prostatic
|
|
D064129||cancers androgen insensitive prostatic
|
|
D064129||cancers androgen resistant prostatic
|
|
D064129||cancers castration resistant prostatic
|
|
D064129||castration resistant prostatic cancer
|
|
D064129||castration resistant prostatic cancers
|
|
D064129||castration resistant prostatic neoplasm
|
|
D064129||castration resistant prostatic neoplasms
|
|
D064129||hormone refractory prostatic cancer
|
|
D064129||hormone refractory prostatic neoplasms
|
|
D064129||neoplasm androgen independent prostatic
|
|
D064129||neoplasm androgen insensitive prostatic
|
|
D064129||neoplasm androgen resistant prostatic
|
|
D064129||neoplasm castration resistant prostatic
|
|
D064129||neoplasms androgen independent prostatic
|
|
D064129||neoplasms androgen insensitive prostatic
|
|
D064129||neoplasms androgen resistant prostatic
|
|
D064129||neoplasms castration resistant prostatic
|
|
D064129||prostatic cancer androgen independent
|
|
D064129||prostatic cancer androgen insensitive
|
|
D064129||prostatic cancer androgen resistant
|
|
D064129||prostatic cancer castration resistant
|
|
D064129||prostatic cancer hormone refractory
|
|
D064129||prostatic cancers androgen independent
|
|
D064129||prostatic cancers androgen insensitive
|
|
D064129||prostatic cancers androgen resistant
|
|
D064129||prostatic cancers castration resistant
|
|
D064129||prostatic neoplasm androgen independent
|
|
D064129||prostatic neoplasm androgen insensitive
|
|
D064129||prostatic neoplasm androgen resistant
|
|
D064129||prostatic neoplasm castration resistant
|
|
D064129||prostatic neoplasms androgen independent
|
|
D064129||prostatic neoplasms androgen insensitive
|
|
D064129||prostatic neoplasms androgen resistant
|
|
D064129||prostatic neoplasms hormone refractory
|
|
C536609||familial capillaro venous leptomeningeal angiomatosis
|
|
C537938||fitzsimmons guilbert syndrome
|
|
C537938||fitzsimmons syndrome
|
|
C537938||spastic paraplegia associated with brachydactyly type e
|
|
D011645||puerperal infection
|
|
D011645||infection puerperal
|
|
D011645||infections puerperal
|
|
D011645||puerperal infections
|
|
D009332||necatoriasis
|
|
D009332||necatoriases
|
|
C537939||boudhina yedes khiari syndrome
|
|
C536608||fallot complex with severe mental and growth retardation
|
|
C536608||bindewald ulmer muller syndrome
|
|
D011644||puerperal disorders
|
|
D011644||disorder puerperal
|
|
D011644||disorders puerperal
|
|
D011644||puerperal disorder
|
|
C537218|268700||saccharopinuria
|
|
C537218|268700|D020167|238700||alpha aminoadipic semialdehyde synthase deficiency
|
|
C537218|268700||hyperlysinemia type ii
|
|
C537218|268700||saccharopine dehydrogenase deficiency
|
|
C554497||non aids related kaposi sarcoma
|
|
D011649||pulmonary alveolar proteinosis
|
|
D011649||alveolar proteinoses pulmonary
|
|
D011649||alveolar proteinosis pulmonary
|
|
D011649||proteinoses pulmonary alveolar
|
|
D011649||proteinosis pulmonary alveolar
|
|
D011649||pulmonary alveolar proteinoses
|
|
D011648||pulmonary adenomatosis ovine
|
|
D011648||adenomatoses ovine pulmonary
|
|
D011648||adenomatoses pulmonary ovine
|
|
D011648||adenomatosis ovine pulmonary
|
|
D011648||adenomatosis pulmonary ovine
|
|
D011648||carcinoma ovine pulmonary
|
|
D011648||carcinomas ovine pulmonary
|
|
D011648||jaagsiekte
|
|
D011648||ovine adenomatoses pulmonary
|
|
D011648||ovine adenomatosis pulmonary
|
|
D011648||ovine pulmonary adenomatoses
|
|
D011648||ovine pulmonary adenomatosis
|
|
D011648||ovine pulmonary carcinoma
|
|
D011648||ovine pulmonary carcinomas
|
|
D011648||pulmonary adenomatoses ovine
|
|
D011648||pulmonary carcinoma ovine
|
|
D011648||pulmonary carcinomas ovine
|
|
D011648||pulmonary ovine adenomatoses
|
|
D011648||pulmonary ovine adenomatosis
|
|
C554498||aids related kaposi sarcoma
|
|
C565140||cryptotia familial
|
|
D053489||mink viral enteritis
|
|
D053489||enteritides mink viral
|
|
D053489||enteritis infectious of mink
|
|
D053489||enteritis mink viral
|
|
D053489||mink viral enteritides
|
|
D053489||viral enteritides mink
|
|
D053489||viral enteritis mink
|
|
C565141||cryoglobulinemia familial mixed
|
|
C565141||meltzer syndrome
|
|
C537933||fine lubinsky syndrome
|
|
C537933||brachycephaly deafness cataract and mental retardation
|
|
C537933||brachycephaly deafness cataract microstomia and mental retardation
|
|
C565142||cryofibrinogenemia familial primary
|
|
C537930||fibular aplasia ectrodactyly
|
|
C537930||brachydactyly ectrodactyly with fibular aplasia or hypoplasia
|
|
C565143||creutzfeldt jakob disease sporadic
|
|
C537987|607734||charcot marie tooth disease type 1f
|
|
C537987|607734||charcot marie tooth disease demyelinating type 1f
|
|
C537987|607734||charcot marie tooth neuropathy type 1f
|
|
C537987|607734||cmt1f
|
|
C537987|607734||cmt 1f
|
|
C537936||fitz hugh curtis syndrome
|
|
C537936||gonococcal perihepatitis
|
|
C537936||perihepatitis syndrome
|
|
C537937||fitzsimmons walson mellor syndrome
|
|
C536606||amelogenesis imperfecta hypomaturation type
|
|
D010310||parovarian cyst
|
|
D010310||cyst paratubal
|
|
D010310||cyst parovarian
|
|
D010310||cysts paratubal
|
|
D010310||cysts parovarian
|
|
D010310||hydatid cyst of morgagni
|
|
D010310||hydatid of morgagni
|
|
D010310||morgagni hydatid
|
|
D010310||morgagni hydatid cyst
|
|
D010310||morgagni hydatid cysts
|
|
D010310||morgagni hydatids
|
|
D010310||paratubal cyst
|
|
D010310||paratubal cysts
|
|
D010310||parovarian cysts
|
|
C566314||adenosine deaminase elevated hemolytic anemia due to
|
|
C566311||adenosine triphosphatase deficiency anemia due to
|
|
C531690|D053579|263800||potassium and magnesium depletion
|
|
C567644||chondrodysplasia megarbane dagher melki type
|
|
C531691||platelet granule deficiency disorder
|
|
D010409||penile diseases
|
|
D010409||disease penile
|
|
D010409||disease penis
|
|
D010409||diseases penile
|
|
D010409||diseases penis
|
|
D010409||penile disease
|
|
D010409||penis disease
|
|
D010409||penis diseases
|
|
C566319||acropectorovertebral dysplasia f form
|
|
C566319|102510||acrpv
|
|
128235|C538001||dystonia 12
|
|
128235|C538001||dystonia parkinsonism rapid onset
|
|
128235|C538001||dyt12
|
|
128235|C538001||rapid onset dystonia parkinsonism
|
|
128235|C538001||rdp
|
|
D009422||nervous system diseases
|
|
D009422||disease nervous system
|
|
D009422||diseases nervous system
|
|
D009422||disorder nervous system
|
|
D009422||disorder neurologic
|
|
D009422||disorder neurological
|
|
D009422||disorders nervous system
|
|
D009422||disorders neurologic
|
|
D009422||disorders neurological
|
|
D009422||nervous system disease
|
|
D009422||nervous system disorder
|
|
D009422||nervous system disorders
|
|
D009422||neurological disorder
|
|
D009422||neurological disorders
|
|
D009422||neurologic disorder
|
|
D009422||neurologic disorders
|
|
D009421||nervous system malformations
|
|
D009421||abnormalities congenital nervous system
|
|
D009421||abnormalities nervous system
|
|
D009421||abnormality nervous system
|
|
D009421||anomalies nervous system
|
|
D009421||anomaly nervous system
|
|
D009421||congenital abnormalities nervous system
|
|
D009421||congenital anomalies nervous system
|
|
D009421||congenital malformations nervous system
|
|
D009421||cranioschises
|
|
D009421||cranioschisis
|
|
D009421||malformation nervous system
|
|
D009421||malformations nervous system
|
|
D009421||malformations nervous system congenital
|
|
D009421||nervous system abnormalities
|
|
D009421||nervous system abnormality
|
|
D009421||nervous system anomalies
|
|
D009421||nervous system anomaly
|
|
D009421||nervous system congenital abnormalities
|
|
D009421||nervous system congenital malformations
|
|
D009421||nervous system malformation
|
|
D009421||nervous system malformations congenital
|
|
C581942||hemoglobin m disease
|
|
C536657|142680||periodic fever familial autosomal dominant
|
|
C536657|142680||autosomal dominant familial periodic fever
|
|
C536657|142680||familial hibernian fever
|
|
C536657|142680||fhf
|
|
C536657|142680||fpf
|
|
C536657|142680||hibernian familial fever
|
|
C536657|142680||hibernian fever familial
|
|
C536657|142680||tnf receptor associated periodic syndrome
|
|
C536657|142680||traps
|
|
C536657|142680||tumor necrosis factor receptor associated periodic syndrome
|
|
604588||never in mitosis gene a related kinase 1
|
|
604588||kiaa1901
|
|
604588||nek1
|
|
604588||nima related kinase 1
|
|
C531684||hereditary spinal ataxia
|
|
C563716|609456||muscular dystrophy congenital merosin positive
|
|
C531689||acute cerebral gaucher disease
|
|
C566325||saethre chotzen syndrome with eyelid anomalies
|
|
C567657||pitt hopkins like syndrome 1
|
|
C567657||pthsl1
|
|
C566327||vogt cephalodactyly
|
|
C567658||polymicrogyria asymmetric
|
|
C566321||pituitary adenoma familial isolated
|
|
C566321||pituitary adenoma predisposition
|
|
C565708|610189||senior loken syndrome 6
|
|
C565708|610189||slsn6
|
|
C566322||acroleukopathy symmetric
|
|
C566323||acrokeratoderma hereditary papulotranslucent
|
|
C536984|610156||morm syndrome
|
|
C536984|610156||mental retardation truncal obesity retinal dystrophy and micropenis
|
|
C565297|605750||exudative vitreoretinopathy 3
|
|
C565297|605750||evr3
|
|
D009423||nervous system neoplasms
|
|
D009423||neoplasm nervous system
|
|
D009423||neoplasms nervous system
|
|
D009423||nervous system neoplasm
|
|
D009423||nervous system tumor
|
|
D009423||nervous system tumors
|
|
D009423||tumor nervous system
|
|
D009423||tumors nervous system
|
|
D009423||tumors of the nervous system
|
|
D010411||penile induration
|
|
D010411||cavernitides fibrous
|
|
D010411||cavernitis fibrous
|
|
D010411||fibromatosis penile
|
|
D010411||fibrous cavernitides
|
|
D010411||fibrous cavernitis
|
|
D010411||penile fibromatosis
|
|
D010411||peyronie disease
|
|
D010411||peyronie apos s disease
|
|
D010411||peyronies disease
|
|
D010411||plastic induration of the penis
|
|
D008101||liver abscess amebic
|
|
D008101||abscess amebic hepatic
|
|
D008101||abscess amebic liver
|
|
D008101||abscess amoebic hepatic
|
|
D008101||abscess amoebic liver
|
|
D008101||abscesses amebic liver
|
|
D008101||abscesses amoebic hepatic
|
|
D008101||abscesses amoebic liver
|
|
D008101||abscess hepatic amebic
|
|
D008101||abscess liver amebic
|
|
D008101||amebiasis hepatic
|
|
D008101||amebic liver abscess
|
|
D008101||amebic liver abscesses
|
|
D008101||amoebiasis hepatic
|
|
D008101||amoebic hepatic abscess
|
|
D008101||amoebic hepatic abscesses
|
|
D008101||amoebic liver abscess
|
|
D008101||amoebic liver abscesses
|
|
D008101||entamoebiases hepatic
|
|
D008101||entamoebiasis hepatic
|
|
D008101||hepatic abscess amoebic
|
|
D008101||hepatic abscesses amoebic
|
|
D008101||hepatic amebiasis
|
|
D008101||hepatic amoebiasis
|
|
D008101||hepatic entamoebiases
|
|
D008101||hepatic entamoebiasis
|
|
D008101||liver abscess amoebic
|
|
D008101||liver abscesses amebic
|
|
D008101||liver abscesses amoebic
|
|
D010412||penile neoplasms
|
|
D010412||cancer of penis
|
|
D010412||cancer of the penis
|
|
D010412||cancer penile
|
|
D010412||cancer penis
|
|
D010412||cancers penile
|
|
D010412||cancers penis
|
|
D010412||neoplasm penile
|
|
D010412||neoplasm penis
|
|
D010412||neoplasms penile
|
|
D010412||neoplasms penis
|
|
D010412||penile cancer
|
|
D010412||penile cancers
|
|
D010412||penile neoplasm
|
|
D010412||penis cancer
|
|
D010412||penis cancers
|
|
D010412||penis neoplasm
|
|
D010412||penis neoplasms
|
|
D008100||liver abscess
|
|
D008100||abscesses hepatic
|
|
D008100||abscesses liver
|
|
D008100||abscess hepatic
|
|
D008100||abscess liver
|
|
D008100||hepatic abscess
|
|
D008100||hepatic abscesses
|
|
D008100||liver abscesses
|
|
C565329|605428||deafness autosomal recessive 26
|
|
C565329|605428||dfnb26
|
|
D047708||myofibroma
|
|
D047708||myofibromas
|
|
C535309|210210||3 methylcrotonyl coa carboxylase 2 deficiency
|
|
C535309|210210||3 alpha methylcrotonyl coa carboxylase 2 deficiency
|
|
C535309|210210||3 alpha methylcrotonylglycinuria 2
|
|
C535309|210210||3 methylcrotonylglycinuria ii
|
|
C535309|210210||mcc2 deficiency
|
|
C535309|210210||methylcrotonoyl coa carboxylase 2 deficiency
|
|
C535309|210210||methylcrotonylglycinuria type 2
|
|
C535309|210210||methylcrotonylglycinuria type ii
|
|
D058497|219000||fraser syndrome
|
|
D058497|219000||cryptophthalmos syndactyly syndrome
|
|
D058497|219000||cryptophthalmos syndactyly syndromes
|
|
D058497|219000||cryptophthalmos with other malformations
|
|
D058497|219000||cryptophthalmos with other malformations cryptophthalmos syndactyly syndrome included
|
|
D058497|219000||syndrome cryptophthalmos syndactyly
|
|
D058497|219000||syndrome fraser
|
|
C567661||progeria syndrome childhood onset
|
|
C531698||intestinal helminthiasis
|
|
C531699||hb c disease
|
|
C567624||mitochondrial dna depletion syndrome encephalomyopathic form with methylmalonic aciduria autosomal recessive
|
|
C567626||chromosome 3q29 duplication syndrome
|
|
C567626||microduplication 3q29 syndrome
|
|
C567620||vertigo benign recurrent 1
|
|
C567762|613090||bartter syndrome type 4b
|
|
C567762|613090||bartter syndrome infantile with sensorineural deafness
|
|
123320||creatine phosphokinase elevated serum
|
|
123320||cpk elevated serum
|
|
123320||hyperckemia idiopathic
|
|
C567627||musician apos s dystonia
|
|
D009400||nephrosclerosis
|
|
D009400||nephroscleroses
|
|
D011711||pyoderma
|
|
D011711||pyodermas
|
|
C566304||alpha 2 macroglobulin deficiency
|
|
C563676|610359||retinitis pigmentosa 33
|
|
C563676|610359||rp33
|
|
C566305||dysalbuminemic hyperthyroxinemia
|
|
C566305||hyperthyroxinemia dysalbuminemic
|
|
C566300||alpha fetoprotein deficiency
|
|
C566301||alopecia familial focal
|
|
C567633||emery dreifuss muscular dystrophy atypical autosomal recessive
|
|
C567633||emery dreifuss muscular dystrophy 3 autosomal recessive
|
|
C567632||growth hormone deficiency with pituitary anomalies
|
|
C567632||pituitary hormone deficiency combined 5
|
|
D047728||myopia degenerative
|
|
D047728||degenerative myopia
|
|
D047728||degenerative myopias
|
|
D047728||myopia pathological
|
|
D047728||myopia progressive
|
|
D047728||myopias degenerative
|
|
D047728||myopias pathological
|
|
D047728||myopias progressive
|
|
D047728||pathological myopia
|
|
D047728||pathological myopias
|
|
D047728||progressive myopia
|
|
D047728||progressive myopias
|
|
D009408||nerve compression syndromes
|
|
D009408||compression syndrome nerve
|
|
D009408||compression syndromes nerve
|
|
D009408||entrapment nerve
|
|
D009408||entrapment neuropathies
|
|
D009408||entrapments nerve
|
|
D009408||external nerve compression syndromes
|
|
D009408||internal nerve compression syndromes
|
|
D009408||nerve compression syndrome
|
|
D009408||nerve compression syndromes external
|
|
D009408||nerve compression syndromes internal
|
|
D009408||nerve entrapment
|
|
D009408||nerve entrapments
|
|
D009408||neuropathies entrapment
|
|
D009408||neuropathy entrapment
|
|
D009408||syndrome nerve compression
|
|
D009408||syndromes nerve compression
|
|
C566307||alacrima congenital
|
|
C566307||alacrimia congenita
|
|
D009404||nephrotic syndrome
|
|
D009404||nephrotic syndromes
|
|
D009404||syndrome nephrotic
|
|
D009404||syndromes nephrotic
|
|
C566308||hypoglossia hypodactylia
|
|
C566308||aglossia adactylia
|
|
C566308||oromandibular limb hypoplasia
|
|
C566308||peromelia with micrognathism
|
|
135150|D058249||birt hogg dube syndrome
|
|
135150|D058249||birt hogg dub 233 syndrome
|
|
135150|D058249||fibrofolliculomas with trichodiscomas and acrochordons
|
|
135150|D058249||hornstein birt hogg dub 233 syndrome
|
|
135150|D058249||hornstein knickenberg syndrome
|
|
C566309||adenine nucleotide translocator deficiency
|
|
D009402||nephrosis lipoid
|
|
D009402||change diseases minimal
|
|
D009402||disease minimal change
|
|
D009402||diseases minimal change
|
|
D009402||glomerulonephritides minimal change
|
|
D009402||glomerulonephritis minimal change
|
|
D009402||glomerulopathies minimal change
|
|
D009402||glomerulopathy minimal change
|
|
D009402||idiopathic minimal change nephrotic syndrome
|
|
D009402||lipoid nephroses
|
|
D009402||lipoid nephrosis
|
|
D009402||minimal change disease
|
|
D009402||minimal change diseases
|
|
D009402||minimal change glomerulonephritides
|
|
D009402||minimal change glomerulonephritis
|
|
D009402||minimal change glomerulopathy
|
|
D009402||minimal change nephropathies
|
|
D009402||minimal change nephropathy
|
|
D009402||minimal change nephrotic syndrome
|
|
D009402||nephropathies minimal change
|
|
D009402||nephropathy minimal change
|
|
D009402||nephroses lipoid
|
|
D009402||nephrotic syndrome minimal change
|
|
D009401||nephrosis
|
|
D009401||nephroses
|
|
C563959|600319||diabetes mellitus insulin dependent 4
|
|
C563959|600319||iddm4
|
|
C563959|600319||insulin dependent diabetes mellitus 4
|
|
D009410||nerve degeneration
|
|
D009410||degeneration nerve
|
|
D009410||degeneration neuron
|
|
D009410||degenerations nerve
|
|
D009410||degenerations neuron
|
|
D009410||nerve degenerations
|
|
D009410||neuron degeneration
|
|
D009410||neuron degenerations
|
|
251880||mitochondrial dna depletion syndrome 3 hepatocerebral type
|
|
251880||mtdps3
|
|
D059707||aliivibrio infections
|
|
D059707||aliivibrio infection
|
|
D059707||infection aliivibrio
|
|
D059707||infections aliivibrio
|
|
C562440|241510||hypophosphatasia childhood
|
|
C563895|608627||amyotrophic lateral sclerosis 8
|
|
C563895|608627||als8
|
|
C567601||gm2 gangliosidosis variant b1
|
|
611134|C567003||meckel syndrome type 4
|
|
611134|C567003||meckel gruber syndrome type 4
|
|
611134|C567003||meckel gruber syndrome type 4 meckel like cerebrorenodigital syndrome included
|
|
611134|C567003||mks4
|
|
C567603||refsum disease adult 2
|
|
C564508|300475||contiguous abcd1 dxs1375e deletion syndrome
|
|
C564508|300475||cadds included
|
|
C564508|300475||contiguous abcd1 dxs1375e deletion syndrome included
|
|
C564508|300475||ddch
|
|
C564508|300475||deafness dystonia and cerebral hypomyelination
|
|
C535456|259680||chronic recurrent multifocal osteomyelitis
|
|
C535456|259680||chronic multifocal osteomyelitis
|
|
C535456|259680||cmo
|
|
C535456|259680||crmo
|
|
C535456|259680||multifocal osteomyelitis chronic
|
|
C535456|259680||osteomyelitis chronic multifocal
|
|
D060705||dyscalculia
|
|
D060705||acalculia
|
|
D060705||acalculias
|
|
D060705||acalculia secondary
|
|
D060705||acalculias secondary
|
|
D060705||acquired dyscalculia
|
|
D060705||acquired dyscalculias
|
|
D060705||developmental dyscalculia
|
|
D060705||developmental dyscalculias
|
|
D060705||dyscalculia acquired
|
|
D060705||dyscalculia developmental
|
|
D060705||dyscalculia primary
|
|
D060705||dyscalculias
|
|
D060705||dyscalculias acquired
|
|
D060705||dyscalculias developmental
|
|
D060705||dyscalculias primary
|
|
D060705||primary dyscalculia
|
|
D060705||primary dyscalculias
|
|
D060705||secondary acalculia
|
|
D060705||secondary acalculias
|
|
C567608||mitochondrial dna depletion syndrome hepatocerebral form autosomal recessive
|
|
601367|D002544||cerebral infarction
|
|
601367|D002544||anterior choroidal artery infarction
|
|
601367|D002544||cerebral infarction left hemisphere
|
|
601367|D002544||cerebral infarction right hemisphere
|
|
601367|D002544||cerebral infarctions
|
|
601367|D002544||cerebral left hemisphere infarction
|
|
601367|D002544||cerebral right hemisphere infarction
|
|
601367|D002544|606799|D020521||cerebrovascular accident
|
|
601367|D002544||infarction cerebral
|
|
601367|D002544||infarction cerebral left hemisphere
|
|
601367|D002544||infarction cerebral right hemisphere
|
|
601367|D002544||infarction left hemisphere cerebral
|
|
601367|D002544||infarction right hemisphere cerebral
|
|
601367|D002544||infarctions cerebral
|
|
601367|D002544||infarctions subcortical
|
|
601367|D002544||infarction subcortical
|
|
601367|D002544||left hemisphere cerebral infarction
|
|
601367|D002544||left hemisphere infarction cerebral
|
|
601367|D002544||posterior choroidal artery infarction
|
|
601367|D002544||right hemisphere cerebral infarction
|
|
601367|D002544||right hemisphere infarction cerebral
|
|
601367|D002544||stroke ischemic
|
|
601367|D002544||subcortical infarction
|
|
601367|D002544||subcortical infarctions
|
|
C531647||caroli disease isolated
|
|
C531647||congenital polycystic dilatation of intrahepatic bile ducts
|
|
C531647||cystic dilatation of the intrahepatic biliary tree
|
|
C531649||neutropenia and hyperlymphocytosis with large granular lymphocytes
|
|
C531649|214500|D002609||chediak steinbrinck higashi syndrome
|
|
211800|C565891||calcification of joints and arteries
|
|
211800|C565891||acdc
|
|
211800|C565891||arterial calcification due to deficiency of cd73
|
|
211800|C565891||calja
|
|
D015299||discitis
|
|
D015299||discitides
|
|
D015299||diskitides
|
|
D015299||diskitis
|
|
D015299||spondylodiscitides
|
|
D015299||spondylodiscitis
|
|
D015299||spondylodiskitides
|
|
D015299||spondylodiskitis
|
|
C531641||monday morning fever
|
|
604547||van der woude syndrome 1 modifier of
|
|
604547||vwsm
|
|
C531642||familial vascular leukoencephalopathy
|
|
C563669|610419||deafness autosomal recessive 68
|
|
C563669|610419||dfnb68
|
|
C567614||demyer sequence
|
|
D011705||pyelonephritis xanthogranulomatous
|
|
D011705||pyelonephritides xanthogranulomatous
|
|
D011705||xanthogranulomatous pyelonephritides
|
|
D011705||xanthogranulomatous pyelonephritis
|
|
D047748||pituitary acth hypersecretion
|
|
D047748||acth hypersecretion pituitary
|
|
D047748||adrenocorticotropic hormone inappropriate secretion
|
|
D047748||cushing disease
|
|
D047748|D049913|219090||cushing disease pituitary
|
|
D047748||cushing diseases pituitary
|
|
D047748||cushing syndrome pituitary
|
|
D047748||cushing syndrome pituitary dependant
|
|
D047748||disease cushing
|
|
D047748||hypercortisolism disorder pituitary dependant
|
|
D047748||hypercortisolism disorders pituitary dependant
|
|
D047748||hypercortisolism pituitary dependant
|
|
D047748||hypercortisolisms pituitary dependant
|
|
D047748||hypersecretion pituitary acth
|
|
D047748||inappropriate acth secretion syndrome
|
|
D047748||inappropriate adrenocorticotropic hormone secretion
|
|
D047748||pituitary cushing disease
|
|
D047748||pituitary cushing diseases
|
|
D047748||pituitary cushing syndrome
|
|
D047748||pituitary dependant cushing syndrome
|
|
D047748||pituitary dependant hypercortisolism
|
|
D047748||pituitary dependant hypercortisolism disorder
|
|
D047748||pituitary dependant hypercortisolism disorders
|
|
D047748||pituitary dependant hypercortisolisms
|
|
D011707||pyloric stenosis
|
|
D011707||stenosis pyloric
|
|
D011702||pyelitis
|
|
D011704||pyelonephritis
|
|
D011704||necrotizing pyelonephritis
|
|
D011704||pyelonephritides
|
|
D011704||pyelonephritis acute necrotizing
|
|
C531652||tcd
|
|
C564703|606482||charcot marie tooth disease dominant intermediate b
|
|
C564703|606482||charcot marie tooth disease axonal autosomal dominant type 2m
|
|
C564703|606482||charcot marie tooth disease axonal autosomal dominant type 2m included
|
|
C564703|606482||charcot marie tooth disease axonal type 2m
|
|
C564703|606482||charcot marie tooth disease dominant intermediate b with neutropenia
|
|
C564703|606482||charcot marie tooth disease dominant intermediate b with neutropenia included
|
|
C564703|606482||charcot marie tooth neuropathy axonal type 2m
|
|
C564703|606482||charcot marie tooth neuropathy axonal type 2m included
|
|
C564703|606482||charcot marie tooth neuropathy dominant intermediate b
|
|
C564703|606482||charcot marie tooth neuropathy dominant intermediate b with neutropenia included
|
|
C564703|606482||cmt2m
|
|
C564703|606482||cmt2m included
|
|
C564703|606482||cmtdi1
|
|
C564703|606482||cmtdi1 charcot marie tooth disease axonal type 2m included
|
|
C564703|606482||cmtdib
|
|
C564703|606482||di cmtb
|
|
C531654||congenital chylous ascites
|
|
242600|C536285||iminoglycinuria
|
|
C537005|609536||complement component 5 deficiency
|
|
C537005|609536||c5d
|
|
C537005|609536||c5 deficiency
|
|
C537005|609536||dysfunction of the fifth component of complement c5
|
|
C537005|609536||leiner disease
|
|
135300||fibromatosis gingival 1
|
|
135300|C562884||fibromatosis gingival hereditary
|
|
135300||ggf1
|
|
135300||gingf
|
|
135300|C562884||gingf1
|
|
135300||hgf
|
|
D060725||uterine retroversion
|
|
D060725||gravid uterus retroverted
|
|
D060725||incarcerated retroverted uterus
|
|
D060725||retroflexed uterus
|
|
D060725||retroflexions uterine
|
|
D060725||retroflexion uterine
|
|
D060725||retroversions uterine
|
|
D060725||retroversion uterine
|
|
D060725||retroverted gravid uterus
|
|
D060725||retroverted uterus
|
|
D060725||retroverted uterus incarcerated
|
|
D060725||tipped uterus
|
|
D060725||uterine retroflexion
|
|
D060725||uterine retroflexions
|
|
D060725||uterine retroversions
|
|
D060725||uterus incarcerated retroverted
|
|
D060725||uterus retroflexed
|
|
D060725||uterus retroverted
|
|
D060725||uterus retroverted gravid
|
|
D060725||uterus tipped
|
|
C537377|265000||multiple pterygium syndrome
|
|
C537377|265000||escobar syndrome
|
|
C537377|265000||evmps
|
|
C537377|265000||familial pterygium syndrome
|
|
C537377|265000||lethal multiple pterygium syndrome
|
|
C537377|265000||multiple pterygium syndrome escobar variant
|
|
C537377|265000||multiple pterygium syndrome nonlethal type
|
|
C537377|265000||pterygium colli syndrome
|
|
C537377|265000||pterygium multiple syndrome lethal type
|
|
C537377|265000||pterygium syndrome
|
|
C537377|265000||pterygium syndrome multiple
|
|
C537377|265000||pterygium universale
|
|
C538262|255960||atrial myxoma familial
|
|
C538262|255960||intracardiac myxoma
|
|
C538262|255960||myxoma intracardiac
|
|
C531660||generalized elastolysis
|
|
C531662||submacular cysticercosis
|
|
D015275||tumor lysis syndrome
|
|
D015275||syndromes tumor lysis
|
|
D015275||syndromes tumour lysis
|
|
D015275||syndrome tumor lysis
|
|
D015275||syndrome tumour lysis
|
|
D015275||tumor lysis syndromes
|
|
D015275||tumour lysis syndrome
|
|
D015275||tumour lysis syndromes
|
|
121300|D046349||coproporphyria hereditary
|
|
121300|D046349||coproporphyrinogen oxidase deficiency
|
|
121300|D046349||cpo deficiency
|
|
121300|D046349||cpox deficiency
|
|
121300|D046349||cpx deficiency harderoporphyria included
|
|
121300|D046349||deficiency coproporphyrinogen oxidase
|
|
121300|D046349||hcp
|
|
121300|D046349||hereditary coproporphyria
|
|
C531664||cystinuria type 1
|
|
181350|D020389||muscular dystrophy emery dreifuss
|
|
181350|D020389||autosomal dominant emery dreifuss muscular dystrophy
|
|
181350|D020389||autosomal recessive emery dreifuss muscular dystrophy
|
|
181350|D020389||benign scapuloperoneal muscular dystrophy with early contractures
|
|
181350|D020389||edmd1
|
|
181350|D020389||edmd2
|
|
181350|D020389||edmd3 included
|
|
181350|D020389||edmd4
|
|
181350|D020389||edmd5
|
|
181350|D020389||emd1
|
|
181350|D020389||emd2
|
|
181350|D020389||emery dreifuss muscular dystrophy
|
|
181350|D020389||emery dreifuss muscular dystrophy 1
|
|
181350|D020389||emery dreifuss muscular dystrophy 1 x linked
|
|
181350|D020389||emery dreifuss muscular dystrophy 2
|
|
181350|D020389||emery dreifuss muscular dystrophy 2 autosomal dominant
|
|
181350|D020389||emery dreifuss muscular dystrophy 3 autosomal recessive included
|
|
181350|D020389|C567831||emery dreifuss muscular dystrophy 4 autosomal dominant
|
|
181350|D020389||emery dreifuss muscular dystrophy 4 with variable features
|
|
181350|D020389||emery dreifuss muscular dystrophy 5 autosomal dominant
|
|
181350|D020389||emery dreifuss muscular dystrophy autosomal dominant
|
|
181350|D020389||emery dreifuss muscular dystrophy autosomal recessive
|
|
181350|D020389||emery dreifuss muscular dystrophy x linked
|
|
181350|D020389||emery dreifuss syndrome
|
|
181350|D020389||emery dreifuss type muscular dystrophy
|
|
181350|D020389||hauptmann thannhauser muscular dystrophy
|
|
181350|D020389||hauptmann thannhauser muscular dystrophy emery dreifuss muscular dystrophy atypical autosomal recessive included
|
|
181350|D020389||humeroperoneal neuromuscular disease formerly
|
|
181350|D020389||muscular dystrophy emery dreifuss autosomal dominant
|
|
181350|D020389||muscular dystrophy emery dreifuss autosomal recessive
|
|
181350|D020389||muscular dystrophy emery dreifuss type
|
|
181350|D020389||muscular dystrophy emery dreifuss x linked
|
|
181350|D020389||muscular dystrophy scapuloperoneal
|
|
181350|D020389|C538478||muscular dystrophy tardive dreifuss emery type with contractures
|
|
181350|D020389||muscular dystrophy with early contractures and cardiomyopathy autosomal dominant
|
|
181350|D020389||myh7 related scapuloperoneal myopathy
|
|
181350|D020389||myopathy myh7 related scapuloperoneal
|
|
181350|D020389||scapuloilioperoneal atrophy with cardiopathy
|
|
181350|D020389|181430||scapuloperoneal muscular dystrophy
|
|
181350|D020389|181430||scapuloperoneal myopathy myh7 related
|
|
181350|D020389||scapuloperoneal syndrome x linked
|
|
181350|D020389||scapuloperoneal syndrome x linked formerly
|
|
181350|D020389||x linked emery dreifuss muscular dystrophy
|
|
181350|D020389||x linked scapuloperoneal syndrome
|
|
C531665|125490|D003811||opalescent dentin
|
|
C531665|125490|D003811||capdepont teeth
|
|
C531665|125490|D003811||dentinogenesis imperfecta 1
|
|
C531665|125490|D003811||dentinogenesis imperfecta shields type ii
|
|
D058405||desmoplastic small round cell tumor
|
|
D058405||desmoplastic small cell tumor
|
|
D058405||desmoplastic small cell tumors
|
|
D058405||small cell tumor desmoplastic
|
|
D058405||small cell tumors desmoplastic
|
|
D058405||tumor desmoplastic small cell
|
|
D058405||tumors desmoplastic small cell
|
|
C531667||5 alpha fluorouracil toxicity
|
|
C537743|258100||oguchi disease
|
|
C537743|258100||csnbo1
|
|
C537743|258100||csnbo2
|
|
C537743|258100||night blindness congenital stationary oguchi type 1
|
|
C537743|258100||night blindness congenital stationary oguchi type 2
|
|
C537743|258100||oguchi disease 1
|
|
C537743|258100||oguchi disease 2
|
|
C537743|258100||stationary night blindness oguchi type
|
|
D006111|275000||graves disease
|
|
D006111|275000||basedow disease
|
|
D006111|275000||basedow apos s disease
|
|
D006111|275000||basedows disease
|
|
D006111|275000||disease basedow
|
|
D006111|275000||disease basedow apos s
|
|
D006111|275000||disease graves
|
|
D006111|275000||disease graves apos
|
|
D006111|275000||exophthalmic goiter
|
|
D006111|275000||exophthalmic goiters
|
|
D006111|275000||goiter exophthalmic
|
|
D006111|275000||goiters exophthalmic
|
|
D006111|275000||graves apos disease
|
|
D006111|275000||graves disease susceptibility to 2
|
|
D006111|275000||grd
|
|
D006111|275000||grd1 included
|
|
D006111|275000||grd2
|
|
D006111|275000||hyperthyroidism autoimmune
|
|
D006111|275000||hyperthyroidism autoimmune graves disease susceptibility to 1 included
|
|
C536655|261650||phosphoenolpyruvate carboxykinase 2 deficiency
|
|
C536655|261650||pck2 deficiency
|
|
C536655|261650||pepck2 deficiency
|
|
C536655|261650|C564890||phosphoenolpyruvate carboxykinase deficiency mitochondrial
|
|
C563391|601086||laterality defects autosomal dominant
|
|
D060737||reproductive tract infections
|
|
D060737||genital tract infection
|
|
D060737||genital tract infections
|
|
D060737||infection genital tract
|
|
D060737||infection reproductive tract
|
|
D060737||infections genital tract
|
|
D060737||infections reproductive tract
|
|
D060737||reproductive tract infection
|
|
C567192|612718||arginine glycine amidinotransferase deficiency
|
|
C567192|612718||agat deficiency
|
|
C567192|612718||arginine glycine amidinotransferase deficiency agat deficiency
|
|
C567192|612718||ccds3
|
|
C567192|612718||cerebral creatine deficiency syndrome 3
|
|
C567192|612718||creatine deficiency syndrome due to agat deficiency
|
|
C567192|612718||gatm deficiency
|
|
C567192|612718||l arginine glycine aminidotransferase deficiency
|
|
C563992|600132||retinitis pigmentosa 14
|
|
C563992|600132||retinitis pigmentosa juvenile tulp1 related
|
|
C563992|600132||rp14
|
|
C531673||familial ependymoma
|
|
C531673||adult intracranial ependymoma
|
|
C531673||childhood ependymoma
|
|
C531673||ependymoma familial
|
|
C567616|225300||split hand foot malformation 6
|
|
C567616|225300||ectrodactyly autosomal recessive
|
|
C567616|225300||shfm6
|
|
D029241|165500||optic atrophy autosomal dominant
|
|
D029241|165500||atrophies juvenile optic
|
|
D029241|165500||atrophies kjer type optic
|
|
D029241|165500||atrophy juvenile optic
|
|
D029241|165500||atrophy kjer apos s optic
|
|
D029241|165500||atrophy kjer type optic
|
|
D029241|165500||autosomal dominant optic atrophy
|
|
D029241|165500||autosomal dominant optic atrophy kjer type
|
|
D029241|165500||dominant optic atrophies
|
|
D029241|165500||dominant optic atrophy
|
|
D029241|165500||juvenile optic atrophies
|
|
D029241|165500||juvenile optic atrophy
|
|
D029241|165500||kjer optic atrophy
|
|
D029241|165500||kjer apos s optic atrophy
|
|
D029241|165500||kjers optic atrophy
|
|
D029241|165500||kjer type optic atrophies
|
|
D029241|165500||kjer type optic atrophy
|
|
D029241|165500||oak
|
|
D029241|165500||opa1
|
|
D029241|165500||optic atrophies dominant
|
|
D029241|165500||optic atrophies juvenile
|
|
D029241|165500||optic atrophies kjer type
|
|
D029241|165500||optic atrophy 1
|
|
D029241|165500||optic atrophy 1s
|
|
D029241|165500||optic atrophy dominant
|
|
D029241|165500||optic atrophy hereditary autosomal dominant
|
|
D029241|165500||optic atrophy juvenile
|
|
D029241|165500||optic atrophy kjer apos s
|
|
D029241|165500||optic atrophy kjer type
|
|
D029241|165500||optic atrophy type 1
|
|
C567471|300712||craniofacioskeletal syndrome
|
|
C562879|104500||amelogenesis imperfecta type ib
|
|
C562879|104500||ai1b
|
|
C562879|104500||aih2
|
|
C562879|104500||amelogenesis imperfecta hypoplastic local autosomal dominant
|
|
C562879|104500||enamel hypoplasia hereditary localized
|
|
C565188|610743||spinocerebellar ataxia autosomal recessive 8
|
|
C565188|610743||ataxia recessive of beauce
|
|
C565188|610743||cerebellar ataxia autosomal recessive type 1
|
|
C565188|610743||scar8
|
|
D046449||hernia abdominal
|
|
D046449||abdominal hernia
|
|
D046449||abdominal hernias
|
|
D046449||hernias abdominal
|
|
C531602||anders apos syndrome
|
|
C531602||dercum vitaut syndrome
|
|
C531604||primary visual agnosia
|
|
C531604||monomodal visual amnesia
|
|
C531604||visual amnesia
|
|
C531607||alexanders leukodystrophy
|
|
C531609||diffuse alopecia
|
|
C531609||alopecia celsi
|
|
C531609||cazenave apos s vitiligo
|
|
C531609||celsus apos vitiligo
|
|
C531609||jonston apos s alopecia
|
|
C531609||marginal alopecia
|
|
C531609||patchy alopecia
|
|
D058429||gnathostomiasis
|
|
D058429||gnathostoma infection
|
|
D058429||gnathostoma infections
|
|
D058429||gnathostomiases
|
|
D058429||infection gnathostoma
|
|
D058429||infections gnathostoma
|
|
D058426||neointima
|
|
D058426||formation neointima
|
|
D058426||neointima formation
|
|
D058426||neointimas
|
|
D016585||vaginosis bacterial
|
|
D016585||bacterial vaginitides
|
|
D016585||bacterial vaginitis
|
|
D016585||bacterial vaginoses
|
|
D016585||bacterial vaginosis
|
|
D016585||nonspecific vaginitis
|
|
D016585||vaginitides bacterial
|
|
D016585||vaginitis bacterial
|
|
D016585||vaginitis nonspecific
|
|
D016585||vaginoses bacterial
|
|
D016586||granular cell tumor
|
|
D016586||cell myoblastoma granular
|
|
D016586||cell myoblastomas granular
|
|
D016586||cell tumor granular
|
|
D016586||cell tumors granular
|
|
D016586||granular cell myoblastoma
|
|
D016586||granular cell myoblastomas
|
|
D016586||granular cell tumors
|
|
D016586||myoblastoma granular cell
|
|
D016586||myoblastomas granular cell
|
|
D016586||tumor granular cell
|
|
D016586||tumors granular cell
|
|
C531600||growth hormone excess
|
|
C531601||tonic sluggishly reacting pupil and hypoactive or absent tendon reflexes
|
|
D015270||mycobacterium avium intracellulare infection
|
|
D015270||infection mycobacterium avium intracellulare
|
|
D015270||infection mycobacterium intracellulare
|
|
D015270||infections mycobacterium avium intracellulare
|
|
D015270||infections mycobacterium intracellulare
|
|
D015270||mycobacterium avium intracellulare infections
|
|
D015270||mycobacterium intracellulare infection
|
|
D015270||mycobacterium intracellulare infections
|
|
C563728|609376||cataract congenital nuclear autosomal recessive 1
|
|
C563728|609376||cataract 35
|
|
C563728|609376||catcn1
|
|
C563728|609376||ctrct35
|
|
D016114|308100||ichthyosis x linked
|
|
D016114|308100||deficiencies steroid sulfatase
|
|
D016114|308100||deficiency steroid sulfatase
|
|
D016114|308100||ichthyoses sex linked
|
|
D016114|308100||ichthyoses x linked
|
|
D016114|308100||ichthyosis sex linked
|
|
D016114|308100||placental steroid sulfatase deficiency
|
|
D016114|308100||steroid sulfatase deficiencies
|
|
D016114|308100||steroid sulfatase deficiency
|
|
D016114|308100||steroid sulfatase deficiency disease
|
|
D016114|308100||steroid sulfatase deficiency disease ssdd ichthyosis x linked complicated included
|
|
D016114|308100||sts deficiency
|
|
D016114|308100||sulfatase deficiencies steroid
|
|
D016114|308100||sulfatase deficiency steroid
|
|
D016114|308100||xli
|
|
D003289||convalescence
|
|
D003289||convalescences
|
|
C565246|606242||mental retardation microcephaly growth retardation joint contractures and facial dysmorphism
|
|
C565246|606242||kondoh syndrome
|
|
D003286||contracture
|
|
D003286||contractures
|
|
D003288||contusions
|
|
D003288||bruise
|
|
D003288||bruises
|
|
D003288||contusion
|
|
C531613||amoebiasis due to entamoeba histolytica
|
|
C537699|256100||nephronophthisis familial juvenile
|
|
C537699|256100||juvenile nephronophthisis
|
|
C537699|256100||nephronophthisis 1
|
|
C537699|256100||nph1
|
|
C537699|256100||nphp1
|
|
C537699|256100||type 1 nephronophthisis
|
|
C531614||amniotic band sequence
|
|
C531614||amniotic bands sequence
|
|
C531614||congenital constricting bands
|
|
C531614||constricting bands congenital
|
|
C531614||familial amniotic bands
|
|
C531614||streeter anomaly
|
|
D003294||seizures febrile
|
|
D003294||convulsion febrile
|
|
D003294||convulsion fever
|
|
D003294||convulsion pyrexial
|
|
D003294||convulsions febrile
|
|
D003294||convulsions fever
|
|
D003294||convulsions pyrexial
|
|
D003294||febrile convulsion
|
|
D003294||febrile convulsions
|
|
D003294||febrile convulsion seizure
|
|
D003294||febrile convulsion seizures
|
|
D003294||febrile fit
|
|
D003294||febrile fits
|
|
D003294||febrile seizure
|
|
D003294||febrile seizures
|
|
D003294||fever convulsion
|
|
D003294||fever convulsions
|
|
D003294||fever seizure
|
|
D003294||fever seizures
|
|
D003294||fit febrile
|
|
D003294||fits febrile
|
|
D003294||pyrexial convulsion
|
|
D003294||pyrexial convulsions
|
|
D003294||pyrexial seizure
|
|
D003294||pyrexial seizures
|
|
D003294||seizure febrile
|
|
D003294||seizure febrile complex
|
|
D003294||seizure febrile convulsion
|
|
D003294||seizure febrile simple
|
|
D003294||seizure fever
|
|
D003294||seizure pyrexial
|
|
D003294||seizures febrile convulsion
|
|
D003294||seizures fever
|
|
D003294||seizures pyrexial
|
|
C531615||amyloid neuropathies primary nonfamilial
|
|
D060751||bone retroversion
|
|
D060751||bone retrotorsion
|
|
D060751||bone retrotorsions
|
|
D060751||bone retroversions
|
|
D060751||retrotorsion bone
|
|
D060751||retrotorsions bone
|
|
D060751||retroversion bone
|
|
D060751||retroversions bone
|
|
C531616||primary amyloidosis
|
|
C531616||amyloidosis primary
|
|
C531616||amyloid primary
|
|
D060750||bone anteversion
|
|
D060750||antetorsion bone
|
|
D060750||antetorsions bone
|
|
D060750||anteversion bone
|
|
D060750||anteversions bone
|
|
D060750||bone antetorsion
|
|
D060750||bone antetorsions
|
|
D060750||bone anteversions
|
|
C566907|611615||cardiomyopathy dilated 1x
|
|
C566907|611615||cardiomyopathy dilated with mild or no proximal muscle weakness
|
|
C566907|611615||cmd1x
|
|
604219|C565815||cataract autosomal dominant
|
|
604219|C565815||cataract 9 multiple types
|
|
604219|C565815||cataract 9 multiple types with or without microcornea
|
|
604219|C565815||catc1
|
|
604219|C565815||ctrct9
|
|
C531619||happy puppet syndrome formerly
|
|
D003291||conversion disorder
|
|
D003291||astasia abasia
|
|
D003291||conversion disorders
|
|
D003291||conversion hysteria
|
|
D003291||conversion hysterias
|
|
D003291||conversion reaction
|
|
D003291||conversion reactions
|
|
D003291||globus hystericus
|
|
D003291||hysteria conversion
|
|
D003291||hysterias conversion
|
|
D003291||reaction conversion
|
|
D003291||reactions conversion
|
|
609015|C566945||trifunctional protein deficiency with myopathy and neuropathy
|
|
609015|C566945||3 hydroxyacyl coa dehydrogenase long chain deficiency
|
|
609015|C566945|609016||lchad deficiency
|
|
609015|C566945|609016||long chain 3 hydroxyacyl coa dehydrogenase deficiency
|
|
609015|C566945||long chain 3 hydroxy acyl coa dehydrogenase deficiency
|
|
609015|C566945||long chain 3 hydroxyacyl coenzyme a dehydrogenase deficiency
|
|
609015|C566945||long chain 3 oh acyl coa dehydrogenase deficiency
|
|
609015|C566945||mitochondrial trifunctional protein deficiency
|
|
609015|C566945||mitochondrial trifunctional protein deficiency trifunctional protein deficiency with myopathy and neuropathy included
|
|
609015|C566945||tfp deficiency
|
|
609015|C566945||trifunctional protein deficiency
|
|
609015|C566945||trifunctional protein deficiency type 1
|
|
609015|C566945||trifunctional protein deficiency type 2
|
|
D015267||churg strauss syndrome
|
|
D015267||allergic angiitides
|
|
D015267||allergic angiitides granulomatous
|
|
D015267||allergic angiitis
|
|
D015267||allergic angiitis and granulomatosis
|
|
D015267||allergic angiitis granulomatous
|
|
D015267||allergic granulomatoses
|
|
D015267||allergic granulomatosis
|
|
D015267||allergic granulomatous and angiitis
|
|
D015267||allergic granulomatous angiitides
|
|
D015267||allergic granulomatous angiitis
|
|
D015267||angiitides allergic
|
|
D015267||angiitides allergic granulomatous
|
|
D015267||angiitides granulomatous allergic
|
|
D015267||angiitis allergic
|
|
D015267||angiitis allergic granulomatous
|
|
D015267||angiitis granulomatous allergic
|
|
D015267||churg strauss vasculitis
|
|
D015267||eosinophilic granulomatous vasculitides
|
|
D015267||eosinophilic granulomatous vasculitis
|
|
D015267||granulomatoses allergic
|
|
D015267||granulomatosis allergic
|
|
D015267||granulomatous allergic angiitides
|
|
D015267||granulomatous allergic angiitis
|
|
D015267||granulomatous angiitides allergic
|
|
D015267||granulomatous angiitis allergic
|
|
D015267||granulomatous vasculitides eosinophilic
|
|
D015267||granulomatous vasculitis eosinophilic
|
|
D015267||syndrome churg strauss
|
|
D015267||vasculitides eosinophilic granulomatous
|
|
D015267||vasculitis churg strauss
|
|
D015267||vasculitis eosinophilic granulomatous
|
|
D015266||carcinoma merkel cell
|
|
D015266||cancer merkel cell
|
|
D015266||cell cancer merkel
|
|
D015266||merkel cell cancer
|
|
D015266||merkel cell carcinoma
|
|
D015266||merkel cell tumor
|
|
D015266||merkle tumors
|
|
D015266||tumor merkel cell
|
|
D015266||tumors merkle
|
|
D058437||hypertensive retinopathy
|
|
D058437||hypertensive retinopathies
|
|
D058437||retinopathies hypertensive
|
|
D058437||retinopathy hypertensive
|
|
C531610||deficiency of aat
|
|
D057108||corneal wavefront aberration
|
|
D057108||aberration corneal wavefront
|
|
D057108||aberrations corneal wavefront
|
|
D057108||corneal wavefront aberrations
|
|
D057108||wavefront aberration corneal
|
|
D057108||wavefront aberrations corneal
|
|
C536545|190300||tremor hereditary essential 1
|
|
C536545|190300||etm1
|
|
C536545|190300||fet1
|
|
C536545|190300||tremor familial essential 1
|
|
C567514|611819||long qt syndrome 10
|
|
C567514|611819||lqt10
|
|
D057112||corneal perforation
|
|
D057112||corneal perforations
|
|
D057112||perforation corneal
|
|
D057112||perforations corneal
|
|
C531624||familial spinal arachnoiditis
|
|
C531624||spinal arachnoiditis
|
|
C531624||spinal tuberculous arachnoiditis
|
|
C531625||chiari malformation type 2
|
|
C531625||chiari malformation type ii
|
|
C531629||human balantidiasis
|
|
C531629||balantidiosis
|
|
C531629||balantidium coli infection
|
|
C531629||b coli infection
|
|
C531629||large intestinal infection with balantidium coli
|
|
D058442||capsule opacification
|
|
D058442||capsule opacifications
|
|
D058442||cataract secondary
|
|
D058442||cataracts secondary
|
|
D058442||opacification capsule
|
|
D058442||opacifications capsule
|
|
D058442||secondary cataract
|
|
D058442||secondary cataracts
|
|
C567709|613204||muscular dystrophy congenital due to integrin alpha 7 deficiency
|
|
C567709|613204||myopathy congenital due to integrin alpha 7 deficiency
|
|
C535979|201910||congenital adrenal hyperplasia due to 21 hydroxylase deficiency
|
|
C535979|201910||21 alpha hydroxylase deficiency
|
|
C535979|201910||21 hydroxylase deficiency
|
|
C535979|201910||adrenal hyperplasia congenital due to 21 hydroxylase deficiency
|
|
C535979|201910||adrenal hyperplasia iii
|
|
C535979|201910||congenital adrenal hyperplasia 1
|
|
C535979|201910||congenital adrenal hyperplasia 1 cah1 hyperandrogenism nonclassic type due to 21 hydroxylase deficiency included
|
|
C535979|201910||cyp21 deficiency
|
|
D015231||sexually transmitted diseases bacterial
|
|
D015231||bacterial sexually transmitted disease
|
|
D015231||bacterial sexually transmitted diseases
|
|
D015231||bacterial venereal disease
|
|
D015231||bacterial venereal diseases
|
|
D015231||disease bacterial venereal
|
|
D015231||diseases bacterial venereal
|
|
D015231||sexually transmitted disease bacterial
|
|
D015231||venereal disease bacterial
|
|
D015231||venereal diseases bacterial
|
|
D016569||blepharophimosis
|
|
D016569||blepharophimoses
|
|
D058447||eye pain
|
|
D058447||eye pains
|
|
D058447||pain eye
|
|
D058447||pains eye
|
|
C531621||cutaneous anthrax
|
|
C531621||anthrax skin type
|
|
C531621||skin anthrax
|
|
C562603|612119||trehalase deficiency
|
|
C562603|612119||trehalose intolerance
|
|
D016582||leukemia feline
|
|
D016582||feline leukemia
|
|
D016582||feline leukemias
|
|
D016582||leukemias feline
|
|
D016583||enzootic bovine leukosis
|
|
D016583||bovine leukemia
|
|
D016583||bovine leukemias
|
|
D016583||bovine leukoses
|
|
D016583||bovine leukoses enzootic
|
|
D016583||bovine leukosis
|
|
D016583||bovine leukosis enzootic
|
|
D016583||bovine lymphoma
|
|
D016583||bovine lymphomas
|
|
D016583||bovine lymphosarcoma
|
|
D016583||bovine lymphosarcomas
|
|
D016583||enzootic bovine leukoses
|
|
D016583||leukemia bovine
|
|
D016583||leukemias bovine
|
|
D016583||leukoses bovine
|
|
D016583||leukoses enzootic bovine
|
|
D016583||leukosis bovine
|
|
D016583||leukosis enzootic bovine
|
|
D016583||lymphoma bovine
|
|
D016583||lymphomas bovine
|
|
D016583||lymphosarcoma bovine
|
|
D016583||lymphosarcomas bovine
|
|
105500||als pdc
|
|
C536404|600995||nephrotic syndrome idiopathic steroid resistant
|
|
C536404|600995||nephrotic syndrome steroid resistant autosomal recessive
|
|
C536404|600995|C535761|256300||nephrotic syndrome type 2
|
|
C536404|600995||nphs2
|
|
C536404|600995||srn1
|
|
D059786||abnormal karyotype
|
|
D059786||abnormal karyotypes
|
|
D059786||karyotype abnormal
|
|
D059786||karyotypes abnormal
|
|
C564888|261740||glycogen storage disease of heart lethal congenital
|
|
C564888|261740||glycogen storage disease of heart
|
|
C564888|261740||phosphorylase kinase deficiency of heart
|
|
C536038|201450||medium chain acyl coa dehydrogenase deficiency
|
|
C536038|201450||acadmd
|
|
C536038|201450||acadm deficiency
|
|
C536038|201450||acyl coa dehydrogenase medium chain deficiency of
|
|
C536038|201450||carnitine deficiency secondary to medium chain acyl coa dehydrogenase deficiency
|
|
C536038|201450||mcad deficiency
|
|
C536038|201450||mcadh deficiency
|
|
C536038|201450||medium chain acyl coenzyme a dehydrogenase deficiency
|
|
D058457||trichiasis
|
|
D058457||trichiases
|
|
D059787||acute pain
|
|
D059787||acute pains
|
|
D059787||pain acute
|
|
D059787||pains acute
|
|
193100|C562791||hypophosphatemic rickets autosomal dominant
|
|
193100|C562791||adhr
|
|
193100|C562791||hypophosphatemia autosomal dominant
|
|
193100|C562791||vitamin d resistant rickets autosomal dominant
|
|
C531638||sudden unexpected nocturnal death syndrome
|
|
C531639||stomatodynia
|
|
C537727|265300||lymphangiectasia pulmonary congenital
|
|
C537727|265300||cpl
|
|
C537727|265300||lymphangiomatosis pulmonary
|
|
C537727|265300||pulmonary cystic lymphangiectasis
|
|
D016574||seasonal affective disorder
|
|
D016574||affective disorder seasonal
|
|
D016574||affective disorders seasonal
|
|
D016574||disorder seasonal affective
|
|
D016574||disorder seasonal mood
|
|
D016574||disorders seasonal affective
|
|
D016574||disorders seasonal mood
|
|
D016574||mood disorder seasonal
|
|
D016574||mood disorders seasonal
|
|
D016574||seasonal affective disorders
|
|
D016574||seasonal mood disorder
|
|
D016574||seasonal mood disorders
|
|
C564501|300505||mental retardation x linked 84
|
|
C564501|300505||mrx84
|
|
D057129||iridocorneal endothelial syndrome
|
|
D057129||chandler apos s syndrome
|
|
D057129||chandlers syndrome
|
|
D057129||chandler syndrome
|
|
D057129||cornea dystrophy endothelial
|
|
D057129||corneas dystrophy endothelial
|
|
D057129||dystrophy endothelial cornea
|
|
D057129||dystrophy endothelial corneas
|
|
D057129||endothelial cornea dystrophy
|
|
D057129||endothelial corneas dystrophy
|
|
D057129||endothelial syndrome iridocorneal
|
|
D057129||endothelial syndromes iridocorneal
|
|
D057129||iridocorneal endothelial syndromes
|
|
D057129||iris atrophy with corneal edema and glaucoma
|
|
300068|D013734||androgen insensitivity syndrome
|
|
300068|D013734|181800||ais
|
|
300068|D013734||androgen insensitivities partial
|
|
300068|D013734||androgen insensitivity partial
|
|
300068|D013734||androgen insensitivity partial with or without breast cancer
|
|
300068|D013734||androgen insensitivity syndrome complete
|
|
300068|D013734||androgen insensitivity syndrome partial
|
|
300068|D013734||androgen insensitivity syndromes
|
|
300068|D013734||androgen insensitivity syndromes complete
|
|
300068|D013734||androgen insensitivity syndromes partial
|
|
300068|D013734||androgen receptor deficiencies
|
|
300068|D013734||androgen receptor deficiency
|
|
300068|D013734||androgen resistance syndrome
|
|
300068|D013734||androgen resistance syndromes
|
|
300068|D013734||ar deficiencies
|
|
300068|D013734||ar deficiency
|
|
300068|D013734||complete androgen insensitivity syndrome
|
|
300068|D013734||complete androgen insensitivity syndromes
|
|
300068|D013734||deficiencies androgen receptor
|
|
300068|D013734||deficiencies ar
|
|
300068|D013734||deficiencies dhtr
|
|
300068|D013734||deficiencies dihydrotestosterone receptor
|
|
300068|D013734||deficiency androgen receptor
|
|
300068|D013734||deficiency ar
|
|
300068|D013734||deficiency dhtr
|
|
300068|D013734||deficiency dihydrotestosterone receptor
|
|
300068|D013734||dhtr deficiencies
|
|
300068|D013734||dhtr deficiency
|
|
300068|D013734||dihydrotestosterone receptor deficiencies
|
|
300068|D013734||dihydrotestosterone receptor deficiency
|
|
300068|D013734||feminizations testicular
|
|
300068|D013734||feminization syndromes testicular
|
|
300068|D013734||feminization syndrome testicular
|
|
300068|D013734||feminization testicular
|
|
300068|D013734||insensitivities partial androgen
|
|
300068|D013734||insensitivity partial androgen
|
|
300068|D013734||insensitivity syndrome androgen
|
|
300068|D013734||insensitivity syndromes androgen
|
|
300068|D013734||male pseudohermaphroditism due to androgen insensitivity
|
|
300068|D013734||pais
|
|
300068|D013734||partial androgen insensitivities
|
|
300068|D013734||partial androgen insensitivity
|
|
300068|D013734||partial androgen insensitivity syndrome
|
|
300068|D013734||partial androgen insensitivity syndromes
|
|
300068|D013734||receptor deficiencies androgen
|
|
300068|D013734||receptor deficiencies dihydrotestosterone
|
|
300068|D013734||receptor deficiency androgen
|
|
300068|D013734||receptor deficiency dihydrotestosterone
|
|
300068|D013734||reifenstein apos s syndrome
|
|
300068|D013734||reifensteins syndrome
|
|
300068|D013734||reifenstein syndrome
|
|
300068|D013734||resistance syndrome androgen
|
|
300068|D013734||resistance syndromes androgen
|
|
300068|D013734||testicular feminization
|
|
300068|D013734||testicular feminizations
|
|
300068|D013734||testicular feminization syndrome
|
|
300068|D013734||testicular feminization syndromes
|
|
300068|D013734||tfm
|
|
D016575||hidradenitis
|
|
D016575||eccrine hidradenitides neutrophilic
|
|
D016575||eccrine hidradenitis neutrophilic
|
|
D016575||hidradenitides
|
|
D016575||hidradenitides neutrophilic eccrine
|
|
D016575||hidradenitis neutrophilic eccrine
|
|
D016575||hidrosadenitides
|
|
D016575||hidrosadenitis
|
|
D016575||hydradenitides
|
|
D016575||hydradenitis
|
|
D016575||neutrophilic eccrine hidradenitides
|
|
D016575||neutrophilic eccrine hidradenitis
|
|
C531633||biotin deficiency
|
|
105550||frontotemporal dementia and or amyotrophic lateral sclerosis
|
|
105550|C566288||alsftd
|
|
105550|C566288||amyotrophic lateral sclerosis and or frontotemporal dementia
|
|
105550||frontotemporal dementia and or motor neuron disease
|
|
105550|C566288||ftdals
|
|
105550|C566288||ftdmnd
|
|
D017880||limb deformities congenital
|
|
D017880||congenital limb deformities
|
|
D017880||congenital limb deformity
|
|
D017880||deformities congenital limb
|
|
D017880||deformity congenital limb
|
|
D017880||limb deformity congenital
|
|
C565198|610687||nemaline myopathy 7
|
|
C565198|610687||nem7
|
|
609055|C537953||ceroid lipofuscinosis neuronal 9
|
|
609055|C537953||cln9
|
|
C536080|300438||hydroxyacyl coa dehydrogenase type 2 deficiency
|
|
C536080|300438||17beta hydroxysteroid dehydrogenase type 10 deficiency
|
|
C536080|300438||17 beta hydroxysteroid dehydrogenase x deficiency
|
|
C536080|300438||2 methyl 3 hydroxybutyric aciduria
|
|
C536080|300438||2 methyl 3 hydroxybutyryl coa dehydrogenase deficiency
|
|
C536080|300438||3 hydroxy 2 methylbutyryl coa dehydrogenase deficiency
|
|
C536080|300438||3 hydroxyacyl coa dehydrogenase ii deficiency
|
|
C536080|300438||3 hydroxyacyl coa dehydrogenase type 2 deficiency
|
|
C536080|300438||hsd10 deficiency
|
|
C536080|300438||hsd17b10 deficiency
|
|
C536080|300438||hydroxyacyl coa dehydrogenase ii deficiency
|
|
C536080|300438||mhbd deficiency
|
|
D003234||conjunctivitis bacterial
|
|
D003234||bacterial conjunctivitides
|
|
D003234||bacterial conjunctivitis
|
|
D003234||conjunctivitides bacterial
|
|
D003234||conjunctivitides mucopurulent
|
|
D003234||conjunctivitides purulent
|
|
D003234||conjunctivitis mucopurulent
|
|
D003234||conjunctivitis purulent
|
|
D003234||mucopurulent conjunctivitides
|
|
D003234||mucopurulent conjunctivitis
|
|
D003234||purulent conjunctivitides
|
|
D003234||purulent conjunctivitis
|
|
D005896||glanders
|
|
D003235||conjunctivitis inclusion
|
|
D003235||blennorrhea inclusion
|
|
D003235||blennorrheas inclusion
|
|
D003235||conjunctivitides inclusion
|
|
D003235||inclusion blennorrhea
|
|
D003235||inclusion blennorrheas
|
|
D003235||inclusion conjunctivitides
|
|
D003235||inclusion conjunctivitis
|
|
D003236||conjunctivitis viral
|
|
D003236||conjunctivitides viral
|
|
D003236||viral conjunctivitides
|
|
D003236||viral conjunctivitis
|
|
C562798||transcobalamin i deficiency
|
|
C562798||cobalamin pseudodeficiency due to transcobalamin deficiency
|
|
C562798||cobalamin r binder protein deficiency
|
|
C562798||transcobalamin i deficiency with lactoferrin deficiency
|
|
178000|C566740||pterygium of conjunctiva and cornea
|
|
D003230||conjunctival neoplasms
|
|
D003230||conjunctival neoplasm
|
|
D003230||neoplasm conjunctival
|
|
D003230||neoplasms conjunctival
|
|
D005892||gingivitis necrotizing ulcerative
|
|
D005892||acute membranous gingivitides
|
|
D005892||acute membranous gingivitis
|
|
D005892||acute necrotizing ulcerative gingivitis
|
|
D005892||anginas vincent
|
|
D005892||angina vincent
|
|
D005892||fusospirillary gingivitides
|
|
D005892||fusospirillary gingivitis
|
|
D005892||fusospirilloses
|
|
D005892||fusospirillosis
|
|
D005892||gingivitides acute membranous
|
|
D005892||gingivitides fusospirillary
|
|
D005892||gingivitides phagedenic
|
|
D005892||gingivitis acute membranous
|
|
D005892||gingivitis fusospirillary
|
|
D005892||gingivitis phagedenic
|
|
D005892||gingivitis vincent apos s
|
|
D005892||infection vincent
|
|
D005892||infection vincent apos s
|
|
D005892||membranous gingivitides acute
|
|
D005892||membranous gingivitis acute
|
|
D005892||mouth trench
|
|
D005892||necrotizing ulcerative gingivitis
|
|
D005892||phagedenic gingivitides
|
|
D005892||phagedenic gingivitis
|
|
D005892||stomatitides ulcerative
|
|
D005892||stomatitis ulcerative
|
|
D005892||stomatitis vincent apos s
|
|
D005892||trench mouth
|
|
D005892||ulcerative gingivitis necrotizing
|
|
D005892||ulcerative stomatitides
|
|
D005892||ulcerative stomatitis
|
|
D005892||vincent angina
|
|
D005892||vincent gingivitis
|
|
D005892||vincent infection
|
|
D005892||vincent apos s gingivitis
|
|
D005892||vincents gingivitis
|
|
D005892||vincent apos s infection
|
|
D005892||vincents infection
|
|
D005892||vincent apos s stomatitis
|
|
D005892||vincents stomatitis
|
|
D005892||vincent stomatitis
|
|
D003231||conjunctivitis
|
|
D003231||conjunctivitides
|
|
D003232||conjunctivitis acute hemorrhagic
|
|
D003232||acute hemorrhagic conjunctivitides
|
|
D003232||acute hemorrhagic conjunctivitis
|
|
D003232||conjunctivitides acute hemorrhagic
|
|
D003232||hemorrhagic conjunctivitides acute
|
|
D003232||hemorrhagic conjunctivitis acute
|
|
D003233||conjunctivitis allergic
|
|
D003233||allergic conjunctivitides
|
|
D003233||allergic conjunctivitis
|
|
D003233||atopic conjunctivitides
|
|
D003233||atopic conjunctivitis
|
|
D003233||conjunctivitides allergic
|
|
D003233||conjunctivitides atopic
|
|
D003233||conjunctivitides giant papillary
|
|
D003233||conjunctivitides vernal
|
|
D003233||conjunctivitis atopic
|
|
D003233||conjunctivitis giant papillary
|
|
D003233||conjunctivitis vernal
|
|
D003233||giant papillary conjunctivitides
|
|
D003233||giant papillary conjunctivitis
|
|
D003233||keratoconjunctivitides vernal
|
|
D003233||keratoconjunctivitis vernal
|
|
D003233||papillary conjunctivitides giant
|
|
D003233||papillary conjunctivitis giant
|
|
D003233||vernal conjunctivitides
|
|
D003233||vernal conjunctivitis
|
|
D003233||vernal keratoconjunctivitides
|
|
D003233||vernal keratoconjunctivitis
|
|
D057135||wet macular degeneration
|
|
D057135||degenerations wet macular
|
|
D057135||degeneration wet macular
|
|
D057135||macular degenerations wet
|
|
D057135||macular degeneration wet
|
|
D057135||wet macular degenerations
|
|
D015218||hyperostosis sternocostoclavicular
|
|
D015218||hyperostoses sternocostoclavicular
|
|
D015218||sternocostoclavicular hyperostoses
|
|
D015218||sternocostoclavicular hyperostosis
|
|
D015217||cholesterol ester storage disease
|
|
D015217|278000|C531854||cholesteryl ester storage disease
|
|
D003240||connective tissue diseases
|
|
D003240||connective tissue disease
|
|
D003240||disease connective tissue
|
|
D003240||diseases connective tissue
|
|
D057130||leber congenital amaurosis
|
|
D057130||abiotrophies leber
|
|
D057130||abiotrophy leber
|
|
D057130||amauroses leber congenital
|
|
D057130||amauroses leber apos s
|
|
D057130||amaurosis leber congenital
|
|
D057130||amaurosis leber apos s
|
|
D057130||blindness congenital retinal
|
|
D057130||blindnesses congenital retinal
|
|
D057130||congenital amauroses leber
|
|
D057130||congenital amaurosis leber
|
|
D057130||congenital amaurosis of retinal origin
|
|
D057130||congenital retinal blindness
|
|
D057130||congenital retinal blindnesses
|
|
D057130||dysgenesis neuroepithelialis retinae
|
|
D057130||hereditary epithelial dysplasia of retina
|
|
D057130||hereditary retinal aplasia
|
|
D057130||heredoretinopathia congenitalis
|
|
D057130||leber abiotrophies
|
|
D057130||leber abiotrophy
|
|
D057130||leber amaurosis
|
|
D057130||leber congenital amauroses
|
|
D057130||leber congenital tapetoretinal degeneration
|
|
D057130||leber apos s amauroses
|
|
D057130||leber apos s amaurosis
|
|
D057130||lebers amaurosis
|
|
D057130||retinal blindnesses congenital
|
|
D016545||choroid plexus neoplasms
|
|
D016545||choroid plexus neoplasm
|
|
D016545||choroid plexus neoplasms primary
|
|
D016545||choroid plexus tumor
|
|
D016545||choroid plexus tumors
|
|
D016545||neoplasm choroid plexus
|
|
D016545||neoplasms choroid plexus
|
|
D016545||primary choroid plexus neoplasms
|
|
D015210||arthritis gouty
|
|
D015210||arthritides gouty
|
|
D015210||gouty arthritides
|
|
D015210||gouty arthritis
|
|
D009447|256700||neuroblastoma
|
|
D009447|256700||nblst1 included
|
|
D009447|256700||nblst2
|
|
D009447|256700||nblst3
|
|
D009447|256700||nblst4
|
|
D009447|256700||nblst5
|
|
D009447|256700||nblst6
|
|
D009447|256700||neuroblastomas
|
|
D009447|256700||neuroblastoma susceptibility to
|
|
D009447|256700||neuroblastoma susceptibility to 1 included
|
|
D009447|256700||neuroblastoma susceptibility to 2
|
|
D009447|256700||neuroblastoma susceptibility to 3
|
|
D009447|256700||neuroblastoma susceptibility to 4
|
|
D009447|256700||neuroblastoma susceptibility to 5
|
|
D009447|256700||neuroblastoma susceptibility to 6
|
|
D009447|256700||neuroblastoma with hirschsprung disease included
|
|
D012516|259500||osteosarcoma
|
|
D012516|259500||osrc
|
|
D012516|259500||osteogenic sarcoma
|
|
D012516|259500||osteogenic sarcomas
|
|
D012516|259500||osteosarcomas
|
|
D012516|259500||osteosarcoma tumor
|
|
D012516|259500||osteosarcoma tumors
|
|
D012516|259500||sarcoma osteogenic
|
|
D012516|259500||sarcomas osteogenic
|
|
D012516|259500||tumor osteosarcoma
|
|
D012516|259500||tumors osteosarcoma
|
|
D016543||central nervous system neoplasms
|
|
D016543||central nervous system neoplasms primary
|
|
D016543||central nervous system tumors
|
|
D016543||neoplasms central nervous system
|
|
D016543||primary central nervous system neoplasms
|
|
D016543||tumors central nervous system
|
|
D007918|246300||leprosy
|
|
D007918|246300||disease hansen
|
|
D007918|246300||disease hansen apos s
|
|
D007918|246300||hansen disease
|
|
D007918|246300||hansen apos s disease
|
|
D007918|246300||hansens disease
|
|
D007918|246300||leprosies
|
|
D007918|246300||leprosy early onset susceptibility to included
|
|
D007918|246300||leprosy paucibacillary type susceptibility to 1
|
|
D007918|246300||leprosy protection against included
|
|
D007918|246300||leprosy susceptibility to 1
|
|
D007918|246300||leprosy susceptibility to 2
|
|
D007918|246300||leprosy susceptibility to 3
|
|
D007918|246300||leprosy susceptibility to 4
|
|
D007918|246300||leprosy susceptibility to 5
|
|
D007918|246300||leprosy susceptibility to 6
|
|
D007918|246300||lprs1
|
|
D007918|246300||lprs2
|
|
D007918|246300||lprs3
|
|
D007918|246300||lprs4
|
|
D007918|246300||lprs5
|
|
D007918|246300||lprs6
|
|
D017890||splenosis
|
|
D017890||splenoses
|
|
D045169||severe acute respiratory syndrome
|
|
D045169||respiratory syndrome acute severe
|
|
D045169||respiratory syndrome severe acute
|
|
C567089|611771||lipoprotein glomerulopathy
|
|
C567089|611771||lpg
|
|
C564926|258450||progressive external ophthalmoplegia with mitochondrial dna deletions autosomal recessive
|
|
C564926|258450||peob
|
|
C564926|258450||progressive external ophthalmoplegia autosomal recessive
|
|
C567730|613135||parkinsonism dystonia infantile
|
|
C567730|613135||dopamine transporter deficiency syndrome
|
|
C567730|613135||dtds
|
|
C567730|613135||pkdys
|
|
C548479||vulvar dysesthesia localized in the vestibule
|
|
105400|C531617||amyotrophic lateral sclerosis 1
|
|
105400|C531617||als1
|
|
105400|C531617||amyotrophic lateral sclerosis 1 autosomal dominant amyotrophic lateral sclerosis 1 autosomal recessive included
|
|
105400|C531617||amyotrophic lateral sclerosis 1 familial
|
|
105400|C531617||amyotrophic lateral sclerosis autosomal dominant
|
|
105400|C531617||amyotrophic lateral sclerosis familial
|
|
105400|C531617||amyotrophic lateral sclerosis sporadic included
|
|
105400|C531617||fals
|
|
C536490|276901||usher syndrome type 2a
|
|
C536490|276901||ush2a
|
|
C536490|276901||usher syndrome type iia
|
|
D003248||constipation
|
|
D003248||colonic inertia
|
|
D003248||dyschezia
|
|
D003244||consciousness disorders
|
|
D003244||altered level of consciousness
|
|
D003244||consciousness disorder
|
|
D003244||consciousness level altered
|
|
D003244||consciousness level depressed
|
|
D003244||depressed level of consciousness
|
|
D003244||semiconsciousness
|
|
D015229||sexually transmitted diseases viral
|
|
D015229||diseases viral venereal
|
|
D015229||disease viral venereal
|
|
D015229||sexually transmitted disease viral
|
|
D015229||venereal diseases viral
|
|
D015229||venereal disease viral
|
|
D015229||viral sexually transmitted disease
|
|
D015229||viral sexually transmitted diseases
|
|
D015229||viral venereal disease
|
|
D015229||viral venereal diseases
|
|
D015228||hypertriglyceridemia
|
|
D015228||hypertriglyceridemias
|
|
D003251||constriction pathologic
|
|
D003251||constriction pathological
|
|
D003251||constrictions pathologic
|
|
D003251||pathological constriction
|
|
D003251||pathologic constriction
|
|
D003251||pathologic constrictions
|
|
D003251||stenoses
|
|
D003251||stenosis
|
|
D003251||stricture
|
|
D003251||strictures
|
|
D015223||wolman disease
|
|
D015223||acid cholesteryl ester hydrolase deficiency wolman type
|
|
D015223||acid lipase deficiency
|
|
D015223||disease wolman
|
|
D015223||disease wolman apos s
|
|
D015223||familial xanthomatoses
|
|
D015223||familial xanthomatosis
|
|
D015223||liposomal acid lipase deficiency wolman type
|
|
D015223||wolman apos s disease
|
|
D015223||wolmans disease
|
|
D015223||wolman apos s xanthomatosis
|
|
D015223||xanthomatoses familial
|
|
D015223||xanthomatosis familial
|
|
D015223||xanthomatosis wolman
|
|
D015223||xanthomatosis wolmans
|
|
D015223||xanthomatosis wolman apos s
|
|
D017887||ossification of posterior longitudinal ligament
|
|
D017887||calcification of posterior longitudinal ligament
|
|
D017887||posterior longitudinal ligament calcification
|
|
D017887||posterior longitudinal ligament ossification
|
|
C548481||periventricular laminar heterotopia
|
|
C548481||heterotopia periventricular
|
|
C536463|611584||waardenburg syndrome type 2
|
|
C536463|611584||hypogonadotropic hypogonadism with anosmia and deafness with or without hypopigmentation
|
|
C536463|611584||waardenburg syndrome type 2e
|
|
C536463|611584||waardenburg syndrome type 2e with or without neurologic involvement
|
|
C536463|611584||waardenburg syndrome type iie
|
|
C536463|611584||ws2e
|
|
C536463|611584||ws2e with or without neurologic involvement
|
|
C562774||muscular atrophy ataxia retinitis pigmentosa and diabetes mellitus
|
|
D003218||condylomata acuminata
|
|
D003218||genital wart
|
|
D003218||genital warts
|
|
D003218||venereal wart
|
|
D003218||venereal warts
|
|
D003218||wart genital
|
|
D003218||warts genital
|
|
D003218||warts venereal
|
|
D003218||wart venereal
|
|
C562773||diabetes mellitus type ii autosomal dominant
|
|
607822|C564330||alzheimer disease familial 3 with spastic paraparesis and apraxia
|
|
607822|C564330||ad3
|
|
607822|C564330|C536598||alzheimer disease 3
|
|
607822|C564330|C536598||alzheimer disease 3 early onset
|
|
607822|C564330||alzheimer disease familial 3 alzheimer disease familial 3 with spastic paraparesis and unusual plaques included
|
|
607822|C564330||alzheimer disease familial 3 with spastic paraparesis and apraxia included
|
|
D005877||gigantism
|
|
D005877||gigantism pituitary
|
|
D005877||pituitary gigantism
|
|
C566494|609968||hyperinsulinemic hypoglycemia familial 5
|
|
C566494|609968||hhf5
|
|
C562776||hyperproinsulinemia
|
|
D004370|126800||duane retraction syndrome
|
|
D004370|126800||acrorenoocular syndrome
|
|
D004370|126800||acrorenoocular syndromes
|
|
D004370|126800||anomalies isolated duane
|
|
D004370|126800||anomaly duane
|
|
D004370|126800||anomaly isolated duane
|
|
D004370|126800||co contractive retraction syndrome
|
|
D004370|126800||co contractive retraction syndromes
|
|
D004370|126800||drrs
|
|
D004370|126800||drs
|
|
D004370|126800||dr syndrome
|
|
D004370|126800||duane anomalies isolated
|
|
D004370|126800||duane anomaly
|
|
D004370|126800||duane anomaly isolated
|
|
D004370|126800||duane anomaly with radial abnormalities and deafness
|
|
D004370|126800||duane anomaly with radial ray abnormalities and deafness
|
|
D004370|126800||duane radial ray syndrome
|
|
D004370|126800||duane retraction syndrome 1
|
|
D004370|126800||duane retraction syndrome 2
|
|
D004370|126800||duane retraction syndrome type 1
|
|
D004370|126800||duane retraction syndrome type 2
|
|
D004370|126800||duane retraction syndrome type 3
|
|
D004370|126800||duane apos s syndrome
|
|
D004370|126800||duanes syndrome
|
|
D004370|126800||duane syndrome
|
|
D004370|126800||durs1
|
|
D004370|126800||durs2
|
|
D004370|126800||dus
|
|
D004370|126800||isolated duane anomalies
|
|
D004370|126800||isolated duane anomaly
|
|
D004370|126800||isolated duane retraction syndrome
|
|
D004370|126800||ocular retraction syndrome
|
|
D004370|126800||ocular retraction syndromes
|
|
D004370|126800||okihiro syndrome
|
|
D004370|126800||retraction syndrome
|
|
D004370|126800||retraction syndrome co contractive
|
|
D004370|126800||retraction syndrome duane
|
|
D004370|126800||retraction syndrome ocular
|
|
D004370|126800||retraction syndromes
|
|
D004370|126800||retraction syndromes co contractive
|
|
D004370|126800||retraction syndromes ocular
|
|
D004370|126800||stilling turk duane syndrome
|
|
D004370|126800||stilling turk duane syndromes
|
|
D004370|126800||syndrome acrorenoocular
|
|
D004370|126800||syndrome co contractive retraction
|
|
D004370|126800||syndrome duane
|
|
D004370|126800||syndrome duane radial ray
|
|
D004370|126800||syndrome duane retraction
|
|
D004370|126800||syndrome duane apos s
|
|
D004370|126800||syndrome ocular retraction
|
|
D004370|126800||syndrome okihiro
|
|
D004370|126800||syndrome retraction
|
|
D004370|126800||syndromes acrorenoocular
|
|
D004370|126800||syndromes co contractive retraction
|
|
D004370|126800||syndromes ocular retraction
|
|
D004370|126800||syndromes retraction
|
|
D004370|126800||syndromes stilling turk duane
|
|
D004370|126800||syndrome stilling turk duane
|
|
D004370|126800||type 1 duane retraction syndrome
|
|
D004370|126800||type 2 duane retraction syndrome
|
|
D004370|126800||type 3 duane retraction syndrome
|
|
300557|C564486||parkinson disease 12
|
|
300557|C564486||park12
|
|
300557|C564486||parkinson disease x linked
|
|
D005871||giant lymph node hyperplasia
|
|
D005871||angiofollicular lymph hyperplasia
|
|
D005871||angiofollicular lymph hyperplasias
|
|
D005871||angiofollicular lymph node hyperplasia
|
|
D005871||angiofollicular lymphoid hyperplasia
|
|
D005871||angiofollicular lymphoid hyperplasias
|
|
D005871||castleman disease
|
|
D005871||castleman apos s disease
|
|
D005871||castlemans disease
|
|
D005871||castleman apos s tumor
|
|
D005871||castlemans tumor
|
|
D005871||castleman tumor
|
|
D005871||glnh
|
|
D005871||hyperplasia angiofollicular lymph
|
|
D005871||hyperplasia angiofollicular lymphoid
|
|
D005871||hyperplasia giant lymph node
|
|
D005871||hyperplasias angiofollicular lymph
|
|
D005871||hyperplasias angiofollicular lymphoid
|
|
D005871||lymph node hyperplasia giant
|
|
D005871||lymphoid hyperplasia angiofollicular
|
|
D005871||lymphoid hyperplasias angiofollicular
|
|
D005871||tumor castleman apos s
|
|
C565202|610320||myopia 14
|
|
C565202|610320||myp14
|
|
D005870||giant cell tumors
|
|
D005870||cell tumor giant
|
|
D005870||cell tumors giant
|
|
D005870||giant cell tumor
|
|
D005870||tumor giant cell
|
|
D005870||tumors giant cell
|
|
D005873||giardiasis
|
|
D005873||giardiases
|
|
D005873||lambliases
|
|
D005873||lambliasis
|
|
D004541||eisenmenger complex
|
|
D004541||complex eisenmenger
|
|
D004541||complex eisenmenger apos s
|
|
D004541||eisenmenger apos s complex
|
|
D004541||eisenmengers complex
|
|
D004541||eisenmenger apos s syndrome
|
|
D004541||eisenmengers syndrome
|
|
D004541||eisenmenger syndrome
|
|
D004541||syndrome eisenmenger
|
|
D004541||syndrome eisenmenger apos s
|
|
D058489||46 xx disorders of sex development
|
|
D058489||46 xx dsd
|
|
D058489||female pseudohermaphroditism
|
|
D058489||female pseudohermaphroditisms
|
|
D058489||pseudohermaphroditism female
|
|
D058489||pseudohermaphroditisms female
|
|
D016523||foot ulcer
|
|
D016523||foot ulcers
|
|
D016523||plantar ulcer
|
|
D016523||plantar ulcers
|
|
D016523||ulcer foot
|
|
D016523||ulcer plantar
|
|
D016523||ulcers foot
|
|
D016523||ulcers plantar
|
|
D005889||gingival recession
|
|
D005889||atrophy of gingiva
|
|
D005889||gingiva atrophies
|
|
D005889||gingiva atrophy
|
|
D005889||gingival atrophies
|
|
D005889||gingival atrophy
|
|
D005889||gingival recessions
|
|
D005889||recession gingival
|
|
D005889||recessions gingival
|
|
C535423|601596||charcot marie tooth disease type 4c
|
|
C535423|601596||charcot marie tooth disease demyelinating autosomal recessive type 4c
|
|
C535423|601596||charcot marie tooth neuropathy type 4c
|
|
C535423|601596||cmt4c
|
|
C535423|601596||cmt 4c
|
|
D003229||conjunctival diseases
|
|
D003229||conjunctival disease
|
|
D003229||disease conjunctival
|
|
D003229||diseases conjunctival
|
|
C562783||hypercalciuric hypocalcemia familial
|
|
C562783||hypocalcemia autosomal dominant
|
|
C562783||hypocalcemia familial
|
|
C562783||hypoparathyroidism autosomal dominant
|
|
C537127|258500||optic atrophy 6
|
|
C537127|258500||opa6
|
|
C537127|258500||optic atrophy congenital or early infantile autosomal recessive
|
|
D005886||gingival hypertrophy
|
|
D005886||gingival hypertrophies
|
|
D005886||hypertrophies gingival
|
|
D005886||hypertrophy gingival
|
|
D005885||gingival hyperplasia
|
|
D005885||gingival hyperplasias
|
|
D005885||hyperplasia gingival
|
|
D005885||hyperplasias gingival
|
|
D005888||gingival pocket
|
|
D005888||gingival pockets
|
|
D005888||pocket gingival
|
|
D005888||pockets gingival
|
|
D005887||gingival neoplasms
|
|
D005887||congenital epulides
|
|
D005887||congenital epulis
|
|
D005887||epulides congenital
|
|
D005887||epulis congenital
|
|
D005887||gingival neoplasm
|
|
D005887||neoplasm gingival
|
|
D005887||neoplasms gingival
|
|
D004556||electric injuries
|
|
D004556||accidental electrocution
|
|
D004556||accidental electrocutions
|
|
D004556||electric injury
|
|
D004556||electrocution accidental
|
|
D004556||electrocutions accidental
|
|
D004556||injuries electric
|
|
D004556||injury electric
|
|
D005882||gingival diseases
|
|
D005882||disease gingival
|
|
D005882||diseases gingival
|
|
D005882||epulides
|
|
D005882||epulis
|
|
D005882||gingival disease
|
|
D005882||gingivoses
|
|
D005882||gingivosis
|
|
D005884||gingival hemorrhage
|
|
D005884||gingival hemorrhages
|
|
D005884||hemorrhage gingival
|
|
D003221||confusion
|
|
D003221||bewilderment
|
|
D003221||confusional state
|
|
D003221||confusional states
|
|
D003221||confusion post ictal
|
|
D003221||confusion reactive
|
|
D003221||disorientation
|
|
D003221||post ictal confusion
|
|
D003221||reactive confusion
|
|
D003221||state confusional
|
|
D003221||states confusional
|
|
D058499||retinal dystrophies
|
|
D058499||dystrophies retinal
|
|
D058499||dystrophy retinal
|
|
D058499||retinal dystrophy
|
|
D015208||smoke inhalation injury
|
|
D015208||inhalation injuries smoke
|
|
D015208||inhalation injury smoke
|
|
D015208||injuries smoke inhalation
|
|
D015208||injury smoke inhalation
|
|
D015208||smoke inhalation injuries
|
|
D005891||gingivitis
|
|
D005891||gingivitides
|
|
D015207||osteoarthritis hip
|
|
D015207||coxarthroses
|
|
D015207||coxarthrosis
|
|
D015207||hip osteoarthritides
|
|
D015207||hip osteoarthritis
|
|
D015207||osteoarthritides hip
|
|
D015207|140600|D010003||osteoarthritis of hip
|
|
D015207||osteoarthritis of hips
|
|
C563709|609508||stickler syndrome type i nonsyndromic ocular
|
|
C563709|609508||drrd included
|
|
C563709|609508||stickler syndrome atypical
|
|
C563709|609508||stickler syndrome atypical rhegmatogenous retinal detachment autosomal dominant included
|
|
C563709|609508||stickler syndrome type i predominantly ocular
|
|
604595||cholesterol level quantitative trait locus 1
|
|
604595||cholesterol level quantitative trait locus on chromosome 13
|
|
604595||cholesterol lowering factor
|
|
604595||clf
|
|
604595||clqtl1
|
|
D057165||proteostasis deficiencies
|
|
D057165||deficiencies proteostasis
|
|
D057165||deficiency proteostasis
|
|
D057165||disease protein folding
|
|
D057165||disease protein misfolding
|
|
D057165||diseases protein folding
|
|
D057165||diseases protein misfolding
|
|
D057165||disorder protein folding
|
|
D057165||disorder protein misfolding
|
|
D057165||disorders protein folding
|
|
D057165||disorders protein misfolding
|
|
D057165||dysfunction proteostasis
|
|
D057165||dysfunctions proteostasis
|
|
D057165||folding disease protein
|
|
D057165||folding diseases protein
|
|
D057165||folding disorder protein
|
|
D057165||folding disorders protein
|
|
D057165||misfolding disease protein
|
|
D057165||misfolding diseases protein
|
|
D057165||misfolding disorder protein
|
|
D057165||misfolding disorders protein
|
|
D057165||protein folding disease
|
|
D057165||protein folding diseases
|
|
D057165||protein folding disorder
|
|
D057165||protein folding disorders
|
|
D057165||protein misfolding disease
|
|
D057165||protein misfolding diseases
|
|
D057165||protein misfolding disorder
|
|
D057165||protein misfolding disorders
|
|
D057165||proteostasis deficiency
|
|
D057165||proteostasis dysfunction
|
|
D057165||proteostasis dysfunctions
|
|
C537457|309580||mental retardation hypotonic facies syndrome x linked 1
|
|
C537457|309580||carpenter waziri syndrome
|
|
C537457|309580||chudley lowry hoar syndrome
|
|
C537457|309580||chudley lowry syndrome
|
|
C537457|309580||chudley mental retardation syndrome
|
|
C537457|309580||chudley syndrome 1
|
|
C537457|309580||holmes gang syndrome
|
|
C537457|309580||jms
|
|
C537457|309580||juberg marsidi mental retardation syndrome
|
|
C537457|309580||juberg marsidi syndrome
|
|
C537457|309580||mental retardation x linked with growth retardation deafness and microgenitalism
|
|
C537457|309580||mental retradation x linked with growth delay deafness microgenitalism
|
|
C537457|309580||mrxhf1
|
|
C537457|309580||sfm1
|
|
C537457|309580||sfms
|
|
C537457|309580||smith fineman myers syndrome 1
|
|
C537457|309580||x linked hypogonadism gynecomastia mental retardation
|
|
C537457|309580||x linked mental retardation hypotonic facies syndrome
|
|
C537457|309580||xlmr hypotonic facies syndrome
|
|
D016534||cardiac output high
|
|
D016534||cardiac outputs high
|
|
D016534||high cardiac output
|
|
D016534||high cardiac outputs
|
|
D016535||bronchial hyperreactivity
|
|
D016535||bronchial hyperreactivities
|
|
D016535||hyperreactivities bronchial
|
|
D016535||hyperreactivity bronchial
|
|
C566397|603221||myopia 3
|
|
C566397|603221||myopia 3 autosomal dominant
|
|
C566397|603221||myp3
|
|
C564284|608133||retinitis pigmentosa 7
|
|
C564284|608133||retinitis pigmentosa 7 digenic included
|
|
C564284|608133||retinitis pigmentosa 7 with bull apos s eye maculopathy included
|
|
C564284|608133||rp7
|
|
C536580||chromosome 18 deletion syndrome
|
|
C536580||18q syndrome
|
|
C536580||chromosome 18 monosomy 18q
|
|
C536580||chromosome 18q deletion syndrome
|
|
C536580||chromosome 18q syndrome
|
|
C536580||monosomy 18q deletion 18q
|
|
C536580||monosomy 18q syndrome
|
|
C536581||chromosome 18 mosaic monosomy
|
|
C536581||monosomy 18 mosaicism
|
|
D004646||emphysema
|
|
D003316||corneal diseases
|
|
D003316||corneal disease
|
|
D003316||disease corneal
|
|
D003316||diseases corneal
|
|
D003317||corneal dystrophies hereditary
|
|
D003317||corneal dystrophy hereditary
|
|
D003317||corneal granular dystrophies
|
|
D003317||corneal granular dystrophy
|
|
D003317||corneal macular dystrophies
|
|
D003317||corneal macular dystrophy
|
|
D003317||corneal stromal dystrophies
|
|
D003317||corneal stromal dystrophy
|
|
D003317||dystrophies corneal granular
|
|
D003317||dystrophies corneal macular
|
|
D003317||dystrophies corneal stromal
|
|
D003317||dystrophies groenouw apos s
|
|
D003317||dystrophies hereditary corneal
|
|
D003317||dystrophy corneal granular
|
|
D003317||dystrophy corneal macular
|
|
D003317||dystrophy corneal stromal
|
|
D003317||dystrophy hereditary corneal
|
|
D003317||granular dystrophies corneal
|
|
D003317||granular dystrophy corneal
|
|
D003317||groenouw dystrophies
|
|
D003317||groenouw apos s dystrophies
|
|
D003317||groenouws dystrophies
|
|
D003317||hereditary corneal dystrophies
|
|
D003317||hereditary corneal dystrophy
|
|
D003317||macular dystrophies corneal
|
|
D003317||macular dystrophy corneal
|
|
D003317||stromal dystrophies corneal
|
|
D003317||stromal dystrophy corneal
|
|
C536584||alpha mannosidosis type 1
|
|
D003318||corneal opacity
|
|
D003318||corneal opacities
|
|
D003318||leukoma
|
|
D003318||leukomas
|
|
D003318||opacities corneal
|
|
D003318||opacity corneal
|
|
C536585||alpha mannosidosis type 2
|
|
C536585||alpha mannosidosis adult onset form
|
|
C562872||tuftsin deficiency
|
|
C565553|231005||gaucher disease type iiic
|
|
C537135|300238||orofaciodigital syndrome shashi type
|
|
C537135|300238||mental retardation x linked shashi type
|
|
C537135|300238||mental retardation x linked syndromic 11
|
|
C537135|300238||mrxs11
|
|
C537135|300238||shashi x linked mental retardation syndrome
|
|
C537135|300238||smrxs
|
|
D003310||cor triatriatum
|
|
D003310||atriums subdivided left
|
|
D003310||atrium subdivided left
|
|
D003310||cor triatriatum sinistrum
|
|
D003310||hearts triatrial
|
|
D003310||heart triatrial
|
|
D003310||left atriums subdivided
|
|
D003310||left atrium subdivided
|
|
D003310||subdivided left atrium
|
|
D003310||subdivided left atriums
|
|
D003310||triatrial heart
|
|
D003310||triatrial hearts
|
|
C563442|600795||frontotemporal dementia chromosome 3 linked
|
|
C563442|600795||dem
|
|
C563442|600795||dementia familial nonspecific
|
|
C563442|600795||dmt1
|
|
C563442|600795|C579991||ftd3
|
|
D058387||candidemia
|
|
D058387||candidemias
|
|
C564547|300271||mental retardation x linked 72
|
|
C564547|300271||mrx72
|
|
C536579||chromosome 17 trisomy 17q22
|
|
C536579||duplication 17q
|
|
C536579||trisomy 17q22
|
|
254110|C535897||limb girdle muscular dystrophy type 2h
|
|
254110|C535897||lgmd2h
|
|
254110|C535897||muscular dystrophy hutterite type
|
|
254110|C535897||muscular dystrophy limb girdle type 2h
|
|
254110|C535897||sarcotubular myopathy
|
|
C536577||borrone di rocco crovato syndrome
|
|
C536577||borrone dermatocardioskeletal syndrome
|
|
C536358|301310||anemia sideroblastic spinocerebellar ataxia
|
|
C536358|301310||anemia sex linked hypochromic siderobla
|
|
C536358|301310||anemia sideroblastic and spinocerebellar ataxia
|
|
C536358|301310||asat
|
|
C536358|301310||pagon bird detter syndrome
|
|
C536358|301310||sideroblastic anemia with spinocerebellar ataxia
|
|
C536358|301310||x linked sideroblastic anemia and ataxia
|
|
C536358|301310||xlsa a
|
|
C564593|607313||gaze palsy familial horizontal with progressive scoliosis
|
|
C564593|607313||familial horizontal gaze palsy with progressive scoliosis
|
|
C564593|607313||familial idiopathic scoliosis associated with congenital encephalopathy
|
|
C564593|607313||familial infantile scoliosis associated with bilateral paralysis of conjugate gaze
|
|
C564593|607313||hgpps
|
|
C564593|607313||horizontal gaze palsy with progressive scoliosis
|
|
C564593|607313||ophthalmoplegia progressive external and scoliosis
|
|
C564593|607313||ophthalmoplegia progressive external and scoliosis included
|
|
C536578||chromosome 17 trisomy 17p11 2
|
|
C536578||duplication 17p11 2
|
|
C536578||trisomy 17p11 2
|
|
C536665|261550||persistent mullerian duct syndrome
|
|
C536665|261550||female genital ducts in otherwise normal male
|
|
C536665|261550||hernia uteri inguinale
|
|
C536665|261550||persistent m 252 llerian duct syndrome
|
|
C536665|261550||persistent mullerian duct syndrome types 1 and 2
|
|
C536665|261550||persistent mullerian duct syndrome types i and ii
|
|
C536665|261550||persistent oviduct syndrome
|
|
C536665|261550||pmds
|
|
C536665|261550||pseudohermaphroditism male internal
|
|
C536593||alves castelo dos santos syndrome
|
|
C536593||ectodermal dysplasia syndrome of hypotrichosis onychodysplasia hyperkeratosis kyphoscoliosis and cataract
|
|
C536594||alzheimer disease type 1
|
|
C536594||alzheimer disease 1
|
|
C536594||early onset familial form of alzheimer disease
|
|
C536591||alveolar echinococcosis
|
|
C562884||fibromatosis gingival type 1
|
|
C536598||alzheimer disease familial type 3
|
|
C536598||alzheimer disease early onset type 3
|
|
C536598||alzheimer disease familial 3
|
|
C536598||alzheimer disease type 3
|
|
C562885||hyperbilirubinemia conjugated type iii
|
|
D003328||coronary thrombosis
|
|
D003328||coronary thromboses
|
|
D003328||thromboses coronary
|
|
D003328||thrombosis coronary
|
|
D003329||coronary vasospasm
|
|
D003329||artery vasospasm coronary
|
|
D003329||artery vasospasms coronary
|
|
D003329||coronary artery vasospasm
|
|
D003329||coronary artery vasospasms
|
|
D003329||coronary vasospasms
|
|
D003329||vasospasm coronary
|
|
D003329||vasospasm coronary artery
|
|
D003329||vasospasms coronary
|
|
D003329||vasospasms coronary artery
|
|
D004654||empyema tuberculous
|
|
D004654||empyema pleural tuberculous
|
|
D004654||empyemas tuberculous
|
|
D004654||tuberculous empyema
|
|
D004654||tuberculous empyemas
|
|
D004653||empyema
|
|
D003323||coronary aneurysm
|
|
D003323||aneurysm coronary
|
|
D003323||aneurysms coronary
|
|
D003323||coronary aneurysms
|
|
D057072||intra articular fractures
|
|
D057072||fracture intraarticular
|
|
D057072||fracture intra articular
|
|
D057072||fractures intraarticular
|
|
D057072||fractures intra articular
|
|
D057072||intraarticular fracture
|
|
D057072||intra articular fracture
|
|
D057072||intraarticular fractures
|
|
D003324||coronary artery disease
|
|
D003324||arterioscleroses coronary
|
|
D003324||arteriosclerosis coronary
|
|
D003324||artery disease coronary
|
|
D003324||artery diseases coronary
|
|
D003324||atheroscleroses coronary
|
|
D003324||atherosclerosis coronary
|
|
D003324||coronary arterioscleroses
|
|
D003324||coronary arteriosclerosis
|
|
D003324||coronary artery diseases
|
|
D003324||coronary atheroscleroses
|
|
D003324||coronary atherosclerosis
|
|
D003324||disease coronary artery
|
|
D003324||diseases coronary artery
|
|
C562886||ichthyosis congenita with biliary atresia
|
|
D004652||empty sella syndrome
|
|
D004652||empty sella syndrome primary
|
|
D004652||empty sella syndromes
|
|
D004652||empty sella syndrome secondary
|
|
D004652||empty sella turcica
|
|
D004652||empty sella turcicas
|
|
D004652||empty sella turcica syndrome
|
|
D004652||primary empty sella syndrome
|
|
D004652||secondary empty sella syndrome
|
|
D004652||sella turcica empty
|
|
D004652||sella turcicas empty
|
|
D003320||corneal ulcer
|
|
D003320||keratitides ulcerative
|
|
D003320||keratitis ulcerative
|
|
D003320||ulcerative keratitides
|
|
D003320||ulcerative keratitis
|
|
D003320||ulcer corneal
|
|
C564710|606407||hypotonia cystinuria syndrome
|
|
C564710|606407||cystinuria with mitochondrial disease
|
|
C564710|606407||homozygous 2p16 deletion syndrome formerly homozygous 2p21 deletion syndrome included
|
|
C564710|606407||homozygous 2p21 deletion syndrome
|
|
609179|D020325||migraine with aura
|
|
609179|D020325||acute onset aura migraine
|
|
609179|D020325||basilar artery migraine
|
|
609179|D020325||basilar migraine
|
|
609179|D020325||basilar migraines
|
|
609179|D020325||basilar type migraine
|
|
609179|D020325||classical migraine
|
|
609179|D020325||classic migraine
|
|
609179|D020325||complicated migraine
|
|
609179|D020325||familial hemiplegic migraine
|
|
609179|D020325||familial hemiplegic migraines
|
|
609179|D020325||hemiplegic migraine familial
|
|
609179|D020325||hemiplegic ophthalmoplegic migraine
|
|
609179|D020325||mgr7
|
|
609179|D020325||mgr9
|
|
609179|D020325||migraine aura without headache
|
|
609179|D020325||migraine basilar
|
|
609179|D020325||migraine basilar artery
|
|
609179|D020325||migraine basilar type
|
|
609179|D020325||migraine classic
|
|
609179|D020325||migraine classical
|
|
609179|D020325||migraine complicated
|
|
609179|D020325||migraine prolonged aura
|
|
609179|D020325||migraine with acute onset aura
|
|
609179|D020325||migraine with auras
|
|
609179|D020325||migraine with aura susceptibility to 7
|
|
609179|D020325||migraine with aura susceptibility to 9
|
|
609179|D020325||migraine with prolonged aura
|
|
609179|D020325||migraine with typical aura
|
|
609179|D020325||prolonged aura migraine
|
|
609179|D020325||typical aura without headache
|
|
D057068||periprosthetic fractures
|
|
D057068||fracture peri implant
|
|
D057068||fracture periprosthetic
|
|
D057068||fractures peri implant
|
|
D057068||fractures periprosthetic
|
|
D057068||peri implant fracture
|
|
D057068||peri implant fractures
|
|
D057068||periprosthetic fracture
|
|
D057066||low tension glaucoma
|
|
D057066||glaucoma low tension
|
|
D057066||glaucoma normal tension
|
|
D057066||glaucomas low tension
|
|
D057066||glaucomas normal tension
|
|
D057066||low tension glaucomas
|
|
D057066||normal tension glaucoma
|
|
D057066||normal tension glaucomas
|
|
D057066||tension glaucoma low
|
|
D057066||tension glaucoma normal
|
|
D057066||tension glaucomas low
|
|
D057066||tension glaucomas normal
|
|
D016638||critical illness
|
|
D016638||critical illnesses
|
|
D016638||critically ill
|
|
D016638||illness critical
|
|
D016638||illnesses critical
|
|
115197|C566169||cardiomyopathy familial hypertrophic 4
|
|
115197|C566169||cardiomyopathy familial hypertrophic 4 susceptibility to included
|
|
115197|C566169||cmh4
|
|
C566550|602433||amyotrophic lateral sclerosis 4 juvenile
|
|
C566550|602433||als4
|
|
C566550|602433||neuronopathy distal hereditary motor with pyramidal features
|
|
C536588||alsing syndrome
|
|
C535272||premature ovarian failure familial
|
|
C535272||familial premature ovarian failure
|
|
C535272||idiopathic familial premature ovarian failure
|
|
C535273||presenile dementia kraepelin type
|
|
C535273||catatonia of kraepelin
|
|
C535273||kraepelin disease
|
|
C535276||primary angiitis of the central nervous system
|
|
C535276||pacns
|
|
D005955||glucosephosphate dehydrogenase deficiency
|
|
D005955||deficiencies g6pd
|
|
D005955||deficiencies glucose 6 phosphate dehydrogenase
|
|
D005955||deficiencies glucosephosphate dehydrogenase
|
|
D005955||deficiencies gpd
|
|
D005955||deficiency g6pd
|
|
D005955||deficiency glucose 6 phosphate dehydrogenase
|
|
D005955||deficiency glucosephosphate dehydrogenase
|
|
D005955||deficiency gpd
|
|
D005955||deficiency of glucose 6 phosphate dehydrogenase
|
|
D005955||dehydrogenase deficiencies glucose 6 phosphate
|
|
D005955||dehydrogenase deficiencies glucosephosphate
|
|
D005955||dehydrogenase deficiency glucose 6 phosphate
|
|
D005955||dehydrogenase deficiency glucosephosphate
|
|
D005955||g6pd deficiencies
|
|
D005955||g6pd deficiency
|
|
D005955||glucose 6 phosphate dehydrogenase deficiencies
|
|
D005955||glucose 6 phosphate dehydrogenase deficiency
|
|
D005955||glucosephosphate dehydrogenase deficiencies
|
|
D005955||gpd deficiencies
|
|
D005955||gpd deficiency
|
|
D005955||hemolytic anemia due to g6pd deficiency
|
|
C535275||primary amebic meningoencephalitis
|
|
C535275||meningoencephalitis caused by naegleria fowleri
|
|
609054|C563801||fanconi anemia complementation group j
|
|
609054|C563801||fancj
|
|
D004620||embolism fat
|
|
D004620||embolisms fat
|
|
D004620||fat embolism
|
|
D004620||fat embolisms
|
|
D042822||genomic instability
|
|
D042822||genome instabilities
|
|
D042822||genome instability
|
|
D042822||genome stabilities
|
|
D042822||genome stability
|
|
D042822||genomic instabilities
|
|
D042822||genomic stabilities
|
|
D042822||genomic stability
|
|
D042822||instabilities genome
|
|
D042822||instabilities genomic
|
|
D042822||instability genome
|
|
D042822||instability genomic
|
|
D042822||stabilities genome
|
|
D042822||stabilities genomic
|
|
D042822||stability genome
|
|
D042822||stability genomic
|
|
D005953||glycogen storage disease type i
|
|
D005953||deficiencies glucose 6 phosphatase
|
|
D005953||deficiencies glucosephosphatase
|
|
D005953||deficiency glucose 6 phosphatase
|
|
D005953||deficiency glucosephosphatase
|
|
D005953||disease gierke
|
|
D005953||disease gierke apos s
|
|
D005953||disease von gierke
|
|
D005953||disease von gierke apos s
|
|
D005953||gierke disease
|
|
D005953||gierke apos s disease
|
|
D005953||gierkes disease
|
|
D005953||glucose 6 phosphatase deficiencies
|
|
D005953|C538655|232200||glucose 6 phosphatase deficiency
|
|
D005953||glucosephosphatase deficiencies
|
|
D005953||glucosephosphatase deficiency
|
|
D005953||glycogenosis 1
|
|
D005953||glycogen storage disease 1 gsd i
|
|
D005953||hepatorenal glycogen storage disease
|
|
D005953|C538655|232200||von gierke disease
|
|
D005953||von gierke apos s disease
|
|
D005953||von gierkes disease
|
|
D057085||tooth wear
|
|
D057085||dental wear
|
|
D057085||dental wears
|
|
D057085||tooth wears
|
|
D057085||wear dental
|
|
D057085||wears dental
|
|
D057085||wears tooth
|
|
D057085||wear tooth
|
|
C538387|145410||autosomal dominant opitz syndrome ados
|
|
C538387|145410||bbb syndrome
|
|
C538387|145410||chromosome 22q11 2 deletion syndrome opitz phenotype
|
|
C538387|145410||gbbb syndrome
|
|
C538387|145410||g syndrome
|
|
C538387|145410||hypertelorism hypospadias sydrome
|
|
C538387|145410||hypertelorism with esophageal abnormalities and hypospadias
|
|
C538387|145410||hypospadias dysphagia syndrome
|
|
C538387|145410||ogs2
|
|
C538387|145410||opitz bbbg syndrome
|
|
C538387|145410||opitz bbb g syndrome
|
|
C538387|145410||opitz bbb syndrome
|
|
C538387|145410||opitz frias syndrome
|
|
C538387|145410||opitz g bbb syndrome
|
|
C538387|145410||opitz gbbb syndrome autosomal dominant
|
|
C538387|145410||opitz gbbb syndrome type ii
|
|
C538387|145410||opitz g syndrome
|
|
C538387|145410||opitz g syndrome type 2
|
|
C538387|145410||opitz g syndrome type ii
|
|
C538387|145410||opitz oculogenitolaryngeal syndrome type ii
|
|
C538387|145410||telecanthus with associated abnormalities
|
|
C535270||premature aging okamoto type
|
|
C562858||cholesteatoma congenital
|
|
C563792|609122||aneurysm intracranial berry 3
|
|
C563792|609122||anib3
|
|
D016609||neoplasms second primary
|
|
D016609||cancer second
|
|
D016609||cancer second primary
|
|
D016609||cancers second
|
|
D016609||cancers second primary
|
|
D016609||cancers therapy associated
|
|
D016609||cancers therapy related
|
|
D016609||cancers treatment associated
|
|
D016609||cancers treatment related
|
|
D016609||cancer therapy associated
|
|
D016609||cancer therapy related
|
|
D016609||cancer treatment associated
|
|
D016609||cancer treatment related
|
|
D016609||malignancies second
|
|
D016609||malignancy second
|
|
D016609||metachronous neoplasm
|
|
D016609||metachronous neoplasms
|
|
D016609||metachronous second primary neoplasms
|
|
D016609||neoplasm metachronous
|
|
D016609||neoplasm second
|
|
D016609||neoplasm second primary
|
|
D016609||neoplasms metachronous
|
|
D016609||neoplasms metachronous second primary
|
|
D016609||neoplasms second
|
|
D016609||neoplasms therapy associated
|
|
D016609||neoplasms therapy related
|
|
D016609||neoplasms treatment associated
|
|
D016609||neoplasms treatment related
|
|
D016609||neoplasm therapy associated
|
|
D016609||neoplasm therapy related
|
|
D016609||neoplasm treatment associated
|
|
D016609||neoplasm treatment related
|
|
D016609||second cancer
|
|
D016609||second cancers
|
|
D016609||second malignancies
|
|
D016609||second malignancy
|
|
D016609||second neoplasm
|
|
D016609||second neoplasms
|
|
D016609||second primary cancer
|
|
D016609||second primary cancers
|
|
D016609||second primary neoplasm
|
|
D016609||second primary neoplasms
|
|
D016609||second primary neoplasms metachronous
|
|
D016609||therapy associated cancer
|
|
D016609||therapy associated cancers
|
|
D016609||therapy associated neoplasm
|
|
D016609||therapy associated neoplasms
|
|
D016609||therapy related cancer
|
|
D016609||therapy related cancers
|
|
D016609||therapy related neoplasm
|
|
D016609||therapy related neoplasms
|
|
D016609||treatment associated cancer
|
|
D016609||treatment associated cancers
|
|
D016609||treatment associated neoplasm
|
|
D016609||treatment associated neoplasms
|
|
D016609||treatment related cancer
|
|
D016609||treatment related cancers
|
|
D016609||treatment related neoplasm
|
|
D016609||treatment related neoplasms
|
|
D016603||eosinophilia myalgia syndrome
|
|
D016603||eosinophilia myalgia syndrome l tryptophan related
|
|
D016603||eosinophilia myalgia syndromes
|
|
D016603||eosinophilia myalgia syndromes l tryptophan related
|
|
D016603||l tryptophan related eosinophilia myalgia syndrome
|
|
D016603||l tryptophan related eosinophilia myalgia syndromes
|
|
D016603||syndrome eosinophilia myalgia
|
|
D016603||syndrome eosinophilia myalgia l tryptophan related
|
|
D016603||syndrome l tryptophan related eosinophilia myalgia
|
|
D016603||syndromes eosinophilia myalgia
|
|
D016603||syndromes l tryptophan related eosinophilia myalgia
|
|
D016606||thyroid nodule
|
|
D016606||nodules thyroid
|
|
D016606||nodule thyroid
|
|
D016606||thyroid nodules
|
|
C535269||preeyasombat varavithya syndrome
|
|
C535269||fanconi syndrome caused by degraded tetracycline
|
|
C536600|204000||amaurosis congenita of leber type 1
|
|
C536600|204000||amaurosis congenita of leber i
|
|
C536600|204000||crb
|
|
C536600|204000||lca
|
|
C536600|204000||lca1
|
|
C536600|204000||leber congenital amaurosis 1
|
|
C536600|204000||leber congenital amaurosis type 1
|
|
C536600|204000||retinal blindness congenital
|
|
C536599||alzheimer apos s disease without neurofibrillary tangles
|
|
C536599||alzheimer disease without neurofibrillary tangles
|
|
C536599||alzheimer apos s disease without tau pathology
|
|
267430|C537048||renal tubular dysgenesis
|
|
267430||primitive renal tubule syndrome renal tubular dysgenesis with choanal atresia and athelia included
|
|
267430||rtd
|
|
D016602||needlestick injuries
|
|
D016602||injuries needlestick
|
|
D016602||injuries needle stick
|
|
D016602||injuries sharps
|
|
D016602||injury needlestick
|
|
D016602||injury needle stick
|
|
D016602||injury sharps
|
|
D016602||needlestick
|
|
D016602||needle stick
|
|
D016602||needle stick injuries
|
|
D016602||needlestick injury
|
|
D016602||needle stick injury
|
|
D016602||needlesticks
|
|
D016602||needle sticks
|
|
D016602||sharps injuries
|
|
D016602||sharps injury
|
|
D001528|109650||behcet syndrome
|
|
D001528|109650||adamantiades behcet disease
|
|
D001528|109650||bd
|
|
D001528|109650||behcet disease
|
|
D001528|109650||beh 231 et disease
|
|
D001528|109650||behcet apos s syndrome
|
|
D001528|109650||behcets syndrome
|
|
D001528|109650||behcet triple symptom complex
|
|
D001528|109650||old silk route disease
|
|
D001528|109650||triple symptom complex
|
|
C535283||rambaud galian syndrome
|
|
C535436|158810||bethlem myopathy
|
|
C535436|158810||benign congenital muscular dystrophy
|
|
C535436|158810||benign congenital myopathy with contractures
|
|
C535436|158810||muscular dystrophy benign congenital
|
|
C535436|158810||myopathy benign congenital with contractures
|
|
C535285||ramon syndrome
|
|
C535285||gingival fibromatosis combined with cherubism
|
|
C565718|610149||macular degeneration age related 7
|
|
C565718|610149||macular degeneration age related 7 armd7 macular degeneration age related neovascular type susceptibility
|
|
C565718|610149||macular degeneration age related wet type susceptibility to included
|
|
C565718|610149|C562694|600669||to included
|
|
C562632|219200||cutis laxa autosomal recessive type iia
|
|
C562632|219200||arcl2
|
|
C562632|219200||arcl2a
|
|
C562632|219200||cutis laxa debre type
|
|
C562632|219200||cutis laxa with bone dystrophy
|
|
C562632|219200||cutis laxa with congenital disorder of glycosylation
|
|
C562632|219200||cutis laxa with growth and developmental delay
|
|
C562632|219200||cutis laxa with joint laxity and retarded development
|
|
C562632|219200||cutis laxa with or without congenital disorder of glycosylation
|
|
C535284||ramer ladda syndrome
|
|
C535284||humero radial synostosis
|
|
C535284||humeroradial synostosis
|
|
C535287||hunt apos s syndrome
|
|
C535287||myoclonus and ataxia
|
|
C535287||ramsay hunt syndrome type 2
|
|
C535286||ramos arroyo clark syndrome
|
|
C535286||ramos arroyo syndrome
|
|
C566951|611451||deafness autosomal recessive 63
|
|
C566951|611451||dfnb63
|
|
D017240|251900||mitochondrial myopathies
|
|
D017240|251900||disease luft
|
|
D017240|251900||disease luft apos s
|
|
D017240|251900||luft disease
|
|
D017240|251900||luft apos s disease
|
|
D017240|251900||lufts disease
|
|
D017240|251900||megaconial myopathies
|
|
D017240|251900||megaconial myopathy
|
|
D017240|251900||mitochondrial myopathy
|
|
D017240|251900||myopathies mitochondrial
|
|
D017240|251900||myopathies pleoconial
|
|
D017240|251900||myopathy megaconial
|
|
D017240|251900||myopathy pleoconial
|
|
D017240|251900||pleoconial myopathies
|
|
D017240|251900||pleoconial myopathy
|
|
C562866||thromboxane synthetase deficiency
|
|
609148|D008288||malaria
|
|
609148|D008288||fever marsh
|
|
609148|D008288||fever remittent
|
|
609148|D008288||infection plasmodium
|
|
609148|D008288||infections plasmodium
|
|
609148|D008288||malaria cerebral resistance to included
|
|
609148|D008288||malaria cerebral susceptibility to included
|
|
609148|D008288||malaria mild susceptibility to
|
|
609148|D008288||malaria resistance to included
|
|
609148|D008288||malaria severe resistance to included
|
|
609148|D008288||malaria severe susceptibility to included
|
|
609148|D008288||malaria susceptibility to
|
|
609148|D008288||mals
|
|
609148|D008288||marsh fever
|
|
609148|D008288||paludism
|
|
609148|D008288||plasmodium infection
|
|
609148|D008288||plasmodium infections
|
|
609148|D008288||remittent fever
|
|
D057096||shellfish poisoning
|
|
D057096||amnesic shellfish poisoning
|
|
D057096||amnesic shellfish poisonings
|
|
D057096||diarrhetic shellfish poisoning
|
|
D057096||diarrhetic shellfish poisonings
|
|
D057096||neurotoxic shellfish poisoning
|
|
D057096||neurotoxic shellfish poisonings
|
|
D057096||paralytic shellfish poisoning
|
|
D057096||paralytic shellfish poisonings
|
|
D057096||poisoning amnesic shellfish
|
|
D057096||poisoning diarrhetic shellfish
|
|
D057096||poisoning neurotoxic shellfish
|
|
D057096||poisoning paralytic shellfish
|
|
D057096||poisonings amnesic shellfish
|
|
D057096||poisonings diarrhetic shellfish
|
|
D057096||poisoning shellfish
|
|
D057096||poisonings neurotoxic shellfish
|
|
D057096||poisonings paralytic shellfish
|
|
D057096||poisonings shellfish
|
|
D057096||shellfish poisoning amnesic
|
|
D057096||shellfish poisoning diarrhetic
|
|
D057096||shellfish poisoning neurotoxic
|
|
D057096||shellfish poisoning paralytic
|
|
D057096||shellfish poisonings
|
|
D057096||shellfish poisonings amnesic
|
|
D057096||shellfish poisonings diarrhetic
|
|
D057096||shellfish poisonings neurotoxic
|
|
D057096||shellfish poisonings paralytic
|
|
D057090||eccrine porocarcinoma
|
|
D057090||eccrine porocarcinomas
|
|
D057090||eccrine poroma malignant
|
|
D057090||eccrine poromas malignant
|
|
D057090||malignant eccrine poroma
|
|
D057090||malignant eccrine poromas
|
|
D057090||porocarcinoma eccrine
|
|
D057090||porocarcinomas eccrine
|
|
D057090||poroma malignant eccrine
|
|
D057090||poromas malignant eccrine
|
|
D004630||emergencies
|
|
D004630||emergency
|
|
D057091||poroma
|
|
D057091||apocrine poroma
|
|
D057091||apocrine poromas
|
|
D057091||eccrine poroma
|
|
D057091||hidracanthoma simplex
|
|
D057091||poroma apocrine
|
|
D057091||poromas
|
|
D057091||poromas apocrine
|
|
D057091||simplex hidracanthoma
|
|
C562868||posttransfusion purpura
|
|
C535281||radius absent anogenital anomalies
|
|
C535281||radial aplasia and anogenital anomalies
|
|
C535281||radial aplasia x linked
|
|
D057092||geographic atrophy
|
|
D057092||atrophies geographic
|
|
D057092||atrophy geographic
|
|
D057092||degeneration dry macular
|
|
D057092||degenerations dry macular
|
|
D057092||dry macular degeneration
|
|
D057092||dry macular degenerations
|
|
D057092||geographic atrophies
|
|
D057092||macular degeneration dry
|
|
D057092||macular degenerations dry
|
|
C562869||secretory component deficiency
|
|
C562869||iga deficiency secretory
|
|
C535280||primary cortisol resistance
|
|
C565227|609800||generalized epilepsy with febrile seizures plus type 4
|
|
C565227|609800||gefs 4
|
|
C565227|609800||gefsp4
|
|
C565227|609800||gefsp type 4
|
|
C565227|609800||gefs type 4
|
|
607482|C564390||cardiomyopathy dilated 1m
|
|
607482|C564390||cmd1m
|
|
D057088||anetoderma
|
|
D057088||anetoderma primary
|
|
D057088||anetodermas
|
|
D057088||anetoderma secondary
|
|
D057088||anetodermas primary
|
|
D057088||anetodermas secondary
|
|
D057088||primary anetoderma
|
|
D057088||primary anetodermas
|
|
D057088||secondary anetoderma
|
|
D057088||secondary anetodermas
|
|
D010040|166800||otosclerosis
|
|
D010040|166800||otoscleroses
|
|
D010040|166800||otosclerosis 1
|
|
D010040|166800||otospongioses
|
|
D010040|166800||otospongiosis
|
|
D010040|166800||ots
|
|
D010040|166800||otsc1
|
|
C536366|300652||angioma serpiginosum x linked
|
|
C536366|300652||angioma serpiginosum
|
|
C566498|609946||deafness autosomal recessive 47
|
|
C566498|609946||dfnb47
|
|
C563688|609915||cardiomyopathy dilated 1q
|
|
C563688|609915||cmd1q
|
|
C537874||larsen syndrome recessive type
|
|
C537874||autosomal recessive larsen syndrome
|
|
C537874||larsen syndrome recessive
|
|
C536543||vertebral body fusion overgrowth
|
|
C536543||progressive anterior vertebral body fusion overgrowth and distinct craniofacial appearance
|
|
C562830||patent ductus venosus
|
|
C562830||portosystemic venous shunt congenital
|
|
D021184||nut hypersensitivity
|
|
D021184||allergies nut
|
|
D021184||allergies tree nut
|
|
D021184||allergy nut
|
|
D021184||allergy tree nut
|
|
D021184||hypersensitivities nut
|
|
D021184||hypersensitivities tree nut
|
|
D021184||hypersensitivity nut
|
|
D021184||hypersensitivity tree nut
|
|
D021184||nut allergies
|
|
D021184||nut allergy
|
|
D021184||nut hypersensitivities
|
|
D021184||nut hypersensitivities tree
|
|
D021184||nut hypersensitivity tree
|
|
D021184||tree nut allergies
|
|
D021184||tree nut allergy
|
|
D021184||tree nut hypersensitivities
|
|
D021184||tree nut hypersensitivity
|
|
D004605||elephantiasis filarial
|
|
D004605||bancroftian elephantiases
|
|
D004605||bancroftian elephantiasis
|
|
D004605||elephantiases bancroftian
|
|
D004605||elephantiases filarial
|
|
D004605||elephantiasis bancroftian
|
|
D004605||filarial elephantiases
|
|
D004605||filarial elephantiasis
|
|
D004605||filariases lymphatic
|
|
D004605||filariasis lymphatic
|
|
D004605||lymphatic filariases
|
|
D004605||lymphatic filariasis
|
|
C536540||verloes van maldergem marneffe syndrome
|
|
C536540||dominantly inherited bone dysplasia with severe eye involvement
|
|
C536540||microspherophakia metaphyseal dysplasia
|
|
D021183||peanut hypersensitivity
|
|
D021183||allergies peanut
|
|
D021183||allergy peanut
|
|
D021183||groundnut hypersensitivity
|
|
D021183||hypersensitivity groundnut
|
|
D021183||hypersensitivity peanut
|
|
D021183||peanut allergies
|
|
D021183||peanut allergy
|
|
D005935||glucagonoma
|
|
D005935||adenoma alpha cell
|
|
D005935||adenomas alpha cell
|
|
D005935||alpha cell adenoma
|
|
D005935||alpha cell adenomas
|
|
D005935||alpha cell tumor
|
|
D005935||alpha cell tumors
|
|
D005935||glucagonomas
|
|
D005935||glucagonoma syndrome
|
|
D005935||glucagonoma syndromes
|
|
D005935||syndrome glucagonoma
|
|
D005935||syndromes glucagonoma
|
|
D005935||tumor alpha cell
|
|
D005935||tumors alpha cell
|
|
250620|C562803||beta hydroxyisobutyryl coa deacylase deficiency
|
|
250620|C562803||3 hydroxyisobutyryl coa hydrolase deficiency
|
|
250620|C562803||hibch deficiency
|
|
250620|C562803||methacrylic acid toxicity
|
|
250620|C562803||methacrylic aciduria
|
|
250620|C562803||valine metabolic defect
|
|
D004604||elephantiasis
|
|
D004604||bigfoot disease
|
|
D004604||bigfoot diseases
|
|
D004604||disease bigfoot
|
|
D004604||disease microcrystal
|
|
D004604||diseases bigfoot
|
|
D004604||diseases microcrystal
|
|
D004604||elephantiases
|
|
D004604||elephantiases endemic
|
|
D004604||elephantiases endemic non filarial
|
|
D004604||elephantiasis endemic
|
|
D004604||elephantiasis endemic non filarial
|
|
D004604||elephantiasis nostras verrucosa
|
|
D004604||elephantiasis nostras verrucosas
|
|
D004604||endemic elephantiases
|
|
D004604||endemic elephantiasis
|
|
D004604||endemic non filarial elephantiases
|
|
D004604||endemic non filarial elephantiasis
|
|
D004604||foot mossy
|
|
D004604||foots mossy
|
|
D004604||lymphostatic verrucoses
|
|
D004604||lymphostatic verrucosis
|
|
D004604||microcrystal disease
|
|
D004604||microcrystal diseases
|
|
D004604||mossy foot
|
|
D004604||mossy foots
|
|
D004604||non filarial elephantiases endemic
|
|
D004604||non filarial elephantiasis endemic
|
|
D004604||nostras verrucosa elephantiasis
|
|
D004604||nostras verrucosas elephantiasis
|
|
D004604||podoconioses
|
|
D004604||podoconiosis
|
|
D004604||verrucosa elephantiasis nostras
|
|
D004604||verrucosas elephantiasis nostras
|
|
D004604||verrucoses lymphostatic
|
|
D004604||verrucosis lymphostatic
|
|
C537872||larsen like syndrome lethal type
|
|
C537872||larsen like multiple joint dislocation syndrome
|
|
C536541||verloove vanhorick brubakk syndrome
|
|
C536541||cleft limb heart malformation syndrome
|
|
D021182||wheat hypersensitivity
|
|
D021182||allergies wheat
|
|
D021182||allergy wheat
|
|
D021182||hypersensitivities wheat
|
|
D021182||hypersensitivity wheat
|
|
D021182||wheat allergies
|
|
D021182||wheat allergy
|
|
D021182||wheat hypersensitivities
|
|
C562833||pulmonary atresia with ventricular septal defect
|
|
C562832||pulmonary atresia with intact ventricular septum
|
|
C562838||comedones familial dyskeratotic
|
|
612954||myopathy myofibrillar 6
|
|
612954||mfm6
|
|
612954|C567843||myopathy myofibrillar bag3 related
|
|
C562835||intestinal malrotation familial
|
|
612953|C567844||parkinson disease 14 autosomal recessive
|
|
612953|C567844||dystonia parkinsonism adult onset
|
|
612953||park14
|
|
611630||epilepsy familial temporal lobe 3
|
|
611630||etl3
|
|
611630||fmtle
|
|
607823|C564327||hypotrichosis lymphedema telangiectasia syndrome
|
|
607823|C564327||hlts
|
|
C537919|228300||fertile eunuch syndrome
|
|
C537866||oculocerebral hypopigmentation syndrome type preus
|
|
C537866||cross syndrome
|
|
C537866||kramer syndrome
|
|
C537866||oculocerebral hypopigmentation syndrome of preus
|
|
C537866||oculocerebral syndrome with hypopigmentation
|
|
C536535||vein of galen aneurysm
|
|
C536535||ectasia or varix of the vein of galen
|
|
C536535||galenic arteriovenous malformation
|
|
C536535||galen vein aneurysm
|
|
C536535||vein of galen aneurysm malformation
|
|
C536536||velofacioskeletal syndrome
|
|
C538324|246450||3 hydroxy 3 methylglutaryl coa lyase deficiency
|
|
C538324|246450||3 hydroxy 3 methylglutaric aciduria
|
|
C538324|246450||3 hydroxy 3 methyl glutaric aciduria
|
|
C538324|246450||3 hydroxy 3 methylglutaryl coenzyme a lyase deficiency
|
|
C538324|246450||3 hydroxyl 3 methyl glutaric aciduria
|
|
C538324|246450||deficiency of hydroxymethylglutaryl coa lyase
|
|
C538324|246450||hl deficiency
|
|
C538324|246450||hmgcld
|
|
C538324|246450||hmgcl deficiency
|
|
C538324|246450||hmg coa lyase deficiency
|
|
C538324|246450||hydroxymethylglutaric aciduria
|
|
C536533||vasquez hurst sotos syndrome
|
|
D011565|177900||psoriasis
|
|
D011565|177900||palmoplantaris pustulosis
|
|
D011565|177900||psoriases
|
|
D011565|177900||psoriasis susceptibility 1
|
|
D011565|177900||psoriasis susceptibility 10
|
|
D011565|177900||psoriasis susceptibility 11
|
|
D011565|177900||psoriasis susceptibility 12
|
|
D011565|177900||psoriasis susceptibility 2
|
|
D011565|177900||psoriasis susceptibility 3
|
|
D011565|177900||psoriasis susceptibility 4
|
|
D011565|177900||psoriasis susceptibility 5
|
|
D011565|177900||psoriasis susceptibility 6
|
|
D011565|177900||psoriasis susceptibility 7
|
|
D011565|177900||psoriasis susceptibility 8
|
|
D011565|177900||psoriasis susceptibility 9
|
|
D011565|177900||psors1
|
|
D011565|177900||psors10
|
|
D011565|177900||psors11
|
|
D011565|177900||psors12
|
|
D011565|177900||psors2
|
|
D011565|177900||psors3
|
|
D011565|177900||psors4
|
|
D011565|177900||psors5
|
|
D011565|177900||psors6
|
|
D011565|177900||psors7
|
|
D011565|177900||psors8
|
|
D011565|177900||psors9
|
|
D011565|177900||pustular psoriasis of palms and soles
|
|
D011565|177900||pustulosis of palms and soles
|
|
D011565|177900||pustulosis palmaris et plantaris
|
|
C537865||oculoauriculofrontonasal syndrome
|
|
C537865||oculoauriculofrontonasal dysplasia
|
|
C536539||verloes gillerot fryns syndrome
|
|
C536539||cerebro acro visceral early lethality multiplex syndrome
|
|
C536537||ventricular extrasystoles perodactyly robin sequence
|
|
612581|C567240||mental retardation autosomal dominant 4
|
|
612581|C567240||mrd4
|
|
C537869||laplane fontaine lagardere syndrome
|
|
C537869||familial syndesmodysplasic dwarfism
|
|
C537869||syndesmodysplasic dwarfism
|
|
C536538||verloes bourguignon syndrome
|
|
C536538||platyspondyly with amelogenesis imperfecta
|
|
C536538||skeletal dysplasia with amelogenesis imperfecta and platyspondyly
|
|
D004618||embolism air
|
|
D004618||air embolism
|
|
D004618||air embolisms
|
|
D004618||embolism gas
|
|
D004618||embolisms air
|
|
D004618||embolisms gas
|
|
D004618||gas embolism
|
|
D004618||gas embolisms
|
|
176620|C531791||priapism familial idiopathic
|
|
176620|C531791||familial idiopathic priapism
|
|
D004617||embolism
|
|
D004617||embolisms
|
|
D004617||embolus
|
|
C536550||tricho dento osseous syndrome 1
|
|
D004619||embolism amniotic fluid
|
|
D004619||amniotic fluid embolism
|
|
D004619||amniotic fluid embolisms
|
|
D004619||embolisms amniotic fluid
|
|
D004614||emaciation
|
|
D004614||emaciations
|
|
C536553||trichofolliculoma
|
|
C536553||congenital trichofolliculoma
|
|
C536553||recurrent trichofolliculoma
|
|
C536553||sebaceous trichofolliculoma
|
|
C562840||breast cancer familial
|
|
C537885||peters anomaly with cataract
|
|
C536554||oliver mcfarlane syndrome
|
|
C536554||congenital trichomegaly pigmentary retinal degeneration and short stature
|
|
C536554||eyelashes long mental retardation
|
|
C536554||trichomegaly retina pigmentary degeneration dwarfism
|
|
C562841||ovarian germ cell cancer
|
|
C537882||laurence prosser rocker syndrome
|
|
C536551||trichodental syndrome
|
|
C536551||tricho dental dysplasia
|
|
C536551||trichodental dysplasia
|
|
C536551||tricho dental syndrome
|
|
300558|C563146||mental retardation x linked 30
|
|
300558|C563146||mrx30
|
|
606049|C535656||acromegaloid features overgrowth cleft palate and hernia
|
|
606049|C535656||aoch
|
|
C563660|610828||holoprosencephaly 7
|
|
C563660|610828||hpe7
|
|
D004612||elliptocytosis hereditary
|
|
D004612||elliptocytoses hereditary
|
|
D004612||hereditary elliptocytoses
|
|
D004612||hereditary elliptocytosis
|
|
D004612||hereditary ovalocytoses
|
|
D004612||hereditary ovalocytosis
|
|
D004612||ovalocytoses hereditary
|
|
D004612||ovalocytosis hereditary
|
|
C535600|223360||dopamine beta hydroxylase deficiency
|
|
C535600|223360||congenital dopamine beta hydroxylase deficiency
|
|
C535600|223360||dopamine beta hydroxylase deficiency congenital
|
|
C535600|223360||dopamine b hydroxylase
|
|
C535600|223360||noradrenaline deficiency
|
|
C535600|223360||norepinephrine deficiency
|
|
C537877||late onset congenital adrenal hyperplasia
|
|
C537877||attenuated congenital adrenal hyperplasia
|
|
C537877||locah
|
|
C537877||nccah
|
|
C537877||non classic congenital adrenal hyperplasia
|
|
D021181||egg hypersensitivity
|
|
D021181||allergies egg
|
|
D021181||allergy egg
|
|
D021181||egg allergies
|
|
D021181||egg allergy
|
|
D021181||egg hypersensitivities
|
|
D021181||hypersensitivities egg
|
|
D021181||hypersensitivity egg
|
|
609308|D058494|236670||muscular dystrophy dystroglycanopathy limb girdle type c 1
|
|
609308|D058494|236670||lgmd2k
|
|
609308||mddgc1
|
|
609308|D058494|236670||muscular dystrophy limb girdle type 2k
|
|
C537878||lateral meningocele syndrome
|
|
C537878||lehman syndrome
|
|
C537875||laryngeal cleft
|
|
C537875||anterior submucous laryngeal cleft
|
|
C537875||congenital laryngeal clefts
|
|
C537875||posterior laryngeal cleft plc
|
|
C536544||treft sanborn carey syndrome
|
|
C536544||dominant optic atrophy deafness ptosis ophthalmoplegia dystaxia and myopathy
|
|
C537876||laryngeal papillomatosis
|
|
C537876||juvenile laryngeal papillomatosis
|
|
C537876||recurrent laryngeal papillomatosis
|
|
C537876||warts in the throat
|
|
C537879||lateral semicircular canal malformation familial with external and middle ear abnormalities
|
|
C567925|147060||hyper ige recurrent infection syndrome autosomal dominant
|
|
C567925|147060|D007589|243700||hies autosomal dominant
|
|
C567925|147060|D007589|243700||hyper ige syndrome autosomal dominant
|
|
C567925|147060|D007589|243700||job syndrome
|
|
C536549||tricho dento osseous syndrome
|
|
C536549|190320||trichodentoosseous syndrome
|
|
C537891||pfeiffer tietze welte syndrome
|
|
C537892||phace association
|
|
C537892||phaces association
|
|
D005918||glomus tumor
|
|
D005918||glomangioma
|
|
D005918||glomangiomas
|
|
D005918||glomus tumors
|
|
D005918||tumor glomus
|
|
D005918||tumors glomus
|
|
C537890||pfeiffer rockelein syndrome
|
|
C537890||asymmetrical coronal synostosis cutaneous syndactyly of fingers and toes and jejunal atresia
|
|
600955|C563423||proprotein convertase 1 3 deficiency
|
|
600955|C563423||obesity and endocrinopathy due to impaired processing of prohormones
|
|
C565089||doughnut lesions of skull familial
|
|
C537895||phenol sulfotransferase deficiency
|
|
C536564||triphalangeal thumbs brachyectrodactyly
|
|
C536564||triphalangeal thumb and brachy ectrodactyly syndrome
|
|
C536564||triphalangeal thumb and brachyectrodactyly syndrome
|
|
C536564||triphalangeal thumbs with brachyectrodactyly
|
|
D005911||gliosis
|
|
D005911||astrocytosis
|
|
D005911||glioses
|
|
C536565||trueb burg bottani syndrome
|
|
C536565||ectodermal dysplasia with corkscrew hairs
|
|
C536565||tricho odonto onychodysplasia with syndactyly
|
|
C537893||phacomatosis pigmentokeratotica
|
|
C536562||triphalangeal thumb non opposable
|
|
C536562||non opposable triphalangeal thumb
|
|
C536562||triphalangeal thumb nonopposable
|
|
C537894||phacomatosis pigmentovascularis
|
|
C535493|609638||epidermolysis bullosa lethal acantholytic
|
|
C535493|609638||ebla
|
|
612936|C567858||spastic paraplegia 50 autosomal recessive
|
|
612936||cerebral palsy spastic quadriplegic 3 formerly
|
|
612936||cpsq3 formerly
|
|
612936||spg50
|
|
C562816||harderoporphyria
|
|
C565240|606263||paget disease of bone 4
|
|
C565240|606263||pdb4
|
|
C565090||double nail for fifth toe
|
|
C562818||glutaric aciduria iii
|
|
C562818||glutaryl coa oxidase deficiency
|
|
D008199||lymphadenitis
|
|
D008199||adenitides
|
|
D008199||adenitis
|
|
D008199||lymphadenitides
|
|
C563295|601543||deafness autosomal dominant 12
|
|
C563295|601543||deafness autosomal dominant 8
|
|
C563295|601543||dfna12
|
|
C563295|601543||dfna8
|
|
C567218|612637||febrile convulsions familial 10
|
|
C567218|612637||convulsions familial febrile 10
|
|
C567218|612637||feb10
|
|
C567218|612637||febrile seizures familial 10
|
|
C567218|612637||seizures familial febrile 10
|
|
C537888||pfeiffer mayer syndrome
|
|
C536557||trichoscyphodysplasia
|
|
C536557||cupped metaphyses and cone shaped epiphyses with alopecia
|
|
C536557||metaphyseal chondrodysplasia with cone shaped epiphyses and alopecia
|
|
C536557||metaphyseal chondrodysplasia with ectodermal dysplasia
|
|
C565097||digitotalar dysmorphism
|
|
C565097||ulnar drift hereditary
|
|
C537889||pfeiffer palm teller syndrome
|
|
C536558||trichostasis spinulosa
|
|
D008193||lyme disease
|
|
D008193||arthritis lyme
|
|
D008193||borreliosis lyme
|
|
D008193||disease lyme
|
|
D008193||lyme arthritis
|
|
D008193||lyme borreliosis
|
|
C565098||diastema dental medial
|
|
C537886||petty laxova wiedemann syndrome
|
|
C537093|113100||brachydactyly type c
|
|
C537093|113100||bdc
|
|
C537093|113100||brachydactyly haws type
|
|
C565099||diarrhea glucose stimulated secretory with common variable immunodeficiency
|
|
C537887||pfeiffer kapferer syndrome
|
|
C537887||short stature mental retardation and multiple dysmorphisms
|
|
C536556||trichorrhexis nodosa syndrome
|
|
C536556||pollitt syndrome
|
|
C536556||trichothiodystrophy neurocutaneous syndrome
|
|
C536556||trichothiodystrophy neurotrichocutaneous syndrome of pollitt
|
|
C565092||distichiasis with congenital anomalies of the heart and peripheral vasculature
|
|
C565093||distal osteosclerosis
|
|
C565093||osteosclerosis distal
|
|
C565094||disproportionate short stature with ptosis and valvular heart lesions
|
|
C565095||megaloblastic anemia due to dihydrofolate reductase deficiency
|
|
C565095||dhfr deficiency
|
|
C536571||boerhaave syndrome
|
|
C536571||boerhaave apos s syndrome
|
|
C536571||boerhave syndrome
|
|
D005926||glossalgia
|
|
D005926||glossalgias
|
|
D005926||glossodynia
|
|
D005926||glossodynias
|
|
D005926||glossopyroses
|
|
D005926||glossopyrosis
|
|
C536572||bone marrow failure syndromes
|
|
D005929||glossitis benign migratory
|
|
D005929||benign migratory glossitis
|
|
D005929||geographic tongue
|
|
D005929||glossitis areata exfoliativa
|
|
D005929||migratory glossitis benign
|
|
D005929||tongue geographic
|
|
D006976|178600||hypertension pulmonary
|
|
D006976|178600||pht
|
|
D006976|178600||pph1
|
|
D006976|178600||pph1 with hht included
|
|
D006976|178600||pulmonary arterial hypertension pah pulmonary hypertension primary dexfenfluramine associated included
|
|
D006976|178600||pulmonary hypertension
|
|
D006976|178600|C536282||pulmonary hypertension primary 1
|
|
D006976|178600||pulmonary hypertension primary 1 with hereditary hemorrhagic telangiectasia included
|
|
D006976|178600||pulmonary hypertension primary fenfluramine associated included
|
|
D005928||glossitis
|
|
D005928||glossitides
|
|
C536576||bork stender schmidt syndrome
|
|
C536576||bork syndrome
|
|
C536576||uncombable hair retinal pigmentary dystrophy dental anomalies and brachydactyly
|
|
D005925||glomus jugulare tumor
|
|
D005925|D010235|168000||glomus jugulare tumors
|
|
D005925|D010235|168000||glomus tumors familial 1
|
|
D005925||jugulare tumor glomus
|
|
D005925||jugulare tumors glomus
|
|
D005925||tumor glomus jugulare
|
|
D005925||tumors glomus jugulare
|
|
612929||mycobacterium tuberculosis susceptibility to 3
|
|
612929||mtbs3
|
|
C536574||bor duane hydrocephalus contiguous gene syndrome
|
|
C536574||branchio oto renal duane hydrocephalus contiguous gene syndrome
|
|
C562823||milia multiple eruptive
|
|
D005921||glomerulonephritis
|
|
D005921||bright disease
|
|
D005921||glomerulonephritides
|
|
D014849|148820||waardenburg syndrome
|
|
D014849|148820||klein apos s syndrome
|
|
D014849|148820||kleins syndrome
|
|
D014849|148820||klein syndrome
|
|
D014849|148820||klein waardenburg syndrome
|
|
D014849|148820||syndrome klein
|
|
D014849|148820||syndrome klein apos s
|
|
D014849|148820||syndrome klein waardenburg
|
|
D014849|148820||syndrome waardenburg
|
|
D014849|148820||syndrome waardenburg klein
|
|
D014849|148820||syndrome waardenburg apos s
|
|
D014849|148820||waardenburg klein syndrome
|
|
D014849|148820||waardenburg apos s syndrome
|
|
D014849|148820||waardenburgs syndrome
|
|
D014849|148820||waardenburg apos s syndrome type 1
|
|
D014849|148820||waardenburg syndrome type 1
|
|
D014849|148820||waardenburg syndrome type 3
|
|
D014849|148820||waardenburg syndrome type iii
|
|
D014849|148820||waardenburg syndrome with dystopia canthorum
|
|
D014849|148820||waardenburg syndrome with upper limb anomalies
|
|
D014849|148820||white forelock poliosis syndrome with multiple congenital malformations
|
|
D014849|148820||ws1
|
|
D014849|148820||ws3
|
|
C562827||alacrima
|
|
C562824||poikiloderma hereditary sclerosing
|
|
C563365|601228||polyposis syndrome hereditary mixed 1
|
|
C563365|601228||chromosome 15q13 q14 duplication syndrome 40 kb
|
|
C563365|601228||colorectal adenoma and carcinoma 1
|
|
C563365|601228||colorectal adenoma and carcinoma 1 crac1 colorectal cancer susceptibility to 4 included
|
|
C563365|601228||colorectal cancer susceptibility to on chromosome 15 included
|
|
C563365|601228||crcs4 included
|
|
C563365|601228||hmps1
|
|
C537899||baker vinters syndrome
|
|
C537899||hydrocephalus with cerebral aqueductal dysgenesis and craniofacial anomalies
|
|
C536568||walker dyson syndrome
|
|
C536568||aniridia associated with mental retardation and other eye abnormalities
|
|
D054853||malignant atrophic papulosis
|
|
D054853||atrophic papuloses malignant
|
|
D054853||atrophic papulosis malignant
|
|
D054853||degos disease
|
|
D054853||degos apos s malignant atrophic papulosis
|
|
D054853||degos syndrome
|
|
D054853||disease degos
|
|
D054853||disease kohlmeier degos
|
|
D054853||erythrokeratoderma en cocardes
|
|
D054853||kohlmeier degos disease
|
|
D054853||malignant atrophic papuloses
|
|
D054853||papuloses malignant atrophic
|
|
D054853||papulosis malignant atrophic
|
|
D054853||syndrome degos
|
|
C537897||phosphoribosylpyrophosphate synthetase deficiency
|
|
C536566||walbaum titran durieux crepin syndrome
|
|
C536567||waldmann disease
|
|
C536567||familial waldmann apos s disease
|
|
C536567||primary intestinal lymphangiectasis
|
|
C536567||waldmann apos s disease
|
|
D054850||osteophyte
|
|
D054850||bone spur
|
|
D054850||bone spurs
|
|
D054850||osteophytes
|
|
D054850||spur bone
|
|
D054850||spurs bone
|
|
C536864|182600||spastic paraplegia 3 autosomal dominant
|
|
C536864|182600||familial spastic paraplegia autosomal dominant 1
|
|
C536864|182600||fsp1
|
|
C536864|182600||spg3
|
|
C536864|182600|C580455||spg3a
|
|
C536864|182600||strumpell disease
|
|
C536595|104310||alzheimer disease type 2
|
|
C536595|104310||ad2
|
|
C536595|104310||alzheimer disease 2
|
|
C536595|104310||alzheimer disease 2 late onset
|
|
C536595|104310||alzheimer disease associated with apoe4
|
|
C536595|104310||alzheimer disease associated with apoe e4
|
|
C536595|104310||late onset familial alzheimer disease
|
|
C565067||ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet
|
|
C567227|612632||usher syndrome type ih
|
|
C567227|612632||ush1h
|
|
C565068||ectodermal dysplasia trichoodontoonychial type
|
|
C537830||macrosomia with lethal microphthalmia
|
|
C537830||macrosomia microphthalmia cleft palate
|
|
C537830||macrosomia with microphthalmia lethal
|
|
C537830||teebi al saleh hassoon syndrome
|
|
C565069||orofacial cleft 8
|
|
D042882||gallstones
|
|
D042882||biliary calculi
|
|
D042882||biliary calculi common bile duct
|
|
D042882||calculi biliary
|
|
D042882||common bile duct calculi
|
|
D042882||common bile duct gallstones
|
|
D042882||common bile duct gall stones
|
|
D042882||gallstone
|
|
D042882||gall stone
|
|
D042882||gall stones
|
|
D042882||gallstones common bile duct
|
|
D042882||gall stones common bile duct
|
|
D042883||choledocholithiasis
|
|
D042883||cholelithiasis common bile duct
|
|
215500|C535358||choroidal dystrophy central areolar
|
|
215500|C535358||cacd
|
|
215500|C535358||cacd1
|
|
215500|C535358||central areolar choroidal sclerosis
|
|
215500|C535358||choroidal dystrophy central areolar 1
|
|
215500|C535358||choroidal sclerosis
|
|
D008169||lung abscess
|
|
D008169||abscesses lung
|
|
D008169||abscesses pulmonary
|
|
D008169||abscess lung
|
|
D008169||abscess pulmonary
|
|
D008169||lung abscesses
|
|
D008169||pulmonary abscess
|
|
D008169||pulmonary abscesses
|
|
612160|C563181||histiocytoma angiomatoid fibrous
|
|
D010488||polyarteritis nodosa
|
|
D010488||arteritides necrotizing
|
|
D010488||arteritis necrotizing
|
|
D010488||essential polyarteritides
|
|
D010488||essential polyarteritis
|
|
D010488||necrotizing arteritides
|
|
D010488||necrotizing arteritis
|
|
D010488||periarteritis nodosa
|
|
D010488||polyarteritides essential
|
|
D010488||polyarteritis essential
|
|
D008178||lupus erythematosus cutaneous
|
|
D008178||cutaneous lupus erythematosus
|
|
D008178||lupus erythematosus cutaneous subacute
|
|
D008178||lupus erythematosus subacute cutaneous
|
|
D008179||lupus erythematosus discoid
|
|
D008179||discoid lupus erythematosus
|
|
D008179||lupus erythematosus chronic cutaneous
|
|
D008179||lupus erythematosus cutaneous chronic
|
|
C537828||chromosome 8 monosomy 8q
|
|
C537828||deletion 8q
|
|
C537828||monosomy 8q
|
|
C537829||macrophagic myofasciitis
|
|
C537829||macrophagic myofasciitis childhood
|
|
D010489||periarthritis
|
|
D010489||periarthritides
|
|
D008177||lupus vulgaris
|
|
D008174||lung diseases parasitic
|
|
D008174||lung disease parasitic
|
|
D008174||lung parasitic infection
|
|
D008174||lung parasitic infections
|
|
D008174||parasitic infection pulmonary
|
|
D008174||parasitic infections of lung
|
|
D008174||parasitic infections pulmonary
|
|
D008174||parasitic lung disease
|
|
D008174||parasitic lung diseases
|
|
D008174||pulmonary parasitic infection
|
|
D008174||pulmonary parasitic infections
|
|
C563882|608658||prostate cancer hereditary 4
|
|
C563882|608658||hpc4
|
|
C563882|608658||prostate cancer hereditary on chromosome 7
|
|
D008172||lung diseases fungal
|
|
D008172||fungal disease pulmonary
|
|
D008172||fungal diseases pulmonary
|
|
D008172||fungal infection pulmonary
|
|
D008172||fungal infections pulmonary
|
|
D008172||fungal lung disease
|
|
D008172||fungal lung diseases
|
|
D008172||lung disease fungal
|
|
D008172||pulmonary fungal disease
|
|
D008172||pulmonary fungal diseases
|
|
D008172||pulmonary fungal infection
|
|
D008172||pulmonary fungal infections
|
|
D008173||lung diseases obstructive
|
|
D008173||lung disease obstructive
|
|
D008173||obstructive lung disease
|
|
D008173||obstructive lung diseases
|
|
D008173||obstructive pulmonary disease
|
|
D008173||obstructive pulmonary diseases
|
|
D008173||pulmonary disease obstructive
|
|
D008173||pulmonary diseases obstructive
|
|
C537822||chromosome 7 trisomy mosaic
|
|
C537822||trisomy 7 mosaicism
|
|
C537822||uniparental disomy of 7
|
|
C537823||chromosome 8 deletion
|
|
C537823||deletions of chromosome 8
|
|
D052202||hydrocolpos
|
|
D008171||lung diseases
|
|
D008171||disease lung
|
|
D008171||disease pulmonary
|
|
D008171||diseases lung
|
|
D008171||diseases pulmonary
|
|
D008171||lung disease
|
|
D008171||pulmonary disease
|
|
D008171||pulmonary diseases
|
|
C565076||dysplasia epiphysealis hemimelica with chondromas and osteochondromas
|
|
C565076||osteochondromatosis dominant carpotarsal
|
|
C537820||chromosome 7 trisomy 7p13 p12 2
|
|
C537820||duplication 7p13 p12 2
|
|
C537820||trisomy 7p13 p12 2
|
|
D010482||periapical abscess
|
|
D010482||abscess apical alveolar
|
|
D010482||abscess apical dentoalveolar
|
|
D010482||abscesses apical alveolar
|
|
D010482||abscesses apical dentoalveolar
|
|
D010482||abscesses periapical
|
|
D010482||abscess periapical
|
|
D010482||alveolar abscess apical
|
|
D010482||alveolar abscesses apical
|
|
D010482||apical alveolar abscess
|
|
D010482||apical alveolar abscesses
|
|
D010482||apical dentoalveolar abscess
|
|
D010482||apical dentoalveolar abscesses
|
|
D010482||dentoalveolar abscess apical
|
|
D010482||dentoalveolar abscesses apical
|
|
D010482||periapical abscesses
|
|
D010482||periapical periodontitides suppurative
|
|
D010482||periapical periodontitis suppurative
|
|
D010482||periodontitides suppurative periapical
|
|
D010482||periodontitis apical suppurative
|
|
D010482||periodontitis suppurative periapical
|
|
D010482||suppurative periapical periodontitides
|
|
D010482||suppurative periapical periodontitis
|
|
C535715|605726||spinal muscular atrophy jerash type
|
|
C535715|605726||dsma2
|
|
C535715|605726||hereditary motor neuropathy jerash type
|
|
C535715|605726||hmnj
|
|
C535715|605726||motor neuropathy distal jerash type
|
|
C535715|605726||neuronopathy distal hereditary motor jerash type
|
|
C535715|605726||neuropathy distal hereditary motor jerash type
|
|
C535715|605726||spinal muscular atrophy distal autosomal recessive 2
|
|
C565077||diffuse lewy body disease with gaze palsy
|
|
C537821||chromosome 7 trisomy 7q
|
|
C537821||duplication 7q
|
|
C537821||trisomy 7q
|
|
C565070||cleft lip with or without cleft palate nonsyndromic 8
|
|
C537826||chromosome 8p deletion syndrome partial
|
|
C537826||8p deletion syndrome partial
|
|
C537826||8p syndrome partial
|
|
C537826||chromosome 8 monosomy 8p2
|
|
C537826||chromosome 8 monosomy 8p21 pter
|
|
C537826||chromosome 8 partial deletion short arm
|
|
C537826||chromosome 8 partial monosomy 8p2
|
|
D010484||periapical granuloma
|
|
D010484||dental granuloma
|
|
D010484||dental granulomas
|
|
D010484||granuloma dental
|
|
D010484||granuloma periapical
|
|
D010484||granulomas dental
|
|
D010484||granulomas periapical
|
|
D010484||periapical granulomas
|
|
D010484||periapical periodontitis chronic nonsuppurative
|
|
D010484||periodontitis apical chronic nonsuppurative
|
|
C537827||chromosome 8 monosomy 8p23 1
|
|
C537827||deletion 8p23 1
|
|
C537827||monosomy 8p23 1
|
|
D010483||periapical diseases
|
|
D010483||disease periapical
|
|
D010483||diseases periapical
|
|
D010483||periapical disease
|
|
C537824||chromosome 8 ring
|
|
C537824||ring chromosome 8
|
|
C537825||chromosome 8 monosomy 8p
|
|
C537825||deletion 8p
|
|
C537825||monosomy 8p
|
|
D010485||periapical periodontitis
|
|
D010485||acute nonsuppurative periodontitides
|
|
D010485||acute nonsuppurative periodontitis
|
|
D010485||apical periodontitides
|
|
D010485||apical periodontitis
|
|
D010485||nonsuppurative periodontitides acute
|
|
D010485||nonsuppurative periodontitis acute
|
|
D010485||periapical periodontitides
|
|
D010485||periodontitides acute nonsuppurative
|
|
D010485||periodontitides apical
|
|
D010485||periodontitides periapical
|
|
D010485||periodontitis acute nonsuppurative
|
|
D010485||periodontitis apical
|
|
D010485||periodontitis periapical
|
|
300604|C564476||premature ovarian failure 2b
|
|
300604|C564476||pof2b
|
|
D005901||glaucoma
|
|
D005901||glaucomas
|
|
C565078||lewy body variant of alzheimer disease
|
|
C537840||mal de debarquement
|
|
C537840||mal de debarquement syndrome
|
|
193510|C536464||waardenburg syndrome type 2a
|
|
193510|C536464||waardenburg syndrome type iia
|
|
193510|C536464||waardenburg syndrome without dystopia canthorum
|
|
193510|C536464||ws2
|
|
193510|C536464||ws2a
|
|
D005902||glaucoma open angle
|
|
D005902||compensated glaucoma
|
|
D005902||compensated glaucomas
|
|
D005902||compensative glaucoma
|
|
D005902||compensative glaucomas
|
|
D005902||glaucoma compensated
|
|
D005902||glaucoma compensative
|
|
D005902||glaucoma pigmentary
|
|
D005902||glaucomas compensated
|
|
D005902||glaucomas compensative
|
|
D005902||glaucoma simple
|
|
D005902||glaucoma simplex
|
|
D005902||glaucomas open angle
|
|
D005902||glaucomas pigmentary
|
|
D005902||glaucomas simple
|
|
D005902||open angle glaucoma
|
|
D005902||open angle glaucomas
|
|
D005902||pigmentary glaucoma
|
|
D005902||pigmentary glaucomas
|
|
D005902||simple glaucoma
|
|
D005902||simple glaucomas
|
|
D005902||simplex glaucoma
|
|
D005902||simplices glaucoma
|
|
611100|C567011||prostate cancer hereditary 10
|
|
611100|C567011||hpc10
|
|
D003057|133540||cockayne syndrome
|
|
D003057|133540||cockayne syndrome a
|
|
D003057|133540||cockayne syndrome b
|
|
D003057|133540||cockayne syndrome group a
|
|
D003057|133540||cockayne syndrome group b
|
|
D003057|133540||cockayne syndrome group c
|
|
D003057|133540||cockayne syndrome type 3
|
|
D003057|133540||cockayne syndrome type a
|
|
D003057|133540||cockayne syndrome type b
|
|
D003057|133540||cockayne syndrome type c
|
|
D003057|133540||cockayne syndrome type i
|
|
D003057|133540||cockayne syndrome type ii
|
|
D003057|133540||cockayne syndrome type iii
|
|
D003057|133540||csa
|
|
D003057|133540||dwarfism retinal atrophy deafness syndrome
|
|
D003057|133540||group a cockayne syndrome
|
|
D003057|133540||group b cockayne syndrome
|
|
D003057|133540||group c cockayne syndrome
|
|
D003057|133540||progeria like syndrome
|
|
D003057|133540||progeria like syndromes
|
|
D003057|133540||progeroid nanism
|
|
D003057|133540||syndrome cockayne
|
|
D003057|133540||syndrome progeria like
|
|
D003057|133540||type a cockayne syndrome
|
|
D003057|133540||type b cockayne syndrome
|
|
D003057|133540||type c cockayne syndrome
|
|
D003057|133540||type i cockayne syndrome
|
|
D003057|133540||type ii cockayne syndrome
|
|
D003057|133540||type iii cockayne syndrome
|
|
608096||epilepsy familial temporal lobe 2
|
|
608096||etl2
|
|
608096||ftle
|
|
607346|C537198||spinocerebellar ataxia 19
|
|
607346|C537198||sca19
|
|
607346|C537198||sca22
|
|
607346|C537198|C542540||spinocerebellar ataxia 22
|
|
C562806||glycogen storage disease id
|
|
C562806||gsd1d
|
|
C565080||dyschondrosteosis and nephritis
|
|
C536509||theodor hertz goodman syndrome
|
|
C536509||symphalangism short stature skeletal anomalies and accessory testis
|
|
D008185||lutembacher syndrome
|
|
D008185||lutembacher apos s syndrome
|
|
D008185||lutembachers syndrome
|
|
D008185||syndrome lutembacher
|
|
D008185||syndrome lutembacher apos s
|
|
C565316|605594||deafness autosomal dominant 39 with dentinogenesis imperfecta 1
|
|
C565316|605594||dfna39 dentinogenesis imperfecta 1 syndrome
|
|
C565316|605594||dfna39 dgi1 syndrome
|
|
C565316|605594||dgi1 dfna39 syndrome
|
|
C536502||tetrasomy x
|
|
C536502||48 xxxx
|
|
C536502||48 xxxx syndrome
|
|
D008181||lupus nephritis
|
|
D008181||glomerulonephritides lupus
|
|
D008181||glomerulonephritis lupus
|
|
D008181||lupus glomerulonephritides
|
|
D008181||lupus glomerulonephritis
|
|
D008181||lupus nephritides
|
|
D008181||nephritides lupus
|
|
D008181||nephritis lupus
|
|
C565086||duodenal ulcer hyperpepsinogenemic i
|
|
C536503||thakker donnai syndrome
|
|
C536503||dysmorphic facial features and multiple structural abnormalities
|
|
C536503||dysmorphism multiple structural anomalies
|
|
D010490||pericardial effusion
|
|
D010490||chylopericardium
|
|
D010490||chylopericardiums
|
|
D010490||effusion pericardial
|
|
D010490||effusions pericardial
|
|
D010490||hemopericardium
|
|
D010490||pericardial effusions
|
|
C536500||tetraamelia multiple malformations
|
|
C536500||zimmer phocomelia
|
|
C536500||zimmer taub sova syndrome
|
|
D010493||pericarditis
|
|
D010493||pleuropericarditis
|
|
C565088||drusen radial autosomal dominant
|
|
C536501||tetralogy of fallot and glaucoma
|
|
C536501||familial tetralogy of fallot and glaucoma
|
|
C567379|612260||myd88 deficiency
|
|
C567379|612260||myd88d
|
|
C567379|612260||pyogenic bacterial infections recurrent due to myd88 deficiency
|
|
C567379|612260||recurrent pyogenic bacterial infections due to myd88 deficiency
|
|
D005909||glioblastoma
|
|
D005909||astrocytoma grade iv
|
|
D005909||astrocytomas grade iv
|
|
D005909||giant cell glioblastoma
|
|
D005909||giant cell glioblastomas
|
|
D005909||glioblastoma giant cell
|
|
D005909||glioblastoma multiforme
|
|
D005909||glioblastomas
|
|
D005909||glioblastomas giant cell
|
|
D005909||grade iv astrocytoma
|
|
D005909||grade iv astrocytomas
|
|
C537837||benign symmetrical lipomatosis
|
|
C537837||launois bensaude syndrome
|
|
C536506||thanatophoric dysplasia glasgow variant
|
|
C536506||neonatally lethal short limb skeletal dysplasia glasgow type
|
|
D010495||pericarditis tuberculous
|
|
D010495||pericarditides tuberculous
|
|
D010495||tuberculous pericarditides
|
|
D010495||tuberculous pericarditis
|
|
C535532|300048||congenital idiopathic intestinal pseudoobstruction
|
|
C535532|300048||ciip
|
|
C535532|300048||ciipx
|
|
C535532|300048||ciip x linked
|
|
C535532|300048||intestinal pseudoobstruction chronic idiopathic
|
|
C535532|300048||intestinal pseudoobstruction neuronal chronic idiopathic with central nervous system involvement
|
|
C535532|300048||intestinal pseudoobstruction neuronal chronic idiopathic with central nervous system involvement congenital short bowel syndrome x linked included
|
|
C535532|300048||intestinal pseudoobstruction neuronal chronic idiopathic x linked
|
|
C535532|300048||ipox
|
|
C537838||madokoro ohdo sonoda syndrome
|
|
C537838||tetra amelia ectodermal dysplasia and lacrimal duct abnormality
|
|
D010494||pericarditis constrictive
|
|
D010494||constrictive pericarditides
|
|
D010494||constrictive pericarditis
|
|
D010494||heart pick apos s disease
|
|
D010494||pericarditides constrictive
|
|
D010494||pick disease heart
|
|
D010494||pick disease of heart
|
|
D010494||picks disease heart
|
|
D010494||pick apos s disease of heart
|
|
C565083||dupuytren contracture 1
|
|
C536504||thalamic degeneration symmetrical infantile
|
|
C536504||symmetrical infantile thalamic degeneration
|
|
C536504||thalamic degeneration symmetric infantile
|
|
D010497||pericoronitis
|
|
D010497||pericoronitides
|
|
C565084||plantar fibromatosis familial
|
|
C565084||plantar fibromas
|
|
C537836||macules hereditary congenital hypopigmented and hyperpigmented
|
|
C537836||congenital hypomelanotic and hypermelanotic macules
|
|
C537836||hereditary congenital hypopigmented and hyperpigmented macules
|
|
C537836||westerhof beemer cormane syndrome
|
|
203750|C535434||beta ketothiolase deficiency
|
|
203750|C535434||2 alpha methyl 3 hydroxybutyricacidemia
|
|
203750|C535434||2 methyl 3 hydroxybutyricacidemia
|
|
203750|C535434||2 methyl 3 hydroxybutyric acidemia
|
|
203750|C535434||3 alpha ketothiolase deficiency
|
|
203750|C535434||3 alpha ktd deficiency
|
|
203750|C535434||3 alpha oxothiolase deficiency
|
|
203750|C535434||3 ketothiolase deficiency
|
|
203750|C535434||3 ktd deficiency
|
|
203750|C535434||3 methylhydroxybutyric acidemia
|
|
203750|C535434||3 oxothiolase deficiency
|
|
203750|C535434||alpha methylacetoaceticaciduria
|
|
203750|C535434||alpha methylacetoacetic aciduria
|
|
203750|C535434||b ketothiolase deficiency
|
|
203750|C535434|C562681|250850||mat deficiency
|
|
203750|C535434||mitochondrial 2 methylacetoacetyl coa thiolase deficiency potassium stimulated
|
|
203750|C535434||mitochondrial acetoacetyl coa thiolase deficiency
|
|
203750|C535434||t2 deficiency
|
|
C565049||epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase
|
|
611105|C567009||leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
|
|
611105|C567009||lbsl
|
|
611105|C567009||mitochondrial aspartyl trna synthetase deficiency
|
|
C562587|613179||purine nucleoside phosphorylase deficiency
|
|
C562587|613179||nucleoside phosphorylase deficiency
|
|
C562587|613179||pnp deficiency
|
|
C566376||tsukahara syndrome
|
|
C566376||radioulnar synostosis with microcephaly short stature scoliosis and mental retardation
|
|
C537851||novak syndrome
|
|
C537851||cleft larynx posterior
|
|
C537851||laryngotracheoesophageal cleft pulmonary hypoplasia
|
|
C566377||microcephaly severe with skeletal anomalies including posterior rib gap defects
|
|
C537852||nuchal bleb familial
|
|
C537852||cystic hygroma fetal
|
|
C537852||familial nuchal bleb
|
|
C537852||fetal cystic hygroma
|
|
C566378||osteosclerotic chondrodysplasia lethal with intracellular inclusions
|
|
C566379||laryngotracheal stenosis progressive with short stature and arthropathy
|
|
C565101|125850||maturity onset diabetes of the young type 1
|
|
C565101|125850||mild juvenile diabetes mellitus
|
|
C565101|125850||mody1
|
|
C565101|125850||mody type 1
|
|
C564741|277450||vitamin k dependent clotting factors combined deficiency of 1
|
|
C564741|277450||factors ii vii ix and x combined deficiency of
|
|
C564741|277450||familial multiple coagulation factor deficiency iii
|
|
C564741|277450||fmfd iii
|
|
C564741|277450||glutamic acid deficient gamma carboxylation of
|
|
C564741|277450||mcfd3
|
|
C564741|277450||multiple coagulation factor deficiency iii
|
|
C564741|277450||vitamin k dependent coagulation defect
|
|
C564741|277450||vkcfd
|
|
C564741|277450||vkcfd1
|
|
C566716|180104||retinitis pigmentosa 9
|
|
C566716|180104||rp9
|
|
204870|C535480||corneal dystrophy gelatinous drop like
|
|
204870|C535480||amyloid corneal dystrophy japanese type
|
|
204870|C535480||amyloidosis corneal
|
|
204870|C535480||cdgdl
|
|
204870|C535480||corneal amyloidosis
|
|
204870|C535480||corneal dystrophy lattice type 3
|
|
204870|C535480||corneal dystrophy lattice type iii
|
|
204870|C535480||gdld
|
|
204870|C535480||gelatinous drop like corneal dystrophy
|
|
204870|C535480||lattice corneal dystrophy type3
|
|
204870|C535480||lattice corneal dystrophy type iii
|
|
204870|C535480||primary familial amyloidosis of the cornea
|
|
C536519||thrombocytopenia chromosome breakage
|
|
C536519||helmerhorst heaton crossen syndrome
|
|
C536519|188000||thrombocytopenia 2
|
|
C536519||thrombocytopenia autosomal dominant
|
|
C536519|188000||thrombocytopenia autosomal dominant 2
|
|
D010468||perceptual disorders
|
|
D010468||discrimination disorder somatosensory
|
|
D010468||discrimination disorders somatosensory
|
|
D010468||hemisensory neglect
|
|
D010468||hemisensory neglects
|
|
D010468||hemispatial neglect
|
|
D010468||hemispatial neglects
|
|
D010468||neglect hemisensory
|
|
D010468||neglect hemispatial
|
|
D010468||neglect sensory
|
|
D010468||neglects hemisensory
|
|
D010468||perceptual disorder
|
|
D010468||sensory neglect
|
|
D010468||sensory neglects
|
|
D010468||somatosensory discrimination disorder
|
|
D010468||somatosensory discrimination disorders
|
|
607091|C535753||congenital disorder of glycosylation type 2d
|
|
607091|C535753|C564625||cdg2d
|
|
607091|C535753|C564625||cdgiid
|
|
607091|C535753|C564625||cdg iid
|
|
607091|C535753||congenital disorder of glycosylation type iid
|
|
D008151||lown ganong levine syndrome
|
|
D008151||short pr normal qrs complex syndrome
|
|
D008151||syndrome lown ganong levine
|
|
C537844||nonseminomatous germ cell tumor
|
|
C537844||non seminomatous germ cell tumors
|
|
C536513||thomas jewett raines syndrome
|
|
C537845||nonsyndromic sensorineural hearing loss
|
|
C537845||autosomal dominant nonsyndromic hereditary hearing impairment
|
|
C537845||nonsyndromic hereditary hearing impairment
|
|
C536514||thomas syndrome
|
|
C537095|112410||brachydactyly with hypertension
|
|
C537095|112410||bilginturan syndrome
|
|
C537095|112410||brachydactyly type e with short stature and hypertension
|
|
C537095|112410||htnb
|
|
C537095|112410||hypertension with brachydactyly
|
|
C536511||schweitzer kemink graham syndrome
|
|
C536511||conductive hearing loss middle ear ossicular anomalies malformed thickened lop auricles and micrognathia
|
|
C536511||thickened earlobes with conductive deafness from incus stapes abnormalities
|
|
C566386||thyroid adenoma hyperfunctioning
|
|
C566386||thyroid carcinoma with thyrotoxicosis
|
|
C536512||thiopurine s methyltranferase deficiency
|
|
C536512||6 alpha mercaptopurine sensitivity
|
|
C536512||thiopurine methyltransferase deficiency
|
|
C536517||thoracolaryngopelvic dysplasia
|
|
C536517||autosomal dominant thoracolaryngopelvic dysplasia
|
|
C536517||barnes syndrome
|
|
C566380||osebold skeletal dysplasia osteolysis syndrome
|
|
C565409|248900||mast syndrome
|
|
C565409|248900||spastic paraplegia 21 autosomal recessive
|
|
C565409|248900||spg21
|
|
C537846||noonan like syndrome
|
|
C537846||noonan like multiple giant cell lesion syndrome
|
|
C537846||noonan syndrome with pigmented villonodular synovitis
|
|
C536515||thompson baraitser syndrome
|
|
C565051||epiblepharon of upper lid
|
|
C565051||epiblepharon of lower lid
|
|
C564524|300372||mental retardation x linked 42
|
|
C564524|300372||mrx42
|
|
C536516||thoraco limb dysplasia rivera type
|
|
C536516||rivera perez salas syndrome
|
|
C566387||peroxisome biogenesis disorder complementation group 9
|
|
C537862||ochronosis hereditary
|
|
C537862||hereditary ochronosis
|
|
C536531||orofaciodigital syndrome 6
|
|
C536531||ofd6
|
|
C536531||ofds vi
|
|
C536531||oral facial digital syndrome type 6
|
|
C536531||oral facial digital syndrome type vi
|
|
C536531||orofaciodigital syndrome vi
|
|
C536531||polydactyly cleft lip palate or lingual lump and psychomotor retardation
|
|
C536531||varadi papp syndrome
|
|
C536531||varadi syndrome
|
|
C566388||peroxisome biogenesis disorder complementation group d
|
|
C536530||van maldergem wetzburger verloes syndrome
|
|
C536530||cerebro facio articular syndrome
|
|
C536530||cerebrofacioarticular syndrome
|
|
C536530||cerebro facio articular syndrome of van maldergem
|
|
C536530||van maldergem syndrome
|
|
C537863|300500||ocular albinism type 1
|
|
C537863|300500||albinism ocular type i
|
|
C537863|300500||nettleship falls type ocular albinism
|
|
C537863|300500||oa1
|
|
C567862|612921||three m syndrome 2
|
|
C567862|612921||3m2
|
|
C567862|612921||3m syndrome 2
|
|
113900|D002037||bundle branch block
|
|
113900||cardiac conduction defect nonprogressive included
|
|
113900||hereditary bundle branch system defect hbbd heart block nonprogressive included
|
|
113900||pccd
|
|
D008158||ludwig apos s angina
|
|
D008158||angina ludwig apos s
|
|
D008158||ludwig angina
|
|
D008158||ludwigs angina
|
|
C563008|261750||glycogen storage disease ixb
|
|
C563008|261750||glycogenosis of liver and muscle autosomal recessive
|
|
C563008|261750||gsd9b
|
|
C563008|261750||gsd ixb
|
|
C563008|261750||phosphorylase kinase deficiency of liver and muscle autosomal recessive
|
|
C567656|610185||cerebellar ataxia mental retardation and dysequilibrium syndrome 2
|
|
C567656|610185||camrq2
|
|
C567656|610185||cerebellar ataxia and mental retardation with or without quadrupedal locomotion 2
|
|
D009497||neurotic disorders
|
|
D009497||disorder neurotic
|
|
D009497||disorders neurotic
|
|
D009497||neuroses
|
|
D009497||neurotic disorder
|
|
D009497||psychoneuroses
|
|
D008166||lumpy skin disease
|
|
D008166||disease lumpy skin
|
|
D008166||diseases lumpy skin
|
|
D008166||lumpy skin diseases
|
|
D008166||skin disease lumpy
|
|
D008166||skin diseases lumpy
|
|
D009494||neurosyphilis
|
|
D009494||asymptomatic neurosyphilis
|
|
D009494||central nervous system syphilis
|
|
D009494||general paralyses
|
|
D009494||general paralysis
|
|
D009494||general pareses
|
|
D009494||general paresis
|
|
D009494||general paresis of the insane
|
|
D009494||gummatous neurosyphilis
|
|
D009494||juvenile neurosyphilis
|
|
D009494||juvenile pareses
|
|
D009494||juvenile paresis
|
|
D009494||neurosyphilis asymptomatic
|
|
D009494||neurosyphilis gummatous
|
|
D009494||neurosyphilis juvenile
|
|
D009494||neurosyphilis paretic
|
|
D009494||neurosyphilis secondary
|
|
D009494||neurosyphilis symptomatic
|
|
D009494||paralyses general
|
|
D009494||paralysis general
|
|
D009494||pareses general
|
|
D009494||pareses juvenile
|
|
D009494||paresis general
|
|
D009494||paresis juvenile
|
|
D009494||paretic neurosyphilis
|
|
D009494||secondary neurosyphilis
|
|
D009494||syphilis central nervous system
|
|
D009494||syphilis cns
|
|
C537042|300700||albinism deafness syndrome
|
|
C537042|300700||adfn
|
|
C537042|300700||alds
|
|
C565063||edema familial idiopathic prepubertal
|
|
C536524||valinemia
|
|
C536524||hypervalinemia
|
|
C536524||valine transaminase deficiency
|
|
C565064||ectrodactyly cleft palate syndrome
|
|
C536525||valproic acid antenatal infection
|
|
C536525||dalpro fetal effects from
|
|
C536525||epival fetal effects from
|
|
C536525||fetal valproate syndrome
|
|
C536525||fetal valproic syndrome
|
|
C536525||valproic acid embryopathy
|
|
D053565||hypercalciuria
|
|
C565065||ectrodactyly and ectodermal dysplasia without cleft lip palate
|
|
C536522||vacuolar myopathy
|
|
C536522||autophagic vacuolar myopathy
|
|
C536522||myopathy autophagic vacuolar infantile onset
|
|
C536523||vagina absence of
|
|
C536523||absence of vagina
|
|
C566391||erythrokeratodermia variabilis autosomal recessive
|
|
C565061||eds viib
|
|
C565061||eds7b
|
|
C566392||muscular dystrophy congenital with cerebellar atrophy
|
|
C537857||hereditary vertical nystagmus
|
|
C537857||congenital hereditary vertical nystagmus
|
|
C537857||nystagmus hereditary vertical
|
|
C536526||van bogaert hozay syndrome
|
|
C536526||acro osteolysis facial dysplasia syndrome
|
|
C536526||hozay apos s syndrome
|
|
C565027||complement factor d deficiency
|
|
C565027||factor d deficiency
|
|
C566358||xanthinuria type ii
|
|
C566358||xanthine dehydrogenase and aldehyde oxidase combined deficiency of
|
|
C565028||facial palsy familial recurrent peripheral
|
|
C566359||parotitis juvenile recurrent
|
|
C536167|245150||keutel syndrome
|
|
C536167|245150||pulmonic stenosis brachytelephalangism and calcification of cartilages
|
|
C565029||facial hypertrichosis
|
|
C563463|608836||carnitine palmitoyltransferase ii deficiency lethal neonatal
|
|
C563463|608836||carnitine palmitoyltransferase ii deficiency antenatal
|
|
C563463|608836||carnitine palmitoyltransferase ii deficiency neonatal
|
|
C563463|608836||cpt2 deficiency lethal neonatal
|
|
C563463|608836||cpt ii deficiency lethal neonatal
|
|
608224|C564272||deafness autosomal dominant 41
|
|
608224|C564272||dfna41
|
|
C565023||factors viii ix and xi combined deficiency of
|
|
C565023||familial multiple coagulation factor deficiency v
|
|
C565023||multiple coagulation factor deficiency v
|
|
C565024||familial multiple coagulation factor deficiency ii
|
|
C565024||f8f9d
|
|
C565024||factor viii and factor ix combined deficiency
|
|
C565024||fmfd ii
|
|
C565025||familial multiple coagulation factor deficiency iv
|
|
C565025||factor vii and factor viii combined deficiency
|
|
C565025||fmfd iv
|
|
C565025||mcfd4
|
|
C565025||multiple coagulation factor deficiency iv
|
|
C566356||osteoma of cranial vault familial
|
|
C565026||factor v excess with spontaneous thrombosis
|
|
C565026||proaccelerin excess
|
|
C566357||craniosynostosis with ectopia lentis
|
|
D009459||neuroleptic malignant syndrome
|
|
D009459||neuroleptic induced neuroleptic malignant syndrome
|
|
D009459||neuroleptic malignant syndrome neuroleptic induced
|
|
D009459||neuroleptic malignant syndromes
|
|
D009459||nms neuroleptic malignant syndrome
|
|
D009459||nmss neuroleptic malignant syndrome
|
|
D009459||syndrome neuroleptic malignant
|
|
D009459||syndromes neuroleptic malignant
|
|
C566473|610455||tumoral calcinosis normophosphatemic familial
|
|
C566473|610455||calcinosis tumoral with normophosphatemia
|
|
C566473|610455||nftc
|
|
C567211|612650||ciliary dyskinesia primary 12
|
|
C567211|612650||cild12
|
|
C567211|612650||ciliary dyskinesia primary 12 without situs inversus
|
|
D009464||neuroma acoustic
|
|
D009464||acoustic neurilemmoma
|
|
D009464||acoustic neurilemmomas
|
|
D009464||acoustic neurilemoma
|
|
D009464||acoustic neurilemomas
|
|
D009464||acoustic neurinoma
|
|
D009464||acoustic neurinomas
|
|
D009464||acoustic neuroma
|
|
D009464||acoustic neuroma cerebellopontine angle
|
|
D009464||acoustic neuromas
|
|
D009464||acoustic schwannoma
|
|
D009464||acoustic schwannomas
|
|
D009464||acoustic tumor
|
|
D009464||acoustic tumors
|
|
D009464||angle tumor
|
|
D009464||cerebellopontine angle acoustic neuroma
|
|
D009464||cerebellopontine angle tumor
|
|
D009464||melanocytic vestibular schwannoma
|
|
D009464||melanocytic vestibular schwannomas
|
|
D009464||neurilemmoma acoustic
|
|
D009464||neurilemmomas acoustic
|
|
D009464||neurilemoma acoustic
|
|
D009464||neurilemomas acoustic
|
|
D009464||neurinoma acoustic
|
|
D009464||neurinoma of the acoustic nerve
|
|
D009464||neurinomas acoustic
|
|
D009464||neuroma acoustic unilateral
|
|
D009464||neuromas acoustic
|
|
D009464||schwannoma acoustic
|
|
D009464||schwannoma melanocytic vestibular
|
|
D009464||schwannomas acoustic
|
|
D009464||schwannomas melanocytic vestibular
|
|
D009464||schwannomas vestibular
|
|
D009464||schwannoma vestibular
|
|
D009464||tumor acoustic
|
|
D009464||tumors acoustic
|
|
D009464||vestibular schwannoma
|
|
D009464||vestibular schwannoma melanocytic
|
|
D009464||vestibular schwannomas
|
|
D009464||vestibular schwannomas melanocytic
|
|
D009463||neuroma
|
|
D009463||neuromas
|
|
D011776||pyuria
|
|
D011776||pyurias
|
|
D008133||long qt syndrome
|
|
219800|D003554||cystinosis
|
|
219800|D003554||ctns
|
|
219800|D003554||cystine diatheses
|
|
219800|D003554||cystine diathesis
|
|
219800|D003554||cystine disease
|
|
219800|D003554||cystine diseases
|
|
219800|D003554||cystine storage disease
|
|
219800|D003554||cystine storage diseases
|
|
219800|D003554||cystinoses
|
|
219800|D003554||cystinoses nephropathic
|
|
219800|D003554||cystinosin defect of
|
|
219800|D003554||cystinosin defect of cystinosis infantile nephropathic included
|
|
219800|D003554||cystinosis atypical nephropathic included
|
|
219800|D003554||cystinosis nephropathic
|
|
219800|D003554||diatheses cystine
|
|
219800|D003554||diathesis cystine
|
|
219800|D003554||disease cystine storage
|
|
219800|D003554||diseases cystine storage
|
|
219800|D003554||lysosomal cystine transport protein defect of
|
|
219800|D003554||nephropathic cystinoses
|
|
219800|D003554||nephropathic cystinosis
|
|
219800|D003554||storage disease cystine
|
|
219800|D003554||storage diseases cystine
|
|
C562785|146110||idiopathic hypogonadotropic hypogonadism
|
|
C562785|146110||hh7
|
|
C562785|146110|D007006||hypogonadism isolated hypogonadotropic
|
|
C562785|146110||hypogonadotropic hypogonadism 7 with or without anosmia
|
|
C562785|146110||ihh
|
|
D009461||neurologic manifestations
|
|
D009461||deficit focal neurologic
|
|
D009461||deficit neurologic
|
|
D009461||deficits focal neurologic
|
|
D009461||deficits neurologic
|
|
D009461||dysfunction neurologic
|
|
D009461||dysfunctions neurologic
|
|
D009461||finding neurologic
|
|
D009461||findings neurologic
|
|
D009461||focal neurologic deficit
|
|
D009461||focal neurologic deficits
|
|
D009461||manifestation neurologic
|
|
D009461||manifestation neurological
|
|
D009461||manifestations neurologic
|
|
D009461||manifestations neurological
|
|
D009461||neurological manifestation
|
|
D009461||neurological manifestations
|
|
D009461||neurologic deficit
|
|
D009461||neurologic deficit focal
|
|
D009461||neurologic deficits
|
|
D009461||neurologic deficits focal
|
|
D009461||neurologic dysfunction
|
|
D009461||neurologic dysfunctions
|
|
D009461||neurologic finding
|
|
D009461||neurologic findings
|
|
D009461||neurologic manifestation
|
|
D009461||neurologic sign
|
|
D009461||neurologic signs
|
|
D009461||neurologic signs and symptoms
|
|
D009461||neurologic symptom
|
|
D009461||neurologic symptoms
|
|
D009461||sign neurologic
|
|
D009461||signs neurologic
|
|
D009461||symptom neurologic
|
|
D009461||symptoms neurologic
|
|
D011778||q fever
|
|
D011778||acute q fever
|
|
D011778||acute q fevers
|
|
D011778||chronic q fever
|
|
D011778||chronic q fevers
|
|
D011778||coxiella burnetii fever
|
|
D011778||coxiella burnetii fevers
|
|
D011778||coxiella burnetii infection
|
|
D011778||coxiella burnetii infections
|
|
D011778||coxiella burnetii vector borne disease
|
|
D011778||fever acute q
|
|
D011778||fever chronic q
|
|
D011778||fever coxiella burnetii
|
|
D011778||fever q
|
|
D011778||fever query
|
|
D011778||fevers acute q
|
|
D011778||fevers chronic q
|
|
D011778||fevers coxiella burnetii
|
|
D011778||fevers q
|
|
D011778||fevers query
|
|
D011778||infection coxiella burnetii
|
|
D011778||infections coxiella burnetii
|
|
D011778||q fever acute
|
|
D011778||q fever chronic
|
|
D011778||q fevers
|
|
D011778||q fevers acute
|
|
D011778||q fevers chronic
|
|
D011778||query fever
|
|
D011778||query fevers
|
|
C566991|119540||cleft palate isolated and mental retardation
|
|
C566991|119540|D002972||cleft palate
|
|
C566991|119540|D002972||cleft palate isolated
|
|
C566991|119540||cp
|
|
C566991|119540||cpi
|
|
D053570||porcine postweaning multisystemic wasting syndrome
|
|
D053570||postweaning multisystemic wasting syndrome porcine
|
|
C566361||microcephaly facial abnormalities micromelia and mental retardation
|
|
C566362||tracheobronchial stenosis congenital
|
|
C567769|613076||myopathy mitochondrial progressive with congenital cataract hearing loss and developmental delay
|
|
C567769|613076||mitochondrial complex deficiency combined
|
|
C567769|613076||myopathy with cataract and combined respiratory chain deficiency
|
|
C565032||extrasystoles multiform ventricular with short stature hyperpigmentation and microcephaly
|
|
C566360||follicular atrophoderma perioral pigmented with milia and epidermoid cysts
|
|
D053578||opsoclonus myoclonus syndrome
|
|
D053578||dancing eyes dancing feet syndrome
|
|
D053578||infants myoclonic encephalopathies
|
|
D053578||infants myoclonic encephalopathy
|
|
D053578||kinsbourne syndrome
|
|
D053578||myoclonic encephalopathy of infants
|
|
D053578||myoclonus opsoclonus
|
|
D053578||opsoclonus myoclonus
|
|
D053578||opsoclonus myoclonus ataxia
|
|
D053578||paraneoplastic opsoclonus myoclonus ataxia
|
|
C565039||erythroleukemia familial
|
|
C565039||di guglielmo disease familial
|
|
C565039||leukemia acute myelogenous m6
|
|
C565034||exostoses with anetodermia and brachydactyly type e
|
|
C565035||cerebrooculofacioskeletal syndrome 3
|
|
C566366||enlarged vestibular aqueduct
|
|
C566366||deafness autosomal recessive 4
|
|
C566366|600791||dilated vestibular aqueduct
|
|
C566366|600791||neurosensory nonsyndromic recessive deafness 4
|
|
C567696||bernard soulier syndrome autosomal dominant
|
|
C565036||exchondrosis of pinna posterior
|
|
C565036||ear bump
|
|
C566367||light fixation seizure syndrome
|
|
C566367||m syndrome
|
|
C566368||dyserythropoiesis congenital with internuclear chromatin bridges and ultrastructurally normal erythroblast heterochromatin
|
|
D009468||neuromuscular diseases
|
|
D009468||amyotonia congenita
|
|
D009468||benign fasciculation cramp syndrome
|
|
D009468||benign fasciculation cramp syndromes
|
|
D009468||cramp fasciculation syndrome
|
|
D009468||cramp fasciculation syndromes
|
|
D009468||fasciculation cramp syndrome benign
|
|
D009468||fasciculation cramp syndromes benign
|
|
D009468||foley denny brown syndrome
|
|
D009468||neuromuscular disease
|
|
D009468||oppenheim disease
|
|
D009468||oppenheim apos s disease
|
|
D009468||oppenheims disease
|
|
D009468||syndrome cramp fasciculation
|
|
D009468||syndrome foley denny brown
|
|
D009468||syndromes cramp fasciculation
|
|
D008146||louping ill
|
|
D008146||ill louping
|
|
D053584||urinoma
|
|
D053584||urinomas
|
|
D008141||lordosis
|
|
610733|C548082||noonan syndrome 4
|
|
610733|C548082||ns4
|
|
D009471||neuromyelitis optica
|
|
D009471||devic disease
|
|
D009471||devic neuromyelitis optica
|
|
D009471||devic apos s disease
|
|
D009471||devics disease
|
|
D009471||devic apos s neuromyelitis optica
|
|
D009471||devics neuromyelitis optica
|
|
D009471||devic apos s neuromyelitis opticas
|
|
D009471||devic apos s syndrome
|
|
D009471||devics syndrome
|
|
D009471||devic apos s syndromes
|
|
D009471||devic syndrome
|
|
D009471||disease devic
|
|
D009471||disease devic apos s
|
|
D009471||neuromyelitis optica devic apos s
|
|
D009471||neuromyelitis opticas devic apos s
|
|
D009471||optica devic apos s neuromyelitis
|
|
D009471||opticas devic apos s neuromyelitis
|
|
D009471||syndrome devic
|
|
D009471||syndrome devic apos s
|
|
D009471||syndromes devic apos s
|
|
C565041||erythema palmare hereditarium
|
|
D052256||tendinopathy
|
|
D052256||tendinitides
|
|
D052256||tendinitis
|
|
D052256||tendinopathies
|
|
D052256||tendinoses
|
|
D052256||tendinosis
|
|
D052256||tendonitides
|
|
D052256||tendonitis
|
|
C566092|186200||syndactyly type iv
|
|
C566092|186200||haas type syndactyly
|
|
C566092|186200||polysyndactyly haas type
|
|
C566092|186200||sd4
|
|
C566092|186200||sdty4
|
|
C566373||hypospadias hypertelorism upper lid coloboma and mixed type hearing loss
|
|
C565043||arene oxide detoxification defect
|
|
C566374||oroacral syndrome verloes koulischer type
|
|
C565044||diphenylhydantoin defect in hydroxylation of
|
|
C566375||expansile bone lesions
|
|
C567684|613251||cardiomyopathy familial hypertrophic 14
|
|
C567684|613251||cmh14
|
|
D011782||quadriplegia
|
|
D011782||flaccid quadriplegia
|
|
D011782||flaccid quadriplegias
|
|
D011782||flaccid tetraplegia
|
|
D011782||flaccid tetraplegias
|
|
D011782||locked in syndrome
|
|
D011782||locked in syndromes
|
|
D011782||paralysis spinal quadriplegic
|
|
D011782||quadripareses
|
|
D011782||quadriparesis
|
|
D011782||quadriplegia flaccid
|
|
D011782||quadriplegias
|
|
D011782||quadriplegias flaccid
|
|
D011782||quadriplegia spastic
|
|
D011782||quadriplegias spastic
|
|
D011782||spastic quadriplegia
|
|
D011782||spastic quadriplegias
|
|
D011782||spastic tetraplegia
|
|
D011782||spastic tetraplegias
|
|
D011782||syndrome locked in
|
|
D011782||syndromes locked in
|
|
D011782||tetraplegia
|
|
D011782||tetraplegia flaccid
|
|
D011782||tetraplegias
|
|
D011782||tetraplegias flaccid
|
|
D011782||tetraplegia spastic
|
|
D011782||tetraplegias spastic
|
|
C566370||muscular dystrophy limb girdle type 1d
|
|
C566370||lgmd1d
|
|
D053589||nuchal cord
|
|
D053589||cord double nuchal
|
|
D053589||cord entanglements fetal
|
|
D053589||cord nuchal
|
|
D053589||double nuchal cord
|
|
D053589||fetal cord entanglement
|
|
D053589||fetal cord entanglements
|
|
D053589||nuchal cord double
|
|
D053589||nuchal cord quadruple
|
|
D053589||nuchal cord single
|
|
D053589||nuchal cord triple
|
|
D053589||quadruple nuchal cord
|
|
D053589||single nuchal cord
|
|
D053589||triple nuchal cord
|
|
C565005||foveal hypoplasia isolated
|
|
C565006||foveal hypoplasia with anterior segment anomalies
|
|
C565007||fourth cranial nerve palsy familial congenital
|
|
C565007||strabismus from superior oblique palsy
|
|
C565007||superior oblique oculomotor palsy familial congenital
|
|
C565007||trochlear nerve palsy familial congenital
|
|
D064250||hypertriglyceridemic waist
|
|
D064250||enlarged waist elevated triglycerides
|
|
D064250||waist hypertriglyceridemic
|
|
C565008||focal epithelial hyperplasia of the oral mucosa
|
|
C565001||fragile site 16p12
|
|
C566332||microcephaly with simplified gyral pattern
|
|
C537831|600208||macrothrombocytopenia progressive deafness
|
|
C537831|600208||brodie chole griffin syndrome
|
|
C537831|600208||macrothrombocytopenia and progressive sensorineural deafness
|
|
C567664||omodysplasia 2
|
|
C567664||omod2
|
|
C567664||omodysplasia autosomal dominant
|
|
603860|C548033||medullary cystic kidney disease 2
|
|
603860|C548033||admckd2
|
|
603860|C548033|C537696||mckd2
|
|
603860|C548033||medullary cystic kidney disease 2 autosomal dominant
|
|
C566334||long qt syndrome 3 6
|
|
C567666||fibrosis of extraocular muscles congenital 3c
|
|
C567666||cfeom3c
|
|
D008109||liver diseases parasitic
|
|
D008109||disease parasitic liver
|
|
D008109||diseases parasitic liver
|
|
D008109||liver disease parasitic
|
|
D008109||parasitic liver disease
|
|
D008109||parasitic liver diseases
|
|
C563738|609322||rhabdoid tumor predisposition syndrome 1
|
|
C563738|609322||at rt included
|
|
C563738|609322||brain tumor posterior fossa of infancy familial
|
|
C563738|609322||brain tumor posterior fossa of infancy familial malignant rhabdoid tumor somatic included
|
|
C563738|609322||malignant rhabdoid tumor somatic
|
|
C563738|609322||rdt included
|
|
C563738|609322||rhabdoid tumor included
|
|
C563738|609322||rtps1
|
|
C563738|609322||teratoid tumor atypical included
|
|
D008107||liver diseases
|
|
D008107||disease liver
|
|
D008107||diseases liver
|
|
D008107||dysfunction liver
|
|
D008107||dysfunctions liver
|
|
D008107||liver disease
|
|
D008107||liver dysfunction
|
|
D008107||liver dysfunctions
|
|
D008108||liver diseases alcoholic
|
|
D008108||alcoholic liver disease
|
|
D008108||alcoholic liver diseases
|
|
D008108||liver disease alcoholic
|
|
C565009||flood factor deficiency
|
|
D009437||neuralgia
|
|
D009437||atypical neuralgia
|
|
D009437||atypical neuralgias
|
|
D009437||iliohypogastric nerve neuralgia
|
|
D009437||iliohypogastric nerve neuralgias
|
|
D009437||ilioinguinal neuralgia
|
|
D009437||ilioinguinal neuralgias
|
|
D009437||nerve neuralgia iliohypogastric
|
|
D009437||nerve neuralgias iliohypogastric
|
|
D009437||nerve pain
|
|
D009437||nerve pain paroxysmal
|
|
D009437||nerve pains
|
|
D009437||nerve pains paroxysmal
|
|
D009437||neuralgia atypical
|
|
D009437||neuralgia iliohypogastric nerve
|
|
D009437||neuralgia ilioinguinal
|
|
D009437||neuralgia perineal
|
|
D009437||neuralgias
|
|
D009437||neuralgias atypical
|
|
D009437||neuralgias iliohypogastric nerve
|
|
D009437||neuralgias ilioinguinal
|
|
D009437||neuralgias perineal
|
|
D009437||neuralgias stump
|
|
D009437||neuralgias supraorbital
|
|
D009437||neuralgia stump
|
|
D009437||neuralgia supraorbital
|
|
D009437||neuralgias vidian
|
|
D009437||neuralgia vidian
|
|
D009437||neurodynia
|
|
D009437||neurodynias
|
|
D009437||neuropathic pain
|
|
D009437||neuropathic pains
|
|
D009437||pain nerve
|
|
D009437||pain neuropathic
|
|
D009437||pain paroxysmal nerve
|
|
D009437||pains nerve
|
|
D009437||pains neuropathic
|
|
D009437||pains paroxysmal nerve
|
|
D009437||paroxysmal nerve pain
|
|
D009437||paroxysmal nerve pains
|
|
D009437||perineal neuralgia
|
|
D009437||perineal neuralgias
|
|
D009437||stump neuralgia
|
|
D009437||stump neuralgias
|
|
D009437||supraorbital neuralgia
|
|
D009437||supraorbital neuralgias
|
|
D009437||vidian neuralgia
|
|
D009437||vidian neuralgias
|
|
D008106||liver cirrhosis experimental
|
|
D008106||cirrhoses experimental liver
|
|
D008106||cirrhosis experimental liver
|
|
D008106||experimental hepatic cirrhosis
|
|
D008106||experimental liver cirrhoses
|
|
D008106||experimental liver cirrhosis
|
|
D008106||hepatic cirrhosis experimental
|
|
D008106||liver cirrhoses experimental
|
|
D008103||liver cirrhosis
|
|
D008103||cirrhoses hepatic
|
|
D008103||cirrhoses liver
|
|
D008103||cirrhosis hepatic
|
|
D008103||cirrhosis liver
|
|
D008103||fibroses liver
|
|
D008103||fibrosis liver
|
|
D008103||hepatic cirrhoses
|
|
D008103||hepatic cirrhosis
|
|
D008103||liver cirrhoses
|
|
D008103||liver fibroses
|
|
D008103||liver fibrosis
|
|
106210|C536372||aniridia type 2
|
|
106210|C536372|606788|D000856||an
|
|
106210|C536372|D015783||aniridia
|
|
106210|C536372||aniridia ii formerly an2 formerly cataract congenital with late onset corneal dystrophy included
|
|
D008104||liver cirrhosis alcoholic
|
|
D008104||alcoholic cirrhosis
|
|
D008104||alcoholic hepatic cirrhosis
|
|
D008104||alcoholic liver cirrhosis
|
|
D008104||hepatic cirrhosis alcoholic
|
|
300448|C563023||alpha thalassemia myelodysplasia syndrome
|
|
300448|C563023||atmds
|
|
300448|C563023||hemoglobin h disease acquired
|
|
C537808||chromosome 6 monosomy 6q1
|
|
C537808||deletion 6q1
|
|
C537808||monosomy 6q1
|
|
D009444||neuritis autoimmune experimental
|
|
D009444||allergic neuritis experimental
|
|
D009444||autoimmune neuritis experimental
|
|
D009444||autoimmune neuropathies experimental
|
|
D009444||autoimmune neuropathy experimental
|
|
D009444||ean experimental allergic neuritis
|
|
D009444||ean experimental autoimmune neuritis
|
|
D009444||experimental allergic neuritis
|
|
D009444||experimental autoimmune neuritis
|
|
D009444||experimental autoimmune neuropathies
|
|
D009444||experimental autoimmune neuropathy
|
|
D009444||neuritis experimental allergic
|
|
D009444||neuritis experimental autoimmune
|
|
D009444||neuropathies experimental autoimmune
|
|
D009444||neuropathy experimental autoimmune
|
|
D053591||pain referred
|
|
D053591||facial pain referred
|
|
D053591||referred facial pain
|
|
D053591||referred pain
|
|
C537809||chromosome 6 monosomy 6q2
|
|
C537809||deletion 6q2
|
|
C537809||monosomy 6q2
|
|
D009443||neuritis
|
|
D009443||motor neuritides
|
|
D009443||motor neuritis
|
|
D009443||neuritides
|
|
D009443||neuritides motor
|
|
D009443||neuritides peripheral
|
|
D009443||neuritides sensory
|
|
D009443||neuritis motor
|
|
D009443||neuritis peripheral
|
|
D009443||neuritis sensory
|
|
D009443||peripheral neuritides
|
|
D009443||peripheral neuritis
|
|
D009443||polyneuritides
|
|
D009443||polyneuritis
|
|
D009443||sensory neuritides
|
|
D009443||sensory neuritis
|
|
D008113||liver neoplasms
|
|
D008113||cancer hepatic
|
|
D008113|114550|D006528||cancer hepatocellular
|
|
D008113||cancer liver
|
|
D008113||cancer of liver
|
|
D008113||cancer of the liver
|
|
D008113||cancers hepatic
|
|
D008113||cancers hepatocellular
|
|
D008113||cancers liver
|
|
D008113||hepatic cancer
|
|
D008113||hepatic cancers
|
|
D008113||hepatic neoplasm
|
|
D008113||hepatic neoplasms
|
|
D008113||hepatocellular cancer
|
|
D008113||hepatocellular cancers
|
|
D008113|114550|D006528||liver cancer
|
|
D008113||liver cancers
|
|
D008113||liver neoplasm
|
|
D008113||neoplasm hepatic
|
|
D008113||neoplasm liver
|
|
D008113||neoplasms hepatic
|
|
D008113||neoplasms liver
|
|
D009442||neurilemmoma
|
|
D009442||malignant neurilemmoma
|
|
D009442||malignant neurilemmomas
|
|
D009442||malignant neurilemoma
|
|
D009442||malignant neurilemomas
|
|
D009442||malignant peripheral nerve sheath tumors
|
|
D009442||malignant schwannoma
|
|
D009442||malignant schwannomas
|
|
D009442||mpnst
|
|
D009442||mpnsts
|
|
D009442||neurilemmoma malignant
|
|
D009442||neurilemmomas
|
|
D009442||neurilemmomas malignant
|
|
D009442||neurilemmosarcoma
|
|
D009442||neurilemmosarcomas
|
|
D009442||neurilemoma
|
|
D009442||neurilemoma malignant
|
|
D009442||neurilemomas
|
|
D009442||neurilemomas malignant
|
|
D009442||neurinoma
|
|
D009442||neurinomas
|
|
D009442||peripheral nerve sheath tumors malignant
|
|
D009442||plexiform schwannomatoses
|
|
D009442||plexiform schwannomatosis
|
|
D009442||schwannoma
|
|
D009442||schwannoma malignant
|
|
D009442||schwannomas
|
|
D009442||schwannomas malignant
|
|
D009442||schwannomatoses plexiform
|
|
D009442||schwannomatosis plexiform
|
|
C537807||chromosome 6 monosomy 6q
|
|
C537807||deletion 6q
|
|
C537807||monosomy 6q
|
|
D009440||neurasthenia
|
|
D009440||neurasthenic neuroses
|
|
D009440||neuroses neurasthenic
|
|
248310||plasmodium falciparum blood infection level
|
|
248310||pfbi
|
|
248310||plasmodium falciparum parasitemia
|
|
142946|C564180||holoprosencephaly 4
|
|
142946|C564180||hpe4
|
|
262890|C563120||scott syndrome
|
|
262890|C563120||bdplt7
|
|
262890|C563120||bleeding abnormality due to deficiency of platelet binding of factor x
|
|
262890|C563120||bleeding disorder platelet type 7
|
|
262890|C563120||prothrombin consumption deficiency
|
|
262890|C563120||prothrombin consumption inhibitor familial
|
|
262890|C563120||prothrombin conversion defect familial
|
|
262890|C563120||scts
|
|
C566340||bile acid synthesis defect congenital 3
|
|
C566340||congenital bile acid synthesis defect type 3 cbas3
|
|
C565010||fingerprints absence of
|
|
C565011||fibula recurrent dislocation of head of
|
|
C537804||chromosome 10q duplication syndrome
|
|
C537804||10q duplication syndrome
|
|
C537804||10q partial trisomy
|
|
C537804||partial trisomy 10q
|
|
C537804||trisomy 10q
|
|
C537803||ghose sachdev kumar syndrome
|
|
C566347||eccrine syringofibroadenomatosis with eyelid abnormalities
|
|
C565017||fibrinolytic defect
|
|
C565018||dysfibrinogenemia causing recurrent thrombosis
|
|
C566345||acromelic frontonasal dysostosis
|
|
C566346||blue nevi familial multiple
|
|
262000|C537633||bjornstad syndrome
|
|
262000|C537633||bjs
|
|
262000|C537633||deafness and pili torti bjornstad type
|
|
262000|C537633||pili torti and nerve deafness
|
|
262000|C537633||pili torti sensorineural hearing loss
|
|
262000|C537633||ptd
|
|
D008118||loiasis
|
|
D008118||loaiases
|
|
D008118||loaiasis
|
|
D008118||loiases
|
|
D009449||asthenia neurocirculatory
|
|
D009449||asthenias neurocirculatory
|
|
D009449||cardiac neuroses
|
|
D009449||cardiac neurosis
|
|
D009449||effort syndrome
|
|
D009449||heart syndrome hyperkinetic
|
|
D009449||hyperkinetic heart syndrome
|
|
D009449||neurocirculatory asthenias
|
|
D009449||neuroses cardiac
|
|
D009449||neurosis cardiac
|
|
D009449||syndrome effort
|
|
D009449||syndrome hyperkinetic heart
|
|
269700|D052497||lipodystrophy congenital generalized
|
|
269700|D052497||agpat2 related brunzell syndrome
|
|
269700|D052497||berardinelli seip congenital lipodystrophy
|
|
269700|D052497||berardinelli seip congenital lipodystrophy type 1
|
|
269700|D052497||berardinelli seip congenital lipodystrophy type 2
|
|
269700|D052497||berardinelli seip syndrome
|
|
269700|D052497||berardinelli syndrome
|
|
269700|D052497||brunzell syndrome
|
|
269700|D052497||brunzell syndrome agpat2 related
|
|
269700|D052497||brunzell syndrome bscl2 related
|
|
269700|D052497||brunzell syndrome with bone cysts
|
|
269700|D052497||bscl1
|
|
269700|D052497||bscl2 related brunzell syndrome
|
|
269700|D052497||cgl1
|
|
269700|D052497||cgl2
|
|
269700|D052497||congenital generalized lipodystrophies
|
|
269700|D052497||congenital generalized lipodystrophy
|
|
269700|D052497||congenital generalized lipodystrophy type 1
|
|
269700|D052497||congenital generalized lipodystrophy type 2
|
|
269700|D052497||congenital lipoatrophic diabete
|
|
269700|D052497||congenital lipoatrophic diabetes
|
|
269700|D052497||congenital lipodystrophy berardinelli seip
|
|
269700|D052497||diabete congenital lipoatrophic
|
|
269700|D052497||diabetes congenital lipoatrophic
|
|
269700|D052497||generalized lipodystrophies
|
|
269700|D052497||generalized lipodystrophies congenital
|
|
269700|D052497||generalized lipodystrophy
|
|
269700|D052497||generalized lipodystrophy congenital
|
|
269700|D052497||lipoatrophic diabete congenital
|
|
269700|D052497||lipoatrophic diabetes congenital
|
|
269700|D052497||lipodystrophies congenital generalized
|
|
269700|D052497||lipodystrophies generalized
|
|
269700|D052497||lipodystrophies total
|
|
269700|D052497||lipodystrophy berardinelli seip congenital
|
|
269700|D052497||lipodystrophy berardinelli seip congenital type 1
|
|
269700|D052497||lipodystrophy berardinelli seip congenital type 2
|
|
269700|D052497||lipodystrophy congenital generalized type 1
|
|
269700|D052497||lipodystrophy congenital generalized type 2
|
|
269700|D052497||lipodystrophy generalized
|
|
269700|D052497||lipodystrophy total
|
|
269700|D052497||lipodystrophy total and acromegaloid gigantism
|
|
269700|D052497||seip syndrome
|
|
269700|D052497||syndrome agpat2 related brunzell
|
|
269700|D052497||syndrome berardinelli
|
|
269700|D052497||syndrome berardinelli seip
|
|
269700|D052497||syndrome brunzell
|
|
269700|D052497||syndrome brunzell with bone cysts
|
|
269700|D052497||syndrome bscl2 related brunzell
|
|
269700|D052497||syndrome seip
|
|
269700|D052497||total lipodystrophies
|
|
269700|D052497||total lipodystrophy
|
|
269700|D052497||total lipodystrophy and acromegaloid gigantism
|
|
D008114||liver neoplasms experimental
|
|
D008114||experimental hepatoma
|
|
D008114||experimental hepatomas
|
|
D008114||experimental liver neoplasm
|
|
D008114||experimental liver neoplasms
|
|
D008114||hepatoma experimental
|
|
D008114||hepatoma morris
|
|
D008114||hepatoma novikoff
|
|
D008114||hepatomas experimental
|
|
D008114||liver neoplasm experimental
|
|
D008114||morris hepatoma
|
|
D008114||neoplasms experimental liver
|
|
D008114||novikoff hepatoma
|
|
C537819||chromosome 7 trisomy 7p
|
|
C537819||duplication 7p
|
|
C537819||trisomy 7p
|
|
D009455||neurofibroma
|
|
D009455||neurofibromas
|
|
608035||melanoma cutaneous malignant susceptibility to 4
|
|
608035||cmm4
|
|
C537817||chromosome 7 monosomy 7q3
|
|
C537817||deletion 7q3
|
|
C537817||monosomy 7q3
|
|
C537818||7p2 monosomy syndrome
|
|
C537818||chromosome 7 monosomy 7p2
|
|
C537818||chromosome 7 partial deletion of short arm 7p2
|
|
C537818||chromosome 7 partial monosomy 7p
|
|
C537818||chromosome 7 terminal 7p deletion del 7p21 p22
|
|
D010437||peptic ulcer
|
|
D010437||gastroduodenal ulcer
|
|
D010437||gastroduodenal ulcers
|
|
D010437||marginal ulcer
|
|
D010437||marginal ulcers
|
|
D010437||peptic ulcers
|
|
D010437||ulcer gastroduodenal
|
|
D010437||ulcer marginal
|
|
D010437||ulcer peptic
|
|
D010437||ulcers gastroduodenal
|
|
D010437||ulcers marginal
|
|
D010437||ulcers peptic
|
|
D009450||neurodermatitis
|
|
D009450||circumscribed neurodermatitides
|
|
D009450||circumscribed neurodermatitis
|
|
D009450||lichen simplex chronicus
|
|
D009450||localized neurodermatitides
|
|
D009450||localized neurodermatitis
|
|
D009450||neurodermatitides
|
|
D009450||neurodermatitides circumscribed
|
|
D009450||neurodermatitides localized
|
|
D009450||neurodermatitis circumscribed
|
|
D009450||neurodermatitis localized
|
|
251110|C537361||methylmalonic aciduria cblb type
|
|
251110|C537361||methylmalonic acidemia cblb type
|
|
251110|C537361||methylmalonic aciduria vitamin b12 responsive due to defect in synthesis of adenosylcobalamin cblb type
|
|
D010439||peptic ulcer perforation
|
|
D010439||peptic ulcer perforations
|
|
D010439||perforation peptic ulcer
|
|
D010439||perforations peptic ulcer
|
|
D010439||ulcer perforation peptic
|
|
D010439||ulcer perforations peptic
|
|
608033||encephalopathy acute infection induced susceptibility to 3
|
|
608033||ane
|
|
608033||encephalopathy acute necrotizing susceptibility to
|
|
608033||iiae3
|
|
D010438||peptic ulcer hemorrhage
|
|
D010438||hemorrhage peptic ulcer
|
|
D010438||peptic ulcer hemorrhages
|
|
D010438||ulcer hemorrhage peptic
|
|
C537811||chromosome 6 trisomy 6p
|
|
C537811||duplication 6p
|
|
C537811||trisomy 6p
|
|
C567682||tsc2 angiomyolipomas renal modifier of
|
|
C562771|274900||thyroid dyshormonogenesis 5
|
|
C562771|274900||hypothyroidism congenital due to dyshormonogenesis 5
|
|
C562771|274900||tdh5
|
|
C562771|274900||thyroid hormonogenesis genetic defect in 5
|
|
C565020||iron overload autosomal dominant
|
|
C566351||atrial septal defect secundum with various cardiac and noncardiac defects
|
|
C537812||chromosome 6 trisomy 6q
|
|
C537812||duplication 6q
|
|
C537812||trisomy 6q
|
|
C566352||neuroendocrine carcinoma of salivary glands sensorineural hearing loss and enamel hypoplasia
|
|
C565022||familial multiple coagulation factor deficiency vi
|
|
C565022||factor ix and factor xi combined deficiency
|
|
C565022||fmfd vi
|
|
C565022||mcfd6
|
|
C565022||multiple coagulation factor deficiency vi
|
|
C537810||6q syndrome partial
|
|
C537810||chromosome 6 partial trisomy 6q
|
|
C537810||chromosome 6 trisomy 6q2
|
|
C537810||distal duplication 6q
|
|
C537810||trisomy 6q partial
|
|
C537810||trisomy 6q syndrome partial
|
|
253200|D009087||mucopolysaccharidosis vi
|
|
253200|D009087||arsb deficiencies
|
|
253200|D009087||arsb deficiency
|
|
253200|D009087||arylsulfatase b deficiencies
|
|
253200|D009087||arylsulfatase b deficiency
|
|
253200|D009087||deficiencies arsb
|
|
253200|D009087||deficiencies arylsulfatase b
|
|
253200|D009087||deficiencies n acetylgalactosamine 4 sulfatase
|
|
253200|D009087||deficiency arsb
|
|
253200|D009087||deficiency arylsulfatase b
|
|
253200|D009087||deficiency n acetylgalactosamine 4 sulfatase
|
|
253200|D009087||dwarfism polydystrophic
|
|
253200|D009087||maroteaux lamy syndrome
|
|
253200|D009087||mps6
|
|
253200|D009087||mps vi
|
|
253200|D009087||mucopolysaccharidosis 6
|
|
253200|D009087||mucopolysaccharidosis type 6
|
|
253200|D009087||mucopolysaccharidosis type vi
|
|
253200|D009087||n acetylgalactosamine 4 sulfatase deficiencies
|
|
253200|D009087||n acetylgalactosamine 4 sulfatase deficiency
|
|
253200|D009087||polydystrophic dwarfism
|
|
253200|D009087||syndrome maroteaux lamy
|
|
253200|D009087||type 6 mucopolysaccharidosis
|
|
253200|D009087||type vi mucopolysaccharidosis
|
|
C537815||chromosome 7 monosomy 7q2
|
|
C537815||deletion 7q2
|
|
C537815||monosomy 7q2
|
|
C537816||chromosome 7 monosomy 7q21
|
|
C537816||deletion 7q21
|
|
C537816||monosomy 7q21
|
|
C567125|611721||combined saposin deficiency
|
|
C567125|611721||combined sap deficiency
|
|
C567125|611721||prosaposin deficiency
|
|
C567125|611721||psapd
|
|
C537813||chromosome 7 ring syndrome
|
|
C537813||ring chromosome 7
|
|
C537813||ring chromosome 7 syndrome
|
|
C537814||chromosome 7 monosomy
|
|
C537814||monosomy 7
|
|
C567461|300770||surfactant metabolism dysfunction pulmonary 4
|
|
C567461|300770||csf2ra deficiency
|
|
C567461|300770||pap due to csf2ra deficiency
|
|
C567461|300770||pulmonary alveolar proteinosis congenital 4
|
|
C567461|300770||smdp4
|
|
D004831|607208||epilepsies myoclonic
|
|
D004831|607208||absence epilepsies myoclonic
|
|
D004831|607208||absence epilepsy myoclonic
|
|
D004831|607208||astatic epilepsies myoclonic
|
|
D004831|607208||astatic epilepsy myoclonic
|
|
D004831|607208||benign infantile myoclonic epilepsy
|
|
D004831|607208||cryptogenic myoclonic epilepsies
|
|
D004831|607208||cryptogenic myoclonic epilepsy
|
|
D004831|607208||disorder myoclonic seizure
|
|
D004831|607208||disorders myoclonic seizure
|
|
D004831|607208||dravet syndrome
|
|
D004831|607208||dravet syndromes
|
|
D004831|607208||early childhood epilepsy myoclonic
|
|
D004831|607208||early childhood myoclonic epilepsy
|
|
D004831|607208||eiee6
|
|
D004831|607208||encephalopathies myoclonic
|
|
D004831|607208||encephalopathy myoclonic
|
|
D004831|607208||epilepsies cryptogenic myoclonic
|
|
D004831|607208||epilepsies idiopathic myoclonic
|
|
D004831|607208||epilepsies infantile myoclonic
|
|
D004831|607208||epilepsies myoclonic absence
|
|
D004831|607208||epilepsies myoclonic astatic
|
|
D004831|607208||epilepsies symptomatic myoclonic
|
|
D004831|607208||epilepsy cryptogenic myoclonic
|
|
D004831|607208||epilepsy early childhood myoclonic
|
|
D004831|607208||epilepsy idiopathic myoclonic
|
|
D004831|607208||epilepsy infantile myoclonic
|
|
D004831|607208||epilepsy myoclonic
|
|
D004831|607208||epilepsy myoclonic absence
|
|
D004831|607208||epilepsy myoclonic astatic
|
|
D004831|607208||epilepsy myoclonic early childhood
|
|
D004831|607208||epilepsy myoclonic infantile
|
|
D004831|607208||epilepsy myoclonic infantile benign
|
|
D004831|607208||epilepsy myoclonic infantile severe
|
|
D004831|607208||epilepsy myoclonus
|
|
D004831|607208||epilepsy symptomatic myoclonic
|
|
D004831|607208||epileptic encephalopathy early infantile 6
|
|
D004831|607208||idiopathic myoclonic epilepsies
|
|
D004831|607208||idiopathic myoclonic epilepsy
|
|
D004831|607208||infantile myoclonic epilepsies
|
|
D004831|607208||infantile myoclonic epilepsy
|
|
D004831|607208||infantile severe myoclonic epilepsy
|
|
D004831|607208||myoclonic absence epilepsies
|
|
D004831|607208||myoclonic absence epilepsy
|
|
D004831|607208||myoclonic astatic epilepsies
|
|
D004831|607208||myoclonic astatic epilepsy
|
|
D004831|607208||myoclonic encephalopathies
|
|
D004831|607208||myoclonic encephalopathy
|
|
D004831|607208||myoclonic epilepsies
|
|
D004831|607208||myoclonic epilepsies cryptogenic
|
|
D004831|607208||myoclonic epilepsies idiopathic
|
|
D004831|607208||myoclonic epilepsies infantile
|
|
D004831|607208||myoclonic epilepsies symptomatic
|
|
D004831|607208||myoclonic epilepsy
|
|
D004831|607208||myoclonic epilepsy benign infantile
|
|
D004831|607208||myoclonic epilepsy cryptogenic
|
|
D004831|607208||myoclonic epilepsy early childhood
|
|
D004831|607208||myoclonic epilepsy idiopathic
|
|
D004831|607208||myoclonic epilepsy infantile
|
|
D004831|607208||myoclonic epilepsy infantile benign
|
|
D004831|607208||myoclonic epilepsy infantile severe
|
|
D004831|607208||myoclonic epilepsy severe infantile
|
|
D004831|607208||myoclonic epilepsy severe of infancy
|
|
D004831|607208||myoclonic epilepsy symptomatic
|
|
D004831|607208||myoclonic seizure disorder
|
|
D004831|607208||myoclonic seizure disorders
|
|
D004831|607208||myoclonus epilepsies
|
|
D004831|607208||myoclonus epilepsy
|
|
D004831|607208||seizure disorder myoclonic
|
|
D004831|607208||seizure disorders myoclonic
|
|
D004831|607208||severe infantile myoclonic epilepsy
|
|
D004831|607208||severe myoclonic epilepsy infantile
|
|
D004831|607208||severe myoclonic epilepsy of infancy
|
|
D004831|607208||smei
|
|
D004831|607208||symptomatic myoclonic epilepsies
|
|
D004831|607208||symptomatic myoclonic epilepsy
|
|
D004831|607208||syndrome dravet
|
|
D004831|607208||syndromes dravet
|
|
C566677||speech development delayed with facial asymmetry strabismus and transverse earlobe crease
|
|
C564014||renal tubulopathy diabetes mellitus and cerebellar ataxia due to duplication of mitochondrial dna
|
|
C566678||elliptocytosis 3
|
|
C566679||spastic paraplegia optic atrophy and dementia
|
|
C564012||wolfram syndrome mitochondrial form
|
|
C564012||diabetes insipidus and mellitus with optic atrophy and deafness mitochondrial form
|
|
C564012||didmoad syndrome mitochondrial form
|
|
C565349||mesomelic dysplasia savarirayan type
|
|
C565349||mesomelic dysplasia with absent fibulas and triangular tibias
|
|
C564011||pancreatic hypoplasia congenital with diabetes mellitus and congenital heart disease
|
|
C566673|C566672|182980||spinal muscular atrophy late onset finkel type
|
|
C566673|C566672|182980||finkel late adult type sma
|
|
C564018||myoglobinuria recurrent
|
|
C566674||spinal muscular atrophy facioscapulohumeral type
|
|
C566674||fshsma
|
|
C537832|153840||macular dystrophy atypical vitelliform
|
|
C537832|153840||vitelliform macular dystrophy atypical
|
|
C537832|153840||vmd1
|
|
C564017||myopathy mitochondrial lethal infantile
|
|
C566675||neuronopathy distal hereditary motor type i
|
|
C566675||charcot marie tooth disease spinal i
|
|
C566675||neuropathy distal hereditary motor type i
|
|
C566675||spinal muscular atrophy distal juvenile autosomal dominant i
|
|
C564016||nephropathy chronic tubulointerstitial
|
|
C564015||parkinson disease mitochondrial
|
|
C579990||childhood myocerebrohepatopathy spectrum
|
|
C579991||chmp2b related frontotemporal dementia
|
|
C579991||chromosome 3 linked frontotemporal dementia
|
|
C579991||dtm1
|
|
C579991||ftd 3
|
|
C579991||ftd chmp2b
|
|
142340|C538080||congenital diaphragmatic hernia
|
|
142340|C538080||agenesis of hemidiaphragm
|
|
142340|C538080|142700||cdh
|
|
142340|C538080||congenital diaphragmatic defect
|
|
142340|C538080||diaphragmatic defect congenital
|
|
142340|C538080||diaphragmatic hernia congenital
|
|
142340|C538080||diaphragm complete agenesis of included
|
|
142340|C538080||diaphragm unilateral agenesis of
|
|
142340|C538080||dih
|
|
142340|C538080||dih1 included
|
|
142340|C538080||hcd
|
|
142340|C538080||hemidiaphragm agenesis of
|
|
142340|C538080||hemidiaphragm agenesis of diaphragmatic hernia 1 included
|
|
142340|C538080||hernia congenital diaphragmatic
|
|
142340|C538080||unilateral agenesis of diaphragm
|
|
D008206||lymphatic diseases
|
|
D008206||disease lymphatic
|
|
D008206||diseases lymphatic
|
|
D008206||lymphadenopathy
|
|
D008206||lymphatic disease
|
|
D008206||lymphatism
|
|
D008206||status lymphaticus
|
|
C536295|608629||joubert syndrome 3
|
|
C536295|608629||jbts3
|
|
C564019||diarrhea chronic with villous atrophy
|
|
D008207||lymphatic metastasis
|
|
D008207||lymphatic metastases
|
|
D008207||metastases lymphatic
|
|
D008207||metastasis lymphatic
|
|
D008204||lymphangiosarcoma
|
|
D008204||lymphangioendothelioma malignant
|
|
D008204||lymphangioendotheliomas malignant
|
|
D008204||lymphangiosarcomas
|
|
D008204||malignant lymphangioendothelioma
|
|
D008204||malignant lymphangioendotheliomas
|
|
D008205||lymphangitis
|
|
D008205||lymphangitides
|
|
C537500|271930||striatonigral degeneration infantile
|
|
C537500|271930||bilateral striatal necrosis infantile
|
|
C537500|271930||ibsn
|
|
C537500|271930||infantile bilateral striatal necrosis
|
|
C537500|271930||sndi
|
|
C537500|271930||striatal degeneration familial
|
|
D008202||lymphangioma
|
|
D008202||cavernous lymphangioma
|
|
D008202||cavernous lymphangiomas
|
|
D008202||endothelioma lymphatic
|
|
D008202||endotheliomas lymphatic
|
|
D008202||lymphangioendothelioma
|
|
D008202||lymphangioendotheliomas
|
|
D008202||lymphangioma cavernous
|
|
D008202||lymphangiomas
|
|
D008202||lymphangiomas cavernous
|
|
D008202||lymphatic endothelioma
|
|
D008202||lymphatic endotheliomas
|
|
D008203||lymphangiomyoma
|
|
D008203||lymphangioleiomyoma
|
|
D008203||lymphangioleiomyomas
|
|
D008203||lymphangiomyomas
|
|
D009542||niemann pick diseases
|
|
D009542||niemann pick disease
|
|
D010523||peripheral nervous system diseases
|
|
D010523||nerve disease peripheral
|
|
D010523||nerve diseases peripheral
|
|
D010523||neuropathy peripheral
|
|
D010523||peripheral nerve disease
|
|
D010523||peripheral nerve diseases
|
|
D010523||peripheral nervous system disease
|
|
D010523||peripheral nervous system disorders
|
|
D010523||peripheral neuropathies
|
|
D010523||peripheral neuropathy
|
|
D010523||pns disease
|
|
D010523||pns diseases
|
|
D010523||pns peripheral nervous system diseases
|
|
D010522||periostitis
|
|
D010522||periostitides
|
|
D008210||lymphocele
|
|
D008210||cyst lymphatic
|
|
D008210||cysts lymphatic
|
|
D008210||lymphatic cyst
|
|
D008210||lymphatic cysts
|
|
D008210||lymphoceles
|
|
D008210||lymphocoele
|
|
D008210||lymphocoeles
|
|
D011855||radiodermatitis
|
|
D011855||dermatitides radiation induced
|
|
D011855||dermatitides radiation recall
|
|
D011855||dermatitis radiation induced
|
|
D011855||dermatitis radiation recall
|
|
D011855||radiation induced dermatitides
|
|
D011855||radiation induced dermatitis
|
|
D011855||radiation recall dermatitides
|
|
D011855||radiation recall dermatitis
|
|
D011855||radiation recall reaction
|
|
D011855||radiation recall reactions
|
|
D011855||radiodermatitides
|
|
D011855||reaction radiation recall
|
|
D011855||reactions radiation recall
|
|
D011855||recall reaction radiation
|
|
D011855||recall reactions radiation
|
|
D010524||peripheral nervous system neoplasms
|
|
D010524||neoplasm peripheral nerve
|
|
D010524||neoplasms peripheral nerve
|
|
D010524||nerve neoplasm peripheral
|
|
D010524||nerve neoplasms peripheral
|
|
D010524||nerve tumor peripheral
|
|
D010524||nerve tumors peripheral
|
|
D010524||peripheral nerve neoplasm
|
|
D010524||peripheral nerve neoplasms
|
|
D010524||peripheral nerve neoplasms benign
|
|
D010524||peripheral nerve neoplasms malignant
|
|
D010524||peripheral nerve neoplastic infiltration
|
|
D010524||peripheral nerve tumor
|
|
D010524||peripheral nerve tumors
|
|
D010524||peripheral nervous system benign neoplasms
|
|
D010524||peripheral nervous system malignant neoplasms
|
|
D010524||tumor peripheral nerve
|
|
D010524||tumors peripheral nerve
|
|
C564694|606593||lig4 syndrome
|
|
C566681||spastic paraplegia with associated extrapyramidal signs
|
|
C566682||spastic paraplegia sensorineural deafness mental retardation and progressive nephropathy
|
|
C564021||leigh syndrome due to mitochondrial complex i deficiency
|
|
C564021||atpase deficiency nuclear encoded
|
|
C564020||ataxia and polyneuropathy adult onset
|
|
231680|D054069||multiple acyl coenzyme a dehydrogenase deficiency
|
|
231680|D054069||aciduria ethylmalonic adipic
|
|
231680|D054069||acidurias ethylmalonic adipic
|
|
231680|D054069||electron transfer flavoprotein alpha subunit deficiency
|
|
231680|D054069||electron transfer flavoprotein beta subunit deficiency
|
|
231680|D054069||electron transfer flavoprotein deficiency
|
|
231680|D054069||electron transfer flavoprotein dehydrogenase deficiency
|
|
231680|D054069||etfa deficiencies
|
|
231680|D054069||etfa deficiency
|
|
231680|D054069||etfa deficiency included
|
|
231680|D054069||etfb deficiencies
|
|
231680|D054069||etfb deficiency
|
|
231680|D054069||etfb deficiency included
|
|
231680|D054069||etfdh deficiencies
|
|
231680|D054069||etfdh deficiency
|
|
231680|D054069||etfdh deficiency included
|
|
231680|D054069||ethylmalonic adipicaciduria
|
|
231680|D054069||ethylmalonic adipic aciduria
|
|
231680|D054069||ethylmalonic adipicaciduria ema glutaric acidemia iia included
|
|
231680|D054069||ethylmalonic adipic acidurias
|
|
231680|D054069||ga ii
|
|
231680|D054069||glutaric acidemia ii
|
|
231680|D054069||glutaric acidemia iib included
|
|
231680|D054069||glutaric acidemia iic included
|
|
231680|D054069||glutaric acidemia type 2
|
|
231680|D054069||glutaric acidemia type ii
|
|
231680|D054069||glutaric aciduria ii
|
|
231680|D054069||glutaric aciduria iia
|
|
231680|D054069||glutaric aciduria iib
|
|
231680|D054069||glutaric aciduria iic
|
|
231680|D054069||glutaric aciduria type 2
|
|
231680|D054069||glutaric aciduria type ii
|
|
231680|D054069||madd
|
|
231680|D054069||madd multiple acyl coa dehydrogenase deficiency
|
|
231680|D054069||madds multiple acyl coa dehydrogenase deficiency
|
|
231680|D054069||multiple acyl coa dehydrogenase deficiency
|
|
231680|D054069||multiple fad dehydrogenase deficiency
|
|
C564025||striatonigral degeneration infantile mitochondrial
|
|
C564025||bilateral striatal necrosis infantile mitochondrial
|
|
C564025||infantile bilateral striatal necrosis mitochondrial
|
|
C565358||growth deficiency and mental retardation with facial dysmorphism
|
|
C564024||hypomagnesemia hypertension and hypercholesterolemia mitochondrial
|
|
C539067||amoebic dysentery due to entamoeba histolytica
|
|
154700|D008382||marfan syndrome
|
|
154700|D008382||marfan apos s syndrome
|
|
154700|D008382||marfans syndrome
|
|
154700|D008382||marfan syndrome type i
|
|
154700|D008382||mfs
|
|
154700|D008382||mfs1
|
|
154700|D008382||syndrome marfan
|
|
154700|D008382||syndrome marfan apos s
|
|
C564023||cyclic vomiting syndrome plus
|
|
C564023||cvs plus
|
|
C564022||cyclic vomiting syndrome with neuromuscular disease
|
|
131300|D003966||camurati engelmann syndrome
|
|
131300|D003966||caend
|
|
131300|D003966||camurati engelmann disease
|
|
131300|D003966||ced
|
|
131300|D003966|C538411||diaphyseal dysplasia 1 progressive
|
|
131300|D003966||diaphyseal dysplasia progressive
|
|
131300|D003966||diaphyseal dysplasias progressive
|
|
131300|D003966||diaphyseal hyperostosis
|
|
131300|D003966||dpd1
|
|
131300|D003966||dysplasia progressive diaphyseal
|
|
131300|D003966||dysplasias progressive diaphyseal
|
|
131300|D003966||engelmann disease
|
|
131300|D003966||engelmann apos s disease
|
|
131300|D003966||pdd
|
|
131300|D003966||progressive diaphyseal dysplasia
|
|
D064386||ankle fractures
|
|
D064386||ankle fracture
|
|
D064386||ankle fracture bimalleolar
|
|
D064386||ankle fractures bimalleolar
|
|
D064386||ankle fractures trimalleolar
|
|
D064386||ankle fracture trimalleolar
|
|
D064386||bimalleolar ankle fracture
|
|
D064386||bimalleolar ankle fractures
|
|
D064386||bimalleolar equivalent ankle fractures
|
|
D064386||bimalleolar equivalent fracture
|
|
D064386||bimalleolar equivalent fractures
|
|
D064386||bimalleolar fracture
|
|
D064386||bimalleolar fractures
|
|
D064386||equivalent fracture bimalleolar
|
|
D064386||equivalent fractures bimalleolar
|
|
D064386||fracture ankle
|
|
D064386||fracture bimalleolar
|
|
D064386||fracture bimalleolar ankle
|
|
D064386||fracture bimalleolar equivalent
|
|
D064386||fracture lateral malleolus
|
|
D064386||fracture medial malleolus
|
|
D064386||fracture posterior malleolus
|
|
D064386||fractures ankle
|
|
D064386||fractures bimalleolar
|
|
D064386||fractures bimalleolar ankle
|
|
D064386||fractures bimalleolar equivalent
|
|
D064386||fractures lateral malleolus
|
|
D064386||fractures medial malleolus
|
|
D064386||fractures posterior malleolus
|
|
D064386||fractures trimalleolar
|
|
D064386||fractures trimalleolar ankle
|
|
D064386||fracture trimalleolar
|
|
D064386||fracture trimalleolar ankle
|
|
D064386||lateral malleolus fracture
|
|
D064386||lateral malleolus fractures
|
|
D064386||malleolus fracture lateral
|
|
D064386||malleolus fracture medial
|
|
D064386||malleolus fracture posterior
|
|
D064386||malleolus fractures lateral
|
|
D064386||malleolus fractures medial
|
|
D064386||malleolus fractures posterior
|
|
D064386||medial malleolus fracture
|
|
D064386||medial malleolus fractures
|
|
D064386||posterior malleolus fracture
|
|
D064386||posterior malleolus fractures
|
|
D064386||trimalleolar ankle fracture
|
|
D064386||trimalleolar ankle fractures
|
|
D064386||trimalleolar fracture
|
|
D064386||trimalleolar fractures
|
|
C566687||skeletal dysplasia with delayed epiphyseal and carpal bone ossification
|
|
C564026||mitochondrial myopathy with diabetes
|
|
C564026||mitochondrial myopathy lipid type
|
|
D008219||lymphogranuloma venereum
|
|
D008219||lymphogranuloma inguinale
|
|
D008218||lymphocytosis
|
|
D008218||lymphocytoses
|
|
D008216||lymphocytic choriomeningitis
|
|
D008216||armstrong apos s syndrome
|
|
D008216||armstrong syndrome
|
|
D008216||choriomeningitis lymphocytic
|
|
D008216||encephalomyelitis lymphocytic choriomeningitis virus
|
|
D008216||lymphocytic choriomeningitis virus encephalomyelitis
|
|
D008216||syndrome armstrong
|
|
D008216||syndrome armstrong apos s
|
|
D010532||peritoneal diseases
|
|
D010532||peritoneal disease
|
|
D008223||lymphoma
|
|
D008223||germinoblastic sarcoma
|
|
D008223||germinoblastic sarcomas
|
|
D008223||germinoblastoma
|
|
D008223||germinoblastomas
|
|
D008223||lymphoma malignant
|
|
D008223||lymphomas
|
|
D008223||lymphomas malignant
|
|
D008223||malignant lymphoma
|
|
D008223||malignant lymphomas
|
|
D008223||reticulolymphosarcoma
|
|
D008223||reticulolymphosarcomas
|
|
D008223||sarcoma germinoblastic
|
|
D008223||sarcomas germinoblastic
|
|
D010534||peritoneal neoplasms
|
|
D010534||neoplasm peritoneal
|
|
D010534||neoplasms peritoneal
|
|
D010534||peritoneal neoplasm
|
|
D010538||peritonitis
|
|
D010538||peritonitis primary
|
|
D010538||peritonitis secondary
|
|
D010538||primary peritonitis
|
|
D010538||secondary peritonitis
|
|
C566692||sclerocornea autosomal dominant
|
|
C565361||muscular dystrophy adult onset with leukoencephalopathy
|
|
C564032||sertoli cell only syndrome type ii
|
|
C566996|600919||cardiac arrhythmia ankyrin b related
|
|
C566996|600919||ankyrin b syndrome
|
|
C566996|600919||ankyrin b syndrome long qt syndrome 4 included
|
|
C566996|600919||lqt4 included
|
|
115430|D002349||carpal tunnel syndrome
|
|
115430|D002349||amyotrophy thenar of carpal origin
|
|
115430|D002349||carpal tunnel syndromes
|
|
115430|D002349||compression neuropathy carpal tunnel
|
|
115430|D002349||cts
|
|
115430|D002349||cts1
|
|
115430|D002349||entrapment neuropathy carpal tunnel
|
|
115430|D002349||median neuropathy carpal tunnel
|
|
115430|D002349||syndrome carpal tunnel
|
|
115430|D002349||syndromes carpal tunnel
|
|
C566690||sinus node disease and myopia
|
|
C566690||sick sinus syndrome and myopia
|
|
C566690||sss myopia syndrome
|
|
C566655||steinfeld syndrome
|
|
C566658||spondyloepiphyseal dysplasia tarda autosomal dominant
|
|
C565327||leber congenital amaurosis 6
|
|
C566651||iris pigment epithelium anomalies
|
|
C566651||cysts of iris pigment epithelium
|
|
C566651||ruffles and cysts of iris pigment epithelium
|
|
C566652||spastic paraplegia and evans syndrome
|
|
C566654||leukoencephalopathy with dystonia and motor neuropathy scpx deficient
|
|
D010509||periodontal cyst
|
|
D010509||cyst dental root
|
|
D010509||cyst dentoalveolar
|
|
D010509||cyst lateral
|
|
D010509||cyst periodontal
|
|
D010509||cysts dental root
|
|
D010509||cysts dentoalveolar
|
|
D010509||cysts lateral
|
|
D010509||cysts periodontal
|
|
D010509||dental root cyst
|
|
D010509||dental root cysts
|
|
D010509||dentoalveolar cyst
|
|
D010509||dentoalveolar cysts
|
|
D010509||lateral cyst
|
|
D010509||lateral cysts
|
|
D010509||periodontal cysts
|
|
D010509||root cyst dental
|
|
D010509||root cysts dental
|
|
D010508||periodontal abscess
|
|
D010508||abscesses periodontal
|
|
D010508||abscess periodontal
|
|
D010508||periodontal abscesses
|
|
C566659||spondyloepiphyseal dysplasia myopia and sensorineural deafness
|
|
C567231|612627||convulsions benign familial infantile 4
|
|
C567231|612627||bfic4
|
|
C567231|612627||bfis4
|
|
C567231|612627||seizures benign familial infantile 4
|
|
C563666|610768||congenital disorder of glycosylation type im
|
|
C563666|610768||cdg1m
|
|
C563666|610768||cdgim
|
|
C563666|610768||cdg im
|
|
C563666|610768||dk1 deficiency
|
|
C563666|610768||dolichol kinase deficiency
|
|
C537179|311510||parkinsonism early onset with mental retardation
|
|
C537179|311510||basal ganglia disorder with mental retardation
|
|
C537179|311510||basal ganglion disorder with mental retardation
|
|
C537179|311510||bgmr
|
|
C537179|311510||laxova brown hogan syndrome
|
|
C537179|311510||waisman syndrome
|
|
C537179|311510||wsn
|
|
C537179|311510||x linked recessive basal ganglia disorder with mental retardation
|
|
D009521||newcastle disease
|
|
D009521||disease newcastle
|
|
D011832||radiation injuries
|
|
D011832||injuries radiation
|
|
D011832||injury radiation
|
|
D011832||radiation injury
|
|
D011832||radiation sickness
|
|
D011832||radiation sicknesses
|
|
D011832||radiation syndrome
|
|
D011832||radiation syndromes
|
|
D011832||sicknesses radiation
|
|
D011832||sickness radiation
|
|
D011832||syndrome radiation
|
|
D011832||syndromes radiation
|
|
D010501||perinephritis
|
|
D010501||inflammation perinephrium
|
|
D010501||inflammations perinephrium
|
|
D010501||perinephritides
|
|
D010501||perinephrium inflammation
|
|
C566459|609647||deafness autosomal recessive 46
|
|
C566459|609647||dfnb46
|
|
D011833||radiation injuries experimental
|
|
D011833||experimental radiation injuries
|
|
D011833||experimental radiation injury
|
|
D011833||injuries experimental radiation
|
|
D011833||radiation injury experimental
|
|
C567326|612381||inflammatory bowel disease 23
|
|
C567326|612381||ibd23
|
|
248360|C535702||malonic aciduria
|
|
248360|C535702||malonicaciduria
|
|
248360|C535702||malonyl coa decarboxylase deficiency
|
|
248360|C535702||malonyl coenzyme a decarboxylase deficiency
|
|
C566660||spondyloepiphyseal dysplasia with punctate corneal dystrophy
|
|
C579969||cap myopathy
|
|
C579969||cap disease
|
|
C579969||congenital myopathy with caps
|
|
C566666||splenomegaly syndrome with splenic germinal center hypoplasia and reduced circulating t helper cells
|
|
C564003||spondyloepiphyseal dysplasia tarda with characteristic facies
|
|
C566668||spinocerebellar atrophy with pupillary paralysis
|
|
C566669||spinocerebellar ataxia with rigidity and peripheral neuropathy
|
|
C564000||retinitis pigmentosa with paraarteriolar preservation of retinal pigment epithelium
|
|
C564000||retinitis pigmentosa prpe type
|
|
C564000||rp with preserved paraarteriole retinal pigment epithelium
|
|
C566662||split hand with obstructive uropathy spina bifida and diaphragmatic defects
|
|
C565331||fibromatosis gingival with hypertrichosis and mental retardation
|
|
C566665||split hand and split foot with hypodontia
|
|
D010518||periodontitis
|
|
D010518||pericementitides
|
|
D010518||pericementitis
|
|
D010518||periodontitides
|
|
C564009||bladder exstrophy and epispadias complex
|
|
C536807||chromosome 3 monosomy 3p25
|
|
C536807||deletion 3p25
|
|
C536807||monosomy 3p25
|
|
C567523|312600||retinitis pigmentosa 2
|
|
C567523|312600||rp2
|
|
D010510||periodontal diseases
|
|
D010510||disease periodontal
|
|
D010510||diseases periodontal
|
|
D010510||parodontoses
|
|
D010510||parodontosis
|
|
D010510||periodontal disease
|
|
D010510||pyorrhea alveolaris
|
|
D008200||lymphangiectasis
|
|
D008200||lymphangiectases
|
|
C536808||chromosome 3 monosomy 3q13
|
|
C536808||deletion 3q13
|
|
C536808||monosomy 3q13
|
|
D008201||lymphangiectasis intestinal
|
|
D008201||intestinal lymphangiectases
|
|
D008201||intestinal lymphangiectasis
|
|
D008201||lymphangiectases intestinal
|
|
D008201||lymphangiectasia intestinal
|
|
C536805||chromosome 3 monosomy 3p14 p11
|
|
C536805||deletion 3p14 p11
|
|
C536805||monosomy 3p14 p11
|
|
D011843||radiculopathy
|
|
D011843||avulsion nerve root
|
|
D011843||avulsions nerve root
|
|
D011843||cervical radiculopathies
|
|
D011843||cervical radiculopathy
|
|
D011843||compression nerve root
|
|
D011843||compressions nerve root
|
|
D011843||inflammation nerve root
|
|
D011843||nerve root avulsion
|
|
D011843||nerve root avulsions
|
|
D011843||nerve root compression
|
|
D011843||nerve root compressions
|
|
D011843||nerve root disorder
|
|
D011843||nerve root disorders
|
|
D011843||nerve root inflammation
|
|
D011843||nerve root inflammations
|
|
D011843||radiculitides
|
|
D011843||radiculitis
|
|
D011843||radiculopathies
|
|
D011843||radiculopathies cervical
|
|
D011843||radiculopathy cervical
|
|
C579978||catsper1 related nonsyndromic male infertility
|
|
C579978||catsper1 related male infertility
|
|
C579978||catsper related nonsyndromic male infertility
|
|
C536806||chromosome 3 monosomy 3p2
|
|
C536806||chromosome 3 deletion of distal 3p
|
|
C536806||chromosome 3 distal 3p monosomy
|
|
C536806||chromosome 3 distal deletion
|
|
C536806||monosomy 3p2
|
|
D011842||radicular cyst
|
|
D011842||apical periodontal cyst
|
|
D011842||apical periodontal cysts
|
|
D011842||cyst apical periodontal
|
|
D011842||cyst periapical
|
|
D011842||cyst radicular
|
|
D011842||cysts apical periodontal
|
|
D011842||cysts periapical
|
|
D011842||cysts radicular
|
|
D011842||periapical cyst
|
|
D011842||periapical cysts
|
|
D011842||periodontal cyst apical
|
|
D011842||periodontal cysts apical
|
|
D011842||radicular cysts
|
|
D010514||periodontal pocket
|
|
D010514||periodontal pockets
|
|
D010514||pocket periodontal
|
|
D010514||pockets periodontal
|
|
C536809||chromosome 3 monosomy 3q21 23
|
|
C536809||deletion 3q21 23
|
|
C536809||monosomy 3q21 23
|
|
C566670||spinal muscular atrophy segmental
|
|
C536800||chromosome 22 trisomy q11 q13
|
|
C536800||duplication 22q11 q13
|
|
C536800||trisomy 22q11 q13
|
|
C566671||spinocerebellar ataxia and plaque like deposits
|
|
C565340||frontoocular syndrome
|
|
C536803||chromosome 3 duplication syndrome
|
|
C536804||chromosome 3 monosomy 3p
|
|
C536804||chromosome 3 deletion 3p
|
|
C536804||deletion 3p
|
|
C536804||monosomy 3p
|
|
C563401|601042||choreoathetosis spasticity episodic
|
|
C563401|601042||choreoathetosis kinesigenic with episodic ataxia and spasticity
|
|
C563401|601042||choreoathetosis paroxysmal with episodic ataxia
|
|
C563401|601042||cse choreoathetosis paroxysmal with episodic ataxia
|
|
C563401|601042||dystonia 9
|
|
C563401|601042||dyt9
|
|
C566633||peroxisome biogenesis disorder complementation group 3
|
|
C566634||peroxisome biogenesis disorder complementation group 11
|
|
C566635||peroxisome biogenesis disorder complementation group r
|
|
D014091||tooth resorption
|
|
D014091||resorptions tooth
|
|
D014091||resorption tooth
|
|
D014091||tooth resorptions
|
|
C565304||multiple mitochondrial dysfunctions syndrome
|
|
D038062||upper extremity deformities congenital
|
|
D038062||upper limb deformities congenital
|
|
C566636||pten hamartoma tumor syndrome with granular cell tumor
|
|
D038061||lower extremity deformities congenital
|
|
D038061||lower limb deformities congenital
|
|
D014097||tooth unerupted
|
|
D014097||teeth unerupted
|
|
D014097||unerupted teeth
|
|
D014097||unerupted tooth
|
|
D014096||tooth supernumerary
|
|
D014096||fourth molar
|
|
D014096||fourth molars
|
|
D014096||molar fourth
|
|
D014096||molars fourth
|
|
D014096||supernumerary teeth
|
|
D014096||supernumerary tooth
|
|
D014096||teeth supernumerary
|
|
208500|C537571||jeune syndrome
|
|
208500|C537571||asphyxiating thoracic chondrodystrophy
|
|
208500|C537571||asphyxiating thoracic dysplasia
|
|
208500|C537571||asphyxiating thoracic dystrophy
|
|
208500|C537571||asphyxiating thoracic dystrophy 1
|
|
208500|C537571||asphyxiating thoracic dystrophy atd
|
|
208500|C537571||atd1
|
|
208500|C537571||chondroectodermal dysplasia like syndrome
|
|
208500|C537571||infantile thoracic dystrophy
|
|
208500|C537571||jeune apos s syndrome
|
|
208500|C537571||jeune thoracic dysplasia
|
|
208500|C537571||jeune thoracic dystrophy
|
|
208500|C537571||short rib thoracic dysplasia 1 with or without polydactyly
|
|
208500|C537571||srtd1
|
|
208500|C537571||thoracic asphyxiant dystrophy
|
|
208500|C537571||thoracic pelvic phalangeal dystrophy
|
|
D014095||tooth impacted
|
|
D014095||impacted teeth
|
|
D014095||impacted tooth
|
|
D014095||teeth impacted
|
|
C566244|611493||atrial fibrillation familial 4
|
|
C566244|611493||atfb4
|
|
C566632||preaxial hallucal polydactyly
|
|
611073|C567022||alzheimer disease 12
|
|
611073|C567022||ad12
|
|
611073|C567022||alzheimer disease familial 12
|
|
C538225|100300||adams oliver syndrome
|
|
C538225|100300||absence defect of limbs scalp and skull
|
|
C538225|100300||adams oliver syndrome 1
|
|
C538225|100300||aos
|
|
C538225|100300||aos1
|
|
C538225|100300||aplasia cutis congenita with terminal transverse limb defects
|
|
C538225|100300||aplasia cutis congenita with terminal transverse limb defects aplasia cutis congenita congenital heart defect and frontonasal cysts included
|
|
C538225|100300||aplasia cutis of the scalp
|
|
C538225|100300||congenital defect of skull and scalp
|
|
C538225|100300||congenital scalp defects with distal limb reduction anomalies
|
|
C538225|100300||familial aplasia cutis congenita of the scalp
|
|
C538225|100300||scalp and head syndrome
|
|
C538225|100300||scalp defect congenital
|
|
C538225|100300||scalp defects with ectrodactyly
|
|
D011818||rabies
|
|
D011818||hydrophobia
|
|
D011818||lyssa
|
|
D011818||lyssas
|
|
D060825||mild cognitive impairment
|
|
D060825||cognitive impairment mild
|
|
D060825||cognitive impairments mild
|
|
D060825||impairment mild cognitive
|
|
D060825||impairments mild cognitive
|
|
D060825||mild cognitive impairments
|
|
C565306||cutis verticis gyrata retinitis pigmentosa and sensorineural deafness
|
|
C566638||superior transverse scapular ligament calcification of familial
|
|
C565308||cerebellar ataxia and hypergonadotropic hypogonadism
|
|
D004613|225500||ellis van creveld syndrome
|
|
D004613|225500||chondroectodermal dysplasia
|
|
D004613|225500||chondroectodermal dysplasias
|
|
D004613|225500||creveld dysplasia ellis van
|
|
D004613|225500||dysplasia chondroectodermal
|
|
D004613|225500||dysplasia ellis van creveld
|
|
D004613|225500||dysplasias chondroectodermal
|
|
D004613|225500||ellis van creveld dysplasia
|
|
D004613|225500||evc
|
|
D004613|225500|C538472||mesoectodermal dysplasia
|
|
D004613|225500||syndrome ellis van creveld
|
|
605751|C565296||seizures benign familial infantile 2
|
|
605751||bfic2
|
|
605751||bfis2
|
|
605751|C565296||convulsions benign familial infantile 2
|
|
C566644||spondyloepimetaphyseal dysplasia with abnormal dentition
|
|
C566644||semdad
|
|
C565313||cerebrooculonasal syndrome
|
|
C565314||tetralogy of fallot syndrome autosomal recessive
|
|
C566640||platelet activating factor acetylhydrolase deficiency
|
|
C566641||glaucoma 1 open angle c
|
|
C566643||ichthyosis congenital with trichothiodystrophy
|
|
C566643||trichothiodystrophy with congenital ichthyosis
|
|
D009508||nevus pigmented
|
|
D009508||melanocytic nevi
|
|
D009508||melanocytic nevus
|
|
D009508||nevi melanocytic
|
|
D009508||nevi pigmented
|
|
D009508||nevus melanocytic
|
|
D009508|162900|C562736||pigmented moles
|
|
D009508||pigmented nevi
|
|
D009508||pigmented nevus
|
|
D009507||nevus of ota
|
|
D009507||nevus ota apos s
|
|
D009507||ota nevus
|
|
D009507||ota apos s nevus
|
|
D009507||otas nevus
|
|
D009506||nevus
|
|
D009506||mole skin
|
|
D009506||moles skin
|
|
D009506||nevi
|
|
D009506||skin mole
|
|
D009506||skin moles
|
|
C565208|610260||pyloric stenosis infantile hypertrophic 2
|
|
C565208|610260||ihps2
|
|
C537134|311200||orofaciodigital syndrome type1
|
|
C537134|311200||ofd1
|
|
C537134|311200||ofds i
|
|
C537134|311200||oral facial digital syndrome type 1
|
|
C537134|311200|D009958||oral facial digital syndrome type i
|
|
C537134|311200|D009958||orofaciodigital syndrome i
|
|
C537134|311200|D009958||papillon leage and psaume syndrome
|
|
C537134|311200||papillon league psaume syndrome
|
|
C566648||spina bifida folate sensitive
|
|
D009503||neutropenia
|
|
D009503||neutropenias
|
|
D047868||pulmonary sclerosing hemangioma
|
|
D047868||hemangioma sclerosing pulmonary
|
|
D047868||lung sclerosing hemangioma
|
|
D047868||lung sclerosing hemangiomas
|
|
D047868||pulmonary sclerosing hemangiomas
|
|
D047868||sclerosing hemangioma lung
|
|
D047868||sclerosing hemangioma of the lung
|
|
D047868||sclerosing hemangioma pulmonary
|
|
D047868||sclerosing hemangiomas lung
|
|
D047868||sclerosing hemangiomas pulmonary
|
|
D060831||hand foot syndrome
|
|
D060831||acral erythema chemotherapy induced
|
|
D060831||acral erythemas chemotherapy induced
|
|
D060831||chemotherapy induced acral erythema
|
|
D060831||chemotherapy induced acral erythemas
|
|
D060831||chemotherapy induced palmoplantar erythrodysesthesia
|
|
D060831||chemotherapy induced palmoplantar erythrodysesthesias
|
|
D060831||hand foot syndromes
|
|
D060831||palmoplantar erythrodysesthesia chemotherapy induced
|
|
D060831||palmoplantar erythrodysesthesias chemotherapy induced
|
|
D060831||syndrome hand foot
|
|
D060831||syndromes hand foot
|
|
114450|C566179||cancer familial with in vitro radioresistance
|
|
C565784|604377||cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency
|
|
C565784|604377||cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency 1
|
|
C565784|604377||cemcox1
|
|
C565784|604377||cytochrome c oxidase deficiency fatal infantile with cardioencephalomyopathy
|
|
303100|D015794||choroideremia
|
|
303100|D015794||choroideremias
|
|
303100|D015794||dystrophies progressive tapetochoroidal
|
|
303100|D015794||dystrophy progressive tapetochoroidal
|
|
303100|D015794||progressive tapetochoroidal dystrophies
|
|
303100|D015794||progressive tapetochoroidal dystrophy
|
|
303100|D015794||tapetochoroidal dystrophies progressive
|
|
303100|D015794||tapetochoroidal dystrophy progressive
|
|
303100|D015794||tapetochoroidal dystrophy progressive tcd choroidal sclerosis included
|
|
C562844|212067||congenital disorder of glycosylation type i iix
|
|
C562844|212067||cdg x
|
|
C562805|232240||glycogen storage disease ic
|
|
C562805|232240||gsd1c glycogen storage disease id included
|
|
C562805|232240||gsd1d included
|
|
C566650||glaucoma iridogoniodysplasia familial
|
|
D014098||toothache
|
|
D014098||odontalgia
|
|
D014098||odontalgias
|
|
D014098||toothaches
|
|
D014071||tooth abnormalities
|
|
D014071||abnormalities teeth
|
|
D014071||abnormalities tooth
|
|
D014071||abnormality teeth
|
|
D014071||abnormality tooth
|
|
D014071||odontome
|
|
D014071||odontomes
|
|
D014071||teeth abnormalities
|
|
D014071||teeth abnormality
|
|
D014071||tooth abnormality
|
|
C566613||autoimmune lymphoproliferative syndrome type ia
|
|
C566613||alps1a
|
|
C566614||autoimmune lymphoproliferative syndrome type ib
|
|
C566614||alps1b
|
|
D014075||tooth discoloration
|
|
D014075||discolorations tooth
|
|
D014075||discoloration tooth
|
|
D014075||tooth discolorations
|
|
C566870|211900||tumoral calcinosis hyperphosphatemic familial
|
|
C566870|211900||calcinosis tumoral with hyperphosphatemia
|
|
C566870|211900|C538381||cortical hyperostosis with hyperphosphatemia
|
|
C566870|211900||hftc
|
|
C566870|211900|C538381||hyperostosis hyperphosphatemia syndrome
|
|
C566870|211900|C538381||hyperostosis with hyperphosphatemia
|
|
C566870|211900||hyperphosphatemia hyperostosis
|
|
C566870|211900||hyperphosphatemia hyperostosis syndrome
|
|
C566870|211900||hyperphosphatemia tumoral calcinosis
|
|
C566870|211900||hyperphosphatemic familial tumoral calcinosis
|
|
C566870|211900||lipocalcinogranulomatosis
|
|
C566870|211900||morbus teutschlaender
|
|
C566870|211900||phptc
|
|
C566870|211900||primary hyperphosphatemic tumoral calcinosis
|
|
C566870|211900||teutschlaender disease familial
|
|
C566870|211900||tumoral calcinosis primary hyperphosphatemic
|
|
C566610||left right axis malformations
|
|
D014072||tooth abrasion
|
|
D014072||abrasion dental
|
|
D014072||abrasion tooth
|
|
D014072||dental abrasion
|
|
C566615||autoimmune lymphoproliferative syndrome type i autosomal recessive
|
|
D060845||obsessive hoarding
|
|
D060845||hoarding
|
|
D060845||hoarding obsessive
|
|
D060845||hoardings
|
|
D060845||hoardings obsessive
|
|
D060845||obsessive hoardings
|
|
D046548||pubic symphysis diastasis
|
|
D046548||diastases pubic symphysis
|
|
D046548||diastases symphysis pubis
|
|
D046548||diastasis pubic symphysis
|
|
D046548||diastasis symphysis pubis
|
|
D046548||pubic symphysis diastases
|
|
D046548||symphysis pubis diastases
|
|
D046548||symphysis pubis diastasis
|
|
C579922||ataxia neuropathy spectrum
|
|
C579922||miras
|
|
C579922||mitochondrial recessive ataxia syndrome
|
|
C579922|607459|C537583||sando
|
|
C579922||sensory ataxia neuropathy dysarthria and ophthalmoplegia
|
|
D002095||byssinosis
|
|
D002095||brown lung
|
|
D002095||brown lung disease
|
|
D002095||brown lung diseases
|
|
D002095||brown lungs
|
|
D002095||byssinoses
|
|
609057|C563798||nephropathy with pretibial epidermolysis bullosa and deafness
|
|
D058529||single umbilical artery
|
|
D058529||single umbilical arteries
|
|
D058529||two vessel cord
|
|
D058529||two vessel cords
|
|
D058529||umbilical artery single
|
|
D014067||tonsillar neoplasms
|
|
D014067||cancer of the tonsil
|
|
D014067||cancer of tonsil
|
|
D014067||cancers tonsil
|
|
D014067||cancers tonsillar
|
|
D014067||cancer tonsil
|
|
D014067||cancer tonsillar
|
|
D014067||neoplasms tonsil
|
|
D014067||neoplasms tonsillar
|
|
D014067||neoplasm tonsil
|
|
D014067||neoplasm tonsillar
|
|
D014067||tonsil cancer
|
|
D014067||tonsil cancers
|
|
D014067||tonsillar cancer
|
|
D014067||tonsillar cancers
|
|
D014067||tonsillar neoplasm
|
|
D014067||tonsil neoplasm
|
|
D014067||tonsil neoplasms
|
|
D006011|232500||glycogen storage disease type iv
|
|
D006011|232500||amylopectinoses
|
|
D006011|232500||amylopectinosis
|
|
D006011|232500||andersen disease
|
|
D006011|232500||andersen apos s disease
|
|
D006011|232500||andersens disease
|
|
D006011|232500||brancher deficiencies
|
|
D006011|232500||brancher deficiency
|
|
D006011|232500||cirrhosis familial with deposition of abnormal glycogen gsd iv classic hepatic included
|
|
D006011|232500||deficiencies brancher
|
|
D006011|232500||deficiencies gbe1
|
|
D006011|232500||deficiency brancher
|
|
D006011|232500||deficiency gbe1
|
|
D006011|232500||disease andersen
|
|
D006011|232500||disease andersen apos s
|
|
D006011|232500||gbe1 deficiencies
|
|
D006011|232500||gbe1 deficiency
|
|
D006011|232500||glycogen branching enzyme deficiency
|
|
D006011|232500||glycogenoses type iv
|
|
D006011|232500||glycogenosis 4
|
|
D006011|232500||glycogenosis 4s
|
|
D006011|232500||glycogenosis iv
|
|
D006011|232500||glycogenosis ivs
|
|
D006011|232500||glycogenosis type iv
|
|
D006011|232500||glycogen storage disease iv
|
|
D006011|232500||glycogen storage disease type 4
|
|
D006011|232500||gsd4
|
|
D006011|232500||gsd iv
|
|
D006011|232500||gsd iv neuromuscular form adult with isolated myopathy included
|
|
D006011|232500||gsd iv neuromuscular form childhood included
|
|
D006011|232500||gsd iv neuromuscular form congenital included
|
|
D006011|232500||gsd iv neuromuscular form fatal perinatal included
|
|
D006011|232500||gsd iv nonprogressive hepatic included
|
|
D006011|232500||type iv glycogenoses
|
|
D006011|232500||type iv glycogenosis
|
|
D005879|137580||tourette syndrome
|
|
D005879|137580||chronic motor and vocal tic disorder
|
|
D005879|137580||combined multiple motor and vocal tic disorder
|
|
D005879|137580||combined vocal and multiple motor tic disorder
|
|
D005879|137580||gilles de la tourette apos s disease
|
|
D005879|137580||gilles de la tourette apos s syndrome
|
|
D005879|137580||gilles de la tourette syndrome
|
|
D005879|137580||gts
|
|
D005879|137580||multiple motor and vocal tic disorder combined
|
|
D005879|137580||syndrome tourette apos s
|
|
D005879|137580||tic disorder combined vocal and multiple motor
|
|
D005879|137580||tourette disease
|
|
D005879|137580||tourette disorder
|
|
D005879|137580||tourette disorder chronic motor tics included
|
|
D005879|137580||tourette apos s disease
|
|
D005879|137580||tourettes disease
|
|
D005879|137580||tourette apos s disorder
|
|
D005879|137580||tourettes disorder
|
|
D005879|137580||tourette apos s syndrome
|
|
D005879|137580||tourettes syndrome
|
|
D058527||enteropathy associated t cell lymphoma
|
|
D058527||enteropathy associated t cell lymphomas
|
|
D058527||lymphomas enteropathy associated t cell
|
|
D058527||lymphoma t cell enteropathy associated
|
|
D058527||t cell lymphoma enteropathy associated
|
|
D058527||t cell lymphomas enteropathy associated
|
|
D014069||tonsillitis
|
|
D014069||tonsillitides
|
|
C579928||atelosteogenesis type 3
|
|
C579928|108721||aoiii
|
|
C579928|108721||atelosteogenesis type iii
|
|
C566622||spondylospinal thoracic dysostosis
|
|
D014082||tooth fractures
|
|
D014082||fractures tooth
|
|
D014082||fracture tooth
|
|
D014082||tooth fracture
|
|
C566623||coloboma obesity hypogenitalism mental retardation syndrome
|
|
C565176|609140||corneal dystrophy posterior polymorphous 2
|
|
C565176|609140||ppcd2
|
|
C566624||peroxisome biogenesis disorder complementation group k
|
|
C566625||peroxisome biogenesis disorder complementation group 13
|
|
D014086||tooth mobility
|
|
D014086||mobilities tooth
|
|
D014086||mobility tooth
|
|
D014086||tooth mobilities
|
|
D014085||tooth migration
|
|
D014085||migration tooth
|
|
D014085||tooth drift
|
|
D014085||tooth drifting
|
|
D014084||tooth avulsion
|
|
D014084||avulsed tooth
|
|
D014084||avulsions tooth
|
|
D014084||avulsion tooth
|
|
D014084||dislocations tooth
|
|
D014084||dislocation tooth
|
|
D014084||luxations tooth
|
|
D014084||luxation tooth
|
|
D014084||tooth avulsed
|
|
D014084||tooth avulsions
|
|
D014084||tooth dislocation
|
|
D014084||tooth dislocations
|
|
D014084||tooth luxation
|
|
D014084||tooth luxations
|
|
C566621||premature aging syndrome okamoto type
|
|
C563692|609887||glaucoma 1 open angle g
|
|
C563692|609887||glc1g
|
|
207410||antley bixler syndrome without genital anomalies or disordered steroidogenesis
|
|
207410||abs2
|
|
C566626||peroxisome biogenesis disorder complementation group h
|
|
C567441|600101||deafness autosomal dominant 2a
|
|
C567441|600101||dfna2a
|
|
C567477|300704||prostate cancer hereditary x linked 2
|
|
C567477|300704||hpcx2
|
|
C579932||autosomal dominant nocturnal frontal lobe epilepsy
|
|
C579932||adnfle
|
|
D058531||46 xx testicular disorders of sex development
|
|
D058531||46 xx gonadal sex reversal
|
|
D058531||46 xx testicular disorder of sex development
|
|
D058531||46 xx testicular dsd
|
|
D058531||gonadal sex reversal 46 xx
|
|
D058531||reversals xx sex
|
|
D058531||reversal xx sex
|
|
D058531||sex reversal gonadal 46 xx
|
|
D058531||sex reversals xx
|
|
D058531||sex reversal xx
|
|
D058531||syndromes xx male
|
|
D058531||syndrome xx male
|
|
D058531||xx male syndrome
|
|
D058531||xx male syndromes
|
|
D058531||xx sex reversal
|
|
D058531||xx sex reversals
|
|
C579934||autosomal recessive cerebellar ataxia type 1
|
|
C579934||arca1
|
|
C579934||autosomal recessive spinocerebellar ataxia 8
|
|
C579934||recessive ataxia of beauce
|
|
D058533||sex chromosome disorders of sex development
|
|
D058533||chromosome dsd sex
|
|
D058533||chromosome dsds sex
|
|
D058533||dsd sex chromosome
|
|
D058533||dsds sex chromosome
|
|
D058533||sex chromosome dsd
|
|
D058533||sex chromosome dsds
|
|
C579935||autosomal recessive primary microcephaly
|
|
C579935||microcephaly primary hereditary
|
|
C579935||primary autosomal recessive microcephaly
|
|
C579935||true microcephaly
|
|
D014079||tooth eruption ectopic
|
|
D014079||ectopic tooth eruption
|
|
D014079||ectopic tooth eruptions
|
|
D014079||eruption ectopic tooth
|
|
D014079||eruptions ectopic tooth
|
|
D014079||tooth eruptions ectopic
|
|
C563481|166780||otofaciocervical syndrome
|
|
C563481|166780|C566121|119530||ofc
|
|
C563481|166780|C566121|119530||ofc1
|
|
C563481|166780||ofc syndrome
|
|
C563481|166780||otofaciocervical syndrome 1
|
|
D014077||tooth erosion
|
|
D014077||erosions tooth
|
|
D014077||erosion tooth
|
|
D014077||tooth erosions
|
|
D014076||tooth diseases
|
|
D014076||diseases tooth
|
|
D014076||disease tooth
|
|
D014076||tooth disease
|
|
D058536||pyelectasis
|
|
D058536||fetal pyelectases
|
|
D058536||fetal pyelectasis
|
|
D058536||prenatal fetal pyelectases
|
|
D058536||prenatal fetal pyelectasis
|
|
D058536||pyelectases
|
|
D058536||pyelectases fetal
|
|
D058536||pyelectasis fetal
|
|
D058535||echogenic bowel
|
|
D058535||echogenic bowels
|
|
D058535||hyperechogenic bowel
|
|
D058535||hyperechogenic bowels
|
|
C536453|122880||craniofacial deafness hand syndrome
|
|
C536453|122880||cdhs
|
|
C564257|608323||charcot marie tooth disease dominant intermediate c
|
|
C564257|608323||charcot marie tooth neuropathy dominant intermediate c
|
|
C564257|608323||cmtdic
|
|
C564257|608323||di cmtc
|
|
602668|C538009||dystrophia myotonica 2
|
|
602668|C538009||dm2
|
|
602668|C538009||myotonic dystrophy 2
|
|
602668|C538009||promm
|
|
602668|C538009||ricker syndrome
|
|
607821|C564331||deafness autosomal recessive 37
|
|
607821|C564331||dfnb37
|
|
D003397||craniopharyngioma
|
|
D003397||adamantinous craniopharyngioma
|
|
D003397||adamantinous craniopharyngiomas
|
|
D003397||adult craniopharyngioma
|
|
D003397||adult craniopharyngiomas
|
|
D003397||child craniopharyngioma
|
|
D003397||child craniopharyngiomas
|
|
D003397||craniopharyngioma adamantinous
|
|
D003397||craniopharyngioma adult
|
|
D003397||craniopharyngioma child
|
|
D003397||craniopharyngioma papillary
|
|
D003397||craniopharyngiomas
|
|
D003397||craniopharyngiomas adamantinous
|
|
D003397||craniopharyngiomas adult
|
|
D003397||craniopharyngiomas child
|
|
D003397||craniopharyngiomas papillary
|
|
D003397||neoplasm rathke cleft
|
|
D003397||neoplasm rathke apos s cleft
|
|
D003397||neoplasm rathkes cleft
|
|
D003397||papillary craniopharyngioma
|
|
D003397||papillary craniopharyngiomas
|
|
D003397||rathke cleft neoplasm
|
|
D003397||rathke pouch tumor
|
|
D003397||rathke apos s cleft neoplasm
|
|
D003397||rathkes cleft neoplasm
|
|
D003397||rathke apos s pouch tumor
|
|
D003397||rathkes pouch tumor
|
|
D003397||tumor rathke pouch
|
|
D003397||tumor rathke apos s pouch
|
|
C566627|601780||ceroid lipofuscinosis neuronal 6
|
|
C566627|601780||ceroid lipofuscinosis neuronal 6 variable age at onset
|
|
C566627|601780||ceroid lipofuscinosis neuronal 6 variable age at onset neuronal ceroid lipofuscinosis late infantile variant included
|
|
C566627|601780||cln6
|
|
C566627|601780||neuronal ceroid lipofuscinosis late infantile variant
|
|
C566627|601780||vlincl included
|
|
D058545||inhalant abuse
|
|
D058545||abuse glue
|
|
D058545||abuse inhalant
|
|
D058545||abuses glue
|
|
D058545||abuses inhalant
|
|
D058545||glue abuse
|
|
D058545||glue abuses
|
|
D058545||glue sniffing
|
|
D058545||glue sniffings
|
|
D058545||inhalant abuses
|
|
C537847|609942||noonan syndrome 3
|
|
C537847|609942||ns3
|
|
D057215||body dysmorphic disorders
|
|
D057215||body dysmorphic disorder
|
|
D057215||body image disfunction
|
|
D057215||body image disfunctions
|
|
D057215||body image disorder
|
|
D057215||body image disorders
|
|
D057215||disfunction body image
|
|
D057215||disfunctions body image
|
|
D057215||disorder body dysmorphic
|
|
D057215||disorders body dysmorphic
|
|
D057215||disorders body image
|
|
D057215||dysmorphic disorder body
|
|
D057215||dysmorphic disorders body
|
|
D057215||image disfunction body
|
|
D057215||image disfunctions body
|
|
D057215||image disorders body
|
|
C537994|607684||charcot marie tooth disease type 2e
|
|
C537994|607684||charcot marie tooth disease axonal type 2e
|
|
C537994|607684||charcot marie tooth neuropathy type 2e
|
|
C537994|607684||cmt2e
|
|
C537994|607684||cmt 2e
|
|
C538203|609952||deafness autosomal recessive 55
|
|
C538203|609952||dfnb55
|
|
D014060||tongue diseases
|
|
D014060||diseases tongue
|
|
D014060||disease tongue
|
|
D014060||microglossia
|
|
D014060||microglossias
|
|
D014060||tongue disease
|
|
C567703|613217||diarrhea 5 with tufting enteropathy congenital
|
|
C567703|613217||cte
|
|
C567703|613217||diar5
|
|
C567703|613217||enteropathy congenital tufting
|
|
C567703|613217||intestinal epithelial cell dysplasia
|
|
D007619|244400||kartagener syndrome
|
|
D007619|244400||bronchiectasis polynesian
|
|
D007619|244400||cild1
|
|
D007619|244400||ciliary dyskinesia primary
|
|
D007619|244400||ciliary dyskinesia primary 1
|
|
D007619|244400||ciliary dyskinesia primary 1 with or without situs inversus
|
|
D007619|244400||dextrocardia bronchiectasis and sinusitis
|
|
D007619|244400||dextrocardia bronchiectasis and sinusitis included
|
|
D007619|244400||dyskinesia primary ciliary
|
|
D007619|244400||ics
|
|
D007619|244400|D002925||immotile cilia syndrome
|
|
D007619|244400||kartagener apos s syndrome
|
|
D007619|244400||kartageners syndrome
|
|
D007619|244400||kartagener apos s triad
|
|
D007619|244400||kartageners triad
|
|
D007619|244400||kartagener triad
|
|
D007619|244400||pcd
|
|
D007619|244400||polynesian bronchiectases
|
|
D007619|244400||polynesian bronchiectasis
|
|
D007619|244400||polynesian bronchiectasis kartagener syndrome included
|
|
D007619|244400||primary ciliary dyskinesia
|
|
D007619|244400||siewert syndrome
|
|
D007619|244400||siewert syndrome included
|
|
D007619|244400||syndrome kartagener
|
|
D007619|244400||syndrome kartagener apos s
|
|
D007619|244400||syndrome siewert
|
|
D014064||tongue hairy
|
|
D014064||hairy tongue
|
|
D014064||hairy tongues
|
|
D014064||tongues hairy
|
|
D014063||tongue fissured
|
|
D014063||fissured tongue
|
|
D014063||fissured tongues
|
|
D014063||furrowed tongue
|
|
D014063||furrowed tongues
|
|
D014063||lingua plicata
|
|
D014063||scrotal tongue
|
|
D014063||tongue furrowed
|
|
D014063||tongues fissured
|
|
D014063||tongues furrowed
|
|
D014062||tongue neoplasms
|
|
D014062||cancer of the tongue
|
|
D014062||cancer of tongue
|
|
D014062||cancers tongue
|
|
D014062||cancer tongue
|
|
D014062||neoplasms tongue
|
|
D014062||neoplasm tongue
|
|
D014062||tongue cancer
|
|
D014062||tongue cancers
|
|
D014062||tongue neoplasm
|
|
C566604||deafness congenital heart defects and posterior embryotoxon
|
|
C564674|606708||split hand foot malformation 5
|
|
C564674|606708||shfm5
|
|
C567418|612099||trichoepithelioma multiple familial 2
|
|
C567418|612099||mft2
|
|
D059885||kasabach merritt syndrome
|
|
D059885||hemangioma thrombocytopenia syndrome
|
|
D059885||hemangioma thrombocytopenia syndromes
|
|
D059885||kasabach merritt phenomenon
|
|
D059885||phenomenon kasabach merritt
|
|
D059885||syndrome hemangioma thrombocytopenia
|
|
D059885||syndrome kasabach merritt
|
|
D059885||syndromes hemangioma thrombocytopenia
|
|
D059885||syndromes thrombocytopenia hemangioma
|
|
D059885||syndrome thrombocytopenia hemangioma
|
|
D059885||thrombocytopenia hemangioma syndrome
|
|
D059885||thrombocytopenia hemangioma syndromes
|
|
C563702|609541||spastic paraplegia optic atrophy and neuropathy
|
|
C563702|609541||spoan
|
|
C566601|613855||episodic ataxia type 5
|
|
C566601|613855||ea5
|
|
D058631|265800||pycnodysostosis
|
|
D058631|265800||pknd
|
|
D058631|265800||pycd
|
|
D058631|265800||pycnodysostoses
|
|
D058631|265800||pyknodysostoses
|
|
D058631|265800||pyknodysostosis
|
|
C537088|112500||brachydactyly type a1
|
|
C537088|112500||bda1
|
|
C537088|112500||brachydactyly farabee type
|
|
C537088|112500||farabee type brachydactyly
|
|
C536053|300373||osteopathia striata cranial sclerosis
|
|
C536053|300373||hyperostosis generalisata with striations
|
|
C536053|300373||oscs
|
|
C536053|300373||osteopathia striata with cranial sclerosis
|
|
D015362||child nutrition disorders
|
|
D015362||child malnutrition
|
|
D015362||child nutrition disorder
|
|
D015362||child overnutrition
|
|
D015362||malnutrition child
|
|
D015362||malnutrition in children
|
|
D015362||nutrition disorder child
|
|
D015362||nutrition disorders child
|
|
D015362||overnutrition child
|
|
C536681|600118||warburg sjo fledelius syndrome
|
|
C536681|600118||micro syndrome
|
|
C536681|600118||warbm1
|
|
C536681|600118||warburg micro syndrome
|
|
C536681|600118||warburg micro syndrome 1
|
|
C538349|256030||nemaline myopathy 2
|
|
C538349|256030||nem2
|
|
C538349|256030||nemaline myopathy caused by mutation in the nebulin gene
|
|
C535374|125595||dermatopathia pigmentosa reticularis
|
|
C535374|125595||dpr
|
|
D053840|601144||brugada syndrome
|
|
D053840|601144||brgda1
|
|
D053840|601144||brugada ecg pattern
|
|
D053840|601144||brugada syndrome 1
|
|
D053840|601144||brugada type ecg pattern
|
|
D053840|601144||ecg pattern brugada
|
|
D053840|601144||right bundle branch block st segment elevation and sudden death syndrome
|
|
D053840|601144||sudden unexplained death syndrome
|
|
D053840|601144||sudden unexplained nocturnal death syndrome
|
|
D053840|601144||sudden unexplained nocturnal death syndrome sunds
|
|
D053840|601144||sudden unexplained nocturnal death syndrome sunds cardiac conduction defect nonspecific included
|
|
D002044||bunyaviridae infections
|
|
D002044||bunyaviridae infection
|
|
D002044||bunyavirus infection
|
|
D002044||bunyavirus infections
|
|
D002044||infections bunyaviridae
|
|
D002044||infections bunyavirus
|
|
D058565||cerebral ventriculitis
|
|
D058565||cerebral ventriculitides
|
|
D058565||infectious ventriculitides
|
|
D058565||infectious ventriculitis
|
|
D058565||ventriculitides cerebral
|
|
D058565||ventriculitides infectious
|
|
D058565||ventriculitis cerebral
|
|
D058565||ventriculitis infectious
|
|
D014029||tobacco use disorder
|
|
D014029||dependence nicotine
|
|
D014029||dependence tobacco
|
|
D014029||disorder nicotine use
|
|
D014029||disorder tobacco use
|
|
D014029||nicotine dependence
|
|
D014029||nicotine use disorder
|
|
D014029||nicotine use disorders
|
|
D014029||tobacco dependence
|
|
D014029||tobacco dependences
|
|
D014029||tobacco use disorders
|
|
D014029||use disorder nicotine
|
|
D058566||sacroiliitis
|
|
D058566||pyogenic sacroiliitides
|
|
D058566||pyogenic sacroiliitis
|
|
D058566||sacroiliitides
|
|
D058566||sacroiliitides pyogenic
|
|
D058566||sacroiliitides septic
|
|
D058566||sacroiliitis pyogenic
|
|
D058566||sacroiliitis septic
|
|
D058566||septic sacroiliitides
|
|
D058566||septic sacroiliitis
|
|
141500|C536890||migraine familial hemiplegic 1
|
|
141500||fhm
|
|
141500||fhm1
|
|
141500||mhp1 migraine familial hemiplegic 1 with progressive cerebellar ataxia included
|
|
141500||migraine sporadic hemiplegic included
|
|
D015355||glaucoma neovascular
|
|
D015355||glaucomas neovascular
|
|
D015355||neovascular glaucoma
|
|
D015355||neovascular glaucomas
|
|
D015354||vision low
|
|
D015354||diminished vision
|
|
D015354||low vision
|
|
D015354||reduced vision
|
|
D015354||subnormal vision
|
|
D015354||vision diminished
|
|
D015354||vision reduced
|
|
D015354||vision subnormal
|
|
D015352||dry eye syndromes
|
|
D015352||dry eye syndrome
|
|
D015352||syndrome dry eye
|
|
D015352||syndromes dry eye
|
|
D013920|187950||thrombocythemia essential
|
|
D013920|187950||autosomal dominant thrombocytoses
|
|
D013920|187950||autosomal dominant thrombocytosis
|
|
D013920|187950||dominant thrombocytoses autosomal
|
|
D013920|187950||dominant thrombocytosis autosomal
|
|
D013920|187950||essential thrombocythemia
|
|
D013920|187950||essential thrombocythemias
|
|
D013920|187950||hemorrhagic thrombocythemia
|
|
D013920|187950||hemorrhagic thrombocythemias
|
|
D013920|187950||idiopathic thrombocythemia
|
|
D013920|187950||idiopathic thrombocythemias
|
|
D013920|187950||primary thrombocythemia
|
|
D013920|187950||primary thrombocythemias
|
|
D013920|187950||primary thrombocytoses
|
|
D013920|187950||primary thrombocytosis
|
|
D013920|187950||thcyt1
|
|
D013920|187950||thrombocythemia 1
|
|
D013920|187950||thrombocythemia hemorrhagic
|
|
D013920|187950||thrombocythemia idiopathic
|
|
D013920|187950||thrombocythemia primary
|
|
D013920|187950||thrombocythemias essential
|
|
D013920|187950||thrombocythemias hemorrhagic
|
|
D013920|187950||thrombocythemias idiopathic
|
|
D013920|187950||thrombocythemias primary
|
|
D013920|187950||thrombocytoses autosomal dominant
|
|
D013920|187950||thrombocytoses primary
|
|
D013920|187950||thrombocytosis 1
|
|
D013920|187950||thrombocytosis autosomal dominant
|
|
D013920|187950||thrombocytosis primary
|
|
D058568||necrolytic migratory erythema
|
|
D058568||erythema necrolytic migratory
|
|
D058568||erythemas necrolytic migratory
|
|
D058568||migratory erythema necrolytic
|
|
D058568||migratory erythemas necrolytic
|
|
D058568||necrolytic migratory erythemas
|
|
D058568||pseudoglucagonoma syndrome
|
|
D058568||pseudoglucagonoma syndromes
|
|
D058568||syndrome pseudoglucagonoma
|
|
D058568||syndromes pseudoglucagonoma
|
|
C563775|609200||myotilinopathy
|
|
C563775|609200||mfm3
|
|
C563775|609200||myopathy myofibrillar 3
|
|
C563775|609200||myopathy myofibrillar myotilin related
|
|
D015356||retinal artery occlusion
|
|
D015356||branch retinal artery occlusion
|
|
D015356||central retinal artery occlusion
|
|
D015356||occlusion retinal artery
|
|
D015356||occlusions retinal artery
|
|
D015356||retinal artery occlusions
|
|
607641|C564362||neuronopathy distal hereditary motor type viib
|
|
607641|C564362||dhmn7b
|
|
607641|C564362||hmn7b
|
|
607641|C564362||hmn viib
|
|
607641|C564362||lower motor neuron disease dynactin type
|
|
607641|C564362||neuropathy distal hereditary motor type viib
|
|
607641|C564362||neuropathy distal hereditary motor with vocal cord paralysis type viib
|
|
D045262||reticulocytosis
|
|
D045262||reticulocytoses
|
|
600901||fanconi anemia complementation group e
|
|
600901||face
|
|
600901||fance
|
|
D002057||burns chemical
|
|
D002057||burn chemical
|
|
D002057||chemical burn
|
|
D002057||chemical burns
|
|
D002058||burns electric
|
|
D002058||burn electric
|
|
D002058||electric burn
|
|
D002058||electric burns
|
|
D003389||cranial nerve diseases
|
|
D003389||cranial nerve disease
|
|
D003389||cranial nerve disorder
|
|
D003389||cranial nerve disorders
|
|
D003389||cranial nerve palsies
|
|
D003389||cranial nerve palsy
|
|
D003389||cranial neuropathies
|
|
D003389||cranial neuropathies multiple
|
|
D003389||cranial neuropathy
|
|
D003389||cranial neuropathy multiple
|
|
D003389||multiple cranial neuropathies
|
|
D003389||multiple cranial neuropathy
|
|
D003389||nervus cranialis disorder
|
|
D003389||nervus cranialis disorders
|
|
D003389||neuropathies cranial
|
|
D003389||neuropathies multiple cranial
|
|
D003389||neuropathy cranial
|
|
D003389||neuropathy multiple cranial
|
|
D003389||palsies cranial nerve
|
|
D003389||palsy cranial nerve
|
|
D002059||burns inhalation
|
|
D002059||burn inhalation
|
|
D002059||inhalation burn
|
|
D002059||inhalation burns
|
|
118700|D002819||chorea
|
|
118700|D002819||bch
|
|
118700|D002819||benign hereditary chorea
|
|
118700|D002819||benign hereditary choreas
|
|
118700|D002819||bhc
|
|
118700|D002819||chorea benign hereditary
|
|
118700|D002819||chorea chronic progressive
|
|
118700|D002819||chorea disorder
|
|
118700|D002819||chorea disorders
|
|
118700|D002819||chorea hereditary
|
|
118700|D002819||chorea rheumatic
|
|
118700|D002819||choreas
|
|
118700|D002819||choreas benign hereditary
|
|
118700|D002819||choreas chronic progressive
|
|
118700|D002819||chorea senile
|
|
118700|D002819||choreas hereditary
|
|
118700|D002819||choreas rheumatic
|
|
118700|D002819||choreas senile
|
|
118700|D002819||choreas sydenham
|
|
118700|D002819||chorea sydenham
|
|
118700|D002819||chorea sydenham apos s
|
|
118700|D002819||chorea syndrome
|
|
118700|D002819||chorea syndromes
|
|
118700|D002819||choreatic disorder
|
|
118700|D002819||choreatic disorders
|
|
118700|D002819||choreatic syndrome
|
|
118700|D002819||choreatic syndromes
|
|
118700|D002819||choreic movement
|
|
118700|D002819||choreic movements
|
|
118700|D002819||choreiform movement
|
|
118700|D002819||choreiform movements
|
|
118700|D002819||chronic progressive chorea
|
|
118700|D002819||chronic progressive choreas
|
|
118700|D002819||disorder chorea
|
|
118700|D002819||disorder choreatic
|
|
118700|D002819||disorders chorea
|
|
118700|D002819||disorders choreatic
|
|
118700|D002819||dyskinesia paroxysmal
|
|
118700|D002819||dyskinesias paroxysmal
|
|
118700|D002819||hereditary chorea
|
|
118700|D002819||hereditary chorea benign
|
|
118700|D002819||hereditary choreas
|
|
118700|D002819||hereditary choreas benign
|
|
118700|D002819||hereditary progressive chorea without dementia
|
|
118700|D002819||movement choreic
|
|
118700|D002819||movement choreiform
|
|
118700|D002819||movements choreic
|
|
118700|D002819||movements choreiform
|
|
118700|D002819||paroxysmal dyskinesia
|
|
118700|D002819||paroxysmal dyskinesias
|
|
118700|D002819||progressive chorea chronic
|
|
118700|D002819||progressive choreas chronic
|
|
118700|D002819||rheumatic chorea
|
|
118700|D002819||rheumatic choreas
|
|
118700|D002819||senile chorea
|
|
118700|D002819||senile choreas
|
|
118700|D002819||st vitus dance
|
|
118700|D002819||st vitus apos s dance
|
|
118700|D002819||st vituss dance
|
|
118700|D002819||st vitus apos s dances
|
|
118700|D002819||sydenham chorea
|
|
118700|D002819||sydenham choreas
|
|
118700|D002819||sydenham apos s chorea
|
|
118700|D002819||sydenhams chorea
|
|
118700|D002819||syndrome chorea
|
|
118700|D002819||syndrome choreatic
|
|
118700|D002819||syndromes chorea
|
|
118700|D002819||syndromes choreatic
|
|
D003384||coxsackievirus infections
|
|
D003384||coxsackievirus infection
|
|
D003384||coxsackie virus infection
|
|
D003384||coxsackie virus infections
|
|
D003384||infections coxsackievirus
|
|
D003384||infections coxsackie virus
|
|
D002054||burning mouth syndrome
|
|
D002054||burning mouth syndromes
|
|
D002054||mouth syndrome burning
|
|
D002054||mouth syndromes burning
|
|
D002054||syndrome burning mouth
|
|
D002054||syndromes burning mouth
|
|
201100|C538178||acrodermatitis enteropathica
|
|
201100|C538178||acrodermatitis enteropathica zinc deficiency type
|
|
201100|C538178||aez
|
|
D002056||burns
|
|
D002056||burn
|
|
D003387||cracked tooth syndrome
|
|
D003387||cracked tooth syndromes
|
|
D003387||syndrome cracked tooth
|
|
D003387||syndromes cracked tooth
|
|
C562750|137760||glaucoma primary open angle
|
|
C562750|137760||glaucoma 1 open angle e included
|
|
C562750|137760||glaucoma primary open angle adult onset included
|
|
C562750|137760||glc1e included
|
|
C562750|137760||poag
|
|
C536300|309510||partington x linked mental retardation syndrome
|
|
C536300|309510||mental retardation dystonic movements ataxia seizures syndrome
|
|
C536300|309510||mental retardation x linked 36
|
|
C536300|309510||mental retardation x linked syndromic 1
|
|
C536300|309510||mental retardation x linked with dystonic movements ataxia and seizures
|
|
C536300|309510||mrx36
|
|
C536300|309510||mrxs1
|
|
C536300|309510||partington syndrome
|
|
C536300|309510||prts
|
|
D002062||bursitis
|
|
D002062||adhesive capsulitides
|
|
D002062||adhesive capsulitis
|
|
D002062||bursitides
|
|
D002062||capsulitides adhesive
|
|
D002062||capsulitis adhesive
|
|
D002062||frozen shoulder
|
|
C536830|606777||de vivo disease
|
|
C536830|606777||encephalopathy due to glut1 deficiency
|
|
C536830|606777||glucose transport defect blood brain barrier
|
|
C536830|606777||glucose transport defect blood brain barrier glut1 deficiency syndrome 1 autosomal recessive included
|
|
C536830|606777||glucose transporter protein syndrome
|
|
C536830|606777||glucose transporter type 1 deficiency syndrome
|
|
C536830|606777||glucose transporter type1 glut 1 deficiency
|
|
C536830|606777||glut1 deficiency syndrome
|
|
C536830|606777||glut 1 deficiency syndrome
|
|
C536830|606777||glut1 deficiency syndrome 1
|
|
C536830|606777||glut1ds1
|
|
D003390||cranial nerve neoplasms
|
|
D003390||benign cranial nerve neoplasms
|
|
D003390||benign cranial nerve tumors
|
|
D003390||benign cranial neuroma
|
|
D003390||benign cranial neuromas
|
|
D003390||cranial nerve neoplasm
|
|
D003390||cranial nerve neoplasms benign
|
|
D003390||cranial nerve neoplasms malignant
|
|
D003390||cranial nerve tumors benign
|
|
D003390||cranial nerve tumors malignant
|
|
D003390||cranial neuroma benign
|
|
D003390||cranial neuromas benign
|
|
D003390||malignant cranial nerve neoplasms
|
|
D003390||malignant cranial nerve tumors
|
|
D003390||neoplasm cranial nerve
|
|
D003390||neoplasms cranial nerve
|
|
D003390||neoplasms cranial nerve benign
|
|
D003390||neoplasms cranial nerve malignant
|
|
D003390||neuroma benign cranial
|
|
D003390||neuromas benign cranial
|
|
D003390||tumors cranial nerve benign
|
|
D003390||tumors cranial nerve malignant
|
|
603188||body mass index quantitative trait locus 8
|
|
603188||bmiq8
|
|
D030981||acro osteolysis
|
|
D030981||acroosteolysis
|
|
D030981||acroosteolysis syndrome
|
|
D030981||acro osteolysis syndrome
|
|
D030981||acro osteolysis syndromes
|
|
D014036||togaviridae infections
|
|
D014036||diseases togaviridae
|
|
D014036||disease togaviridae
|
|
D014036||infections togaviridae
|
|
D014036||infections togavirus
|
|
D014036||infection togaviridae
|
|
D014036||infection togavirus
|
|
D014036||togaviridae disease
|
|
D014036||togaviridae diseases
|
|
D014036||togaviridae infection
|
|
D014036||togavirus infection
|
|
D014036||togavirus infections
|
|
C566931|611497||osteopetrosis autosomal recessive 6
|
|
C566931|611497||optb6
|
|
C566931|611497||osteopetrosis autosomal recessive intermediate form
|
|
C563315|601450||dislocation of hip congenital with hyperextensibility of fingers and facial dysmorphism
|
|
C563315|601450||hip congenital dislocation of with hyperextensibility of fingers and facial dysmorphism
|
|
148190|C537022||keratitis hereditary
|
|
148190|C537022||dominantly inherited keratitis
|
|
D016697||herpes zoster oticus
|
|
D016697||auricular syndrome of ramsay hunt
|
|
D016697||ganglionitis herpetic geniculate
|
|
D016697||geniculate ganglionitides herpetic
|
|
D016697||geniculate ganglionitis herpetic
|
|
D016697||geniculate herpes zoster
|
|
D016697||geniculate neuralgia
|
|
D016697||geniculate neuralgias
|
|
D016697||herpes zoster auricularis
|
|
D016697||herpes zoster cephalicus
|
|
D016697||herpes zoster geniculate
|
|
D016697||herpetic geniculate ganglionitides
|
|
D016697||herpetic geniculate ganglionitis
|
|
D016697||neuralgia geniculate
|
|
D016697||neuralgias geniculate
|
|
D016697||ramsay hunt auricular syndrome
|
|
D016697||ramsay hunt syndrome
|
|
D016697||syndrome ramsay hunt
|
|
C536766|278750||xeroderma pigmentosum variant type
|
|
C536766|278750||photosensitivity with defective dna synthesis
|
|
C536766|278750||xeroderma pigmentosum with normal dna repair rates
|
|
C536766|278750||xpv
|
|
C538375|606762||hyperinsulinemic hypoglycemia familial 6
|
|
C538375|606762||hhf6
|
|
C538375|606762||hyperinsulinism hyperammonemia syndrome
|
|
D004688||encopresis
|
|
D004683||encephalomyelitis equine
|
|
D004683||encephalitis equine
|
|
D004683||equine encephalitis
|
|
D004683||equine encephalomyelitis
|
|
D004683||equine encephalomyelitis viral infections
|
|
D004683||equine encephalomyelitis virus infections
|
|
D004683||infections equine encephalomyelitis virus
|
|
D004682||encephalomyelitis enzootic porcine
|
|
D004682||disease talfan
|
|
D004682||disease teschen
|
|
D004682||enzootic porcine encephalomyelitis
|
|
D004682||poliomyelitis porcine
|
|
D004682||porcine encephalomyelitis enzootic
|
|
D004682||porcine poliomyelitis
|
|
D004682||talfan disease
|
|
D004682||teschen disease
|
|
D004685||encephalomyelitis venezuelan equine
|
|
D004685||encephalitis venezuelan equine
|
|
D004685||encephalomyelitides venezuelan equine
|
|
D004685||equine encephalitis venezuelan
|
|
D004685||equine encephalomyelitides venezuelan
|
|
D004685||equine encephalomyelitis venezuelan
|
|
D004685||venezuelan equine encephalitis
|
|
D004685||venezuelan equine encephalomyelitides
|
|
D004685||venezuelan equine encephalomyelitis
|
|
D004684||leukoencephalitis acute hemorrhagic
|
|
D004684||acute hemorrhagic leukoencephalitides
|
|
D004684||acute hemorrhagic leukoencephalitis
|
|
D004684||acute necrotizing encephalitides
|
|
D004684||acute necrotizing encephalitis
|
|
D004684||disease hurst
|
|
D004684||disease hurst apos s
|
|
D004684||encephalitides acute necrotizing
|
|
D004684||encephalitis acute necrotizing
|
|
D004684||encephalomyelitides hemorrhagic necrotizing
|
|
D004684||encephalomyelitis acute necrotizing hemorrhagic
|
|
D004684||encephalomyelitis hemorrhagic necrotizing
|
|
D004684||encephalomyelitis necrotizing hemorrhagic
|
|
D004684||hemorrhagic encephalomyelitides necrotizing
|
|
D004684||hemorrhagic encephalomyelitis necrotizing
|
|
D004684||hemorrhagic leukoencephalitides acute
|
|
D004684||hemorrhagic leukoencephalitides subacute
|
|
D004684||hemorrhagic leukoencephalitis acute
|
|
D004684||hemorrhagic leukoencephalitis subacute
|
|
D004684||hemorrhagic necrotizing encephalomyelitis
|
|
D004684||hurst disease
|
|
D004684||hurst apos s disease
|
|
D004684||hursts disease
|
|
D004684||hurst syndrome
|
|
D004684||leukoencephalitides acute hemorrhagic
|
|
D004684||leukoencephalitides subacute hemorrhagic
|
|
D004684||leukoencephalitis acuta hemorrhagica
|
|
D004684||leukoencephalitis subacute hemorrhagic
|
|
D004684||necrotizing encephalitides acute
|
|
D004684||necrotizing encephalitis acute
|
|
D004684||necrotizing encephalomyelitides hemorrhagic
|
|
D004684||necrotizing encephalomyelitis hemorrhagic
|
|
D004684||necrotizing hemorrhagic encephalomyelitides
|
|
D004684||necrotizing hemorrhagic encephalomyelitis
|
|
D004684||subacute hemorrhagic leukoencephalitides
|
|
D004684||subacute hemorrhagic leukoencephalitis
|
|
D004684||syndrome hurst
|
|
D003354||corynebacterium infections
|
|
D003354||corynebacterium infection
|
|
D003354||infection corynebacterium
|
|
D003354||infections corynebacterium
|
|
D014009||onychomycosis
|
|
D014009||fungus nail
|
|
D014009||nail fungus
|
|
D014009||onychomycoses
|
|
D014009||tinea ungui
|
|
D014009||tinea unguis
|
|
D014009||tinea unguium
|
|
D014009||tinea unguiums
|
|
D014009||unguis tinea
|
|
D014009||ungui tinea
|
|
D014009||unguiums tinea
|
|
D014009||unguium tinea
|
|
C535301|605253||charcot marie tooth disease type 4e
|
|
C535301|605253||charcot marie tooth neuropathy type 4e
|
|
C535301|605253||charcot marie tooth neuropathy type 4e neuropathy congenital hypomyelinating autosomal dominant included
|
|
C535301|605253||chn
|
|
C535301|605253||cmt4e
|
|
C535301|605253||congenital hypomyelinating neuropathy
|
|
C535301|605253||congenital hypomyelinating neuropathy chn
|
|
C535301|605253||hypomyelination severe congenital
|
|
C535301|605253||neuropathy congenital hypomyelinating
|
|
C535301|605253||neuropathy congenital hypomyelinating or amyelinating autosomal recessive
|
|
D004692||endarteritis
|
|
D004692||endarteritides
|
|
D014008||tinea pedis
|
|
D014008||athlete foot
|
|
D014008||athlete apos s foot
|
|
D014008||athletes foot
|
|
D014007||tinea favosa
|
|
D014007||favus
|
|
C537990|605588||charcot marie tooth disease type 2b1
|
|
C537990|605588||charcot marie tooth disease axonal autosomal recessive 2b1
|
|
C537990|605588||charcot marie tooth disease axonal autosomal recessive b1
|
|
C537990|605588||charcot marie tooth disease axonal type 2b1
|
|
C537990|605588||charcot marie tooth disease neuronal type 2b1
|
|
C537990|605588||charcot marie tooth neuropathy type 2b1
|
|
C537990|605588||cmt2b1
|
|
154400|C538184||acrofacial dysostosis nager type
|
|
154400|C538184||acrofacial dysostosis 1 nager type
|
|
154400|C538184||afd1
|
|
154400|C538184||afd nager type
|
|
154400|C538184||mandibulofacial dysostosis treacher collins type with limb anomalies
|
|
154400|C538184||nager acrofacial dysostosis
|
|
154400|C538184||nager acrofacial dysostosis syndrome
|
|
154400|C538184||nager syndrome
|
|
154400|C538184||preaxial acrofacial dysostosis
|
|
154400|C538184||preaxial mandibulofacial dysostosis
|
|
D014006||tinea capitis
|
|
D014006||barbae trichophytia profunda
|
|
D014006||capitides trichophytia profunda
|
|
D014006||capitis profundas tinea
|
|
D014006||capitis profunda tinea
|
|
D014006||capitis trichophytia profunda
|
|
D014006||kerion celsi
|
|
D014006||profunda barbae trichophytia
|
|
D014006||profunda capitides trichophytia
|
|
D014006||profunda capitis trichophytia
|
|
D014006||profundas tinea capitis
|
|
D014006||profunda tinea capitis
|
|
D014006||tinea capitis profunda
|
|
D014006||tinea capitis profundas
|
|
D014006||trichophytia profunda barbae
|
|
D014006||trichophytia profunda capitides
|
|
D014006||trichophytia profunda capitis
|
|
D014005||tinea
|
|
D014005||dermatophytoses
|
|
D014005||dermatophytosis
|
|
D014005||epidermophytoses
|
|
D014005||epidermophytosis
|
|
D014005||ringworm
|
|
D014005||tineas
|
|
D014005||trichophytoses
|
|
D014005||trichophytosis
|
|
C566587|602078||fibrosis of extraocular muscles congenital 2
|
|
C566587|602078||cfeom2
|
|
C566587|602078||feom2 locus
|
|
C566587|602078||fibrosis of extraocular muscles congenital autosomal recessive
|
|
D004698||endocarditis subacute bacterial
|
|
D004698||bacterial endocarditides subacute
|
|
D004698||bacterial endocarditis subacute
|
|
D004698||endocarditides subacute bacterial
|
|
D004698||endocarditis lenta
|
|
D004698||subacute bacterial endocarditides
|
|
D004698||subacute bacterial endocarditis
|
|
D004697||endocarditis bacterial
|
|
D004697||bacterial endocarditides
|
|
D004697||bacterial endocarditis
|
|
D004697||endocarditides bacterial
|
|
C564921|259440||osteogenesis imperfecta type ix
|
|
C564921|259440||oi9
|
|
C564921|259440||oi type ix
|
|
C564921|259440||osteogenesis imperfecta sillence type ii iii without abnormality of type i collagen
|
|
D002037||anterior fascicular block
|
|
D002037||anterior fascicular blocks
|
|
D002037||block anterior fascicular
|
|
D002037||block bundle branch
|
|
D002037||block fascicular
|
|
D002037||block left bundle branch
|
|
D002037||block posterior fascicular
|
|
D002037||block right bundle branch
|
|
D002037||blocks anterior fascicular
|
|
D002037||blocks bundle branch
|
|
D002037||blocks fascicular
|
|
D002037||blocks left bundle branch
|
|
D002037||blocks posterior fascicular
|
|
D002037||blocks right bundle branch
|
|
D002037||branch block bundle
|
|
D002037||branch blocks bundle
|
|
D002037||bundle branch block left
|
|
D002037||bundle branch block right
|
|
D002037||bundle branch blocks
|
|
D002037||bundle branch blocks left
|
|
D002037||bundle branch blocks right
|
|
D002037||fascicular block
|
|
D002037||fascicular block anterior
|
|
D002037||fascicular block posterior
|
|
D002037||fascicular blocks
|
|
D002037||fascicular blocks anterior
|
|
D002037||fascicular blocks posterior
|
|
D002037||left bundle branch block
|
|
D002037||left bundle branch blocks
|
|
D002037||posterior fascicular block
|
|
D002037||posterior fascicular blocks
|
|
D002037||right bundle branch block
|
|
D002037||right bundle branch blocks
|
|
C537250|603553||hemophagocytic lymphohistiocytosis familial 2
|
|
C537250|603553||fhl2
|
|
C537250|603553||hlh2
|
|
C537250|603553||hplh2
|
|
D004694||endocardial cushion defects
|
|
D004694||cushion defect endocardial
|
|
D004694||cushion defects endocardial
|
|
D004694||defect endocardial cushion
|
|
D004694||defects endocardial cushion
|
|
D004694||endocardial cushion defect
|
|
D004694||persistent common atrioventricular canal
|
|
D002032||bulimia
|
|
D002032||binge eating
|
|
D002032||bulimias
|
|
D002032||eating binge
|
|
D004696||endocarditis
|
|
D004696||endocarditides
|
|
D004696||endocarditides infective
|
|
D004696||endocarditis infective
|
|
D004696||infective endocarditides
|
|
D004696||infective endocarditis
|
|
D004695||endocardial fibroelastosis
|
|
D004695||endocardial fibroelastoses
|
|
D004695||endomyocardial fibroelastosis
|
|
D004695||fibroelastoses endocardial
|
|
D004695||fibroelastosis endocardial
|
|
C567090|611762||familial cold autoinflammatory syndrome 2
|
|
C567090|611762||fcas2
|
|
D003371||cough
|
|
D003371||coughs
|
|
219750|C535765||cystinosis ocular nonnephropathic
|
|
219750|C535765||cystinosis adult nonnephropathic
|
|
219750|C535765||cystinosis benign nonnephropathic
|
|
219750|C535765||ocular nonnephropathic cystinosis
|
|
D014012||tinnitus
|
|
D014012||clicking tinnitus
|
|
D014012||induced tinnitus noise
|
|
D014012||leudet apos s tinnitus
|
|
D014012||leudet tinnitus
|
|
D014012||noise induced tinnitus
|
|
D014012||objective tinnitus
|
|
D014012||pulsatile tinnitus
|
|
D014012||ringing buzzing tinnitus
|
|
D014012||spontaneous oto acoustic emission tinnitus
|
|
D014012||subjective tinnitus
|
|
D014012||tensor palatini induced tinnitus
|
|
D014012||tensor tympani induced tinnitus
|
|
D014012||tinnitus clicking
|
|
D014012||tinnitus leudet
|
|
D014012||tinnitus leudets
|
|
D014012||tinnitus leudet apos s
|
|
D014012||tinnitus noise induced
|
|
D014012||tinnitus objective
|
|
D014012||tinnitus of vascular origin
|
|
D014012||tinnitus pulsatile
|
|
D014012||tinnitus spontaneous oto acoustic emission
|
|
D014012||tinnitus subjective
|
|
D014012||tinnitus tensor palatini induced
|
|
D014012||tinnitus tensor tympani induced
|
|
D014012||tinnitus vascular origin
|
|
D014012||vascular origin tinnitus
|
|
D014010||tinea versicolor
|
|
D014010||pityriasis versicolor
|
|
C565016|135400||hypertrichosis terminalis generalized with or without gingival hyperplasia
|
|
C565016|135400||chromosome 17q24 2 q24 3 deletion syndrome
|
|
C565016|135400||fibromatosis gingival with hypertrichosis
|
|
C565016|135400||microdeletion 17q24 2 q24 3 syndrome
|
|
D016672||zenker diverticulum
|
|
D016672||diverticula esophago pharyngeal
|
|
D016672||diverticula pharyngeal
|
|
D016672||diverticula pharyngoesophageal
|
|
D016672||diverticula pharyngo esophageal
|
|
D016672||diverticula pharyngoesophageal pulsion
|
|
D016672||diverticula zenker apos s
|
|
D016672||diverticulum esophagopharyngeal
|
|
D016672||diverticulum esophago pharyngeal
|
|
D016672||diverticulum pharyngeal
|
|
D016672||diverticulum pharyngoesophageal
|
|
D016672||diverticulum pharyngo esophageal
|
|
D016672||diverticulum pharyngoesophageal pulsion
|
|
D016672||diverticulums esophagopharyngeal
|
|
D016672||diverticulum zenker
|
|
D016672||diverticulum zenker apos s
|
|
D016672||esophago pharyngeal diverticula
|
|
D016672||esophagopharyngeal diverticulum
|
|
D016672||esophago pharyngeal diverticulum
|
|
D016672||esophagopharyngeal diverticulums
|
|
D016672||pharyngeal diverticula
|
|
D016672||pharyngeal diverticulum
|
|
D016672||pharyngoesophageal diverticula
|
|
D016672||pharyngo esophageal diverticula
|
|
D016672||pharyngoesophageal diverticulum
|
|
D016672||pharyngo esophageal diverticulum
|
|
D016672||pharyngoesophageal pulsion diverticula
|
|
D016672||pharyngoesophageal pulsion diverticulum
|
|
D016672||pulsion diverticula pharyngoesophageal
|
|
D016672||pulsion diverticulum pharyngoesophageal
|
|
D016672||zenker diverticula
|
|
D016672||zenker apos s diverticula
|
|
D016672||zenkers diverticula
|
|
D016672||zenker apos s diverticulum
|
|
D016672||zenkers diverticulum
|
|
D002006||brucellosis
|
|
D002006||brucelloses
|
|
D002006||brucelloses pulmonary
|
|
D002006||brucellosis pulmonary
|
|
D002006||cyprus fever
|
|
D002006||cyprus fevers
|
|
D002006||fever cyprus
|
|
D002006||fever gibraltar
|
|
D002006||fever malta
|
|
D002006||fever rock
|
|
D002006||fevers cyprus
|
|
D002006||fevers rock
|
|
D002006||fevers undulant
|
|
D002006||fever undulant
|
|
D002006||gibraltar fever
|
|
D002006||malta fever
|
|
D002006||pulmonary brucelloses
|
|
D002006||pulmonary brucellosis
|
|
D002006||rock fever
|
|
D002006||rock fevers
|
|
D002006||undulant fever
|
|
D002006||undulant fevers
|
|
D002007||brucellosis bovine
|
|
D002007||bang disease
|
|
D002007||bang apos s disease
|
|
D002007||bangs disease
|
|
D002007||bovine brucelloses
|
|
D002007||bovine brucellosis
|
|
D002007||brucelloses bovine
|
|
D002007||disease bang
|
|
D002007||disease bang apos s
|
|
D004660||encephalitis
|
|
D004660||brain inflammation
|
|
D004660||brain inflammations
|
|
D004660||encephalitides infectious
|
|
D004660||encephalitis infectious
|
|
D004660||encephalitis rasmussen
|
|
D004660||infectious encephalitides
|
|
D004660||infectious encephalitis
|
|
D004660||inflammation brain
|
|
D004660||rasmussen encephalitis
|
|
D004660||rasmussen apos s syndrome
|
|
D004660||rasmussen syndrome
|
|
D003330||coronary vessel anomalies
|
|
D003330||anomalies coronary vessel
|
|
D003330||anomaly coronary vessel
|
|
D003330||coronary vessel anomaly
|
|
D015318||fructose metabolism inborn errors
|
|
500004|D052245||usher syndromes
|
|
500004|D052245||deafness retinitis pigmentosa syndrome
|
|
500004|D052245||deafness retinitis pigmentosa syndromes
|
|
500004|D052245||dystrophia retinae pigmentosa dysostosis syndrome
|
|
500004|D052245||graefe usher syndrome
|
|
500004|D052245||hallgren syndrome
|
|
500004|D052245||pigmentosa syndromes deafness retinitis
|
|
500004|D052245||retinitis pigmentosa 21 formerly
|
|
500004|D052245||retinitis pigmentosa 8 formerly
|
|
500004|D052245||retinitis pigmentosa and congenital deafness
|
|
500004|D052245||retinitis pigmentosa deafness syndrome
|
|
500004|D052245||retinitis pigmentosa deafness syndromes
|
|
500004|D052245||rp21 formerly
|
|
500004|D052245||rp8 formerly
|
|
500004|D052245||syndrome deafness retinitis pigmentosa
|
|
500004|D052245||syndrome graefe usher
|
|
500004|D052245||syndrome hallgren
|
|
500004|D052245||syndrome retinitis pigmentosa deafness
|
|
500004|D052245||syndromes deafness retinitis pigmentosa
|
|
500004|D052245||syndromes retinitis pigmentosa deafness
|
|
500004|D052245||syndromes usher
|
|
500004|D052245||syndrome usher
|
|
500004|D052245||syndrome usher apos s
|
|
500004|D052245||usher apos s syndrome
|
|
500004|D052245||ushers syndrome
|
|
500004|D052245||usher syndrome
|
|
500004|D052245||usher syndrome type 1
|
|
500004|D052245||usher syndrome type 1a
|
|
500004|D052245||usher syndrome type 3
|
|
500004|D052245|C536485|276900||usher syndrome type i
|
|
500004|D052245||usher syndrome type i french variety
|
|
500004|D052245||usher syndrome type ii
|
|
500004|D052245|611383||usher syndrome type iid
|
|
500004|D052245|276902||usher syndrome type iii
|
|
D004670||encephalitis california
|
|
D004670||california encephalitis
|
|
D004670||california viral encephalitides
|
|
D004670||california viral encephalitis
|
|
D004670||encephalitides california viral
|
|
D004670||encephalitis california viral
|
|
D004670||viral encephalitides california
|
|
D004670||viral encephalitis california
|
|
D006432|235200||hemochromatosis
|
|
D006432|235200||bronzed cirrhoses
|
|
D006432|235200||bronzed cirrhosis
|
|
D006432|235200||bronze diabetes
|
|
D006432|235200||cirrhoses bronzed
|
|
D006432|235200||cirrhoses pigmentary
|
|
D006432|235200||cirrhosis bronzed
|
|
D006432|235200||cirrhosis pigmentary
|
|
D006432|235200||diabetes bronze
|
|
D006432|235200||diseases von recklenhausen applebaum
|
|
D006432|235200||disease von recklenhausen applebaum
|
|
D006432|235200||disorder iron storage
|
|
D006432|235200||disorders iron storage
|
|
D006432|235200||familial hemochromatoses
|
|
D006432|235200||familial hemochromatosis
|
|
D006432|235200||genetic hemochromatoses
|
|
D006432|235200||genetic hemochromatosis
|
|
D006432|235200||haemochromatoses
|
|
D006432|235200||haemochromatosis
|
|
D006432|235200||hemochromatose
|
|
D006432|235200||hemochromatoses
|
|
D006432|235200||hemochromatoses familial
|
|
D006432|235200||hemochromatoses genetic
|
|
D006432|235200||hemochromatosis familial
|
|
D006432|235200||hemochromatosis genetic
|
|
D006432|235200||hemochromatosis hereditary
|
|
D006432|235200||hemochromatosis type 1
|
|
D006432|235200||hfe
|
|
D006432|235200||hfe1
|
|
D006432|235200||hh
|
|
D006432|235200||iron storage disorder
|
|
D006432|235200||iron storage disorders
|
|
D006432|235200||pigmentary cirrhoses
|
|
D006432|235200||pigmentary cirrhosis
|
|
D006432|235200||primary hemochromatosis
|
|
D006432|235200||recklenhausen applebaum diseases von
|
|
D006432|235200||recklenhausen applebaum disease von
|
|
D006432|235200||storage disorder iron
|
|
D006432|235200||storage disorders iron
|
|
D006432|235200||syndromes troisier hanot chauffard
|
|
D006432|235200||syndrome troisier hanot chauffard
|
|
D006432|235200||troisier hanot chauffard syndrome
|
|
D006432|235200||troisier hanot chauffard syndromes
|
|
D006432|235200||von recklenhausen applebaum disease
|
|
D006432|235200||von recklenhausen applebaum diseases
|
|
C535279|608646||primary ciliary dyskinesia 4
|
|
C535279|608646||cild4
|
|
C535279|608646||ciliary dyskinesia primary 4
|
|
C535279|608646||ciliary dyskinesia primary 4 with or without situs inversus
|
|
D016643||encephalopathy bovine spongiform
|
|
D016643||bovine spongiform encephalitis
|
|
D016643||bovine spongiform encephalopathy
|
|
D016643||bse bovine spongiform encephalopathy
|
|
D016643||bses bovine spongiform encephalopathy
|
|
D016643||encephalitis bovine spongiform
|
|
D016643||mad cow disease
|
|
D016643||mad cow diseases
|
|
D016643||spongiform encephalopathy bovine
|
|
D016640||diabetes gestational
|
|
D016640||diabetes mellitus gestational
|
|
D016640||diabetes pregnancy induced
|
|
D016640||gestational diabetes
|
|
D016640||gestational diabetes mellitus
|
|
D016640||pregnancy induced diabetes
|
|
C566425|602772||retinitis pigmentosa 25
|
|
C566425|602772||rp25
|
|
D004679||encephalomyelitis
|
|
D004679||encephalomyelitis inflammatory
|
|
D004679||inflammatory encephalomyelitis
|
|
D004679||myeloencephalitides
|
|
D004679||myeloencephalitis
|
|
C567191|146450||hypospadias 3 autosomal
|
|
C567191|146450||hysp3
|
|
D004675||encephalitis tick borne
|
|
D004675||central european encephalitis
|
|
D004675||encephalitides european tick borne
|
|
D004675||encephalitides louping ill
|
|
D004675||encephalitides powassan
|
|
D004675||encephalitides tick borne
|
|
D004675||encephalitis central european
|
|
D004675||encephalitis european tick borne
|
|
D004675||encephalitis far eastern russian
|
|
D004675||encephalitis louping ill
|
|
D004675||encephalitis powassan
|
|
D004675||encephalitis russian spring summer
|
|
D004675||european tick borne encephalitides
|
|
D004675||european tick borne encephalitis
|
|
D004675||far eastern russian encephalitis
|
|
D004675||louping ill encephalitides
|
|
D004675||louping ill encephalitis
|
|
D004675||powassan encephalitides
|
|
D004675||powassan encephalitis
|
|
D004675||russian spring summer encephalitis
|
|
D004675||spring summer encephalitis russian
|
|
D004675||tick borne encephalitides
|
|
D004675||tick borne encephalitides european
|
|
D004675||tick borne encephalitis
|
|
D004675||tick borne encephalitis european
|
|
D004678||encephalomalacia
|
|
D004678||cerebromalacia
|
|
D004678||cerebromalacias
|
|
D004678||encephalomalacia multicystic
|
|
D004678||encephalomalacias
|
|
D004678||encephalomalacias multicystic
|
|
D004678||multicystic encephalomalacia
|
|
D004678||multicystic encephalomalacias
|
|
D004677||encephalocele
|
|
D004677||acquired encephalocele
|
|
D004677||acquired encephaloceles
|
|
D004677||bifid cranium
|
|
D004677||bifid craniums
|
|
D004677||bifidum cranium
|
|
D004677||bifidums cranium
|
|
D004677||cephalocele
|
|
D004677||cephaloceles
|
|
D004677||cerebellar hernia
|
|
D004677||cerebellar hernias
|
|
D004677||cerebellar herniation
|
|
D004677||cerebellar herniations
|
|
D004677||cerebral hernia
|
|
D004677||cerebral hernias
|
|
D004677||cranial meningoencephalocele
|
|
D004677||cranial meningoencephaloceles
|
|
D004677||craniocele
|
|
D004677||cranioceles
|
|
D004677||cranium bifid
|
|
D004677||cranium bifidum
|
|
D004677||cranium bifidums
|
|
D004677||craniums bifid
|
|
D004677||encephalocele acquired
|
|
D004677||encephalocele frontal
|
|
D004677||encephalocele occipital
|
|
D004677||encephaloceles
|
|
D004677||encephaloceles acquired
|
|
D004677||encephaloceles frontal
|
|
D004677||encephalocele sincipital
|
|
D004677||encephaloceles occipital
|
|
D004677||encephaloceles sincipital
|
|
D004677||frontal encephalocele
|
|
D004677||frontal encephaloceles
|
|
D004677||hernia cerebellar
|
|
D004677||hernia cerebral
|
|
D004677||hernias cerebellar
|
|
D004677||hernias cerebral
|
|
D004677||hernias tonsillar
|
|
D004677||herniation cerebellar
|
|
D004677||herniations cerebellar
|
|
D004677||herniations tonsillar
|
|
D004677||herniation tonsillar
|
|
D004677||hernia tonsillar
|
|
D004677||meningoencephalocele cranial
|
|
D004677||meningoencephaloceles cranial
|
|
D004677||notoencephalocele
|
|
D004677||notoencephaloceles
|
|
D004677||occipital encephalocele
|
|
D004677||occipital encephaloceles
|
|
D004677||sincipital encephalocele
|
|
D004677||sincipital encephaloceles
|
|
D004677||tonsillar hernia
|
|
D004677||tonsillar hernias
|
|
D004677||tonsillar herniation
|
|
D004677||tonsillar herniations
|
|
D004672||encephalitis japanese
|
|
D004672||encephalitis japanese b
|
|
D004672||japanese b encephalitis
|
|
D004672||japanese b viral encephalitis
|
|
D004672||japanese encephalitis
|
|
D004672||viral encephalitis japanese b
|
|
C562591|278730||xeroderma pigmentosum complementation group d
|
|
C562591|278730||trichothiodystrophy type 1 included
|
|
C562591|278730||ttd1 included
|
|
C562591|278730||xeroderma pigmentosum iv
|
|
C562591|278730||xeroderma pigmentosum iv xp4 trichothiodystrophy with sun sensitivity included
|
|
C562591|278730||xeroderma pigmentosum viii formerly
|
|
C562591|278730||xp4
|
|
C562591|278730||xp8 formerly
|
|
C562591|278730||xpd
|
|
C562591|278730||xpdc
|
|
C562591|278730||xp group d
|
|
C562591|278730||xp group h formerly
|
|
C562591|278730||xph formerly
|
|
D004671||encephalitis arbovirus
|
|
D004671||arbovirus encephalitides
|
|
D004671||arbovirus encephalitis
|
|
D004671||arthropod borne encephalitides
|
|
D004671||arthropod borne encephalitis
|
|
D004671||arthropod borne viral encephalitides
|
|
D004671||arthropod borne viral encephalitis
|
|
D004671||encephalitides arbovirus
|
|
D004671||encephalitides arthropod borne
|
|
D004671||encephalitides arthropod borne viral
|
|
D004671||encephalitides epidemic
|
|
D004671||encephalitides mosquito borne
|
|
D004671||encephalitis arthropod borne
|
|
D004671||encephalitis arthropod borne viral
|
|
D004671||encephalitis epidemic
|
|
D004671||encephalitis mosquito borne
|
|
D004671||epidemic encephalitides
|
|
D004671||epidemic encephalitis
|
|
D004671||mosquito borne encephalitides
|
|
D004671||mosquito borne encephalitis
|
|
D004671||viral encephalitides arthropod borne
|
|
D004671||viral encephalitis arthropod borne
|
|
D004674||encephalitis st louis
|
|
D004674||encephalitis saint louis
|
|
D004674||encephalitis viral st louis
|
|
D004674||lethargic encephalitis type c
|
|
D004674||louis meningoencephalitides st
|
|
D004674||meningoencephalitides st louis
|
|
D004674||meningoencephalitis st louis
|
|
D004674||saint louis encephalitis
|
|
D004674||st louis encephalitis
|
|
D004674||st louis meningoencephalitides
|
|
D004674||st louis meningoencephalitis
|
|
D004674||st louis viral encephalitis
|
|
D004674||type c lethargic encephalitis
|
|
C567729|613144||choroidal dystrophy central areolar 3
|
|
C567729|613144||cacd3
|
|
C567729|613144||choroidal dystrophy central areolar with or without drusen
|
|
D004673||encephalomyelitis acute disseminated
|
|
D004673||acute disseminated encephalomyelitides
|
|
D004673||acute disseminated encephalomyelitis
|
|
D004673||disseminated encephalomyelitides acute
|
|
D004673||disseminated encephalomyelitis acute
|
|
D004673||encephalitides post vaccinal
|
|
D004673||encephalitis postvaccinal
|
|
D004673||encephalitis post vaccinal
|
|
D004673||encephalitis vaccination
|
|
D004673||encephalomyelitides acute disseminated
|
|
D004673||encephalomyelitides post vaccinal
|
|
D004673||encephalomyelitis postexanthem
|
|
D004673||encephalomyelitis postinfectious
|
|
D004673||encephalomyelitis post vaccinal
|
|
D004673||postexanthem encephalomyelitis
|
|
D004673||postinfectious encephalomyelitis
|
|
D004673||post vaccinal encephalitides
|
|
D004673||postvaccinal encephalitis
|
|
D004673||post vaccinal encephalitis
|
|
D004673||post vaccinal encephalomyelitides
|
|
D004673||post vaccinal encephalomyelitis
|
|
D004673||vaccination encephalitis
|
|
D002012||bruxism
|
|
D002012||disorders teeth grinding
|
|
D002012||disorder teeth grinding
|
|
D002012||grinding disorders teeth
|
|
D002012||grinding disorder teeth
|
|
D002012||teeth grinding disorder
|
|
D002012||teeth grinding disorders
|
|
D004681||encephalomyelitis autoimmune experimental
|
|
D004681||allergic encephalomyelitis
|
|
D004681||allergic encephalomyelitis experimental
|
|
D004681||autoimmune encephalomyelitis experimental
|
|
D004681||autoimmune experimental encephalomyelitis
|
|
D004681||encephalomyelitis allergic
|
|
D004681||encephalomyelitis experimental allergic
|
|
D004681||encephalomyelitis experimental autoimmune
|
|
D004681||experimental allergic encephalomyelitides
|
|
D004681||experimental allergic encephalomyelitis
|
|
D004681||experimental autoimmune encephalomyelitis
|
|
D004681||experimental encephalomyelitis autoimmune
|
|
C536510|249270||thiamine responsive megaloblastic anemia syndrome
|
|
C536510|249270||abboud syndrome
|
|
C536510|249270||megaloblastic anemia thiamine responsive with diabetes mellitus and sensorineural deafness
|
|
C536510|249270||rogers syndrome
|
|
C536510|249270||thiamine metabolism dysfunction syndrome 1 megaloblastic anemia diabetes mellitus and deafness type
|
|
C536510|249270||thiamine responsive anemia syndrome
|
|
C536510|249270||thiamine responsive myelodysplasia
|
|
C536510|249270||thmd1
|
|
C536510|249270||trma
|
|
C562908|187260||telangiectasia hereditary benign
|
|
C562908|187260||hbt
|
|
D016659||psoas abscess
|
|
D016659||abscesses iliopsoas
|
|
D016659||abscesses psoas
|
|
D016659||abscesses pyogenic iliopsoas
|
|
D016659||abscess iliopsoas
|
|
D016659||abscess psoas
|
|
D016659||abscess pyogenic iliopsoas
|
|
D016659||iliopsoas abscess
|
|
D016659||iliopsoas abscesses
|
|
D016659||iliopsoas abscesses pyogenic
|
|
D016659||iliopsoas abscess pyogenic
|
|
D016659||psoas abscesses
|
|
D016659||pyogenic iliopsoas abscess
|
|
D016659||pyogenic iliopsoas abscesses
|
|
C567498|611897||nanophthalmos 3
|
|
C567498|611897||nanophthalmia 3
|
|
C567498|611897||nno3
|
|
D016657||cerebral amyloid angiopathy
|
|
D016657||amyloid angiopathy cerebral
|
|
D016657||angiopathy cerebral amyloid
|
|
D016657||angiopathy congophilic
|
|
D016657||cerebral amyloid angiopathies
|
|
D016657||congophilic angiopathies
|
|
D016657||congophilic angiopathy
|
|
D016657||sporadic cerebral amyloid angiopathy
|
|
D015323||pyruvate metabolism inborn errors
|
|
C536190|225280||ectodermal dysplasia ectrodactyly and macular dystrophy
|
|
C536190|225280||ectodermal dysplasia ectrodactyly macular dystrophy
|
|
C536190|225280||eem syndrome
|
|
C537527|245050||succinyl coa 3 oxoacid coa transferase deficiency
|
|
C537527|245050||3 oxoacid coa transferase deficiency
|
|
C537527|245050||ketoacidosis due to scot deficiency
|
|
C537527|245050||scot deficiency
|
|
C537527|245050||succinyl coa 3 ketoacid coa transferase deficiency
|
|
C537527|245050||succinyl coa 3 oxoacid transferase deficiency
|
|
C537527|245050||succinyl coa acetoacetate transferase deficiency
|
|
D002105||cadmium poisoning
|
|
D002105||cadmium poisonings
|
|
D002105||itai itai
|
|
D002105||poisoning cadmium
|
|
D002105||poisonings cadmium
|
|
D004767||enterotoxemia
|
|
D004767||enterotoxemias
|
|
D054908||extensively drug resistant tuberculosis
|
|
D054908||drug resistant tuberculoses extensively
|
|
D054908||drug resistant tuberculoses extremely
|
|
D054908||drug resistant tuberculosis extensively
|
|
D054908||drug resistant tuberculosis extremely
|
|
D054908||extensively drug resistant tuberculoses
|
|
D054908||extremely drug resistant tuberculoses
|
|
D054908||extremely drug resistant tuberculosis
|
|
D054908||tuberculoses extensively drug resistant
|
|
D054908||tuberculoses extremely drug resistant
|
|
D054908||tuberculosis extensively drug resistant
|
|
D054908||tuberculosis extremely drug resistant
|
|
D054908||xdr tb
|
|
D004769||enterovirus infections
|
|
D004769||enterovirus infection
|
|
D004769||infection enterovirus
|
|
D004769||infections enterovirus
|
|
C567306|612447||skeletal defects genital hypoplasia and mental retardation
|
|
128100|C538005||dystonia musculorum deformans type 1
|
|
128100|C538005||dystonia 1 torsion autosomal dominant
|
|
128100|C538005||dystonia musculorum deformans 1
|
|
128100|C538005||dyt1
|
|
128100|C538005||early onset generalized torsion dystonia
|
|
128100|C538005||early onset primary dystonia
|
|
128100|C538005||early onset torsion dystonia
|
|
128100|C538005||eotd
|
|
128100|C538005||oppenheim dystonia
|
|
128100|C538005||oppenheim apos s dystonia
|
|
128100|C538005||primary torsion dystonia
|
|
128100|C538005||torsion dystonia 1 autosomal dominant
|
|
D002102||cadaver
|
|
D002102||cadavers
|
|
D002102||corpse
|
|
D002102||corpses
|
|
D004760||enterocolitis
|
|
D004760||enterocolitides
|
|
610217||neuroaxonal dystrophy atypical karak syndrome included
|
|
C536044|259420||osteogenesis imperfecta type 3
|
|
C536044|259420||oi3
|
|
C536044|259420||oi type iii
|
|
C536044|259420||osteogenesis imperfecta progressively deforming with normal sclerae
|
|
C536044|259420||osteogenesis imperfecta type iii
|
|
D004761||enterocolitis pseudomembranous
|
|
D004761||antibiotic associated colitis
|
|
D004761||clostridium enterocolitis
|
|
D004761||colitis antibiotic associated
|
|
D004761||colitis pseudomembranous
|
|
D004761||enteritis pseudomembranous
|
|
D004761||pseudomembranous colitis
|
|
D004761||pseudomembranous enteritis
|
|
D004761||pseudomembranous enterocolitis
|
|
D002100||cachexia
|
|
C567422|612095||retinitis pigmentosa 41
|
|
C567422|612095||retinal degeneration autosomal recessive prominin related
|
|
C567422|612095||rp41
|
|
D015418||optic atrophies hereditary
|
|
D015418||atrophies hereditary optic
|
|
D015418||atrophy hereditary optic
|
|
D015418||hereditary optic atrophies
|
|
D015418||hereditary optic atrophy
|
|
D015418||optic atrophy hereditary
|
|
D057178||primary progressive nonfluent aphasia
|
|
D057178||aphasia progressive nonfluent
|
|
D057178||aphasias progressive nonfluent
|
|
D057178||nonfluent aphasia progressive
|
|
D057178||nonfluent aphasias progressive
|
|
D057178||non fluent primary progressive aphasia
|
|
D057178||ppa syndrome
|
|
D057178||ppa syndromes
|
|
D057178||progressive nonfluent aphasia
|
|
D057178||progressive nonfluent aphasias
|
|
D057178||syndrome ppa
|
|
D057178||syndromes ppa
|
|
C566437|610131||progressive external ophthalmoplegia with mitochondrial dna deletions autosomal dominant 4
|
|
C566437|610131||peoa4
|
|
C566437|610131||progressive external ophthalmoplegia autosomal dominant 4
|
|
D057174||frontotemporal lobar degeneration
|
|
D057174||degeneration frontotemporal lobar
|
|
D057174||degenerations frontotemporal lobar
|
|
D057174||frontotemporal lobar degenerations
|
|
D057174||ftld
|
|
D057174||ftlds
|
|
D057174||lobar degeneration frontotemporal
|
|
D057174||lobar degenerations frontotemporal
|
|
C563924|608456||colorectal adenomatous polyposis autosomal recessive
|
|
C563924|608456||adenomas multiple colorectal autosomal recessive
|
|
C563924|608456||familial adenomatous polyposis 2
|
|
C563924|608456||fap2
|
|
D015419||spastic paraplegia hereditary
|
|
D015419||autosomal dominant hereditary spastic paraplegia
|
|
D015419||autosomal dominant spastic paraplegia hereditary
|
|
D015419||autosomal recessive hereditary spastic paraplegia
|
|
D015419||autosomal recessive spastic paraplegia hereditary
|
|
D015419||charcot marie tooth disease with pyramidal features autosomal dominant
|
|
D015419||cmt with pyramidal features
|
|
D015419||hereditary autosomal dominant spastic paraplegia
|
|
D015419||hereditary autosomal recessive spastic paraplegia
|
|
D015419||hereditary motor and sensory neuropathy 5
|
|
D015419||hereditary motor and sensory neuropathy v
|
|
D015419||hereditary motor sensory neuropathy with pyramidal signs
|
|
D015419||hereditary spastic paraplegia
|
|
D015419||hereditary spastic paraplegia autosomal dominant
|
|
D015419||hereditary spastic paraplegia autosomal recessive
|
|
D015419||hereditary spastic paraplegias
|
|
D015419||hereditary spastic paraplegia x linked recessive
|
|
D015419||hereditary x linked recessive spastic paraplegia
|
|
D015419||hmsn 5
|
|
D015419||hmsn type v
|
|
D015419||hmsn v
|
|
D015419||hmsn v hereditary motor and sensory neuropathy type v
|
|
D015419||hypertrophic motor sensory neuropathy spastic paraplegia
|
|
D015419||paraplegia hereditary spastic
|
|
D015419||paraplegias hereditary spastic
|
|
D015419||paraplegia spastic hereditary
|
|
D015419||peroneal muscular atrophy with pyramidal features autosomal dominant
|
|
D015419||spastic paraplegia 2
|
|
D015419||spastic paraplegia autosomal dominant hereditary
|
|
D015419||spastic paraplegia autosomal recessive hereditary
|
|
D015419||spastic paraplegia hereditary autosomal dominant
|
|
D015419||spastic paraplegia hereditary autosomal recessive
|
|
D015419||spastic paraplegia hereditary x linked recessive
|
|
D015419||spastic paraplegia hypertrophic motor sensory neuropathy
|
|
D015419||spastic paraplegias hereditary
|
|
D015419||spastic paraplegia type 2
|
|
D015419||spastic paraplegia x linked recessive hereditary
|
|
D015419||type v hereditary motor and sensory neuropathy
|
|
D015419||type v hmsn
|
|
D015419||x linked recessive hereditary spastic paraplegia
|
|
D015419||x linked spastic paraplegia hereditary
|
|
D057177||tdp 43 proteinopathies
|
|
D057177||proteinopathies tdp 43
|
|
D057177||proteinopathy tdp 43
|
|
D057177||tdp 43 proteinopathy
|
|
D013398|272120||sudden infant death
|
|
D013398|272120||cot death
|
|
D013398|272120||cot deaths
|
|
D013398|272120||crib death
|
|
D013398|272120||death cot
|
|
D013398|272120||death crib
|
|
D013398|272120||death sudden infant
|
|
D013398|272120||infant death sudden
|
|
D013398|272120||sid
|
|
D013398|272120||sids
|
|
D013398|272120||sudden infant death syndrome
|
|
C566333|613693||long qt syndrome 6
|
|
C566333|613693|C565840|603830||long qt syndrome 3 6 digenic included lqt3 6 digenic included
|
|
C566333|613693||long qt syndrome 6 acquired susceptibility to included
|
|
C566333|613693||lqt6
|
|
D003449||cryoglobulinemia
|
|
D003449||cryoglobulinemias
|
|
D004775||enuresis
|
|
D004774||entropion
|
|
D004774||entropions
|
|
D003444||crush syndrome
|
|
D003444||crush syndromes
|
|
D003444||syndrome crush
|
|
D003444||syndromes crush
|
|
D002114||calcinosis
|
|
D002114||calcification pathologic
|
|
D002114||calcinoses
|
|
D002114||calcinoses tumoral
|
|
D002114||calcinosis tumoral
|
|
D002114||pathologic calcification
|
|
D002114||tumoral calcinoses
|
|
D002114||tumoral calcinosis
|
|
D002115||calciphylaxis
|
|
D002115||calciphylaxes
|
|
D002115||calciphylaxis idiopathic
|
|
D002115||idiopathic calciphylaxis
|
|
611038|C567025||microphthalmia isolated 3
|
|
611038|C567025||mcop3
|
|
C567037|604559||progressive familial heart block type ib
|
|
C567037|604559||pfhb1b
|
|
C567037|604559||pfhbib
|
|
D003440||croup
|
|
D003440||croup postintubation
|
|
D003440||croup spasmodic
|
|
D003440||croup viral
|
|
D003440||postintubation croup
|
|
D003440||spasmodic croup
|
|
D003440||viral croup
|
|
D015428||myocardial reperfusion injury
|
|
D015428||injuries myocardial reperfusion
|
|
D015428||injury myocardial reperfusion
|
|
D015428||myocardial ischemic reperfusion injury
|
|
D015428||myocardial reperfusion injuries
|
|
D015428||reperfusion injuries myocardial
|
|
D015428||reperfusion injury myocardial
|
|
D015427||reperfusion injury
|
|
D015427||damage reperfusion
|
|
D015427||damages reperfusion
|
|
D015427||injuries ischemia reperfusion
|
|
D015427||injuries reperfusion
|
|
D015427||injury ischemia reperfusion
|
|
D015427||injury reperfusion
|
|
D015427||ischemia reperfusion injuries
|
|
D015427||ischemia reperfusion injury
|
|
D015427||reperfusion damage
|
|
D015427||reperfusion damages
|
|
D015427||reperfusion injuries
|
|
C565323|605544||fibromatosis gingival 2
|
|
C565323|605544||fibromatosis gingival hereditary 2
|
|
C565323|605544||ggf2
|
|
C565323|605544||gingf2
|
|
C565323|605544||hgf2
|
|
D016757||death sudden cardiac
|
|
D016757||arrest sudden cardiac
|
|
D016757||cardiac arrests sudden
|
|
D016757||cardiac arrest sudden
|
|
D016757||cardiac death sudden
|
|
D016757||cardiac sudden death
|
|
D016757||death cardiac sudden
|
|
D016757||sudden cardiac arrest
|
|
D016757||sudden cardiac death
|
|
D016757||sudden death cardiac
|
|
D007566|237500||jaundice chronic idiopathic
|
|
D007566|237500||chronic idiopathic jaundice
|
|
D007566|237500||chronic idiopathic jaundices
|
|
D007566|237500||djs
|
|
D007566|237500||dubin johnson syndrome
|
|
D007566|237500||hblrdj
|
|
D007566|237500||hyperbilirubinemia 2
|
|
D007566|237500||hyperbilirubinemia 2s
|
|
D007566|237500||hyperbilirubinemia dubin johnson type
|
|
D007566|237500||hyperbilirubinemia ii
|
|
D007566|237500||hyperbilirubinemia iis
|
|
D007566|237500||idiopathic jaundice chronic
|
|
D007566|237500||idiopathic jaundices chronic
|
|
D007566|237500||jaundices chronic idiopathic
|
|
D007566|237500||syndrome dubin johnson
|
|
C573898||triphalangeal thumb
|
|
D015423||scleritis
|
|
D015423||episcleritides
|
|
D015423||episcleritis
|
|
D015423||necrotizing scleritides
|
|
D015423||necrotizing scleritis
|
|
D015423||scleritides
|
|
D015423||scleritides necrotizing
|
|
D015423||scleritis necrotizing
|
|
D016751||hepatitis e
|
|
D016751||enterically transmitted non a non b hepatitis
|
|
D016751||epidemic non a non b hepatitis
|
|
D016751||et nanbh
|
|
D016751||hepatitides water borne
|
|
D016751||hepatitis viral non a non b enterically transmitted
|
|
D016751||hepatitis water borne
|
|
D016751||water borne hepatitides
|
|
D016751||water borne hepatitis
|
|
D015422||scleral diseases
|
|
D015422||disease sclera
|
|
D015422||disease scleral
|
|
D015422||diseases sclera
|
|
D015422||diseases scleral
|
|
D015422||sclera disease
|
|
D015422||sclera diseases
|
|
D015422||scleral disease
|
|
D004749||entamoebiasis
|
|
D004749||entamoebiases
|
|
C567043|610965||xfe progeroid syndrome
|
|
C567043|610965||xpf ercc1 progeroid syndrome
|
|
C536612|125630||familial dermographism
|
|
C536612|125630||ddu
|
|
C536612|125630||dermatographism familial
|
|
C536612|125630||dermo distortive urticaria
|
|
C536612|125630||dermodistortive urticaria
|
|
C536612|125630||dermographism familial
|
|
C536612|125630||familial dermatographism
|
|
C566977|611274||glaucoma 1 open angle n
|
|
C566977|611274||glc1n
|
|
C566874|603516||spinocerebellar ataxia 10
|
|
C566874|603516||sca10
|
|
612862||pulmonary hypertension chronic thromboembolic without deep vein thrombosis susceptibility to
|
|
612862||cteph dvt negative susceptibility to
|
|
D016724||empyema pleural
|
|
D016724||empyemas pleural
|
|
D016724||empyemas thoracic
|
|
D016724||empyema thoracic
|
|
D016724||pleural empyema
|
|
D016724||pleural empyemas
|
|
D016724||pyothorax
|
|
D016724||thoracic empyema
|
|
D016724||thoracic empyemas
|
|
D016726||plasma cell granuloma pulmonary
|
|
D016726||granuloma plasma cell pulmonary
|
|
D016726||inflammatory pseudotumor of lung
|
|
D016726||inflammatory pseudotumor pulmonary
|
|
D016726||inflammatory pseudotumors pulmonary
|
|
D016726||inflammatory pulmonary pseudotumor
|
|
D016726||inflammatory pulmonary pseudotumors
|
|
D016726||plasma cell granuloma of lung
|
|
D016726||pseudotumor inflammatory pulmonary
|
|
D016726||pseudotumor pulmonary inflammatory
|
|
D016726||pulmonary granuloma plasma cell
|
|
D016726||pulmonary inflammatory pseudotumor
|
|
D016726||pulmonary inflammatory pseudotumors
|
|
D016726||pulmonary plasma cell granuloma
|
|
D016726||pulmonary pseudotumor inflammatory
|
|
D016726||pulmonary pseudotumors inflammatory
|
|
D016727||orbital pseudotumor
|
|
D016727||granuloma plasma cell orbital
|
|
D016727||inflammatory pseudotumor of orbit
|
|
D016727||inflammatory pseudotumor orbital
|
|
D016727||inflammatory pseudotumors orbital
|
|
D016727||orbital granuloma plasma cell
|
|
D016727||orbital inflammatory pseudotumor
|
|
D016727||orbital inflammatory pseudotumors
|
|
D016727||orbital pseudotumors
|
|
D016727||plasma cell granuloma orbital
|
|
D016727||pseudotumor inflammatory orbital
|
|
D016727||pseudotumor orbital
|
|
D016727||pseudotumor orbital inflammatory
|
|
D016727||pseudotumors orbital
|
|
D016720||pneumocystis infections
|
|
D016720||infection pneumocystis
|
|
D016720||infections pneumocystis
|
|
D016720||pneumocystis carinii infection
|
|
D016720||pneumocystis carinii infections
|
|
D016720||pneumocystis infection
|
|
C567677|613268||corneal dystrophy fuchs endothelial 4
|
|
C567677|613268||fecd4
|
|
300705|C563140||mental retardation x linked 17
|
|
300705|C563140||mrx17
|
|
300705|C563140||mrx31
|
|
D004756||enterobacteriaceae infections
|
|
D004756||enterobacteriaceae infection
|
|
D004756||enterobacterial infection
|
|
D004756||enterobacterial infections
|
|
D004756||infection enterobacteriaceae
|
|
D004756||infection enterobacterial
|
|
D004756||infections enterobacteriaceae
|
|
D004756||infections enterobacterial
|
|
D053609||lethargy
|
|
D003428||cross infection
|
|
D003428||cross infections
|
|
D003428||hospital infection
|
|
D003428||hospital infections
|
|
D003428||infection cross
|
|
D003428||infection hospital
|
|
D003428||infection nosocomial
|
|
D003428||infections cross
|
|
D003428||infections hospital
|
|
D003428||infections nosocomial
|
|
D003428||nosocomial infection
|
|
D003428||nosocomial infections
|
|
D053608||stupor
|
|
D053608||narcosis
|
|
D004753||enteritis transmissible of turkeys
|
|
D004753||bluecomb of turkeys
|
|
D004753||transmissible enteritis of turkeys
|
|
C563663|610798||immunodeficiency due to defect in mapbp interacting protein
|
|
D003424||crohn disease
|
|
D003424||colitis granulomatous
|
|
D003424||crohn apos s disease
|
|
D003424||crohns disease
|
|
D003424||crohn apos s enteritis
|
|
D003424||enteritis granulomatous
|
|
D003424||enteritis regional
|
|
D003424||granulomatous colitis
|
|
D003424||granulomatous enteritis
|
|
D003424||ileitis regional
|
|
D003424||ileitis terminal
|
|
D003424||ileocolitis
|
|
D003424||regional enteritis
|
|
D003424||regional ileitides
|
|
D003424||regional ileitis
|
|
D003424||terminal ileitis
|
|
D004751||enteritis
|
|
D004751||enteritides
|
|
D003420||crisscross heart
|
|
D003420||criss cross heart
|
|
D003420||criss cross hearts
|
|
D003420||crisscross hearts
|
|
D003420||heart crisscross
|
|
D003420||heart criss cross
|
|
D003420||hearts crisscross
|
|
D003420||hearts criss cross
|
|
612852||osteomyelitis sterile multifocal with periostitis and pustulosis
|
|
612852||dira
|
|
612852|C557815||interleukin 1 receptor antagonist deficiency
|
|
612852||ompp
|
|
C563435|600881||cataract congenital zonular with sutural opacities
|
|
C563435|600881||cataract 10 multiple types
|
|
C563435|600881||cczs
|
|
C563435|600881||ctrct10
|
|
D016736||antiphospholipid syndrome
|
|
D016736||antibody syndrome antiphospholipid
|
|
D016736||antibody syndrome anti phospholipid
|
|
D016736||antiphospholipid antibody syndrome
|
|
D016736||anti phospholipid antibody syndrome
|
|
D016736||antiphospholipid antibody syndromes
|
|
D016736||anti phospholipid syndrome
|
|
D016736||syndrome antiphospholipid
|
|
D016736||syndrome anti phospholipid
|
|
D016736||syndrome antiphospholipid antibody
|
|
D016736||syndrome anti phospholipid antibody
|
|
D015408||gastrinoma
|
|
D015408||gastrinomas
|
|
D015408||gastrin producing tumor
|
|
D015408||gastrin producing tumors
|
|
D015408||islet cell tumor ulcerogenic
|
|
D015408||tumor gastrin producing
|
|
D015408||tumors gastrin producing
|
|
D015408||ulcerogenic islet cell tumor
|
|
D016731||erythema infectiosum
|
|
D016731||fifth disease
|
|
C567706|613211||amelogenesis imperfecta hypomaturation type iia3
|
|
C567706|613211||ai2a3
|
|
C535571||cantu sanchez corona fragoso syndrome
|
|
C535571||severe mental deficiency proportionate dwarfism and delayed sexual maturation
|
|
C566856|613697||cardiomyopathy dilated 1v
|
|
C566856|613697||cmd1v
|
|
C535570||acalvaria
|
|
159000|C535906||muscular dystrophy limb girdle type 1a
|
|
159000|C535906||lgmd1
|
|
159000|C535906||lgmd1a
|
|
159000|C535906||muscular dystrophy limb girdle type1a
|
|
159000|C535906||muscular dystrophy proximal type 1a
|
|
C535573||capillary leak syndrome with monoclonal gammopathy
|
|
C535573||periodic systemic capillary leak syndrome
|
|
C535572||cantu syndrome
|
|
C535572||hypertrichosis osteochondrodysplasia cardiomegaly syndrome
|
|
C535572||hypertrichotic osteochondrodysplasia
|
|
C535574||carbamoyl phosphate synthase 1 deficiency
|
|
202200|C565974||familial glucocorticoid deficiency 1
|
|
202200|C565974||acth resistance
|
|
202200|C565974||adrenal unresponsiveness to acth
|
|
202200|C565974||fgd1
|
|
202200|C565974||gccd1
|
|
202200|C565974||glucocorticoid deficiency 1
|
|
C536181|300291||ectodermal dysplasia hypohidrotic with immune deficiency
|
|
C536181|300291||ectodermal dysplasia anhidrotic with immune deficiency
|
|
C536181|300291||eda id included
|
|
C536181|300291||hed id ectodermal dysplasia anhidrotic with immune deficiency included
|
|
C536181|300291||hyper igm immunodeficiency x linked with hypohidrotic ectodermal dysplasia included
|
|
C536181|300291||xhm ed included
|
|
D016706||still apos s disease adult onset
|
|
D016706||adult onset still disease
|
|
D016706||adult onset still apos s disease
|
|
D016706||adult onset stills disease
|
|
D016706||still disease adult onset
|
|
D016706||stills disease adult onset
|
|
C565249|606217||atrioventricular septal defect partial with heterotaxy syndrome
|
|
C565249|606217||atrioventricular septal defect susceptibility to 2 avsd2 atrioventricular septal defect partial with heterotaxy syndrome
|
|
C565249|606217|C567485|300123|C567429|612069|C537139|600376|606346||included
|
|
C536898||thrombocytopenia robin sequence
|
|
C536898||braddock carey syndrome
|
|
C535566||absent corpus callosum cataract immunodeficiency
|
|
C535566||vici syndrome
|
|
C536899||thrombocytopenia cyclic
|
|
C535565||absent breasts and nipples
|
|
C535565||athelia
|
|
C535565||complete absence of breasts
|
|
C536896||tamari goodman syndrome
|
|
C536896||congenital heart disease radio ulnar synostos mental retardation
|
|
C536896||upper limb cardiovascular syndromes
|
|
C536897||tang hsi ryu syndrome
|
|
C536897||ascitis splenomegaly lymphadenopathy
|
|
C536897||polyneuropathy hepatosplenomegaly hyperpigmentation
|
|
C536897||syndrome of polyneuropathy skin hyperpigmentation oedema and hepatosplenomegaly
|
|
C535567||absent duct of santorini
|
|
C535567||absent accessory pancreatic duct of santorini
|
|
D010520|170650||aggressive periodontitis
|
|
D010520|170650||circumpubertal periodontitis
|
|
D010520|170650||early onset periodontitis
|
|
D010520|170650||jp
|
|
D010520|170650|239000||jpd
|
|
D010520|170650||juvenile periodontitis
|
|
D010520|170650||periodontitis aggressive
|
|
D010520|170650||periodontitis aggressive 1
|
|
D010520|170650||periodontitis circumpubertal
|
|
D010520|170650||periodontitis juvenile
|
|
D010520|170650||periodontitis prepubertal
|
|
D010520|170650||periodontoses
|
|
D010520|170650||periodontosis
|
|
D010520|170650||ppp
|
|
D010520|170650||prepubertal periodontitis
|
|
C563475|167400||paroxysmal extreme pain disorder
|
|
C563475|167400||familial rectal pain
|
|
C563475|167400||pain submandibular ocular and rectal with flushing
|
|
C563475|167400||pain submandibular ocular wnd rectal with flushing
|
|
C563475|167400||pepd
|
|
C563475|167400||pexpd
|
|
C563475|167400||rectal pain familial
|
|
C563475|167400||submandibular ocular and rectal pain with flushing
|
|
C535569||abuse dwarfism syndrome
|
|
C535569||child abuse dwarfism
|
|
C535569||psychosocial dwarfism
|
|
C535580||najjar syndrome
|
|
C535580||cardiogenital syndrome
|
|
C535580||genital anomaly with cardiomyopathy
|
|
C567651|613307||deafness autosomal recessive 79
|
|
C567651|613307||dfnb79
|
|
D003409||congenital hypothyroidism
|
|
D003409||cretinism
|
|
D003409||cretinism endemic
|
|
D003409||endemic cretinism
|
|
D003409||fetal iodine deficiency disorder
|
|
D003409||hypothyroidism congenital
|
|
D003409||myxedema congenital
|
|
D053627||asthenozoospermia
|
|
604117|C565826||vohwinkel syndrome variant form
|
|
604117|C565826||loricrin keratoderma
|
|
604117|C565826||mutilating keratoderma with ichthyosis
|
|
604117|C565826||vohwinkel syndrome with ichthyosis
|
|
C535582||cardiomyopathy hypogonadism collagenoma syndrome
|
|
204200|D009472||neuronal ceroid lipofuscinoses
|
|
204200|D009472||adult neuronal ceroid lipofuscinosis
|
|
204200|D009472||amaurotic idiocy adult type
|
|
204200|D009472||batten disease
|
|
204200|D009472||batten disease juvenile
|
|
204200|D009472||batten diseases juvenile
|
|
204200|D009472||batten mayou disease
|
|
204200|D009472||batten spielmeyer vogt disease
|
|
204200|D009472||cerebroretinal degeneration juvenile
|
|
204200|D009472||cerebroretinal degenerations juvenile
|
|
204200|D009472||ceroid lipofuscinoses cln3 related neuronal
|
|
204200|D009472||ceroid lipofuscinosis cln3 related neuronal
|
|
204200|D009472||ceroid lipofuscinosis neuronal
|
|
204200|D009472||ceroid lipofuscinosis neuronal 3
|
|
204200|D009472||ceroid lipofuscinosis neuronal 3 juvenile
|
|
204200|D009472||ceroid lipofuscinosis neuronal 4
|
|
204200|D009472||ceroid lipofuscinosis neuronal 4a autosomal recessive
|
|
204200|D009472||ceroid lipofuscinosis neuronal 4b autosomal dominant
|
|
204200|D009472||ceroid lipofuscinosis neuronal parry type
|
|
204200|D009472||ceroid storage disease
|
|
204200|D009472||ceroid storage diseases
|
|
204200|D009472||cln3
|
|
204200|D009472||cln3 related neuronal ceroid lipofuscinoses
|
|
204200|D009472||cln3 related neuronal ceroid lipofuscinosis
|
|
204200|D009472||cln4a
|
|
204200|D009472||cln4as
|
|
204200|D009472||cln4b
|
|
204200|D009472||cln4bs
|
|
204200|D009472||disease ceroid storage
|
|
204200|D009472||disease juvenile batten
|
|
204200|D009472||disease kuf apos s
|
|
204200|D009472||disease lipofuscin storage
|
|
204200|D009472||diseases ceroid storage
|
|
204200|D009472||diseases juvenile batten
|
|
204200|D009472||diseases kuf apos s
|
|
204200|D009472||diseases lipofuscin storage
|
|
204200|D009472||disease spielmeyer sjogren
|
|
204200|D009472||diseases spielmeyer sjogren
|
|
204200|D009472||diseases vogt spielmeyer
|
|
204200|D009472||disease vogt spielmeyer
|
|
204200|D009472||infantile neuronal ceroid lipofuscinosis
|
|
204200|D009472||jansky bielschowsky disease
|
|
204200|D009472||jncl
|
|
204200|D009472||juvenile batten disease
|
|
204200|D009472||juvenile batten diseases
|
|
204200|D009472||juvenile cerebroretinal degeneration
|
|
204200|D009472||juvenile cerebroretinal degenerations
|
|
204200|D009472||juvenile neuronal ceroid lipofuscinosis
|
|
204200|D009472||kuf disease
|
|
204200|D009472||kuf apos s disease
|
|
204200|D009472||kufs disease
|
|
204200|D009472||kufs disease autosomal dominant
|
|
204200|D009472||kufs disease autosomal recessive
|
|
204200|D009472||kuf apos s diseases
|
|
204200|D009472||kufs type neuronal ceroid lipofuscinosis
|
|
204200|D009472||late infantile neuronal ceroid lipofuscinosis
|
|
204200|D009472||lipofuscinosis neuronal ceroid
|
|
204200|D009472||lipofuscin storage disease
|
|
204200|D009472||lipofuscin storage diseases
|
|
204200|D009472||neuronal ceroid lipofuscinoses cln3 related
|
|
204200|D009472||neuronal ceroid lipofuscinosis
|
|
204200|D009472||neuronal ceroid lipofuscinosis adult
|
|
204200|D009472||neuronal ceroid lipofuscinosis adult type
|
|
204200|D009472||neuronal ceroid lipofuscinosis cln3 related
|
|
204200|D009472||neuronal ceroid lipofuscinosis infantile
|
|
204200|D009472||neuronal ceroid lipofuscinosis juvenile
|
|
204200|D009472||neuronal ceroid lipofuscinosis juvenile type
|
|
204200|D009472||neuronal ceroid lipofuscinosis late infantile
|
|
204200|D009472||santavuori haltia disease
|
|
204200|D009472||spielmeyer disease vogt
|
|
204200|D009472||spielmeyer sjogren disease
|
|
204200|D009472||spielmeyer sjogren diseases
|
|
204200|D009472||spielmeyer vogt disease
|
|
204200|D009472||storage disease ceroid
|
|
204200|D009472||storage disease lipofuscin
|
|
204200|D009472||storage diseases ceroid
|
|
204200|D009472||storage diseases lipofuscin
|
|
204200|D009472||vogt spielmeyer disease
|
|
204200|D009472||vogt spielmeyer diseases
|
|
C535584||cardiomyopathy infantile histiocytoid
|
|
C535584||cardiomyopathy focal lipid
|
|
C535584||cardiomyopathy infantile xanthomatous
|
|
C535584||cardiomyopathy oncocytic
|
|
C535584||foamy myocardial transformation of infancy
|
|
C535584||focal lipid cardiomyopathy
|
|
C535584||infantile xanthomatous cardiomyopathy
|
|
C535584||oncocytic cardiomyopathy
|
|
C535586||carnevale syndrome
|
|
C535586||carnevale krajewska fischetto syndrome
|
|
C535586||oculo skeletal abdominal syndrome
|
|
C535586||ptosis of eyelids with diastasis recti and hip dysplasia
|
|
C535585||carnevale hernandez castillo syndrome
|
|
C535585||triphalyngeal thumbs and brachyectrodactyly
|
|
C566914|611571||otosclerosis 4
|
|
C566914|611571||otsc4
|
|
C535577||cardioauditory syndrome of sanchez cascos
|
|
C535577||sanchez cascos cardioauditory syndrome
|
|
D016710||yin deficiency
|
|
D016710||deficiency yin
|
|
D016710||hsu yin
|
|
D016710||xu yin
|
|
D016710||yin deficiencies
|
|
D016710||yin hsu
|
|
D016710||yinxu
|
|
D016710||yin xu
|
|
D016711||yang deficiency
|
|
D016711||deficiency yang
|
|
D016711||hsu yang
|
|
D016711||xu yang
|
|
D016711||yang hsu
|
|
D016711||yangxu
|
|
D016711||yang xu
|
|
C535578||cardiocranial syndrome
|
|
C535578||pfeiffer cardiocranial syndrome
|
|
C535578||pfeiffer singer zschiesche syndrome
|
|
C535578||pfeiffer syndrome 2
|
|
C535578||pfeiffer type cardiocranial syndrome
|
|
C565737|604901||north american indian childhood cirrhosis
|
|
C565737|604901||naic
|
|
C535591||chromosome 1 monosomy 1p
|
|
C535591||deletion 1p
|
|
C535591||monosomy 1p
|
|
C535590||carrington syndrome
|
|
C535590||carrington apos s disease
|
|
C535590||carrington apos s pulmonary eosinophilia
|
|
C535590||chronic eosinophilic pneumonia cep
|
|
C535590||chronic idiopathic eosinophilic pneumonia
|
|
C535590||eosinophilic idiopathic chronic pneumopathy
|
|
C535593||chromosome 1 monosomy 1p31 p22
|
|
C535593||deletion 1p31 p22
|
|
C535593||monosomy 1p31 p22
|
|
D054969||primary dysautonomias
|
|
D054969||dysautonomia
|
|
D054969||dysautonomia primary
|
|
D054969||dysautonomias
|
|
D054969||dysautonomias primary
|
|
D054969||primary dysautonomia
|
|
C567588|300778||corneal dystrophy lisch epithelial
|
|
C567588|300778||band shaped and whorled microcystic corneal epithelial dystrophy
|
|
C567588|300778||lecd
|
|
C567588|300778||lisch epithelial corneal dystrophy
|
|
C535592||chromosome 1 monosomy 1p22 p13
|
|
C535592||deletion 1p22 p13
|
|
C535592||monosomy 1p22 p13
|
|
C535595||chromosome 1 monosomy 1p34 p32
|
|
C535595||deletion 1p34 p32
|
|
C535595||monosomy 1p34 p32
|
|
D004701||endocrine gland neoplasms
|
|
D004701||cancer endocrine
|
|
D004701||cancer endocrine gland
|
|
D004701||cancer of endocrine gland
|
|
D004701||cancer of the endocrine gland
|
|
D004701||cancers endocrine
|
|
D004701||carcinoma endocrine gland
|
|
D004701||carcinoma of endocrine gland
|
|
D004701||endocrine cancer
|
|
D004701||endocrine cancers
|
|
D004701||endocrine gland cancer
|
|
D004701||endocrine gland carcinoma
|
|
D004701||endocrine gland neoplasm
|
|
D004701||neoplasm endocrine gland
|
|
D004701||neoplasms endocrine gland
|
|
C535594||chromosome 1 monosomy 1p32
|
|
C535594||deletion 1p32
|
|
C535594||monosomy 1p32
|
|
C535597||craniotelencephalic dysplasia
|
|
C535597||complex of anomalies involving the cranium and brain
|
|
C535596||chromosome 1 monosomy 1q25 q32
|
|
C535596||deletion 1q25 q32
|
|
C535596||monosomy 1q25 q32
|
|
D004700||endocrine system diseases
|
|
D004700||disease endocrine
|
|
D004700||disease endocrine system
|
|
D004700||diseases endocrine
|
|
D004700||diseases endocrine system
|
|
D004700||diseases of endocrine system
|
|
D004700||endocrine disease
|
|
D004700||endocrine diseases
|
|
D004700||endocrine system disease
|
|
D004700||system disease endocrine
|
|
D004700||system diseases endocrine
|
|
C537465|300166||microphthalmia syndromic 2
|
|
C537465|300166||anop2 formerly
|
|
C537465|300166||cataracts microphthalmia radiculomegaly and septal heart defects
|
|
C537465|300166||maa2 formerly
|
|
C537465|300166||marashi gorlin syndrome
|
|
C537465|300166||mcops2
|
|
C537465|300166||microphthalmia cataracts radiculomegaly and septal heart defects
|
|
C537465|300166||oculo facio cardio dental syndrome
|
|
C537465|300166||oculofaciocardiodental syndrome
|
|
C537465|300166||ofcd syndrome
|
|
C535589||carnitine palmitoyl transferase 2 deficiency
|
|
C535589||carnitine palmitoyltransferase 2 deficiency
|
|
C535589||carnitine palmitoyltransferase deficiency type 2
|
|
C535589||carnitine palmitoyltransferase ii deficiency
|
|
C535589||cpt2 deficiency
|
|
C535589||cpt ii deficiency
|
|
C535589||muscle form of carnitine palmitoyltransferase deficiency
|
|
182000|D017492||keratosis seborrheic
|
|
182000|D017492||keratoses seborrheic
|
|
182000|D017492||keratosis seborrheica
|
|
182000|D017492||seborrheic keratoses
|
|
182000|D017492||seborrheic keratosis
|
|
D004716||endometritis
|
|
D004716||endomyometritis
|
|
C567554|612841||hypotrichosis 5
|
|
C567554|612841||hypt5
|
|
C567554|612841||marie unna hereditary hypotrichosis 2
|
|
C567554|612841||muhh2
|
|
D004719||endomyocardial fibrosis
|
|
D004719||endomyocardial fibroses
|
|
D004719||fibroses endomyocardial
|
|
D004719||fibrosis endomyocardial
|
|
D004714||endometrial hyperplasia
|
|
D004714||atypical endometrial hyperplasia
|
|
D004714||atypical endometrial hyperplasias
|
|
D004714||complex endometrial hyperplasia
|
|
D004714||complex endometrial hyperplasias
|
|
D004714||endometrial hyperplasia atypical
|
|
D004714||endometrial hyperplasia complex
|
|
D004714||endometrial hyperplasias
|
|
D004714||endometrial hyperplasias atypical
|
|
D004714||endometrial hyperplasias complex
|
|
D004714||endometrial hyperplasia simple
|
|
D004714||endometrial hyperplasias simple
|
|
D004714||hyperplasia atypical endometrial
|
|
D004714||hyperplasia complex endometrial
|
|
D004714||hyperplasia endometrial
|
|
D004714||hyperplasias atypical endometrial
|
|
D004714||hyperplasias complex endometrial
|
|
D004714||hyperplasias endometrial
|
|
D004714||hyperplasia simple endometrial
|
|
D004714||hyperplasias simple endometrial
|
|
D004714||simple endometrial hyperplasia
|
|
D004714||simple endometrial hyperplasias
|
|
201300|C567738|613115||neuropathy hereditary sensory and autonomic type iia
|
|
201300|C567738|613115||hsan2a
|
|
201300|C567738|613115||hsan iia
|
|
201300|C567738|613115||hsn2a
|
|
201300|C567738|613115||hsn iia
|
|
201300|D013595||morvan disease
|
|
201300|C567738|613115||neuropathy hereditary sensory type iia
|
|
D054970||pure autonomic failure
|
|
D054970||autonomic failure pure
|
|
D054970||bradbury eggleston syndrome
|
|
D054970||syndrome bradbury eggleston
|
|
C566239|108800||atrial septal defect 1
|
|
C566239|108800||asd1
|
|
C566239|108800||asd ii included
|
|
C566239|108800||asd i included
|
|
C566239|108800||atrial septal defect primum type included
|
|
C566239|108800||atrial septal defect secundum type included
|
|
D019851|188050||thrombophilia
|
|
D019851|188050||hypercoagulabilities
|
|
D019851|188050||hypercoagulability
|
|
D019851|188050||thph1
|
|
D019851|188050||thrombophilia due to factor 2 defect
|
|
D019851|188050||thrombophilia due to thrombin defect
|
|
D019851|188050||thrombophilias
|
|
D019851|188050||venous thromboembolism thrombosis protection against included
|
|
D019851|188050|D020246||venous thrombosis
|
|
D054973||perivascular epithelioid cell neoplasms
|
|
D054973||ccmmt
|
|
D054973||clear cell myomelanocytic tumor
|
|
D054973||clear cell myomelanocytic tumors
|
|
D054973||clear cell sugar tumor
|
|
D054973||clear cell sugar tumors
|
|
D054973||myomelanocytic tumor clear cell
|
|
D054973||myomelanocytic tumors clear cell
|
|
D054973||neoplasms perivascular epithelioid cell
|
|
D054973||pecoma
|
|
D054973||pecomas
|
|
D054973||perivascular epithelioid cell tumors
|
|
D054973||sugar tumor clear cell
|
|
D054973||sugar tumors clear cell
|
|
D054973||tumor clear cell myomelanocytic
|
|
D054973||tumor clear cell sugar
|
|
D054973||tumors clear cell myomelanocytic
|
|
D054973||tumors clear cell sugar
|
|
C537734|164280||oculodigitoesophagoduodenal syndrome
|
|
C537734|164280||brunner winter syndrome
|
|
C537734|164280||digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
|
|
C537734|164280||feingold syndrome
|
|
C537734|164280||feingold syndrome 1
|
|
C537734|164280||fglds1
|
|
C537734|164280||microcephaly and digital abnormalities with normal intelligence
|
|
C537734|164280||microcephaly mental retardation and tracheoesophageal fistula syndrome
|
|
C537734|164280||microcephaly mesobrachyphalangy tracheoesophageal fistula mmt syndrome
|
|
C537734|164280||microcephaly oculo digito esophageal duodenal moded syndrome
|
|
C537734|164280||microcephaly oculo digito esophageal duodenal syndrome
|
|
C537734|164280||mmt syndrome
|
|
C537734|164280||moded
|
|
C537734|164280||oculo digito esophagoduodental oded syndrome
|
|
C537734|164280||oded
|
|
C537734|164280||oded syndrome
|
|
D054972||postural orthostatic tachycardia syndrome
|
|
D054972||postural tachycardia syndrome
|
|
D054972||syndrome postural tachycardia
|
|
D054972||tachycardia syndrome postural
|
|
C564099||mental retardation with spastic paraplegia
|
|
238600||hyperlipoproteinemia type i lipoprotein lipase deficiency
|
|
238600|207750|D008072||lpl deficiency
|
|
238600|207750|D008072||hyperchylomicronemia familial
|
|
238600|207750|D008072||hyperlipemia idiopathic burger grutz type
|
|
238600|207750|D008072||hyperlipemia essential familial
|
|
238600|207750|D008072||lipase d deficiency
|
|
238600|207750|D008072||lipd deficiency
|
|
238600|207750|D008072||hyperlipoproteinemia type ia
|
|
238600|207750|D008072||chylomicronemia familial
|
|
C535530||interferon gamma receptor 1 deficiency
|
|
C576084||bleeding disorder due to p2rx1 defect
|
|
C538361|267500||reticular dysgenesis
|
|
C538361|267500||aleukocytosis
|
|
C538361|267500||congenital aleukia
|
|
C538361|267500||devaal disease
|
|
C538361|267500||de vaal disease
|
|
C538361|267500||hematopoietic hypoplasia generalized
|
|
C538361|267500||immunoerythromyeloid hypoplasia
|
|
C538361|267500||reticular dysgenesia
|
|
C538361|267500||severe combined immunodeficiency with leukopenia
|
|
C536970|314300||torticollis keloids cryptorchidism renal dysplasia
|
|
C536970|314300||goeminne syndrome
|
|
C536970|314300||tkc
|
|
C536970|314300||tkcr
|
|
C536970|314300||tkcr syndrome
|
|
C536970|314300||torticollis keloids cryptorchidism and renal dysplasia
|
|
C537404|262400||pituitary dwarfism 1
|
|
C537404|262400||growth hormone deficiency isolated autosomal recessive
|
|
C537404|262400||ighd1a
|
|
C537404|262400||ighd ia
|
|
C537404|262400||illig type growth hormone deficiency
|
|
C537404|262400||isolated growth hormone deficiency type 1b
|
|
C537404|262400||isolated growth hormone deficiency type ia
|
|
C537404|262400||nanism due to growth hormone isolated deficiency
|
|
C537404|262400||pituitary dwarfism i
|
|
C537404|262400||primordial dwarfism
|
|
C537404|262400||sexual ateleiotic dwarfism
|
|
D012779|263520||short rib polydactyly syndrome
|
|
D012779|263520||majewski syndrome
|
|
D012779|263520||polydactyly with neonatal chondrodystrophy type 1
|
|
D012779|263520||polydactyly with neonatal chondrodystrophy type 2
|
|
D012779|263520||polydactyly with neonatal chondrodystrophy type ii
|
|
D012779|263520||short rib polydactyly syndrome majewski type
|
|
D012779|263520||short rib polydactyly syndromes
|
|
D012779|263520||short rib polydactyly syndrome saldino noonan type
|
|
D012779|263520||short rib polydactyly syndrome type 1
|
|
D012779|263520||short rib polydactyly syndrome type ii
|
|
D012779|263520||short rib polydactyly syndrome type iia
|
|
D012779|263520||short rib thoracic dysplasia 6 with or without polydactyly
|
|
D012779|263520||srps2a
|
|
D012779|263520||srps type ii
|
|
D012779|263520||srtd6
|
|
D012779|263520||syndrome majewski
|
|
D012779|263520||syndrome saldino noonan
|
|
D012779|263520||syndrome short rib polydactyly
|
|
C536855||fanconi like syndrome
|
|
D053653||pyelocystitis
|
|
D053653||cystopyelitis
|
|
C536852||familial streblodactyly
|
|
C536852||crooked little finger familial
|
|
C536852||minor streblomicrodactyly familial
|
|
C535524||infantile polymyoclonus
|
|
C535524||polymyoclonus infantile
|
|
C535523||infantile onset spinocerebellar ataxia
|
|
C535523|271245||ohaha syndrome
|
|
C535523|271245||ophthalmoplegia hypotonia ataxia hypacusis and athetosis
|
|
C535523|271245||spinocerebellar ataxia infantile with sensory neuropathy
|
|
C535526||infection with mycobacterium marinum
|
|
C535526||fish tank granuloma
|
|
C535526||mycobacterium marinum infection
|
|
D054989||nephrogenic fibrosing dermopathy
|
|
D054989||dermopathies nephrogenic fibrosing
|
|
D054989||dermopathy nephrogenic fibrosing
|
|
D054989||fibroses nephrogenic systemic
|
|
D054989||fibrosing dermopathies nephrogenic
|
|
D054989||fibrosing dermopathy nephrogenic
|
|
D054989||fibrosis nephrogenic systemic
|
|
D054989||nephrogenic fibrosing dermopathies
|
|
D054989||nephrogenic systemic fibroses
|
|
D054989||nephrogenic systemic fibrosis
|
|
D054989||systemic fibroses nephrogenic
|
|
D054989||systemic fibrosis nephrogenic
|
|
D054988||idiopathic interstitial pneumonias
|
|
D054988||idiopathic interstitial pneumonia
|
|
D054988||interstitial pneumonia idiopathic
|
|
D054988||interstitial pneumonias idiopathic
|
|
D054988||pneumonia idiopathic interstitial
|
|
D054988||pneumonias idiopathic interstitial
|
|
C535528||infundibulopelvic dysgenesis
|
|
605711||multiple mitochondrial dysfunctions syndrome 1
|
|
605711||mmds
|
|
605711||mmds1
|
|
C563888|608645||deafness autosomal dominant 31
|
|
C563888|608645||dfna31
|
|
C536873||spastic paraplegia with kallmann syndrome
|
|
C536873||familial spastic paraplegia with kallmann apos s syndrome
|
|
C536873||kallmann syndrome with spastic paraplegia
|
|
C536873||spastic paraplegia kallmann syndrome
|
|
C536870||spastic paraplegia neuropathy poikiloderma
|
|
C536870||familial spastic paraplegia with neuropathy and poikiloderma
|
|
C536870||spastic paraplegia with neuropathy and poikiloderma
|
|
C535542||isotretinoin embryopathy like syndrome
|
|
C535542||isotretinoin teratogen syndrome
|
|
C535542||microtia aortic arch syndrome
|
|
C535542||syndrome of microtia and aortic arch anomalies
|
|
D058747|214800||charge syndrome
|
|
D058747|214800||association charge
|
|
D058747|214800||associations charge
|
|
D058747|214800||charge association
|
|
D058747|214800||charge association coloboma heart anomaly choanal atresia retardation genital and ear anomalies
|
|
D058747|214800||charge associations
|
|
D058747|214800||charge syndrome familial
|
|
D058747|214800||charge syndromes
|
|
D058747|214800||charge syndromes familial
|
|
D058747|214800||familial charge syndrome
|
|
D058747|214800||familial charge syndromes
|
|
D058747|214800||hall hittner syndrome
|
|
D058747|214800||syndrome charge
|
|
D058747|214800||syndrome hall hittner
|
|
164160||leptin
|
|
164160||lep obese mouse homolog of
|
|
164160||ob
|
|
214300|C536888||klippel feil syndrome recessive type
|
|
214300|C536888||cervical vertebral fusion autosomal recessive
|
|
214300|C536888||kfs2
|
|
214300|C536888||kfs autosomal recessive
|
|
214300|C536888||klippel feil syndrome 2 autosomal recessive
|
|
214300|C536888||klippel feil syndrome autosomal recessive
|
|
610297||parkinson disease 13 autosomal dominant susceptibility to
|
|
610297|C565204||park13
|
|
C536489|602083||usher syndrome type 1f
|
|
C536489|602083||ush1f
|
|
C536489|602083|C566586||usher syndrome type if
|
|
C548841||parasitic infection caused by dracunculus medinensis
|
|
C535533||intrahepatic cholangiocarcinoma
|
|
C563020|105580||anal canal carcinoma
|
|
C563020|105580||cloacogenic carcinoma included
|
|
C535534||iridogoniodysgenesis and skeletal anomalies
|
|
C536869||spastic paraplegia epilepsy mental retardation
|
|
C536869||spastic paraplegia epilepsy and mental retardation
|
|
C535537||iris dysplasia hypertelorism deafness
|
|
C565533|233690||granulomatous disease chronic autosomal recessive cytochrome b negative
|
|
C565533|233690||cgd autosomal recessive cytochrome b negative
|
|
C565533|233690||cgd due to deficiency of the alpha subunit of cytochrome b
|
|
C565533|233690||chronic granulomatous disease autosomal recessive cytochrome b negative
|
|
C565533|233690||chronic granulomatous disease due to deficiency of the alpha subunit of cytochrome b
|
|
C565533|233690||cyba deficiency
|
|
C535539||irons bhan syndrome
|
|
C535539||autosomal recessive syndrome of lymphedema hydroceles atrial septal defect and characteristic facial changes
|
|
C535539||lymphedema atrial septal defect and characteristic facial changes
|
|
C564078||pierre robin sequence with facial and digital anomalies
|
|
300559|C564485||glycogen storage disease type ixd
|
|
300559|C564485||gsd9d
|
|
300559|C564485||gsd ixd
|
|
300559|C564485||muscle glycogenosis x linked
|
|
300559|C564485||muscle phosphorylase kinase deficiency
|
|
C536883||king denborough syndrome
|
|
C536883||anesthetic induced malignant hyperpyrexia in children
|
|
C536883||king syndrome
|
|
C535551||pemphigus and fogo selvagem
|
|
C535551||brazilian pemphigus
|
|
C535551||brazilian pemphigus foliaceus
|
|
C535551||endemic pemphigus foliaceus
|
|
C535551||south american pemphigus
|
|
C536884||kleeblattschaedel syndrome
|
|
C536884||cloverleaf skull syndrome
|
|
C536884||kleeblattschaedel deformity syndrome
|
|
305100|D053358||ectodermal dysplasia 1 anhidrotic
|
|
305100|D053358||anhidrotic ectodermal dysplasia x linked
|
|
305100|D053358||anhydrotic ectodermal dysplasia x linked
|
|
305100|D053358||christ siemens touraine syndrome
|
|
305100|D053358||cst syndrome
|
|
305100|D053358||cst syndromes
|
|
305100|D053358||dysplasia 1 ectodermal
|
|
305100|D053358||ectd1
|
|
305100|D053358||ectodermal dysplasia 1
|
|
305100|D053358||ectodermal dysplasia 1 anhydrotic
|
|
305100|D053358||ectodermal dysplasia 1 hypohidrotic hair tooth type x linked
|
|
305100|D053358||ectodermal dysplasia 1 hypohidrotic x linked
|
|
305100|D053358||ectodermal dysplasia 1s
|
|
305100|D053358||ectodermal dysplasia anhidrotic x linked
|
|
305100|D053358||ectodermal dysplasia hypohidrotic 1
|
|
305100|D053358||ectodermal dysplasia hypohidrotic x linked
|
|
305100|D053358||ectodermal dysplasia hypohydridic x linked
|
|
305100|D053358||ed1
|
|
305100|D053358||eda1
|
|
305100|D053358||hed1
|
|
305100|D053358||hypohidrotic ectodermal dysplasia
|
|
305100|D053358||syndrome cst
|
|
305100|D053358||syndromes cst
|
|
305100|D053358||xhed
|
|
305100|D053358||xlhed
|
|
305100|D053358||x linked hypohydridic ectodermal dysplasia
|
|
C535550|260660||pelviscapular dysplasia
|
|
C535550|260660||cousin syndrome
|
|
C535550|260660||craniofacial dysmorphism hypoplasia of scapula and pelvis and short stature
|
|
C535550||pelvic shoulder dysplasia
|
|
C536881||spinal muscular atrophy ryukyuan type
|
|
C536881||ryukyuan muscular atrophy
|
|
C535553||abdominal cystic lymphangioma
|
|
C535553||abdominal retroperitoneal lymphangioma
|
|
C535553||retroperitoneal cystic lymphangioma
|
|
C535552||abdominal chemodectomas with cutaneous angiolipomas
|
|
C535552||chemodectoma intraabdominal with cutaneous angiolipomas
|
|
C535552||familial abdominal chemodectomas with cutaneous angiolipomas
|
|
C536582|203740||alpha ketoglutarate dehydrogenase deficiency
|
|
C536582|203740||2 alpha ketoglutarate dehydrogenase deficiency
|
|
C536582|203740||2 ketoglutarate dehydrogenase deficiency
|
|
C536582|203740||alpha kgd deficiency
|
|
C536582|203740||oxoglutaricaciduria
|
|
C536582|203740||oxoglutaric aciduria
|
|
C535750|608776||congenital disorder of glycosylation type 1l
|
|
C535750|608776||cdg1l
|
|
C535750|608776||cdgil
|
|
C535750|608776||cdg il
|
|
C535750|608776||congenital disorder of glycosylation type il
|
|
D008268||macular degeneration
|
|
D008268||age related macular degeneration
|
|
D008268||age related macular degenerations
|
|
D008268||age related maculopathies
|
|
D008268||age related maculopathy
|
|
D008268||degeneration age related macular
|
|
D008268||degeneration macular
|
|
D008268||degenerations age related macular
|
|
D008268||degenerations macular
|
|
D008268||dystrophies macular
|
|
D008268||dystrophy macular
|
|
D008268||macular degeneration age related
|
|
D008268||macular degenerations
|
|
D008268||macular degenerations age related
|
|
D008268||macular dystrophies
|
|
D008268||macular dystrophy
|
|
D008268||maculopathies age related
|
|
D008268||maculopathy age related
|
|
D008275||magnesium deficiency
|
|
D008275||deficiencies magnesium
|
|
D008275||deficiency magnesium
|
|
D008275||magnesium deficiencies
|
|
C567059|610755||multiple endocrine neoplasia type iv
|
|
C567059|610755||men4
|
|
C562618|612740||porphyria acute hepatic
|
|
C562618|612740||alad deficiency
|
|
C562618|612740||delta aminolevulinate dehydratase deficiency
|
|
C562618|612740||doss porphyria
|
|
C562618|612740||doss porphyria lead poisoning susceptibility to included
|
|
C562618|612740||porphobilinogen synthase deficiency
|
|
C562618|612740||porphyria alad
|
|
114550|D006528||carcinoma hepatocellular
|
|
114550|D006528||adult liver cancer
|
|
114550|D006528||adult liver cancers
|
|
114550|D006528||cancer adult liver
|
|
114550|D006528||cancers adult liver
|
|
114550|D006528||carcinoma liver cell
|
|
114550|D006528||carcinomas hepatocellular
|
|
114550|D006528||carcinomas liver cell
|
|
114550|D006528||cell carcinoma liver
|
|
114550|D006528||cell carcinomas liver
|
|
114550|D006528||hcc
|
|
114550|D006528||hepatoblastoma caused by somatic mutation included
|
|
114550|D006528||hepatocellular carcinoma
|
|
114550|D006528||hepatocellular carcinomas
|
|
114550|D006528||hepatoma
|
|
114550|D006528||hepatoma hepatoblastoma included
|
|
114550|D006528||hepatomas
|
|
114550|D006528||lcc
|
|
114550|D006528||liver cancer adult
|
|
114550|D006528||liver cancers adult
|
|
114550|D006528||liver cell carcinoma
|
|
114550|D006528||liver cell carcinoma adult
|
|
114550|D006528||liver cell carcinomas
|
|
D008271||mycetoma
|
|
D008271||actinomycetoma
|
|
D008271||actinomycetomas
|
|
D008271||eumycetoma
|
|
D008271||eumycetomas
|
|
D008271||foot madura
|
|
D008271||madura foot
|
|
D008271||maduromycoses
|
|
D008271||maduromycosis
|
|
D008271||mycetomas
|
|
607371|C537704||juvenile onset dystonia
|
|
607371|C537704||dystonia juvenile onset
|
|
C536874||spastic paraplegia with precocious puberty
|
|
C536874||familial spastic paraplegia mental retardation and precocious puberty
|
|
C536874||precocious puberty with spastic paraplegia
|
|
C562567|238320||leydig cell hypoplasia
|
|
C562567|238320||46 xy disorder of sex development due to lh defects
|
|
C562567|238320||hypergonadotropic hypogonadism male due to lhcgr defect
|
|
C562567|238320||hypergonadotropic hypogonadism male due to lhcgr defect included
|
|
C562567|238320||leydig cell agenesis
|
|
C562567|238320||leydig cell agenesis leydig cell hypoplasia type ii included
|
|
C562567|238320||leydig cell hypoplasia complete
|
|
C562567|238320||leydig cell hypoplasia partial
|
|
C562567|238320||leydig cell hypoplasia partial included
|
|
C562567|238320||leydig cell hypoplasia type i
|
|
C562567|238320||leydig cell hypoplasia type ii
|
|
C562567|238320||leydig cell hypoplasia with male pseudohermaphroditism
|
|
C562567|238320||lh resistance due to lh receptor deactivation
|
|
C562567|238320||luteinizing hormone resistance female
|
|
C562567|238320||luteinizing hormone resistance female included
|
|
C562567|238320||male hypergonadotropic hypogonadism due to lhcgr defect
|
|
146510|D054975||pallister hall syndrome
|
|
146510|D054975||cave complex
|
|
146510|D054975||cave complices
|
|
146510|D054975||cerebroacrovisceral early lethality complex
|
|
146510|D054975||complex cave
|
|
146510|D054975||complices cave
|
|
146510|D054975||hall pallister syndrome
|
|
146510|D054975||hamartoblastoma syndrome hypothalamic
|
|
146510|D054975||hamartoblastoma syndromes hypothalamic
|
|
146510|D054975||hypothalamic hamartoblastoma hypopituitarism imperforate anus and postaxial polydactyly
|
|
146510|D054975||hypothalamic hamartoblastoma syndrome
|
|
146510|D054975||hypothalamic hamartoblastoma syndromes
|
|
146510|D054975||pallister hall syndrome 1
|
|
146510|D054975||phs
|
|
146510|D054975||phs1
|
|
146510|D054975||syndrome hall pallister
|
|
146510|D054975||syndrome hypothalamic hamartoblastoma
|
|
146510|D054975||syndrome pallister hall
|
|
146510|D054975||syndromes hypothalamic hamartoblastoma
|
|
C536875||arrest of spermatogenesis
|
|
C536875||spermatogenesis arrest
|
|
C535548||pelvic dysplasia arthrogryposis of lower limbs
|
|
C535548||pelvic hypoplasia with arthrogryposis of lower limbs
|
|
C535548||pelvic hypoplasia with lower limb arthrogryposis
|
|
C536878||spinal intradural arachnoid cysts
|
|
C536878||arachnoid cysts spinal intradural
|
|
D010585||phagocyte bactericidal dysfunction
|
|
D010585||bactericidal dysfunction phagocyte
|
|
D010585||bactericidal dysfunctions phagocyte
|
|
D010585||dysfunction phagocyte bactericidal
|
|
D010585||dysfunctions phagocyte bactericidal
|
|
D010585||phagocyte bactericidal dysfunctions
|
|
C535549||pelvic lipomatosis
|
|
C564084||optic atrophy spastic paraplegia syndrome
|
|
C536890||hemiplegic migraine familial type 1
|
|
C536890||migraine familial hemiplegic 1 with progressive cerebellar ataxia
|
|
C535520|137920||renal cysts and diabetes syndrome
|
|
C535520|137920||cakut with diabetes
|
|
C535520|137920||congenital anomalies of the kidney and urinary tract with diabetes
|
|
C535520|137920||fjhn atypical
|
|
C535520|137920||glomerulocystic kidney disease hypoplastic type
|
|
C535520|137920||glomerulocystic kidney familial hypoplastic
|
|
C535520|137920||hyperuricemic nephropathy familial juvenile atypical
|
|
C535520|137920||maturity onset diabetes of the young type 5
|
|
C535520|137920||mody5
|
|
C535520|137920||rcad
|
|
D021921|185500||aortic stenosis supravalvular
|
|
D021921|185500||aortic supravalvular stenoses
|
|
D021921|185500||aortic supravalvular stenosis
|
|
D021921|185500||stenoses aortic supravalvular
|
|
D021921|185500||stenosis aortic supravalvular
|
|
D021921|185500||stenosis supravalvular aortic
|
|
D021921|185500||supravalvar aortic stenosis
|
|
D021921|185500|C538461||supravalvar aortic stenosis eisenberg type
|
|
D021921|185500||supravalvular aortic stenosis
|
|
D021921|185500||supravalvular stenoses aortic
|
|
D021921|185500||supravalvular stenosis aortic
|
|
D021921|185500||svas
|
|
C564088||nystagmus myoclonic
|
|
C536894||talo patello scaphoid osteolysis synovitis and short fourth metacarpals
|
|
C535562||absence of septum pellucidum
|
|
C536895||talonavicular coalition
|
|
C535561||congenital absence of gluteal muscles
|
|
C536892||kaplan plauchu fitch syndrome
|
|
C536892||acrocraniofacial dysostosis
|
|
C535564||absence of tibia with polydactyly
|
|
C535564||polydactyly with absent tibia
|
|
C535564||tibia absence of with polydactyly
|
|
C536893||kaplowitz bodurtha syndrome
|
|
C536893||congenital hypopituitarism and microphthalmia
|
|
C536893||hypopituitarism microphthalmia
|
|
C535932|147480||intrahepatic cholestasis of pregnancy
|
|
C535932|147480||cholestasis intrahepatic of pregnancy
|
|
C535932|147480||cholestasis intrahepatic of pregnancy 1
|
|
C535932|147480||cholestasis pregnancy related
|
|
C535932|147480||cholestasis pregnancy related 1
|
|
C535932|147480||familial intrahepatic cholestasis of pregnancy
|
|
C535932|147480||familial recurrent intrahepatic cholestasis of pregnancy
|
|
C535932|147480||icp1
|
|
C535932|147480||obstetric cholestasis
|
|
C535932|147480||pregnancy related cholestasis
|
|
C535932|147480||recurrent intrahepatic cholestasis of pregnancy
|
|
C567234|612621||mental retardation autosomal dominant 5
|
|
C567234|612621||mrd5
|
|
C566394|603284||cerebral cavernous malformations 2
|
|
C566394|603284||ccm2
|
|
D008289||malaria avian
|
|
D008289||avian malaria
|
|
D008289||avian malarias
|
|
D008289||malarias avian
|
|
D008286||malabsorption syndromes
|
|
D008286||malabsorption syndrome
|
|
D008286||syndrome malabsorption
|
|
D008286||syndromes malabsorption
|
|
D008287||malacoplakia
|
|
D008287||malacoplakias
|
|
D008287||malakoplakia
|
|
D008287||malakoplakias
|
|
C564090||neuropathy hereditary sensory x linked
|
|
D053682||tendon entrapment
|
|
D053682||entrapments tendon
|
|
D053682||entrapment tendon
|
|
D053682||stenosing tendovaginitides
|
|
D053682||stenosing tendovaginitis
|
|
D053682||stenosing tenosynovitides
|
|
D053682||stenosing tenosynovitis
|
|
D053682||stenosing tenovaginitides
|
|
D053682||stenosing tenovaginitis
|
|
D053682||tendon entrapments
|
|
D053682||tendovaginitides stenosing
|
|
D053682||tendovaginitis stenosing
|
|
D053682||tenosynovitides stenosing
|
|
D053682||tenosynovitis stenosing
|
|
D053682||tenovaginitides stenosing
|
|
D053682||tenovaginitis stenosing
|
|
C563838|608895||macular degeneration age related 3
|
|
C563838|608895||armd3
|
|
C535555||aberrant subclavian artery
|
|
C535555||aberrant left subclavian artery
|
|
C535555||aberrant right subclavian artery
|
|
C536885||kleiner holmes syndrome
|
|
C536885||hallux varus and preaxial polysyndactyly
|
|
C535557||ablepharon macrostomia syndrome
|
|
D053684||de quervain disease
|
|
D053684||de quervain apos s disease
|
|
D053684||de quervains disease
|
|
D053684||de quervain stenosing tenosynovitis
|
|
D053684||disease de quervain
|
|
D053684||stenosing tenosynovitis de quervain
|
|
D010591||phantom limb
|
|
D010591||limb pain phantom
|
|
D010591||limb pains phantom
|
|
D010591||limb phantom
|
|
D010591||limbs phantom
|
|
D010591||pain phantom
|
|
D010591||pain phantom limb
|
|
D010591||pains phantom
|
|
D010591||pains phantom limb
|
|
D010591||phantom limb pain
|
|
D010591||phantom limb pains
|
|
D010591||phantom limbs
|
|
D010591||phantom pain
|
|
D010591||phantom pains
|
|
D010591||phantom sensation
|
|
D010591||phantom sensations
|
|
D010591||pseudomelia
|
|
D010591||pseudomelias
|
|
D010591||sensation phantom
|
|
D010591||sensations phantom
|
|
C535559||abruzzo erickson syndrome
|
|
C535559||charge like syndrome x linked
|
|
C564098||modifier x linked for neurofunctional defects
|
|
C564098||tourette syndrome modifier of
|
|
C535558||abrikosov apos s tumor
|
|
C535558||abrikosoff apos s granulous cell tumor
|
|
C535558||abrikosoff apos s tumor
|
|
C535558||giant granulo cellular abrikosov apos s tumor
|
|
C535558||malignant variant of abrikosov apos s tumor
|
|
C564097||muscular dystrophy hemizygous lethal type
|
|
C536889||weber klippel trenaunay
|
|
C564096||muscular dystrophy mabry type
|
|
C537403|610954||pitt hopkins syndrome
|
|
C537403|610954||encephalopathy severe epileptic with autonomic dysfunction
|
|
C537403|610954||mental retardation syndromal with intermittent hyperventilation
|
|
C537403|610954||pths
|
|
190440||trigonocephaly 1
|
|
190440||trigno1
|
|
C564095||muscular dystrophy progressive pectorodorsal
|
|
C564095||muscular dystrophy progressive involving shoulder girdle and back
|
|
C564058||turner syndrome associated neurocognitive phenotype
|
|
C564056||split hand foot anomaly x linked
|
|
C564056||split hand foot malformation x linked
|
|
C565387||methylmalonyl coa epimerase deficiency with sepiapterin reductase deficiency
|
|
D015325|312170||pyruvate dehydrogenase complex deficiency disease
|
|
D015325|312170||ataxia intermittent with abnormal pyruvate metabolism
|
|
D015325|312170||ataxia intermittent with pyruvate dehydrogenase deficiency
|
|
D015325|312170||ataxia intermittent with pyruvate dehydrogenase or decarboxylase deficiency
|
|
D015325|312170||ataxia with lactic acidosis
|
|
D015325|312170||ataxia with lactic acidosis i
|
|
D015325|312170||ataxia with lactic acidosis i lactic acidemia thiamine responsive included
|
|
D015325|312170||ataxia with lactic acidosis type i
|
|
D015325|312170||deficiency pdh
|
|
D015325|312170||deficiency pdhc
|
|
D015325|312170||deficiency pyruvate decarboxylase
|
|
D015325|312170||deficiency pyruvate dehydrogenase
|
|
D015325|312170||intermittent ataxia with pyruvate dehydrogenase deficiency
|
|
D015325|312170||juvenile pyruvate dehydrogenase complex deficiency disease
|
|
D015325|312170||lactic acidosis with ataxia type i
|
|
D015325|312170||neonatal pyruvate dehydrogenase complex deficiency disease
|
|
D015325|312170||pdhad
|
|
D015325|312170||pdhc deficiency
|
|
D015325|312170||pdhc deficiency disease
|
|
D015325|312170||pdh deficiency
|
|
D015325|312170||pyruvate decarboxylase deficiency
|
|
D015325|312170||pyruvate dehydrogenase complex deficiency
|
|
D015325|312170||pyruvate dehydrogenase complex deficiency disease juvenile
|
|
D015325|312170||pyruvate dehydrogenase complex deficiency disease neonatal
|
|
D015325|312170||pyruvate dehydrogenase deficiency
|
|
D015325|312170|C564071||pyruvate dehydrogenase e1 alpha deficiency
|
|
D015325|312170||type i ataxia with lactic acidosis
|
|
C564697|606554||episodic ataxia type 3
|
|
C564697|606554||ataxia episodic with vertigo and tinnitus
|
|
C564697|606554||ea3
|
|
C565754|604717||deafness autosomal dominant 20
|
|
C565754|604717||dfna20
|
|
C565754|604717||dfna26
|
|
C536818||giant mammary hamartoma
|
|
C536818||giant hamartoma of the breast
|
|
C536819||giant pigmented hairy nevus
|
|
C536817||al gazali syndrome
|
|
611091|C567018||mental retardation autosomal recessive 5
|
|
611091|C567018||mrt5
|
|
C565393||3 methylglutaconic aciduria type iv
|
|
C565393||mga4
|
|
C565393||mga type iv
|
|
C536810||chromosome 3 monosomy 3q27
|
|
C536810||deletion 3q27
|
|
C536810||monosomy 3q27
|
|
C536811||chromosome 3 trisomy 3p
|
|
C536811||duplication 3p
|
|
C536811||trisomy 3p
|
|
C565395||metaphyseal dysplasia anetoderma and optic atrophy
|
|
C565396||metaphyseal dysostosis mental retardation and conductive deafness
|
|
C535420|601382||charcot marie tooth disease type 4b1
|
|
C535420|601382||charcot marie tooth disease autosomal recessive with focally folded myelin sheaths autosomal recessive type 4b1
|
|
C535420|601382||charcot marie tooth disease type 4b
|
|
C535420|601382||charcot marie tooth neuropathy type 4b1
|
|
C535420|601382||cmt4b
|
|
C535420|601382||cmt4b1
|
|
C536814||distal arthrogryposis moore weaver type
|
|
C536814||moore weaver syndrome
|
|
C536859|270750||spastic paraplegia 23
|
|
C536859|270750||abdallat davis farrage syndrome
|
|
C536859|270750||abdallat syndrome
|
|
C536859|270750||lison syndrome
|
|
C536859|270750||spastic paraparesis vitiligo premature graying characteristic facies
|
|
C536859|270750||spastic paraplegia and pigmentary abnormalities
|
|
C536859|270750||spastic paraplegia vitiligo premature graying and characteristic facies
|
|
C536859|270750||spastic paraplegia with pigmentary abnormalities
|
|
C536859|270750||spg23
|
|
C536812||chromosome 3 trisomy 3p25
|
|
C536812||duplication 3p25
|
|
C536812||trisomy 3p25
|
|
C564063||rett syndrome preserved speech variant
|
|
D000326|300100||adrenoleukodystrophy
|
|
D000326|300100|C538676||addison disease and cerebral sclerosis
|
|
D000326|300100||adrenoleukodystrophy x linked
|
|
D000326|300100||adrenomyeloneuropathy
|
|
D000326|300100||ald
|
|
D000326|300100||ald adrenoleukodystrophy
|
|
D000326|300100||amn included
|
|
D000326|300100|C538676||bronze schilder disease
|
|
D000326|300100||melanodermic leukodystrophy adrenomyeloneuropathy included
|
|
D000326|300100||schilder addison complex
|
|
D000326|300100|C538676||siemerling creutzfeldt disease
|
|
D000326|300100||x ald
|
|
D000326|300100||x ald x linked adrenoleukodystrophy
|
|
D000326|300100||x linked adrenoleukodystrophy
|
|
C536813||chromosome 3 trisomy 3q
|
|
C536813||duplication 3q
|
|
C536813||trisomy 3q
|
|
C567855|612940||cutis laxa autosomal recessive type iib
|
|
C567855|612940||arcl2b
|
|
C567855|612940||cutis laxa with progeroid features
|
|
C564069||mental retardation x linked syndromic ube2a related
|
|
C564066||radiation sensitivity of natural killer activity
|
|
C564066||x ray nk sensitivity
|
|
C565398||metaphyseal chondrodysplasia with retinitis pigmentosa
|
|
C565399||metaphyseal chondrodysplasia pena type
|
|
D010190|260350||pancreatic neoplasms
|
|
D010190|260350||cancer of pancreas
|
|
D010190|260350||cancer of the pancreas
|
|
D010190|260350||cancer pancreas
|
|
D010190|260350||cancer pancreatic
|
|
D010190|260350||cancers pancreas
|
|
D010190|260350||cancers pancreatic
|
|
D010190|260350||neoplasm pancreas
|
|
D010190|260350||neoplasm pancreatic
|
|
D010190|260350||neoplasms pancreas
|
|
D010190|260350||neoplasms pancreatic
|
|
D010190|260350||pancreas cancer
|
|
D010190|260350||pancreas cancers
|
|
D010190|260350||pancreas neoplasm
|
|
D010190|260350||pancreas neoplasms
|
|
D010190|260350||pancreatic cancer
|
|
D010190|260350||pancreatic cancers
|
|
D010190|260350||pancreatic cancer susceptibility to 1
|
|
D010190|260350||pancreatic cancer susceptibility to 2
|
|
D010190|260350||pancreatic cancer susceptibility to 3
|
|
D010190|260350|C562463||pancreatic carcinoma
|
|
D010190|260350||pancreatic neoplasm
|
|
D010190|260350||pnca1
|
|
D010190|260350||pnca2
|
|
D010190|260350||pnca3
|
|
C537340|312870||simpson golabi behmel syndrome
|
|
C537340|312870||bulldog syndrome
|
|
C537340|312870||dgsx
|
|
C537340|312870||dysplasia gigantism syndrome x linked
|
|
C537340|312870||golabi rosen syndrome
|
|
C537340|312870||mental retardation overgrowth syndrome
|
|
C537340|312870||sdys
|
|
C537340|312870||sgbs
|
|
C537340|312870||sgbs1
|
|
C537340|312870||simpson dysmorphia syndrome
|
|
C537340|312870||simpson dysplasia syndrome
|
|
C537340|312870||simpson golabi behmel syndrome type 1
|
|
C537340|312870||simpson syndrome
|
|
609261|C563756||stuttering familial persistent 2
|
|
609261||stut2
|
|
C563865|608758||cardiomyopathy familial hypertrophic 10
|
|
C563865|608758||cardiomyopathy hypertrophic mid left ventricular chamber type 2
|
|
C563865|608758||cmh10
|
|
611588||muscular dystrophy dystroglycanopathy limb girdle type c 4
|
|
611588||mddgc4
|
|
310400||myopathy centronuclear x linked
|
|
310400||cnmx
|
|
310400||mtm1
|
|
310400||mtmx
|
|
310400|C538647||myotubular myopathy x linked
|
|
D008260||macroglossia
|
|
D008260||macroglossias
|
|
610251||alcohol sensitivity acute
|
|
610251||hangover susceptibility to included
|
|
C536821||gigantomastia
|
|
C536821||gestational gigantomastia
|
|
C536821||gigantomastia juvenile
|
|
C536821||hypertrophy of the breast juvenile
|
|
C536821||juvenile gigantomastia
|
|
C536821||macromastia
|
|
276902||usher syndrome type iiia
|
|
276902||ush3
|
|
276902||ush3a
|
|
C564072||multiple pterygium syndrome x linked
|
|
C564072||pterygium syndrome multiple x linked
|
|
C564071||lactic acidemia thiamine responsive
|
|
C536820||giedion syndrome
|
|
C536820||trichorhinophalangeal dysplasia 1
|
|
C536820|190350||trichorhinophalangeal syndrome type i
|
|
C536820||trichorhinophalangeal trp syndrome 1
|
|
C536825||glomerulonephritis sparse hair telangiectases
|
|
C536825||cutaneous telangiectasia sparse hair and membranoproliferative glomerulonephritis
|
|
C536825||glomerulonephritis with sparse hair and telangiectases
|
|
C536825||telangiectatic membranoproliferative glomerulonephritis
|
|
C564076||properdin deficiency type iii
|
|
C564075||properdin deficiency type ii
|
|
C536823||glassy cell carcinoma of the cervix
|
|
C536823||glassy cell adenocarcinoma of the uterine cervix
|
|
C537406|259450||bruck syndrome 1
|
|
C537406|259450||brks1
|
|
C537406|259450|C537407|609220||osteogenesis imperfecta with congenital joint contractures
|
|
C564036||mental retardation x linked 89
|
|
C564034||hodgkin disease y linked pseudoautosomal
|
|
C564033||incomplete sertoli cell only syndrome
|
|
C562839|156240||mesothelioma malignant
|
|
C562839|156240||mesom
|
|
C565365|253260|D028921||multiple carboxylase deficiency juvenile onset
|
|
C536840||aplasia cutis congenita of limbs recessive
|
|
C536840||congenital absence of skin on the upper or lower limbs
|
|
C536840||recessive aplasia cutis congenita of the limbs
|
|
C565366||mucus inspissation of respiratory tract
|
|
C564038||neuroacanthocytosis mcleod type
|
|
C564038|300842||mcleod syndrome
|
|
C535499|608105||epilepsy rolandic with paroxysmal exercise induced dystonia and writer apos s cramp
|
|
C535499|608105||eprpdc
|
|
C535499|608105||re ped wc
|
|
C536025|154780||marshall syndrome
|
|
C536025|154780||deafness myopia cataract saddle nose marshall type
|
|
C536025|154780||mrshs
|
|
610239||high density lipoprotein cholesterol level quantitative trait locus 4
|
|
610239||hdlcq4
|
|
C535522|602066||infantile convulsions and paroxysmal choreoathetosis familial
|
|
C535522|602066||convulsions familial infantile with paroxysmal choreoathetosis
|
|
C535522|602066||convulsions infantile with paroxysmal choreoathetosis familial
|
|
C535522|602066||icca
|
|
C535522|602066||icca syndrome
|
|
C535522|602066||paroxysmal kinesigenic dyskinesia with infantile convulsions
|
|
C535522|602066||pkd ic
|
|
C535508||ermine phenotype
|
|
C535508||cutaneous albinism hermine phenotype
|
|
C535508||o apos doherty syndrome
|
|
C535508||pigmentary disorder with hearing loss
|
|
D001321|209850||autistic disorder
|
|
D001321|209850||asd included
|
|
D001321|209850||autism
|
|
D001321|209850||autism early infantile
|
|
D001321|209850||autism infantile
|
|
D001321|209850||autism related speech delay
|
|
D001321|209850||autisms
|
|
D001321|209850||autism spectrum disorder included
|
|
D001321|209850||autism susceptibility to 10
|
|
D001321|209850||autism susceptibility to 11
|
|
D001321|209850||autism susceptibility to 12
|
|
D001321|209850||autism susceptibility to 13
|
|
D001321|209850||autism susceptibility to 14a included
|
|
D001321|209850||autism susceptibility to 15
|
|
D001321|209850||autism susceptibility to 16
|
|
D001321|209850||autism susceptibility to 17
|
|
D001321|209850||autism susceptibility to 3
|
|
D001321|209850||autism susceptibility to 5
|
|
D001321|209850||autism susceptibility to 6
|
|
D001321|209850||autism susceptibility to 7
|
|
D001321|209850||autism susceptibility to 8
|
|
D001321|209850||autism susceptibility to 9
|
|
D001321|209850||autism with or without seizures
|
|
D001321|209850||autistic disorder autism susceptibility to 1 included
|
|
D001321|209850||auts10
|
|
D001321|209850||auts11
|
|
D001321|209850||auts12
|
|
D001321|209850||auts13
|
|
D001321|209850||auts14a included
|
|
D001321|209850||auts15
|
|
D001321|209850||auts16
|
|
D001321|209850||auts17
|
|
D001321|209850||auts1 included
|
|
D001321|209850||auts2 formerly
|
|
D001321|209850||auts3
|
|
D001321|209850||auts4 included
|
|
D001321|209850||auts5
|
|
D001321|209850||auts6
|
|
D001321|209850||auts7
|
|
D001321|209850||auts8
|
|
D001321|209850||auts9
|
|
D001321|209850||chromosome 15q11 2 duplication syndrome included
|
|
D001321|209850|C557830||chromosome 15q11 q13 duplication syndrome
|
|
D001321|209850||chromosome 16p11 2 deletion syndrome 593 kb
|
|
D001321|209850||disorder autistic
|
|
D001321|209850||disorders autistic
|
|
D001321|209850||duplication 15q11 q13 syndrome autism susceptibility to 4 included
|
|
D001321|209850||early infantile autism
|
|
D001321|209850||infantile autism
|
|
D001321|209850||infantile autism early
|
|
D001321|209850||kanner apos s syndrome
|
|
D001321|209850||kanners syndrome
|
|
D001321|209850||kanner syndrome
|
|
D001321|209850||phrase speech delay autism related
|
|
D001321|209850||syndrome kanner apos s
|
|
D008231||lymphopenia
|
|
D008231||lymphocytopenia
|
|
D008231||lymphocytopenias
|
|
D008231||lymphopenias
|
|
C536839||cardiac form of generalized glycogenosis
|
|
C536839|D006009|232300||cardiomegalia glycogenica diffusa
|
|
C536839|D006009|232300||glycogenosis generalized cardiac form
|
|
C535509||erythema elevatum diutinum
|
|
C535509||extracellular cholesterosis
|
|
C535509||leukocytoclastic vasculitis
|
|
D010547||persistent fetal circulation syndrome
|
|
D010547||acd mpv
|
|
D010547||circulation persistent fetal
|
|
D010547||familial persistent pulmonary hypertension of the newborn
|
|
D010547||fetal circulation persistent
|
|
D010547||hypertension pulmonary of newborn persistent
|
|
D010547||misalignment of the pulmonary vessels
|
|
D010547||persistent fetal circulation
|
|
D010547||persistent pulmonary hypertension of newborn
|
|
D010547||pulmonary hypertension familial persistent of the newborn
|
|
D055728|254450||primary myelofibrosis
|
|
D055728|254450||agnogenic myeloid metaplasia
|
|
D055728|254450||agnogenic myeloid metaplasias
|
|
D055728|254450||bone marrow fibroses
|
|
D055728|254450||bone marrow fibrosis
|
|
D055728|254450||chronic idiopathic myelofibrosis
|
|
D055728|254450||fibroses bone marrow
|
|
D055728|254450||fibrosis bone marrow
|
|
D055728|254450||idiopathic myelofibrosis
|
|
D055728|254450||metaplasia agnogenic myeloid
|
|
D055728|254450||metaplasia myeloid
|
|
D055728|254450||metaplasias agnogenic myeloid
|
|
D055728|254450||metaplasias myeloid
|
|
D055728|254450||mmm included
|
|
D055728|254450||myelofibroses
|
|
D055728|254450||myelofibroses primary
|
|
D055728|254450||myelofibrosis
|
|
D055728|254450||myelofibrosis primary
|
|
D055728|254450||myelofibrosis with myeloid metaplasia
|
|
D055728|254450||myelofibrosis with myeloid metaplasia included
|
|
D055728|254450||myeloid metaplasia
|
|
D055728|254450||myeloid metaplasia agnogenic
|
|
D055728|254450||myeloid metaplasias
|
|
D055728|254450||myeloid metaplasias agnogenic
|
|
D055728|254450||myeloscleroses
|
|
D055728|254450||myelosclerosis
|
|
D055728|254450||myeloses nonleukemic
|
|
D055728|254450||myelosis nonleukemic
|
|
D055728|254450||nonleukemic myeloses
|
|
D055728|254450||nonleukemic myelosis
|
|
D055728|254450||primary myelofibroses
|
|
C567123|225250||hypothyroidism congenital nongoitrous 5
|
|
C567123|225250||chng5
|
|
D008230||lymphomatoid granulomatosis
|
|
D008230||granulomatoses lymphomatoid
|
|
D008230||granulomatosis lymphomatoid
|
|
D008230||lymphomatoid granulomatoses
|
|
C567356|612293||porokeratosis disseminated superficial actinic 3
|
|
C567356|612293||dsap3
|
|
C567356|612293||porok5
|
|
C567356|612293||porokeratosis 5 disseminated superficial actinic type
|
|
C565371||monocyte chemotactic disorder
|
|
300578|C564481||chromosome xp11 3 deletion syndrome
|
|
300578|C564481||mental retardation x linked with retinitis pigmentosa
|
|
C565373||molybdenum cofactor deficiency complementation group b
|
|
C565374||molybdenum cofactor deficiency complementation group c
|
|
C564603|607236||hypoprebetalipoproteinemia acanthocytosis retinitis pigmentosa and pallidal degeneration
|
|
C564603|607236||harp syndrome
|
|
C536831||glucose 6 phosphate translocase deficiency
|
|
C536837||glyceraldehyde 3 phosphate dehydrogenase deficiency
|
|
C564042||vesicoureteral reflux x linked
|
|
C536834||glutaric aciduria 2
|
|
C536834||glutaric acidemia 2 a
|
|
C564041||von willebrand disease x linked form
|
|
C565370||monosomy 7 of bone marrow
|
|
C565370||myelodysplasia and leukemia syndrome with monosomy 7
|
|
C564040||widow apos s peak syndrome
|
|
C564040||widow apos s peak ptosis and skeletal anomalies
|
|
C565379||microcephaly with chorioretinopathy autosomal recessive
|
|
D016481|600263||helicobacter infections
|
|
D016481|600263||helicobacter infection
|
|
D016481|600263||helicobacter pylori infection susceptibility to
|
|
D016481|600263||infection helicobacter
|
|
D016481|600263||infections helicobacter
|
|
C565376||mitochondrial myopathy with a defect in mitochondrial protein transport
|
|
C536851||familial renal cell carcinoma
|
|
C536851||familial renal carcinoma
|
|
D007888|256000||leigh disease
|
|
D007888|256000||disease leigh apos s
|
|
D007888|256000||encephalomyelitides subacute necrotizing
|
|
D007888|256000||encephalomyelitis subacute necrotizing
|
|
D007888|256000||encephalomyelopathies subacute necrotizing
|
|
D007888|256000||encephalomyelopathy subacute necrotizing
|
|
D007888|256000||encephalopathies subacute necrotizing
|
|
D007888|256000||encephalopathy subacute necrotizing
|
|
D007888|256000||encephalopathy subacute necrotizing infantile
|
|
D007888|256000||encephalopathy subacute necrotizing juvenile
|
|
D007888|256000||infantile leigh disease
|
|
D007888|256000||infantile subacute necrotizing encephalopathy
|
|
D007888|256000||juvenile leigh disease
|
|
D007888|256000||juvenile subacute necrotizing encephalopathy
|
|
D007888|256000||leigh disease infantile
|
|
D007888|256000||leigh disease juvenile
|
|
D007888|256000||leigh apos s disease
|
|
D007888|256000||leighs disease
|
|
D007888|256000||leigh syndrome
|
|
D007888|256000||leigh syndrome due to mitochondrial complex ii deficiency included
|
|
D007888|256000||leigh syndrome due to mitochondrial complex iii deficiency included
|
|
D007888|256000||leigh syndrome due to mitochondrial complex iv deficiency included
|
|
D007888|256000||leigh syndrome due to mitochondrial complex v deficiency included
|
|
D007888|256000||ls
|
|
D007888|256000||necrotizing encephalomyelitides subacute
|
|
D007888|256000||necrotizing encephalomyelitis subacute
|
|
D007888|256000||necrotizing encephalomyelopathies subacute
|
|
D007888|256000||necrotizing encephalomyelopathy subacute
|
|
D007888|256000||necrotizing encephalopathies subacute
|
|
D007888|256000||necrotizing encephalopathy infantile subacute of leigh sne leigh syndrome due to mitochondrial complex i deficiency included
|
|
D007888|256000||necrotizing encephalopathy subacute
|
|
D007888|256000||subacute necrotizing encephalomyelitides
|
|
D007888|256000||subacute necrotizing encephalomyelitis
|
|
D007888|256000||subacute necrotizing encephalomyelitis infantile
|
|
D007888|256000||subacute necrotizing encephalomyelopathies
|
|
D007888|256000||subacute necrotizing encephalomyelopathy
|
|
D007888|256000||subacute necrotizing encephalopathies
|
|
D007888|256000||subacute necrotizing encephalopathy
|
|
D007888|256000||subacute necrotizing encephalopathy infantile
|
|
D007888|256000||subacute necrotizing encephalopathy juvenile
|
|
C564049||thyroxine binding globulin deficiency
|
|
C565378||microphthalmia isolated with coloboma 4
|
|
C565378||mcopcb4
|
|
C565378||microphthalmia with colobomatous cyst
|
|
C536561|602079||trimethylaminuria
|
|
C536561|602079||fish malodor syndrome
|
|
C536561|602079||fish odor syndrome
|
|
C536561|602079||stale fish syndrome
|
|
C536561|602079||tmau
|
|
C536561|602079||tmauria
|
|
241550|D018636||hypoplastic left heart syndrome
|
|
241550|D018636||hlhs
|
|
241550|D018636||hlhs1
|
|
241550|D018636||hypoplastic left heart syndrome 1
|
|
241550|D018636||left heart hypoplasia syndrome
|
|
241550|D018636||left heart syndrome hypoplastic
|
|
C564254|608354||capillary malformation arteriovenous malformation
|
|
C564254|608354||capillary malformation arteriovenous malformation syndrome
|
|
C564254|608354||capillary malformation without arteriovenous malformation
|
|
C564254|608354||capillary malformation without arteriovenous malformation included
|
|
C564254|608354||cm avm
|
|
C564254|608354||cmavm
|
|
D011885||radius fractures
|
|
D011885||fracture radius
|
|
D011885||fractures radius
|
|
D011885||radius fracture
|
|
D010554||personality disorders
|
|
D010554||as if personality
|
|
D010554||avoidant personality disorder
|
|
D010554||avoidant personality disorders
|
|
D010554||impulse ridden personality
|
|
D010554||inadequate personality
|
|
D010554||narcissistic personality disorder
|
|
D010554||personality as if
|
|
D010554||personality disorder
|
|
D010554||personality disorder avoidant
|
|
D010554||personality disorder narcissistic
|
|
D010554||personality disorders avoidant
|
|
D010554||personality impulse ridden
|
|
D010554||personality inadequate
|
|
C535519||reginato schiapachasse syndrome
|
|
300400|D053632||x linked combined immunodeficiency diseases
|
|
300400|D053632||cidx
|
|
300400|D053632||combined immunodeficiency x linked
|
|
300400|D053632||imd4
|
|
300400|D053632||imd6
|
|
300400|D053632||immunodeficiency 4
|
|
300400|D053632||immunodeficiency 6
|
|
300400|D053632||immunodeficiency diseases x linked
|
|
300400|D053632||immunodeficiency diseases x linked combined
|
|
300400|D053632||immunodeficiency disease x linked
|
|
300400|D053632||immunodeficiency syndromes x linked
|
|
300400|D053632||immunodeficiency syndrome x linked
|
|
300400|D053632||immunodeficiency x linked combined
|
|
300400|D053632||scids x linked
|
|
300400|D053632||scidx
|
|
300400|D053632||scidx1
|
|
300400|D053632||scid x linked
|
|
300400|D053632||severe combined immunodeficiency x linked
|
|
300400|D053632||severe combined immunodeficiency x linked t cell negative b cell positive nk cell negative
|
|
300400|D053632||syndromes x linked immunodeficiency
|
|
300400|D053632||xcid
|
|
300400|D053632||x linked combined immunodeficiencies
|
|
300400|D053632||x linked combined immunodeficiency
|
|
300400|D053632||x linked immunodeficiency disease
|
|
300400|D053632||x linked immunodeficiency diseases
|
|
300400|D053632||x linked immunodeficiency syndrome
|
|
300400|D053632||x linked immunodeficiency syndromes
|
|
300400|D053632||x linked scid
|
|
300400|D053632||x linked scids
|
|
300400|D053632||x linked severe combined immunodeficiency
|
|
300400|D053632||xscid
|
|
300400|D053632||x scid
|
|
C536849||familial neurocardiogenic syncope
|
|
C536849||familial vasovagal syncope
|
|
C536849||syncope familial neurocardiogenic
|
|
C536849||syncope familial vasovagal
|
|
C535331|305400||aarskog syndrome
|
|
C535331|305400||aarskog disease
|
|
C535331|305400||aarskog like syndrome
|
|
C535331|305400||aarskog scott syndrome
|
|
C535331|305400||aarskog syndrome x linked faciogenital dysplasia with attention deficit hyperactivity disorder included
|
|
C535331|305400||aas
|
|
C535331|305400||facio digito genital dysplasia
|
|
C535331|305400||faciodigitogenital syndrome
|
|
C535331|305400||faciodigitogenital syndrome recessive
|
|
C535331|305400||faciogenital dysplasia
|
|
C535331|305400||fgdy
|
|
C535331|305400||kuwait type faciodigitogenital syndrome
|
|
C535331|305400||mental retardation x linked syndromic 16 included
|
|
C535331|305400||mrxs16 included
|
|
C535331|305400||scott aarskog syndrome
|
|
D047808||adrenogenital syndrome
|
|
D047808||adrenogenital syndromes
|
|
D047808||syndrome adrenogenital
|
|
D047808||syndromes adrenogenital
|
|
C565382||microcephaly micromelia syndrome
|
|
C535511||erythema nodosum idiopathic
|
|
C535511||erythema nodosum of unknown etiology
|
|
C535511||idiopathic erythema nodosum
|
|
C535510||erythema nodosum familial
|
|
C535510||familial erythema nodosum
|
|
C565384||microcephaly primary autosomal recessive 1
|
|
C565384|251200||premature chromosome condensation syndrome
|
|
C565384|251200||premature chromosome condensation with microcephaly and mental retardation
|
|
C535513||lethal congenital erythroderma
|
|
C535513||erythroderma lethal congenital
|
|
C535512||erythroderma desquamativa of leiner
|
|
C535512||erythroderma desquamativum of infancy
|
|
C535512||generalized erythroderma diarrhea and failure to thrive
|
|
C535512||leiner moussous desquamative erythroderma
|
|
C536847||familial multiple trichodiscomas
|
|
C536847||hereditary multiple trichodiscomas
|
|
C536847||trichodiscomas familial multiple
|
|
300605|C564475||retinitis pigmentosa 34
|
|
300605|C564475||rp34
|
|
C535515||red skin pigment anomaly of new guinea
|
|
C535515||red skin pigment new guinea type
|
|
C564054||midline defects x linked
|
|
C536848||familial myelofibrosis
|
|
C564053||thrombocytopenia x linked intermittent
|
|
C565380||ataxia telangiectasia variant v2
|
|
C536845||familial hypersecretion of adrenal androgens
|
|
C536845||hypersecretion of adrenal androgens familial
|
|
C535517||refsum disease with increased pipecolic acidemia
|
|
C565381||microcephaly with chemotactic defect and transient hypogammaglobulinemia
|
|
C536846||familial hypersensitivity pneumonitis
|
|
C536846||hypersensitivity pneumonitis familial
|
|
C535516||reed apos s syndrome
|
|
C535516||cutaneous leiomyomata with uterine leiomyomata
|
|
C535516|150800||hereditary leiomyomatosis and renal cell cancer
|
|
C535516||leiomyoma hereditary multiple of skin
|
|
C535516|150800||leiomyoma multiple cutaneous
|
|
C535516|150800||leiomyomatosis and renal cell cancer hereditary
|
|
C535516||multiple cutaneous and uterine leiomyomata 1
|
|
C535516||multiple cutaneous and uterine leiomyomatosis
|
|
C564051||thrombocytopenia with elevated serum iga and renal disease
|
|
C565226||hamartoma precalcaneal congenital fibrolipomatous
|
|
C564600|607258||hypercalciuria absorptive 1
|
|
C564600|607258||hca1
|
|
C566559||plantar lipomatosis unusual facies and developmental delay
|
|
212050|C537979|613108||candidiasis familial 2
|
|
212050|C537979|613108||candf2
|
|
212050|C537979|613108||candidiasis familial chronic mucocutaneous autosomal recessive
|
|
212050||card9 immunodeficiency
|
|
C566553||ectodermal dysplasia hidrotic autosomal recessive
|
|
C565222||vasculitis lymphocytic cutaneous small vessel
|
|
C566554||ichthyosis follicular atrophoderma hypotrichosis and hypohidrosis
|
|
D060906||coxa valga
|
|
D060906||acquired coxa valga
|
|
D060906||acquired coxa valgas
|
|
D060906||acquired coxa valgus
|
|
D060906||congenital coxa valga
|
|
D060906||congenital coxa valgas
|
|
D060906||congenital coxa valgus
|
|
D060906||coxa valga acquired
|
|
D060906||coxa valga congenital
|
|
D060906||coxa valga developmental
|
|
D060906||coxa valgas
|
|
D060906||coxa valgas acquired
|
|
D060906||coxa valgas congenital
|
|
D060906||coxa valgas developmental
|
|
D060906||coxa valgus
|
|
D060906||coxa valgus acquired
|
|
D060906||coxa valgus congenital
|
|
D060906||coxa valgus developmental
|
|
D060906||developmental coxa valga
|
|
D060906||developmental coxa valgas
|
|
D060906||developmental coxa valgus
|
|
D060906||valga coxa
|
|
D060906||valgas coxa
|
|
D060906||valgus coxa
|
|
D060905||coxa vara
|
|
D060905||acquired coxa vara
|
|
D060905||acquired coxa varas
|
|
D060905||acquired coxa varus
|
|
D060905||congenital coxa vara
|
|
D060905||congenital coxa varas
|
|
D060905||congenital coxa varus
|
|
D060905||coxa vara acquired
|
|
D060905||coxa vara congenital
|
|
D060905||coxa vara developmental
|
|
D060905||coxa vara infantile
|
|
D060905||coxa varas
|
|
D060905||coxa varas acquired
|
|
D060905||coxa varas congenital
|
|
D060905||coxa varas developmental
|
|
D060905||coxa varas infantile
|
|
D060905||coxa varus
|
|
D060905||coxa varus acquired
|
|
D060905||coxa varus congenital
|
|
D060905||coxa varus developmental
|
|
D060905||developmental coxa vara
|
|
D060905||developmental coxa varas
|
|
D060905||developmental coxa varus
|
|
D060905||infantile coxa vara
|
|
D060905||infantile coxa varas
|
|
D060905||vara coxa
|
|
D060905||varas coxa
|
|
D060905||varus coxa
|
|
128200|C566847||episodic kinesigenic dyskinesia 1
|
|
128200|C566847||dystonia 10
|
|
128200|C566847|C537180||dystonia familial paroxysmal
|
|
128200|C566847||dyt10
|
|
128200|C566847||ekd1
|
|
128200|C566847||familial paroxysmal kinesigenic dyskinesia
|
|
128200|C566847|C537180||paroxysmal kinesigenic choreoathetosis
|
|
128200|C566847||paroxysmal kinesigenic dyskinesia
|
|
128200|C566847||pkc
|
|
128200|C566847||pkd
|
|
C579872||6q24 related transient neonatal diabetes mellitus
|
|
C579872||6q24 tndm
|
|
C579872||tndm type 1
|
|
D008325||mammary neoplasms experimental
|
|
D008325||experimental mammary neoplasm
|
|
D008325||experimental mammary neoplasms
|
|
D008325||mammary neoplasm experimental
|
|
D008325||neoplasm experimental mammary
|
|
D008325||neoplasms experimental mammary
|
|
C537369|602849||muenke syndrome
|
|
C537369|602849||fgfr3 associated coronal synostosis
|
|
C537369|602849||mnkes
|
|
C537369|602849||muenke nonsyndromic coronal craniosynostosis
|
|
C537369|602849||syndrome of coronal craniosynostosis
|
|
D023961||gonadal dysgenesis 46 xx
|
|
D023961|233300||gonadal dysgenesis xx type
|
|
D023961||pure gonadal dysgenesis 46 xx
|
|
C579867||3 methylglutaconic aciduria
|
|
C579867||3mga 3 methylglutaconic aciduria
|
|
C536214|272430||crisponi syndrome
|
|
C536214|272430||ciss1
|
|
C536214|272430||cntf receptor related disorders
|
|
C536214|272430||cold induced sweating syndrome
|
|
C536214|272430|C564791|610313||cold induced sweating syndrome 1
|
|
C536214|272430||muscle contractions tetanoform with characteristic face camptodactyly hyperthermia and sudden death
|
|
C536214|272430||sohar crisponi syndrome
|
|
C567349|612335||spastic paraplegia 38 autosomal dominant
|
|
C567349|612335||spg38
|
|
D007000||hypodermyiasis
|
|
D007000||hypodermyiases
|
|
C579862||3b hydroxysteroid dehydrogenase deficiency
|
|
C579862||3beta hsd deficiency
|
|
C579862|C538236|201810||3 beta hsd deficiency
|
|
C579862||3beta hsd deficiency congenital adrenal hyperplasia
|
|
C579862||3beta hydroxysteroid dehydrogenase deficiency
|
|
C579862|C538236|201810||3 beta hydroxysteroid dehydrogenase deficiency
|
|
C579862||3 beta ol dehydrogenase deficiency
|
|
C579862||type ii 3beta hydroxysteroid dehydrogenase deficiency
|
|
D046608||synkinesis
|
|
D046608||synkineses
|
|
C566560||sensorineural hearing loss retinal pigment epithelium lesions discolored teeth
|
|
C565230|100070||aortic aneurysm familial abdominal 1
|
|
C536056|607634||osteopetrosis autosomal dominant type 1
|
|
C536056|607634||opta1
|
|
C536056|607634||osteopetrosis autosomal dominant 1
|
|
C536056|607634||osteopetrosis autosomal dominant type i
|
|
C565236||deafness sensorineural with hypertrophic cardiomyopathy
|
|
C566568||peroxisome biogenesis disorder complementation group 1
|
|
173600|C566795||pneumothorax primary spontaneous
|
|
173600|C566795|D013494|601104||psp
|
|
C566569||peroxisome biogenesis disorder complementation group e
|
|
608516|D003865||depressive disorder major
|
|
608516|D003865||depression involutional
|
|
608516|D003865||depressive disorders major
|
|
608516|D003865||disorder major depressive
|
|
608516|D003865||disorders major depressive
|
|
608516|D003865||involutional depression
|
|
608516|D003865||involutional melancholia
|
|
608516|D003865||involutional psychoses
|
|
608516|D003865||involutional psychosis
|
|
608516|D003865||major depressive disorder
|
|
608516|D003865||major depressive disorders
|
|
608516|D003865||mdd
|
|
608516|D003865||melancholia involutional
|
|
608516|D003865||paraphrenia involutional
|
|
608516|D003865||psychoses involutional
|
|
608516|D003865||psychosis involutional
|
|
608516|D003865||sad included
|
|
608516|D003865||unipolar depression seasonal affective disorder included
|
|
C566563||progeroid facial appearance with hand anomalies
|
|
C566469|610489||pigmented nodular adrenocortical disease primary 1
|
|
C566469|610489||adrenocortical nodular dysplasia primary
|
|
C566469|610489||cushing syndrome adrenal due to ppnad1
|
|
C566469|610489||pigmented micronodular adrenocortical disease primary 1
|
|
C566469|610489||ppnad1
|
|
C566611|601869||deafness autosomal recessive 15
|
|
C566611|601869||deafness autosomal recessive 72
|
|
C566611|601869||deafness autosomal recessive 95
|
|
C566611|601869||dfmb15
|
|
C566611|601869||dfnb15
|
|
C566611|601869||dfnb72
|
|
C566611|601869||dfnb95
|
|
D063173||retrognathia
|
|
D063173||mandibular retroposition
|
|
D063173||mandibular retropositions
|
|
D063173||mandibular retrusion
|
|
D063173||mandibular retrusions
|
|
D063173||maxillary retroposition
|
|
D063173||maxillary retropositions
|
|
D063173||maxillary retrusion
|
|
D063173||maxillary retrusions
|
|
D063173||retrognathias
|
|
D063173||retrognathism
|
|
D063173||retrognathisms
|
|
D063173||retroposition mandibular
|
|
D063173||retroposition maxillary
|
|
D063173||retropositions mandibular
|
|
D063173||retropositions maxillary
|
|
D063173||retrusion mandibular
|
|
D063173||retrusion maxillary
|
|
D063173||retrusions mandibular
|
|
D063173||retrusions maxillary
|
|
C566565||ventriculomegaly with defects of the radius and kidney
|
|
C566566||medium chain 3 ketoacyl coa thiolase deficiency
|
|
C537470|251850||microvillus inclusion disease
|
|
C537470|251850||congenital familial protracted diarrhea with enterocyte brush border abnormalities
|
|
C537470|251850||davidson disease
|
|
C537470|251850||diar2
|
|
C537470|251850||diarrhea 2 with microvillus atrophy
|
|
C537470|251850||intractable diarrhea of infancy
|
|
C537470|251850||microvillus atrophy congenital
|
|
C537470|251850||mvid
|
|
C579880||actin accumulation myopathy
|
|
C579880||actin filament aggregate myopathy
|
|
C579880||actin myopathy
|
|
C579880||congenital myopathy with excess of thin filaments
|
|
D007009||hypolipoproteinemias
|
|
D007009||hypolipoproteinemia
|
|
D007009||hypoprebetalipoproteinemia
|
|
D007007||hypohidrosis
|
|
D007007||anhidrosis
|
|
D008338||mandibular injuries
|
|
D008338||injuries mandibular
|
|
D008338||injury mandibular
|
|
D008338||mandibular injury
|
|
D009669||nose neoplasms
|
|
D009669||cancer nasal
|
|
D009669||cancer nose
|
|
D009669||cancer of nose
|
|
D009669||cancer of the nose
|
|
D009669||cancers nasal
|
|
D009669||cancers nose
|
|
D009669||nasal cancer
|
|
D009669||nasal cancers
|
|
D009669||nasal neoplasm
|
|
D009669||nasal neoplasms
|
|
D009669||neoplasm nasal
|
|
D009669||neoplasm nose
|
|
D009669||neoplasms nasal
|
|
D009669||neoplasms nose
|
|
D009669||nose cancer
|
|
D009669||nose cancers
|
|
D009669||nose neoplasm
|
|
D007008||hypokalemia
|
|
D007008||hypokalemias
|
|
D007008||hypopotassemia
|
|
D007008||hypopotassemias
|
|
D008339||mandibular neoplasms
|
|
D008339||mandibular neoplasm
|
|
D008339||neoplasm mandibular
|
|
D008339||neoplasms mandibular
|
|
D009668||nose diseases
|
|
D009668||disease nasal
|
|
D009668||disease nose
|
|
D009668||diseases nasal
|
|
D009668||diseases nose
|
|
D009668||disorder nasal
|
|
D009668||disorders nasal
|
|
D009668||nasal disease
|
|
D009668||nasal diseases
|
|
D009668||nasal disorder
|
|
D009668||nasal disorders
|
|
D009668||nose disease
|
|
D008336||mandibular diseases
|
|
D008336||disease mandibular
|
|
D008336||diseases mandibular
|
|
D008336||mandibular disease
|
|
D009667||nose deformities acquired
|
|
D009667||acquired nasal deformities
|
|
D009667||acquired nasal deformity
|
|
D009667||acquired nose deformities
|
|
D009667||acquired nose deformity
|
|
D009667||nasal deformities acquired
|
|
D009667||nasal deformity acquired
|
|
D009667||nose deformity acquired
|
|
D007006||hypogonadism
|
|
D007006||hypergonadotropic hypogonadism
|
|
D007006||hypogonadism hypergonadotropic
|
|
D007006||hypogonadism hypogonadotropic
|
|
D007006||hypogonadotropic hypogonadism
|
|
D008337||mandibular fractures
|
|
D008337||fracture mandibular
|
|
D008337||fractures mandibular
|
|
D008337||mandibular fracture
|
|
D007003||hypoglycemia
|
|
D007003||fasting hypoglycemia
|
|
D007003||hypoglycemia fasting
|
|
D007003||hypoglycemia postabsorptive
|
|
D007003||hypoglycemia postprandial
|
|
D007003||hypoglycemia reactive
|
|
D007003||postabsorptive hypoglycemia
|
|
D007003||postprandial hypoglycemia
|
|
D007003||reactive hypoglycemia
|
|
C535752|212066||congenital disorder of glycosylation type 2a
|
|
C535752|212066||alkuraya syndrome
|
|
C535752|212066||carbohydrate deficient glycoprotein syndrome type 2
|
|
C535752|212066||carbohydrate deficient glycoprotein syndrome type ii formerly
|
|
C535752|212066||cdg2a
|
|
C535752|212066||cdgiia
|
|
C535752|212066||cdg iia
|
|
C535752|212066||cdgs2 formerly
|
|
C535752|212066||congenital disorder of glycosylation type iia
|
|
C535752|212066||mental retardation growth retardation prominent columella and open mouth
|
|
D007012||hypopharyngeal neoplasms
|
|
D007012||cancer hypopharyngeal
|
|
D007012||cancers hypopharyngeal
|
|
D007012||hypopharyngeal cancer
|
|
D007012||hypopharyngeal cancers
|
|
D007012||hypopharyngeal neoplasm
|
|
D007012||neoplasm hypopharyngeal
|
|
D007012||neoplasms hypopharyngeal
|
|
C579878||achondrogenesis
|
|
C579878||achondrogenesis syndrome
|
|
D007010||hyponatremia
|
|
D007010||hyponatremias
|
|
D007011||hypoparathyroidism
|
|
D007011||hypoparathyroidism idiopathic
|
|
D007011||idiopathic hypoparathyroidism
|
|
C579873||9q22 3 microdeletion
|
|
C579873||9q22 3 deletion
|
|
C579873||9q22 deletion syndrome
|
|
C579873||microdeletion 9q22 3 syndrome
|
|
C566572||cervical dystonia primary
|
|
C566572||dystonia primary cervical
|
|
C566573||nephropathy progressive tubulointerstitial with cholestatic liver disease
|
|
C566535|D006950|144250||hyperlipidemia combined 1
|
|
C566535|D006950|144250||fchl1
|
|
C566535|D006950|144250||hyperlipidemia familial combined 1
|
|
C566535|D006950|144250||hyplip1
|
|
D013967|608173||thyroiditis autoimmune
|
|
D013967|608173||aitd1
|
|
D013967|608173||aitd2
|
|
D013967|608173||aitd3
|
|
D013967|608173||aitd4
|
|
D013967|608173||autoimmune thyroid disease susceptibility to 1
|
|
D013967|608173||autoimmune thyroid disease susceptibility to 2
|
|
D013967|608173||autoimmune thyroid disease susceptibility to 3
|
|
D013967|608173||autoimmune thyroid disease susceptibility to 4
|
|
D013967|608173||autoimmune thyroiditides
|
|
D013967|608173||autoimmune thyroiditis
|
|
D013967|608173||lymphocytic thyroiditides
|
|
D013967|608173||lymphocytic thyroiditis
|
|
D013967|608173||lymphomatous thyroiditides
|
|
D013967|608173||lymphomatous thyroiditis
|
|
D013967|608173||thyroiditides autoimmune
|
|
D013967|608173||thyroiditides lymphocytic
|
|
D013967|608173||thyroiditides lymphomatous
|
|
D013967|608173||thyroiditis lymphocytic
|
|
D013967|608173||thyroiditis lymphomatous
|
|
C565204||parkinson disease 13
|
|
C567865||zechi ceide syndrome
|
|
C567865||occipital atretic cephalocele unusual facies and large feet
|
|
C538111|600089||pancreatic beta cell agenesis with neonatal diabetes mellitus
|
|
C538111|600089||congenital absence of insulin producing beta cells with diabetes mellitus
|
|
C566531||pseudoacromegaly with severe insulin resistance
|
|
C567864||giacheti syndrome
|
|
C567864||marfanoid habitus and specific language and learning disabilities
|
|
D008309||mallory weiss syndrome
|
|
D008309||gastroesophageal laceration hemorrhage
|
|
D008309||gastroesophageal laceration hemorrhages
|
|
D008309||junction mucosal lacerations gastroesophageal
|
|
D008309||junctions mucosal lacerations gastroesophageal
|
|
D008309||laceration hemorrhage gastroesophageal
|
|
D008309||laceration hemorrhages gastroesophageal
|
|
D008309||laceration mallory weiss
|
|
D008309||lacerations gastroesophageal junction mucosal
|
|
D008309||lacerations gastroesophageal junctions mucosal
|
|
D008309||mallory weiss laceration
|
|
D008309||mallory weiss tear
|
|
D008309||mucosal lacerations gastroesophageal junction
|
|
D008309||mucosal lacerations gastroesophageal junctions
|
|
D008309||syndrome mallory weiss
|
|
C567863||congenital lipomatous overgrowth vascular malformations and epidermal nevi
|
|
C567863||cloves syndrome
|
|
C567863||clove syndrome
|
|
C567863||congenital lipomatous overgrowth vascular malformations epidermal nevi and skeletal spinal abnormalities
|
|
604286|C535902||limb girdle muscular dystrophy type 2e
|
|
604286|C535902||beta sarcoglycan limb girdle muscular dystrophy
|
|
604286|C535902||lgmd2e
|
|
604286|C535902||muscular dystrophy limb girdle type 2e
|
|
604286|C535902||muscular dystrophy limb girdle with beta sarcoglycan deficiency
|
|
192315|C566007||vasculopathy retinal with cerebral leukodystrophy
|
|
192315|C566007||cerebroretinal vasculopathy hereditary
|
|
192315|C566007||crv
|
|
192315|C566007||retinopathy vascular with cerebral and renal involvement and raynaud and migraine phenomena
|
|
192315|C566007||rvcl
|
|
D046628||sphincter of oddi dysfunction
|
|
D046628||sphincter of oddi dyskinesia
|
|
D046628||sphincter of oddi stenosis
|
|
D008305||malignant hyperthermia
|
|
D008305||anesthesia hyperthermia
|
|
D008305||anesthesia hyperthermias
|
|
D008305||anesthesia related hyperthermia
|
|
D008305||anesthesia related hyperthermias
|
|
D008305||hyperpyrexia malignant
|
|
D008305||hyperpyrexias malignant
|
|
D008305||hyperthermia anesthesia related
|
|
D008305||hyperthermia malignant
|
|
D008305|145600|C535694||hyperthermia of anesthesia
|
|
D008305||hyperthermias anesthesia related
|
|
D008305||malignant hyperpyrexia
|
|
D008305||malignant hyperpyrexias
|
|
D008305||malignant hyperthermias
|
|
D008305||related hyperthermia anesthesia
|
|
D008305||related hyperthermias anesthesia
|
|
C579850||16p11 2 deletion syndrome
|
|
D008303||malignant carcinoid syndrome
|
|
D008303||carcinoid syndrome malignant
|
|
D008303||carcinoid syndromes malignant
|
|
D008303||malignant carcinoid syndromes
|
|
D008303||syndrome malignant carcinoid
|
|
D008303||syndromes malignant carcinoid
|
|
D008304||malignant catarrh
|
|
D008304||catarrh malignant
|
|
D008304||catarrhs malignant
|
|
D008304||malignant catarrhs
|
|
C565209||sclerocornea
|
|
D008310||malocclusion
|
|
D008310||angle classification
|
|
D008310||angle apos s classification
|
|
D008310||angles classification
|
|
D008310||bite cross
|
|
D008310||bites cross
|
|
D008310||classification angle apos s
|
|
D008310||crossbite
|
|
D008310||cross bite
|
|
D008310||crossbites
|
|
D008310||cross bites
|
|
D008310||crowdings tooth
|
|
D008310||crowding tooth
|
|
D008310||malocclusions
|
|
D008310||tooth crowding
|
|
D008311||malocclusion angle class i
|
|
D008311||angle class i
|
|
D008311||class i angle
|
|
D010623||phencyclidine abuse
|
|
D010623||abuse angel dust
|
|
D010623||abuse pcp
|
|
D010623||abuse phencyclidine
|
|
D010623||angel dust abuse
|
|
D010623||pcp abuse
|
|
D010623||phencyclidine abuses
|
|
D010623||phencyclidine related disorder
|
|
D010623||phencyclidine related disorders
|
|
D058606||accessory atrioventricular bundle
|
|
D058606||accessory atrioventricular bundles
|
|
D058606||accessory atrioventricular pathway
|
|
D058606||accessory atrioventricular pathways
|
|
D058606||accessory conducting pathway
|
|
D058606||accessory conducting pathways
|
|
D058606||accessory pathway concealed
|
|
D058606||accessory pathway fasciculoventricular
|
|
D058606||accessory pathway nodoventricular
|
|
D058606||accessory pathways concealed
|
|
D058606||accessory pathways fasciculoventricular
|
|
D058606||accessory pathways nodoventricular
|
|
D058606||atrio hisian bypass tract
|
|
D058606||atrio hisian bypass tracts
|
|
D058606||atriohisian fiber
|
|
D058606||atriohisian fibers
|
|
D058606||atriohisian tract
|
|
D058606||atriohisian tracts
|
|
D058606||atrioventricular bundle accessory
|
|
D058606||atrioventricular bundles accessory
|
|
D058606||atrioventricular pathway accessory
|
|
D058606||atrioventricular pathways accessory
|
|
D058606||bundle accessory atrioventricular
|
|
D058606||bundle kent
|
|
D058606||bundle of kent
|
|
D058606||bundles accessory atrioventricular
|
|
D058606||bypass tract atrio hisian
|
|
D058606||bypass tracts atrio hisian
|
|
D058606||concealed accessory pathway
|
|
D058606||concealed accessory pathways
|
|
D058606||conducting pathway accessory
|
|
D058606||conducting pathways accessory
|
|
D058606||fasciculoventricular accessory pathway
|
|
D058606||fasciculoventricular accessory pathways
|
|
D058606||fasciculoventricular pathway
|
|
D058606||fasciculoventricular pathways
|
|
D058606||fiber atriohisian
|
|
D058606||fibers atriohisian
|
|
D058606||fibers james
|
|
D058606||fibers mahaim
|
|
D058606||james fibers
|
|
D058606||kent bundle
|
|
D058606||mahaim fibers
|
|
D058606||nodoventricular accessory pathway
|
|
D058606||nodoventricular accessory pathways
|
|
D058606||nodoventricular pathway
|
|
D058606||nodoventricular pathways
|
|
D058606||pathway accessory atrioventricular
|
|
D058606||pathway accessory conducting
|
|
D058606||pathway concealed accessory
|
|
D058606||pathway fasciculoventricular
|
|
D058606||pathway fasciculoventricular accessory
|
|
D058606||pathway nodoventricular
|
|
D058606||pathway nodoventricular accessory
|
|
D058606||pathways accessory atrioventricular
|
|
D058606||pathways accessory conducting
|
|
D058606||pathways concealed accessory
|
|
D058606||pathways fasciculoventricular
|
|
D058606||pathways fasciculoventricular accessory
|
|
D058606||pathways nodoventricular
|
|
D058606||pathways nodoventricular accessory
|
|
D058606||tract atriohisian
|
|
D058606||tract atrio hisian bypass
|
|
D058606||tracts atriohisian
|
|
D058606||tracts atrio hisian bypass
|
|
604321||microcephaly 4 primary autosomal recessive
|
|
604321||mcph4
|
|
C566540||migraine familial basilar
|
|
C579849||15q24 microdeletion
|
|
C579849||15q24 deletion
|
|
C579849||15q24 microdeletion syndrome
|
|
C579849||interstitial deletion of chromosome 15q24
|
|
D063192||pregnancy heterotopic
|
|
D063192||cornual heterotopic pregnancies
|
|
D063192||cornual heterotopic pregnancy
|
|
D063192||heterotopic pregnancies
|
|
D063192||heterotopic pregnancies cornual
|
|
D063192||heterotopic pregnancies tubal
|
|
D063192||heterotopic pregnancy
|
|
D063192||heterotopic pregnancy cornual
|
|
D063192||heterotopic pregnancy tubal
|
|
D063192||pregnancies cornual heterotopic
|
|
D063192||pregnancies heterotopic
|
|
D063192||pregnancies tubal heterotopic
|
|
D063192||pregnancy cornual heterotopic
|
|
D063192||pregnancy tubal heterotopic
|
|
D063192||tubal heterotopic pregnancies
|
|
D063192||tubal heterotopic pregnancy
|
|
C567878||erythrocyte amp deaminase deficiency
|
|
C566543||creases infra auricular cutaneous with tall stature and advanced bone age
|
|
C566544||short stature auditory canal atresia mandibular hypoplasia skeletal abnormalities
|
|
C566544||sams
|
|
C563415|600977||cone rod dystrophy 5
|
|
C563415|600977||cord5
|
|
D008312||malocclusion angle class ii
|
|
D008312||angle class ii
|
|
D008312||class ii angle
|
|
210710|C537577||microcephalic osteodysplastic primordial dwarfism type 1
|
|
210710|C537577||brachymelic primordial dwarfism
|
|
210710|C537577||cephaloskeletal dysplasia
|
|
210710|C537577||low birth weight dwarfism with skeletal dysplasia
|
|
210710|C537577||microcephalic osteodysplastic primordial dwarfism type i
|
|
210710|C537577||mopd
|
|
210710|C537577||mopd1
|
|
210710|C537577||mopd i
|
|
210710|C537577||osteodysplastic primordial dwarfism type 1
|
|
210710|C537577||osteodysplastic primordial dwarfism type i
|
|
210710|C537577||tals
|
|
210710|C537577||taybi linder syndrome
|
|
D008313||malocclusion angle class iii
|
|
D008313||angle class iii
|
|
D008313||class iii angle
|
|
D008313||underbite
|
|
D008313||underbites
|
|
C535494|131850||epidermolysis bullosa pretibial
|
|
C535494|131850||deb pretibial
|
|
C535494|131850||dystrophic epidermolysis bullosa pretibial
|
|
C535494|131850||epidermolysis bullosa dystrophica pretibial
|
|
C535494|131850||pretibial epidermolysis bullosa
|
|
208400|D054880||aspartylglucosaminuria
|
|
208400|D054880||aga deficiencies
|
|
208400|D054880||aga deficiency
|
|
208400|D054880||agu
|
|
208400|D054880||aspartylglucosamidase deficiencies
|
|
208400|D054880||aspartylglucosamidase deficiency
|
|
208400|D054880|C538402||aspartylglucosaminidase deficiency
|
|
208400|D054880||aspartylglucosaminurias
|
|
208400|D054880||aspartylglycosaminuria
|
|
208400|D054880||aspartylglycosaminurias
|
|
208400|D054880||deficiencies aga
|
|
208400|D054880||deficiencies aspartylglucosamidase
|
|
208400|D054880||deficiency aga
|
|
208400|D054880||deficiency aspartylglucosamidase
|
|
208400|D054880||glycoasparaginase
|
|
208400|D054880||glycoasparaginases
|
|
208400|D054880|C538402||glycosylasparaginase deficiency
|
|
C567835|612968||cataract autosomal recessive congenital 3
|
|
C567835|612968||cataract 34 multiple types
|
|
C567835|612968||cataract 34 multiple types with or without microcornea
|
|
C567835|612968||catc3
|
|
C567835|612968||ctrct34
|
|
D058617||composite lymphoma
|
|
D058617||composite lymphomas
|
|
D058617||lymphoma composite
|
|
D058617||lymphomas composite
|
|
D001327|109100||autoimmune diseases
|
|
D001327|109100||ais6
|
|
D001327|109100||autoimmune disease
|
|
D001327|109100||autoimmune disease susceptibility to 6
|
|
D001327|109100||disease autoimmune
|
|
D001327|109100||diseases autoimmune
|
|
C567492|262700||pituitary hormone deficiency combined 4
|
|
C567492|262700||cphd4
|
|
C567492|262700||pituitary hormone deficiency combined with or without cerebellar defects
|
|
C567492|262700||short stature pituitary and cerebellar defects and small sella turcica
|
|
203300|C538539||albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
|
|
203300|C538539||delta storage pool disease
|
|
203300|C538539||hermansky pudlak syndrome 1
|
|
203300|C538539||hps1
|
|
C565220||bleeding disorder due to p2ry12 defect
|
|
106280|C562396||ankyloglossia
|
|
106280|C562396||tongue tie
|
|
106280|C562396||apos tongue tie apos
|
|
604317||microcephaly 2 primary autosomal recessive with or without cortical malformations
|
|
604317||mcph2
|
|
C537746|258315||omodysplasia type 1
|
|
C537746|258315|C537557||micromelic dysplasia congenital with dislocation of radius
|
|
C537746|258315||omod1
|
|
C537746|258315||omodysplasia 1
|
|
C537746|258315||omodysplasia autosomal recessive
|
|
C537746|258315||omodysplasia autosomal recessive form
|
|
C537746|258315||omodysplasia generalized form
|
|
C537746|258315||omodysplasia maroteaux
|
|
C566514||skeletal dysplasia and progressive central nervous system degeneration lethal
|
|
C566515||spondyloepiphyseal dysplasia with coronal craniosynostosis cataracts cleft palate and mental retardation
|
|
D023921||coronary stenosis
|
|
D023921||artery stenoses coronary
|
|
D023921||artery stenosis coronary
|
|
D023921||coronary artery stenoses
|
|
D023921||coronary artery stenosis
|
|
D023921||coronary stenoses
|
|
D023921||stenoses coronary
|
|
D023921||stenoses coronary artery
|
|
D023921||stenosis coronary
|
|
D023921||stenosis coronary artery
|
|
C562405|265100||pulmonary alveolar microlithiasis
|
|
D009617||nocardia infections
|
|
D009617||cerebral nocardioses
|
|
D009617||cerebral nocardiosis
|
|
D009617||cutaneous nocardioses primary
|
|
D009617||cutaneous nocardiosis primary
|
|
D009617||infection nocardia
|
|
D009617||infections nocardia
|
|
D009617||nocardia infection
|
|
D009617||nocardioses
|
|
D009617||nocardioses cerebral
|
|
D009617||nocardioses primary cutaneous
|
|
D009617||nocardioses pulmonary
|
|
D009617||nocardiosis
|
|
D009617||nocardiosis cerebral
|
|
D009617||nocardiosis primary cutaneous
|
|
D009617||nocardiosis pulmonary
|
|
D009617||primary cutaneous nocardioses
|
|
D009617||primary cutaneous nocardiosis
|
|
D009617||pulmonary nocardioses
|
|
D009617||pulmonary nocardiosis
|
|
209920|C537079||bare lymphocyte syndrome 2
|
|
209920|C537079||bare lymphocyte syndrome type 2
|
|
209920|C537079||bare lymphocyte syndrome type ii
|
|
209920|C537079||bare lymphocyte syndrome type ii complementation group b included
|
|
209920|C537079||bare lymphocyte syndrome type ii complementation group c included
|
|
209920|C537079||bare lymphocyte syndrome type ii complementation group d included
|
|
209920|C537079||bare lymphocyte syndrome type ii complementation group e included
|
|
209920|C537079|210900|D001816||bls
|
|
209920|C537079||bls type ii
|
|
209920|C537079||scid hla class 2 negative
|
|
209920|C537079||scid hla class ii negative
|
|
209920|C537079||scid hla class ii negative bare lymphocyte syndrome type ii complementation group a included
|
|
209920|C537079||severe combined immunodeficiency hla class ii negative
|
|
D046648||hematoma subdural intracranial
|
|
D046648||hematoma intracranial subdural
|
|
D046648||hematomas intracranial subdural
|
|
D046648||hematoma subdural cranial
|
|
D046648||intracranial subdural hematoma
|
|
D046648||intracranial subdural hematomas
|
|
D046648||intracranial subdural hematoma traumatic
|
|
D046648||subdural hematoma intracranial
|
|
D046648||subdural hematomas intracranial
|
|
D046648||subdural hematoma traumatic intracranial
|
|
D046648||traumatic intracranial subdural hematoma
|
|
D010608||pharyngeal diseases
|
|
D010608||disease pharyngeal
|
|
D010608||disease pharynx
|
|
D010608||diseases of pharynx
|
|
D010608||diseases pharyngeal
|
|
D010608||diseases pharynx
|
|
D010608||pharyngeal disease
|
|
D010608||pharynx disease
|
|
D010608||pharynx diseases
|
|
254210|C535759||congenital myasthenic syndrome with episodic apnea
|
|
254210|C535759||cms1a2
|
|
254210|C535759||cms ea
|
|
254210|C535759||cms ia2
|
|
254210|C535759||congenital myasthenic syndrome type 1a
|
|
254210|C535759||congenital myasthenic syndrome type ia
|
|
254210|C535759||congenital myasthenic syndrome type ia2
|
|
254210|C535759||fim
|
|
254210|C535759||fimg2 formerly
|
|
254210|C535759||myasthenia familial infantile
|
|
254210|C535759||myasthenia gravis familial infantile 2 formerly
|
|
254210|C535759||myasthenic syndrome congenital associated with episodic apnea
|
|
254210|C535759||myasthenic syndrome presynaptic congenital associated with episodic apnea
|
|
D046649||hematoma subdural spinal
|
|
D046649||hematoma spinal subdural
|
|
D046649||hematomas spinal subdural
|
|
D046649||spinal subdural hematoma
|
|
D046649||spinal subdural hematomas
|
|
D046649||spinal subdural hematoma traumatic
|
|
D046649||subdural hematoma spinal
|
|
D046649||subdural hematoma spinal traumatic
|
|
D046649||subdural hematomas spinal
|
|
D046649||traumatic spinal subdural hematoma
|
|
C535428|606798||benign essential blepharospasm
|
|
C535428|606798||blepharospasm benign essential
|
|
C535428|606798||essential blepharospasm
|
|
C535428|606798||eyelid twitching
|
|
C535428|606798||primary blepharospasm
|
|
C535428|606798||spasm of eyelids
|
|
C566516||pancreatic lymphoma familial
|
|
C566519||emphysema congenital with deafness penoscrotal web and mental retardation
|
|
C567849||microcephaly growth retardation cataract hearing loss and unusual appearance
|
|
C537119|127300||leri weil syndrome
|
|
C537119|127300||dyschondrosteosis
|
|
C537119|127300||dyschondrosteosis dco madelung deformity included
|
|
C537119|127300||leri weill dyschondrosteosis
|
|
C537119|127300||l 233 ri weill dyschondrosteosis
|
|
C537119|127300||lwd
|
|
D017204|105830||angelman syndrome
|
|
D017204|105830||ancr included
|
|
D017204|105830||as
|
|
D017204|105830||children puppet
|
|
D017204|105830||happy puppet syndrome
|
|
D017204|105830||happy puppet syndrome formerly angelman syndrome chromosome region included
|
|
D017204|105830||puppet children
|
|
D017204|105830||syndrome angelman
|
|
D017204|105830||syndrome happy puppet
|
|
D059952||pelvic floor disorders
|
|
D059952||disease pelvic floor
|
|
D059952||diseases pelvic floor
|
|
D059952||disorder pelvic floor
|
|
D059952||disorders pelvic floor
|
|
D059952||pelvic floor disease
|
|
D059952||pelvic floor diseases
|
|
D059952||pelvic floor disorder
|
|
C567551|612847||spondyloepimetaphyseal dysplasia pakistani type
|
|
C567551|612847||brachyolmia type 4 with mild epiphyseal and metaphyseal changes
|
|
C567551|612847||semd pakistani type
|
|
C567551|612847|C567552||spondylodysplasia and premature pubarche
|
|
D058627||macrocephaly
|
|
D058627||macrocephalies
|
|
C563448|600757||orofacial cleft 3
|
|
C563448|600757||cleft lip with or without cleft palate nonsyndromic 3
|
|
C563448|600757||ofc3
|
|
C537150|240800||hypoglycemia leucine induced
|
|
C537150|240800||leucine sensitive hypoglycemia of infancy
|
|
C537150|240800||lih
|
|
D058625||end stage liver disease
|
|
D058625||chronic liver failure
|
|
D058625||chronic liver failures
|
|
D058625||failure chronic liver
|
|
D058625||failures chronic liver
|
|
D058625||liver failure chronic
|
|
D058625||liver failures chronic
|
|
C566523||spondyloepimetaphyseal dysplasia shohat type
|
|
C566523||semd shohat type
|
|
C566524||facial dysmorphism cleft palate hearing loss and camptodactyly
|
|
C566525||microcephaly macrotia and mental retardation
|
|
C566526||anal atresia hypospadias and penoscrotal inversion
|
|
C566520||mandibulofacial dysostosis with macroblepharon and macrostomia
|
|
C567850||hadziselimovic syndrome
|
|
C567850||microcephaly faciocardioskeletal syndrome
|
|
115195|C566171||cardiomyopathy familial hypertrophic 2
|
|
115195|C566171||cmh2
|
|
C566521||brachydactyly intraventricular septal defect and deafness
|
|
C566522||craniomicromelic syndrome
|
|
C564531|300345||microphthalmia isolated with coloboma 1
|
|
C564531|300345||mcopcb1
|
|
C564531|300345||microphthalmia colobomatous isolated 1
|
|
604232|C565814||leber congenital amaurosis 3
|
|
604232|C565814||lca3
|
|
604232|C565814||retinitis pigmentosa juvenile spata7 related
|
|
604232|C565814||retinitis pigmentosa juvenile spata7 related included
|
|
D009625||noma
|
|
D009625||cancrum oris
|
|
D009625||gangrenous stomatitides
|
|
D009625||gangrenous stomatitis
|
|
D009625||nomas
|
|
D009625||stomatitides gangrenous
|
|
D009625||stomatitis gangrenous
|
|
D010024|166710||osteoporosis
|
|
D010024|166710||age related bone loss
|
|
D010024|166710||age related bone losses
|
|
D010024|166710||age related osteoporoses
|
|
D010024|166710||age related osteoporosis
|
|
D010024|166710||bmnd
|
|
D010024|166710||bone loss age related
|
|
D010024|166710||bone losses age related
|
|
D010024|166710||bone mineral density quantitative trait locus
|
|
D010024|166710||osteoporoses
|
|
D010024|166710||osteoporoses age related
|
|
D010024|166710||osteoporoses senile
|
|
D010024|166710||osteoporosis age related
|
|
D010024|166710||osteoporosis involutional
|
|
D010024|166710||osteoporosis involutional fracture hip susceptibility to included
|
|
D010024|166710|D015663||osteoporosis postmenopausal
|
|
D010024|166710||osteoporosis post traumatic
|
|
D010024|166710||osteoporosis senile
|
|
D010024|166710||post traumatic osteoporoses
|
|
D010024|166710||post traumatic osteoporosis
|
|
D010024|166710||senile osteoporoses
|
|
D010024|166710||senile osteoporosis
|
|
C566527||muscular dystrophy congenital megaconial type
|
|
C566529||arterial occlusive disease progressive with hypertension heart defects bone fragility and brachysyndactyly
|
|
C566529||grange occlusive arterial syndrome
|
|
C563752|609271||keratoconus 4
|
|
C563752|609271||ktcn4
|
|
D009631||nonodontogenic cysts
|
|
D009631||cyst nonodontogenic
|
|
D009631||cysts nonodontogenic
|
|
D009631||nonodontogenic cyst
|
|
D009630||nondisjunction genetic
|
|
D009630||genetic nondisjunction
|
|
D009630||genetic non disjunction
|
|
D009630||genetic nondisjunctions
|
|
D009630||genetic non disjunctions
|
|
D009630||non disjunction genetic
|
|
D009630||nondisjunctions genetic
|
|
D009630||non disjunctions genetic
|
|
C567647|613312||hypophosphatemic rickets autosomal recessive 2
|
|
C567647|613312||arhr2
|
|
D010610||pharyngeal neoplasms
|
|
D010610||cancer of pharynx
|
|
D010610||cancer of the pharynx
|
|
D010610||cancer pharnyx
|
|
D010610||cancer pharyngeal
|
|
D010610||cancers pharnyx
|
|
D010610||cancers pharyngeal
|
|
D010610||neoplasm pharyngeal
|
|
D010610||neoplasm pharynx
|
|
D010610||neoplasms pharyngeal
|
|
D010610||neoplasms pharynx
|
|
D010610||pharnyx cancer
|
|
D010610||pharnyx cancers
|
|
D010610||pharyngeal cancer
|
|
D010610||pharyngeal cancers
|
|
D010610||pharyngeal neoplasm
|
|
D010610||pharynx cancer
|
|
D010610||pharynx cancers
|
|
D010610||pharynx neoplasm
|
|
D010610||pharynx neoplasms
|
|
D010612||pharyngitis
|
|
D010612||pharyngitides
|
|
D010612||sore throat
|
|
D010612||sore throats
|
|
D010612||throat sore
|
|
C535476|608470||corneal dystrophy of bowman layer type 1
|
|
C535476|608470||cdb1
|
|
C535476|608470||cdrb
|
|
C535476|608470||corneal dystrophy geographic
|
|
C535476|608470||corneal dystrophy of bowman layer type i
|
|
C535476|608470||corneal dystrophy reis bucklers type
|
|
C535476|608470||granular corneal dystrophy type iii
|
|
C535476|608470||rbcd
|
|
C535476|608470||reis bucklers corneal dystrophy
|
|
C535476|608470||reis bucklers dystrophy
|
|
C567821||febrile convulsions familial 3b
|
|
607595|C564372||brain small vessel disease with hemorrhage
|
|
607595|C564372||brain small vessel disease with axenfeld rieger anomaly
|
|
607595|C564372||col4a1 related brain small vessel disease
|
|
607595|C564372||infantile hemiparesis
|
|
607595|C564372||leukoencephalopathy with axenfeld rieger anomaly
|
|
607595|C564372||leukoencephalopathy with axenfeld rieger anomaly included
|
|
607595|C564372||retinal arteriolar tortuosity infantile hemiparesis and leukoencephalopathy autosomal dominant
|
|
607595|C564372||retinal arteriolar tortuosity infantile hemiparesis and leukoencephalopathy autosomal dominant brain small vessel disease with axenfeld rieger anomaly included
|
|
D014190||transvestism
|
|
D014190||fetishisms transvestic
|
|
D014190||fetishism transvestic
|
|
D014190||transvestic fetishism
|
|
D014190||transvestic fetishisms
|
|
D014190||transvestisms
|
|
C567820||febrile convulsions familial 3a
|
|
C567820||convulsions familial febrile 3a
|
|
C567820||seizures familial febrile 3a
|
|
C567046|610921||surfactant metabolism dysfunction pulmonary 3
|
|
C567046|610921||interstitial lung disease due to abca3 deficiency
|
|
C567046|610921||pulmonary alveolar proteinosis congenital 3
|
|
C567046|610921||smdp3
|
|
D023903||coronary restenosis
|
|
D023903||coronary restenoses
|
|
D023903||restenoses coronary
|
|
D023903||restenosis coronary
|
|
C565390|251000||methylmalonic aciduria due to methylmalonyl coa mutase deficiency
|
|
C565390|251000||methylmalonic acidemia due to methylmalonyl coa mutase deficiency
|
|
C565390|251000||methylmalonic acidemia due to methylmalonyl coa mutase deficiency mma due to mcm deficiency
|
|
C565390|251000||methylmalonic aciduria mut 0 type
|
|
C565390|251000||methylmalonic aciduria mut type
|
|
C565390|251000||methylmalonic aciduria mut type included
|
|
C565390|251000||methylmalonic aciduria mut type methylmalonic aciduria mut 0 type included
|
|
C565390|251000||mma due to mcm deficiency
|
|
C565310|605642||thyroid carcinoma papillary with papillary renal neoplasia
|
|
C565310|605642||prn1
|
|
C565310|605642||ptcprn
|
|
C565320|605582||cardiomyopathy dilated 1k
|
|
C565320|605582||cmd1k
|
|
C567827||generalized epilepsy with febrile seizures plus 7
|
|
C567827||gefsp7
|
|
C567827||generalized epilepsy with febrile seizures plus type 7
|
|
190350||trps1
|
|
190350||trps i
|
|
D014189||transsexualism
|
|
D014189||transsexualisms
|
|
D014188||transposition of great vessels
|
|
D014188||dextro looped transposition of the great arteries
|
|
D014188||great arteries transposition
|
|
D014188||great arteries transpositions
|
|
D014188||great vessels transposition
|
|
D014188||great vessels transpositions
|
|
D014188||transposition of great arteries
|
|
302045|300376|D020388||cardiomyopathy dilated 3b
|
|
302045|300376|D020388||cardiomyopathy dilated x linked
|
|
302045||xlcm
|
|
C563322|601410||diabetes mellitus transient neonatal 1
|
|
C563322|601410||dmtn
|
|
C563322|601410||tndm
|
|
C563322|601410||tndm1
|
|
C566502||visceral neuropathy familial autosomal dominant
|
|
C566502||enteric neuropathy familial
|
|
C566502||pseudoobstruction chronic intestinal neuropathic
|
|
C566502|155310||pseudoobstruction idiopathic intestinal
|
|
C567053|610878||vesicoureteral reflux 2
|
|
C567053|610878||vur2
|
|
C567831||emery dreifuss muscular dystrophy 4
|
|
C567830||emery dreifuss muscular dystrophy 5
|
|
C566509||external ophthalmoplegia synergistic divergence jaw winking and oculocutaneous hypopigmentation
|
|
D011928||raynaud disease
|
|
D011928||cold fingers hereditary
|
|
D011928||raynaud phenomenon
|
|
D011928||raynaud apos s disease
|
|
D011928||raynauds disease
|
|
C566507||spondylomegaepiphyseal dysplasia with upper limb mesomelia punctate calcifications and deafness
|
|
C566508||fibrosis of extraocular muscles congenital with synergistic divergence
|
|
C566508||congenital fibrosis syndrome with synergistic divergence
|
|
C566508||external ophthalmoplegia with synergistic divergence
|
|
C567425|612079||alopecia neurologic defects and endocrinopathy syndrome
|
|
C567425|612079||ane syndrome
|
|
607676|C564352||irak4 deficiency
|
|
607676|C564352||irak4d
|
|
607676|C564352||irak 4 deficiency
|
|
C535323|153550||5q syndrome
|
|
C535323|153550||5q deletion syndrome
|
|
C535323|153550||chromosome 5q deletion syndrome
|
|
C535323|153550||macrocytic anemia refractory due to 5q deletion
|
|
C535323|153550||macrocytic anemia refractory due to 5q deletion mar megakaryocytes unilobular nucleated included
|
|
C535323|153550||refractory macrocytic anemia due to 5q deletion
|
|
C537589|602450||severe combined immunodeficiency with sensitivity to ionizing radiation
|
|
C537589|602450||athabaskan severe combined immunodeficiency included
|
|
C537589|602450||rs scid
|
|
C537589|602450||scida included
|
|
C537589|602450||scid autosomal recessive t cell negative b cell negative nk cell positive with sensitivity to ionizing radiation
|
|
C537589|602450||scid autosomal recessive t cell negative b cell negative nk cell positive with sensitivity to ionizing radiation severe combined immunodeficiency athabaskan type included
|
|
C537589|602450||severe combined immunodeficiency partial included
|
|
C566411|603075||macular degeneration age related 1
|
|
C566411|603075||armd1
|
|
C566411|603075||maculopathy age related 1
|
|
D002189||marijuana abuse
|
|
D002189||abuse cannabis
|
|
D002189||abuse hashish
|
|
D002189||abuse marihuana
|
|
D002189||abuse marijuana
|
|
D002189||cannabis abuse
|
|
D002189||cannabis dependence
|
|
D002189||cannabis related disorder
|
|
D002189||dependence cannabis
|
|
D002189||dependence marijuana
|
|
D002189||disorder cannabis related
|
|
D002189||hashish abuse
|
|
D002189||marihuana abuse
|
|
D002189||marijuana dependence
|
|
C565360|613791||masp2 deficiency
|
|
C567804||dursun syndrome
|
|
C567804||pulmonary arterial hypertension leukopenia and atrial septal defect
|
|
C531844||von willebrand factor deficiency
|
|
D002194||capgras syndrome
|
|
D002194||syndrome capgras
|
|
C531847||wallerian degeneration of the pyramidal tract
|
|
C531849||intestinal lipophagic granulomatosis
|
|
C531849||secondary non tropical sprue
|
|
D056005||leprosy paucibacillary
|
|
D056005||borderline tuberculoid
|
|
D056005||borderline tuberculoids
|
|
D056005||indeterminate tuberculoid
|
|
D056005||indeterminate tuberculoids
|
|
D056005||leprosies paucibacillary
|
|
D056005||paucibacillary leprosies
|
|
D056005||paucibacillary leprosy
|
|
D056005||tuberculoid borderline
|
|
D056005||tuberculoid indeterminate
|
|
D056005||tuberculoids borderline
|
|
D056005||tuberculoids indeterminate
|
|
D056006||leprosy multibacillary
|
|
D056006||borderline lepromatous
|
|
D056006||lepromatous borderline
|
|
D056006||lepromatous midborderline
|
|
D056006||leprosies multibacillary
|
|
D056006||midborderline lepromatous
|
|
D056006||multibacillary leprosies
|
|
D056006||multibacillary leprosy
|
|
C531841||benign non infected urachal cyst
|
|
C531841||giant urachal cyst
|
|
C531841||infected urachal cyst
|
|
C531841||inflamed urachal cyst
|
|
D015499||renal tubular transport inborn errors
|
|
D015499||kidney tubular transport inborn error
|
|
D015499||kidney tubular transport inborn errors
|
|
D015499||renal tubular transport errors
|
|
D015499||renal tubular transport inborn error
|
|
132000|C562638||epidermolysis bullosa with congenital localized absence of skin and deformity of nails
|
|
132000|C562638||epidermolysis bullosa dystrophica bart type
|
|
C567810||chromosome 19q13 11 deletion syndrome
|
|
226670|C535955||epidermolysa bullosa simplex and limb girdle muscular dystrophy
|
|
226670|C535955||ebs md
|
|
226670|C535955||epidermolysis bullosa simplex and limb girdle muscular dystrophy
|
|
226670|C535955||epidermolysis bullosa simplex with muscular dystrophy
|
|
226670|C535955||mdebs
|
|
226670|C535955||md ebs
|
|
600803||gallbladder disease 1
|
|
600803||cholelithiasis low phospholipid associated
|
|
600803||gbd1
|
|
600803||lpac
|
|
C567819||santos syndrome
|
|
C567819||fibular agenesis hypoplasia oligodactylous clubfeet and anonychia nail hypoplasia syndrome
|
|
D011906||rat bite fever
|
|
D011906||fever ratbite
|
|
D011906||fever rat bite
|
|
D011906||fevers ratbite
|
|
D011906||fevers rat bite
|
|
D011906||ratbite fever
|
|
D011906||ratbite fevers
|
|
D011906||rat bite fevers
|
|
D011906||sodoku
|
|
C537466|309801||microphthalmia syndromic 7
|
|
C537466|309801||mcops7
|
|
C537466|309801||microphthalmia dermal aplasia and sclerocornea
|
|
C537466|309801||microphthalmia with linear skin defects
|
|
C537466|309801||microphthalmia with linear skin defects syndrome
|
|
C537466|309801||microphthalmia with linear skin lesions syndrome
|
|
C537466|309801||midas syndrome
|
|
C537466|309801||mls
|
|
C537466|309801||syndromic microphthalmia 7
|
|
607785|D054429||leukemia myelomonocytic juvenile
|
|
607785|D054429||cmml included
|
|
607785|D054429||jmml
|
|
607785|D054429||juvenile chronic myelogenous leukemia
|
|
607785|D054429||juvenile myelomonocytic leukemia
|
|
607785|D054429||juvenile myelomonocytic leukemias
|
|
607785|D054429||leukemia juvenile myelomonocytic
|
|
607785|D054429||leukemia juvenile myelomonocytic leukemia chronic myelomonocytic included
|
|
607785|D054429||myelomonocytic leukemia juvenile
|
|
607785|D054429||myelomonocytic leukemias juvenile
|
|
D058674||chromosome duplication
|
|
D058674||chromosomal duplication
|
|
D058674||chromosomal duplications
|
|
D058674||chromosome duplications
|
|
D058674||duplication chromosomal
|
|
D058674||duplication chromosome
|
|
D058674||duplications chromosomal
|
|
D058674||duplications chromosome
|
|
C531857||zellweger leukodystrophy
|
|
D011900||ranula
|
|
D011900||ranulas
|
|
D058670||tetrasomy
|
|
D058670||partial tetrasomies
|
|
D058670||partial tetrasomy
|
|
D058670||tetrasomies
|
|
D058670||tetrasomies partial
|
|
D058670||tetrasomy partial
|
|
D014178||translocation genetic
|
|
D014178||chromosomal translocation
|
|
D014178||chromosomal translocations
|
|
D014178||genetic translocation
|
|
D014178||genetic translocations
|
|
D014178||translocation chromosomal
|
|
D014178||translocations chromosomal
|
|
D014178||translocations genetic
|
|
142700||developmental dysplasia of the hip 1
|
|
142700||acetabular dysplasia
|
|
142700||ddh
|
|
142700||ddh1
|
|
142700||hip dysplasia developmental
|
|
D000437|103780||alcoholism
|
|
D000437|103780||abuse alcohol
|
|
D000437|103780||addiction alcohol
|
|
D000437|103780||alcohol abuse
|
|
D000437|103780||alcohol addiction
|
|
D000437|103780||alcohol dependence
|
|
D000437|103780||alcoholic intoxication chronic
|
|
D000437|103780||chronic alcoholic intoxication
|
|
D000437|103780||dependence alcohol
|
|
D000437|103780||intoxication chronic alcoholic
|
|
C563848|608810||alpha b crystallinopathy
|
|
C563848|608810||mfm2
|
|
C563848|608810||myopathy cardioskeletal desmin related with cataract
|
|
C563848|608810||myopathy desmin related associated with mutation in the cryab gene
|
|
C563848|608810||myopathy myofibrillar 2
|
|
C563848|608810||myopathy myofibrillar alpha b crystallin related
|
|
C563848|608810||myopathy myofibrillar with or without cataract and or cardiomyopathy
|
|
D002169||campylobacter infections
|
|
D002169||campylobacter infection
|
|
D002169||infection campylobacter
|
|
D002169||infections campylobacter
|
|
D058686||coronary subclavian steal syndrome
|
|
D058686||syndrome coronary subclavian steal
|
|
D058686||syndromes coronary subclavian steal
|
|
D058687||out of hospital cardiac arrest
|
|
D058687||cardiac arrest out of hospital
|
|
D058687||cardiac arrests out of hospital
|
|
D058687||heart arrest out of hospital
|
|
D058687||heart arrests out of hospital
|
|
D058687||out of hospital cardiac arrests
|
|
D058687||out of hospital heart arrest
|
|
D058687||out of hospital heart arrests
|
|
C537505|262650||kowarski syndrome
|
|
C537505|262650||biodefective growth hormone
|
|
C537505|262650||nanism due to growth hormone qualitative anomaly
|
|
C537505|262650||pituitary dwarfism 4
|
|
C537505|262650||pituitary dwarfism with normal immunoreactive growth hormone
|
|
C537505|262650||pituitary dwarfism with normal immunoreactive growth hormone and low somatomedin
|
|
D015479||leukemia myelomonocytic acute
|
|
D015479||acute myelomonocytic leukemia
|
|
D015479||acute myelomonocytic leukemias
|
|
D015479||leukemia acute myelomonocytic
|
|
D015479||leukemia myeloid acute m4
|
|
D015479||leukemia myeloid naegeli type
|
|
D015479||leukemia naegeli type myeloid
|
|
D015479||leukemias acute myelomonocytic
|
|
D015479||myeloid leukemia acute m4
|
|
D015479||myeloid leukemia naegeli type
|
|
D015479||myelomonocytic leukemia acute
|
|
D015479||myelomonocytic leukemias acute
|
|
D015479||naegeli type myeloid leukemia
|
|
209950|D009165||mycobacterium infections nontuberculous
|
|
209950|D009165||atypical mycobacterial infection disseminated
|
|
209950|D009165||atypical mycobacterioses familial
|
|
209950|D009165||atypical mycobacteriosis familial
|
|
209950|D009165||atypical mycobacteriosis familial disseminated
|
|
209950|D009165||atypical mycobacterium infection
|
|
209950|D009165||atypical mycobacterium infections
|
|
209950|D009165||bcg and salmonella infection disseminated included
|
|
209950|D009165||bcg infection generalized familial semibenign autosomal dominant included
|
|
209950|D009165||familial atypical mycobacterioses
|
|
209950|D009165||familial atypical mycobacteriosis
|
|
209950|D009165||infection atypical mycobacterium
|
|
209950|D009165||infection nontuberculous mycobacterium
|
|
209950|D009165||infections atypical mycobacterium
|
|
209950|D009165||infections nontuberculous mycobacterium
|
|
209950|D009165||mycobacterial disease mendelian susceptibility to msmd bcg infection generalized familial included
|
|
209950|D009165||mycobacterioses familial atypical
|
|
209950|D009165||mycobacteriosis familial atypical
|
|
209950|D009165||mycobacterium infection atypical
|
|
209950|D009165||mycobacterium infection nontuberculous
|
|
209950|D009165||mycobacterium infections atypical
|
|
209950|D009165||nontuberculous mycobacterium infection
|
|
209950|D009165||nontuberculous mycobacterium infections
|
|
D015477||leukemia myelomonocytic chronic
|
|
D015477||chronic myelomonocytic leukemia
|
|
D015477||chronic myelomonocytic leukemias
|
|
D015477||leukemia chronic myelomonocytic
|
|
D015477||leukemias chronic myelomonocytic
|
|
D015477||myelomonocytic leukemia chronic
|
|
D015477||myelomonocytic leukemias chronic
|
|
D015490||htlv i infections
|
|
D015490||htlv i infection
|
|
D015490||infection htlv i
|
|
D015490||infections htlv i
|
|
D015494||salivary gland calculi
|
|
D015494||calculi salivary gland
|
|
D015494||calculus salivary gland
|
|
D015494||gland calculi salivary
|
|
D015494||gland calculus salivary
|
|
D015494||gland stone salivary
|
|
D015494||gland stones salivary
|
|
D015494||salivary gland calculus
|
|
D015494||salivary gland stone
|
|
D015494||salivary gland stones
|
|
D015494||sialolith
|
|
D015494||sialolithiasis
|
|
D015494||sialoliths
|
|
D015494||stone salivary gland
|
|
D015494||stones salivary gland
|
|
D015491||htlv ii infections
|
|
D015491||htlv ii infection
|
|
D015491||infection htlv ii
|
|
D015491||infections htlv ii
|
|
D002178||candidiasis chronic mucocutaneous
|
|
D002178||candidiases chronic mucocutaneous
|
|
D002178||chronic mucocutaneous candidiases
|
|
D002178||chronic mucocutaneous candidiasis
|
|
D002178||mucocutaneous candidiases chronic
|
|
D002178||mucocutaneous candidiasis chronic
|
|
D002179||candidiasis cutaneous
|
|
D002179||candidiases cutaneous
|
|
D002179||cutaneous candidiases
|
|
D002179||cutaneous candidiasis
|
|
D002179||cutaneous moniliases
|
|
D002179||cutaneous moniliasis
|
|
D002179||moniliases cutaneous
|
|
D002179||moniliasis cutaneous
|
|
D002177||candidiasis
|
|
D002177||candidiases
|
|
D002177||moniliases
|
|
D002177||moniliasis
|
|
D002181||candidiasis vulvovaginal
|
|
D002181||monilial vaginitides
|
|
D002181||monilial vaginitis
|
|
D002181||moniliasis vulvovaginal
|
|
D002181||vaginitides monilial
|
|
D002181||vaginitis monilial
|
|
D002181||vulvovaginal candidiases
|
|
D002181||vulvovaginal candidiasis
|
|
D002181||vulvovaginal moniliases
|
|
D002181||vulvovaginal moniliasis
|
|
604391||atld
|
|
C564747|277380||methylmalonic aciduria and homocystinuria cblf type
|
|
C564747|277380||cblf
|
|
C564747|277380||cobalamin defect in lysosomal release of
|
|
C564747|277380||cobalamin f disease
|
|
C564747|277380||methylmalonic acidemia and homocystinuria cblf type
|
|
C564747|277380||methylmalonic aciduria due to vitamin b12 release defect
|
|
C564747|277380||vitamin b12 lysosomal release defect
|
|
C564747|277380||vitamin b12 storage disease
|
|
D002180||candidiasis oral
|
|
D002180||candidiases oral
|
|
D002180||moniliases oral
|
|
D002180||moniliasis oral
|
|
D002180||oral candidiases
|
|
D002180||oral candidiasis
|
|
D002180||oral moniliases
|
|
D002180||oral moniliasis
|
|
D002180||thrush
|
|
C575214|613371||spinocerebellar ataxia 30
|
|
C575214|613371||sca30
|
|
D015461||leukemia prolymphocytic t cell
|
|
D015461||leukemia lymphocytic chronic t cell
|
|
D015461||leukemias t cell prolymphocytic
|
|
D015461||leukemia t cell chronic
|
|
D015461||leukemia t cell prolymphocytic
|
|
D015461||lymphocytic leukemia t cell chronic
|
|
D015461||prolymphocytic leukemias t cell
|
|
D015461||prolymphocytic leukemia t cell
|
|
D015461||t cell leukemia chronic
|
|
D015461||t cell prolymphocytic leukemia
|
|
D015461||t cell prolymphocytic leukemias
|
|
D015461||t lymphocytic leukemia chronic
|
|
304730|C535376||dermoids of cornea
|
|
304730|C535376||bilateral corneal dermoids
|
|
304730|C535376||cnd
|
|
304730|C535376||corneal dermoids and short stature
|
|
304730|C535376||guizar vazquez luengas munoz syndrome
|
|
615031||spastic paraplegia 49 autosomal recessive
|
|
615031||spg49
|
|
D002145||callosities
|
|
D002145||callosity
|
|
D002145||corns
|
|
D003480||cushing syndrome
|
|
D003480||cushing apos s syndrome
|
|
D003480||hypercortisolism
|
|
D003480||syndrome cushing
|
|
D003480||syndrome cushing apos s
|
|
D015459||leukemia lymphoma adult t cell
|
|
D015459||adult t cell leukemia
|
|
D015459||adult t cell leukemia lymphoma
|
|
D015459||adult t cell leukemia lymphomas
|
|
D015459||adult t cell leukemias
|
|
D015459||atll
|
|
D015459||htlv associated leukemia lymphoma
|
|
D015459||htlv associated leukemia lymphomas
|
|
D015459||htlv i associated t cell leukemia lymphoma
|
|
D015459||htlv i associated t cell leukemia lymphomas
|
|
D015459||human t cell leukemia lymphoma
|
|
D015459||human t cell leukemia lymphomas
|
|
D015459||human t lymphotropic virus associated leukemia lymphoma
|
|
D015459||leukemia adult t cell
|
|
D015459||leukemia lymphoma htlv associated
|
|
D015459||leukemia lymphoma htlv i associated t cell
|
|
D015459||leukemia lymphoma human t cell
|
|
D015459||leukemia lymphomas adult t cell
|
|
D015459||leukemia lymphomas htlv associated
|
|
D015459||leukemia lymphomas htlv i associated t cell
|
|
D015459||leukemia lymphomas human t cell
|
|
D015459||leukemia lymphoma t cell acute htlv i associated
|
|
D015459||leukemias adult t cell
|
|
D015459||t cell leukemia adult
|
|
D015459||t cell leukemia lymphoma adult
|
|
D015459||t cell leukemia lymphoma htlv i associated
|
|
D015459||t cell leukemia lymphoma human
|
|
D015459||t cell leukemia lymphomas adult
|
|
D015459||t cell leukemia lymphomas htlv i associated
|
|
D015459||t cell leukemia lymphomas human
|
|
D015459||t cell leukemias adult
|
|
C564791|610313||ciss2
|
|
C564791|610313||cold induced sweating syndrome 2
|
|
C564791|610313||sweating cold induced
|
|
D014123||toxoplasmosis
|
|
D014123||infections toxoplasma gondii
|
|
D014123||infection toxoplasma gondii
|
|
D014123||toxoplasma gondii infection
|
|
D014123||toxoplasma gondii infections
|
|
D014123||toxoplasmoses
|
|
D011546|145260||pseudohypoaldosteronism
|
|
D011546|145260||familial hyperpotassemia and hypertension
|
|
D011546|145260||familial hypertensive hyperkalemia
|
|
D011546|145260||familial hypertensive hyperkalemias
|
|
D011546|145260||gordon hyperkalemia hypertension syndrome
|
|
D011546|145260||hyperkalemia familial hypertensive
|
|
D011546|145260||hyperkalemia hypertension syndrome gordon
|
|
D011546|145260||hyperkalemias familial hypertensive
|
|
D011546|145260||hyperpotassemia and hypertension familial
|
|
D011546|145260||hypertensive hyperkalemia familial
|
|
D011546|145260||hypertensive hyperkalemias familial
|
|
D011546|145260||i pseudohypoaldosteronism type
|
|
D011546|145260||is pseudohypoaldosteronism type
|
|
D011546|145260||pha1a
|
|
D011546|145260||pha1b
|
|
D011546|145260||pha2a
|
|
D011546|145260||pha i autosomal dominant
|
|
D011546|145260||pha i autosomal recessive
|
|
D011546|145260||php1b
|
|
D011546|145260|C548076||php1c
|
|
D011546|145260||php ib
|
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D011546|145260|C548076||php ic
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D011546|145260||pseudohypoaldosteronisms
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D011546|145260||pseudohypoaldosteronisms type i
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D011546|145260||pseudohypoaldosteronisms type ii
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D011546|145260||pseudohypoaldosteronism type 1
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D011546|145260||pseudohypoaldosteronism type 1 autosomal dominant
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D011546|145260||pseudohypoaldosteronism type 1 autosomal recessive
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D011546|145260||pseudohypoaldosteronism type 1s
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D011546|145260||pseudohypoaldosteronism type 2
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D011546|145260||pseudohypoaldosteronism type 2s
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D011546|145260||pseudohypoaldosteronism type i
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D011546|145260||pseudohypoaldosteronism type i autosomal dominant
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D011546|145260||pseudohypoaldosteronism type i autosomal recessive
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D011546|145260||pseudohypoaldosteronism type ii
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D011546|145260||pseudohypoaldosteronism type is
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D011546|145260|C548076||pseudohypoparathyroidism type ic
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D011546|145260||syndrome gordon hyperkalemia hypertension
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D011546|145260||type 1 pseudohypoaldosteronism
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D011546|145260||type ii pseudohypoaldosteronism
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D011546|145260||type ii pseudohypoaldosteronisms
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D011546|145260||type i pseudohypoaldosteronism
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D011546|145260||type is pseudohypoaldosteronism
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D015452||precursor b cell lymphoblastic leukemia lymphoma
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D015452||leukemia pre b cell
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D015452||leukemias pre b cell
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D015452||pre b all
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D015452||pre b cell leukemia
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D015452||pre b cell leukemias
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D015452||precursor b cell lymphoblastic leukemia
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D015452||precursor b cell lymphoblastic lymphoma
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D014120||toxocariasis
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D014120||toxocariases
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D015458||leukemia t cell
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D015458||leukemia lymphocytic t cell
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D015458||leukemias t cell
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D015458||leukemias t cell lymphocytic
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D015458||leukemias t lymphocytic
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D015458||leukemia t cell lymphocytic
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D015458||leukemia t lymphocytic
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D015458||lymphocytic leukemias t
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D015458||lymphocytic leukemias t cell
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D015458||lymphocytic leukemia t
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D015458||lymphocytic leukemia t cell
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D015458||t cell leukemia
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D015458||t cell leukemias
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D015458||t cell lymphocytic leukemia
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D015458||t cell lymphocytic leukemias
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D015458||t lymphocytic leukemia
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D015458||t lymphocytic leukemias
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D014126||toxoplasmosis ocular
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D014126||ocular toxoplasmoses
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D014126||ocular toxoplasmosis
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D014126||toxoplasmoses ocular
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D015456||leukemia biphenotypic acute
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D015456||acute biphenotypic leukemia
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D015456||acute biphenotypic leukemias
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D015456||acute leukemia biphenotypic
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D015456||acute leukemia hybrid
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D015456||acute leukemia mixed lineage
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D015456||acute leukemias biphenotypic
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D015456||acute leukemias hybrid
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D015456||acute leukemias mixed lineage
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D015456||b and t cell acute lymphoblastic leukemia
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D015456||b and t cell leukemia acute
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D015456||biphenotypic acute leukemia
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D015456||biphenotypic acute leukemias
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D015456||biphenotypic leukemia acute
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D015456||biphenotypic leukemias acute
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D015456||hybrid acute leukemia
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D015456||hybrid acute leukemias
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D015456||leukemia acute biphenotypic
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D015456||leukemia hybrid acute
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D015456||leukemia lymphocytic acute mixed cell
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D015456||leukemia mixed b and t cell
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D015456||leukemia mixed cell
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D015456||leukemia mixed lineage acute
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D015456||leukemias acute biphenotypic
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D015456||leukemias biphenotypic acute
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D015456||leukemias hybrid acute
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D015456||leukemias mixed cell
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D015456||leukemias mixed lineage acute
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D015456||lymphocytic leukemia acute b and t cell
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D015456||mixed cell leukemia
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D015456||mixed cell leukemias
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D015456||mixed lineage acute leukemia
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D015456||mixed lineage acute leukemias
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D014125||toxoplasmosis congenital
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D014125||congenital infection toxoplasma gondii
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D014125||congenital toxoplasma gondii infection
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D014125||congenital toxoplasma infection
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D014125||congenital toxoplasma infections
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D014125||congenital toxoplasmoses
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D014125||congenital toxoplasmosis
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D014125||fetal toxoplasmoses
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D014125||fetal toxoplasmosis
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D014125||infection congenital toxoplasma
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D014125||infections congenital toxoplasma
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D014125||prenatal toxoplasmoses
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D014125||prenatal toxoplasmosis
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D014125||toxoplasma infection congenital
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D014125||toxoplasma infections congenital
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D014125||toxoplasmoses congenital
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D014125||toxoplasmoses fetal
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D014125||toxoplasmoses prenatal
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D014125||toxoplasmosis fetal
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D014125||toxoplasmosis prenatal
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D014124||toxoplasmosis animal
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D014124||animal toxoplasmoses
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D014124||animal toxoplasmosis
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D014124||toxoplasmoses animal
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C565747|604802||huntington disease like 3
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C565747|604802||hdl3
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C565747|604802||huntington disease like neurodegenerative disorder autosomal recessive
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D011535|100100||prune belly syndrome
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D011535|100100||abdominal muscle deficiency syndrome
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D011535|100100||abdominal muscles absence of with urinary tract abnormality and cryptorchidism
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D011535|100100||congenital absence of the abdominal muscles
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D011535|100100||eagle barrett syndrome
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D011535|100100||egbrs
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D011535|100100||obrinsky syndrome
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D011535|100100||prune belly syndromes
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D011535|100100||syndrome eagle barrett
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D011535|100100||syndrome obrinsky
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D011535|100100||syndrome prune belly
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D011535|100100||syndromes prune belly
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D015472||leukemia eosinophilic acute
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D015472||acute eosinophilic leukemia
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D015472||acute eosinophilic leukemias
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D015472||eosinophilic leukemia acute
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D015472||eosinophilic leukemias acute
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D015472||leukemia acute eosinophilic
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D015472||leukemias acute eosinophilic
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D014141||trachoma
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D014141||egyptian ophthalmia
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D014141||ophthalmia egyptian
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D014141||trachomas
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D015471||leukemia basophilic acute
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D015471||acute basophilic leukemia
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D015471||acute basophilic leukemias
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D015471||basophilic leukemia acute
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D015471||basophilic leukemias acute
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D015471||leukemia acute basophilic
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D015471||leukemias acute basophilic
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205100|C565957||amyotrophic lateral sclerosis 2 juvenile
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205100|C565957||als2
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205100|C565957||alsj
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205100|C565957||als juvenile
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C537492|108300||stickler syndrome type 1
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C537492|108300||aom
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C537492|108300||arthroophthalmopathy hereditary progressive
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C537492|108300||stickler syndrome membranous vitreous type
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C537492|108300||stickler syndrome type i
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C537492|108300||stickler syndrome vitreous type 1
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C537492|108300||stl1
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D003483||cutis laxa
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D003483||dermatolyses
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D003483||dermatolysis
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D003483||dermatomegaly
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604370||breast ovarian cancer familial susceptibility to 1
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604370||breast cancer familial susceptibility to 1 included
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604370||brovca1
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604370||ovarian cancer familial susceptibility to 1 included
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D003490||cyanosis
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D003490||cyanoses
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C562733|136880||fundus albipunctatus
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C562733|136880||retinitis punctata albescens
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C562733|136880||retinitis punctata albescens included
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603040||tumor suppressor gene on chromosome 11
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603040||nonsmall cell lung cancer suppressor
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603040||tsg11
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203100|C537728||oculocutaneous albinism type 1
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203100|C537728||albinism 1
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203100|C537728||albinism i
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203100|C537728||albinism oculocutaneous type ia
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203100|C537728||atn
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203100|C537728||oca1
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203100|C537728||oca1a
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203100|C537728||oculocutaneous albinism type 1a
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203100|C537728||oculocutaneous albinism type i
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203100|C537728||oculocutaneous albinism tyrosinase negative
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145701|C536605||ambras syndrome
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145701|C536605||htc1
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145701|C536605||hypertrichosis universalis congenita ambras type
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603041||mitochondrial dna depletion syndrome 1 mngie type
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603041||mitochondrial neurogastrointestinal encephalopathy syndrome tymp related
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603041||mngie tymp related
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603041||mtdps1
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603041|C537477||myoneurogastrointestinal encephalopathy syndrome
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603041|C537477||polip syndrome
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603041|C537477||polyneuropathy ophthalmoplegia leukoencephalopathy and intestinal pseudoobstruction
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607085|C564628||myasthenia gravis with thymus hyperplasia
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607085|C564628||myas1
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D015465||leukemia myeloid accelerated phase
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D015465||leukemia myelogenous aggressive phase
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D015465||leukemia myeloid aggressive phase
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D015465||myelogenous leukemia chronic aggressive phase
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D015465||myeloid leukemia chronic accelerated phase
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D015465||myeloid leukemia chronic aggressive phase
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D014134||tracheal neoplasms
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D014134||neoplasms tracheal
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D014134||neoplasm tracheal
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D014134||tracheal neoplasm
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D014133||tracheal diseases
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D014133||diseases tracheal
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D014133||disease tracheal
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D014133||tracheal disease
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D015463||leukemia prolymphocytic
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D015463||leukemias prolymphocytic
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D015463||prolymphocytic leukemia
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D015463||prolymphocytic leukemias
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D014138||tracheoesophageal fistula
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D014138||esophagotracheal fistula
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D014138||esophagotracheal fistulas
|
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D014138||fistula esophagotracheal
|
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D014138||fistulas esophagotracheal
|
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D014138||fistulas tracheoesophageal
|
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D014138||fistula tracheoesophageal
|
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D014138||tracheoesophageal fistulas
|
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171200||thiourea tasting
|
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171200||phenylthiocarbamide tasting included
|
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171200||prop tasting included
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171200||propylthiouracil tasting included
|
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171200||ptc tasting included
|
|
D014137||tracheobronchomegaly
|
|
D014137||congenital tracheobronchomegalies
|
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D014137||congenital tracheobronchomegaly
|
|
D014137||mounier kuhn syndrome
|
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D014137||tracheobronchomegalies
|
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D014137||tracheobronchomegalies congenital
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D014137||tracheobronchomegaly congenital
|
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D015467||leukemia neutrophilic chronic
|
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D015467||chronic neutrophilic leukemia
|
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D015467||chronic neutrophilic leukemias
|
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D015467||leukemia chronic neutrophilic
|
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D015467||leukemias chronic neutrophilic
|
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D015467||neutrophilic leukemia chronic
|
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D015467||neutrophilic leukemias chronic
|
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D014136||tracheitis
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D014136||tracheitides
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D015466||leukemia myeloid chronic phase
|
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D015466||granulocytic leukemia chronic stable phase
|
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D015466||leukemia granulocytic chronic phase
|
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D015466||leukemia myelogenous chronic phase
|
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D015466||leukemia myeloid stable phase
|
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D015466||myelogenous leukemia chronic chronic phase
|
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D015466||myeloid leukemia chronic chronic phase
|
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D015466||myeloid leukemia chronic stable phase
|
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D014135||tracheal stenosis
|
|
D014135||stenoses tracheal
|
|
D014135||stenosis tracheal
|
|
D014135||tracheal stenoses
|
|
C567359|612290||microtia hearing impairment and cleft palate
|
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C567359|612290||microtia with or without hearing impairment included
|
|
D016770||ciliophora infections
|
|
D016770||ciliophora infection
|
|
D016770||infection ciliophora
|
|
D016770||infections ciliophora
|
|
D002128||calcium metabolism disorders
|
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D002128||calcium metabolism disorder
|
|
D002128||disorder calcium metabolism
|
|
D002128||disorders calcium metabolism
|
|
D015493|159580||paraparesis tropical spastic
|
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D015493|159580||familial spastic paraparesis htlv 1 associated
|
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D015493|159580||ham
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D015493|159580||htlv 1 associated myelopathies
|
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D015493|159580||htlv 1 associated myelopathy
|
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D015493|159580||htlv i associated myelopathies
|
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D015493|159580||htlv i associated myelopathy
|
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D015493|159580||htlv i associated myelopathy tropical spastic paraparesis
|
|
D015493|159580||human t lymphotropic virus type 1 associated myelopathy
|
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D015493|159580||myelopathies htlv 1 associated
|
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D015493|159580||myelopathies htlv i associated
|
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D015493|159580||myelopathy htlv 1 associated
|
|
D015493|159580||myelopathy htlv i associated
|
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D015493|159580||myelopathy human t lymphotropic virus type 1 associated
|
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D015493|159580||parapareses tropical spastic
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D015493|159580||paraplegias tropical spastic
|
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D015493|159580||paraplegia tropical spastic
|
|
D015493|159580||spastic parapareses tropical
|
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D015493|159580||spastic paraparesis tropical
|
|
D015493|159580||spastic paraplegias tropical
|
|
D015493|159580||spastic paraplegia tropical
|
|
D015493|159580||tropical spastic parapareses
|
|
D015493|159580||tropical spastic paraparesis
|
|
D015493|159580||tropical spastic paraplegia
|
|
D015493|159580||tropical spastic paraplegias
|
|
D003457||cryptosporidiosis
|
|
D003457||cryptosporidioses
|
|
D003453||cryptococcosis
|
|
D003453||cryptococcoses
|
|
D003453||toruloses
|
|
D003453||torulosis
|
|
D015439||leprosy borderline
|
|
D015439||borderline leprosies
|
|
D015439||borderline leprosy
|
|
D015439||dimorphous leprosies
|
|
D015439||dimorphous leprosy
|
|
D015439||leprosies borderline
|
|
D015439||leprosies dimorphous
|
|
D015439||leprosy dimorphous
|
|
D016769||embolism and thrombosis
|
|
D016769||thrombosis and embolism
|
|
140600|D010003||osteoarthritis
|
|
140600|D010003||arthritides degenerative
|
|
140600|D010003||arthritis degenerative
|
|
140600|D010003||degenerative arthritides
|
|
140600|D010003||degenerative arthritis
|
|
140600|D010003||dipoa
|
|
140600|D010003||goa1
|
|
140600|D010003||hand osteoarthritis hoa heberden nodes included
|
|
140600|D010003||oa
|
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140600|D010003||oadip
|
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140600|D010003||os1
|
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140600|D010003||os2
|
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140600|D010003||os3
|
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140600|D010003||os4
|
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140600|D010003||os5
|
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140600|D010003||os6
|
|
140600|D010003||osteoarthritides
|
|
140600|D010003||osteoarthritis generalized without dysplasia
|
|
140600|D010003||osteoarthritis of distal interphalangeal joints
|
|
140600|D010003||osteoarthritis of hip female specific susceptibility to
|
|
140600|D010003|D020370||osteoarthritis of knee
|
|
140600|D010003||osteoarthritis of knee hip
|
|
140600|D010003||osteoarthritis susceptibility 1
|
|
140600|D010003||osteoarthritis susceptibility 2
|
|
140600|D010003||osteoarthritis susceptibility 3
|
|
140600|D010003||osteoarthritis susceptibility 4
|
|
140600|D010003||osteoarthritis susceptibility 5
|
|
140600|D010003||osteoarthritis susceptibility 6
|
|
140600|D010003||osteoarthroses
|
|
140600|D010003||osteoarthrosis
|
|
140600|D010003||osteoarthrosis deformans
|
|
D015432||glomerulonephritis membranoproliferative
|
|
D015432||ddd mpgnii
|
|
D015432||dense deposit disease
|
|
D015432||glomerulonephritides hypocomplementemic
|
|
D015432||glomerulonephritides membranoproliferative
|
|
D015432||glomerulonephritides mesangiocapillary
|
|
D015432||glomerulonephritis hypocomplementemic
|
|
D015432||glomerulonephritis mesangiocapillary
|
|
D015432||hypocomplementemic glomerulonephritides
|
|
D015432||hypocomplementemic glomerulonephritis
|
|
D015432||membranoproliferative glomerulonephritides
|
|
D015432||membranoproliferative glomerulonephritis
|
|
D015432||membranoproliferative glomerulonephritis subendothelial
|
|
D015432||membranoproliferative glomerulonephritis type i
|
|
D015432||membranoproliferative glomerulonephritis type ii
|
|
D015432||membranoproliferative glomerulonephritis type iii
|
|
D015432||mesangiocapillary glomerulonephritides
|
|
D015432||mesangiocapillary glomerulonephritis
|
|
D015432||mesangiocapillary glomerulonephritis type i
|
|
D015432||mesangiocapillary glomerulonephritis type ii
|
|
D015432||mpgn
|
|
D015432||mpgnii
|
|
D015432||subendothelial membranoproliferative glomerulonephritis
|
|
D015432||type ii mpgn
|
|
C565171|120502||branchiootic syndrome 2
|
|
C565171|120502||bos2
|
|
C565171|120502||bo syndrome 2
|
|
D015431||weight loss
|
|
D015431||losses weight
|
|
D015431||loss weight
|
|
D015431||reductions weight
|
|
D015431||reduction weight
|
|
D015431||weight losses
|
|
D015431||weight reduction
|
|
D015431||weight reductions
|
|
D015430||weight gain
|
|
D015430||gains weight
|
|
D015430||gain weight
|
|
D015430||weight gains
|
|
D016766||feline infectious peritonitis
|
|
D016766||feline infectious peritonitides
|
|
D016766||infectious peritonitides feline
|
|
D016766||infectious peritonitis feline
|
|
D016766||peritonitis feline infectious
|
|
D016766||peritonitis infectious feline
|
|
C538154|186100||syndactyly type 3
|
|
C538154|186100||familial syndactyly type 3
|
|
C538154|186100||ring and little finger syndactyly
|
|
C538154|186100||sdty3
|
|
C538154|186100||syndactyly of fingers four and five
|
|
C538154|186100||syndactyly of fingers iv and v
|
|
C538154|186100||syndactyly of the ring and little finger
|
|
C538154|186100||syndactyly type iii
|
|
D016767||caroli disease
|
|
D016767||caroli apos s disease
|
|
D016767||carolis disease
|
|
D016767||caroli apos s syndrome
|
|
D016767||carolis syndrome
|
|
D016767||caroli syndrome
|
|
D016767||disease caroli
|
|
D016767||disease caroli apos s
|
|
D016767||syndrome caroli apos s
|
|
D015436||panniculitis peritoneal
|
|
D015436||lipodystrophy mesenteric
|
|
D015436||liposclerotic mesenteritis
|
|
D015436||mesenteric lipodystrophy
|
|
D015436||mesenteric panniculitis
|
|
D015436||mesenteric weber christian disease
|
|
D015436||mesenteritis liposclerotic
|
|
D015436||mesenteritis retractile
|
|
D015436||mesenteritis sclerosing
|
|
D015436||omental panniculitis
|
|
D015436||panniculitis mesenteric
|
|
D015436||panniculitis omental
|
|
D015436||peritoneal panniculitis
|
|
D015436||retractile mesenteritis
|
|
D015436||sclerosing mesenteritis
|
|
209300|C538259||congenital atransferrinemia
|
|
209300|C538259||atransferrinemia
|
|
209300|C538259||familial hypotransferrinemia
|
|
209300|C538259||hypotransferrinemia familial
|
|
209300|C538259||hypotransferrinemia familial transferrin serum level quantitative trait locus 1 included
|
|
209300|C538259||tfqtl1 included
|
|
D015435||panniculitis lupus erythematosus
|
|
D015435||lupus erythematosus panniculitides
|
|
D015435||lupus erythematosus panniculitis
|
|
D015435||lupus erythematosus profundus
|
|
D015435||lupus panniculitides
|
|
D015435||lupus panniculitis
|
|
D015435||lupus profundus
|
|
D015435||panniculitides lupus
|
|
D015435||panniculitides lupus erythematosus
|
|
D015435||panniculitis lupus
|
|
D015434||panniculitis
|
|
D015434||cold panniculitides
|
|
D015434||cold panniculitis
|
|
D015434||panniculitides
|
|
D015434||panniculitides cold
|
|
D015434||panniculitis cold
|
|
D015434||panniculitis subacute nodular migratory
|
|
D014103||torticollis
|
|
D014103||cervical dystonia
|
|
D014103||intermittent torticollis
|
|
D014103||psychogenic torticollis
|
|
D014103||spasmodic torticollis
|
|
D014103||torticollis intermittent
|
|
D014103||torticollis psychogenic
|
|
D014103||torticollis spasmodic
|
|
D014103||wryneck
|
|
D015433||glomerulonephritis membranous
|
|
D015433||extramembranous glomerulopathy
|
|
D015433||glomerulonephritides idiopathic membranous
|
|
D015433||glomerulonephritides membranous
|
|
D015433||glomerulonephritis idiopathic membranous
|
|
D015433||glomerulonephropathy membranous
|
|
D015433||glomerulopathy extramembranous
|
|
D015433||glomerulopathy membranous
|
|
D015433||heymann nephritis
|
|
D015433||idiopathic membranous glomerulonephritides
|
|
D015433||idiopathic membranous glomerulonephritis
|
|
D015433||idiopathic membranous nephropathy
|
|
D015433||membranous glomerulonephritides
|
|
D015433||membranous glomerulonephritides idiopathic
|
|
D015433||membranous glomerulonephritis
|
|
D015433||membranous glomerulonephritis idiopathic
|
|
D015433||membranous glomerulonephropathy
|
|
D015433||membranous glomerulopathy
|
|
D015433||membranous nephropathy
|
|
D015433||membranous nephropathy idiopathic
|
|
D015433||nephritis heymann
|
|
D015433||nephropathy idiopathic membranous
|
|
D015433||nephropathy membranous
|
|
D014102||torsion abnormality
|
|
D014102||abnormalities torsion
|
|
D014102||abnormality torsion
|
|
D014102||torsion abnormalities
|
|
C537842|603386||nonmedullary thyroid carcinoma with or without cell oxyphilia
|
|
C537842|603386||tco
|
|
C537842|603386||tco1
|
|
C537842|603386||thyroid carcinoma nonmedullary with or without cell oxyphilia
|
|
C531821||stenotrophomonas maltophilia bacteremia
|
|
C566857|204500||ceroid lipofuscinosis neuronal 2
|
|
C566857|204500||ceroid lipofuscinosis neuronal 2 variable age at onset
|
|
C566857|204500||cln2
|
|
C566857|204500||jansky bielschowsky disease neuronal ceroid lipofuscinosis late infantile included
|
|
C566857|204500||lincl included
|
|
300554|D053098||familial hypophosphatemic rickets
|
|
300554|D053098||hereditary hypophosphatemic rickets
|
|
300554|D053098||hereditary vitamin d resistant rickets
|
|
300554|D053098||hpdr
|
|
300554|D053098||hyp
|
|
300554|D053098||hypophosphatemia x linked
|
|
300554|D053098||hypophosphatemic rickets familial
|
|
300554|D053098||hypophosphatemic rickets hereditary
|
|
300554|D053098||hypophosphatemic rickets x linked
|
|
300554|D053098||hypophosphatemic rickets x linked dominant
|
|
300554|D053098||hypophosphatemic rickets x linked recessive
|
|
300554|D053098|D063730||hypophosphatemic vitamin d resistant rickets
|
|
300554|D053098||rickets familial hypophosphatemic
|
|
300554|D053098||rickets hereditary hypophosphatemic
|
|
300554|D053098||rickets x linked hypophosphatemic
|
|
300554|D053098|D063730||vitamin d resistant rickets
|
|
300554|D053098||vitamin d resistant rickets hereditary
|
|
300554|D053098||vitamin d resistant rickets x linked
|
|
300554|D053098||xlh
|
|
300554|D053098||xlhr
|
|
300554|D053098||x linked hypophosphatemia
|
|
300554|D053098||x linked hypophosphatemic rickets
|
|
D016780||malaria vivax
|
|
D016780||malaria plasmodium vivax
|
|
D016780||plasmodium vivax malaria
|
|
D016780||vivax malaria
|
|
D016781||toxoplasmosis cerebral
|
|
D016781||central nervous system toxoplasmosis
|
|
D016781||cerebral toxoplasmosis
|
|
D016781||intracranial toxoplasmosis
|
|
D016781||neurotoxoplasmosis
|
|
D016781||toxoplasmoses cerebral
|
|
D016781||toxoplasmosis central nervous system
|
|
D016781||toxoplasmosis intracranial
|
|
247200|D054221||classical lissencephalies and subcortical band heterotopias
|
|
247200|D054221||agyria pachygyria band spectrum
|
|
247200|D054221||band heterotopia lissencephaly subcortical
|
|
247200|D054221||chromosome 17p13 3 deletion syndrome
|
|
247200|D054221||classical lissencephalies
|
|
247200|D054221||classical lissencephaly
|
|
247200|D054221||classical lissencephaly syndrome
|
|
247200|D054221||classic lissencephaly
|
|
247200|D054221||dc syndrome included
|
|
247200|D054221||double cortex syndrome
|
|
247200|D054221||double cortex syndrome included
|
|
247200|D054221||heterotopia lissencephaly subcortical band
|
|
247200|D054221||heterotopias lissencephaly subcortical band
|
|
247200|D054221||heterotopias subcortical band
|
|
247200|D054221||heterotopias subcortical laminar
|
|
247200|D054221||heterotopia subcortical band
|
|
247200|D054221||heterotopia subcortical laminar
|
|
247200|D054221||isolated lissencephaly sequence
|
|
247200|D054221||lissencephalies classical
|
|
247200|D054221||lissencephalies type 1
|
|
247200|D054221||lissencephalies x linked
|
|
247200|D054221|607432|D054082||lissencephaly 1
|
|
247200|D054221||lissencephaly and agenesis of corpus callosum subcortical laminar heterotopia x linked included
|
|
247200|D054221||lissencephaly classic
|
|
247200|D054221||lissencephaly classical
|
|
247200|D054221||lissencephaly miller dieker
|
|
247200|D054221|607432|D054082||lissencephaly sequence isolated
|
|
247200|D054221||lissencephaly subcortical band heterotopia
|
|
247200|D054221||lissencephaly subcortical band heterotopias
|
|
247200|D054221||lissencephaly syndrome miller dieker
|
|
247200|D054221||lissencephaly type 1
|
|
247200|D054221||lissencephaly x linked
|
|
247200|D054221||lissencephaly x linked 1
|
|
247200|D054221||lisx1
|
|
247200|D054221||mdcr included
|
|
247200|D054221||mdls
|
|
247200|D054221||mds chromosome 17p13 3 deletion syndrome included
|
|
247200|D054221||miller dieker lissencephaly
|
|
247200|D054221||miller dieker lissencephaly syndrome
|
|
247200|D054221||miller dieker syndrome
|
|
247200|D054221||miller dieker syndrome chromosome region included
|
|
247200|D054221|607432|D054082||sbh included
|
|
247200|D054221|607432|D054082||sclh included
|
|
247200|D054221||subcortical band heterotopia
|
|
247200|D054221||subcortical band heterotopias
|
|
247200|D054221||subcortical band heterotopia x linked included
|
|
247200|D054221||subcortical laminar heterotopia
|
|
247200|D054221||syndrome double cortex
|
|
247200|D054221||syndrome miller dieker
|
|
247200|D054221||syndrome miller dieker lissencephaly
|
|
247200|D054221||type 1 lissencephalies
|
|
247200|D054221||type 1 lissencephaly
|
|
247200|D054221||x linked lissencephalies
|
|
247200|D054221||x linked lissencephaly
|
|
247200|D054221||xlis
|
|
D002137||calculi
|
|
D002137||biliary or urinary stones
|
|
D002137||calculus
|
|
C531833||ophthalmoplegia painful
|
|
C531833||nonspecific inflammation of the cavernous sinus or superior orbital fissure
|
|
C531834||toxocara canis infection canine roundworms
|
|
C531834||human infection with the larvae of canine or feline roundworms
|
|
C531834||toxocara catis infection feline roundworms
|
|
D015448||leukemia b cell
|
|
D015448||b cell leukemia
|
|
D015448||b cell leukemias
|
|
D015448||b cell lymphocytic leukemia
|
|
D015448||b cell lymphocytic leukemias
|
|
D015448||b lymphocytic leukemia
|
|
D015448||b lymphocytic leukemias
|
|
D015448||leukemia b cell lymphocytic
|
|
D015448||leukemia b lymphocytic
|
|
D015448||leukemia lymphocytic b cell
|
|
D015448||leukemias b cell
|
|
D015448||leukemias b cell lymphocytic
|
|
D015448||leukemias b lymphocytic
|
|
D015448||lymphocytic leukemia b cell
|
|
D015448||lymphocytic leukemias b cell
|
|
C531836||congenital agenesis of the tricuspid valve
|
|
C562963|113500||brachyolmia type 3
|
|
C562963|113500||brachyolmia autosomal dominant
|
|
C562963|113500||brachyrachia
|
|
D016779||malaria cerebral
|
|
D016779||cerebral malaria
|
|
D016779||malaria meningitis
|
|
D016779||meningitis malaria
|
|
C565394|250940||methylcobalamin deficiency cblg type
|
|
C565394|250940||hmag
|
|
C565394|250940||homocystinuria megaloblastic anemia cblg complementation type
|
|
C565394|250940||homocystinuria megaloblastic anemia due to defect in cobalamin metabolism cblg complementation type
|
|
C565394|250940|C537426||methionine synthase deficiency
|
|
D016776||blastocystis infections
|
|
D016776||blastocystis infection
|
|
D016776||infection blastocystis
|
|
D016776||infections blastocystis
|
|
D015441||leprosy tuberculoid
|
|
D015441||leprosies macular
|
|
D015441||leprosies neural
|
|
D015441||leprosies tuberculoid
|
|
D015441||leprosy macular
|
|
D015441||leprosy neural
|
|
D015441||macular leprosies
|
|
D015441||macular leprosy
|
|
D015441||neural leprosies
|
|
D015441||neural leprosy
|
|
D015441||tuberculoid leprosies
|
|
D015441||tuberculoid leprosy
|
|
D015440||leprosy lepromatous
|
|
D015440||cutaneous leprosies
|
|
D015440||cutaneous leprosy
|
|
D015440||lepromatous leprosies
|
|
D015440||lepromatous leprosy
|
|
D015440||leprosies cutaneous
|
|
D015440||leprosies lepromatous
|
|
D015440||leprosies nodular
|
|
D015440||leprosy cutaneous
|
|
D015440||leprosy nodular
|
|
D015440||nodular leprosies
|
|
D015440||nodular leprosy
|
|
D016778||malaria falciparum
|
|
D016778||malaria plasmodium falciparum
|
|
D016778||plasmodium falciparum malaria
|
|
D014115||toxemia
|
|
D014115||toxemias
|
|
D016773||leishmaniasis cutaneous
|
|
D016773||american leishmaniasis
|
|
D016773||cutaneous leishmaniases
|
|
D016773||cutaneous leishmaniasis
|
|
D016773||leishmaniases cutaneous
|
|
D016773||leishmaniasis american
|
|
D016773||leishmaniasis new world
|
|
D016773||leishmaniasis old world
|
|
D016773||new world leishmaniasis
|
|
D016773||old world leishmaniasis
|
|
D016773||oriental sore
|
|
D016773||sore oriental
|
|
D016774||leishmaniasis diffuse cutaneous
|
|
D016774||cutaneous leishmaniases diffuse
|
|
D016774||cutaneous leishmaniasis diffuse
|
|
D016774||diffuse cutaneous leishmaniases
|
|
D016774||diffuse cutaneous leishmaniasis
|
|
D016774||leishmaniases diffuse cutaneous
|
|
C535492||epidermolysis bullosa late onset localized junctional with mental retardation
|
|
C535492||epidermolysis bullosa simplex localisata associated with anodontia hair and nail disorders
|
|
D004889||erysipelothrix infections
|
|
D004889||erysipelothrix infection
|
|
D004889||infection erysipelothrix
|
|
D004889||infections erysipelothrix
|
|
D003557||phyllodes tumor
|
|
D003557||cystosarcoma phyllodes
|
|
D003557||cystosarcoma phyllodes malignant
|
|
D003557||cystosarcoma phylloides
|
|
D003557||malignant cystosarcoma phyllodes
|
|
D003557||phyllodes tumors
|
|
D003557||tumor phyllodes
|
|
D003557||tumors phyllodes
|
|
C535496||epilepsy occipital calcifications
|
|
C535496||bilateral occipital calcifications with epilepsy
|
|
C535496||epilepsy with bilateral occipital calcifications
|
|
C535496||familial unilateral and bilateral occipital calcifications and epilepsy
|
|
C535497||epilepsy telangiectasia
|
|
D004884||eructation
|
|
D004884||belching
|
|
D004884||belchings
|
|
D004884||eructations
|
|
D004887||erysipeloid
|
|
D004887||erysipeloids
|
|
308230|D053307||hyper igm immunodeficiency syndrome type 1
|
|
308230|D053307||higm
|
|
308230|D053307||higm1
|
|
308230|D053307||higm1 syndrome
|
|
308230|D053307||higm1 syndromes
|
|
308230|D053307||hyper igm immunodeficiencies x linked
|
|
308230|D053307||hyper igm immunodeficiency x linked
|
|
308230|D053307|605258|D053306||hyper igm syndrome
|
|
308230|D053307||hyper igm syndrome 1
|
|
308230|D053307||ihis
|
|
308230|D053307||immunodeficiencies x linked hyper igm
|
|
308230|D053307||immunodeficiency with hyper igm type 1
|
|
308230|D053307||immunodeficiency x linked hyper igm
|
|
308230|D053307||syndrome 1 hyper igm
|
|
308230|D053307||syndrome higm1
|
|
308230|D053307||syndromes higm1
|
|
308230|D053307||xhim
|
|
308230|D053307||x linked hyper igm immunodeficiencies
|
|
308230|D053307||x linked hyper igm immunodeficiency
|
|
308230|D053307||x linked hyper igm syndrome
|
|
D004886||erysipelas
|
|
219900|C562683||cystinosis late onset juvenile or adolescent nephropathic type
|
|
219900|C562683||cystinosis intermediate
|
|
D003556||cystitis
|
|
D003556||cystitides
|
|
D004881||ergotism
|
|
D004881||ergotisms
|
|
D004881||ergot poisoning
|
|
D004881||ergot poisonings
|
|
D004881||fire st anthonys
|
|
D004881||poisoning ergot
|
|
D004881||poisonings ergot
|
|
D004881||saint anthony fire
|
|
D004881||saint anthony apos s fire
|
|
D004881||saint anthonys fire
|
|
D004881||st anthony fire
|
|
D004881||st anthony apos s fire
|
|
D004881||st anthonys fire
|
|
D003551||cysticercosis
|
|
D003551||cysticercoses
|
|
D004890||erythema
|
|
D004890||erythemas
|
|
D014205||trench fever
|
|
D014205||fevers trench
|
|
D014205||fever trench
|
|
D014205||trench fevers
|
|
C536887|118100||klippel feil syndrome dominant type
|
|
C536887|118100||cervical vertebral fusion autosomal dominant
|
|
C536887|118100||kfs
|
|
C536887|118100||kfs1
|
|
C536887|118100||klippel feil syndrome 1 autosomal dominant
|
|
C536887|118100||klippel feil syndrome autosomal dominant
|
|
D016868||serratia infections
|
|
D016868||infection serratia
|
|
D016868||infections serratia
|
|
D016868||serratia infection
|
|
D016869||ureaplasma infections
|
|
D016869||infections ureaplasma
|
|
D016869||infection ureaplasma
|
|
D016869||ureaplasma infection
|
|
C535489||chromosome 14 trisomy mosaic
|
|
C535489||trisomy 14 mosaic
|
|
C535489||trisomy 14 mosaicism
|
|
C535489||trisomy 14 mosaicism syndrome
|
|
D016863||bacillaceae infections
|
|
D016863||bacillaceae infection
|
|
D016863||infection bacillaceae
|
|
D016863||infections bacillaceae
|
|
C535488||chromosome 14 trisomy
|
|
C535488||trisomy 14
|
|
D016864||li fraumeni syndrome
|
|
167959||human papillomavirus type 18 integration site 1
|
|
167959||hpv18i1
|
|
167959||papillomavirus type 18 integration site 1
|
|
D016866||bacteroidaceae infections
|
|
D016866||bacteroidaceae infection
|
|
D016866||infection bacteroidaceae
|
|
D016866||infections bacteroidaceae
|
|
D014202||tremor
|
|
D014202||action tremor
|
|
D014202||action tremors
|
|
D014202||coarse tremor
|
|
D014202||coarse tremors
|
|
D014202||continuous tremor
|
|
D014202||continuous tremors
|
|
D014202||darkness tremor
|
|
D014202||darkness tremors
|
|
D014202||fine tremor
|
|
D014202||fine tremors
|
|
D014202||intention tremor
|
|
D014202||intention tremors
|
|
D014202||intermittent tremor
|
|
D014202||intermittent tremors
|
|
D014202||involuntary quiver
|
|
D014202||involuntary quivers
|
|
D014202||limb tremor
|
|
D014202||limb tremors
|
|
D014202||massive tremor
|
|
D014202||massive tremors
|
|
D014202||muscle tremor
|
|
D014202||muscle tremors
|
|
D014202||neonatal tremor
|
|
D014202||neonatal tremors
|
|
D014202||nerve tremor
|
|
D014202||nerve tremors
|
|
D014202||passive tremor
|
|
D014202||passive tremors
|
|
D014202||perioral tremor
|
|
D014202||perioral tremors
|
|
D014202||persistent tremor
|
|
D014202||persistent tremors
|
|
D014202||pill rolling tremor
|
|
D014202||pill rolling tremors
|
|
D014202||quiver involuntary
|
|
D014202||quivers involuntary
|
|
D014202||resting tremor
|
|
D014202||resting tremors
|
|
D014202||rest tremor
|
|
D014202||rest tremors
|
|
D014202||rolling tremor pill
|
|
D014202||rolling tremors pill
|
|
D014202||saturnine tremor
|
|
D014202||saturnine tremors
|
|
D014202||semirhythmic tremor
|
|
D014202||semirhythmic tremors
|
|
D014202||senile tremor
|
|
D014202||senile tremors
|
|
D014202||static tremor
|
|
D014202||static tremors
|
|
D014202||tremor action
|
|
D014202||tremor coarse
|
|
D014202||tremor continuous
|
|
D014202||tremor darkness
|
|
D014202||tremor fine
|
|
D014202||tremor intention
|
|
D014202||tremor intermittent
|
|
D014202||tremor limb
|
|
D014202||tremor massive
|
|
D014202||tremor muscle
|
|
D014202||tremor neonatal
|
|
D014202||tremor nerve
|
|
D014202||tremor passive
|
|
D014202||tremor perioral
|
|
D014202||tremor persistent
|
|
D014202||tremor pill rolling
|
|
D014202||tremor rest
|
|
D014202||tremor resting
|
|
D014202||tremors
|
|
D014202||tremors action
|
|
D014202||tremor saturnine
|
|
D014202||tremors coarse
|
|
D014202||tremors continuous
|
|
D014202||tremors darkness
|
|
D014202||tremor semirhythmic
|
|
D014202||tremor senile
|
|
D014202||tremors fine
|
|
D014202||tremors intention
|
|
D014202||tremors intermittent
|
|
D014202||tremors limb
|
|
D014202||tremors massive
|
|
D014202||tremors muscle
|
|
D014202||tremors neonatal
|
|
D014202||tremors nerve
|
|
D014202||tremors passive
|
|
D014202||tremors perioral
|
|
D014202||tremors persistent
|
|
D014202||tremors pill rolling
|
|
D014202||tremors rest
|
|
D014202||tremors resting
|
|
D014202||tremors saturnine
|
|
D014202||tremors semirhythmic
|
|
D014202||tremors senile
|
|
D014202||tremors static
|
|
D014202||tremor static
|
|
D014201||trematode infections
|
|
D014201||fasciolopsiases
|
|
D014201||fasciolopsiasis
|
|
D014201||infections trematode
|
|
D014201||infection trematode
|
|
D014201||metagonimiases
|
|
D014201||metagonimiasis
|
|
D014201||trematode infection
|
|
604233|C565809||generalized epilepsy with febrile seizures plus type 1
|
|
604233|C565809||gefs 1
|
|
604233|C565809||gefsp1
|
|
604233|C565809||gefs type 1
|
|
D016862||tuberculoma intracranial
|
|
D016862||abscess tubercular intracranial
|
|
D016862||intracranial tuberculoma
|
|
D016862||intracranial tuberculomas
|
|
D016862||tuberculomas intracranial
|
|
D053706||typhlitis
|
|
D053706||cecitis
|
|
D053706||neutropenic typhlitis
|
|
D053706||typhlitis neutropenic
|
|
C563762|609255||febrile convulsions familial 5
|
|
C563762|609255||convulsions familial febrile 5
|
|
C563762|609255||feb5
|
|
C563762|609255||febrile seizures familial 5
|
|
C563762|609255||seizures familial febrile 5
|
|
D004899||erythroblastosis fetal
|
|
D004899||erythroblastoses fetal
|
|
D004899||erythroblastosis fetali
|
|
D004899||erythroblastosis fetalis
|
|
D004899||fetal erythroblastoses
|
|
D004899||fetal erythroblastosis
|
|
D004899||fetali erythroblastosis
|
|
D004899||fetalis erythroblastosis
|
|
D004899||hemolytic disease of newborn
|
|
D004899||newborn hemolytic disease
|
|
D004899||newborn hemolytic diseases
|
|
122470|D003635||de lange syndrome
|
|
122470|D003635||amstelodamensis typus degenerativus
|
|
122470|D003635||bdls
|
|
122470|D003635||brachmann de lange syndrome
|
|
122470|D003635||cdl
|
|
122470|D003635||cdls
|
|
122470|D003635||cdls1
|
|
122470|D003635||cdls2
|
|
122470|D003635||cdls3
|
|
122470|D003635||cdls x linked
|
|
122470|D003635||cornelia de lange syndrome
|
|
122470|D003635||cornelia de lange syndrome 1
|
|
122470|D003635||cornelia de lange syndrome 2
|
|
122470|D003635||cornelia de lange syndrome 3
|
|
122470|D003635||cornelia de lange syndrome x linked
|
|
122470|D003635||de lange apos s syndrome
|
|
122470|D003635||syndrome brachmann de lange
|
|
122470|D003635||syndrome de lange
|
|
122470|D003635||syndrome de lange apos s
|
|
122470|D003635||typus degenerativus amstelodamensis
|
|
300428|C563135||mental retardation x linked 2
|
|
300428|C563135||mrx2
|
|
D002239||carbohydrate metabolism inborn errors
|
|
D002239||carbohydrate metabolism inborn error
|
|
187500|D013771||tetralogy of fallot
|
|
187500|D013771||fallot apos s tetralogy
|
|
187500|D013771||fallots tetralogy
|
|
187500|D013771||fallot tetralogy
|
|
187500|D013771||tetralogy fallot
|
|
187500|D013771||tetralogy fallots
|
|
187500|D013771||tetralogy fallot apos s
|
|
187500|D013771||tof
|
|
D004892||erythema multiforme
|
|
D003560||cysts
|
|
D003560||cyst
|
|
D004891||erythema induratum
|
|
D004891||bazin disease
|
|
D004891||bazin apos s disease
|
|
D004891||bazins disease
|
|
D004891||disease bazin
|
|
D004891||disease bazin apos s
|
|
D004891||tuberculosis cutis indurativa
|
|
D004894||erythrasma
|
|
D004893||erythema nodosum
|
|
D016878||poems syndrome
|
|
D016878||crow fukase syndrome
|
|
D016878||organomegalies polyneuropathy
|
|
D016878||organomegaly polyneuropathy
|
|
D016878||polyneuropathy organomegalies
|
|
D016878||polyneuropathy organomegaly
|
|
D016878||polyneuropathy organomegaly endocrinopathy m protein and skin changes syndrome
|
|
D016878||syndrome crow fukase
|
|
D016878||syndrome poems
|
|
D016878||syndrome takatsuki apos s
|
|
D016878||takatsuki apos s syndrome
|
|
D016878||takatsuki syndrome
|
|
D014211||treponemal infections
|
|
D014211||bejel
|
|
D014211||bejels
|
|
D014211||infections treponemal
|
|
D014211||infection treponemal
|
|
D014211||treponemal infection
|
|
D016870||neisseriaceae infections
|
|
D016870||infection neisseriaceae
|
|
D016870||infections neisseriaceae
|
|
D016870||neisseriaceae infection
|
|
D016871||pasteurellaceae infections
|
|
D016871||infection pasteurellaceae
|
|
D016871||infections pasteurellaceae
|
|
D016871||pasteurellaceae infection
|
|
D016873||ehrlichiosis
|
|
D016873||ehrlichioses
|
|
D053717||pneumonia ventilator associated
|
|
D053717||ventilator associated pneumonia
|
|
D053716||female athlete triad syndrome
|
|
D053716||female athlete triad
|
|
D053714||aspermia
|
|
D002205||caplan syndrome
|
|
D002205||caplan apos s syndrome
|
|
D002205||caplans syndrome
|
|
D002205||caplan syndromes
|
|
D003536||cystadenocarcinoma
|
|
D003536||cystadenocarcinomas
|
|
D003537||cystadenoma
|
|
D003537||cystadenomas
|
|
D053718||scleromyxedema
|
|
D053718||lichen myxedematosus
|
|
D053718||mucinosis papular
|
|
D053718||myxedematosus lichen
|
|
D053718||papular mucinosis
|
|
D004863||equinus deformity
|
|
D004863||contracture equinus
|
|
D004863||contractures equinus
|
|
D004863||deformities equinus
|
|
D004863||deformity equinus
|
|
D004863||equinus contracture
|
|
D004863||equinus contractures
|
|
D004863||equinus deformities
|
|
D004863||talipes equinus
|
|
300257|D052120||glycogen storage disease type iib
|
|
300257|D052120||antopol disease
|
|
300257|D052120||cardiomyopathies glycogen storage
|
|
300257|D052120||cardiomyopathy glycogen storage
|
|
300257|D052120||danon disease
|
|
300257|D052120||disease antopol
|
|
300257|D052120||glycogen storage cardiomyopathies
|
|
300257|D052120||glycogen storage cardiomyopathy
|
|
300257|D052120||glycogen storage disease iib
|
|
300257|D052120||glycogen storage disease limited to the heart
|
|
300257|D052120||glycogen storage disease type 2b
|
|
300257|D052120||gsd2b formerly
|
|
300257|D052120||gsd iib formerly
|
|
300257|D052120||lysosomal glycogen storage disease with normal acid maltase
|
|
300257|D052120||lysosomal glycogen storage disease without acid maltase deficiency
|
|
300257|D052120||lysosomal glycogen storage disease without acid maltase deficiency formerly
|
|
300257|D052120||pseudoglycogenosis 2
|
|
300257|D052120||pseudoglycogenosis 2s
|
|
300257|D052120||pseudoglycogenosis ii
|
|
300257|D052120||pseudoglycogenosis iis
|
|
300257|D052120||vacuolar cardiomyopathy and myopathy x linked
|
|
300257|D052120||x linked vacuolar cardiomyopathy and myopathy
|
|
254800|D020194||unverricht lundborg syndrome
|
|
254800|D020194||baltic myoclonic epilepsies
|
|
254800|D020194||baltic myoclonic epilepsy
|
|
254800|D020194||baltic myoclonus
|
|
254800|D020194||baltic myoclonus epilepsies
|
|
254800|D020194||baltic myoclonus epilepsy
|
|
254800|D020194||diseases unverricht
|
|
254800|D020194||diseases unverricht lundborg
|
|
254800|D020194||disease unverricht
|
|
254800|D020194||disease unverricht lundborg
|
|
254800|D020194||epilepsies baltic myoclonic
|
|
254800|D020194||epilepsies baltic myoclonus
|
|
254800|D020194||epilepsy baltic myoclonic
|
|
254800|D020194||epilepsy baltic myoclonus
|
|
254800|D020194||epilepsy mediterranean myoclonic
|
|
254800|D020194||epilepsy progressive myoclonic 1
|
|
254800|D020194||epilepsy progressive myoclonic 1a
|
|
254800|D020194||epilepsy progressive myoclonic type 1
|
|
254800|D020194||epilepsy progressive myoclonus 1
|
|
254800|D020194||epm1
|
|
254800|D020194||epm1a
|
|
254800|D020194||lundborg unverricht syndrome
|
|
254800|D020194||mediterranean myoclonic epilepsy
|
|
254800|D020194||myoclonic epilepsies baltic
|
|
254800|D020194||myoclonic epilepsy baltic
|
|
254800|D020194||myoclonic epilepsy mediterranean
|
|
254800|D020194||myoclonic epilepsy of unverricht and lundborg
|
|
254800|D020194||myoclonus baltic
|
|
254800|D020194||myoclonus epilepsies baltic
|
|
254800|D020194||myoclonus epilepsy baltic
|
|
254800|D020194||myoclonus progressive epilepsy of unverricht and lundborg
|
|
254800|D020194||pme
|
|
254800|D020194|D020191|125370||progressive myoclonic epilepsy
|
|
254800|D020194||progressive myoclonus epilepsy 1
|
|
254800|D020194||progressive myoclonus epilepsybaltic myoclonic epilepsy
|
|
254800|D020194||syndrome lundborg unverricht
|
|
254800|D020194||syndrome unverricht lundborg
|
|
254800|D020194||uld
|
|
254800|D020194||unverricht disease
|
|
254800|D020194||unverricht diseases
|
|
254800|D020194||unverricht lundborg disease
|
|
254800|D020194||unverricht lundborg diseases
|
|
611403||asthma related traits susceptibility to 6
|
|
611403||asrt6
|
|
D016849||keratitis herpetic
|
|
D016849||herpes simplex keratitides
|
|
D016849||herpes simplex keratitis
|
|
D016849||herpes simplex ocular
|
|
D016849||herpetic keratitides
|
|
D016849||herpetic keratitis
|
|
D016849||keratitides herpes simplex
|
|
D016849||keratitides herpetic
|
|
D016849||keratitis herpes simplex
|
|
D016849||ocular herpes simplex
|
|
C567832|612997||spermatogenic failure 7
|
|
C567832|612997||male infertility nonsyndromic autosomal recessive
|
|
C567832|612997||miar
|
|
C567832|612997||spgf7
|
|
D053713||azoospermia
|
|
D015511||goat diseases
|
|
D015511||caprine disease
|
|
D015511||caprine diseases
|
|
D015511||disease caprine
|
|
D015511||disease goat
|
|
D015511||diseases caprine
|
|
D015511||diseases goat
|
|
D015511||goat disease
|
|
161200|D009261||nail patella syndrome
|
|
161200|D009261||disease fong
|
|
161200|D009261||fong disease
|
|
161200|D009261||hereditary onycho osteodysplasia
|
|
161200|D009261||hereditary osteo onychodysplasia
|
|
161200|D009261||hereditary osteo onychodysplasias
|
|
161200|D009261||nps
|
|
161200|D009261||nps1
|
|
161200|D009261||onychoosteodysplasia
|
|
161200|D009261||osteo onychodysplasia hereditary
|
|
161200|D009261||osteo onychodysplasias hereditary
|
|
161200|D009261||osterreicher syndrome
|
|
161200|D009261||pelvic horn syndrome
|
|
161200|D009261||syndrome nail patella
|
|
161200|D009261||syndrome osterreicher
|
|
161200|D009261||syndrome pelvic horn
|
|
161200|D009261||syndrome turner kieser
|
|
161200|D009261||turner kieser syndrome
|
|
167960||human papillomavirus type 18 integration site 2
|
|
167960||hpv18i2
|
|
167960||papillomavirus type 18 integration site 2
|
|
D015526||aids dementia complex
|
|
D015526||acquired immune deficiency syndrome dementia complex
|
|
D015526||aids encephalopathies
|
|
D015526||aids encephalopathy
|
|
D015526||aids related dementia complex
|
|
D015526||complex aids dementia
|
|
D015526||complex aids related dementia
|
|
D015526||dementia complex acquired immune deficiency syndrome
|
|
D015526||dementia complex aids
|
|
D015526||dementia complex aids related
|
|
D015526||dementia hiv
|
|
D015526||dementias hiv
|
|
D015526||encephalopathies aids
|
|
D015526||encephalopathies hiv
|
|
D015526||encephalopathy aids
|
|
D015526||encephalopathy hiv
|
|
D015526||hiv 1 associated cognitive motor complex
|
|
D015526||hiv 1 cognitive and motor complex
|
|
D015526||hiv associated cognitive motor complex
|
|
D015526||hiv dementia
|
|
D015526||hiv dementias
|
|
D015526||hiv encephalopathies
|
|
D015526||hiv encephalopathy
|
|
C565058|130600||elliptocytosis 2
|
|
C565058|130600||el2
|
|
C565058|130600||elliptocytosis rhesus unlinked type
|
|
D016857||hypocapnia
|
|
D016857||hypocapnias
|
|
255200||myopathy centronuclear 2
|
|
255200||cnm2
|
|
D015529||choledochal cyst
|
|
D015529||bile duct cyst
|
|
D015529||bile duct cysts
|
|
D015529||choledochal cyst congenital
|
|
D015529||choledochal cyst diverticulum
|
|
D015529||choledochal cyst intrahepatic
|
|
D015529||choledochal cyst multiple
|
|
D015529||choledochal cysts
|
|
D015529||choledochal cysts congenital
|
|
D015529||choledochal cysts diverticulum
|
|
D015529||choledochal cysts intrahepatic
|
|
D015529||choledochal cysts multiple
|
|
D015529||choledochal cyst type i
|
|
D015529||choledochal cyst type ii
|
|
D015529||choledochal cyst type iii
|
|
D015529||choledochal cyst type iv
|
|
D015529||choledochal cyst type v
|
|
D015529||choledochal diverticulum
|
|
D015529||choledochal diverticulums
|
|
D015529||choledochocele
|
|
D015529||choledochoceles
|
|
D015529||common bile duct cyst
|
|
D015529||congenital choledochal cyst
|
|
D015529||congenital choledochal cysts
|
|
D015529||cyst bile duct
|
|
D015529||cyst choledochal
|
|
D015529||cyst common bile duct
|
|
D015529||cyst congenital choledochal
|
|
D015529||cyst intrahepatic choledochal
|
|
D015529||cyst multiple choledochal
|
|
D015529||cysts bile duct
|
|
D015529||cysts choledochal
|
|
D015529||cysts common bile duct
|
|
D015529||cysts congenital choledochal
|
|
D015529||cysts intrahepatic choledochal
|
|
D015529||cysts multiple choledochal
|
|
D015529||diverticulum choledochal
|
|
D015529||diverticulum choledochal cyst
|
|
D015529||diverticulum choledochal cysts
|
|
D015529||diverticulums choledochal
|
|
D015529||duct cyst bile
|
|
D015529||duct cysts bile
|
|
D015529||intrahepatic choledochal cyst
|
|
D015529||intrahepatic choledochal cysts
|
|
D015529||multiple choledochal cyst
|
|
D015529||multiple choledochal cysts
|
|
D015524||sphenoid sinusitis
|
|
D015524||sinusitides sphenoid
|
|
D015524||sinusitides sphenoidal
|
|
D015524||sinusitis sphenoid
|
|
D015524||sinusitis sphenoidal
|
|
D015524||sphenoidal sinusitides
|
|
D015524||sphenoidal sinusitis
|
|
D015524||sphenoid sinusitides
|
|
C567065|300660||leukoencephalopathy with metaphyseal chondrodysplasia
|
|
C567065|300660||lkmcd
|
|
D015523||maxillary sinusitis
|
|
D015523||maxillary sinusitides
|
|
D015523||sinusitides maxillary
|
|
D015523||sinusitis maxillary
|
|
D015522||frontal sinusitis
|
|
D015522||frontal sinusitides
|
|
D015522||sinusitides frontal
|
|
D015522||sinusitis frontal
|
|
D015521||ethmoid sinusitis
|
|
D015521||ethmoidal sinusitides
|
|
D015521||ethmoidal sinusitis
|
|
D015521||ethmoid sinusitides
|
|
D015521||sinusitides ethmoid
|
|
D015521||sinusitides ethmoidal
|
|
D015521||sinusitis ethmoid
|
|
D015521||sinusitis ethmoidal
|
|
C536780||t cell immunodeficiency primary
|
|
C536780||primary t cell immunodeficiency disorders
|
|
C567595|300455||retinitis pigmentosa x linked and sinorespiratory infections with or without deafness
|
|
C535450||chromosome 13p duplication
|
|
C535450||chromosome 13p trisomy
|
|
C535450||duplication 13p
|
|
C535450||trisomy 13p
|
|
C536784||tabatznik syndrome
|
|
C536784||heart hand syndrome 2
|
|
D020096||zygomycosis
|
|
D020096||entomophthoramycoses
|
|
D020096||entomophthoramycosis
|
|
D020096||phycomycoses
|
|
D020096||phycomycosis
|
|
D020096||zygomycoses
|
|
D004844||epistaxis
|
|
D004844||bleeding nasal
|
|
D004844||bleedings nasal
|
|
D004844||nasal bleeding
|
|
D004844||nasal bleedings
|
|
D004844||nosebleed
|
|
D004844||nose bleed
|
|
D004844||nose bleeds
|
|
C536782||t cell lymphoma 1a
|
|
C536105|608908||myopia 6
|
|
C536105|608908||myopia susceptibility to
|
|
C536105|608908||myp6
|
|
C535454||chromosome 9 trisomy mosaic
|
|
C535454||trisomy 9 mosaic
|
|
C535454||trisomy 9 mosaicism
|
|
C535454||uniparental disomy of 9
|
|
C536783||t lymphocytopenia
|
|
C537533|210600||seckel syndrome 1
|
|
C537533|210600||bird headed dwarfism
|
|
C537533|210600||microcephalic primordial dwarfism 1
|
|
C537533|210600||microcephalic primordial dwarfism i
|
|
C537533|210600||nanocephalic dwarfism
|
|
C537533|210600||sckl
|
|
C537533|210600||sckl1
|
|
C537533|210600||seckel type dwarfism
|
|
C535453||chromosome 9 trisomy 9q32
|
|
C535453||duplication 9q32
|
|
C535453||trisomy 9q32
|
|
C563335|601369||deafness autosomal dominant 9
|
|
C563335|601369||dfna9
|
|
D004842||epispadias
|
|
D004842||epispadia
|
|
C567654|613286||cardiomyopathy dilated 1ff
|
|
C567654|613286||cmd1ff
|
|
D010661|261600||phenylketonurias
|
|
D010661|261600||atypical phenylketonuria
|
|
D010661|261600||atypical pku
|
|
D010661|261600||bh4 deficiency
|
|
D010661|261600||classical phenylketonuria
|
|
D010661|261600||deficiency bh4
|
|
D010661|261600||deficiency dhpr
|
|
D010661|261600||deficiency dihydropteridine reductase
|
|
D010661|261600||deficiency disease dihydropteridine reductase
|
|
D010661|261600||deficiency disease phenylalanine hydroxylase
|
|
D010661|261600||deficiency disease phenylalanine hydroxylase severe
|
|
D010661|261600||deficiency pah
|
|
D010661|261600||deficiency phenylalanine hydroxylase
|
|
D010661|261600||deficiency qdpr
|
|
D010661|261600||deficiency tetrahydrobiopterin
|
|
D010661|261600||dihydropteridine reductase deficiency disease
|
|
D010661|261600||disease folling
|
|
D010661|261600||disease folling apos s
|
|
D010661|261600||folling disease
|
|
D010661|261600||folling disease hyperphenylalaninemia non pku mild included
|
|
D010661|261600||folling apos s disease
|
|
D010661|261600||hpa non pku mild included
|
|
D010661|261600||hyperphenylalaninaemia
|
|
D010661|261600||hyperphenylalaninemia caused by a defect in biopterin metabolism
|
|
D010661|261600||hyperphenylalaninemia non phenylketonuric
|
|
D010661|261600||non phenylketonuric hyperphenylalaninemia
|
|
D010661|261600||non phenylketonuric hyperphenylalaninemias
|
|
D010661|261600||oligophrenia phenylpyruvica
|
|
D010661|261600||pah deficiency
|
|
D010661|261600||phenylalanine hydroxylase deficiency
|
|
D010661|261600||phenylalanine hydroxylase deficiency disease
|
|
D010661|261600||phenylalanine hydroxylase deficiency disease severe
|
|
D010661|261600||phenylketonuria
|
|
D010661|261600||phenylketonuria atypical
|
|
D010661|261600||phenylketonuria classical
|
|
D010661|261600||phenylketonuria i
|
|
D010661|261600||phenylketonuria ii
|
|
D010661|261600||phenylketonuria maternal included
|
|
D010661|261600||phenylketonuria type 2
|
|
D010661|261600||pku
|
|
D010661|261600||pku atypical
|
|
D010661|261600||tetrahydrobiopterin deficiency
|
|
304110|C536456||craniofrontonasal dysplasia
|
|
304110|C536456||cfnd
|
|
304110|C536456||cfns
|
|
304110|C536456||craniofrontonasal dysostosis
|
|
304110|C536456||craniofrontonasal syndrome
|
|
C536777||systemic candidiasis
|
|
C536777||systemic candida infections
|
|
C573722||acrocephalopolydactylous dysplasia
|
|
C573722||elejalde syndrome
|
|
C538243|301200||amelogenesis imperfecta hypoplastic hypomaturation x linked 1
|
|
C538243|301200||ai1e
|
|
C538243|301200||aih1
|
|
C538243|301200||amelogenesis imperfecta type ie
|
|
C538243|301200||amelogenesis imperfecta x linked 1
|
|
C536775||syphilitic aseptic meningitis
|
|
C536775||meningeal syphilis
|
|
C536775||meningitis syphilitic
|
|
C536775||syphilitic meningitis
|
|
C564567|300209||simpson golabi behmel syndrome type 2
|
|
C564567|300209||sgbs2
|
|
C536776||syphilitic myelopathy tabes dorsalis
|
|
250950|C562801||3 methylglutaconic aciduria type i
|
|
250950|C562801||3 methylglutaconyl coa hydratase deficiency
|
|
250950|C562801||3 mg coa hydratase deficiency
|
|
250950|C562801||mga type i
|
|
250950|C562801||mgca1
|
|
C535449||deletion 13q syndrome partial
|
|
C535449||13q syndrome partial
|
|
C535449||chromosome 13 partial monosomy 13q
|
|
C535449||monosomy 13q partial
|
|
C535449||partial monosomy of the long arm of chromosome 13
|
|
300577|C564482||mental retardation x linked 91
|
|
300577|C564482||mrx91
|
|
C535448||bird headed dwarfism montreal type
|
|
C535448||bird headed dwarfism with features of premature senility
|
|
C536779||systemic necrotizing angiitis
|
|
C536779||systemic necrotizing angitis
|
|
D003528||carcinoma adenoid cystic
|
|
D003528||adenocystic carcinoma
|
|
D003528||adenocystic carcinomas
|
|
D003528||adenoid cystic carcinoma
|
|
D003528||adenoid cystic carcinomas
|
|
D003528||carcinoma adenocystic
|
|
D003528||carcinomas adenocystic
|
|
D003528||carcinomas adenoid cystic
|
|
D003528||cylindroma
|
|
D003528||cylindromas
|
|
D003528||cystic carcinoma adenoid
|
|
D003528||cystic carcinomas adenoid
|
|
D004859||equine infectious anemia
|
|
D004859||anemia equine infectious
|
|
D004859||anemias equine infectious
|
|
D004859||equine infectious anemias
|
|
D004859||fevers swamp
|
|
D004859||fever swamp
|
|
D004859||infectious anemia equine
|
|
D004859||infectious anemias equine
|
|
D004859||swamp fever
|
|
D004859||swamp fevers
|
|
C563845|608837||carney complex variant
|
|
C536790||craniosynostosis sagittal with dandy walker malformation and hydrocephalus
|
|
C536790||sagittal craniosynostosis dandy walker malformation and hydrocephalus
|
|
C536795||chromosome 22 ring
|
|
C536795||ring 22 chromosome
|
|
C535463||mainzer saldino disease
|
|
C535463||conorenal syndrome
|
|
C535463||mainzer saldino syndrome
|
|
C535463||renal dysplasia retinal pigmentary dystrophy cerebellar ataxia and skeletal dysplasia
|
|
C535463||saldino mainzer disease
|
|
C536796||trisomy 22 mosaicism syndrome
|
|
C536796||chromosome 22 trisomy mosaic
|
|
C536796||trisomy 22 mosaic
|
|
C536796||trisomy mosaic 22
|
|
C536796||uniparental disomy of 22
|
|
C536793||chromosome 21 tetrasomy 21q
|
|
C536793||tetrasomy 21q
|
|
C567320|612394||bone fragility with contractures arterial rupture and deafness
|
|
C567320|612394||lh3 deficiency
|
|
C567320|612394||lysyl hydroxylase 3 deficiency
|
|
C535465||contractures ectodermal dysplasia cleft lip palate
|
|
D020083||acquired hyperostosis syndrome
|
|
D020083||acquired hyperostosis syndromes
|
|
D020083||hyperostosis syndrome acquired
|
|
D020083||hyperostosis syndromes acquired
|
|
D020083||sapho syndrome
|
|
D020083||sapho syndromes
|
|
D020083||syndrome acquired hyperostosis
|
|
D020083||syndromes acquired hyperostosis
|
|
D020083||syndrome sapho
|
|
D020083||syndromes sapho
|
|
D020083||synovitis acne pustlosis hyperostosis and osteomyelitis
|
|
C536794||chromosome 21 uniparental disomy of
|
|
C536794||mosaic trisomy 21
|
|
C536794||uniparental disomy of 21
|
|
D003527||cyclothymic disorder
|
|
D003527||cyclothymic disorders
|
|
D003527||cyclothymic personalities
|
|
D003527||cyclothymic personality
|
|
D003527||disorder cyclothymic
|
|
D003527||disorders cyclothymic
|
|
D003527||personalities cyclothymic
|
|
D003527||personality cyclothymic
|
|
C535464||conotruncal cardiac defects
|
|
C535464||truncus arteriosus communis
|
|
300640|C564468||invasive pneumococcal disease recurrent isolated 2
|
|
300640|C564468||ipd2
|
|
C563989|610951||ceroid lipofuscinosis neuronal 7
|
|
C563989|610951||cln7
|
|
612703||microcephaly 7 primary autosomal recessive
|
|
612703||mcph7
|
|
D041761||cholecystolithiasis
|
|
153480|D006223||hamartoma syndrome multiple
|
|
153480|D006223||bannayan riley ruvalcaba syndrome
|
|
153480|D006223||bannayan ruvalcaba riley syndrome
|
|
153480|D006223||bannayan zonana syndrome
|
|
153480|D006223||brrs
|
|
153480|D006223||bzs
|
|
153480|D006223||cerebellar granule cell hypertrophy and megalencephaly included
|
|
153480|D006223||cerebelloparenchymal disorder vi included
|
|
153480|D006223||cerebellum dysplastic gangliocytoma
|
|
153480|D006223||cerebellum dysplastic gangliocytomas
|
|
153480|D006223||cowden disease
|
|
153480|D006223||cowden apos s disease
|
|
153480|D006223||cowdens disease
|
|
153480|D006223||cowden apos s syndrome
|
|
153480|D006223||cowdens syndrome
|
|
153480|D006223||cowden syndrome
|
|
153480|D006223||cowden syndrome 1
|
|
153480|D006223||cpd6 included
|
|
153480|D006223||cs
|
|
153480|D006223||cws1
|
|
153480|D006223||dysplastic gangliocytoma of cerebellum
|
|
153480|D006223||dysplastic gangliocytoma of the cerebellum
|
|
153480|D006223||hamartoma syndromes multiple
|
|
153480|D006223|C535531|603932||ldd included
|
|
153480|D006223||lhermitte duclos disease
|
|
153480|D006223||lhermitte duclos disease included
|
|
153480|D006223||macrocephaly multiple lipomas and hemangiomata
|
|
153480|D006223||macrocephaly pseudopapilledema and multiple hemangiomas
|
|
153480|D006223||macrocephaly pseudopapilledema and multiple hemangiomata
|
|
153480|D006223||multiple hamartoma syndrome
|
|
153480|D006223||multiple hamartoma syndrome mham dysplastic gangliocytoma of the cerebellum included
|
|
153480|D006223||multiple hamartoma syndromes
|
|
153480|D006223||myhre riley smith syndrome
|
|
153480|D006223||proteus like syndrome included
|
|
153480|D006223||pten hamartoma tumor syndrome
|
|
153480|D006223||riley smith syndrome
|
|
153480|D006223||rmss
|
|
153480|D006223||ruvalcaba myhre smith syndrome
|
|
153480|D006223||ruvalcaba myhre syndrome
|
|
D004402|223900||dysautonomia familial
|
|
D004402|223900||dominant hereditary sensory neuropathy type iii
|
|
D004402|223900||dys
|
|
D004402|223900||familial dysautonomia
|
|
D004402|223900||fd
|
|
D004402|223900||hereditary sensory and autonomic neuropathy 3
|
|
D004402|223900||hereditary sensory and autonomic neuropathy type iii
|
|
D004402|223900||hereditary sensory neuropathy dominant type 3
|
|
D004402|223900||hereditary sensory neuropathy dominant type iii
|
|
D004402|223900||hereditary sensory neuropathy type 3
|
|
D004402|223900||hereditary sensory neuropathy type 3 dominant
|
|
D004402|223900||hsan3
|
|
D004402|223900||hsan 3
|
|
D004402|223900||hsan hereditary sensory and autonomic neuropathy type iii
|
|
D004402|223900||hsan iii
|
|
D004402|223900||hsan type iii
|
|
D004402|223900||hsn iii
|
|
D004402|223900||neuropathy hereditary and autonomic type iii
|
|
D004402|223900||neuropathy hereditary sensory and autonomic type iii
|
|
D004402|223900||riley day syndrome
|
|
D004402|223900||type 3 hereditary sensory neuropathy dominant
|
|
D004402|223900||type iii hereditary sensory neuropathy dominant
|
|
D015508||nasal obstruction
|
|
D015508||airway obstruction nasal
|
|
D015508||bilateral nasal obstruction
|
|
D015508||blockage nasal
|
|
D015508||blockages nasal
|
|
D015508||nasal airway obstruction
|
|
D015508||nasal blockage
|
|
D015508||nasal blockages
|
|
D015508||nasal obstruction bilateral
|
|
D015508||nasal obstruction unilateral
|
|
D015508||obstruction bilateral nasal
|
|
D015508||obstruction nasal
|
|
D015508||obstruction nasal airway
|
|
D015508||obstructions nasal
|
|
D015508||unilateral nasal obstruction
|
|
C535455||chromosomes 1 and 2 monosomy 2q duplication 1p
|
|
C535455||deletion 2q duplication 1p
|
|
C535455||monosomy 2q duplication 1p
|
|
C536786||athabaskan severe combined immunodeficiency
|
|
C535458||chudley rozdilsky syndrome
|
|
C535458||chudley syndrome
|
|
D004827||epilepsy
|
|
D004827||aura
|
|
D004827||auras
|
|
D004827||awakening epilepsy
|
|
D004827||cryptogenic epilepsies
|
|
D004827||cryptogenic epilepsy
|
|
D004827||epilepsies
|
|
D004827||epilepsies cryptogenic
|
|
D004827||epilepsy awakening
|
|
D004827||epilepsy cryptogenic
|
|
D004827||epileptic seizure
|
|
D004827||epileptic seizures
|
|
D004827||seizure disorder
|
|
D004827||seizure disorders
|
|
D004827||seizure epileptic
|
|
D004827||seizures epileptic
|
|
D004827||seizure single
|
|
D004827||seizures single
|
|
D004827||single seizure
|
|
D004827||single seizures
|
|
C535470||coq responsive oxphos deficiency
|
|
D020078||neurogenic inflammation
|
|
D020078||inflammation neurogenic
|
|
D020078||inflammations neurogenic
|
|
D020078||neurogenic inflammations
|
|
D004826||epiglottitis
|
|
D004826||epiglottitides
|
|
D004829||epilepsy generalized
|
|
D004829||akinetic epilepsies
|
|
D004829||akinetic epilepsy
|
|
D004829||atonic epilepsies
|
|
D004829||atonic epilepsy
|
|
D004829||convulsive epilepsies generalized
|
|
D004829||convulsive epilepsy generalized
|
|
D004829||convulsive generalized seizure disorder
|
|
D004829||convulsive seizure disorder generalized
|
|
D004829||epilepsies akinetic
|
|
D004829||epilepsies atonic
|
|
D004829||epilepsies generalized
|
|
D004829||epilepsies generalized convulsive
|
|
D004829||epilepsies tonic
|
|
D004829||epilepsy akinetic
|
|
D004829||epilepsy atonic
|
|
D004829||epilepsy generalized convulsive
|
|
D004829||epilepsy generalized nonconvulsive
|
|
D004829||epilepsy symptomatic generalized
|
|
D004829||epilepsy tonic
|
|
D004829||generalized convulsive epilepsies
|
|
D004829||generalized convulsive epilepsy
|
|
D004829||generalized epilepsies
|
|
D004829||generalized epilepsy
|
|
D004829||generalized epilepsy symptomatic
|
|
D004829||generalized nonconvulsive epilepsy
|
|
D004829||generalized nonconvulsive seizure disorder
|
|
D004829||generalized onset seizure disorder
|
|
D004829||generalized seizure disorder
|
|
D004829||generalized seizure disorder convulsive
|
|
D004829||generalized seizure disorder nonconvulsive
|
|
D004829||generalized seizure disorders
|
|
D004829||nonconvulsive epilepsy generalized
|
|
D004829||nonconvulsive generalized seizure disorder
|
|
D004829||nonconvulsive seizure disorder generalized
|
|
D004829||seizure disorder convulsive generalized
|
|
D004829||seizure disorder generalized
|
|
D004829||seizure disorder generalized convulsive
|
|
D004829||seizure disorder generalized nonconvulsive
|
|
D004829||seizure disorder generalized onset
|
|
D004829||seizure disorder nonconvulsive generalized
|
|
D004829||seizure disorders generalized
|
|
D004829||symptomatic generalized epilepsy
|
|
D004829||tonic epilepsies
|
|
D004829||tonic epilepsy
|
|
C537608|600121||rhizomelic chondrodysplasia punctata type 3
|
|
C537608|600121||agps deficiency
|
|
C537608|600121||alkyldihydroxyacetonephosphate synthase deficiency
|
|
C537608|600121||alkylglycerone phosphate synthase deficiency
|
|
C537608|600121||rcdp3
|
|
C535472||corneal cerebellar syndrome
|
|
C535472||corneal dystrophy with spinocerebellar degeneration
|
|
C535472||der kaloustian jarudi khoury syndrome
|
|
C535472||spinocerebellar degeneration and corneal dystrophy
|
|
D004828||epilepsies partial
|
|
D004828||abdominal epilepsies
|
|
D004828||abdominal epilepsy
|
|
D004828||amygdalo hippocampal epilepsies
|
|
D004828||amygdalo hippocampal epilepsy
|
|
D004828||benign focal epilepsy childhood
|
|
D004828||benign occipital epilepsies
|
|
D004828||benign occipital epilepsy
|
|
D004828||benign occipital epilepsy childhood
|
|
D004828||childhood benign focal epilepsy
|
|
D004828||childhood benign occipital epilepsy
|
|
D004828||digestive epilepsies
|
|
D004828||digestive epilepsy
|
|
D004828||disorders focal seizure
|
|
D004828||disorders partial seizure
|
|
D004828||epilepsies abdominal
|
|
D004828||epilepsies amygdalo hippocampal
|
|
D004828||epilepsies benign occipital
|
|
D004828||epilepsies digestive
|
|
D004828||epilepsies focal
|
|
D004828||epilepsies gelastic
|
|
D004828||epilepsies localization related
|
|
D004828||epilepsies occipital lobe
|
|
D004828||epilepsies rhinencephalic
|
|
D004828||epilepsies simple partial
|
|
D004828||epilepsy abdominal
|
|
D004828||epilepsy benign occipital
|
|
D004828||epilepsy focal
|
|
D004828||epilepsy localization related
|
|
D004828||epilepsy partial
|
|
D004828||epilepsy simple partial
|
|
D004828||focal epilepsies
|
|
D004828||focal epilepsy
|
|
D004828||focal seizure disorder
|
|
D004828||focal seizure disorders
|
|
D004828||gelastic epilepsies
|
|
D004828||gelastic epilepsy
|
|
D004828||lobe epilepsy occipital
|
|
D004828||localization related epilepsies
|
|
D004828||localization related epilepsy
|
|
D004828||occipital epilepsies benign
|
|
D004828||occipital epilepsy benign
|
|
D004828||occipital lobe epilepsies
|
|
D004828||occipital lobe epilepsy
|
|
D004828||partial epilepsies
|
|
D004828||partial epilepsies simple
|
|
D004828||partial epilepsy
|
|
D004828||partial seizure disorder
|
|
D004828||partial seizure disorders
|
|
D004828||partial seizures simple
|
|
D004828||partial seizures simple consciousness preserved
|
|
D004828||rhinencephalic epilepsies
|
|
D004828||rhinencephalic epilepsy
|
|
D004828||seizure disorder focal
|
|
D004828||seizure disorder partial
|
|
D004828||seizure disorders focal
|
|
D004828||seizure disorders partial
|
|
D004828||seizures simple partial
|
|
D004828||seizures subclinical
|
|
D004828||seizure subclinical
|
|
D004828||seizures uncinate
|
|
D004828||seizure uncinate
|
|
D004828||simple partial epilepsies
|
|
D004828||simple partial seizures
|
|
D004828||subclinical seizure
|
|
D004828||subclinical seizures
|
|
D004828||uncinate seizures
|
|
C535471||cornea guttata with anterior polar cataract
|
|
C535471||cornea guttata with anterior polar cataracts
|
|
C535471||familial congenital cornea guttata with anterior polar cataracts
|
|
D004823||epididymitis
|
|
D004823||epididymitides
|
|
120435|C537261||lynch syndrome i site specific colonic cancer
|
|
120435|C537261||coca1 lynch syndrome ii included
|
|
120435|C537261||fcc1
|
|
120435|C537261||hnpcc1
|
|
C536254|266100||pyridoxine dependent epilepsy
|
|
C536254|266100||aasa dehydrogenase deficiency
|
|
C536254|266100||epd
|
|
C536254|266100||epilepsy pyridoxine dependent
|
|
C536254|266100||pde
|
|
C536254|266100||pyridoxine dependency
|
|
C536254|266100||pyridoxine dependency with seizures
|
|
C536254|266100||pyridoxine dependent seizures
|
|
C536254|266100||vitamin b6 dependent seizures
|
|
D019080||cafe au lait spots
|
|
D019080||cafe au lait spot
|
|
D019080||spot cafe au lait
|
|
D019080||spots cafe au lait
|
|
D004820||epidermolysis bullosa
|
|
D004820||acantholysis bullosa
|
|
C535443|235555||bile acid synthesis defect congenital 2
|
|
C535443|235555||cbas2
|
|
C535443|235555||cholestasis with delta 4 3 oxosteroid 5 beta reductase deficiency
|
|
C535443|235555||congenital bile acid synthesis defect type 2 cbas2
|
|
D064419||chemically induced disorders
|
|
D064419||chemically induced disorder
|
|
D064419||disorder chemically induced
|
|
D064419||disorders chemically induced
|
|
C535737|602473||ethylmalonic encephalopathy
|
|
C535737|602473|610247|D057765||ee
|
|
C535737|602473||encephalopathy ethylmalonic
|
|
C535737|602473||encephalopathy petechiae and ethylmalonic aciduria
|
|
C535737|602473||epema syndrome
|
|
C535737|602473||syndrome of encephalopathy petechiae and ethylmalonic aciduria
|
|
C567310|612444||ciliary dyskinesia primary 9
|
|
C567310|612444||cild9
|
|
C567310|612444||ciliary dyskinesia primary 9 with or without situs inversus
|
|
C536799||chromosome 22 trisomy
|
|
C536799||duplication 22
|
|
C536799||trisomy 22
|
|
C562626|130080||ehlers danlos syndrome type viii
|
|
C562626|130080||eds8
|
|
C562626|130080||eds viii
|
|
C562626|130080||ehlers danlos syndrome periodontitis type
|
|
C562626|130080||ehlers danlos syndrome periodontosis type
|
|
C536296|609583||joubert syndrome 4
|
|
C536296|609583||jbts4
|
|
C535466||convulsions benign familial neonatal dominant form
|
|
C535466||autosomal dominant form of benign neonatal seizures
|
|
C535466||autosomal dominant spheroid body myopathy
|
|
C535466||benign familial neonatal seizures
|
|
C535466||epilepsy benign neonatal 2
|
|
C535466||seizures benign familial neonatal
|
|
C535466||spheroid body myopathy
|
|
C536797||chromosome 22 microdeletion 22 q11
|
|
C536797||microdeletion 22 q11
|
|
C535469||coproporphyria
|
|
C535469||hereditary coproporphyria porphyria
|
|
C535469||porphyria hepatica coproporphyria
|
|
C535469||porphyria hepatica ii
|
|
C536798||chromosome 22 monosome mosaic
|
|
C536798||chromosome 22 mosaic monosomy
|
|
C536798||mosaic monosome 22
|
|
C535468||copper deficiency familial benign
|
|
C535468||familial benign copper deficiency
|
|
C535468||familial benign hypocupremia
|
|
C563788|609141||corneal dystrophy posterior polymorphous 3
|
|
C563788|609141||ppcd3
|
|
C535481||fraser jequier chen syndrome
|
|
D020065||hepatopulmonary syndrome
|
|
D020065||hepato pulmonary syndrome
|
|
D020065||hepatopulmonary syndromes
|
|
D020065||hepato pulmonary syndromes
|
|
D020065||syndrome hepatopulmonary
|
|
D020065||syndrome hepato pulmonary
|
|
D020065||syndromes hepatopulmonary
|
|
D020065||syndromes hepato pulmonary
|
|
D004839||epiphyses slipped
|
|
D004839||epiphysiolyses
|
|
D004839||epiphysiolysis
|
|
D004839||slipped epiphyses
|
|
D052439||lipid metabolism disorders
|
|
D052439||lipid metabolism disorder
|
|
D052439||metabolism disorder lipid
|
|
D052439||metabolism disorders lipid
|
|
D041781||jaundice obstructive
|
|
D041781||cholestatic jaundice
|
|
D041781||jaundice cholestatic
|
|
D041781||jaundice mechanical
|
|
D041781||mechanical jaundice
|
|
D041781||obstructive jaundice
|
|
D004834||epilepsy post traumatic
|
|
D004834||concussive convulsion
|
|
D004834||concussive convulsions
|
|
D004834||convulsion concussive
|
|
D004834||convulsions concussive
|
|
D004834||disorder post traumatic seizure
|
|
D004834||disorders post traumatic seizure
|
|
D004834||early post traumatic seizure
|
|
D004834||early post traumatic seizures
|
|
D004834||epilepsies post traumatic
|
|
D004834||epilepsies traumatic
|
|
D004834||epilepsy traumatic
|
|
D004834||impact seizure
|
|
D004834||impact seizures
|
|
D004834||late post traumatic seizure
|
|
D004834||late post traumatic seizures
|
|
D004834||post traumatic epilepsies
|
|
D004834||post traumatic epilepsy
|
|
D004834||post traumatic seizure disorder
|
|
D004834||post traumatic seizure disorders
|
|
D004834||post traumatic seizure early
|
|
D004834||post traumatic seizure late
|
|
D004834||post traumatic seizures early
|
|
D004834||post traumatic seizures late
|
|
D004834||seizure disorder post traumatic
|
|
D004834||seizure disorders post traumatic
|
|
D004834||seizure early post traumatic
|
|
D004834||seizure late post traumatic
|
|
D004834||seizures early post traumatic
|
|
D004834||seizures late post traumatic
|
|
D004834||traumatic epilepsies
|
|
D004834||traumatic epilepsy
|
|
C535485||chromosome 13q trisomy
|
|
C535485||duplication 13q
|
|
C535485||trisomy 13q
|
|
D004833||epilepsy temporal lobe
|
|
D004833||benign psychomotor epilepsy childhood
|
|
D004833||childhood benign psychomotor epilepsy
|
|
D004833||epilepsies lateral temporal
|
|
D004833||epilepsies temporal lobe
|
|
D004833||epilepsies uncinate
|
|
D004833||epilepsy benign psychomotor childhood
|
|
D004833||epilepsy lateral temporal
|
|
D004833||epilepsy uncinate
|
|
D004833||lateral temporal epilepsies
|
|
D004833||lateral temporal epilepsy
|
|
D004833||temporal lobe epilepsies
|
|
D004833||temporal lobe epilepsy
|
|
D004833||uncinate epilepsies
|
|
D004833||uncinate epilepsy
|
|
C535484||13q deletion syndrome
|
|
C535484||chromosome 13q deletion
|
|
C535484|613884||chromosome 13q deletion syndrome
|
|
C535484||chromosome 13q monosomy
|
|
C535484||chromosome 13q syndrome
|
|
C535484||deletion 13q
|
|
C535484||deletion 13q syndrome
|
|
C535484||monosomy 13q
|
|
C535484||monosomy 13q syndrome
|
|
C535484||orbeli apos s syndrome
|
|
C535484||orbeli syndrome
|
|
C535487||ring chromosome 14 syndrome
|
|
C535487||chromosome 14 ring
|
|
C535487||ring 14
|
|
C535487||ring 14 syndrome
|
|
C535487||ring chromosome 14
|
|
C535486||chromosome 13q mosaicism
|
|
C535486||mosiacism of chromosome 13q
|
|
D004830||epilepsy tonic clonic
|
|
D004830||convulsion disorders tonic clonic
|
|
D004830||convulsion disorder tonic clonic
|
|
D004830||convulsion grand mal
|
|
D004830||convulsions grand mal
|
|
D004830||convulsions tonic clonic
|
|
D004830||convulsion syndromes tonic clonic
|
|
D004830||convulsion syndrome tonic clonic
|
|
D004830||convulsion tonic clonic
|
|
D004830||cryptogenic tonic clonic epilepsies
|
|
D004830||cryptogenic tonic clonic epilepsy
|
|
D004830||disorders tonic clonic convulsion
|
|
D004830||disorders tonic clonic seizure
|
|
D004830||disorder tonic clonic convulsion
|
|
D004830||disorder tonic clonic seizure
|
|
D004830||epilepsies cryptogenic tonic clonic
|
|
D004830||epilepsies familial tonic clonic
|
|
D004830||epilepsies symptomatic tonic clonic
|
|
D004830||epilepsies tonic clonic
|
|
D004830||epilepsy cryptogenic tonic clonic
|
|
D004830||epilepsy familial tonic clonic
|
|
D004830||epilepsy grand mal
|
|
D004830||epilepsy major
|
|
D004830||epilepsy symptomatic tonic clonic
|
|
D004830||epilepsy tonic clonic cryptogenic
|
|
D004830||epilepsy tonic clonic familial
|
|
D004830||epilepsy tonic clonic symptomatic
|
|
D004830||familial tonic clonic epilepsies
|
|
D004830||familial tonic clonic epilepsy
|
|
D004830||grand mal convulsion
|
|
D004830||grand mal convulsions
|
|
D004830||grand mal epilepsy
|
|
D004830||grand mal seizure disorder
|
|
D004830||major epilepsies
|
|
D004830||major epilepsy
|
|
D004830||major motor seizure disorder
|
|
D004830||seizure disorder grand mal
|
|
D004830||seizure disorder major motor
|
|
D004830||seizure disorders tonic clonic
|
|
D004830||seizure disorder tonic clonic
|
|
D004830||seizure syndromes tonic clonic
|
|
D004830||seizure syndrome tonic clonic
|
|
D004830||symptomatic tonic clonic epilepsies
|
|
D004830||symptomatic tonic clonic epilepsy
|
|
D004830||syndromes tonic clonic convulsion
|
|
D004830||syndromes tonic clonic seizure
|
|
D004830||syndrome tonic clonic convulsion
|
|
D004830||syndrome tonic clonic seizure
|
|
D004830||tonic clonic convulsion
|
|
D004830||tonic clonic convulsion disorder
|
|
D004830||tonic clonic convulsion disorders
|
|
D004830||tonic clonic convulsions
|
|
D004830||tonic clonic convulsion syndrome
|
|
D004830||tonic clonic convulsion syndromes
|
|
D004830||tonic clonic epilepsies
|
|
D004830||tonic clonic epilepsies cryptogenic
|
|
D004830||tonic clonic epilepsies familial
|
|
D004830||tonic clonic epilepsies symptomatic
|
|
D004830||tonic clonic epilepsy
|
|
D004830||tonic clonic epilepsy cryptogenic
|
|
D004830||tonic clonic epilepsy familial
|
|
D004830||tonic clonic epilepsy symptomatic
|
|
D004830||tonic clonic seizure disorder
|
|
D004830||tonic clonic seizure disorders
|
|
D004830||tonic clonic seizure syndrome
|
|
D004830||tonic clonic seizure syndromes
|
|
D020069||shoulder pain
|
|
D020069||pain shoulder
|
|
D020069||pains shoulder
|
|
D020069||shoulder pains
|
|
612566|C567252||inflammatory bowel disease 24
|
|
612566|C567252||ibd24
|
|
204650|C567147||amelogenesis imperfecta type ic
|
|
204650|C567147||ai1c
|
|
204650|C567147||amelogenesis imperfecta hypoplastic with or without openbite malocclusion autosomal recessive
|
|
204650|C567147||amelogenesis imperfecta local hypoplastic type autosomal recessive
|
|
607017|C564634||deafness autosomal dominant 21
|
|
607017|C564634||dfna21
|
|
204700|C538242||amelogenesis imperfecta pigmented hypomaturation type
|
|
204700|C538242|C567146||ai2a1
|
|
204700|C538242|C567146||amelogenesis imperfecta hypomaturation type iia1
|
|
204700|C538242|C567146||amelogenesis imperfecta pigmented hypomaturation type 1
|
|
C563835|608902||drug metabolism poor cyp2d6 related
|
|
C563835|608902||codeine ultrarapid metabolism of included
|
|
C563835|608902||debrisoquine poor metabolism of included
|
|
C563835|608902||debrisoquine ultrarapid metabolism of included
|
|
C563835|608902||drug metabolism ultrarapid cyp2d6 related included
|
|
C563835|608902||nortriptyline poor metabolism of included
|
|
C563835|608902||sparteine poor metabolism of included
|
|
106600|D000848||anodontia
|
|
106600|D000848||hyd1
|
|
106600|D000848||hypodontia
|
|
106600|D000848||hypodontia oligodontia 1
|
|
106600|D000848||hypodontia oligodontia with orofacial cleft included
|
|
106600|D000848||second premolars and third molars absence of
|
|
106600|D000848||sthag1
|
|
106600|D000848||tooth agenesis familial
|
|
106600|D000848||tooth agenesis familial tooth agenesis selective with orofacial cleft included
|
|
106600|D000848||tooth agenesis selective 1
|
|
D019066||facies
|
|
C535444|214950||bile acid synthesis defect congenital 4
|
|
C535444|214950||cbas4
|
|
C535444|214950||cholestasis intrahepatic with defective conversion of trihydroxycoprostanic acid to cholic acid
|
|
C535444|214950||trihydroxycoprostanic acid in bile
|
|
D004806||ependymoma
|
|
D004806||anaplastic ependymoma
|
|
D004806||anaplastic ependymomas
|
|
D004806||cellular ependymoma
|
|
D004806||clear cell ependymoma
|
|
D004806||ependymoma anaplastic
|
|
D004806||ependymoma myxopapillary
|
|
D004806||ependymoma papillary
|
|
D004806||ependymomas
|
|
D004806||ependymomas anaplastic
|
|
D004806||ependymomas myxopapillary
|
|
D004806||ependymomas papillary
|
|
D004806||myxopapillary ependymoma
|
|
D004806||myxopapillary ependymomas
|
|
D004806||papillary ependymoma
|
|
D004806||papillary ependymomas
|
|
C536741||wolffian tumor
|
|
C536741||female adnexal tumor of probable wolffian origin
|
|
C536741||wolffian adenoma
|
|
C536741||wolffian adnexal tumor
|
|
C567845|612951||leukoencephalopathy cystic without megalencephaly
|
|
D004803||eosinophilic granuloma
|
|
D004803||eosinophilic granulomas
|
|
D004803||granuloma eosinophilic
|
|
D004803||granulomas eosinophilic
|
|
D004802||eosinophilia
|
|
D004802||eosinophilias
|
|
D004802||eosinophilias tropical
|
|
D004802||eosinophilia tropical
|
|
D004802||tropical eosinophilia
|
|
D004802||tropical eosinophilias
|
|
C563418|600971||deafness autosomal recessive 6
|
|
C563418|600971||dfnb6
|
|
C563418|600971||neurosensory nonsyndromic recessive deafness 6
|
|
C563418|600971||nsrd6
|
|
C563858|608787||otosclerosis 5
|
|
C563858|608787||otsc5
|
|
D007088||illusions
|
|
D007088||auditory illusion
|
|
D007088||auditory illusions
|
|
D007088||autokinetic effect
|
|
D007088||autokinetic effects
|
|
D007088||autokinetic illusion
|
|
D007088||autokinetic illusions
|
|
D007088||effect autokinetic
|
|
D007088||effects autokinetic
|
|
D007088||illusion
|
|
D007088||illusion auditory
|
|
D007088||illusion autokinetic
|
|
D007088||illusion kinesthetic
|
|
D007088||illusions auditory
|
|
D007088||illusions autokinetic
|
|
D007088||illusions kinesthetic
|
|
D007088||illusions tactile
|
|
D007088||illusions visual
|
|
D007088||illusion tactile
|
|
D007088||illusion visual
|
|
D007088||kinesthetic illusion
|
|
D007088||kinesthetic illusions
|
|
D007088||tactile illusion
|
|
D007088||tactile illusions
|
|
D007088||visual illusion
|
|
D007088||visual illusions
|
|
607791|C564333||charcot marie tooth disease dominant intermediate d
|
|
607791|C564333||charcot marie tooth neuropathy dominant intermediate d
|
|
607791|C564333||cmtdid
|
|
607791|C564333||di cmtd
|
|
C536733||x chromosome trisomy xq25
|
|
C536733||duplication xq25
|
|
C536733||trisomy xq25
|
|
C535401||charcot marie tooth disease dominant intermediate 3
|
|
C535400||charcot marie tooth disease dominant intermediate 2
|
|
C536731||x chromosome trisomy xpter xq13
|
|
C536731||duplication xpter xq13
|
|
C536731||trisomy xpter xq13
|
|
C536732||chromosome xq duplication syndrome
|
|
C536732||chromosome xq trisomy
|
|
C536732||duplication xq
|
|
C536732||dup xq syndrome
|
|
C536732||trisomy xq
|
|
C536732||x chromosome trisomy xq
|
|
C535402||galactorrhea hyperprolactinemia
|
|
C535402||galactorrhoea hyperprolactinaemia
|
|
C535607|225750||aicardi goutieres syndrome
|
|
C535607|225750||ags
|
|
C535607|225750||ags1
|
|
C535607|225750||ags2
|
|
C535607|225750||aicardi goutieres syndrome 1
|
|
C535607|225750||aicardi goutieres syndrome 2
|
|
C535607|225750||cree encephalitis
|
|
C535607|225750||encephalopathy familial infantile with intracranial calcification and chronic cerebrospinal fluid lymphocytosis
|
|
C535607|225750||encephalopathy with basal ganglia calcification
|
|
C535607|225750||familial infantile encephalopathy with intracranial calcification and chronic cerebrospinal fluid lymphocytosis
|
|
C535607|225750|251290||pseudo torch syndrome
|
|
C535607|225750||pseudotoxoplasmosis syndrome
|
|
C535607|225750||pseudotoxoplasmosis syndrome aicardi goutieres syndrome 1 autosomal dominant included
|
|
C536735||winter shortland temple syndrome
|
|
C536735||craniofacial malformations asymmetric with polysyndactyly and abnormal skin and gut development
|
|
C536735||curry jones syndrome
|
|
226900|C535504||epiphyseal dysplasia multiple 4
|
|
226900|C535504||autosomal recessive multiple epiphyseal dysplasia
|
|
226900|C535504||edm4
|
|
226900|C535504||multiple epiphyseal dysplasia 4
|
|
226900|C535504||multiple epiphyseal dysplasia autosomal recessive
|
|
226900|C535504||multiple epiphyseal dysplasia with bilayered patellae
|
|
226900|C535504||multiple epiphyseal dysplasia with clubfoot
|
|
226900|C535504||multiple epiphyseal dysplasia with double layered patella
|
|
C535406||game friedman paradice syndrome
|
|
C535406||hydrocephalus with associated malformations
|
|
D004818||epidermitis exudative of swine
|
|
D004818||disease greasy pig
|
|
D004818||exudative dermatitis of swine
|
|
D004818||greasy pig disease
|
|
D004818||swine exudative dermatitides
|
|
D004818||swine exudative dermatitis
|
|
D020042||histiocytic necrotizing lymphadenitis
|
|
D020042||disease kikuchi
|
|
D020042||disease kikuchi fujimoto
|
|
D020042||disease kikuchi fujimoto apos s
|
|
D020042||disease kikuchi apos s
|
|
D020042||histiocytic necrotising lymphadenitides
|
|
D020042||histiocytic necrotising lymphadenitis
|
|
D020042||kikuchi disease
|
|
D020042||kikuchi fujimoto disease
|
|
D020042||kikuchi fujimoto apos s disease
|
|
D020042||kikuchi fujimotos disease
|
|
D020042||kikuchi necrotizing lymphadenitis
|
|
D020042||kikuchi apos s disease
|
|
D020042||kikuchis disease
|
|
D020042||kikuchi apos s disease nosocomial
|
|
D020042||lymphadenitides histiocytic necrotising
|
|
D020042||lymphadenitis histiocytic necrotising
|
|
D020042||lymphadenitis histiocytic necrotizing
|
|
D020042||lymphadenitis kikuchi necrotizing
|
|
D020042||necrotising lymphadenitides histiocytic
|
|
D020042||necrotising lymphadenitis histiocytic
|
|
D020042||necrotizing lymphadenitis histiocytic
|
|
D020042||necrotizing lymphadenitis kikuchi
|
|
D020042||nosocomial kikuchi disease
|
|
D020042||nosocomial kikuchi apos s disease
|
|
D020042||nosocomial kikuchis disease
|
|
C536751||wt limb blood syndrome
|
|
C536751||radial ulnar hypoplasia with bone marrow failure and or leukemia
|
|
C536752||wyburn mason apos s syndrome
|
|
C536752||arteriovenous aneurysm of mid brain and retina facial nevi and mental changes
|
|
C536752||wyburn mason syndrome
|
|
D004814||epidermal cyst
|
|
D004814||cyst epidermal
|
|
D004814||cyst epidermoid
|
|
D004814||cyst pilar
|
|
D004814||cyst sebaceous
|
|
D004814||cysts epidermal
|
|
D004814||cysts epidermoid
|
|
D004814||cysts pilar
|
|
D004814||cysts sebaceous
|
|
D004814||epidermal cysts
|
|
D004814||epidermoid cyst
|
|
D004814||epidermoid cysts
|
|
D004814||pilar cysts
|
|
D004814||sebaceous cyst
|
|
D004814||sebaceous cysts
|
|
C567641|613328||roifman chitayat syndrome
|
|
C567641|613328||combined immunodeficiency facial dysmorphism optic nerve atrophy skeletal anomalies and developmental delay
|
|
D064420||drug related side effects and adverse reactions
|
|
D064420||adverse drug event
|
|
D064420||adverse drug events
|
|
D064420||adverse drug reaction
|
|
D064420||adverse drug reactions
|
|
D064420||drug event adverse
|
|
D064420||drug events adverse
|
|
D064420||drug reaction adverse
|
|
D064420||drug reactions adverse
|
|
D064420||drug toxicities
|
|
D064420||drug toxicity
|
|
D064420||event adverse drug
|
|
D064420||events adverse drug
|
|
D064420||reaction adverse drug
|
|
D064420||reactions adverse drug
|
|
D064420||toxicities drug
|
|
D064420||toxicity drug
|
|
D004810||ephemeral fever
|
|
D004810||fever ephemeral
|
|
D004810||sickness three day
|
|
D004810||three day sickness
|
|
D020047||rectocele
|
|
D020047||proctocele
|
|
D020047||proctoceles
|
|
D020047||rectoceles
|
|
C565300|605738||microphthalmia isolated with coloboma 2
|
|
C565300|605738||mcopcb2
|
|
C565300|605738||microphthalmia colobomatous isolated 2
|
|
255120|C535588||carnitine palmitoyl transferase 1a deficiency
|
|
255120|C535588||carnitine palmitoyltransferase 1 deficiency
|
|
255120|C535588||carnitine palmitoyltransferase ia deficiency
|
|
255120|C535588||carnitine palmitoyltransferase i deficiency
|
|
255120|C535588||cpt 1a deficiency
|
|
255120|C535588||cpt deficiency hepatic type i
|
|
255120|C535588||cpt i deficiency
|
|
255120|C535588||hepatic carnitine palmitoyltransferase 1 deficiency
|
|
255120|C535588||liver form of carnitine palmitoyltransferase deficiency
|
|
C566331|603813||hypercholesterolemia autosomal recessive
|
|
C566331|603813||arh
|
|
C566331|603813||arh1 formerly
|
|
C566331|603813||arh2 formerly
|
|
C566331|603813||fhcb1 formerly
|
|
C566331|603813||fhcb2 formerly
|
|
C566331|603813||hypercholesterolemia autosomal recessive 1 formerly
|
|
C566331|603813||hypercholesterolemia autosomal recessive 2 formerly
|
|
C536744||woods leversha rogers syndrome
|
|
C536744||intrauterine growth retardation with increased mitomycin c sensitivity
|
|
C536744||severe intrauterine growth retardation with increased mitomycin c sensitivity
|
|
C536745||woolly hair congenital
|
|
C536745||frizzy hair syndrome
|
|
C536745||woolly hair syndrome
|
|
607936|C564309||exfoliative ichthyosis autosomal recessive ichthyosis bullosa of siemens like
|
|
607936|C564309||arei
|
|
607936|C564309||exfoliative ichthyosis autosomal recessive ibs like
|
|
C536749||wright dyck syndrome
|
|
C536749||hearing loss ankle anomalies and neurological regression dementia
|
|
C536749||sensory neuropathy with deafness and dementia
|
|
C535326|142900||holt oram syndrome
|
|
C535326|142900||atriodigital dysplasia
|
|
C535326|142900||atrio digital syndrome
|
|
C535326|142900||cardiac limb syndrome
|
|
C535326|142900||cervico oculo acoustic syndrome
|
|
C535326|142900||heart hand syndrome
|
|
C535326|142900||heart hand syndrome type 1
|
|
C535326|142900||hos
|
|
C535326|142900||hos1
|
|
C535326|142900||ventriculo radial syndrome
|
|
C535326|142900||wildervanck syndrome
|
|
C536746||woolly hair hypotrichosis everted lower lip and outstanding ears
|
|
C536746||salamon syndrome
|
|
C536747||worster drought syndrome
|
|
C536747||congenital suprabulbar paresis
|
|
C536747||suprabulbar paresis congenital
|
|
C565764|604519||inflammatory bowel disease 3
|
|
C565764|604519||ibd3
|
|
D019046||bone marrow neoplasms
|
|
D019046||bone marrow neoplasm
|
|
D019046||neoplasm bone marrow
|
|
D019046||neoplasms bone marrow
|
|
D020031||epstein barr virus infections
|
|
D020031||ebv infection
|
|
D020031||ebv infections
|
|
D020031||herpesvirus 4 infections human
|
|
D020031||human herpesvirus 4 infections
|
|
D020031||human herpes virus 4 infections
|
|
D020031||infections ebv
|
|
D020031||infections epstein barr virus
|
|
D020031||virus infections epstein barr
|
|
C536762||xanthogranulomatous cholecystitis
|
|
C536763||xanthogranulomatous sialadenitis
|
|
C536763||sialadenitis xanthogranulomatous
|
|
C536760||x linked mental retardation type wittwer
|
|
C536760||x linked mental retardation syndrome wittwer tpe
|
|
D019043||vascular neoplasms
|
|
D019043||neoplasms vascular
|
|
D019043||neoplasm vascular
|
|
D019043||vascular neoplasm
|
|
C535432||berk tabatznik syndrome
|
|
C535432||cleft nare brachydactyly short stature dwarfism
|
|
C535432||congenital optic atrophy and brachytelephalangy
|
|
C535432||kyphosis brachyphalangy optic atrophy
|
|
D019042||muscle neoplasms
|
|
D019042||cancer muscle
|
|
D019042||cancer of muscle
|
|
D019042||cancer of the muscle
|
|
D019042||cancers muscle
|
|
D019042||muscle cancer
|
|
D019042||muscle cancers
|
|
D019042||muscle neoplasm
|
|
D019042||neoplasm muscle
|
|
D019042||neoplasms muscle
|
|
C564859|266120||uridine 5 prime monophosphate hydrolase deficiency hemolytic anemia due to
|
|
C564859|266120||hemolytic anemia due to p5n deficiency
|
|
C564859|266120||hemolytic anemia due to umph1 deficiency
|
|
C564859|266120||hemolytic anemia due to uridine 5 prime monophosphate hydrolase deficiency
|
|
C564859|266120||p5n deficiency
|
|
C564859|266120||pyrimidine 5 prime nucleotidase deficiency hemolytic anemia due to
|
|
C564859|266120||umph1 deficiency
|
|
D063129||parental death
|
|
D063129||death parental
|
|
D063129||death paternal
|
|
D063129||deaths parental
|
|
D063129||deaths paternal
|
|
D063129||parental deaths
|
|
D063129||paternal death
|
|
D063129||paternal deaths
|
|
610168||loeys dietz syndrome 2
|
|
610168||aat3
|
|
610168|C537783||aortic aneurysm familial thoracic 3
|
|
610168||lds2
|
|
610168||marfan syndrome type ii formerly
|
|
D008398||masochism
|
|
D008398||masochisms
|
|
D008398||masochism sexual
|
|
D008398||masochisms sexual
|
|
D008398||sexual masochism
|
|
D008398||sexual masochisms
|
|
188000||thc2
|
|
C536755||x chromosome monosomy xq28
|
|
C536755||deletion xq28
|
|
C536755||monosomy xq28
|
|
C565295||gonadal dysgenesis hypergonadotropic xx type short stature and recurrent metabolic acidosis
|
|
C536756||x chromosome trisomy xp3
|
|
C536756||duplication xp3
|
|
C536756||trisomy xp3
|
|
C535422||charcot marie tooth disease type 4b2 with early onset glaucoma
|
|
C536753||x chromosome duplication xq13 1 q21 1
|
|
C536753||duplication xq13 1 q21 1
|
|
C536753||trisomy xq13 1 q21 1
|
|
611490||optb4
|
|
C535425||congenital torticollis
|
|
C535425||congenital muscular torticollis
|
|
C535425||familial spasmodic torticollis
|
|
C535425||familial torticollis
|
|
C535425||torticollis congenital
|
|
C535425||torticollis familial
|
|
C536754||x chromosome monosomy xp22 pter
|
|
C536754||deletion xp22 pter
|
|
C536754||monosomy xp22 pter
|
|
C535427||ben ari shuper mimouni syndrome
|
|
C535426||congenitally corrected transposition of the great arteries
|
|
C535426||congenitally corrected transposition of the great vessels
|
|
C535426||transposition of the great arteries congenitally corrected
|
|
C535426||transposition of the great vessels congenitally corrected
|
|
C536757||x linked adrenal hypoplasia congenita
|
|
C536757|300200||addison disease x linked
|
|
C536757||adrenal hypoplasia congenita
|
|
C536757|300200||adrenal hypoplasia congenital
|
|
C536757|300200||adrenal hypoplasia congenital with hypogonadotropic hypogonadism
|
|
C536757||ahc with isolated gonadotropin deficiency
|
|
C536757||congenital adrenal hypoplasia
|
|
C536757|300200||cytomegalic adrenocortical hypoplasia
|
|
C536757||x linked congenital adrenal hypoplasia
|
|
611090|C567019||mental retardation autosomal recessive 12
|
|
611090|C567019||mrt12
|
|
164400|D020754||spinocerebellar ataxia 1
|
|
164400|D020754||sca1 spinocerebellar atrophy i
|
|
164400|D020754||olivopontocerebellar atrophy i
|
|
164400|D020754||opca i
|
|
164400|D020754||opca1
|
|
164400|D020754||cerebelloparenchymal disorder i
|
|
164400|D020754||cpd1
|
|
164400|D020754||menzel type opca
|
|
164400|D020754||olivopontocerebellar atrophy iv
|
|
164400|D020754||opca iv
|
|
164400|D020754||opca4
|
|
164400|D020754||schut haymaker type opca
|
|
D020022||genetic predisposition to disease
|
|
D020022||genetic predisposition
|
|
D020022||genetic predispositions
|
|
D020022||genetic susceptibilities
|
|
D020022||genetic susceptibility
|
|
D020022||predisposition genetic
|
|
D020022||predispositions genetic
|
|
D020022||susceptibilities genetic
|
|
D020022||susceptibility genetic
|
|
241200|C537651||bartter syndrome antenatal type 2
|
|
241200|C537651||hyperprostaglandin e syndrome 2
|
|
241200|C537651||hypokalemic alkalosis with hypercalciuria antenatal 2
|
|
C536773||syphilis secondary
|
|
C536773||secondary syphilis
|
|
D019052||depression postpartum
|
|
D019052||depression postnatal
|
|
D019052||depression post natal
|
|
D019052||depression post partum
|
|
D019052||postnatal depression
|
|
D019052||post natal depression
|
|
D019052||postpartum depression
|
|
D019052||post partum depression
|
|
C535441||bifid nose
|
|
C535441||bifid nose autosomal recessive
|
|
C535441||median fissure of nose
|
|
C535441||nose median cleft of
|
|
C536774||syphilis tertiary
|
|
C536774||late syphilis
|
|
C536774||tertiary syphilis
|
|
C536772||syphilis primary
|
|
C536772||primary syphilis
|
|
D019053||hiv enteropathy
|
|
D019053||aids associated enteropathies
|
|
D019053||aids associated enteropathy
|
|
D019053||aids enteropathies
|
|
D019053||aids enteropathies idiopathic
|
|
D019053||aids enteropathy
|
|
D019053||aids enteropathy idiopathic
|
|
D019053||enteropathies aids
|
|
D019053||enteropathies aids associated
|
|
D019053||enteropathies hiv
|
|
D019053||enteropathies hiv associated
|
|
D019053||enteropathies idiopathic aids
|
|
D019053||enteropathy aids
|
|
D019053||enteropathy aids associated
|
|
D019053||enteropathy hiv
|
|
D019053||enteropathy hiv associated
|
|
D019053||enteropathy idiopathic aids
|
|
D019053||hiv associated enteropathies
|
|
D019053||hiv associated enteropathy
|
|
D019053||hiv enteropathies
|
|
D019053||idiopathic aids enteropathies
|
|
D019053||idiopathic aids enteropathy
|
|
C566404|603165||dermatitis atopic 1
|
|
C566404|603165||atod
|
|
C566404|603165||atod1 included
|
|
C566404|603165|D003876||dermatitis atopic
|
|
C566404|603165||eczema atopic dermatitis atopic 1 included
|
|
D007078||ileal neoplasms
|
|
D007078||cancer ileal
|
|
D007078||cancer of ileum
|
|
D007078||cancer of the ileum
|
|
D007078||cancers ileal
|
|
D007078||ileal cancer
|
|
D007078||ileal cancers
|
|
D007078||ileal neoplasm
|
|
D007078||ileum cancer
|
|
D007078||ileum cancers
|
|
D007078||neoplasm ileal
|
|
D007078||neoplasms ileal
|
|
D007079||ileitis
|
|
C566637|601718||retinitis pigmentosa 19
|
|
C566637|601718||rp19
|
|
D007077||ileal diseases
|
|
D007077||disease ileal
|
|
D007077||diseases ileal
|
|
D007077||ileal disease
|
|
C535689|135750||laurin sandrow syndrome
|
|
C535689|135750||fibula and ulna duplication of with absence of tibia and radius
|
|
C535689|135750||fibula and ulna duplication of with absence of tibia and radius laurin sandrow syndrome segmental included
|
|
C535689|135750||fibula ulna duplication tibia radius absence
|
|
C535689|135750||laurin sandrow syndrome segmental
|
|
C535689|135750||lss
|
|
C535689|135750||mip
|
|
C535689|135750||mirror hands and feet with nasal defects
|
|
C535689|135750||mirror image polydactyly
|
|
C535689|135750||sandrow syndrome
|
|
C535689|135750||tetramelic mirror image polydactyly
|
|
C535689|135750||tmip
|
|
609165||erythroderma ichthyosiform congenital reticular
|
|
609165||aarau disease included
|
|
609165||crie
|
|
609165||ichthyosis variegata erythrokeratoderma reticular included
|
|
609165||ichthyosis with confetti
|
|
609165||iwc
|
|
D052476||hypobetalipoproteinemia familial apolipoprotein b
|
|
D052476||abetalipoproteinemia normotriglyceridemic steinbert type
|
|
D052476||apolipoprotein b deficiencies
|
|
D052476||apolipoprotein b deficiency
|
|
D052476||apolipoprotein b deficiency disease
|
|
D052476||hypobetalipoproteinemia familial apo b
|
|
C536767||xk aprosencephaly
|
|
C536767||aprosencephaly atelencephaly syndrome
|
|
C536767||aprosencephaly syndrome
|
|
C536767||garcia lurie syndrome
|
|
C536767||xk aprosencephaly syndrome
|
|
C536767||xk syndrome
|
|
C536764|194380|C566369||xerocytosis hereditary
|
|
C536764|194380|C566369||dehydrated hereditary stomatocytosis
|
|
C536764|194380|C566369||desiccytosis hereditary
|
|
C536764||hereditary xerocytosis
|
|
C536765||xeroderma pigmentosum type 9
|
|
C536765||xeroderma pigmentosum complementation group 1
|
|
C535435||beta sarcoglycanopathy
|
|
D053579|263800||gitelman syndrome
|
|
D053579|263800||familial hypokalemia hypomagnesemia
|
|
D053579|263800||familial hypokalemia hypomagnesemias
|
|
D053579|263800||gitelman apos s syndrome
|
|
D053579|263800||gitelmans syndrome
|
|
D053579|263800||hypokalemia hypomagnesemia familial
|
|
D053579|263800||hypokalemia hypomagnesemia primary renotubular with hypocalciuria
|
|
D053579|263800||hypokalemia hypomagnesemias familial
|
|
D053579|263800||hypomagnesemia hypokalemia primary renotubular with hypocalciuria
|
|
D053579|263800||primary renotubular hypokalemia hypomagnesemia with hypocalciuria
|
|
D053579|263800||primary renotubular hypomagnesemia hypokalemia with hypocalciuria
|
|
D053579|263800||syndrome gitelman
|
|
D053579|263800||syndrome gitelman apos s
|
|
D053579|263800||tubular hypomagnesemia hypokalemia with hypocalcuria
|
|
C535438||bidirectional tachycardia
|
|
C535438||bidirectional ventricular tachycardia
|
|
D019048||prostatic intraepithelial neoplasia
|
|
D019048||intraepithelial neoplasia prostatic
|
|
D019048||intraepithelial neoplasm prostatic
|
|
D019048||intraepithelial neoplasms prostatic
|
|
D019048||intraepithelial prostatic neoplasia
|
|
D019048||intraepithelial prostatic neoplasias
|
|
D019048||neoplasia intraepithelial prostatic
|
|
D019048||neoplasia prostatic intraepithelial
|
|
D019048||neoplasm prostatic intraepithelial
|
|
D019048||neoplasms prostatic intraepithelial
|
|
D019048||prostatic intraepithelial neoplasias
|
|
D019048||prostatic intraepithelial neoplasm
|
|
D019048||prostatic intraepithelial neoplasms
|
|
D019048||prostatic neoplasia intraepithelial
|
|
C535437||bhaskar jagannathan syndrome
|
|
145600|C535694||malignant hyperthermia susceptibility type 1
|
|
145600|C535694||hyperpyrexia malignant mh king syndrome included
|
|
145600|C535694||king denborough syndrome included
|
|
145600|C535694||malignant hyperthermia susceptibility to 1
|
|
145600|C535694||mhs
|
|
145600|C535694||mhs1
|
|
190320||tdo
|
|
190320||tdo syndrome
|
|
C566052|613740||cardiomyopathy dilated 1t
|
|
C566052|613740||cmd1t
|
|
C536769||46 xy female
|
|
C536769||xy female
|
|
C535439||biemond syndrome type 2
|
|
182900|C567159||spherocytosis type 1
|
|
182900|C567159||congenital spherocytic hemolytic anemia
|
|
182900|C567159||congenital spherocytosis
|
|
182900|C567159||hereditary spherocytosis
|
|
182900|C567159||hs
|
|
182900|C567159||hs1
|
|
182900|C567159||sph
|
|
182900|C567159||sph1
|
|
182900|C567159||spherocytic anemia
|
|
182900|C567159||spherocytosis hereditary 1
|
|
304120|C538089||oto palato digital syndrome type 2
|
|
304120|C538089||andre syndrome
|
|
304120|C538089||cranio oro digital syndrome
|
|
304120|C538089||cranioorodigital syndrome
|
|
304120|C538089||faciopalatoosseous syndrome
|
|
304120|C538089||fpo
|
|
304120|C538089||opd2
|
|
304120|C538089||opd ii syndrome
|
|
304120|C538089||opd syndrome 2
|
|
304120|C538089||opd syndrome type 2
|
|
304120|C538089||otopalatodigital syndrome type 2
|
|
304120|C538089||otopalatodigital syndrome type ii
|
|
C536221|176450||currarino triad
|
|
C536221|176450||currarino syndrome
|
|
C536221|176450||currarino triad sacral agenesis syndrome included
|
|
C536221|176450||sacral agenesis hereditary with presacral mass anterior meningocele and or teratoma and anorectal malformation included
|
|
C536221|176450||scra1 included
|
|
C566596||thrombocytosis benign familial microcytic
|
|
249700|C537267||langer mesomelic dysplasia
|
|
249700|C537267||dyschondrosteosis homozygous
|
|
249700|C537267||langer mesomelic dwarfism
|
|
249700|C537267||langer mesomelic dyspalsia
|
|
249700|C537267||langer type of mesomelic dwarfism
|
|
249700|C537267||lmd
|
|
249700|C537267||mesomelic dwarfism langer type
|
|
249700|C537267||mesomelic dwarfism of the hypoplastic ulna fibula and mandible type
|
|
C565724|609745||glaucoma 1 open angle i
|
|
C565724|609745||glc1i
|
|
C566597||otofacioosseous gonadal syndrome
|
|
C567068|300645||atypical mycobacteriosis familial x linked 2
|
|
C567068|300645||amcbx2
|
|
C567068|300645||atypical mycobacterial infection disseminated x linked 2
|
|
C567068|300645||atypical mycobacterial infection familial disseminated x linked 2
|
|
C567068|300645||mycobacterial disease mendelian susceptibility to x linked recessive 2
|
|
C567068|300645||mycobacterial disease susceptibility to x linked 2
|
|
C567068|300645||xrmsmd2
|
|
C566598||odontotrichoungual digital palmar syndrome
|
|
C536192|229200||ehlers danlos syndrome 6b
|
|
C536192|229200||adducted thumb club foot syndrome
|
|
C536192|229200|601776||adducted thumb clubfoot syndrome
|
|
C536192|229200||adducted thumbs dundar type
|
|
C536192|229200|601776||arthrogryposis distal with peculiar facies and hydronephrosis
|
|
C536192|229200||bcs1
|
|
C536192|229200||brittle cornea syndrome
|
|
C536192|229200||brittle cornea syndrome 1
|
|
C536192|229200||corneal fragility keratoglobus blue sclerae joint hyperextensibility
|
|
C536192|229200||dysgenesis mesodermalis corneae et sclerae
|
|
C536192|229200|601776||eds6b formerly
|
|
C536192|229200||ehlers danlos syndrome type vib
|
|
C536192|229200|601776||ehlers danlos syndrome type vib formerly
|
|
C536192|229200||fragilitas oculi with joint hyperextensibility
|
|
C536965|162500||tomaculous neuropathy
|
|
C536965|162500||compression neuropathy
|
|
C536965|162500||entrapment neuropathy
|
|
C536965|162500||familial pressure sensitive neuropathy
|
|
C536965|162500||hereditary neuropathy with liability to pressure palsies
|
|
C536965|162500||hereditary neuropathy with liability to pressure palsy
|
|
C536965|162500||hereditary pressure sensitive neuropathy
|
|
C536965|162500||hnpp
|
|
C536965|162500||inherited tendency to pressure palsies
|
|
C536965|162500||neuropathy hereditary with liability to pressure palsies
|
|
C536965|162500||polyneuropathy familial recurrent
|
|
C564637|606995||senior loken syndrome 3
|
|
C564637|606995||slsn3
|
|
D020019||neurocysticercosis
|
|
D020019||brain cysticercosis
|
|
D020019||central nervous system cysticercosis
|
|
D020019||cysticercosis brain
|
|
D020019||cysticercosis central nervous system
|
|
D020019||neurocysticercoses
|
|
D020018||sexual dysfunctions psychological
|
|
D020018||arousal disorders sexual
|
|
D020018||aversion disorders sexual
|
|
D020018||disorder psychosexual
|
|
D020018||disorders orgasmic
|
|
D020018||disorders psychosexual
|
|
D020018||disorders sexual arousal
|
|
D020018||disorders sexual aversion
|
|
D020018||dysfunction psychological sexual
|
|
D020018||dysfunction psychosexual
|
|
D020018||dysfunctions psychological sexual
|
|
D020018||dysfunctions psychosexual
|
|
D020018||frigidity
|
|
D020018||hypoactive sexual desire disorder
|
|
D020018||orgasmic disorder
|
|
D020018||orgasmic disorders
|
|
D020018||psychological sexual dysfunction
|
|
D020018||psychological sexual dysfunctions
|
|
D020018||psychosexual disorder
|
|
D020018||psychosexual disorders
|
|
D020018||psychosexual dysfunction
|
|
D020018||psychosexual dysfunctions
|
|
D020018||sexual arousal disorder
|
|
D020018||sexual arousal disorders
|
|
D020018||sexual aversion disorder
|
|
D020018||sexual aversion disorders
|
|
D020018||sexual dysfunction psychological
|
|
D020016|188055|C566056||activated protein c resistance
|
|
D020016|188055|C566056||apc resistance
|
|
D020016||resistance apc
|
|
C536913|607464||thyroid cancer hurthle cell
|
|
C536913|607464||follicular thyroid cancer hurthle cell type
|
|
C536913|607464||hurthle cell carcinoma of the thyroid
|
|
C536913|607464||hurthle cell thyroid neoplasia
|
|
C536913|607464||thyroid cancer follicular hurthle cell type
|
|
C536913|607464||thyroid carcinoma hurthle cell
|
|
D007037||hypothyroidism
|
|
D007037||hypothyroidisms
|
|
D008368||mansonelliasis
|
|
D008368||acanthocheilonema perstans infection
|
|
D008368||acanthocheilonema perstans infections
|
|
D008368||dipetalonema perstans infection
|
|
D008368||dipetalonema perstans infections
|
|
D008368||infection acanthocheilonema perstans
|
|
D008368||infection dipetalonema perstans
|
|
D008368||infection mansonella perstans
|
|
D008368||infections acanthocheilonema perstans
|
|
D008368||infections dipetalonema perstans
|
|
D008368||infections mansonella perstans
|
|
D008368||mansonella perstans infection
|
|
D008368||mansonella perstans infections
|
|
D008368||mansonelliases
|
|
D008368||mansonelloses
|
|
D008368||mansonellosis
|
|
D008368||perstans infection acanthocheilonema
|
|
D008368||perstans infection dipetalonema
|
|
D008368||perstans infection mansonella
|
|
D008368||perstans infections acanthocheilonema
|
|
D008368||perstans infections dipetalonema
|
|
D008368||perstans infections mansonella
|
|
201000|C563187||acrocephalopolysyndactyly type ii
|
|
201000|C563187||acps ii
|
|
201000|C563187||carpenter syndrome
|
|
201000|C563187||carpenter syndrome 1
|
|
201000|C563187||crpt1
|
|
D007046||hysteria
|
|
D007046||hysterical neuroses
|
|
D007046||neuroses hysterical
|
|
D010688||phimosis
|
|
D010688||phimoses
|
|
D010689||phlebitis
|
|
D010689||periphlebitides
|
|
D010689||periphlebitis
|
|
D010689||phlebitides
|
|
610141||qt interval variation in
|
|
D007040||hypoventilation
|
|
D007040||hypoventilations
|
|
C565272||liver fibrocystic disease and polydactyly
|
|
C565273||arthropathy erosive
|
|
C565271||metaphyseal dysplasia braun tinschert type
|
|
D063130||maternal death
|
|
D063130||death maternal
|
|
D063130||deaths maternal
|
|
D063130||maternal deaths
|
|
C536063|259770||osteoporosis pseudoglioma syndrome
|
|
C536063|259770||oppg
|
|
C536063|259770||ops
|
|
C536063|259770||osteogenesis imperfecta ocular form
|
|
C536063|259770||pseudoglioma with bone fragility
|
|
C565277||cardiomyopathy dilated with left ventricular noncompaction
|
|
C563562|158580||neuropathy distal hereditary motor type viia
|
|
C563562|158580||dhmn7a
|
|
C563562|158580||dhmnvp
|
|
C563562|158580||harper young myopathy
|
|
C563562|158580||hmn7a
|
|
C563562|158580||hmn viia
|
|
C563562|158580||neuronopathy distal hereditary motor type viia
|
|
C563562|158580||spinal muscular atrophy distal with vocal cord paralysis
|
|
C562447|313400||spondyloepiphyseal dysplasia tarda x linked
|
|
C562447|313400||sedt
|
|
C562447|313400||sed tarda x linked
|
|
C562447|313400||spondyloepiphyseal dysplasia late
|
|
C564551|300261||armfield x linked mental retardation syndrome
|
|
C564551|300261||mental retardation x linked armfield type
|
|
C564551|300261||mental retardation x linked syndromic armfield type
|
|
C564551|300261||mrxsa
|
|
D007049||iatrogenic disease
|
|
D007049||disease iatrogenic
|
|
D007049||diseases iatrogenic
|
|
D007049||iatrogenic diseases
|
|
264300|C537805||17 hydroxysteroid dehydrogenase deficiency
|
|
264300|C537805||17 alpha ketosteroid reductase deficiency of testis
|
|
264300|C537805||17 beta hydroxysteroid dehydrogenase 3 deficiency
|
|
264300|C537805||17 beta hydroxysteroid dehydrogenase deficiency
|
|
264300|C537805||17 beta hydroxysteroid dehydrogenase iii deficiency
|
|
264300|C537805||17 ketosteroid reductase deficiency of testis
|
|
264300|C537805||17 ksr deficiency
|
|
264300|C537805||male pseudohermaphroditism with gynecomastia
|
|
264300|C537805||neutral 17 beta hydroxysteroid oxidoreductase deficiency
|
|
264300|C537805||pseudohermaphroditism male with gynecomastia
|
|
264300|C537805||pseudohermaphroditism male with gynecomastia polycystic ovarian disease due to 17 ketosteroid reductase deficiency included
|
|
C535356|600790||chorioretinal atrophy progressive bifocal
|
|
C535356|600790||crapb
|
|
C535356|600790||pbcra
|
|
C535356|600790||progressive bifocal chorioretinal atrophy
|
|
D008379||marburg virus disease
|
|
D008379||disease marburg
|
|
D008379||fever marburg hemorrhagic
|
|
D008379||hemorrhagic fever marburg
|
|
D008379||marburg disease
|
|
D008379||marburg hemorrhagic fever
|
|
C536709||winchester syndrome
|
|
C536709||winchester disease
|
|
C536709||winchester grossman disease
|
|
C536709||winchester grossman syndrome
|
|
C562694|600669||epilepsy idiopathic generalized
|
|
C562694|600669||eig
|
|
C562694|600669||eig11
|
|
C562694|600669||eig1 included
|
|
C562694|600669||eig2
|
|
C562694|600669||eig3
|
|
C562694|600669||eig4
|
|
C562694|600669||eig5
|
|
C562694|600669||eig8
|
|
C562694|600669||eig9
|
|
C562694|600669||eja2 included
|
|
C562694|600669||ejm6
|
|
C562694|600669||ejm6 included
|
|
C562694|600669||ejm7 included
|
|
C562694|600669||ejm8
|
|
C562694|600669||ejm8 included
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 10 eig10 generalized epilepsy with febrile seizures plus type 5 susceptibility
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 11
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 2
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 3
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 4
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 5
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 8
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to 9
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to locus on chromosome 10
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to locus on chromosome 14
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to locus on chromosome 8 included
|
|
C562694|600669||epilepsy idiopathic generalized susceptibility to locus on chromosome 9
|
|
C562694|600669||epilepsy juvenile absence susceptibility to 2 included
|
|
C562694|600669||epilepsy juvenile myoclonic susceptibility to 6 included
|
|
C562694|600669||epilepsy juvenile myoclonic susceptibility to 7 included
|
|
C562694|600669||epilepsy juvenile myoclonic susceptibility to 8 included
|
|
C562694|600669||gefs5 included
|
|
C562694|600669||gefs 5 susceptibility to included
|
|
C562694|600669||gefsp5 susceptibility to included
|
|
C562694|600669||gefs type 5 susceptibility to included
|
|
C562694|600669||idiopathic generalized epilepsy
|
|
C562694|600669||idiopathic generalized epilepsy ige epilepsy idiopathic generalized susceptibility to 1 included
|
|
612797||high density lipoprotein cholesterol level quantitative trait locus 12
|
|
612797||hdlcq12
|
|
D007057||ichthyosis
|
|
D007057||ichthyoses
|
|
D007057||xeroderma
|
|
D007057||xerodermas
|
|
C536707||wilms tumor and radial bilateral aplasia
|
|
C536707||bilateral radial aplasia with wilms tumor
|
|
C536707|601583||wilms tumor 5
|
|
C564101|309620||mental retardation skeletal dysplasia and abducens palsy
|
|
C564101|309620||christian syndrome
|
|
C564101|309620||chrs
|
|
C564101|309620||mrsd
|
|
D010698||phobic disorders
|
|
D010698||claustrophobia
|
|
D010698||claustrophobias
|
|
D010698||disorder phobic
|
|
D010698||disorders phobic
|
|
D010698||neuroses phobic
|
|
D010698||phobia
|
|
D010698||phobias
|
|
D010698||phobia school
|
|
D010698||phobia social
|
|
D010698||phobias school
|
|
D010698||phobias social
|
|
D010698||phobic disorder
|
|
D010698||phobic neuroses
|
|
D010698||school phobia
|
|
D010698||school phobias
|
|
D010698||social phobia
|
|
D010698||social phobias
|
|
C536700||white forelock with malformations
|
|
C565284||basaloid follicular hamartoma syndrome generalized autosomal dominant
|
|
C536701||curatolo cilio pessagno syndrome
|
|
C536701||white matter hypoplasia corpus callosum agenesia and mental retardation
|
|
C535310|231530||3 hydroxyacyl coa dehydrogenase deficiency
|
|
C535310|231530||3 alpha hydroxyacyl coenzyme a dehydrogenase deficiency
|
|
C535310|231530||3 hydroxyacyl coenzyme a dehydrogenase deficiency
|
|
C535310|231530||had deficiency
|
|
C535310|231530||hadh deficiency
|
|
C535310|231530||hadhsc deficiency
|
|
C535310|231530||l 3 alpha hydroxyacyl coa dehydrogenase short chain deficiency
|
|
C535310|231530||m schad deficiency
|
|
C535310|231530||schad deficiency
|
|
C535310|231530||schad deficiency formerly
|
|
D008380||marek disease
|
|
D008380||fowl paralyses
|
|
D008380||fowl paralysis
|
|
D008380||marek apos s disease
|
|
D008380||mareks disease
|
|
D008380||neurolymphomatoses
|
|
D008380||neurolymphomatosis
|
|
D008380||paralyses fowl
|
|
D008380||paralysis fowl
|
|
C565285||spondyloocular syndrome autosomal recessive
|
|
C536704||wiedemann grosse dibbern syndrome
|
|
C535531|603932||intervertebral disc disease
|
|
C535531|603932||idd
|
|
C535531|603932||lumbar disc degeneration susceptibility to included
|
|
C535531|603932||lumbar disc disease
|
|
C535531|603932||lumbar disc disease included
|
|
C535531|603932||lumbar disc herniation susceptibility to included
|
|
C536705||wiedemann oldigs oppermann syndrome
|
|
C536705||hirsutism skeletal dysplasia mental retardation syndrome
|
|
C536702||white platelet syndrome
|
|
C565282||baby rattle pelvis dysplasia
|
|
C565247||thyroid carcinoma nonmedullary 1
|
|
C565247|606240||nonmedullary thyroid carcinoma 1
|
|
C565248||mental retardation short stature facial anomalies and joint dislocations
|
|
C566575||neuropathy hereditary thermosensitive
|
|
C566577|C536488|602097||usher syndrome type ie
|
|
D063169||dentofacial deformities
|
|
D063169||abnormalities dentofacial
|
|
D063169||abnormality dentofacial
|
|
D063169||deformities dentofacial
|
|
D063169||deformity dentofacial
|
|
D063169||dentofacial abnormalities
|
|
D063169||dentofacial abnormality
|
|
D063169||dentofacial deformity
|
|
D063169||dentofacial dyplasia
|
|
D063169||dentofacial dyplasias
|
|
D063169||dyplasia dentofacial
|
|
D063169||dyplasias dentofacial
|
|
D007018||hypopituitarism
|
|
D007018||adenohypophyseal hyposecretion
|
|
D007018||anterior pituitary hyposecretion syndrome
|
|
D007018||disease simmonds
|
|
D007018||hypopituitarism postpartum
|
|
D007018||hyposecretion adenohypophyseal
|
|
D007018||hyposecretion syndrome anterior pituitary
|
|
D007018||insufficiency pituitary
|
|
D007018||panhypopituitarism postpartum
|
|
D007018||pituitary insufficiency
|
|
D007018||pituitary insufficiency postpartum
|
|
D007018||postpartum hypopituitarism
|
|
D007018||postpartum panhypopituitarism
|
|
D007018||postpartum pituitary insufficiency
|
|
D007018||sheehan apos s syndrome
|
|
D007018||sheehans syndrome
|
|
D007018||sheehan syndrome
|
|
D007018||simmond apos s disease
|
|
D007018||simmonds disease
|
|
D007018||simmonds apos disease
|
|
D007018||syndrome sheehan
|
|
D007018||syndrome sheehan apos s
|
|
D007019||hypoproteinemia
|
|
D007019||hypoproteinemias
|
|
D023981||sarcoma myeloid
|
|
D023981||chloroma
|
|
D023981||chloromas
|
|
D023981||extramedullary myeloid cell tumor
|
|
D023981||granulocytic sarcoma
|
|
D023981||granulocytic sarcomas
|
|
D023981||myeloid cell tumor extramedullary
|
|
D023981||myeloid sarcoma
|
|
D023981||myeloid sarcomas
|
|
D023981||sarcoma granulocytic
|
|
D023981||sarcomas granulocytic
|
|
D023981||sarcomas myeloid
|
|
D007014||hypophosphatasia
|
|
D007014||hypophosphatasias
|
|
D007015||hypophosphatemia familial
|
|
D007015||diabetes phosphate
|
|
D007015||familial hypophosphatemia
|
|
D007015||familial hypophosphatemias
|
|
D007015||hyperphosphaturia
|
|
D007015||hypophosphatemias familial
|
|
D007015||phosphate diabetes
|
|
D007015||phosphaturia
|
|
C536719||yunis varon syndrome
|
|
C536719||cleidocranial dysplasia micrognathia absent thumbs amp distal aphalangia
|
|
C536719||cleidocranial dysplasia with micrognathia absent thumbs and distal aphalangia
|
|
D007024||hypotension orthostatic
|
|
D007024||hypotension postural
|
|
D007024||orthostatic hypotension
|
|
D007024||postural hypotension
|
|
C536717||young simpson syndrome
|
|
C536717||blepharophimosis and mental retardation syndrome say barber biesecker young simpson type
|
|
C536717||blepharophimosis intellectual deficit syndrome say barber biesecker young simpson type
|
|
C536717||mental retardation unusual facies hypothyroidism
|
|
C536717||ohdo syndrome say barber biesecker variant
|
|
C536717||ohdo syndrome say barber biesecker young simpson variant
|
|
C536717||ohdo syndrome sbbys variant
|
|
C536717||say barber biesecker young simpson syndrome
|
|
C536717||say barber biesecker young simpson variant of ohdo syndrome
|
|
C536717||sbbys variant of ohdo syndrome
|
|
D007021||hypospadias
|
|
D007021||hypospadia
|
|
C536718||young syndrome
|
|
C536718||azoospermia obstructive and chronic sinopulmonary infections
|
|
C536718||azoospermia sinopulmonary infections
|
|
C536718||barry perkins young syndrome
|
|
C536718||sinusitis infertility syndrome
|
|
D007022||hypotension
|
|
D007022||blood pressure low
|
|
D007022||hypotension vascular
|
|
D007022||low blood pressure
|
|
D007022||vascular hypotension
|
|
D034062|600072||insomnia fatal familial
|
|
D034062|600072||familial fatal insomnia
|
|
D034062|600072||familial fatal insomnias
|
|
D034062|600072||familial fatals insomnia
|
|
D034062|600072||fatal familial insomnia
|
|
D034062|600072||fatal familial insomnias
|
|
D034062|600072||fatal insomnia familial
|
|
D034062|600072||fatal insomnias familial
|
|
D034062|600072||fatals insomnia familial
|
|
D034062|600072||ffi
|
|
D034062|600072||insomnia familial fatal
|
|
D034062|600072||insomnia familial fatals
|
|
D034062|600072||insomnias familial fatal
|
|
D034062|600072||insomnias fatal familial
|
|
D007020||hypoprothrombinemias
|
|
D007020||deficiencies factor ii
|
|
D007020||deficiencies prothrombin
|
|
D007020||deficiency factor ii
|
|
D007020||deficiency prothrombin
|
|
D007020||factor ii deficiencies
|
|
D007020||factor ii deficiency
|
|
D007020||hypoprothrombinemia
|
|
D007020||prothrombin deficiencies
|
|
D007020||prothrombin deficiency
|
|
C579887||african hemochromatosis
|
|
C579887||african siderosis
|
|
C536711||winship viljoen leary syndrome
|
|
C536711||microcephaly cardiomyopathy
|
|
C536711||microcephaly cardiomyopathy syndrome
|
|
C536711||microcephaly with cardiomyopathy
|
|
C536711||microcephaly with mental retardation and dilated cardiomyopathy
|
|
C536711||severe microcephaly and self limiting dilated cardiomyopathy
|
|
C536711||severe microcephaly with mental retardation and dilated cardiomyopathy
|
|
C536712||winter harding hyde syndrome
|
|
C536712||pachygyria joint contractures facial abnormalities
|
|
C565252||laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy
|
|
C565253||developmental delay epilepsy and neonatal diabetes
|
|
C536715||young hughes syndrome
|
|
C536715||sex linked mental retardation short stature obesity and hypogonadism
|
|
C536716||young mckeever squier syndrome
|
|
C536716||olivopontocerebellar hypoplasia lethal type
|
|
C536713||yim ebbin syndrome
|
|
C536713||amelia cleft lip palate hydrocephalus iris coloboma
|
|
C536713||brachial amelia forebrain defects and facial clefts
|
|
C536714||yorifuji okuno syndrome
|
|
C536714||pancreatic hypoplasia diabetes heart disease
|
|
C565258||fryns aftimos syndrome
|
|
C565258||cerebrooculofacial lymphatic syndrome
|
|
C565258||mental retardation with epilepsy and characteristic facies
|
|
C565258||pachygyria mental retardation epilepsy and characteristic facies
|
|
C565255||genitopatellar syndrome
|
|
C565255||absent patellae scrotal hypoplasia renal anomalies facial dysmorphism and mental retardation
|
|
C536730||zuska apos s disease
|
|
C536730||lactation and squamous metaplasia of lactiferous ducts
|
|
C536730||lactiferous fistula
|
|
C536730||zuska disease
|
|
C565256||diamond blackfan anemia with microtia and cleft palate
|
|
C566588||broad terminal phalanges familial
|
|
D007029||hypothalamic neoplasms
|
|
D007029||benign hypothalamic neoplasm
|
|
D007029||benign hypothalamic neoplasms
|
|
D007029||cancer hypothalamic
|
|
D007029||cancers hypothalamic
|
|
D007029||hypothalamic cancer
|
|
D007029||hypothalamic cancers
|
|
D007029||hypothalamic chiasmatic neoplasm
|
|
D007029||hypothalamic chiasmatic neoplasms
|
|
D007029||hypothalamic neoplasm
|
|
D007029||hypothalamic neoplasm malignant
|
|
D007029||hypothalamic neoplasms benign
|
|
D007029||hypothalamic neoplasms malignant
|
|
D007029||hypothalamic pituitary neoplasm
|
|
D007029||hypothalamic pituitary neoplasms
|
|
D007029||hypothalamic teratoma
|
|
D007029||hypothalamic teratomas
|
|
D007029||hypothalamic tumor
|
|
D007029||hypothalamic tumors
|
|
D007029||hypothalamo neurohypophysial region neoplasm
|
|
D007029||hypothalamo neurohypophysial region neoplasms
|
|
D007029||hypothalamus neoplasm
|
|
D007029||hypothalamus neoplasms
|
|
D007029||hypothalamus tumor
|
|
D007029||hypothalamus tumors
|
|
D007029||malignant hypothalamic neoplasm
|
|
D007029||malignant hypothalamic neoplasms
|
|
D007029||neoplasm benign hypothalamic
|
|
D007029||neoplasm hypothalamic
|
|
D007029||neoplasm hypothalamic chiasmatic
|
|
D007029||neoplasm hypothalamic pituitary
|
|
D007029||neoplasm hypothalamo neurohypophysial region
|
|
D007029||neoplasm hypothalamus
|
|
D007029||neoplasm malignant hypothalamic
|
|
D007029||neoplasms hypothalamic
|
|
D007029||neoplasms hypothalamic benign
|
|
D007029||neoplasms hypothalamic chiasmatic
|
|
D007029||neoplasms hypothalamic malignant
|
|
D007029||neoplasms hypothalamic pituitary
|
|
D007029||neoplasms hypothalamo neurohypophysial region
|
|
D007029||neoplasms hypothalamus
|
|
D007029||neoplasms malignant hypothalamic
|
|
D007029||teratoma hypothalamic
|
|
D007029||teratomas hypothalamic
|
|
D007029||tumor hypothalamic
|
|
D007029||tumor hypothalamus
|
|
D007029||tumors hypothalamic
|
|
D007029||tumors hypothalamus
|
|
C567726|613164||parkinson disease 16
|
|
C567726|613164||park16
|
|
D007027||hypothalamic diseases
|
|
D007027||diencephalic syndrome pituitary
|
|
D007027||diencephalic syndromes pituitary
|
|
D007027||disease hypothalamic
|
|
D007027||diseases hypothalamic
|
|
D007027||disorder hypothalamic adenohypophyseal
|
|
D007027||disorder hypothalamic neurohypophyseal
|
|
D007027||disorders hypothalamic adenohypophyseal
|
|
D007027||disorders hypothalamic neurohypophyseal
|
|
D007027||dysfunction syndrome hypothalamic
|
|
D007027||dysfunction syndromes hypothalamic
|
|
D007027||dysinhibition syndrome hypothalamic
|
|
D007027||dysinhibition syndromes hypothalamic
|
|
D007027||froehlich apos s syndrome
|
|
D007027||froehlichs syndrome
|
|
D007027||froehlich syndrome
|
|
D007027||hypothalamic adenohypophyseal disorder
|
|
D007027||hypothalamic adenohypophyseal disorders
|
|
D007027||hypothalamic disease
|
|
D007027||hypothalamic dysfunction syndrome
|
|
D007027||hypothalamic dysfunction syndromes
|
|
D007027||hypothalamic dysinhibition syndrome
|
|
D007027||hypothalamic dysinhibition syndromes
|
|
D007027||hypothalamic neurohypophyseal disorder
|
|
D007027||hypothalamic neurohypophyseal disorders
|
|
D007027||hypothalamic overactivity syndrome
|
|
D007027||hypothalamic overactivity syndromes
|
|
D007027||hypothalamic pseudopuberties
|
|
D007027||hypothalamic pseudopuberty
|
|
D007027||overactivity syndrome hypothalamic
|
|
D007027||overactivity syndromes hypothalamic
|
|
D007027||pituitary diencephalic syndrome
|
|
D007027||pituitary diencephalic syndromes
|
|
D007027||pseudopuberties hypothalamic
|
|
D007027||pseudopuberty hypothalamic
|
|
D007027||syndrome froehlich apos s
|
|
D007027||syndrome hypothalamic dysfunction
|
|
D007027||syndrome hypothalamic dysinhibition
|
|
D007027||syndrome hypothalamic overactivity
|
|
D007027||syndromes hypothalamic dysfunction
|
|
D007027||syndromes hypothalamic dysinhibition
|
|
D007027||syndromes hypothalamic overactivity
|
|
D007027||syndromes pituitary diencephalic
|
|
612775||cone rod dystrophy 9
|
|
612775||cord9
|
|
D007035||hypothermia
|
|
D007035||accidental hypothermia
|
|
D007035||accidental hypothermias
|
|
D007035||hypothermia accidental
|
|
D007035||hypothermias
|
|
D007035||hypothermias accidental
|
|
C536728||zori stalker williams syndrome
|
|
C536728||familial short stature developmental delay pectus abnormalities distinctive facies and dysplastic nails
|
|
C536728||pectus excavatum macrocephaly and dysplastic nails
|
|
D010677||philadelphia chromosome
|
|
D010677||1 chromosome ph
|
|
D010677||1 chromosomes ph
|
|
D010677||chromosome ph1
|
|
D010677||chromosome ph 1
|
|
D010677||chromosome philadelphia
|
|
D010677||chromosomes ph1
|
|
D010677||chromosomes ph 1
|
|
D010677||ph 1 chromosome
|
|
D010677||ph1 chromosome
|
|
D010677||ph 1 chromosomes
|
|
D010677||ph1 chromosomes
|
|
C536729||zunich neuroectodermal syndrome
|
|
C536729||chime syndrome
|
|
310500|C536122||night blindness congenital stationary type 1a
|
|
310500|C536122||csnb1a
|
|
310500|C536122||csnb complete x linked
|
|
310500|C536122||hemeralopia myopia
|
|
310500||myopia night blindness nbm1 nyctalopia included
|
|
310500|C536122||night blindness congenital stationary with myopia
|
|
C537761|309500||renpenning syndrome 1
|
|
C537761|309500||golabi ito hall syndrome
|
|
C537761|309500||hamel cerebropalatocardiac syndrome
|
|
C537761|309500||mental retardation x linked 55
|
|
C537761|309500||mental retardation x linked renpenning type
|
|
C537761|309500||mental retardation x linked syndromic 3
|
|
C537761|309500||mental retardation x linked syndromic 8
|
|
C537761|309500||mental retardation x linked with spastic diplegia
|
|
C537761|309500||mrx55
|
|
C537761|309500||mrxs3
|
|
C537761|309500||mrxs8
|
|
C537761|309500||porteous syndrome
|
|
C537761|309500||renpenning syndrome
|
|
C537761|309500||rens1
|
|
C537761|309500|C538400|601680||shs
|
|
C537761|309500||sutherland haan syndrome
|
|
C537761|309500||sutherland haan x linked mental retardation syndrome
|
|
C537761|309500||x linked intellectual deficit due to pqbp1 mutations
|
|
C537761|309500||x linked intellectual deficit renpenning type
|
|
C537761|309500||x linked mental retardation syndromic 3
|
|
C537761|309500||x linked mental retardation with spastic diplegia
|
|
C567405|612162||aneurysm intracranial berry 8
|
|
C567405|612162||anib8
|
|
D047928||premature birth
|
|
D047928||birth premature
|
|
D047928||birth preterm
|
|
D047928||births premature
|
|
D047928||births preterm
|
|
D047928||premature births
|
|
D047928||preterm birth
|
|
D047928||preterm births
|
|
C566592||ectodermal dysplasia pure hair nail type
|
|
C536722||zap70 deficiency
|
|
C536722||selective t cell defect
|
|
C536722||zap70 related scid
|
|
C536722||zap70 related severe combined immunodeficiency
|
|
C536722||zeta associated protein 70 deficiency
|
|
C565429|247640||lymphoblastic leukemia acute with lymphomatous features
|
|
C565429|247640||lall
|
|
C565429|247640||lymphomatous all
|
|
C565262||myopathy distal 2
|
|
C565262||distal myopathy with vocal cord and pharyngeal signs
|
|
C565262||distal myopathy with vocal cord weakness
|
|
C565262||matrin 3 distal myopathy
|
|
C565262||mpd2
|
|
C565262||myopathia distalis type 2
|
|
C565262||vcpdm
|
|
C565262||vocal cord and pharyngeal dysfunction with distal myopathy
|
|
C565262||vocal cord and pharyngeal weakness with distal myopathy
|
|
C536723||zazam sheriff phillips syndrome
|
|
C536723||aniridia ectopia lentis abnormal upper incisors and mental retardation
|
|
C536723||aniridia lens luxation mental retardation
|
|
C536529|606713||van der woude syndrome 2
|
|
C536529|606713||vws2
|
|
600791||deafness autosomal recessive 4 with enlarged vestibular aqueduct
|
|
600791||dfnb4
|
|
600791||dva
|
|
600791||nsrd4
|
|
C536720||yusho disease
|
|
D059905||endocarditis non infective
|
|
D059905||endocarditides marantic
|
|
D059905||endocarditides non infective
|
|
D059905||endocarditis marantic
|
|
D059905||endocarditis non bacterial thrombotic
|
|
D059905||marantic endocarditides
|
|
D059905||marantic endocarditis
|
|
D059905||non bacterial thrombotic endocarditis
|
|
D059905||non infective endocarditides
|
|
D059905||non infective endocarditis
|
|
C566595||hyperzincemia with functional zinc depletion
|
|
C536721||zadik barak levin syndrome
|
|
C536721||dermoid cysts hypothyroidism cleft palate and hypodontia
|
|
C536727||zonular cataract and nystagmus
|
|
C536727||nystagmus with congenital zonular cataract
|
|
C536724||zerres rietschel majewski syndrome
|
|
C536528|119300||van der woude syndrome
|
|
C536528|119300||cleft lip and or palate with mucous cysts of lower lip
|
|
C536528|119300||lip pit syndrome
|
|
C536528|119300||lps
|
|
C536528|119300||pit
|
|
C536528|119300||van der woude syndrome 1
|
|
C536528|119300||vdws
|
|
C536528|119300||vws1
|
|
D007119||immunoblastic lymphadenopathy
|
|
D007119||angioimmunoblastic lymphadenopathies
|
|
D007119||angioimmunoblastic lymphadenopathy
|
|
D007119||immunoblastic lymphadenopathies
|
|
D007119||lymphadenopathies angioimmunoblastic
|
|
D007119||lymphadenopathies immunoblastic
|
|
D007119||lymphadenopathy angioimmunoblastic
|
|
D007119||lymphadenopathy immunoblastic
|
|
D046728||colitis microscopic
|
|
D046728||microscopic colitis
|
|
D008446||maxillofacial injuries
|
|
D008446||injuries maxillofacial
|
|
D008446||injury maxillofacial
|
|
D008446||maxillofacial injury
|
|
C566454|609698||thyroid hormone metabolism abnormal
|
|
D008444||maxillary sinus neoplasms
|
|
D008444||cancer maxillary sinus
|
|
D008444||cancer of maxillary sinus
|
|
D008444||cancers maxillary sinus
|
|
D008444||maxillary sinus cancer
|
|
D008444||maxillary sinus cancers
|
|
D008444||maxillary sinus neoplasm
|
|
D008444||neoplasm maxillary sinus
|
|
D008444||neoplasms maxillary sinus
|
|
D054067|274270||dihydropyrimidine dehydrogenase deficiency
|
|
D054067|274270||deficiencies dihydropyrimidine dehydrogenase
|
|
D054067|274270||deficiencies dpd
|
|
D054067|274270||deficiency dihydropyrimidine dehydrogenase
|
|
D054067|274270||deficiency dpd
|
|
D054067|274270||dehydrogenase deficiencies dihydropyrimidine
|
|
D054067|274270||dehydrogenase deficiency dihydropyrimidine
|
|
D054067|274270||dihydropyrimidine dehydrogenase deficiencies
|
|
D054067|274270|C562815|222748||dihydropyrimidinuria
|
|
D054067|274270||dihydropyrimidinurias
|
|
D054067|274270||dpd deficiencies
|
|
D054067|274270||dpd deficiency
|
|
D054067|274270||dpyd deficiency
|
|
D054067|274270||familial pyrimidemia
|
|
D054067|274270||familial pyrimidemias
|
|
D054067|274270||familial pyrimidinemia
|
|
D054067|274270||familial pyrimidinemias
|
|
D054067|274270||hereditary thymine uraciluria
|
|
D054067|274270||hereditary thymine uracilurias
|
|
D054067|274270||pyrimidemia familial
|
|
D054067|274270||pyrimidemias familial
|
|
D054067|274270||pyrimidinemia familial
|
|
D054067|274270||pyrimidinemia familial 5 fluorouracil toxicity included
|
|
D054067|274270||pyrimidinemias familial
|
|
D054067|274270||thymine uraciluria hereditary
|
|
D054067|274270||thymine uracilurias hereditary
|
|
D009784||occupational diseases
|
|
D009784||disease occupational
|
|
D009784||diseases occupational
|
|
D009784||illnesse occupational
|
|
D009784||illnesses occupational
|
|
D009784||occupational disease
|
|
D009784||occupational illnesse
|
|
D009784||occupational illnesses
|
|
D009783||dermatitis occupational
|
|
D009783||dermatitides occupational
|
|
D009783||dermatoses industrial
|
|
D009783||dermatosis industrial
|
|
D009783||industrial dermatoses
|
|
D009783||industrial dermatosis
|
|
D009783||occupational dermatitides
|
|
D009783||occupational dermatitis
|
|
308240|D008232||lymphoproliferative disorders
|
|
308240|D008232||disease duncan
|
|
308240|D008232||diseases x linked lymphoproliferative
|
|
308240|D008232||disease x linked lymphoproliferative
|
|
308240|D008232||disorder lymphoproliferative
|
|
308240|D008232||disorders lymphoproliferative
|
|
308240|D008232||disorders x linked lymphoproliferative
|
|
308240|D008232||disorder x linked lymphoproliferative
|
|
308240|D008232||duncan disease
|
|
308240|D008232||duncan apos s syndrome
|
|
308240|D008232||ebv infection severe susceptibility to
|
|
308240|D008232||ebvs
|
|
308240|D008232||epstein barr virus induced lymphoproliferative disease in males
|
|
308240|D008232||epstein barr virus infection familial fatal
|
|
308240|D008232||familial fatal epstein barr infection
|
|
308240|D008232||imd5
|
|
308240|D008232||immunodeficiency 5
|
|
308240|D008232||immunodeficiency 5s
|
|
308240|D008232||immunodeficiency x linked progressive combined variable
|
|
308240|D008232||infectious mononucleosis severe susceptibility to
|
|
308240|D008232||lymphoproliferative diseases x linked
|
|
308240|D008232||lymphoproliferative disease x linked
|
|
308240|D008232||lymphoproliferative disorder
|
|
308240|D008232||lymphoproliferative disorders x linked
|
|
308240|D008232||lymphoproliferative disorder x linked
|
|
308240|D008232||lymphoproliferative syndromes x linked
|
|
308240|D008232||lymphoproliferative syndrome x linked
|
|
308240|D008232||lymphoproliferative syndrome x linked 1
|
|
308240|D008232||lyp
|
|
308240|D008232||purtilo syndrome
|
|
308240|D008232||purtilo syndromes
|
|
308240|D008232||syndrome purtilo
|
|
308240|D008232||syndromes purtilo
|
|
308240|D008232||syndromes x linked lymphoproliferative
|
|
308240|D008232||syndrome x linked lymphoproliferative
|
|
308240|D008232||x linked lymphoproliferative disease
|
|
308240|D008232||x linked lymphoproliferative diseases
|
|
308240|D008232||x linked lymphoproliferative disorder
|
|
308240|D008232||x linked lymphoproliferative disorders
|
|
308240|D008232||x linked lymphoproliferative syndrome
|
|
308240|D008232||x linked lymphoproliferative syndromes
|
|
308240|D008232||xlp
|
|
308240|D008232||xlp1
|
|
308240|D008232||xlpd
|
|
202370||peroxisome biogenesis disorder 2b
|
|
202370||pbd2b
|
|
D046729||colitis collagenous
|
|
D046729||collagenous colitis
|
|
C535938|600668||chondrocalcinosis 1
|
|
C535938|600668||ccal1
|
|
C535938|600668||chondrocalcinosis with early onset osteoarthritis
|
|
C562476|141200||hematuria benign familial
|
|
C562476|141200||bfh
|
|
C562476|141200||thin basement membrane nephropathy
|
|
C562476|141200||thin membrane nephropathy
|
|
C562476|141200||tmn
|
|
D010760||phosphorus metabolism disorders
|
|
D010760||disorder phosphorus metabolism
|
|
D010760||disorders phosphorus metabolism
|
|
D010760||metabolism disorder phosphorus
|
|
D010760||metabolism disorders phosphorus
|
|
D010760||phosphorus metabolism disorder
|
|
D046730||colitis lymphocytic
|
|
D046730||lymphocytic colitis
|
|
C563672|610374||diabetes mellitus transient neonatal 2
|
|
C563672|610374||tndm2
|
|
C565448|245348||pyruvate dehydrogenase e2 deficiency
|
|
C565448|245348||lactic acidemia due to defect of e2 lipoyl transacetylase of the pyruvate dehydrogenase complex
|
|
C565448|245348||pdhdd
|
|
300802||mental retardation x linked 96
|
|
300802||mrx96
|
|
106250|C536373||ankyloblepharon filiforme adnatum cleft palate
|
|
106250|C536373||afa
|
|
106250|C536373||ankyloblepharon filiforme adnatum
|
|
106250|C536373||ankyloblepharon filiforme adnatum and cleft palate
|
|
106250|C536373||ankyloblepharon filiforme congenitum
|
|
106250|C536373||congenital filiform fusion of the eyelids with cleft palate and or cleft lip
|
|
D008457||measles
|
|
D008457||rubeola
|
|
C566530|602522||bartter syndrome type 4a
|
|
C566530|602522||bartter syndrome infantile with sensorineural deafness bsnd sensorineural deafness with mild renal dysfunction included
|
|
608027|C548072||pontocerebellar hypoplasia type 3
|
|
608027|C548072||cerebellar atrophy with progressive microcephaly
|
|
608027|C548072||clam
|
|
608027|C548072||pch3
|
|
608027|C548072||pch with optic atrophy
|
|
D009794||ochronosis
|
|
D009794||ochronoses
|
|
607906|C535747||congenital disorder of glycosylation type ii
|
|
607906|C535747||cdg1i
|
|
607906|C535747||cdgii
|
|
607906|C535747||cdg ii
|
|
607906|C535747||congenital disorder of glycosylation type 1i
|
|
D019106||postoperative hemorrhage
|
|
D019106||blood loss postoperative
|
|
D019106||hemorrhage postoperative
|
|
D019106||hemorrhages postoperative
|
|
D019106||loss postoperative blood
|
|
D019106||postoperative blood loss
|
|
D019106||postoperative hemorrhages
|
|
D034721||mastocytosis systemic
|
|
D034721||aggressive systemic mastocytoses
|
|
D034721||aggressive systemic mastocytosis
|
|
D034721||indolent systemic mastocytoses
|
|
D034721||indolent systemic mastocytosis
|
|
D034721||mast cell diseases systemic
|
|
D034721||mast cell disease systemic
|
|
D034721||mastocytoses aggressive systemic
|
|
D034721||mastocytoses indolent systemic
|
|
D034721||mastocytoses systemic
|
|
D034721||mastocytosis aggressive systemic
|
|
D034721||mastocytosis indolent systemic
|
|
D034721||systemic mast cell disease
|
|
D034721||systemic mast cell diseases
|
|
D034721||systemic mastocytoses
|
|
D034721||systemic mastocytoses aggressive
|
|
D034721||systemic mastocytoses indolent
|
|
D034721||systemic mastocytosis
|
|
D034721||systemic mastocytosis aggressive
|
|
D034721||systemic mastocytosis indolent
|
|
D004687|166000||enchondromatosis
|
|
D004687|166000||chondrodysplasia with hemangioma
|
|
D004687|166000||chondroplasia angiomatosis
|
|
D004687|166000||disease ollier
|
|
D004687|166000||disease ollier apos s
|
|
D004687|166000||dyschondrodysplasia with hemangiomas
|
|
D004687|166000|239100|D010009||dyschondroplasia
|
|
D004687|166000||dyschondroplasia and cavernous hemangioma
|
|
D004687|166000||enchondroma multiple
|
|
D004687|166000||enchondromas multiple
|
|
D004687|166000||enchondromatoses
|
|
D004687|166000||enchondromatosis multiple
|
|
D004687|166000||enchondromatosis multiple ollier type
|
|
D004687|166000||enchondromatosis with hemangiomata
|
|
D004687|166000||enchondromatosis with multiple cavernous hemangiomas
|
|
D004687|166000||enchondroses multiple
|
|
D004687|166000||enchondrosis multiple
|
|
D004687|166000||hemangiomata with dyschondroplasia
|
|
D004687|166000||hemangiomatosis chondrodystrophica
|
|
D004687|166000||kast syndrome
|
|
D004687|166000||maffucci syndrome
|
|
D004687|166000||multiple angiomas and endochondromas
|
|
D004687|166000||multiple enchondroma
|
|
D004687|166000||multiple enchondromas
|
|
D004687|166000||multiple enchondroses
|
|
D004687|166000||multiple enchondrosis
|
|
D004687|166000||ollier disease
|
|
D004687|166000||ollier apos s disease
|
|
D004687|166000||olliers disease
|
|
D004687|166000|D018216|133700||osteochondromatosis
|
|
D004687|166000||syndrome maffucci
|
|
C564306|608013||gaucher disease perinatal lethal
|
|
C564306|608013||gaucher disease collodion type
|
|
C537952|600143||ceroid lipofuscinosis neuronal 8
|
|
C537952|600143||ceroid lipofuscinosis neuronal 8 northern epilepsy variant
|
|
C537952|600143||cln8
|
|
C537952|600143||epilepsy progressive with mental retardation
|
|
C537952|600143||epmr
|
|
C537952|600143||northern epilepsy
|
|
C537952|600143||northern epilepsy syndrome
|
|
C563137|309549||mental retardation x linked 9
|
|
C563137|309549||mental retardation x linked 44
|
|
C563137|309549||mrx44
|
|
C563137|309549||mrx9
|
|
D009759||nystagmus pathologic
|
|
D009759||alternating nystagmus periodic
|
|
D009759||conjugate nystagmus
|
|
D009759||convergence nystagmus
|
|
D009759||dissociated nystagmus
|
|
D009759||fatigable positional nystagmus
|
|
D009759||horizontal nystagmus
|
|
D009759||jerk nystagmus
|
|
D009759||multidirectional nystagmus
|
|
D009759||non fatigable positional nystagmus
|
|
D009759||nystagmus conjugate
|
|
D009759||nystagmus convergence
|
|
D009759||nystagmus dissociated
|
|
D009759||nystagmus fatigable positional
|
|
D009759||nystagmus horizontal
|
|
D009759||nystagmus jerk
|
|
D009759||nystagmus multidirectional
|
|
D009759||nystagmus non fatigable positional
|
|
D009759||nystagmus pendular
|
|
D009759||nystagmus periodic alternating
|
|
D009759||nystagmus permanent
|
|
D009759||nystagmus rebound
|
|
D009759||nystagmus retraction
|
|
D009759||nystagmus rotary
|
|
D009759||nystagmus rotational
|
|
D009759||nystagmus see saw
|
|
D009759||nystagmus spontaneous ocular
|
|
D009759||nystagmus symptomatic
|
|
D009759||nystagmus temporary
|
|
D009759||nystagmus unidirectional
|
|
D009759||nystagmus vertical
|
|
D009759||ocular nystagmus spontaneous
|
|
D009759||pathologic nystagmus
|
|
D009759||pendular nystagmus
|
|
D009759||periodic alternating nystagmus
|
|
D009759||permanent nystagmus
|
|
D009759||positional nystagmus fatigable
|
|
D009759||positional nystagmus non fatigable
|
|
D009759||rebound nystagmus
|
|
D009759||retraction nystagmus
|
|
D009759||rotary nystagmus
|
|
D009759||rotational nystagmus
|
|
D009759||see saw nystagmus
|
|
D009759||spontaneous ocular nystagmus
|
|
D009759||symptomatic nystagmus
|
|
D009759||temporary nystagmus
|
|
D009759||unidirectional nystagmus
|
|
D009759||vertical nystagmus
|
|
C563422|600962||palmoplantar keratoderma nonepidermolytic
|
|
C563422|600962||keratoderma nonepidermolytic palmoplantar
|
|
C563422|600962||neppk
|
|
C563422|600962||nonepidermolytic palmoplantar keratoderma
|
|
D046748||hematoma epidural spinal
|
|
D046748||epidural hematoma spinal
|
|
D046748||epidural hematomas spinal
|
|
D046748||epidural hemorrhage spinal
|
|
D046748||epidural hemorrhages spinal
|
|
D046748||hematoma spinal epidural
|
|
D046748||hematomas spinal epidural
|
|
D046748||hemorrhage spinal epidural
|
|
D046748||hemorrhages spinal epidural
|
|
D046748||spinal epidural hematoma
|
|
D046748||spinal epidural hematomas
|
|
D046748||spinal epidural hemorrhage
|
|
D046748||spinal epidural hemorrhages
|
|
C535612|276820||al awadi syndrome
|
|
C535612|276820||aarrs
|
|
C535612|276820||al awadi raas rothschild syndrome
|
|
C535612|276820||al awadi rass rothschild syndrome
|
|
C535612|276820||limb pelvis hypoplasia aplasia syndrome
|
|
C535612|276820||lphas
|
|
C535612|276820||schinzel phocomelia syndrome
|
|
C535612|276820||ulna and fibula absence of with severe limb deficiency
|
|
106700|D012587||scimitar syndrome
|
|
106700|D012587||anomalous pulmonary venous return
|
|
106700|D012587||anomaly scimitar
|
|
106700|D012587||apvr
|
|
106700|D012587||pulmonary venous return anomaly
|
|
106700|D012587||scimitar anomaly
|
|
106700|D012587||syndrome scimitar
|
|
106700|D012587||tapvr
|
|
106700|D012587||tapvr1
|
|
106700|D012587||total anomalous pulmonary venous return
|
|
106700|D012587||total anomalous pulmonary venous return 1
|
|
D009755||night blindness
|
|
D009755||blindness night
|
|
D009755||nyctalopia
|
|
C563659|610829||holoprosencephaly 9
|
|
C563659|610829|C567278||holoprosencephaly with microphthalmia and first branchial arch anomalies
|
|
C563659|610829||hpe9
|
|
C563659|610829||pituitary anomalies with holoprosencephaly like features
|
|
188055|C566056||thrombophilia due to activated protein c resistance
|
|
188055|C566056||apc resistance leiden type
|
|
188055|C566056||factor v leiden thrombophilia
|
|
188055|C566056||hereditary resistance to activated protein c
|
|
188055|C566056||pccf deficiency
|
|
188055|C566056||proc cofactor deficiency
|
|
188055|C566056||protein c cofactor deficiency
|
|
188055|C566056||thph2
|
|
188055|C566056||thrombophilia due to deficiency of activated protein c cofactor
|
|
188055|C566056||thrombophilia due to factor v leiden
|
|
188055|C566056||thrombophilia v
|
|
188055|C566056||thrombophilia v thrombophilia due to factor v leiden included
|
|
252600|252650|D009081||mucolipidosis iii alpha beta
|
|
252600||ml iii
|
|
252600||ml iiia
|
|
252600|252650|D009081||ml iii alpha beta
|
|
252600|252650|D009081||mucolipidosis iii
|
|
252600|252650|D009081||mucolipidosis iiia
|
|
252600||pseudo hurler polydystrophy mucolipidosis iii alpha beta atypical included
|
|
C565145|123000||craniometaphyseal dysplasia autosomal dominant
|
|
C565145|123000||autosomal dominant craniometaphyseal dysplasia
|
|
C565145|123000||autosomal recessive craniometaphyseal dysplasia
|
|
C565145|123000||cmd
|
|
C565145|123000||cmdd
|
|
C565145|123000||cmdj
|
|
C565145|123000||craniometaphyseal dysplasia dominant type
|
|
C565145|123000||craniometaphyseal dysplasia jackson type
|
|
D058729||peripheral arterial disease
|
|
D058729||arterial disease peripheral
|
|
D058729||arterial diseases peripheral
|
|
D058729||artery disease peripheral
|
|
D058729||artery diseases peripheral
|
|
D058729||disease peripheral arterial
|
|
D058729||disease peripheral artery
|
|
D058729||diseases peripheral arterial
|
|
D058729||diseases peripheral artery
|
|
D058729||peripheral arterial diseases
|
|
D058729||peripheral artery disease
|
|
D058729||peripheral artery diseases
|
|
604201||hepatic fibrosis severe susceptibility to due to schistosoma mansoni infection
|
|
604201||sm2 hepatic fibrosis severe susceptibility to due to schistosoma japonicum infection included
|
|
600886|C538137||hyperferritinemia hereditary with congenital cataracts
|
|
600886|C538137||bonneau beaumont syndrome
|
|
600886|C538137||dominant hyperferritinemia and cataract
|
|
600886|C538137||hereditary hyperferritinemia cataract syndrome
|
|
600886|C538137||hereditary hyperferritinemia with congenital cataracts
|
|
600886|C538137||hhcs
|
|
600886|C538137||hyperferritinemia cataract syndrome
|
|
600886|C538137||hyperferritinemia with or without cataract
|
|
610064|D009293||opioid related disorders
|
|
610064|D009293||abuse narcotic
|
|
610064|D009293||abuses narcotic
|
|
610064|D009293||addiction narcotic
|
|
610064|D009293||addiction opiate
|
|
610064|D009293||dependence narcotic
|
|
610064|D009293||dependence opiate
|
|
610064|D009293||disorder opioid related
|
|
610064|D009293||narcotic abuse
|
|
610064|D009293||narcotic abuses
|
|
610064|D009293||narcotic addiction
|
|
610064|D009293||narcotic dependence
|
|
610064|D009293||ods1
|
|
610064|D009293||opiate addiction
|
|
610064|D009293||opiate dependence
|
|
610064|D009293||opioid dependence susceptibility to 1
|
|
144650|D006954||hyperlipoproteinemia type v
|
|
144650|D006954||hyperchylomicronemia late onset
|
|
144650|D006954||hyperchylomicronemia late onsets
|
|
144650|D006954||hyperchylomicronemias late onset
|
|
144650|D006954||hyperchylomicronemia with hyperprebetalipoproteinemia familial
|
|
144650|D006954||hyperlipemia combined fat and carbohydrate induced
|
|
144650|D006954||hyperlipemia mixed
|
|
144650|D006954||hyperlipemias mixed
|
|
144650|D006954||hyperlipidemias type v
|
|
144650|D006954||hyperlipidemia type v
|
|
144650|D006954||hyperlipoproteinemias type v
|
|
144650|D006954||hyperlipoproteinemia type 5
|
|
144650|D006954||hyperlipoproteinemia type 5s
|
|
144650|D006954||late onset hyperchylomicronemia
|
|
144650|D006954||late onset hyperchylomicronemias
|
|
144650|D006954||mixed hyperlipemia
|
|
144650|D006954||mixed hyperlipemias
|
|
144650|D006954||type v hyperlipidemia
|
|
144650|D006954||type v hyperlipidemias
|
|
144650|D006954||type v hyperlipoproteinemia
|
|
144650|D006954||type v hyperlipoproteinemias
|
|
D008439||maxillary diseases
|
|
D008439||disease maxillary
|
|
D008439||diseases maxillary
|
|
D008439||maxillary disease
|
|
C567628|611225||spastic paraplegia 18 autosomal recessive
|
|
C567628|611225||idmdc
|
|
C567628|611225||intellectual disability motor dysfunction and joint contractures
|
|
C567628|611225||spg18
|
|
D009767||obesity morbid
|
|
D009767||morbid obesities
|
|
D009767||morbid obesity
|
|
D009767||obesities morbid
|
|
D009767||obesities severe
|
|
D009767||obesity severe
|
|
D009767||severe obesities
|
|
D009767||severe obesity
|
|
D007105||immune complex diseases
|
|
D007105||disease immune complex
|
|
D007105||diseases immune complex
|
|
D007105||hypersensitivities type iii
|
|
D007105||hypersensitivity type iii
|
|
D007105||immune complex disease
|
|
D007105||type iii hypersensitivities
|
|
D007105||type iii hypersensitivity
|
|
D007102||immersion foot
|
|
D007102||feet immersion
|
|
D007102||feet trench
|
|
D007102||foot immersion
|
|
D007102||foot trench
|
|
D007102||immersion feet
|
|
D007102||trench feet
|
|
D007102||trench foot
|
|
D008441||maxillary neoplasms
|
|
D008441||maxillary neoplasm
|
|
D008441||neoplasm maxillary
|
|
D008441||neoplasms maxillary
|
|
D008440||maxillary fractures
|
|
D008440||fracture maxillary
|
|
D008440||fractures maxillary
|
|
D008440||maxillary fracture
|
|
C536085|308205||ichthyosis follicularis atrichia photophobia syndrome
|
|
C536085|308205||ichthyosis follicularis atrichia and photophobia syndrome
|
|
C536085|308205||ichthyosis follicularis atrichia and photophobia with or without brain anomalies retardation ectodermal dysplasia skeletal malformations hirschsprung disease ear eye anomalies cleft palate cryptorchidism and kidney dysplasia hypoplasia
|
|
C536085|308205||ifap syndrome with or without bresheck syndrome
|
|
607683|C564348||deafness autosomal dominant 52
|
|
607683|C564348||deafness autosomal dominant 42
|
|
607683|C564348||dfna42
|
|
607683|C564348||dfna52
|
|
252650|D009081||mucolipidoses
|
|
252650|D009081||alpha beta ml iii
|
|
252650|D009081||alpha beta mucolipidosis iii
|
|
252650|D009081||alpha betas mucolipidosis iii
|
|
252650|D009081||cell disease inclusion
|
|
252650|D009081||cell diseases inclusion
|
|
252650|D009081||cherry red spot myoclonus syndrome
|
|
252650|D009081||deficiencies glycoprotein neuraminidase
|
|
252650|D009081||deficiency disease ganglioside sialidase
|
|
252650|D009081||deficiency glycoprotein neuraminidase
|
|
252650|D009081||disease i cell
|
|
252650|D009081||disease inclusion cell
|
|
252650|D009081||disease psuedo hurler
|
|
252650|D009081||diseases i cell
|
|
252650|D009081||diseases inclusion cell
|
|
252650|D009081||diseases psuedo hurler
|
|
252650|D009081||ganglioside sialidase deficiency disease
|
|
252650|D009081||glycoprotein neuraminidase deficiencies
|
|
252650|D009081|256550|C537366||glycoprotein neuraminidase deficiency
|
|
252650|D009081|252500||i cell disease
|
|
252650|D009081||i cell diseases
|
|
252650|D009081||iii alpha beta mucolipidosis
|
|
252650|D009081||iii alpha betas mucolipidosis
|
|
252650|D009081||iiia mucolipidosis
|
|
252650|D009081||inclusion cell disease
|
|
252650|D009081||inclusion cell diseases
|
|
252650|D009081||lipomucopolysaccharidoses
|
|
252650|D009081|256550|C537366||lipomucopolysaccharidosis
|
|
252650|D009081||ml4
|
|
252650|D009081||ml iv
|
|
252650|D009081||mucolipidoses type i
|
|
252650|D009081||mucolipidoses type ii
|
|
252650|D009081||mucolipidoses type iii
|
|
252650|D009081||mucolipidoses type iv
|
|
252650|D009081||mucolipidosis
|
|
252650|D009081|256550|C537366||mucolipidosis i
|
|
252650|D009081|252500||mucolipidosis ii
|
|
252650|D009081|252500|C567100||mucolipidosis ii alpha beta
|
|
252650|D009081||mucolipidosis iiis
|
|
252650|D009081||mucolipidosis is
|
|
252650|D009081||mucolipidosis iv
|
|
252650|D009081||mucolipidosis type 1
|
|
252650|D009081||mucolipidosis type 1s
|
|
252650|D009081||mucolipidosis type i
|
|
252650|D009081||mucolipidosis type ii
|
|
252650|D009081||mucolipidosis type iii
|
|
252650|D009081||mucolipidosis type is
|
|
252650|D009081||mucolipidosis type iv
|
|
252650|D009081||mucolipidosis type ivs
|
|
252650|D009081||myoclonus cherry red spot syndrome
|
|
252650|D009081||neuraminidase deficiencies glycoprotein
|
|
252650|D009081||neuraminidase deficiency glycoprotein
|
|
252650|D009081||polydystrophy pseudo hurler
|
|
252650|D009081||pseudo hurler polydystrophy
|
|
252650|D009081||psuedo hurler disease
|
|
252650|D009081||psuedo hurler diseases
|
|
252650|D009081||sialidoses
|
|
252650|D009081||sialidosis
|
|
252650|D009081||sialolipidoses
|
|
252650|D009081||sialolipidosis
|
|
252650|D009081||type iii mucolipidoses
|
|
252650|D009081||type iii mucolipidosis
|
|
252650|D009081||type ii mucolipidoses
|
|
252650|D009081||type ii mucolipidosis
|
|
252650|D009081||type i mucolipidoses
|
|
252650|D009081||type i mucolipidosis
|
|
252650|D009081||type iv mucolipidoses
|
|
252650|D009081||type iv mucolipidosis
|
|
D016537|230500||gangliosidosis gm1
|
|
D016537|230500||adult gm1 gangliosidosis
|
|
D016537|230500||beta galactosidase 1 deficiency
|
|
D016537|230500||beta galactosidase 1 deficiency disease
|
|
D016537|230500||beta galactosidase 1 glb1 deficiency
|
|
D016537|230500||beta galactosidase deficiency
|
|
D016537|230500||beta galactosidosis
|
|
D016537|230500||deficiencies glb1
|
|
D016537|230500||deficiency beta galactosidase
|
|
D016537|230500||deficiency beta galactosidase 1
|
|
D016537|230500||deficiency glb1
|
|
D016537|230500||gangliosidosis adult gm1
|
|
D016537|230500||gangliosidosis generalized gm1 adult type
|
|
D016537|230500||gangliosidosis generalized gm1 chronic type
|
|
D016537|230500||gangliosidosis generalized gm1 infantile form
|
|
D016537|230500||gangliosidosis generalized gm1 juvenile type
|
|
D016537|230500||gangliosidosis generalized gm1 type 1
|
|
D016537|230500||gangliosidosis generalized gm1 type 2
|
|
D016537|230500||gangliosidosis generalized gm1 type 2 gangliosidosis generalized gm1 late infantile type included
|
|
D016537|230500||gangliosidosis generalized gm1 type 3
|
|
D016537|230500||gangliosidosis generalized gm1 type i
|
|
D016537|230500||gangliosidosis generalized gm1 type ii
|
|
D016537|230500||gangliosidosis generalized gm1 type iii
|
|
D016537|230500||gangliosidosis generalized gm1 type i with cardiac involvement included
|
|
D016537|230500||gangliosidosis g m1
|
|
D016537|230500||gangliosidosis gm1 adult
|
|
D016537|230500||gangliosidosis gm1 infantile
|
|
D016537|230500||gangliosidosis gm1 juvenile
|
|
D016537|230500||gangliosidosis gm1 type 1
|
|
D016537|230500||gangliosidosis gm1 type 2
|
|
D016537|230500||gangliosidosis gm1 type 3
|
|
D016537|230500||generalized gangliosidosis
|
|
D016537|230500||glb1 deficiency
|
|
D016537|230500||glb1 deficiency gm1 gangliosidosis type i with cardiac involvement included
|
|
D016537|230500||gm1 gangliosidoses type i
|
|
D016537|230500||gm1 gangliosidoses type ii
|
|
D016537|230500||gm1 gangliosidoses type iii
|
|
D016537|230500||g m1 gangliosidosis
|
|
D016537|230500||gm1 gangliosidosis
|
|
D016537|230500||gm1 gangliosidosis adult
|
|
D016537|230500||gm1 gangliosidosis type i
|
|
D016537|230500||gm1 gangliosidosis type ii
|
|
D016537|230500||gm1 gangliosidosis type iii
|
|
D016537|230500||infantile gangliosidosis gm1
|
|
D016537|230500||juvenile gangliosidosis gm1
|
|
D016537|230500||type 3 adult gm1 gangliosidosis
|
|
D016537|230500||type i gm1 gangliosidoses
|
|
D016537|230500||type i gm1 gangliosidosis
|
|
D016537|230500||type ii gm1 gangliosidoses
|
|
D016537|230500||type ii gm1 gangliosidosis
|
|
D016537|230500||type iii gm1 gangliosidoses
|
|
D016537|230500||type iii gm1 gangliosidosis
|
|
C567766|613080||46 xy sex reversal 5
|
|
C567766|613080||46 xy gonadal dysgenesis complete cbx2 related
|
|
C567766|613080||46 xy sex reversal cbx2 related
|
|
C567766|613080||disorder of sex development 46 xy cbx2 related
|
|
C567766|613080||sex reversal xy cbx2 related
|
|
C567766|613080||srxy5
|
|
D058739||aberrant crypt foci
|
|
D058739||crypt foci aberrant
|
|
D058739||foci aberrant crypt
|
|
D034701||mastocytosis cutaneous
|
|
D034701||bullous mastocytoses
|
|
D034701||bullous mastocytosis
|
|
D034701||cutaneous mastocytoses
|
|
D034701||cutaneous mastocytoses diffuse
|
|
D034701||cutaneous mastocytosis
|
|
D034701||cutaneous mastocytosis diffuse
|
|
D034701||mastocytoses bullous
|
|
D034701||mastocytoses cutaneous
|
|
D034701||mastocytoses skin
|
|
D034701||mastocytosis bullous
|
|
D034701||mastocytosis diffuse cutaneous
|
|
D034701||mastocytosis skin
|
|
D034701||skin mastocytoses
|
|
D034701||skin mastocytosis
|
|
D058734||exsanguination
|
|
D058734||exsanguinating hemorrhage
|
|
D058734||exsanguinating hemorrhages
|
|
D058734||hemorrhage exsanguinating
|
|
D058734||hemorrhages exsanguinating
|
|
C537206|117360||spinocerebellar ataxia 29
|
|
C537206|117360||acv
|
|
C537206|117360||aplasia of cerebellar vermis
|
|
C537206|117360||cerebellar ataxia congenital nonprogressive autosomal dominant
|
|
C537206|117360||cerebellar ataxia early onset nonprogressive
|
|
C537206|117360||cerebellar vermis aplasia
|
|
C537206|117360||cnpca
|
|
C537206|117360||sca29
|
|
D058736||intrauterine device migration
|
|
D058736||device migration intrauterine
|
|
D058736||device migrations intrauterine
|
|
D058736||intrauterine device migrations
|
|
D058736||iud migration
|
|
D058736||iud migrations
|
|
D058736||migration intrauterine device
|
|
D058736||migration iud
|
|
D058736||migrations intrauterine device
|
|
D058736||migrations iud
|
|
135290|C535944||desmoid disease hereditary
|
|
135290|C535944||desmoid tumor caused by somatic mutation
|
|
135290|C535944||familial infiltrative fibromatosis
|
|
135290|C535944||fibromatosis familial infiltrative
|
|
135290|C535944||fibromatosis familial infiltrative fif desmoid tumor caused by somatic mutation included
|
|
C536697|193670||whim syndrome
|
|
C536697|193670||warts hypogammaglobulinemia infections and myelokathexis
|
|
C564252|608361||spondyloepiphyseal dysplasia kimberley type
|
|
C564252|608361||sedk
|
|
D046768|D044903|256450||nesidioblastosis
|
|
D046768|D044903|256450||hyperinsulinism familial with pancreatic nesidioblastosis
|
|
D046768||nesidioblastoses
|
|
D046768||nesidioblastoses pancreatic
|
|
D046768|D044903|256450||nesidioblastosis of pancreas
|
|
D046768||nesidioblastosis pancreatic
|
|
D046768||pancreas nesidioblastoses
|
|
D046768||pancreas nesidioblastosis
|
|
D046768||pancreatic nesidioblastoses
|
|
D046768||pancreatic nesidioblastosis
|
|
D058745||iliotibial band syndrome
|
|
D058745||syndrome iliotibial band
|
|
C566645|601666||diabetes mellitus insulin dependent 15
|
|
C566645|601666||iddm15
|
|
C566645|601666||insulin dependent diabetes mellitus 15
|
|
C562812|212138||carnitine acylcarnitine translocase deficiency
|
|
C562812|212138||cactd
|
|
C562812|212138||cact deficiency
|
|
C562812|212138||carnitine acylcarnitine carrier deficiency
|
|
D009748||nutrition disorders
|
|
D009748||nutritional disorder
|
|
D009748||nutritional disorders
|
|
D009748||nutrition disorder
|
|
D008417||mastoiditis
|
|
D008417||mastoiditides
|
|
607507|D015535||arthritis psoriatic
|
|
607507|D015535||arthritic psoriasis
|
|
607507|D015535||arthropathies psoriatic
|
|
607507|D015535||arthropathy psoriatic
|
|
607507|D015535||psoras1
|
|
607507|D015535||psoriasis arthritic
|
|
607507|D015535||psoriasis arthropathica
|
|
607507|D015535||psoriatic arthritis
|
|
607507|D015535||psoriatic arthritis susceptibility to psoriatic arthritis susceptibility to 1
|
|
607507|D015535||psoriatic arthropathies
|
|
607507|D015535||psoriatic arthropathy
|
|
D008415||mastocytosis
|
|
D008415||disease mast cell
|
|
D008415||diseases mast cell
|
|
D008415||mast cell disease
|
|
D008415||mast cell diseases
|
|
D008415||mastocytoses
|
|
D008414||mastitis bovine
|
|
D008414||bovine mastitides
|
|
D008414||bovine mastitis
|
|
D008414||mastitides bovine
|
|
D008413||mastitis
|
|
D009750||nutritional and metabolic diseases
|
|
C563310|601458||inflammatory bowel disease 2
|
|
C563310|601458||ibd2
|
|
D005645|230000||fucosidosis
|
|
D005645|230000||1 fucosidosis type
|
|
D005645|230000||alpha fucosidase deficiency
|
|
D005645|230000||alpha fucosidase deficiency disease
|
|
D005645|230000||alpha fucosidase deficiency diseases
|
|
D005645|230000||alpha l fucosidase deficiency
|
|
D005645|230000||alpha l fucosidase deficiency disease
|
|
D005645|230000||alpha l fucosidase deficiency diseases
|
|
D005645|230000||deficiency disease alpha fucosidase
|
|
D005645|230000||deficiency disease alpha l fucosidase
|
|
D005645|230000||deficiency disease fucosidase
|
|
D005645|230000||deficiency diseases alpha fucosidase
|
|
D005645|230000||deficiency diseases alpha l fucosidase
|
|
D005645|230000||deficiency diseases fucosidase
|
|
D005645|230000||disease alpha fucosidase deficiency
|
|
D005645|230000||disease alpha l fucosidase deficiency
|
|
D005645|230000||disease fucosidase deficiency
|
|
D005645|230000||diseases alpha fucosidase deficiency
|
|
D005645|230000||diseases alpha l fucosidase deficiency
|
|
D005645|230000||diseases fucosidase deficiency
|
|
D005645|230000||fucosidase deficiency
|
|
D005645|230000||fucosidase deficiency disease
|
|
D005645|230000||fucosidase deficiency diseases
|
|
D005645|230000||fucosidosis infantile
|
|
D005645|230000||fucosidosis juvenile
|
|
D005645|230000||fucosidosis type 1
|
|
D005645|230000||fucosidosis type 1s
|
|
D005645|230000||fucosidosis type i
|
|
D005645|230000||fucosidosis type ii
|
|
D005645|230000||infantile fucosidosis
|
|
D005645|230000||juvenile fucosidosis
|
|
D005645|230000||type 1 fucosidosis
|
|
D005645|230000||type 1s fucosidosis
|
|
C564522|300387||mental retardation x linked 63
|
|
C564522|300387||mental retardation x linked 68
|
|
C564522|300387||mrx63
|
|
C564522|300387||mrx68
|
|
C562735|166350||osseous heteroplasia progressive
|
|
C562735|166350||cutaneous ossification
|
|
C562735|166350||ectopic ossification familial
|
|
C562735|166350||osteodermia
|
|
C562735|166350||osteoma cutis
|
|
C562735|166350||osteosis cutis
|
|
C562735|166350||poh
|
|
C562735|166350||progressive osseous heteroplasia
|
|
C537409|300755||bruton type agammaglobulinemia
|
|
C537409|300755||agammaglobulinemia bruton tyrosine kinase
|
|
C537409|300755||agammaglobulinemia btk
|
|
C537409|300755||agammaglobulinemia x linked
|
|
C537409|300755||agammaglobulinemia x linked type 1
|
|
C537409|300755||agammaglobulinemia x linked type i
|
|
C537409|300755||agmx1
|
|
C537409|300755||bruton apos s agammaglobulinemia
|
|
C537409|300755||bruton type congenital x linked agammaglobulinemia
|
|
C537409|300755||congenital agammaglobulinemia
|
|
C537409|300755||immunodeficiency 1
|
|
C537409|300755||immunodeficiency 1 imd1 hypogammaglobulinemia x linked included
|
|
C537409|300755||xla
|
|
C537409|300755||x linked agammaglobulinemia
|
|
C567818|613006||diabetes mellitus insulin dependent 24
|
|
C567818|613006||iddm24
|
|
C565261|606071||hereditary motor and sensory neuropathy type iic
|
|
C565261|606071||charcot marie tooth disease axonal autosomal dominant type 2c
|
|
C565261|606071||charcot marie tooth neuropathy type 2c
|
|
C565261|606071||cmt2c
|
|
C565261|606071||hmsn2c
|
|
C565261|606071||hmsn iic
|
|
D046789||chondromalacia patellae
|
|
D046789||patella chondromalacia of
|
|
C567691|613225||factor xiii a subunit deficiency of
|
|
C565232|606367||interleukin 2 receptor alpha deficiency of
|
|
C565232|606367||cd25 deficiency
|
|
C565232|606367||il2ra deficiency
|
|
D046788||patellofemoral pain syndrome
|
|
D046788||anterior knee pain syndrome
|
|
D046788||pain syndrome patellofemoral
|
|
D046788||patellofemoral syndrome
|
|
151900||fml
|
|
151900||lipo
|
|
151900||lipomatosis familial multiple
|
|
C563922|608474||myopia 5
|
|
C563922|608474||myopia 5 autosomal dominant
|
|
C563922|608474||myp5
|
|
184250|C537501||strudwick syndrome
|
|
184250|C537501||dappled metaphysis syndrome
|
|
184250|C537501||sed strudwick
|
|
184250|C537501||semdc
|
|
184250|C537501||semd strudwick type
|
|
184250|C537501||semdstwk
|
|
184250|C537501||smd
|
|
184250|C537501||smed strudwick type
|
|
184250|C537501||smed type i
|
|
184250|C537501||spondyloepimetaphyseal dysplasia strudwick type
|
|
184250|C537501||spondylometaepiphyseal dysplasia congenita strudwick type
|
|
184250|C537501||spondylometaphyseal dysplasia
|
|
184250|C537501||spondylometaphyseal dysplasia smd
|
|
D056104||commotio cordis
|
|
D056104||cardiac concussion
|
|
D056104||cardiac concussions
|
|
D056104||concussion cardiac
|
|
D056104||concussions cardiac
|
|
C567034|610978||choreoathetosis hypothyroidism and neonatal respiratory distress
|
|
C567034|610978||brain lung thyroid syndrome
|
|
C567034|610978||cahtp
|
|
C567034|610978||choreoathetosis and congenital hypothyroidism
|
|
C567034|610978||choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction
|
|
C563685|609923||retinitis pigmentosa 31
|
|
C563685|609923||rp31
|
|
D045463||avulavirus infections
|
|
D045463||avulavirus infection
|
|
D045463||infection avulavirus
|
|
D045463||infections avulavirus
|
|
D045464||henipavirus infections
|
|
D045464||henipavirus infection
|
|
D045464||infection henipavirus
|
|
D045464||infections henipavirus
|
|
C535274|309610||prieto x linked mental retardation syndrome
|
|
C535274|309610||mental retardation x linked syndromic 2
|
|
C535274|309610||mental retardation x linked with dysmorphism and cerebral atrophy
|
|
C535274|309610||mrxs2
|
|
C535274|309610||prieto syndrome
|
|
C535274|309610||prs
|
|
C535274|309610||x linked dysmorphic syndrome with mental retardation
|
|
300511|C564498||premature ovarian failure 2a
|
|
300511|C564498||pof2a
|
|
C538212|300009||dent disease 1
|
|
C538212|300009||nephrolithiasis 2
|
|
C538212|300009||nephrolithiasis hypercalciuria x linked
|
|
C538212|300009||nephrolithiasis hypercalciuric x linked
|
|
C538212|300009||nphl2
|
|
C538212|300009||urolithiasis hypercalciuric x linked
|
|
256540|C536411||neuraminidase deficiency with beta galactosidase deficiency
|
|
256540|C536411||cathepsin a deficiency
|
|
256540|C536411||cathepsin a deficiency of
|
|
256540|C536411||deficiency of cathepsin a
|
|
256540|C536411||galactosialidosis
|
|
256540|C536411||goldberg syndrome
|
|
256540|C536411||gsl
|
|
256540|C536411||lysosomal protective protein deficiency
|
|
256540|C536411||lysosomal protective protein deficiency of
|
|
256540|C536411||neuraminidase beta galactosidase expression
|
|
256540|C536411||ngbe
|
|
256540|C536411||ppca deficiency
|
|
256540|C536411||protective protein cathepsin a deficiency
|
|
607655|C564359||skin fragility woolly hair syndrome
|
|
607655|C564359||sfwhs
|
|
310460|C564091||myopia 1
|
|
310460|C564091||myopia 1 x linked
|
|
310460|C564091||myopia x linked
|
|
310460|C564091||myp1
|
|
249900|C562609||metachromatic leukodystrophy due to saposin b deficiency
|
|
249900|C562609||metachromatic leukodystrophy due to cerebroside sulfatase activator deficiency
|
|
249900|C562609||saposin b deficiency
|
|
C536187||ectrodactyly cardiopathy dysmorphism
|
|
C536187||ectrodactyly of lower limbs congenital heart defect and characteristic facies
|
|
C536187||van den ende brunner syndrome
|
|
C536184||familial ectopia lentis
|
|
C536184||ectopia lentis familial
|
|
C536184||ectopia lentis isolated
|
|
C536184||isolated ectopia lentis
|
|
C562472||teratoma testicular
|
|
C562477||halothane hepatitis
|
|
C562478||hypogammaglobulinemia x linked
|
|
C536188||blepharo cheilo dontic syndrome
|
|
C536188||blepharocheilodontic syndrome
|
|
C536188||clefting ectropion and conical teeth
|
|
C536188||elschnig syndrome
|
|
C536188||lagophthalmia with bilateral cleft lip and palate
|
|
C536189||ectrodactyly cleft lip palate syndrome
|
|
C536189||cleft lip cleft palate lobster claw deformity syndrome
|
|
C536189||ectrodactyly ectodermal dysplasia clefting eec syndrome
|
|
C536189||eec syndrome
|
|
C536189||rudiger syndrome 1
|
|
C536189||walker clodius syndrome
|
|
C567305|612448||age related hearing impairment 1
|
|
C567305|612448||arhi1
|
|
C567305|612448||presbycusis 1
|
|
611093|C567016||mental retardation autosomal recessive 7
|
|
611093|C567016||mental retardation autosomal recessive 22
|
|
611093|C567016||mrt22
|
|
611093|C567016||mrt7
|
|
C537537|605407||segawa syndrome autosomal recessive
|
|
C537537|605407||autosomal recessive infantile parkinsonism
|
|
C537537|605407||dopa responsive dystonia autosomal recessive
|
|
C537537|605407||dystonia dopa responsive autosomal recessive
|
|
C537537|605407||dystonia dopa responsive with or without hyperphenylalaninemia autosomal recessive
|
|
C537537|605407||parkinsonism infantile autosomal recessive
|
|
C537537|605407||th deficient drd
|
|
C537537|605407||tyrosine hydroxylase deficiency
|
|
C566236|108985||sveinsson chorioretinal atrophy
|
|
C566236|108985||aa
|
|
C566236|108985||atrophia areata
|
|
C566236|108985||helicoidal peripapillary chorioretinal degeneration
|
|
C566236|108985||hpcd
|
|
C566236|108985||peripapillary chorioretinal degeneration icelandic type
|
|
C566236|108985||scra
|
|
D044148||lymphatic abnormalities
|
|
D044148||abnormalities lymphatic
|
|
D044148||abnormality lymphatic
|
|
D044148||lymphatic abnormality
|
|
C536182||ectodermal dysplasia sensorineural hearing loss and distinctive facial features
|
|
275350||transcobalamin ii deficiency
|
|
275350||tc ii deficiency
|
|
275350||tcn2 deficiency
|
|
C536180||ectodermal dysplasia hidrotic christianson fourie type
|
|
C566921|611548||premature ovarian failure 5
|
|
C566921|611548||pof5
|
|
607196|C538247||amish lethal microcephaly
|
|
607196|C538247||amish microcephaly
|
|
607196|C538247||mcpha
|
|
607196|C538247||microcephaly amish type
|
|
607196|C538247||thiamine metabolism dysfunction syndrome 3 microcephaly type
|
|
607196|C538247||thmd3
|
|
D056124||slit ventricle syndrome
|
|
D056124||slit ventricle syndromes
|
|
D056124||syndrome slit ventricle
|
|
D056124||syndromes slit ventricle
|
|
D006010|232400||glycogen storage disease type iii
|
|
D006010|232400||agl deficiency
|
|
D006010|232400||amylo 1 6 glucosidase deficiencies
|
|
D006010|232400||amylo 1 6 glucosidase deficiency
|
|
D006010|232400||cori disease
|
|
D006010|232400||cori apos s disease
|
|
D006010|232400||coris disease
|
|
D006010|232400||debrancher deficiencies
|
|
D006010|232400||debrancher deficiencies glycogen
|
|
D006010|232400||debrancher deficiency
|
|
D006010|232400||debrancher deficiency glycogen
|
|
D006010|232400||deficiencies amylo 1 6 glucosidase
|
|
D006010|232400||deficiencies debrancher
|
|
D006010|232400||deficiencies glycogen debrancher
|
|
D006010|232400||deficiency amylo 1 6 glucosidase
|
|
D006010|232400||deficiency debrancher
|
|
D006010|232400||deficiency glycogen debrancher
|
|
D006010|232400||dextrinoses limit
|
|
D006010|232400||dextrinosis limit
|
|
D006010|232400||disease cori
|
|
D006010|232400||disease cori apos s
|
|
D006010|232400||disease forbes
|
|
D006010|232400||forbes disease
|
|
D006010|232400||gde deficiency glycogen storage disease iiia included
|
|
D006010|232400||glycogen debrancher deficiencies
|
|
D006010|232400||glycogen debrancher deficiency
|
|
D006010|232400||glycogen debranching enzyme deficiency
|
|
D006010|232400||glycogenosis 3
|
|
D006010|232400||glycogenosis 3s
|
|
D006010|232400||glycogen storage disease iii
|
|
D006010|232400||glycogen storage disease iiib included
|
|
D006010|232400||glycogen storage disease iiic included
|
|
D006010|232400||glycogen storage disease iiid included
|
|
D006010|232400||glycogen storage disease type 3
|
|
D006010|232400||gsd3
|
|
D006010|232400||gsd iiia included
|
|
D006010|232400||gsd iiib included
|
|
D006010|232400||gsd iiic included
|
|
D006010|232400||gsd iiid included
|
|
D006010|232400||limit dextrinoses
|
|
D006010|232400||limit dextrinosis
|
|
D014286||trilogy of fallot
|
|
D014286||fallot apos s trilogy
|
|
D014286||fallots trilogy
|
|
D014286||fallot trilogy
|
|
D014286||trilogy fallot apos s
|
|
C562481||urticaria aquagenic
|
|
D056128||obesity abdominal
|
|
D056128||abdominal obesities
|
|
D056128||abdominal obesity
|
|
D056128||central obesities
|
|
D056128||central obesity
|
|
D056128||obesities abdominal
|
|
D056128||obesities central
|
|
D056128||obesities visceral
|
|
D056128||obesity central
|
|
D056128||obesity visceral
|
|
D056128||visceral obesities
|
|
D056128||visceral obesity
|
|
139393|D020275||guillain barre syndrome
|
|
139393|D020275||acute autoimmune neuropathies
|
|
139393|D020275||acute autoimmune neuropathy
|
|
139393|D020275||acute infectious polyneuritis
|
|
139393|D020275||acute inflammatory demyelinating polyneuropathy
|
|
139393|D020275||acute inflammatory demyelinating polyradiculoneuropathy
|
|
139393|D020275||acute inflammatory polyneuropathies
|
|
139393|D020275||acute inflammatory polyneuropathy
|
|
139393|D020275||acute inflammatory polyradiculoneuropathies
|
|
139393|D020275||acute inflammatory polyradiculoneuropathy
|
|
139393|D020275||autoimmune neuropathies acute
|
|
139393|D020275||autoimmune neuropathy acute
|
|
139393|D020275||cidp included
|
|
139393|D020275||demyelinating polyradiculoneuropathy acute inflammatory
|
|
139393|D020275||gbs
|
|
139393|D020275||guillain barr 233 syndrome
|
|
139393|D020275||guillain barre syndrome familial
|
|
139393|D020275||guillaine barre syndrome
|
|
139393|D020275||inflammatory demyelinating polyradiculoneuropathy acute
|
|
139393|D020275||inflammatory polyneuropathies acute
|
|
139393|D020275||inflammatory polyneuropathy acute
|
|
139393|D020275||inflammatory polyneuropathy acutes
|
|
139393|D020275||inflammatory polyradiculoneuropathies acute
|
|
139393|D020275||landry guillain barre syndrome
|
|
139393|D020275||neuropathies acute autoimmune
|
|
139393|D020275||neuropathy acute autoimmune
|
|
139393|D020275||polyneuropathies acute inflammatory
|
|
139393|D020275||polyneuropathy acute inflammatory
|
|
139393|D020275||polyneuropathy inflammatory demyelinating acute
|
|
139393|D020275||polyneuropathy inflammatory demyelinating acute aidp polyneuropathy inflammatory demyelinating chronic included
|
|
139393|D020275||polyradiculoneuropathies acute inflammatory
|
|
139393|D020275||polyradiculoneuropathy acute inflammatory
|
|
139393|D020275||polyradiculoneuropathy acute inflammatory demyelinating
|
|
139393|D020275||syndrome guillain barre
|
|
139393|D020275||syndrome guillaine barre
|
|
139393|D020275||syndrome landry guillain barre
|
|
C562484||hairy ears
|
|
C562484||hypertrichosis pinnae auris
|
|
C536197||ehlers danlos syndrome type 5
|
|
C536197||ehlers danlos syndrome type v
|
|
C562485||pili torti
|
|
C562485||twisted hair
|
|
C567377|612262||inflammatory bowel disease 18
|
|
C567377|612262||ibd18
|
|
C562483||granulosis rubra nasi
|
|
C562489||lymphoid interstitial pneumonia
|
|
C562486||perifolliculitis capitis abscedens et suffodiens familial
|
|
C562486||dissecting cellulitis of the scalp
|
|
C564596|607304||cataract nuclear progressive
|
|
C564596|607304||cataract 27
|
|
C564596|607304||cataract 27 nuclear progressive
|
|
C564596|607304||cataract congenital nuclear progressive
|
|
C564596|607304||ccnp
|
|
C564596|607304||ctrct27
|
|
C536199||ehlers danlos syndrome beasley cohen type
|
|
C536199||ehlers danlos syndrome with mental retardation deafness and cataract
|
|
C562487||eosinophilic fasciitis
|
|
D007645|248300||keratoderma palmoplantar
|
|
D007645|248300||de meleda mal
|
|
D007645|248300||disease meleda
|
|
D007645|248300||hyperkeratosis palmaris et plantaris
|
|
D007645|248300||keratodermas palmoplantar
|
|
D007645|248300||keratoses palmoplantar
|
|
D007645|248300||keratosis palmaris et plantaris
|
|
D007645|248300||keratosis palmoplantar
|
|
D007645|248300||keratosis palmoplantaris transgradiens of siemens
|
|
D007645|248300||keratosis palmoplantaris transgrediens of siemens
|
|
D007645|248300||mal de meleda
|
|
D007645|248300||mdm
|
|
D007645|248300||meleda disease
|
|
D007645|248300||meleda mal de
|
|
D007645|248300||palmoplantar keratoderma
|
|
D007645|248300||palmoplantar keratodermas
|
|
D007645|248300||palmoplantar keratoses
|
|
D007645|248300||palmoplantar keratosis
|
|
222800||bisphosphoglycerate mutase deficiency
|
|
222800||bisphosphoglyceromutase deficiency
|
|
222800||bpgm deficiency
|
|
222800||diphosphoglycerate mutase deficiency of erythrocyte
|
|
222800||dpgm deficiency
|
|
C536742|241080||woodhouse sakati syndrome
|
|
C536742|241080||extrapyramidal disorder progressive with primary hypogonadism mental retardation and alopecia
|
|
C536742|241080||hypogonadism alopecia diabetes mellitus mental retardation and extrapyramidal syndrome
|
|
C536742|241080||hypogonadism alopecia diabetes mellitus mental retardation deafness and extrapyramidal syndrome
|
|
C562492||robinow syndrome autosomal dominant
|
|
C562492||acral dysostosis with facial and genital abnormalities
|
|
C562492||fetal face syndrome
|
|
C562492||mesomelic dwarfism small genitalia syndrome
|
|
C562492||robinow dwarfism
|
|
C562492||robinow silverman smith syndrome
|
|
C562492||robinow syndrome
|
|
C562451||hyperbilirubinemia shunt
|
|
C563781||erythrokeratoderma reticular
|
|
C563781||aarau disease
|
|
C563780||branchiogenic deafness syndrome
|
|
C563787||tibia bowing of with pseudarthrosis and pectus excavatum
|
|
C562456||volvulus of midgut
|
|
C567686|613243||cardiomyopathy familial hypertrophic 13
|
|
C567686|613243||cmh13
|
|
C563784||arrhythmogenic right ventricular dysplasia familial 7
|
|
C563784||arrhythmogenic right ventricular cardiomyopathy 7
|
|
C563784|601419||desmin related myopathy with arrhythmogenic right ventricular cardiomyopathy
|
|
C563784|601419||myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy
|
|
C563784||myopathy desmin related with arrhythmogenic right ventricular cardiomyopathy
|
|
C566381|603387||megalanecephaly polymicrogyria polydactyly hydrocephalus syndrome
|
|
C566381|603387||megalencephaly mega corpus callosum and complete lack of motor development
|
|
C566381|603387||megalencephaly polymicrogyria mega corpus callosum syndrome
|
|
C566381|603387||megalencephaly polymicrogyria polydactyly hydrocephalus syndrome
|
|
C566381|603387||meg pmg megacc syndrome
|
|
C566381|603387||mpph
|
|
D002288||adenocarcinoma mucinous
|
|
D002288||adenocarcinomas mucinous
|
|
D002288||carcinoma colloid
|
|
D002288||carcinoma mucinous
|
|
D002288||carcinomas colloid
|
|
D002288||carcinomas mucinous
|
|
D002288||colloid carcinoma
|
|
D002288||colloid carcinomas
|
|
D002288||mucinous adenocarcinoma
|
|
D002288||mucinous adenocarcinomas
|
|
D002288||mucinous carcinoma
|
|
D002288||mucinous carcinomas
|
|
D002289||carcinoma non small cell lung
|
|
D002289||carcinomas non small cell lung
|
|
D002289||lung carcinoma non small cell
|
|
D002289||lung carcinomas non small cell
|
|
D002289||nonsmall cell lung cancer
|
|
D002289||non small cell lung cancer
|
|
D002289||non small cell lung carcinoma
|
|
D002289||non small cell lung carcinomas
|
|
D056150||acute generalized exanthematous pustulosis
|
|
D056150||acute localized exanthematous pustulosis
|
|
D056150||pustulosis exanthematous acute generalized
|
|
D056150||pustulosis exanthematous acute localized
|
|
D002284||carcinoma brown pearce
|
|
D002284||brown pearce carcinoma
|
|
D002284||brown pearce epithelioma
|
|
D002284||epithelioma brown pearce
|
|
D002285||carcinoma intraductal noninfiltrating
|
|
D002285||carcinoma intraductal
|
|
D002285||carcinoma noninfiltrating intraductal
|
|
D002285||carcinomas intraductal
|
|
D002285||carcinomas noninfiltrating intraductal
|
|
D002285||dcis
|
|
D002285||ductal carcinoma in situ
|
|
D002285||intraductal carcinoma
|
|
D002285||intraductal carcinoma noninfiltrating
|
|
D002285||intraductal carcinomas
|
|
D002285||intraductal carcinomas noninfiltrating
|
|
D002285||noninfiltrating intraductal carcinoma
|
|
D002285||noninfiltrating intraductal carcinomas
|
|
D002286||carcinoma ehrlich tumor
|
|
D002286||ascites tumor ehrlich
|
|
D002286||ehrlich ascites tumor
|
|
D002286||ehrlich tumor carcinoma
|
|
D002286||tumor ehrlich ascites
|
|
C535896|601287||limb girdle muscular dystrophy type 2f
|
|
C535896|601287||lgmd2f
|
|
C535896|601287||muscular dystrophy limb girdle type 2f
|
|
C535896|601287||muscular dystrophy limb girdle with delta sarcoglyan deficiency
|
|
D002287||carcinoma krebs 2
|
|
D002287||krebs 2 carcinoma
|
|
C563690|609909||cardiomyopathy dilated 1p
|
|
C563690|609909||cmd1p
|
|
D002291||carcinoma papillary
|
|
D002291||carcinomas papillary
|
|
D002291||papillary carcinoma
|
|
D002291||papillary carcinomas
|
|
D056146||corpse dismemberment
|
|
D056146||cadaver dismemberment
|
|
D056146||cadaver dismemberments
|
|
D056146||corpse dismemberments
|
|
D056146||dismemberment cadaver
|
|
D056146||dismemberment corpse
|
|
D056146||dismemberments cadaver
|
|
D056146||dismemberments corpse
|
|
D002293||adenocarcinoma scirrhous
|
|
D002293||adenocarcinomas scirrhous
|
|
D002293||carcinoma scirrhous
|
|
D002293||carcinomas scirrhous
|
|
D002293||scirrhous adenocarcinoma
|
|
D002293||scirrhous adenocarcinomas
|
|
D002293||scirrhous carcinoma
|
|
D002293||scirrhous carcinomas
|
|
D002294||carcinoma squamous cell
|
|
D002294||carcinoma epidermoid
|
|
D002294||carcinoma planocellular
|
|
D002294||carcinomas epidermoid
|
|
D002294||carcinomas planocellular
|
|
D002294||carcinoma squamous
|
|
D002294||carcinomas squamous
|
|
D002294||carcinomas squamous cell
|
|
D002294||epidermoid carcinoma
|
|
D002294||epidermoid carcinomas
|
|
D002294||planocellular carcinoma
|
|
D002294||planocellular carcinomas
|
|
D002294||squamous carcinoma
|
|
D002294||squamous carcinomas
|
|
D002294||squamous cell carcinoma
|
|
D002294||squamous cell carcinomas
|
|
D015597||pregnancy complications parasitic
|
|
D015597||complication parasitic pregnancy
|
|
D015597||complications parasitic pregnancy
|
|
D015597||complications pregnancies parasitic
|
|
D015597||complications pregnancy parasitic
|
|
D015597||parasitic complications pregnancies
|
|
D015597||parasitic complications pregnancy
|
|
D015597||parasitic pregnancy complication
|
|
D015597||parasitic pregnancy complications
|
|
D015597||pregnancies parasitic complications
|
|
D015597||pregnancy complication parasitic
|
|
D015597||pregnancy parasitic complications
|
|
D014264||tricuspid valve stenosis
|
|
D014264||stenoses tricuspid valve
|
|
D014264||stenosis tricuspid valve
|
|
D014264||tricuspid valve stenoses
|
|
D014264||valve stenoses tricuspid
|
|
D014264||valve stenosis tricuspid
|
|
D014263||tricuspid valve prolapse
|
|
D014263||prolapses tricuspid valve
|
|
D014263||prolapse tricuspid valve
|
|
D014263||tricuspid valve prolapses
|
|
D014263||valve prolapses tricuspid
|
|
D014263||valve prolapse tricuspid
|
|
D015594||optic disk drusen
|
|
D015594||drusen optic disc
|
|
D015594||drusen optic disk
|
|
D015594||drusen optic nerve
|
|
D015594||optic disc drusen
|
|
D015594||optic disc drusens
|
|
D015594||optic disk drusens
|
|
D015594||optic nerve drusen
|
|
182212|C537328||shprintzen golberg craniosynostosis
|
|
182212|C537328||craniosynostosis and marfanoid disorder type 1
|
|
182212|C537328||craniosynostosis with arachnodactyly and abdominal hernias
|
|
182212|C537328||marfanoid craniosynostosis syndrome
|
|
182212|C537328||marfanoid disorder with craniosynostosis type i
|
|
182212|C537328|C536632|269150||sgs
|
|
182212|C537328||shprintzen golberg craniosynostosis syndrome
|
|
182212|C537328||shprintzen goldberg craniosynostosis syndrome
|
|
182212|C537328||shprintzen goldberg syndrome
|
|
C536632|269150||schinzel giedion syndrome
|
|
C536632|269150||schinzel giedion midface retraction syndrome
|
|
C562461||annular erythema
|
|
C567475|300707||toe syndactyly telecanthus and anogenital and renal malformations
|
|
C567475|300707||star
|
|
C567475|300707||star syndrome
|
|
C567475|300707||syndactyly with renal and anogenital malformations
|
|
226730|C535377||epidermolysis bullosa with pyloric atresia
|
|
226730|C535377||aplasia cutis congenita with gastrointestinal atresia
|
|
226730|C535377||carmi syndrome
|
|
226730|C535377||eb pa
|
|
226730|C535377||eb pa acc
|
|
226730|C535377||epidermolysis bullosa junctionalis with pyloric atresia
|
|
226730|C535377||epidermolysis bullosa junctional with pyloric atresia
|
|
226730|C535377||epidermylosis bullosa junctional with pyloric atresia and aplasia cutis congenita
|
|
226730|C535377||jeb pa
|
|
226730|C535377||junctional epidermolysis bullosa with pyloric atresia
|
|
226730|C535377||pa jeb
|
|
C562464||polyposis gastric
|
|
208540||renal hepatic pancreatic dysplasia 1
|
|
208540||rhpd
|
|
208540||rhpd1
|
|
C562469||paralysis agitans juvenile of hunt
|
|
C562469||parkinson disease juvenile of hunt
|
|
C565551|231095||ghosal hematodiaphyseal dysplasia
|
|
C565551|231095||ghdd
|
|
C565551|231095||ghosal syndrome
|
|
D002295||carcinoma transitional cell
|
|
D002295||carcinomas transitional cell
|
|
D002295||cell carcinomas transitional
|
|
D002295||cell carcinoma transitional
|
|
D002295||transitional cell carcinoma
|
|
D002295||transitional cell carcinomas
|
|
D002296||carcinosarcoma
|
|
D002296||carcinosarcomas
|
|
180550|C535684||ring dermoid of cornea
|
|
180550|C535684||bilateral annular limbal dermoids with corneal and conjunctival extension
|
|
180550|C535684||rdc
|
|
180550|C535684||ring dermoid syndrome
|
|
C537393|601321||neurofibromatosis noonan syndrome
|
|
C537393|601321||neurofibromatosis with noonan phenotype
|
|
C537393|601321||nfns
|
|
C537393|601321||noonan neurofibromatosis syndrome
|
|
C565324|605543||parkinson disease 4 autosomal dominant lewy body
|
|
C565324|605543||park4
|
|
C565324|605543||parkinson disease 4 autosomal dominant
|
|
300607|C564474||hyperekplexia and epilepsy
|
|
300607|C564474||eiee8
|
|
300607|C564474||epileptic encephalopathy early infantile 8
|
|
D056151||airway remodeling
|
|
D056151||airway remodeling asthmatic
|
|
D056151||airway remodelings
|
|
D056151||airway remodelings asthmatic
|
|
D056151||airway remodeling small
|
|
D056151||airway remodelings small
|
|
D056151||airway remodelling
|
|
D056151||airway remodelling asthmatic
|
|
D056151||airway remodellings
|
|
D056151||airway remodellings asthmatic
|
|
D056151||airway remodelling small
|
|
D056151||airway remodellings small
|
|
D056151||airway wall remodelling
|
|
D056151||airway wall remodellings
|
|
D056151||asthmatic airway remodeling
|
|
D056151||asthmatic airway remodelings
|
|
D056151||asthmatic airway remodelling
|
|
D056151||asthmatic airway remodellings
|
|
D056151||asthmatic airway wall remodeling
|
|
D056151||asthmatic airway wall remodelling
|
|
D056151||remodeling airway
|
|
D056151||remodeling asthmatic airway
|
|
D056151||remodelings airway
|
|
D056151||remodelings asthmatic airway
|
|
D056151||remodeling small airway
|
|
D056151||remodelings small airway
|
|
D056151||remodelling airway
|
|
D056151||remodelling airway wall
|
|
D056151||remodelling asthmatic airway
|
|
D056151||remodellings airway
|
|
D056151||remodellings airway wall
|
|
D056151||remodellings asthmatic airway
|
|
D056151||remodelling small airway
|
|
D056151||remodellings small airway
|
|
D056151||small airway remodeling
|
|
D056151||small airway remodelings
|
|
D056151||small airway remodelling
|
|
D056151||small airway remodellings
|
|
D056151||wall remodelling airway
|
|
D056151||wall remodellings airway
|
|
604273||mitochondrial complex v atp synthase deficiency nuclear type 1 mc5dn1 mitochondrial complex v atp synthase deficiency atpaf2 type
|
|
D014277||trigeminal neuralgia
|
|
D014277||disease fothergill
|
|
D014277||epileptiform neuralgia
|
|
D014277||epileptiform neuralgias
|
|
D014277||fothergill disease
|
|
D014277||idiopathic trigeminal neuralgia
|
|
D014277||idiopathic trigeminal neuralgias
|
|
D014277||neuralgia epileptiform
|
|
D014277||neuralgia idiopathic trigeminal
|
|
D014277||neuralgia secondary trigeminal
|
|
D014277||neuralgias epileptiform
|
|
D014277||neuralgias idiopathic trigeminal
|
|
D014277||neuralgias secondary trigeminal
|
|
D014277||neuralgias trifacial
|
|
D014277||neuralgias trigeminal
|
|
D014277||neuralgia trifacial
|
|
D014277||neuralgia trigeminal
|
|
D014277||secondary trigeminal neuralgia
|
|
D014277||secondary trigeminal neuralgias
|
|
D014277||tic douloureux
|
|
D014277||trifacial neuralgia
|
|
D014277||trifacial neuralgias
|
|
D014277||trigeminal neuralgia idiopathic
|
|
D014277||trigeminal neuralgias
|
|
D014277||trigeminal neuralgia secondary
|
|
D014277||trigeminal neuralgias idiopathic
|
|
D014277||trigeminal neuralgias secondary
|
|
D038223||post concussion syndrome
|
|
D038223||chronic post concussive syndrome
|
|
D038223||chronic post concussive syndromes
|
|
D038223||post concussion symptom
|
|
D038223||post concussion symptoms
|
|
D038223||post concussive symptom
|
|
D038223||post concussive symptoms
|
|
D038223||post concussive syndrome
|
|
D038223||post concussive syndrome chronic
|
|
D038223||post concussive syndromes
|
|
D038223||post concussive syndromes chronic
|
|
D038223||symptom post concussive
|
|
D038223||syndrome chronic post concussive
|
|
D038223||syndrome post concussive
|
|
D038223||syndromes chronic post concussive
|
|
D038223||syndromes post concussive
|
|
C567435|612017||pyloric stenosis infantile hypertrophic 3
|
|
C567435|612017||ihps3
|
|
C566916|611560||joubert syndrome 7
|
|
C566916|611560||jbts7
|
|
C537473||milner khallouf gibson syndrome
|
|
C536142||megalencephaly cutis marmorata telangiectatica congenita
|
|
C536142||macrocephaly capillary malformation
|
|
C536142||macrocephaly cutis marmorata telangiectatica congenita
|
|
C536142||megalocephaly cutis marmorata telangiectatica congenita
|
|
C537474||minicore myopathy antenatal onset with arthrogryposis
|
|
C537474||multicore myopathy antenatal onset with arthrogryposis
|
|
C537474||multiminicore myopathy antenatal onset with arthrogryposis
|
|
C536143||neuhauser syndrome
|
|
C536143||cerebral palsy hypotonic seizures megalcornea syndrome
|
|
C536143||megalocornea macrocephaly mental and motor retardation mmmm syndrome
|
|
C536143||megalocornea mental retardation syndrome
|
|
C536143||mmr syndrome
|
|
C536143||seizures hypotonic cerebral palsy megalocornea mental retardation syndrome
|
|
C536915|188550||thyroid cancer papillary
|
|
C536915|188550||familial nonmedullary thyroid cancer
|
|
C536915|188550||familial nonmedullary thyroid cancer papillary
|
|
C536915|188550||nonmedullary thyroid carcinoma
|
|
C536915|188550||nonmedullary thyroid carcinoma papillary
|
|
C536915|188550||pact
|
|
C536915|188550||papillary carcinoma of thyroid
|
|
C536915|188550||papillary thyroid carcinoma
|
|
C536915|188550||ptc
|
|
C536915|188550||thyroid carcinoma papillary
|
|
C536915|188550||tpc
|
|
C537471||midphalangeal hair
|
|
C537471||middigital hair
|
|
C536140||megaepiphyseal dwarfism
|
|
C536140|215150||chondrodystrophy with sensorineural deafness
|
|
C536140||insley astley syndrome
|
|
C536140||mega epiphyseal dwarfism
|
|
C536140|215150||nance insley syndrome
|
|
C536140|215150||nance sweeney chondrodysplasia
|
|
C536140|215150||otospondylomegaepiphyseal dysplasia
|
|
C536140||oto spondylo megaepiphyseal dysplasia
|
|
C536140||oto spondylo mega epiphyseal dysplasia
|
|
C563765||hypotrichosis progressive patterned scalp with wiry hair onycholysis and cleft lip palate
|
|
C563765||marie unna like scalp hypotrichosis
|
|
C537477||mitochondrial neurogastrointestinal encephalopathy syndrome
|
|
C537477||mitochondrial dna depletion syndrome 1
|
|
C537477||mitochondrial dna depletion syndrome 8a
|
|
C537477||mitochondrial dna depletion syndrome encephalomyopathic form with renal tubulopathy autosomal recessive
|
|
C537477||mitochondrial myopathy with sensorimotor polyneuropathy ophthalmoplegia and pseudo obstruction
|
|
C537477||mitochondrial neurogastrointestinal encephalopathy disease
|
|
C537477||mitochondrial neurogastrointestinal encephalopathy syndrome rrm2b related
|
|
C537477||mngie disease
|
|
C537477||mngie rrm2b related
|
|
C537477||mngie syndrome
|
|
C537477||mngie without leukoencephalopathy
|
|
C537477||oculogastrointestinal muscular dystrophy
|
|
C537477||polyneuropathy ophthalmoplegia leukoencephalopathy and intestinal pseudo obstruction
|
|
C537477||thymidine phosphorylase deficiency
|
|
C536146||mehes syndrome
|
|
C537478||mitral valve prolapse familial x linked
|
|
C537478|157700||barlow syndrome
|
|
C537478|157700||mitral regurgitation familial
|
|
C537478|157700||myxomatous valvular disease familial
|
|
C536147||mehta lewis patton syndrome
|
|
C536147||congenital heart disease ptosis hypodontia and craniosynostosis
|
|
C536144||megalocytic interstitial nephritis
|
|
C536144||interstitial megalocytic nephritis
|
|
C536144||transplant megalocytic interstitial nephritis type
|
|
137440|D016098||gerstmann straussler scheinker disease
|
|
137440|D016098||disease gerstmann straussler
|
|
137440|D016098||diseases gerstmann straussler
|
|
137440|D016098||encephalopathy subacute spongiform gerstmann straussler type
|
|
137440|D016098||gerstmann straussler disease
|
|
137440|D016098||gerstmann straussler diseases
|
|
137440|D016098||gerstmann straussler inherited spongiform encephalopathy
|
|
137440|D016098||gerstmann straussler scheinker syndrome
|
|
137440|D016098||gerstmann straussler syndrome
|
|
137440|D016098||gsd
|
|
137440|D016098||gss
|
|
137440|D016098||inherited spongiform encephalopathy gerstmann straussler
|
|
137440|D016098||prion dementia cerebral amyloid angiopathy prnp related included
|
|
C537476||mitochondrial myopathy with lactic acidosis
|
|
C536145||megarbane syndrome
|
|
C562438||hemangiomatosis cutaneous with associated features
|
|
C562435||choanal atresia posterior
|
|
603622|C538050||deafness autosomal dominant nonsyndromic sensorineural 17
|
|
603622|C538050||cochleosaccular degeneration included
|
|
603622|C538050|153640|C535507||deafness autosomal dominant 17
|
|
603622|C538050|153640|C535507||dfna17
|
|
603622|C538050||late onset progressive hereditary hearing impairment due to cochleosaccular degeneration
|
|
C537483|604360||spastic paraplegia 11 autosomal recessive
|
|
C537483|604360|C580453||hsp tcc
|
|
C537483|604360||spastic paraplegia autosomal recessive complicated with thin corpus callosum
|
|
C537483|604360||spastic paraplegia autosomal recessive with mental impairment and thin corpus callosum
|
|
C537483|604360||spg11
|
|
C567408|612138||epidermolysis bullosa simplex with pyloric atresia
|
|
C567408|612138||ebs pa
|
|
C567408|612138||ebs with pyloric atresia
|
|
C567382|612247||crouzon syndrome with acanthosis nigricans
|
|
C567382|612247||can
|
|
C567382|612247||crouzonodermoskeletal syndrome
|
|
D002270||carbuncle
|
|
D002270||carbuncles
|
|
C566617|601846||vacuolar neuromyopathy
|
|
C566617|601846||mdrv
|
|
C566617|601846||muscular dystrophy autosomal dominant with rimmed vacuoles
|
|
191181||suppressor of tumorigenicity 3
|
|
191181||ccts
|
|
191181||cervical carcinoma tumor suppressor gene involved in
|
|
191181||st3
|
|
191181||tshl
|
|
191181||tumor suppressor gene hela cell type
|
|
C567057|610852||ciliary dyskinesia primary 6
|
|
C567057|610852||cild6
|
|
C536139||megaduodenum
|
|
C536139||fetal megacystis
|
|
C536139||megacystis
|
|
C565629|222400||diaphragmatic hernia 2
|
|
C565629|222400||dih2
|
|
C537468||microspherophakia with hernia
|
|
C537469||microtia meatal atresia and conductive deafness
|
|
C537469||familial microtia and meatal atresia
|
|
C537469||familial microtia with meatal atresia and conductive deafness
|
|
C537469||gupta patton syndrome
|
|
C537469||microtia meatal atresia deafness dominant
|
|
C537469||microtia with meatal atresia and conductive deafness
|
|
C536138|155310||megacystis microcolon intestinal hypoperistalsis syndrome
|
|
C536138|155310||berdon syndrome
|
|
C563375|239200||hyperparathyroidism neonatal severe primary
|
|
C563375|239200||hyperparathyroidism neonatal severe
|
|
C563375|239200||nhpt
|
|
C563375|239200||nshpt
|
|
C563375|239200||nsph
|
|
D014247||trichomonas vaginitis
|
|
D014247||trichomonas vaginitides
|
|
D014247||vaginitides trichomonas
|
|
D014247||vaginitis trichomonas
|
|
D014245||trichomonas infections
|
|
D014245||infections trichomonas
|
|
D014245||infection trichomonas
|
|
D014245||trichomonas infection
|
|
D015576||hyperostosis
|
|
D015576||bone hypertrophies
|
|
D015576||bone hypertrophy
|
|
D015576||hyperostoses
|
|
D015576||hypertrophies bone
|
|
D015576||hypertrophy bone
|
|
C563772||spondyloepiphyseal dysplasia tarda autosomal recessive leroy spranger type
|
|
C536153||keratoderma palmoplantar spastic paralysis
|
|
C536153||axonal neuropathy with palmoplantar keratoderma
|
|
C536153||charcot marie tooth disease with palmoplantar keratoderma and nail dystrophy
|
|
C536153||keratoderma palmoplantar with nail dystrophy and hereditary motor sensory neuropathy
|
|
C536154||keratoderma palmoplantaris transgrediens
|
|
C536154||erythrokeratodermia variabilis with erythema gyratum repens
|
|
C536154||keratosis palmoplantaris transgrediens et progrediens
|
|
248600|D008375||maple syrup urine disease
|
|
248600|D008375||bckd deficiency
|
|
248600|D008375||branched chain alpha keto acid dehydrogenase deficiency
|
|
248600|D008375||branched chain ketoaciduria
|
|
248600|D008375||branched chain ketoacidurias
|
|
248600|D008375||classical maple syrup urine disease
|
|
248600|D008375||classic maple syrup urine disease
|
|
248600|D008375||intermediate maple syrup urine disease
|
|
248600|D008375||intermittent maple syrup urine disease
|
|
248600|D008375||keto acid decarboxylase deficiency
|
|
248600|D008375||keto acid decarboxylase deficiency maple syrup urine disease classic included
|
|
248600|D008375||ketoaciduria branched chain
|
|
248600|D008375||ketoacidurias branched chain
|
|
248600|D008375||maple syrup urine disease classic
|
|
248600|D008375||maple syrup urine disease classical
|
|
248600|D008375||maple syrup urine disease intermediate
|
|
248600|D008375||maple syrup urine disease intermediate included
|
|
248600|D008375||maple syrup urine disease intermittent
|
|
248600|D008375||maple syrup urine disease intermittent included
|
|
248600|D008375||maple syrup urine disease thiamine responsive
|
|
248600|D008375||maple syrup urine disease thiamine responsive included
|
|
248600|D008375||maple syrup urine disease type ia included
|
|
248600|D008375||maple syrup urine disease type ib included
|
|
248600|D008375||maple syrup urine disease type ii included
|
|
248600|D008375||msud
|
|
248600|D008375||msud1a included
|
|
248600|D008375||msud1b included
|
|
248600|D008375||msud2 included
|
|
248600|D008375||msud maple syrup urine disease
|
|
248600|D008375||thiamine responsive maple syrup urine disease
|
|
C536151||keratoconus posticus circumscriptus
|
|
C537488||stern lubinsky durrie syndrome
|
|
C536157||keratosis focal palmoplantar gingival
|
|
C536157||focal palmoplantar and gingival hyperkeratosis syndrome
|
|
C536157||focal palmoplantar and oral mucosa hyperkeratosis
|
|
C536157||keratosis focal palmoplantar and gingival
|
|
D014262||tricuspid valve insufficiency
|
|
D014262||incompetence tricuspid
|
|
D014262||incompetence tricuspid valve
|
|
D014262||insufficiency tricuspid valve
|
|
D014262||regurgitation tricuspid
|
|
D014262||regurgitation tricuspid valve
|
|
D014262||tricuspid incompetence
|
|
D014262||tricuspid regurgitation
|
|
D014262||tricuspid valve incompetence
|
|
D014262||tricuspid valve regurgitation
|
|
D014262||valve incompetence tricuspid
|
|
D014262||valve insufficiency tricuspid
|
|
D014262||valve regurgitation tricuspid
|
|
D015593||retinal drusen
|
|
D015593||drusen retinal
|
|
C537489||sternal cleft
|
|
C537489||congenital sternal cleft
|
|
C536158||keratosis follicularis dwarfism cerebral atrophy
|
|
C536158||keratosis follicularis dwarfism and cerebral atrophy
|
|
C537277|610293||glycosylphosphatidylinositol deficiency
|
|
C537277|610293||gpi deficiency
|
|
C562442||mucopolysaccharidoses unclassified types
|
|
C567543|613079||deafness autosomal recessive 77
|
|
C567543|613079||dfnb77
|
|
D018814|162300||multiple endocrine neoplasia type 2b
|
|
D018814|162300||mea 2b
|
|
D018814|162300||mea iib
|
|
D018814|162300||men2b
|
|
D018814|162300||men 2b
|
|
D018814|162300||men 3
|
|
D018814|162300||men iib
|
|
D018814|162300||men iii
|
|
D018814|162300||mucosal neuroma syndrome
|
|
D018814|162300||mucosal neuroma syndromes
|
|
D018814|162300||multiple endocrine neoplasia type iib
|
|
D018814|162300||multiple endocrine neoplasia type iii formerly men3 formerly mucosal neuroma syndrome included
|
|
D018814|162300||multiple endocrine neoplasms type 2b
|
|
D018814|162300||neoplasia multiple endocrine type 2b
|
|
D018814|162300||neoplasms multiple endocrine type 2b
|
|
D018814|162300||neuroma syndrome mucosal
|
|
D018814|162300||neuromata mucosal with endocrine tumors
|
|
D018814|162300||syndrome wagenmann froboese
|
|
D018814|162300||wagenmann froboese syndrome
|
|
C562443||weaver like syndrome
|
|
C537487||steatocystoma multiplex with natal teeth
|
|
C537487||natal teeth and steatocystoma multiplex
|
|
C536156||keratomalacia
|
|
C536156||retinol deficiency
|
|
C536156||xerotic keratitis
|
|
D002277||carcinoma
|
|
D002277||anaplastic carcinoma
|
|
D002277||anaplastic carcinomas
|
|
D002277||carcinoma anaplastic
|
|
D002277||carcinomas
|
|
D002277||carcinomas anaplastic
|
|
D002277||carcinoma spindle cell
|
|
D002277||carcinomas spindle cell
|
|
D002277||carcinomas undifferentiated
|
|
D002277||carcinomatoses
|
|
D002277||carcinomatosis
|
|
D002277||carcinoma undifferentiated
|
|
D002277||epithelial neoplasm malignant
|
|
D002277||epithelial neoplasms malignant
|
|
D002277||epithelial tumor malignant
|
|
D002277||epithelial tumors malignant
|
|
D002277||epithelioma
|
|
D002277||epitheliomas
|
|
D002277||malignant epithelial neoplasm
|
|
D002277||malignant epithelial neoplasms
|
|
D002277||malignant epithelial tumor
|
|
D002277||malignant epithelial tumors
|
|
D002277||neoplasm malignant epithelial
|
|
D002277||neoplasms malignant epithelial
|
|
D002277||spindle cell carcinoma
|
|
D002277||spindle cell carcinomas
|
|
D002277||tumor malignant epithelial
|
|
D002277||tumors malignant epithelial
|
|
D002277||undifferentiated carcinoma
|
|
D002277||undifferentiated carcinomas
|
|
C537880|607330||lathosterolosis
|
|
C537880|607330||3 beta hydroxysteroid delta 5 desaturase deficiency
|
|
C537880|607330||deficiency of 3 beta hydroxysteroid delta 5 desaturase
|
|
C537880|607330||sc5d deficiency
|
|
C537880|607330||sterol c5 desaturase deficiency
|
|
D002278||carcinoma in situ
|
|
D002278||carcinoma intraepithelial
|
|
D002278||carcinoma preinvasive
|
|
D002278||intraepithelial carcinoma
|
|
D002278||intraepithelial neoplasm
|
|
D002278||intraepithelial neoplasms
|
|
D002278||neoplasm intraepithelial
|
|
D002278||neoplasms intraepithelial
|
|
D002278||preinvasive carcinoma
|
|
C562446||russell silver syndrome x linked
|
|
C562446||russell silver like syndrome with skin pigmentation
|
|
D002279||carcinoma 256 walker
|
|
D002279||carcinosarcoma 256 walker
|
|
D002279||walker carcinoma 256
|
|
D002279||walker carcinosarcoma 256
|
|
D002275||carcinoid heart disease
|
|
D002275||carcinoid heart diseases
|
|
D002275||heart disease carcinoid
|
|
D002275||heart diseases carcinoid
|
|
D002276||carcinoid tumor
|
|
D002276||argentaffinoma
|
|
D002276||argentaffinomas
|
|
D002276||carcinoid
|
|
D002276||carcinoid goblet cell
|
|
D002276||carcinoids
|
|
D002276||carcinoids goblet cell
|
|
D002276||carcinoid tumors
|
|
D002276||goblet cell carcinoid
|
|
D002276||goblet cell carcinoids
|
|
D002276||tumor carcinoid
|
|
D002276||tumors carcinoid
|
|
D002281||carcinoma basosquamous
|
|
D002281||basosquamous carcinoma
|
|
D002281||basosquamous carcinomas
|
|
D002281||carcinomas basosquamous
|
|
D002282||adenocarcinoma bronchiolo alveolar
|
|
D002282||adenocarcinoma alveolar
|
|
D002282||adenocarcinomas alveolar
|
|
D002282||adenocarcinomas bronchiolo alveolar
|
|
D002282||alveolar adenocarcinoma
|
|
D002282||alveolar adenocarcinomas
|
|
D002282||alveolar carcinoma
|
|
D002282||alveolar carcinomas
|
|
D002282||alveolar cell carcinoma
|
|
D002282||bronchiolar carcinoma
|
|
D002282||bronchiolar carcinomas
|
|
D002282||bronchiolo alveolar adenocarcinoma
|
|
D002282||bronchiolo alveolar adenocarcinomas
|
|
D002282||bronchioloalveolar carcinoma
|
|
D002282||bronchiolo alveolar carcinoma
|
|
D002282||bronchioloalveolar carcinomas
|
|
D002282||bronchiolo alveolar carcinomas
|
|
D002282||carcinoma alveolar
|
|
D002282||carcinoma bronchiolar
|
|
D002282||carcinoma bronchioloalveolar
|
|
D002282||carcinoma bronchiolo alveolar
|
|
D002282||carcinomas alveolar
|
|
D002282||carcinomas bronchiolar
|
|
D002282||carcinomas bronchioloalveolar
|
|
D002282||carcinomas bronchiolo alveolar
|
|
D002283||carcinoma bronchogenic
|
|
D002283||bronchial carcinoma
|
|
D002283||bronchial carcinomas
|
|
D002283||bronchogenic carcinoma
|
|
D002283||bronchogenic carcinomas
|
|
D002283||carcinoma bronchial
|
|
D002283||carcinomas bronchial
|
|
D002283||carcinomas bronchogenic
|
|
C562664|300600||aland island eye disease
|
|
C562664|300600||aied
|
|
C562664|300600||forsius eriksson type ocular albinism
|
|
C537479||mixed sclerosing bone dystrophy
|
|
C536148||meier blumberg imahorn syndrome
|
|
C536148||idiopathic hypercalciuria with bilateral macular colobomata
|
|
D014253||trichostrongylosis
|
|
D014253||trichostrongyloses
|
|
D014252||trichostrongyloidiasis
|
|
D014252||trichostrongyloidiases
|
|
D014257||trichuriasis
|
|
D014257||trichocephaliases
|
|
D014257||trichocephaliasis
|
|
D014257||trichuriases
|
|
202400|C531603||afibrinogenemia congenital
|
|
202400|C531603||congenital afibrinogenaemia
|
|
202400|C531603||dysfibrinogenemia congenital included
|
|
202400|C531603||hypodysfibrinogenemia congenital included
|
|
202400|C531603||hypofibrinogenemia congenital
|
|
202400|C531603||hypofibrinogenemia congenital included
|
|
C537496||stoelinga de koomen davis syndrome
|
|
C537496||multiple non erupting teeth maxillo zygomatical hypoplasia and other congenital defects
|
|
C537496||non erupted teeth with maxillary hypoplasia and genu valgum
|
|
D016890||encephalitozoonosis
|
|
D016890||encephalitozoonoses
|
|
D002249||carbon monoxide poisoning
|
|
D002249||carbon monoxide poisonings
|
|
D002249||gas poisoning illuminating
|
|
D002249||gas poisonings illuminating
|
|
D002249||illuminating gas poisoning
|
|
D002249||illuminating gas poisonings
|
|
D002249||monoxide poisoning carbon
|
|
D002249||monoxide poisonings carbon
|
|
D002249||poisoning carbon monoxide
|
|
D002249||poisoning illuminating gas
|
|
D002249||poisonings carbon monoxide
|
|
D002249||poisonings illuminating gas
|
|
C537497||stoll alembik dott syndrome
|
|
C537497||ventricular extrasystoles with syncope perodactyly and robin sequence
|
|
C536166||keshan disease
|
|
C537498||stoll levy francfort syndrome
|
|
C537498||facioauriculoradial dysplasia
|
|
C537498||phocomelia ectrodactyly ear malformation deafness and sinus arrhythmia
|
|
C563745||b cell immunodeficiency distal limb anomalies and urogenital malformations
|
|
C563745||bilu syndrome
|
|
C537491||stewart treves syndrome
|
|
C537491||angiosarcoma associated with chronic lymphedema
|
|
C537491||lymphangiosarcoma following mastectomy
|
|
C537491||postmastectomy extremity angiosarcoma
|
|
306900|D002836||hemophilia b
|
|
306900|D002836||b hemophilia
|
|
306900|D002836||bs hemophilia
|
|
306900|D002836||christmas disease
|
|
306900|D002836||deficiencies f9
|
|
306900|D002836||deficiencies factor ix
|
|
306900|D002836||deficiency f9
|
|
306900|D002836||deficiency factor ix
|
|
306900|D002836||disease christmas
|
|
306900|D002836||f9 deficiencies
|
|
306900|D002836||f9 deficiency
|
|
306900|D002836||factor ix deficiencies
|
|
306900|D002836||factor ix deficiency
|
|
306900|D002836||haemophilia b
|
|
306900|D002836||haemophilia bs
|
|
306900|D002836||hemb
|
|
306900|D002836||hemophilia b leyden
|
|
306900|D002836||hemophilia b leyden included
|
|
306900|D002836||hemophilia b m
|
|
306900|D002836||hemophilia bs
|
|
306900|D002836||hemophilia bs m
|
|
306900|D002836||plasma thromboplastin component deficiency
|
|
306900|D002836||plasma thromboplastin component deficiency hemophilia b m included
|
|
C562417||adactylia unilateral
|
|
C562417||terminal transverse defects of hand unilateral
|
|
C537490||lyngstadaas syndrome
|
|
C537490||steroid dehydrogenase deficiency dental anomalies
|
|
D029503|105650||anemia diamond blackfan
|
|
D029503|105650|612561|C538442||aase smith syndrome ii
|
|
D029503|105650|C538442||aase syndrome
|
|
D029503|105650||anemia blackfan diamond
|
|
D029503|105650|C538442||anemia congenital erythroid hypoplastic
|
|
D029503|105650||anemia congenital hypoplastic of blackfan and diamond
|
|
D029503|105650||anemia diamond blackfan type
|
|
D029503|105650||anemias hypoplastic congenital
|
|
D029503|105650|C538442||aregenerative anemia chronic congenital
|
|
D029503|105650||bds
|
|
D029503|105650||blackfan diamond anemia
|
|
D029503|105650||blackfan diamond disease
|
|
D029503|105650||blackfan diamond syndrome
|
|
D029503|105650||chronic congenital agenerative anemia
|
|
D029503|105650||congenital anemia hypoplastic
|
|
D029503|105650||congenital anemias hypoplastic
|
|
D029503|105650||congenital erythroid hypoplastic anemia
|
|
D029503|105650||congenital hypoplastic anemia of blackfan and diamond
|
|
D029503|105650||congenital pure red cell anemia
|
|
D029503|105650||congenital pure red cell aplasia
|
|
D029503|105650||dba
|
|
D029503|105650||dba1
|
|
D029503|105650||diamond anemia blackfan
|
|
D029503|105650||diamond blackfan anemia
|
|
D029503|105650|C567302||diamond blackfan anemia 1
|
|
D029503|105650||diamond blackfan type anemia
|
|
D029503|105650||disease blackfan diamond
|
|
D029503|105650||erythroblastopenia inherited
|
|
D029503|105650||erythroblastopenias inherited
|
|
D029503|105650||erythrogenesis imperfecta
|
|
D029503|105650||erythrogenesis imperfectas
|
|
D029503|105650||hypoplastic congenital anemia
|
|
D029503|105650||hypoplastic congenital anemias
|
|
D029503|105650||imperfecta erythrogenesis
|
|
D029503|105650||imperfectas erythrogenesis
|
|
D029503|105650||inherited erythroblastopenia
|
|
D029503|105650||inherited erythroblastopenias
|
|
D029503|105650||pure hereditary red cell aplasia
|
|
D029503|105650||red cell aplasia pure hereditary
|
|
D016888||angiodysplasia
|
|
D016888||angiodysplasias
|
|
D016881||microsporidiosis
|
|
D016881||infection microspora
|
|
D016881||infections microspora
|
|
D016881||microspora infection
|
|
D016881||microspora infections
|
|
D016881||microsporidioses
|
|
C562880|130900||amelogenesis imperfecta type iii
|
|
C562880|130900||adhcai
|
|
C562880|130900||ai3
|
|
C562880|130900||amelogenesis imperfecta hypocalcification type autosomal dominant
|
|
C562880|130900||amelogenesis imperfecta hypomineralization type
|
|
D016883||diabetic ketoacidosis
|
|
D016883||acidoses diabetic
|
|
D016883||acidosis diabetic
|
|
D016883||diabetic acidoses
|
|
D016883||diabetic acidosis
|
|
D016883||diabetic ketoacidoses
|
|
D016883||diabetic ketoses
|
|
D016883||diabetic ketosis
|
|
D016883||ketoacidoses diabetic
|
|
D016883||ketoacidosis diabetic
|
|
D016883||ketoses diabetic
|
|
D016883||ketosis diabetic
|
|
D016884||polyendocrinopathies autoimmune
|
|
D016884||aire deficiencies
|
|
D016884||aire deficiency
|
|
D016884|C538275|240300||apeced
|
|
D016884||aps type 1
|
|
D016884||autoimmune polyendocrine syndrome type 2
|
|
D016884||autoimmune polyendocrine syndrome type ii
|
|
D016884||autoimmune polyendocrinopathy
|
|
D016884|C538275|240300||autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
|
|
D016884|C538275|240300||autoimmune polyendocrinopathy syndrome type 1
|
|
D016884||autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy
|
|
D016884||autoimmune polyglandular syndrome type 1
|
|
D016884||autoimmune polyglandular syndrome type 3
|
|
D016884|C538275|240300||autoimmune polyglandular syndrome type i
|
|
D016884||autoimmune polyglandular syndrome type ii
|
|
D016884||autoimmune polyglandular syndrome type iii
|
|
D016884||autoimmune syndrome type iii polyglandular
|
|
D016884||autoimmune syndrome type ii polyglandular
|
|
D016884||autoimmune syndrome type i polyglandular
|
|
D016884||deficiency aire
|
|
D016884||diabetes mellitus addison disease myxedema
|
|
D016884||diabetes mellitus addison apos s disease myxedema
|
|
D016884||multiple endocrine deficiency syndrome type 2
|
|
D016884||polyendocrine autoimmune syndrome type ii
|
|
D016884||polyendocrinopathy autoimmune
|
|
D016884||polyendocrinopathy candidiasis ectodermal dystrophy autoimmune
|
|
D016884||polyglandular autoimmune syndrome type 1
|
|
D016884||polyglandular autoimmune syndrome type 2
|
|
D016884||polyglandular autoimmune syndrome type 3
|
|
D016884|C538275|240300||polyglandular autoimmune syndrome type i
|
|
D016884||polyglandular deficiency syndrome type 2
|
|
D016884||polyglandular type i autoimmune syndrome
|
|
D016884||polyglandular type ii autoimmune syndrome
|
|
D016884||polyglandular type iii autoimmune syndrome
|
|
D016884||schmidt apos s syndrome
|
|
D016884||schmidt syndrome
|
|
D016884||syndrome schmidt
|
|
D016884||syndrome schmidt apos s
|
|
C563469|600624||cone rod dystrophy 1
|
|
C563469|600624||cord1
|
|
C563469|600624||crd1
|
|
C563030|140700||heinz body anemias
|
|
C536179||feingold trainer syndrome
|
|
C536179||unusual facies cleft palate short stature and mental retardation
|
|
C562423||deafness progressive high tone neural
|
|
C536177||dincsoy salih patel syndrome
|
|
C536177||dincsoy syndrome
|
|
C536177||midline malformations multiple with limb abnormalities and hypopituitarism
|
|
C536178||feigenbaum bergeron richardson syndrome
|
|
D003586||cytomegalovirus infections
|
|
D003586||cytomegalic inclusion disease
|
|
D003586||cytomegalic inclusion diseases
|
|
D003586||cytomegalovirus infection
|
|
D003586||disease cytomegalic inclusion
|
|
D003586||diseases cytomegalic inclusion
|
|
D003586||inclusion disease
|
|
D003586||inclusion disease cytomegalic
|
|
D003586||inclusion diseases
|
|
D003586||inclusion diseases cytomegalic
|
|
D003586||infection cytomegalovirus
|
|
D003586||infections cytomegalovirus
|
|
D003586||salivary gland virus disease
|
|
C562424||ehlers danlos syndrome autosomal dominant type unspecified
|
|
C562424||ehlers danlos syndrome friedman harrod type
|
|
D002252||carbon tetrachloride poisoning
|
|
D002252||carbon tetrachloride poisonings
|
|
D002252||ccl4 poisoning
|
|
D002252||ccl4 poisonings
|
|
D002252||poisoning carbon tetrachloride
|
|
D002252||poisoning ccl4
|
|
D002252||poisonings carbon tetrachloride
|
|
C536172||dieterich apos s disease
|
|
C536172||avascular necrosis of the metacarpal head
|
|
C536172||dieterich disease
|
|
314250|C564048||dystonia 3 torsion x linked
|
|
314250|C564048||dystonia parkinsonism x linked
|
|
314250|C564048||dyt3
|
|
314250|C564048||lubag
|
|
314250|C564048||lubag syndrome
|
|
314250|C564048||torsion dystonia parkinsonism filipino type
|
|
314250|C564048||xdp
|
|
314250|C564048||x linked dystonia parkinsonism
|
|
314250|C564048||x linked dystonia parkinsonism syndrome
|
|
314250|C564048||x linked torsion dystonia parkinsonism syndrome
|
|
D016893||carotid stenosis
|
|
D016893||artery narrowing carotid
|
|
D016893||artery narrowings carotid
|
|
D016893||artery plaque carotid
|
|
D016893||artery plaques carotid
|
|
D016893||artery stenoses carotid
|
|
D016893||artery stenosis carotid
|
|
D016893||carotid artery narrowing
|
|
D016893||carotid artery narrowings
|
|
D016893||carotid artery plaque
|
|
D016893||carotid artery plaques
|
|
D016893||carotid artery stenoses
|
|
D016893||carotid artery stenosis
|
|
D016893||carotid artery ulcerating plaque
|
|
D016893||carotid stenoses
|
|
D016893||carotid ulcer
|
|
D016893||carotid ulcers
|
|
D016893||common carotid artery stenosis
|
|
D016893||external carotid artery stenosis
|
|
D016893||internal carotid artery stenosis
|
|
D016893||narrowing carotid artery
|
|
D016893||narrowings carotid artery
|
|
D016893||plaque carotid artery
|
|
D016893||plaques carotid artery
|
|
D016893||plaque ulcerating carotid artery
|
|
D016893||stenoses carotid
|
|
D016893||stenoses carotid artery
|
|
D016893||stenosis carotid
|
|
D016893||stenosis carotid artery
|
|
D016893||stenosis common carotid artery
|
|
D016893||stenosis external carotid artery
|
|
D016893||ulcerating plaque carotid artery
|
|
D016893||ulcer carotid
|
|
D016893||ulcers carotid
|
|
D014235||trichinellosis
|
|
D014235||human trichinelloses
|
|
D014235||human trichinellosis
|
|
D014235||trichinelliases
|
|
D014235||trichinelliasis
|
|
D014235||trichinelloses
|
|
D014235||trichinelloses human
|
|
D014235||trichinellosis human
|
|
D014235||trichinoses
|
|
D014235||trichinosis
|
|
D001019||aortic rupture
|
|
D001019||aneurysm ruptured aortic
|
|
D001019||aneurysms ruptured aortic
|
|
D001019||aortic aneurysm ruptured
|
|
D001019||aortic aneurysms ruptured
|
|
D001019||aortic ruptures
|
|
D001019||rupture aortic
|
|
D001019||ruptured aortic aneurysm
|
|
D001019||ruptured aortic aneurysms
|
|
D001019||ruptures aortic
|
|
D001018||aortic diseases
|
|
D001018||aortic disease
|
|
D001018||disease aortic
|
|
D001018||diseases aortic
|
|
C537551||microcornea corectopia macular hypoplasia
|
|
C536220||curly hair acral keratoderma caries syndrome
|
|
D001017||aortic coarctation
|
|
D001017||aorta coarctation
|
|
D001017||aorta coarctations
|
|
D001017||aorta dominant coarctation
|
|
D001017||aorta dominant coarctations
|
|
D001017||aortic coarctations
|
|
D001017||coarctation aortic
|
|
D001017||coarctation of aorta
|
|
D001017||coarctation of aorta dominant
|
|
D001017||coarctation of the aorta
|
|
D001017||coarctations aortic
|
|
C537554||microgastria limb reduction defect
|
|
C537554||congenital microgastria and limb reduction defects
|
|
C537554||microgastria limb reduction defects association
|
|
C536224||cutaneous photosensitivity and colitis lethal
|
|
C536224||early cutaneous photosensitivity and severe colitis
|
|
C563840||cryohydrocytosis stomatin deficient with mental retardation seizures cataracts and massive hepatosplenomegaly
|
|
C563840||stomatin deficient cryohydrocytosis with neurologic defects
|
|
C537552||microcornea glaucoma and absent frontal sinuses
|
|
C537552||hereditary microcornea glaucoma and absent frontal sinuses
|
|
C537553||microdontia hypodontia short stature
|
|
C537315|301790||spinocerebellar ataxia x linked 3
|
|
C537315|301790||ataxia deafness syndrome x linked
|
|
C537315|301790||scax3
|
|
C537315|301790||schmidley syndrome
|
|
D001010||anxiety separation
|
|
D001010||anxiety disorder separation
|
|
D001010||separation anxiety
|
|
D001010||separation anxiety disorder
|
|
C563844|608840||muscular dystrophy congenital type 1d
|
|
D002345||carotid body tumor
|
|
D002345||carotid body paraganglioma
|
|
D002345||carotid body paragangliomas
|
|
D002345|D010235|168000||carotid body tumors
|
|
D002345|D010235|168000||paraganglioma carotid body
|
|
D002345||paragangliomas carotid body
|
|
D002345||tumor carotid body
|
|
D002345||tumors carotid body
|
|
D003677||deficiency diseases
|
|
D003677||deficiency disease
|
|
D003677||disease deficiency
|
|
D003677||diseases deficiency
|
|
D001015||aortic arch syndromes
|
|
D001015||aortic arch syndrome
|
|
D001015||syndrome aortic arch
|
|
D001015||syndromes aortic arch
|
|
C563849||alpha b crystallinopathy with cataract
|
|
C563849||desmin related myopathy with cataract
|
|
D001014||aortic aneurysm
|
|
D001014||aneurysm aortic
|
|
D001014||aneurysms aortic
|
|
D001014||aortic aneurysms
|
|
D002340||carotid artery diseases
|
|
D002340||arterial disease carotid
|
|
D002340||arterial diseases carotid
|
|
D002340||arterial diseases common carotid
|
|
D002340||arterial diseases external carotid
|
|
D002340||arterial diseases internal carotid
|
|
D002340||artery disease carotid
|
|
D002340||artery diseases carotid
|
|
D002340||artery disorder carotid
|
|
D002340||artery disorders carotid
|
|
D002340||atherosclerotic disease carotid
|
|
D002340||atherosclerotic diseases carotid
|
|
D002340||carotid arterial disease
|
|
D002340||carotid arterial diseases
|
|
D002340||carotid artery disease
|
|
D002340||carotid artery disorder
|
|
D002340||carotid artery disorders
|
|
D002340||carotid atheroscleroses
|
|
D002340||carotid atherosclerosis
|
|
D002340||carotid atherosclerotic disease
|
|
D002340||carotid atherosclerotic diseases
|
|
D002340||common carotid artery diseases
|
|
D002340||disorders carotid artery
|
|
D002340||external carotid artery diseases
|
|
D002340||internal carotid artery diseases
|
|
C565301|605728||cataract central saccular with sutural opacities
|
|
C565301|605728||cataract 25
|
|
C565301|605728||cataract central pouch like with sutural opacities
|
|
C565301|605728||ccsso
|
|
C565301|605728||ctrct25
|
|
C563747|609286||progressive external ophthalmoplegia with mitochondrial dna deletions autosomal dominant 3
|
|
C563747|609286||peoa3
|
|
C563747|609286||progressive external ophthalmoplegia autosomal dominant 3
|
|
612635||microvascular complications of diabetes susceptibility to 7
|
|
612635||mvcd7
|
|
612635|612634|612628|612624||nephropathy diabetic susceptibility to
|
|
612635||nonproliferative retinopathy diabetic susceptibility to
|
|
612635|612623|603933||proliferative retinopathy diabetic susceptibility to
|
|
D002341||carotid artery thrombosis
|
|
D002341||carotid artery thromboses
|
|
D002341||carotid thrombosis
|
|
D002341||common carotid artery thrombosis
|
|
D002341||external carotid artery thrombosis
|
|
D002341||internal carotid artery thrombosis
|
|
D002341||thrombosis carotid
|
|
D002341||thrombosis carotid artery
|
|
D002341||thrombosis common carotid artery
|
|
D002341||thrombosis external carotid artery
|
|
D002341||thrombosis internal carotid artery
|
|
612634||microvascular complications of diabetes susceptibility to 6
|
|
612634||mvcd6
|
|
D014328||trophoblastic neoplasms
|
|
D014328||cancers trophoblast
|
|
D014328||cancers trophoblastic
|
|
D014328||cancer trophoblast
|
|
D014328||cancer trophoblastic
|
|
D014328||neoplasms trophoblast
|
|
D014328||neoplasms trophoblastic
|
|
D014328||neoplasm trophoblast
|
|
D014328||neoplasm trophoblastic
|
|
D014328||trophoblast cancer
|
|
D014328||trophoblast cancers
|
|
D014328||trophoblastic cancer
|
|
D014328||trophoblastic cancers
|
|
D014328||trophoblastic neoplasm
|
|
D014328||trophoblastic tumor
|
|
D014328||trophoblastic tumors
|
|
D014328||trophoblast neoplasm
|
|
D014328||trophoblast neoplasms
|
|
D014328||trophoblast tumor
|
|
D014328||trophoblast tumors
|
|
D014328||tumors trophoblast
|
|
D014328||tumors trophoblastic
|
|
D014328||tumor trophoblast
|
|
D014328||tumor trophoblastic
|
|
D003327|300464||coronary disease
|
|
D003327|300464||chds1
|
|
D003327|300464||chds2
|
|
D003327|300464||chds3
|
|
D003327|300464||chds4
|
|
D003327|300464||chds5
|
|
D003327|300464||chds7
|
|
D003327|300464||chds8
|
|
D003327|300464||chds9
|
|
D003327|300464||coronary artery disease early onset
|
|
D003327|300464||coronary diseases
|
|
D003327|300464||coronary heart disease
|
|
D003327|300464||coronary heart diseases
|
|
D003327|300464||coronary heart disease susceptibility to 1
|
|
D003327|300464||coronary heart disease susceptibility to 2
|
|
D003327|300464||coronary heart disease susceptibility to 3
|
|
D003327|300464||coronary heart disease susceptibility to 4
|
|
D003327|300464||coronary heart disease susceptibility to 5
|
|
D003327|300464||coronary heart disease susceptibility to 7
|
|
D003327|300464||coronary heart disease susceptibility to 8
|
|
D003327|300464||coronary heart disease susceptibility to 9
|
|
D003327|300464||disease coronary
|
|
D003327|300464||disease coronary heart
|
|
D003327|300464||diseases coronary
|
|
D003327|300464||diseases coronary heart
|
|
D003327|300464||heart disease coronary
|
|
D003327|300464||heart diseases coronary
|
|
C537060|228960||flaujeac factor deficiency
|
|
C537060|228960||fitzgerald trait
|
|
C537060|228960||fitzgerald trait kininogen deficiency total included
|
|
C537060|228960||flaujeac trait included
|
|
C537060|228960||high molecular weight kininogen deficiency
|
|
C537060|228960||hmwk deficiency
|
|
C537060|228960||kininogen deficiency high molecular weight
|
|
C537060|228960||kininogen deficiency high molecular weight and low molecular weight included
|
|
C537060|228960||kininogen deficiency total
|
|
C537060|228960||williams trait included
|
|
D003680||deglutition disorders
|
|
D003680||deglutition disorder
|
|
D003680||disorders deglutition
|
|
D003680||dysphagia
|
|
D003680||dysphagia esophageal
|
|
D003680||dysphagia oropharyngeal
|
|
D003680||esophageal dysphagia
|
|
D003680||oropharyngeal dysphagia
|
|
D003680||swallowing disorder
|
|
D003680||swallowing disorders
|
|
613969||myopia 19 autosomal dominant
|
|
613969||myp19
|
|
C566136|118300||charcot marie tooth disease demyelinating type 1e
|
|
C566136|118300||charcot marie tooth neuropathy and deafness autosomal dominant
|
|
C566136|118300||cmt1e
|
|
C538258|301040||atr x syndrome
|
|
C538258|301040||alpha thalassemia mental retardation syndrome nondeletion type
|
|
C538258|301040||alpha thalassemia mental retardation syndrome non deletion type x linked
|
|
C538258|301040||alpha thalassemia mental retardation syndrome nondeletion type x linked
|
|
C538258|301040||alpha thalassemia mental retardation syndrome x linked
|
|
C538258|301040||alpha thalassemia mental retardation x linked
|
|
C538258|301040||alpha thalassemia x linked intellectual disability syndrome
|
|
C538258|301040||alpha thalassemia x linked mental retardation syndrome
|
|
C538258|301040||atr non deletion type
|
|
C538258|301040||atr nondeletion type
|
|
C538258|301040||atrx
|
|
C538258|301040||atrx syndrome
|
|
C538258|301040||x linked alpha thalassemia mental retardation syndrome
|
|
C538258|301040||xlmr hypotonic face syndrome
|
|
C537547||microcephaly corpus callosum dysgenesis and cleft lip palate
|
|
C537547||microcephaly facial clefting and preaxial polydactyly
|
|
C536216||crome syndrome
|
|
C537548||galloway mowat syndrome
|
|
C537548||galloway syndrome
|
|
C537548||microcephaly hiatal hernia and nephrotic syndrome
|
|
C537548||microcephaly hiatus hernia and nephrotic syndrome
|
|
C537548||microcephaly nephrosis syndrome
|
|
C537548||nephrosis microcephaly syndrome
|
|
C537548||nephrosis neuronal dysmigration syndrome
|
|
C536217||crumpled helices and small mouth
|
|
C536217||sparse hair prominent nose small mouth micrognathia cleft palate crumpled upper helices digit anomaly and mild developmental delay
|
|
D015651||mycotoxicosis
|
|
D015651||fungus poisoning
|
|
D015651||fungus poisonings
|
|
D015651||mycotoxicoses
|
|
D015651||poisoning fungus
|
|
D015651||poisonings fungus
|
|
C537545||microcephaly sparse hair mental retardation seizures
|
|
C537546||microcephaly with spastic quadriplegia
|
|
C537546||recessive microcephaly with spastic quadriplegia
|
|
C536215||pediatric crohn apos s disease
|
|
C536215||crohn apos s disease pediatric
|
|
C536215||pediatric onset crohn apos s disease
|
|
C537549||lambotte syndrome
|
|
C537549||microcephaly holoprosencephaly and intrauterine growth retardation
|
|
C536218||cryofibrinogenemia
|
|
D014323||trombiculiasis
|
|
D014323||trombiculiases
|
|
C536219||cryptomicrotia brachydactyly syndrome
|
|
C536219||cryptomicrotia brachydactyly syndrome excess fingertip arch
|
|
C536219||tonoki ohura niikawa syndrome
|
|
C537561||jaffer beighton syndrome
|
|
C537561||arachnodactyly joint laxity and spondylolisthesis
|
|
C536230||cystic medial necrosis of aorta
|
|
C536230||erdheim cystic medial necrosis of aorta
|
|
C537562||jamaican vomiting sickness
|
|
C537562||ackee poisoning
|
|
D001028||aortopulmonary septal defect
|
|
D001028||aorticopulmonary septal defect
|
|
D001028||aorticopulmonary septal defects
|
|
D001028||aortopulmonary septal defects
|
|
D001028||septal defect aorticopulmonary
|
|
D001028||septal defect aortopulmonary
|
|
D001028||septal defects aorticopulmonary
|
|
D001028||septal defects aortopulmonary
|
|
C537565|277300||jarcho levin syndrome
|
|
C537565|277300||costovertebral dysplasia
|
|
C537565||spondylocostal dysostosis
|
|
C537565|277300||spondylocostal dysostosis 1 autosomal recessive
|
|
C537565||spondylocostal dysplasia recessive form
|
|
C537565|277300||spondylothoracic dysostosis
|
|
C537565|277300||spondylothoracic dysplasia
|
|
608367|D009216||myopia
|
|
608367|D009216||myopia 17 autosomal dominant
|
|
608367|D009216||myopia 4 formerly
|
|
608367|D009216||myopias
|
|
608367|D009216||myp17
|
|
608367|D009216||myp4 formerly
|
|
608367|D009216||nearsightedness
|
|
608367|D009216||nearsightednesses
|
|
C536234||blepharophimosis syndrome type 2
|
|
C536234||blepharophimosis ptosis and epicanthus inversus type 2
|
|
C536234||blepharophimosis ptosis and epicanthus inversus without premature ovarian failure
|
|
C563852||leukoencephalopathy arthritis colitis and hypogammaglobulinema
|
|
C536235||blepharophimosis with ptosis syndactyly and short stature
|
|
C537563||jankovic rivera syndrome
|
|
C537563||hereditary myoclonus and progressive distal muscular atrophy
|
|
C537563||myoclonus hereditary with progressive distal muscular atrophy
|
|
C536232||blepharophimosis syndrome ohdo type
|
|
C536232||mental retardation congenital heart disease blepharophimosis blepharoptosis and hypoplastic teeth
|
|
C536232||ohdo blepharophimosis syndrome
|
|
C536232||ohdo madokoro sonoda syndrome
|
|
C536233||blepharophimosis syndrome type 1
|
|
C536233||blepharophimosis ptosis epicanthus inversus type 1
|
|
C536233||blepharophimosis ptosis epicanthus inversus with ovarian failure
|
|
D001022||aortic valve insufficiency
|
|
D001022||aortic incompetence
|
|
D001022||aortic regurgitation
|
|
D001022||aortic valve incompetence
|
|
D001022||incompetence aortic
|
|
D001022||incompetence aortic valve
|
|
D001022||insufficiency aortic valve
|
|
D001022||regurgitation aortic
|
|
D001022||regurgitation aortic valve
|
|
D001020||aortic stenosis subvalvular
|
|
D001020||aortic stenoses subvalvular
|
|
D001020||aortic subvalvular stenoses
|
|
D001020||aortic subvalvular stenosis
|
|
D001020||stenoses aortic subvalvular
|
|
D001020||stenoses subvalvular aortic
|
|
D001020||stenosis aortic subvalvular
|
|
D001020||stenosis subvalvular aortic
|
|
D001020||subvalvular aortic stenoses
|
|
D001020||subvalvular aortic stenosis
|
|
D001020||subvalvular stenoses aortic
|
|
D001020||subvalvular stenosis aortic
|
|
612628||microvascular complications of diabetes susceptibility to 4
|
|
612628||mvcd4
|
|
C562524||fibrochondrogenesis
|
|
D002357||cartilage diseases
|
|
D002357||cartilage disease
|
|
D002357||chondromalacia
|
|
D002357||chondromalacias
|
|
D003681||dehydration
|
|
D003681||stress water
|
|
D003681||water stress
|
|
D001025||aortitis
|
|
D001025||aortitides
|
|
D001024||aortic valve stenosis
|
|
D001024||aortic stenosis
|
|
D001024||aortic valve stenoses
|
|
D001024||stenoses aortic
|
|
D001024||stenoses aortic valve
|
|
D001024||stenosis aortic
|
|
D001024||stenosis aortic valve
|
|
D001024||valve stenoses aortic
|
|
D001024||valve stenosis aortic
|
|
612624||microvascular complications of diabetes susceptibility to 3
|
|
612624|612623||end stage renal disease diabetic susceptibility to
|
|
612624||mvcd3
|
|
184500|D062685||steatocystoma multiplex
|
|
184500|D062685||cyst multiple sebaceous
|
|
184500|D062685||cysts multiple sebaceous
|
|
184500|D062685||multiple sebaceous cyst
|
|
184500|D062685||multiple sebaceous cysts
|
|
184500|D062685||multiplex steatocystoma
|
|
184500|D062685||multiplex steatocystomas
|
|
184500|D062685||sebaceous cyst multiple
|
|
184500|D062685||sebaceous cysts multiple
|
|
184500|D062685||steatocystoma multiplices
|
|
184500|D062685||steatocystomas multiplex
|
|
D001023||aortic valve prolapse
|
|
D001023||aortic valve prolapses
|
|
D001023||prolapse aortic valve
|
|
D001023||prolapses aortic valve
|
|
D001023||valve prolapse aortic
|
|
D001023||valve prolapses aortic
|
|
612623||microvascular complications of diabetes susceptibility to 2
|
|
612623||mvcd2
|
|
612633||microvascular complications of diabetes susceptibility to 5
|
|
612633||mvcd5
|
|
612633||retinopathy diabetic susceptibility to
|
|
611302||spastic ataxia 2 autosomal recessive
|
|
611302||spax2
|
|
D014339||truncus arteriosus persistent
|
|
D014339||persistent truncus arteriosus
|
|
C536011|200400||achalasia familial esophageal
|
|
C536011|200400||familial esophageal achalasia
|
|
C537558||osteogenesis imperfecta congenita microcephaly and cataracts
|
|
D015663||bone losses perimenopausal
|
|
D015663||bone losses postmenopausal
|
|
D015663||bone loss perimenopausal
|
|
D015663||bone loss postmenopausal
|
|
D015663||osteoporoses postmenopausal
|
|
D015663||osteoporoses post menopausal
|
|
D015663||osteoporosis post menopausal
|
|
D015663||perimenopausal bone loss
|
|
D015663||perimenopausal bone losses
|
|
D015663||postmenopausal bone loss
|
|
D015663||postmenopausal bone losses
|
|
D015663||postmenopausal osteoporoses
|
|
D015663||post menopausal osteoporoses
|
|
D015663||postmenopausal osteoporosis
|
|
D015663||post menopausal osteoporosis
|
|
D013001||somatoform disorders
|
|
D013001||briquet syndrome
|
|
D013001||pain disorder
|
|
D013001||somatization disorder
|
|
D013001||somatization disorders
|
|
D013001||somatoform disorder
|
|
D013001||syndrome briquet
|
|
C536228||familial cyclic vomiting syndrome
|
|
C536228||cyclical vomiting
|
|
C536228||cyclical vomiting syndrome
|
|
C536228||cyclic vomiting syndrome
|
|
C536228||periodic vomiting
|
|
C537556||micromelic dwarfism fryns type
|
|
C537556||dwarfism micromelic with cone epiphyses metaphyseal dysplasia and vertebral segmentation defects
|
|
C537556||micromelic dwarfism with cone epiphyses metaphyseal dysplasia and vertebral segmentation defects
|
|
C537556||spondyloepimetaphyseal dysplasia micromelic
|
|
C536225||cutis laxa recessive
|
|
C536225||cutis laxa type 1
|
|
C537557||micromelic dysplasia dislocation of radius
|
|
C536226||cutis marmorata telangiectatica congenita
|
|
C536226||hereditary cutis marmorata telangiectatica congenita
|
|
600652||deafness autosomal dominant 4a
|
|
600652|C563460||deafness autosomal dominant 4
|
|
600652||dfna4
|
|
600652||dfna4a
|
|
D013005||somatostatinoma
|
|
D013005||somatostatinomas
|
|
D053821||cardiovascular infections
|
|
D053821||cardiovascular infection
|
|
D053821||infection cardiovascular
|
|
D053821||infections cardiovascular
|
|
C536229||cyprus facial neuromusculoskeletal syndrome
|
|
C537572||jeune syndrome situs inversus
|
|
C536241||bobble head doll syndrome
|
|
C537573||methylmalonyl coenzyme a mutase deficiency
|
|
C536242||brachymorphism onychodysplasia dysphalangism syndrome
|
|
D053836||dna degradation necrotic
|
|
D053836||necrotic dna degradation
|
|
C536240||blue rubber bleb nevus syndrome
|
|
C536240||bean syndrome
|
|
C536240||blue rubber bleb nevus
|
|
C537576||michels caskey syndrome
|
|
C537576||mullerian aplasia with hypoplastic thumbs
|
|
C536245||nondystrophic myotonia
|
|
C536246||noninsulin dependent diabetes mellitus with deafness
|
|
C536246||ballinger wallace syndrome
|
|
C536246||diabetes and deafness maternally inherited
|
|
C536246||diabetes deafness syndrome maternally transmitted
|
|
C536246||diabetes mellitus type 2 with deafness
|
|
C536246||diabetes mellitus type ii with deafness
|
|
C536246||maternally inherited diabetes and deafness
|
|
C536246||maternally transmitted diabetes deafness syndrome
|
|
C536246||mitochondrial inherited diabetes and deafness
|
|
C536246||niddm with deafness
|
|
D050197|108725||atherosclerosis
|
|
D050197|108725||alp
|
|
D050197|108725||atherogenesis
|
|
D050197|108725||atherogenic lipoprotein phenotype
|
|
D050197|108725||atheroscleroses
|
|
D050197|108725||atherosclerosis susceptibility
|
|
D050197|108725||aths
|
|
C537574||meyenburg altherr uehlinger syndrome
|
|
C537574||ashkenazi syndrome
|
|
C537574||atrophic polychondritis cartilagenous arthritic deafness syndrome
|
|
C537574||jaksch apos syndrome
|
|
C537574||jaksch wartenhorst apos s syndrome
|
|
C537574||von jaksch wartenhorst apos s syndrome
|
|
C536243||non lissencephalic cortical dysplasia
|
|
C537575||michelin tire baby syndrome
|
|
C537575||kunze riehm syndrome
|
|
C537575||skin creases multiple benign ring shaped of limbs
|
|
C563822|608971||severe combined immunodeficiency autosomal recessive t cell negative b cell positive nk cell positive
|
|
C563822|608971||scid autosomal recessive t cell negative b cell positive nk cell positive
|
|
C563821|C538162|608978||meacham syndrome
|
|
D003655||decerebrate state
|
|
D003655||decerebrate posturing
|
|
D003655||decerebrate posturings
|
|
D003655||decerebrate rigidity
|
|
D003655||decerebrate states
|
|
D003655||decorticate rigidities
|
|
D003655||decorticate rigidity
|
|
D003655||decorticate state
|
|
D003655||decorticate states
|
|
D003655||posturing decerebrate
|
|
D003655||posturings decerebrate
|
|
D003655||rigidities decorticate
|
|
D003655||rigidity decerebrate
|
|
D003655||rigidity decorticate
|
|
D003655||state decerebrate
|
|
D003655||states decerebrate
|
|
C563825||spondylometaphyseal dysplasia with cone rod dystrophy
|
|
C563825||smdcrd
|
|
C563829||myasthenic syndrome congenital with facial dysmorphism associated with acetylcholine receptor deficiency
|
|
C537407|609220||bruck syndrome 2
|
|
C537407|609220||brks2
|
|
184700|D011085||polycystic ovary syndrome
|
|
184700|D011085||hyperandrogenemia
|
|
184700|D011085||ovarian degeneration sclerocystic
|
|
184700|D011085||ovarian syndrome polycystic
|
|
184700|D011085||ovary sclerocystic
|
|
184700|D011085||ovary syndrome polycystic
|
|
184700|D011085||pco
|
|
184700|D011085||pco1
|
|
184700|D011085||pcos
|
|
184700|D011085||pcos1
|
|
184700|D011085||polycystic ovarian syndrome
|
|
184700|D011085||polycystic ovary syndrome 1
|
|
184700|D011085||sclerocystic ovarian degeneration
|
|
184700|D011085||sclerocystic ovaries
|
|
184700|D011085||sclerocystic ovary
|
|
184700|D011085||sclerocystic ovary syndrome
|
|
184700|D011085||stein leventhal syndrome
|
|
184700|D011085||syndrome polycystic ovary
|
|
184700|D011085||syndrome stein leventhal
|
|
C537569||jequier kozlowski skeletal dysplasia
|
|
C537569||cloverleaf skull and bone dysplasias
|
|
C537569||facies unusual arthrogryposis advanced skeletal maturation
|
|
C537569||round face short small nose advanced bone age enlarged diaphysis
|
|
C536239||blue diaper syndrome
|
|
C536239||hypercalcemia familial with nephrocalcinosis and indicanuria
|
|
C537567||jejunal atresia with renal adysplasia
|
|
C536236||blepharoptosis myopia ectopia lentis
|
|
C536236||blepharoptosis myopia and ectopia lentis
|
|
C536236||dominantly inherited blepharoptosis high myopia and ectopia lentis
|
|
C536237||blount disease
|
|
C536237||osteochondrosis deformans tibiae
|
|
C536237||osteochondrosis deformans tibiae familial infantile type
|
|
C536237||tibia vara
|
|
C536252||pyle disease
|
|
C536252||edwin pyle disease
|
|
C536252||metaphyseal dysplasia
|
|
C536252||metaphyseal dysplasia with little involvement of the cranial bones
|
|
C537584||seow najjar syndrome
|
|
C537584||enamel hypoplasia capsular cataracts and ductal stenosis
|
|
D001006||anus imperforate
|
|
D001006||anal atresia
|
|
D001006||anal atresias
|
|
D001006||atresia anal
|
|
D001006||atresias anal
|
|
D001006||imperforate anus
|
|
D052516||sulfatidosis
|
|
D052516||sulfatidoses
|
|
D001005||anus neoplasms
|
|
D001005||anal cancer
|
|
D001005||anal cancers
|
|
D001005||anal neoplasm
|
|
D001005||anal neoplasms
|
|
D001005||anus cancer
|
|
D001005||anus cancers
|
|
D001005||anus neoplasm
|
|
D001005||cancer anal
|
|
D001005||cancer of anus
|
|
D001005||cancer of the anus
|
|
D001005||cancers anal
|
|
D001005||neoplasm anal
|
|
D001005||neoplasm anus
|
|
D001005||neoplasms anal
|
|
D001005||neoplasms anus
|
|
C537582||sennetsu fever
|
|
C537582||human ehrlichial infection sennetsu type
|
|
C536251||pyknoachondrogenesis
|
|
C563831||myasthenic syndrome congenital ie
|
|
C563830||myasthenic syndrome congenital associated with facial dysmorphism
|
|
D003668||pressure ulcer
|
|
D003668||bedsore
|
|
D003668||bed sore
|
|
D003668||bedsores
|
|
D003668||bed sores
|
|
D003668||decubitus ulcer
|
|
D003668||decubitus ulcers
|
|
D003668||pressure sore
|
|
D003668||pressure sores
|
|
D003668||pressure ulcers
|
|
D003668||sore bed
|
|
D003668||sore pressure
|
|
D003668||sores bed
|
|
D003668||sores pressure
|
|
D003668||ulcer decubitus
|
|
D003668||ulcer pressure
|
|
D003668||ulcers decubitus
|
|
D003668||ulcers pressure
|
|
C537588||androblastoma of ovary
|
|
C537588||sertoli leydig cell tumor of the ovary
|
|
C537585||seres santamaria arimany muniz syndrome
|
|
C537585||cleft palate ankyloblepharon alveolar synechiae and ectodermal defects
|
|
C537586||serpentine fibula polycystic kidney syndrome
|
|
C537586||serpentine fibula syndrome
|
|
C536255|D015324|266150||leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency
|
|
C536255|D015324|266150||leigh syndrome due to pyruvate carboxylase deficiency
|
|
C536781|601705||t cell immunodeficiency congenital alopecia and nail dystrophy
|
|
C536781|601705||congenital alopecia and nail dystrophy associated with severe functional t cell immunodeficiency
|
|
C536781|601705||pignata guarino syndrome
|
|
D003665||decompression sickness
|
|
D003665||bends
|
|
D003665||caisson disease
|
|
D003665||caisson diseases
|
|
D003665||disease caisson
|
|
D003665||diseases caisson
|
|
D003665||sickness decompression
|
|
D001004||anus diseases
|
|
D001004||anus disease
|
|
D001004||disease anus
|
|
D001004||diseases anus
|
|
D001002||anuria
|
|
D001002||anurias
|
|
C536249||purpura simplex
|
|
C536249||hereditary familial purpura simplex
|
|
605067|D018785||tricuspid atresia
|
|
605067|D018785||absent right atrioventricular connection
|
|
605067|D018785||atresias tricuspid
|
|
605067|D018785||atresias tricuspid valve
|
|
605067|D018785||atresia tricuspid
|
|
605067|D018785||atresia tricuspid valve
|
|
605067|D018785||tricuspid atresias
|
|
605067|D018785||tricuspid valve atresia
|
|
605067|D018785||tricuspid valve atresias
|
|
605067|D018785||valve atresias tricuspid
|
|
605067|D018785||valve atresia tricuspid
|
|
C536247||nonkeratan sulfate excreting morquio syndrome
|
|
C536247||morquio syndrome c
|
|
C536247||morquio syndrome nonkeratan sulfate excreting type
|
|
C536247||morquio syndrome nonkeratosulfate excreting type
|
|
C537579||sener syndrome
|
|
C537579||frontonasal dysplasia and dilated virchow robin spaces
|
|
D014314||trisomy
|
|
D014314||chromosomal triplication
|
|
D014314||chromosomal triplications
|
|
D014314||partial trisomies
|
|
D014314||partial trisomy
|
|
D014314||trisomies
|
|
D014314||trisomies partial
|
|
D014314||trisomy partial
|
|
600630||uv sensitive syndrome 1
|
|
600630||uvss1
|
|
D014313||trismus
|
|
D014313||lockjaw
|
|
D014313||lock jaw
|
|
D014313||masseter muscle spasm
|
|
D014313||masseter muscle spasms
|
|
D014313||masseter spasm
|
|
D014313||masseter spasms
|
|
D014313||muscle spasm masseter
|
|
D014313||muscle spasms masseter
|
|
D014313||spasm masseter
|
|
D014313||spasm masseter muscle
|
|
D014313||spasms masseter
|
|
D014313||spasms masseter muscle
|
|
D053842||microsatellite instability
|
|
D053842||error phenotype replication
|
|
D053842||error phenotypes replication
|
|
D053842||instability microsatellite
|
|
D053842||phenotype replication error
|
|
D053842||phenotypes replication error
|
|
D053842||replication error phenotype
|
|
D053842||replication error phenotypes
|
|
D003638||deafness
|
|
D003638||acquired deafness
|
|
D003638||bilateral deafness
|
|
D003638||complete hearing loss
|
|
D003638||deaf mutism
|
|
D003638||deafness acquired
|
|
D003638||deafness bilateral
|
|
D003638||deafness prelingual
|
|
D003638||extreme hearing loss
|
|
D003638||hearing loss complete
|
|
D003638||hearing loss extreme
|
|
D003638||prelingual deafness
|
|
D003639||hearing loss sudden
|
|
D003639||deafness sudden
|
|
D003639||sudden deafness
|
|
D003639||sudden hearing loss
|
|
C537510||kozlowski tsuruta taki syndrome
|
|
C537510||achondrogenesis kozlowski type
|
|
C537510||chondrodysplasia lethal neonatal
|
|
D002303||cardiac output low
|
|
D002303||low cardiac output
|
|
D002303||low cardiac output syndrome
|
|
D002303||output low cardiac
|
|
C566079||cd4 lymphocyte deficiency
|
|
C537511||piussan lenaerts mathieu syndrome
|
|
C537511||thumb ankylosis with mental retardation
|
|
D002305||cardiac tamponade
|
|
D002305||cardiac tamponades
|
|
D002305||pericardial tamponade
|
|
D002305||pericardial tamponades
|
|
D002305||tamponade cardiac
|
|
D002305||tamponade pericardial
|
|
D002305||tamponades cardiac
|
|
D002305||tamponades pericardial
|
|
C563806||skeletal dysplasia rhizomelic with retinitis pigmentosa
|
|
D027601||polyomavirus infections
|
|
D027601||polyomavirus infection
|
|
C563805||nephrotic syndrome congenital with or without ocular abnormalities
|
|
613930||alopecia mental retardation syndrome 3
|
|
613930||apmr3
|
|
C563803||spondylometaphyseal dysplasia type a4
|
|
C579395||ruvalcaba syndrome
|
|
D015616||histiocytosis non langerhans cell
|
|
D015616||disseminatum xanthoma
|
|
D015616||non langerhans cell histiocytosis
|
|
D015616||reticulohistiocytoma
|
|
D015616||reticulohistiocytomas
|
|
D015616||xanthoma disseminatum
|
|
D015615||cystic adenomatoid malformation of lung congenital
|
|
D015615||congenital cystic adenomatoid malformation
|
|
D015615||congenital cystic adenomatoid malformation of lung
|
|
D015615||congenital cystic adenomatoid malformation type 1
|
|
D015615||congenital cystic adenomatoid malformation type 2
|
|
D015615||congenital cystic adenomatoid malformation type 3
|
|
D015615||congenital cystic adenomatoid malformation type i
|
|
D015615||congenital cystic adenomatoid malformation type ii
|
|
D015615||congenital cystic adenomatoid malformation type iii
|
|
D015615||cystic adenomatoid malformation of lung
|
|
D015615||lung malformation congenital cystic adenomatoid
|
|
D015615||lung malformation cystic adenomatoid congenital
|
|
C537509||kozlowski rafinski klicharska syndrome
|
|
C537509||metaphyseal and epiphyseal dysplasia with unusual facies and cataract
|
|
C566080||t cell okt4 deficiency
|
|
D015614||histiocytosis
|
|
D015614||histiocytoses
|
|
D015619||respiratory system abnormalities
|
|
D015619||abnormalities respiratory system
|
|
D015619||abnormality respiratory system
|
|
D015619||respiratory system abnormality
|
|
D015619||system abnormalities respiratory
|
|
D015619||system abnormality respiratory
|
|
D015618||histiocytosis sinus
|
|
D015618||destombes rosai dorfman syndrome
|
|
D015618||disease rosai dorfman
|
|
D015618||histiocytoses sinus
|
|
D015618||rosai dorfman disease
|
|
D015618||sinus histiocytoses
|
|
D015618||sinus histiocytosis
|
|
D015618||sinus histiocytosis with massive lymphadenopathy
|
|
D015618||syndrome destombes rosai dorfman
|
|
C537503||subcutaneous panniculitis like t cell lymphoma
|
|
C537504||kousseff nichols syndrome
|
|
C537504||noonan like contracture myopathy hyperpyrexia
|
|
C566087||synovial chondromatosis familial with dwarfism
|
|
C566089||synostosis of talus and calcaneus with short stature
|
|
C566082||immunodeficiency due to defect in cd3 epsilon
|
|
C537508||kozlowski ouvrier syndrome
|
|
C537508||agenesis of the corpus callosum with mental retardation and osseous lesions
|
|
C566083||immunodeficiency due to defect in cd3 gamma
|
|
C566084||syringomyelia isolated
|
|
C537506||kozlowski brown hardwick syndrome
|
|
C566085||syringomas multiple
|
|
D003649||decalcification pathologic
|
|
D003649||decalcification pathological
|
|
D003649||pathological decalcification
|
|
D003649||pathologic decalcification
|
|
D002318||cardiovascular diseases
|
|
D002318||cardiovascular disease
|
|
D002318||disease cardiovascular
|
|
D002318||diseases cardiovascular
|
|
D003645||death sudden
|
|
D003645||sudden death
|
|
C563813||peripheral cone dystrophy
|
|
D002310||cardiomyopathy alcoholic
|
|
D002310||alcoholic cardiomyopathy
|
|
D003643||death
|
|
D003643||cardiac death
|
|
D003643||death cardiac
|
|
D003643||determination of death
|
|
D003643||near death experience
|
|
D002312||cardiomyopathy hypertrophic
|
|
D002312||asymmetric septal hypertrophies
|
|
D002312||cardiomyopathies hypertrophic
|
|
D002312||cardiomyopathies hypertrophic obstructive
|
|
D002312||cardiomyopathies hypertrophic obstructive hocm
|
|
D002312||cardiomyopathies idiopathic hypertrophic
|
|
D002312||cardiomyopathy hypertrophic obstructive
|
|
D002312||cardiomyopathy hypertrophic obstructive hocm
|
|
D002312||cardiomyopathy idiopathic hypertrophic
|
|
D002312||hypertrophic cardiomyopathies
|
|
D002312||hypertrophic cardiomyopathies idiopathic
|
|
D002312||hypertrophic cardiomyopathy
|
|
D002312||hypertrophic cardiomyopathy idiopathic
|
|
D002312||hypertrophic obstructive cardiomyopathies
|
|
D002312||hypertrophic obstructive cardiomyopathies hocm
|
|
D002312||hypertrophic obstructive cardiomyopathy
|
|
D002312||hypertrophic obstructive cardiomyopathy hocm
|
|
D002312||hypertrophies asymmetric septal
|
|
D002312||hypertrophy asymmetric septal
|
|
D002312||idiopathic hypertrophic cardiomyopathies
|
|
D002312||idiopathic hypertrophic cardiomyopathy
|
|
D002312||idiopathic hypertrophic subaortic stenosis
|
|
D002312||idiopathic hypertrophic subaortic stenosis ihss
|
|
D002312||idiopathic hypertrophic subvalvular stenosis
|
|
D002312||ihss
|
|
D002312||ihsss
|
|
D002312||obstructive cardiomyopathies hypertrophic
|
|
D002312||obstructive cardiomyopathy hypertrophic
|
|
D002312||septal hypertrophies asymmetric
|
|
D002312||septal hypertrophy asymmetric
|
|
D002312||subvalvular stenosis idiopathic hypertrophic
|
|
C563810||mental retardation with optic atrophy facial dysmorphism microcephaly and short stature
|
|
D002313||cardiomyopathy restrictive
|
|
D002313||cardiomyopathies restrictive
|
|
D002313||familial restrictive cardiomyopathy
|
|
D002313||restrictive cardiomyopathies
|
|
D002313||restrictive cardiomyopathy
|
|
D041881||cholecystitis acute
|
|
D041881||acute cholecystitis
|
|
203700||mitochondrial dna depletion syndrome 4a alpers type
|
|
203700|D002549||alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
|
203700|D002549||alpers huttenlocher syndrome
|
|
203700|D002549||alpers progressive infantile poliodystrophy
|
|
203700|D002549||alpers syndrome
|
|
203700||mtdps4a
|
|
203700|D002549||neuronal degeneration of childhood with liver disease progressive
|
|
203700||pndc
|
|
D041882||emphysematous cholecystitis
|
|
D041882||cholecystitis emphysematous
|
|
314050|C564050||thrombocytopenia platelet dysfunction hemolysis and imbalanced globin synthesis
|
|
314050|C564050||thrombocytopenia with beta thalassemia x linked
|
|
314050|C564050||xltt
|
|
C563815||deafness autosomal recessive 36
|
|
C563815|609006||dfnb36
|
|
C563814||marfanoid habitus with situs inversus
|
|
C567716|613177||cutis laxa with severe pulmonary gastrointestinal and urinary abnormalities
|
|
C567716|613177||arcl1c
|
|
C567716|613177||cutis laxa autosomal recessive type ic
|
|
C567716|613177||urban rifkin davis syndrome
|
|
C567716|613177||urds
|
|
C566090||synostosis carpal with dysplastic elbow joints and brachydactyly
|
|
C566090||brachydactyly with joint dysplasia
|
|
C566090||liebenberg syndrome
|
|
C563819|115700||cataract congenital cerulean type 3
|
|
C563819||cataract congenital blue dot type 3
|
|
C566091||syndactyly polydactyly earlobe syndrome
|
|
C563818||ataxia sensory autosomal dominant
|
|
D015624||lambert eaton myasthenic syndrome
|
|
D015624||eaton lambert myasthenic myopathic syndrome
|
|
D015624||eaton lambert myasthenic syndrome
|
|
D015624||eaton lambert myopathic myasthenic syndrome
|
|
D015624||eaton lambert myopathic myasthenic syndromes
|
|
D015624||eaton lambert syndrome
|
|
D015624||lambert eaton myasthenic myopathic syndrome
|
|
D015624||lambert eaton myasthenic myopathic syndromes
|
|
D015624||lambert eaton myopathic myasthenic syndrome
|
|
D015624||lambert eaton myopathic myasthenic syndromes
|
|
D015624||lambert eaton syndrome
|
|
D015624||myasthenic myopathic syndrome of eaton lambert
|
|
D015624||myasthenic myopathic syndrome of lambert eaton
|
|
D015624||myasthenic syndrome eaton lambert
|
|
D015624||myasthenic syndrome lambert eaton
|
|
D015624||myopathic myasthenic syndrome of eaton lambert
|
|
D015624||myopathic myasthenic syndrome of lambert eaton
|
|
D015624||syndrome eaton lambert
|
|
D015624||syndrome eaton lambert myasthenic
|
|
D015624||syndrome lambert eaton
|
|
D015624||syndrome lambert eaton myasthenic
|
|
613916||deafness autosomal recessive 89
|
|
613916||dfnb89
|
|
C580387||ppm x syndrome
|
|
C580388||prickle1 related progressive myoclonus epilepsy with ataxia
|
|
C580388||pme with ataxia
|
|
C580388||prickle1 related progressive myoclonic epilepsy with ataxia
|
|
C580388||progressive myoclonic epilepsy 1b
|
|
C580388||progressive myoclonus epilepsy with ataxia
|
|
C537514||plasmacytoma anaplastic
|
|
C537514||anaplastic skeletal plasmacytoma type
|
|
C537514||anaplastic solitary extramedullary plasmacytoma of the cecum type
|
|
C537514||extramedullary anaplastic plasmacytoma type
|
|
C566098||symphalangism with multiple anomalies of hands and feet
|
|
C537512||plagiocephaly and x linked mental retardation
|
|
C537512||hyde forster mccarthy berry syndrome
|
|
C537512||mental retardation plagiocephaly brachycephaly prominent forehead and coarse facial features
|
|
C537512||mental retardation x linked hyde forster type
|
|
C537512||mental retardation x linked with craniofacial dysmorphism
|
|
C580383||pontocerebellar hypoplasia
|
|
C580383||congenital pontocerebellar hypoplasia
|
|
C566099||symphalangism distal
|
|
C537518||podder tolmie syndrome
|
|
C537518||meningoencephalocele arthrogryposis and hypoplastic thumbs
|
|
C537519||schwartz lelek syndrome
|
|
C537519||craniometaphyseal dysplasia
|
|
C537519||genetic craniotubular bone dysplasias and hyperostoses
|
|
C566095||synpolydactyly with foot anomalies
|
|
C566822|168605||perry syndrome
|
|
C566822|168605||parkinsonism with alveolar hypoventilation and mental depression
|
|
C537517||plexosarcoma
|
|
C537517||gastrointestinal autonomic nerve tumor
|
|
D015620||histiocytic disorders malignant
|
|
D015620||disorder malignant histiocytic
|
|
D015620||disorders malignant histiocytic
|
|
D015620||histiocytic disorder malignant
|
|
D015620||malignant histiocytic disorder
|
|
D015620||malignant histiocytic disorders
|
|
D020199||hematoma subdural acute
|
|
D020199||acute subdural hematoma
|
|
D020199||acute subdural hematomas
|
|
D020199||hematoma acute subdural
|
|
D020199||hematomas acute subdural
|
|
D020199||hemorrhage subdural acute
|
|
D020199||subdural hematoma acute
|
|
D020199||subdural hematomas acute
|
|
D004948||esotropia
|
|
D004948||convergent strabismus
|
|
D004948||cross eye
|
|
D004948||cross eyes
|
|
D004948||esodeviation
|
|
D004948||esodeviations
|
|
D004948||esophoria
|
|
D004948||esophorias
|
|
D004948||esotropia intermittent
|
|
D004948||esotropia monocular
|
|
D004948||esotropia primary
|
|
D004948||esotropias
|
|
D004948||esotropia secondary
|
|
D004948||esotropias intermittent
|
|
D004948||esotropias monocular
|
|
D004948||esotropias primary
|
|
D004948||esotropias secondary
|
|
D004948||intermittent esotropia
|
|
D004948||intermittent esotropias
|
|
D004948||internal strabismus
|
|
D004948||monocular esotropia
|
|
D004948||monocular esotropias
|
|
D004948||primary esotropia
|
|
D004948||primary esotropias
|
|
D004948||secondary esotropia
|
|
D004948||secondary esotropias
|
|
D004948||strabismus convergent
|
|
D004948||strabismus internal
|
|
D020198||intracranial hemorrhage traumatic
|
|
D020198||hematomas traumatic intracranial
|
|
D020198||hematoma traumatic intracranial
|
|
D020198||hemorrhage intracranial traumatic
|
|
D020198||hemorrhages traumatic intracranial
|
|
D020198||hemorrhage traumatic intracranial
|
|
D020198||intracranial hematomas traumatic
|
|
D020198||intracranial hematoma traumatic
|
|
D020198||intracranial hemorrhages traumatic
|
|
D020198||traumatic intracranial hematoma
|
|
D020198||traumatic intracranial hematomas
|
|
D020198||traumatic intracranial hemorrhage
|
|
D020198||traumatic intracranial hemorrhages
|
|
247100|D008065||lipoid proteinosis of urbach and wiethe
|
|
247100|D008065||hyalinosis cutis et mucosae
|
|
247100|D008065||lipoidproteinosis
|
|
247100|D008065||lipoid proteinosis
|
|
247100|D008065||lipoid proteinosis urbach wiethe
|
|
247100|D008065||lipoproteinosis
|
|
247100|D008065||urbach wiethe disease
|
|
247100|D008065||urbach wiethe lipoid proteinosis
|
|
247100|D008065||urbach wiethe syndrome
|
|
D015658|609423||hiv infections
|
|
D015658|609423||acquired immunodeficiency syndrome progression to included
|
|
D015658|609423||aids progression to included
|
|
D015658|609423||hiv 1 resistance to included
|
|
D015658|609423||hiv 1 susceptibility to human immunodeficiency virus type 1 resistance to included
|
|
D015658|609423||hiv infection
|
|
D015658|609423||htlv iii infection
|
|
D015658|609423||htlv iii infections
|
|
D015658|609423||htlv iii lav infection
|
|
D015658|609423||htlv iii lav infections
|
|
D015658|609423||human immunodeficiency virus type 1 susceptibility to
|
|
D015658|609423||infection hiv
|
|
D015658|609423||infection htlv iii
|
|
D015658|609423||infection htlv iii lav
|
|
D015658|609423||infections hiv
|
|
D015658|609423||infections htlv iii
|
|
D015658|609423||infections htlv iii lav
|
|
D015658|609423||t lymphotropic virus type iii infections human
|
|
D020197||head injuries penetrating
|
|
D020197||brain injuries penetrating
|
|
D020197||brain injury penetrating
|
|
D020197||cranial trauma penetrating
|
|
D020197||cranial traumas penetrating
|
|
D020197||craniocerebral trauma penetrating
|
|
D020197||craniocerebral traumas penetrating
|
|
D020197||head injuries penetrating missile
|
|
D020197||head injury penetrating
|
|
D020197||head trauma penetrating
|
|
D020197||head traumas penetrating
|
|
D020197||injuries penetrating head
|
|
D020197||injury penetrating head
|
|
D020197||missile injuries penetrating head
|
|
D020197||penetrating brain injuries
|
|
D020197||penetrating brain injury
|
|
D020197||penetrating cranial trauma
|
|
D020197||penetrating cranial traumas
|
|
D020197||penetrating craniocerebral trauma
|
|
D020197||penetrating craniocerebral traumas
|
|
D020197||penetrating head injuries
|
|
D020197||penetrating head injury
|
|
D020197||penetrating head trauma
|
|
D020197||penetrating head traumas
|
|
D020197||penetrating missile injuries head
|
|
D020197||trauma penetrating cranial
|
|
D020197||trauma penetrating craniocerebral
|
|
D020197||trauma penetrating head
|
|
D020197||traumas penetrating cranial
|
|
D020197||traumas penetrating craniocerebral
|
|
D020197||traumas penetrating head
|
|
C567771|613073||metaphyseal anadysplasia 2
|
|
C567771|613073||mandp2
|
|
C564276|608189||tropical calcific pancreatitis
|
|
C564276|608189||tcp
|
|
D020196||trauma nervous system
|
|
D020196||craniocervical injuries
|
|
D020196||craniocervical injury
|
|
D020196||injuries craniocervical
|
|
D020196||injuries nervous system
|
|
D020196||injury craniocervical
|
|
D020196||injury nervous system
|
|
D020196||nervous system injuries
|
|
D020196||nervous system injury
|
|
D020196||nervous system trauma
|
|
D020196||nervous system traumas
|
|
D020195||epilepsy reflex
|
|
D020195||audiogenic epilepsies
|
|
D020195||audiogenic epilepsy
|
|
D020195||audiogenic reflex epilepsies
|
|
D020195||audiogenic reflex epilepsy
|
|
D020195||cursive epilepsy
|
|
D020195||cursive reflex epilepsies running
|
|
D020195||cursive reflex epilepsy running
|
|
D020195||decision making reflex epilepsy
|
|
D020195||eating induced epilepsies
|
|
D020195||eating induced epilepsy
|
|
D020195||eating induced reflex epilepsies
|
|
D020195||eating induced reflex epilepsy
|
|
D020195||epilepsies audiogenic reflex
|
|
D020195||epilepsies cursive
|
|
D020195||epilepsies eating induced
|
|
D020195||epilepsies eating induced reflex
|
|
D020195||epilepsies immersion related
|
|
D020195||epilepsies musicogenic
|
|
D020195||epilepsies musicogenic reflex
|
|
D020195||epilepsies photosensitive
|
|
D020195||epilepsies photosensitive reflex
|
|
D020195||epilepsies reading
|
|
D020195||epilepsies reading reflex
|
|
D020195||epilepsies reflex
|
|
D020195||epilepsies tactile reflex
|
|
D020195||epilepsies writing induced reflex
|
|
D020195||epilepsy audiogenic
|
|
D020195||epilepsy audiogenic reflex
|
|
D020195||epilepsy cursive
|
|
D020195||epilepsy cursive reflex running
|
|
D020195||epilepsy eating induced
|
|
D020195||epilepsy eating induced reflex
|
|
D020195||epilepsy immersion related
|
|
D020195||epilepsy musicogenic
|
|
D020195||epilepsy musicogenic reflex
|
|
D020195||epilepsy photosensitive
|
|
D020195||epilepsy photosensitive reflex
|
|
D020195||epilepsy reading
|
|
D020195||epilepsy reading reflex
|
|
D020195||epilepsy tactile reflex
|
|
D020195||epilepsy writing induced reflex
|
|
D020195||immersion related epilepsies
|
|
D020195||immersion related epilepsy
|
|
D020195||musicogenic epilepsies
|
|
D020195||musicogenic epilepsy
|
|
D020195||musicogenic reflex epilepsies
|
|
D020195||musicogenic reflex epilepsy
|
|
D020195||photosensitive epilepsies
|
|
D020195||photosensitive epilepsy
|
|
D020195||photosensitive reflex epilepsies
|
|
D020195||photosensitive reflex epilepsy
|
|
D020195||reading epilepsies
|
|
D020195||reading epilepsy
|
|
D020195||reading reflex epilepsies
|
|
D020195||reading reflex epilepsy
|
|
D020195||reflex epilepsies
|
|
D020195||reflex epilepsies audiogenic
|
|
D020195||reflex epilepsies cursive running
|
|
D020195||reflex epilepsies eating induced
|
|
D020195||reflex epilepsies musicogenic
|
|
D020195||reflex epilepsies photosensitive
|
|
D020195||reflex epilepsies reading
|
|
D020195||reflex epilepsies tactile
|
|
D020195||reflex epilepsies writing induced
|
|
D020195||reflex epilepsy
|
|
D020195||reflex epilepsy audiogenic
|
|
D020195||reflex epilepsy cursive running
|
|
D020195||reflex epilepsy eating induced
|
|
D020195||reflex epilepsy musicogenic
|
|
D020195||reflex epilepsy photosensitive
|
|
D020195||reflex epilepsy reading
|
|
D020195||reflex epilepsy tactile
|
|
D020195||reflex epilepsy visual pattern
|
|
D020195||reflex epilepsy writing induced
|
|
D020195||tactile reflex epilepsies
|
|
D020195||tactile reflex epilepsy
|
|
D020195||visual pattern reflex epilepsy
|
|
D020195||writing induced reflex epilepsies
|
|
D020195||writing induced reflex epilepsy
|
|
C537532||seckel like syndrome type buebel
|
|
C566057||thrombophilia due to thrombomodulin defect
|
|
C536202||elastosis perforans serpiginosa
|
|
C536202||elastoma intrapapillare perforans verruciformis
|
|
C536202||miescher elastoma
|
|
C537530||sebaceous gland hyperplasia familial presenile
|
|
D004940||esophageal stenosis
|
|
D004940||esophageal stenoses
|
|
D004940||esophageal stricture
|
|
D004940||stenoses esophageal
|
|
D004940||stenosis esophageal
|
|
D004940||stricture esophageal
|
|
D004942||esophagitis peptic
|
|
D004942||esophagitides peptic
|
|
D004942||esophagitides reflux
|
|
D004942||esophagitis reflux
|
|
D004942||peptic esophagitides
|
|
D004942||peptic esophagitis
|
|
D004942||reflux esophagitides
|
|
D004942||reflux esophagitis
|
|
D004941||esophagitis
|
|
D004941||esophagitides
|
|
C562592|278760||xeroderma pigmentosum complementation group f
|
|
C562592|278760||xeroderma pigmentosum vi
|
|
C562592|278760||xeroderma pigmentosum vi xp6 xeroderma pigmentosum type f cockayne syndrome included
|
|
C562592|278760||xp6
|
|
C562592|278760||xpf
|
|
C562592|278760||xpf cs included
|
|
C562592|278760||xp group f
|
|
C567938|107100||anorectal anomalies
|
|
D063205||pneumorrhachis
|
|
D063205||epidural pneumorrhachi
|
|
D063205||epidural pneumorrhachis
|
|
D063205||pneumorrhachi
|
|
D063205||pneumorrhachi epidural
|
|
D063205||pneumorrhachis epidural
|
|
D063205||pneumorrhachis subarachnoid
|
|
D063205||pneumorrhachi subarachnoid
|
|
D063205||subarachnoid pneumorrhachi
|
|
D063205||subarachnoid pneumorrhachis
|
|
C580359||palmoplantar keratoderma with deafness
|
|
C580359||palmoplantar hyperkeratosis deafness syndrome
|
|
C580359||palmoplantar hyperkeratosis hearing loss syndrome
|
|
C580359||palmoplantar keratoderma deafness syndrome
|
|
C580359||palmoplantar keratoderma hearing loss syndrome
|
|
C580359||ppk deafness syndrome
|
|
C580359||ppk with deafness
|
|
141750|C563050||alpha thalassemia mental retardation syndrome deletion type
|
|
141750|C563050||alpha thalassemia mental retardation syndrome chromosome 16 related
|
|
141750|C563050||atr 16 syndrome
|
|
141750|C563050||atr deletion type
|
|
141750|C563050||chromosome 16p deletion syndrome
|
|
141750|C563050||hbhr
|
|
141750|C563050||hemoglobin h related mental retardation
|
|
141750|C563050||mental retardation with hemoglobin h
|
|
C566065||thalassemia beta silent allele
|
|
D016920||meningitis bacterial
|
|
D016920||bacterial meningitides
|
|
D016920||bacterial meningitis
|
|
D016920||meningitides bacterial
|
|
C567398||lymphedema cardiac septal defects and characteristic facies
|
|
C567398||irons bianchi syndrome
|
|
C567398||lymphedema atrial septal defect and characteristic facies
|
|
C537523||sclerosing bone dysplasia mental retardation
|
|
C537523||mixed sclerosing bone dysplasia and mental retardation
|
|
C566066||tetramelic monodactyly
|
|
D016921||meningitis fungal
|
|
D016921||fungal meningitides
|
|
D016921||fungal meningitis
|
|
D016921||fungal pachymeningitides
|
|
D016921||fungal pachymeningitis
|
|
D016921||meningitides fungal
|
|
D016921||pachymeningitides fungal
|
|
D016921||pachymeningitis fungal
|
|
C537524||sclerosing lymphocytic lobulitis
|
|
C537524||sclerosing lymphocytic lobulitis of the breast
|
|
C566067||forebrain defects
|
|
C537529||seaver cassidy syndrome
|
|
C566060||thrombasthenia thrombocytopenia hereditary
|
|
C566062||thoracopelvic dysostosis
|
|
C537528||scott bryant graham syndrome
|
|
C537528||craniodigital syndrome mental retardation scott type
|
|
C537528||craniodigital syndrome with mental retardation
|
|
C537528||scott craniodigital syndrome with mental retardation
|
|
C566063||thoracic dysostosis isolated
|
|
D020188||sleep paralysis
|
|
D020188||paralysis sleep
|
|
D020187||rem sleep behavior disorder
|
|
D020187||behavior disorder rapid eye movement sleep
|
|
D020187||behavior disorder rem
|
|
D020187||behavior disorders rem
|
|
D020187||rapid eye movement sleep behavior disorder
|
|
D020187||rem behavior disorder
|
|
D020187||rem behavior disorders
|
|
C537540||microcephaly seizures genital hypoplasia
|
|
C537540||microcephaly micropenis convulsions
|
|
C537540||microcephaly micropenis seizures
|
|
D020186||sleep bruxism
|
|
D020186||adult sleep bruxism
|
|
D020186||adult sleep bruxisms
|
|
D020186||bruxism nocturnal
|
|
D020186||bruxism sleep
|
|
D020186||bruxism sleep related
|
|
D020186||bruxisms nocturnal
|
|
D020186||bruxisms sleep
|
|
D020186||bruxisms sleep related
|
|
D020186||childhood sleep bruxism
|
|
D020186||childhood sleep bruxisms
|
|
D020186||nocturnal bruxism
|
|
D020186||nocturnal bruxisms
|
|
D020186||nocturnal teeth grinding disorder
|
|
D020186||sleep bruxism adult
|
|
D020186||sleep bruxism childhood
|
|
D020186||sleep bruxisms
|
|
D020186||sleep bruxisms adult
|
|
D020186||sleep bruxisms childhood
|
|
D020186||sleep related bruxism
|
|
D020186||sleep related bruxisms
|
|
D020186||teeth grinding disorder nocturnal
|
|
C535330|214900||aagenaes syndrome
|
|
C535330|214900||chls
|
|
C535330|214900||cholestasis lymphedema syndrome
|
|
C535330|214900||lcs
|
|
C535330|214900||lcs1
|
|
C535330|214900||lymphedema cholestasis syndrome
|
|
D020184||night terrors
|
|
D020184||adult night terror
|
|
D020184||adult night terrors
|
|
D020184||adult pavor nocturnus
|
|
D020184||childhood night terror
|
|
D020184||childhood night terrors
|
|
D020184||childhood pavor nocturnus
|
|
D020184||night terror adult
|
|
D020184||night terror childhood
|
|
D020184||night terror primary
|
|
D020184||night terrors adult
|
|
D020184||night terrors childhood
|
|
D020184||night terror secondary
|
|
D020184||night terrors primary
|
|
D020184||night terrors secondary
|
|
D020184||nocturnus adult pavor
|
|
D020184||nocturnus childhood pavor
|
|
D020184||pavor nocturnus
|
|
D020184||pavor nocturnus adult
|
|
D020184||pavor nocturnus childhood
|
|
D020184||primary night terror
|
|
D020184||primary night terrors
|
|
D020184||secondary night terror
|
|
D020184||secondary night terrors
|
|
D020184||sleep terror
|
|
D020184||sleep terror disorder
|
|
D020184||sleep terrors
|
|
D020184||terror adult night
|
|
D020184||terror childhood night
|
|
D020184||terror primary night
|
|
D020184||terrors adult night
|
|
D020184||terrors childhood night
|
|
D020184||terror secondary night
|
|
D020184||terror sleep
|
|
D020184||terrors primary night
|
|
D020184||terrors secondary night
|
|
D020184||terrors sleep
|
|
C537543||microcephaly pontocerebellar hypoplasia dyskinesia
|
|
C566068||tendons extensor of fingers anomalous insertion of
|
|
D020183||nocturnal paroxysmal dystonia
|
|
D020183||dystonia hypnogenic paroxysmal
|
|
D020183||dystonia nocturnal paroxysmal
|
|
D020183||dystonias hypnogenic paroxysmal
|
|
D020183||dystonia sleep related
|
|
D020183||dystonias nocturnal paroxysmal
|
|
D020183||dystonias sleep related
|
|
D020183||hypnogenic paroxysmal dystonia
|
|
D020183||hypnogenic paroxysmal dystonias
|
|
D020183||nocturnal paroxysmal dystonias
|
|
D020183||paroxysmal dystonia hypnogenic
|
|
D020183||paroxysmal dystonia nocturnal
|
|
D020183||paroxysmal dystonias hypnogenic
|
|
D020183||paroxysmal dystonias nocturnal
|
|
D020183||sleep related dystonia
|
|
D020183||sleep related dystonias
|
|
C537544||microcephaly seizures mental retardation heart disorders
|
|
C537544||microcephaly seizures mental retardation congenital heart disease and skeletal abnormalities
|
|
C566069||arthrogryposis distal type 10
|
|
C566069||tendo calcaneus short
|
|
D020182||sleep apnea central
|
|
D020182||alveolar hypoventilation central
|
|
D020182||alveolar hypoventilations central
|
|
D020182||apnea central
|
|
D020182||apnea central sleep
|
|
D020182||apneas central
|
|
D020182||apneas central sleep
|
|
D020182||apnea sleep central
|
|
D020182||breathing central sleep disordered
|
|
D020182||breathings central sleep disordered
|
|
D020182||central alveolar hypoventilation
|
|
D020182||central alveolar hypoventilation syndrome
|
|
D020182||central apnea
|
|
D020182||central apneas
|
|
D020182||central sleep apnea
|
|
D020182||central sleep apnea primary
|
|
D020182||central sleep apneas
|
|
D020182||central sleep apnea secondary
|
|
D020182||central sleep apnea syndrome
|
|
D020182||central sleep disordered breathing
|
|
D020182||central sleep disordered breathings
|
|
D020182||hypoventilation central alveolar
|
|
D020182||hypoventilations central alveolar
|
|
D020182||newborn primary sleep apneas
|
|
D020182||ondine syndrome
|
|
D020182||primary central sleep apnea
|
|
D020182||primary sleep apneas of newborn
|
|
D020182||secondary central sleep apnea
|
|
D020182||sleep apnea lethal central
|
|
D020182||sleep apnea newborn primary
|
|
D020182||sleep apneas central
|
|
D020182||sleep disordered breathing central
|
|
D020182||sleep disordered breathings central
|
|
C537541||microcephaly microphthalmos blindness
|
|
D020181||sleep apnea obstructive
|
|
D020181||apnea hypopnea syndrome sleep
|
|
D020181||apnea hypopnea syndromes sleep
|
|
D020181||apnea obstructive sleep
|
|
D020181||apneas obstructive sleep
|
|
D020181||obstructive sleep apnea
|
|
D020181||obstructive sleep apneas
|
|
D020181||obstructive sleep apnea syndrome
|
|
D020181||osahs
|
|
D020181||sleep apnea hypopnea syndrome
|
|
D020181||sleep apnea hypopnea syndromes
|
|
D020181||sleep apneas obstructive
|
|
D020181||sleep apnea syndrome obstructive
|
|
D020181||syndrome obstructive sleep apnea
|
|
D020181||syndrome sleep apnea hypopnea
|
|
D020181||syndrome sleep apnea obstructive
|
|
D020181||syndromes sleep apnea hypopnea
|
|
D020181||syndrome upper airway resistance sleep apnea
|
|
D020181||upper airway resistance sleep apnea syndrome
|
|
C537542||microcephaly nonsyndromal
|
|
C537542||nonsyndromal microcephaly
|
|
C537542||nonsyndromic microcephaly
|
|
D020189||nocturnal myoclonus syndrome
|
|
D020189||excessive periodic sleep related leg movements
|
|
D020189||myoclonus syndrome nocturnal
|
|
D020189||myoclonus syndrome sleep
|
|
D020189||myoclonus syndromes sleep
|
|
D020189||nocturnal myoclonus syndromes
|
|
D020189||periodic leg movements excessive sleep related
|
|
D020189||periodic limb movement disorder
|
|
D020189||periodic movement disorder sleep
|
|
D020189||sleep disorder periodic movements
|
|
D020189||sleep myoclonus syndrome
|
|
D020189||sleep myoclonus syndromes
|
|
D020189||sleep related periodic leg movements excessive
|
|
D020189||syndrome nocturnal myoclonus
|
|
D020189||syndrome sleep myoclonus
|
|
D020189||syndromes sleep myoclonus
|
|
D015605||cowpox
|
|
D015605||cow pox
|
|
D015605||pox cow
|
|
C563957|600321||diabetes mellitus insulin dependent 7
|
|
C563957|600321||iddm7
|
|
C563957|600321||insulin dependent diabetes mellitus 7
|
|
C567636|613341||leber congenital amaurosis 14
|
|
C567636|613341||lca14
|
|
C567636|613341||retinal dystrophy early onset severe lrat related
|
|
C567636|613341||retinal dystrophy early onset severe lrat related included
|
|
C567636|613341||retinitis pigmentosa juvenile lrat related
|
|
C567636|613341||retinitis pigmentosa juvenile lrat related included
|
|
607475|C564392||bothnia retinal dystrophy
|
|
607475|C564392||vasterbotten dystrophy
|
|
612527|C567281||diamond blackfan anemia 4
|
|
612527|C567281||dba4
|
|
C580365||pdgfrb associated chronic eosinophilic leukemia
|
|
C580365||atypical philadelphia negative chronic myeloid leukemia
|
|
C580365||chronic myeloproliferative disorder with eosinophilia
|
|
C580365||clonal eosinophilia with chronic myeloproliferative disorder
|
|
C580365||primary eosinophilia with chronic myeloproliferative disorder
|
|
C565353|605225||inflammatory bowel disease 7
|
|
C565353|605225||ibd7
|
|
C537536||seemanova lesny syndrome
|
|
C536205||ellis yale winter syndrome
|
|
C580364||pdgfra associated chronic eosinophilic leukemia
|
|
C580364||chronic eosinophilic leukemia
|
|
C580364||pdgfra associated myeloproliferative neoplasm
|
|
C566076||teeth odd shapes of
|
|
C566076||conical teeth multiple
|
|
C566076||lobodontia
|
|
C536203||elejalde disease
|
|
C536203||melanolysosomal neurocutaneous syndrome
|
|
C536203||neuroectodermal melanolysosomal disease
|
|
C536203||neuro ectodermal melanolysosomal syndrome
|
|
C537535||secretory breast carcinoma
|
|
C536204||elliott ludman teebi syndrome
|
|
C537538||segmentation syndrome 1
|
|
C537538||klippel feil syndrome with laryngeal malformation
|
|
C536207||citrulline transport defect
|
|
C567354|612301||osteopetrosis autosomal recessive 7
|
|
C567354|612301||optb7
|
|
C567354|612301||osteopetrosis osteoclast poor with hypogammaglobulinemia
|
|
C537539||microcephaly microcornea syndrome seemanova type
|
|
C536208||clark baraitser syndrome
|
|
C536208||baraitser syndrome
|
|
D020177||hypersomnolence idiopathic
|
|
D020177||cns hypersomnolence idiopathic
|
|
D020177||cns hypersomnolences idiopathic
|
|
D020177||hypersomnia idiopathic
|
|
D020177||hypersomnias idiopathic
|
|
D020177||hypersomnolence cns idiopathic
|
|
D020177||hypersomnolence idiopathic cns
|
|
D020177||hypersomnolences idiopathic
|
|
D020177||hypersomnolences idiopathic cns
|
|
D020177||idiopathic central nervous system hypersomnolence
|
|
D020177||idiopathic cns hypersomnolence
|
|
D020177||idiopathic cns hypersomnolences
|
|
D020177||idiopathic hypersomnia
|
|
D020177||idiopathic hypersomnias
|
|
D020177||idiopathic hypersomnolence
|
|
D020177||idiopathic hypersomnolences
|
|
C566039||colorectal cancer hereditary nonpolyposis type 6
|
|
C566039||colon cancer hereditary nonpolyposis type 6
|
|
C566039||hnpcc6
|
|
D019189||iron metabolism disorders
|
|
D019189||disorder iron metabolism
|
|
D019189||disorders iron metabolism
|
|
D019189||iron metabolism disorder
|
|
D019189||metabolism disorder iron
|
|
D019189||metabolism disorders iron
|
|
D004927||escherichia coli infections
|
|
D004927||e coli infection
|
|
D004927||e coli infections
|
|
D004927||escherichia coli infection
|
|
D004927||infection e coli
|
|
D004927||infection escherichia coli
|
|
D004927||infections e coli
|
|
D004927||infections escherichia coli
|
|
C567369||retinitis pigmentosa late onset dominant
|
|
C566038||tremor of intention ataxia and lipofuscinosis
|
|
C567500|611892||aneurysm intracranial berry 6
|
|
C567500|611892||anib6
|
|
C567481|300695||scapuloperoneal myopathy x linked dominant
|
|
C567481|300695||scapuloperoneal myopathy fhl1 related
|
|
C567481|300695||spm
|
|
C536415|260000||primary hyperoxaluria type 2
|
|
C536415|260000||d glycerate dehydrogenase deficiency
|
|
C536415|260000||glyceric aciduria
|
|
C536415|260000||glyoxylate reductase hydroxypyruvate reductase deficiency
|
|
C536415|260000||hp2
|
|
C536415|260000||hyperoxaluria primary type ii
|
|
C536415|260000||oxalosis 2
|
|
C536415|260000||oxalosis ii
|
|
D016908||gram positive bacterial infections
|
|
D016908||bacterial infection gram positive
|
|
D016908||bacterial infections gram positive
|
|
D016908||gram positive bacterial infection
|
|
D016908||infection gram positive bacterial
|
|
D016908||infections gram positive bacterial
|
|
D020179||jet lag syndrome
|
|
D020179||jet lag syndromes
|
|
D020179||time zone change syndrome
|
|
D020179||time zone syndrome
|
|
D020179||time zone syndromes
|
|
C565168|120790||complement component 4 partial deficiency of
|
|
D020178||sleep disorders circadian rhythm
|
|
D020178||advanced sleep phase syndrome
|
|
D020178||circadian rhythm sleep disorders
|
|
D020178||cycle disorder sleep wake
|
|
D020178||cycle disorders sleep wake
|
|
D020178||delayed sleep phase syndrome
|
|
D020178||disturbed nyctohemeral rhythm
|
|
D020178||disturbed nyctohemeral rhythms
|
|
D020178||non 24 hour sleep wake disorder
|
|
D020178||nonorganic sleep wake cycle disorders
|
|
D020178||nyctohemeral rhythm disturbed
|
|
D020178||nyctohemeral rhythms disturbed
|
|
D020178||shift work sleep disorder
|
|
D020178||shift work sleep disorders
|
|
D020178||sleep disorder shift work
|
|
D020178||sleep disorders shift work
|
|
D020178||sleep wake cycle disorder
|
|
D020178||sleep wake cycle disorders
|
|
D020178||sleep wake disorder non 24 hour
|
|
D020178||sleep wake schedule disorder
|
|
D020178||sleep wake schedule disorders
|
|
143470||hyperalphalipoproteinemia 1
|
|
143470||cetp deficiency high density lipoprotein cholesterol level quantitative trait locus 10 included
|
|
143470||cholesterol ester transfer protein deficiency
|
|
143470||halp1
|
|
143470||hdlcq10 included
|
|
D016905||gram negative bacterial infections
|
|
D016905||bacterial infection gram negative
|
|
D016905||bacterial infections gram negative
|
|
D016905||gram negative bacterial infection
|
|
D016905||infection gram negative bacterial
|
|
D016905||infections gram negative bacterial
|
|
C580334||nonsyndromic deafness
|
|
C580334||isolated deafness
|
|
C580334||nonsyndromic hearing impairment
|
|
C580334||nonsyndromic hearing loss
|
|
C580334||undifferentiated deafness
|
|
C580335||nonsyndromic holoprosencephaly
|
|
C580335||isolated holoprosencephaly
|
|
C580335||isolated hpe
|
|
C580335||nonsyndromic hpe
|
|
C580335||non syndromic non chromosomal holoprosencephaly
|
|
C580335||non syndromic non chromosomal hpe
|
|
C567374||skin hair eye pigmentation variation in 11
|
|
C567374||shep11
|
|
C567374||skin hair eye pigmentation 11 blue nonblue eyes
|
|
C566043||torus palatinus and torus mandibularis
|
|
C567376||skin hair eye pigmentation variation in 10
|
|
C567376||shep10
|
|
C567376||skin hair eye pigmentation 10 blond brown hair
|
|
611390||spastic ataxia 3 autosomal recessive
|
|
611390||arsal
|
|
611390||spax3
|
|
C566045||tibial torsion bilateral medial
|
|
C567370||ichthyosis congenital autosomal recessive ichthyin related
|
|
C567370||arcii
|
|
609056|C563799||amish infantile epilepsy syndrome
|
|
609056|C563799||epilepsy syndrome infantile onset symptomatic
|
|
609056|C563799||gm3 synthase deficiency
|
|
C563236|273300||testicular germ cell tumor
|
|
C563236|273300||embryonal cell carcinoma included
|
|
C563236|273300||endodermal sinus tumor included
|
|
C563236|273300||male germ cell tumor mgct seminoma included
|
|
C563236|273300||nonseminomatous germ cell tumors included
|
|
C563236|273300||spermatocytic seminoma included
|
|
C563236|273300||teratoma testicular included
|
|
C563236|273300||tgct
|
|
C538331|161000||naegeli syndrome
|
|
C538331|161000||naegeli franceschetti jadassohn syndrome
|
|
C538331|161000||nfjs
|
|
C538331|161000||nfj syndrome
|
|
C567195|612714||exocrine pancreatic insufficiency dyserythropoietic anemia and calvarial hyperostosis
|
|
D004937||esophageal fistula
|
|
D004937||esophageal fistulas
|
|
D004937||fistula esophageal
|
|
D004937||fistulas esophageal
|
|
181750||scleroderma familial progressive
|
|
181750||systemic sclerosis susceptibility to crest syndrome included
|
|
D004936||diverticulum esophageal
|
|
D004936||diverticula esophageal
|
|
D004936||esophageal diverticula
|
|
D004936||esophageal diverticulum
|
|
C566511|609579||scaphocephaly maxillary retrusion and mental retardation
|
|
D003607||dacryocystitis
|
|
D003607||dacryoadenitides
|
|
D003607||dacryoadenitis
|
|
D003607||dacryocystitides
|
|
D004939||esophageal perforation
|
|
D004939||esophageal perforations
|
|
D004939||perforation esophageal
|
|
D004939||perforations esophageal
|
|
D020163||ornithine carbamoyltransferase deficiency disease
|
|
D020163||deficiencies ornithine transcarbamylase
|
|
D020163||deficiencies otc
|
|
D020163||deficiency disease ornithine carbamoyltransferase
|
|
D020163||deficiency disease ornithine transcarbamylase
|
|
D020163||deficiency ornithine transcarbamylase
|
|
D020163||deficiency otc
|
|
D020163|311250||ornithine carbamoyltransferase deficiency
|
|
D020163||ornithine transcarbamylase deficiencies
|
|
D020163||ornithine transcarbamylase deficiency
|
|
D020163||ornithine transcarbamylase deficiency disease
|
|
D020163|311250||ornithine transcarbamylase deficiency hyperammonemia due to
|
|
D020163||otc deficiencies
|
|
D020163||otc deficiency
|
|
C566046||tibia hypoplasia of with polydactyly
|
|
C566046||tibial hemimelia polydactyly triphalangeal thumbs with fibular dimelia
|
|
D004933||esophageal atresia
|
|
D004933||atresia esophageal
|
|
D004933||atresias esophageal
|
|
D004933||esophageal atresias
|
|
D004932||esophageal and gastric varices
|
|
D004932||esophageal varices
|
|
D004932||esophageal varix
|
|
D004932||gastric varices
|
|
D004932||gastric varix
|
|
D004932||varices esophageal
|
|
D004932||varices gastric
|
|
D004932||varix esophageal
|
|
D004932||varix gastric
|
|
D004935||esophageal diseases
|
|
D004935||disease esophageal
|
|
D004935||diseases esophageal
|
|
D004935||esophageal disease
|
|
C566049||thyrotropin releasing hormone resistance generalized
|
|
D004934||esophageal cyst
|
|
D004934||cyst esophageal
|
|
D004934||cysts esophageal
|
|
D004934||esophageal cysts
|
|
D019190||iron overload
|
|
D019190||overload iron
|
|
C562420|113200||brachydactyly type d
|
|
C562420|113200||bdd
|
|
C562420|113200||stub thumb
|
|
D004931||esophageal achalasia
|
|
D004931||achalasia
|
|
D004931||achalasia esophageal
|
|
D004931||achalasias
|
|
D004931||achalasias esophageal
|
|
D004931||cardiospasm
|
|
D004931||cardiospasms
|
|
D004931||esophageal achalasias
|
|
D004931||megaesophagus
|
|
D016919||meningitis cryptococcal
|
|
D016919||cerebral cryptococcoses
|
|
D016919||cerebral cryptococcoses granulomous
|
|
D016919||cerebral cryptococcosis
|
|
D016919||cerebral cryptococcosis granulomous
|
|
D016919||cryptococcal meningitides
|
|
D016919||cryptococcal meningitis
|
|
D016919||cryptococcoses cerebral
|
|
D016919||cryptococcoses granulomous cerebral
|
|
D016919||cryptococcosis cerebral
|
|
D016919||cryptococcosis granulomous cerebral
|
|
D016919||granulomous cerebral cryptococcoses
|
|
D016919||granulomous cerebral cryptococcosis
|
|
D016919||meningitides cryptococcal
|
|
D016919||toruloma
|
|
D016919||torulomas
|
|
C567876|612881||heterotopia periventricular associated with chromosome 5q deletion
|
|
C567876|612881||periventricular nodular heterotopia 5
|
|
C567876|612881||pvnh5
|
|
310200|300376|D020388||muscular dystrophy duchenne type
|
|
310200||dmd duchenne muscular dystrophy
|
|
310200|300376|D020388||muscular dystrophy pseudohypertrophic progressive duchenne type
|
|
D016916||joint deformities acquired
|
|
D016916||acquired joint deformities
|
|
D016916||acquired joint deformity
|
|
D016916||deformities acquired joint
|
|
D016916||deformity acquired joint
|
|
D016916||joint deformity acquired
|
|
D016917||angiomatosis bacillary
|
|
D016917||angiomatoses bacillary
|
|
D016917||angiomatoses bacillary epithelioid
|
|
D016917||angiomatoses epithelioid
|
|
D016917||angiomatosis bacillary epithelioid
|
|
D016917||angiomatosis epithelioid
|
|
D016917||bacillary angiomatoses
|
|
D016917||bacillary angiomatosis
|
|
D016917||bacillary epithelioid angiomatoses
|
|
D016917||bacillary epithelioid angiomatosis
|
|
D016917||epithelioid angiomatoses
|
|
D016917||epithelioid angiomatoses bacillary
|
|
D016917||epithelioid angiomatosis
|
|
D016917||epithelioid angiomatosis bacillary
|
|
D016918||arthritis reactive
|
|
D016918||arthritides postinfectious
|
|
D016918||arthritides post infectious
|
|
D016918||arthritides reactive
|
|
D016918||arthritis postinfectious
|
|
D016918||arthritis post infectious
|
|
D016918||disease reiter
|
|
D016918||disease reiter apos s
|
|
D016918||postinfectious arthritides
|
|
D016918||post infectious arthritides
|
|
D016918||postinfectious arthritis
|
|
D016918||post infectious arthritis
|
|
D016918||reactive arthritides
|
|
D016918||reactive arthritis
|
|
D016918||reiter disease
|
|
D016918||reiter apos s disease
|
|
D016918||reiters disease
|
|
D016918||reiter syndrome
|
|
D016918||syndrome reiter
|
|
C563886|608647||ciliary dyskinesia primary 5
|
|
C563886|608647||cild5
|
|
C563886|608647||ciliary dyskinesia primary 5 with or without situs inversus
|
|
C563886|608647||ciliary dyskinesia primary 5 without situs inversus
|
|
611383||ush2d
|
|
C567385||chromosome 10q23 deletion syndrome
|
|
C566053||thumbs stiff with brachydactyly type a1 and developmental delay
|
|
607602|C564367||ichthyosis cyclic with epidermolytic hyperkeratosis
|
|
607602|C564367||aei
|
|
607602|C564367||ciehk
|
|
607602|C564367||epidermolytic ichthyosis annular
|
|
C566054||thumb deformity and alopecia
|
|
C566055||bleeding disorder due to defective thromboxane a2 receptor
|
|
607087|C564627||aortic aneurysm familial thoracic 2
|
|
607087|C564627||aat2
|
|
607087|C564627||faa2
|
|
C564664|606768||myopathy distal with anterior tibial onset
|
|
C564664|606768||dmat
|
|
C566051||takao vcf syndrome
|
|
C566017||parkinson disease 5
|
|
C567348||thrombophilia hereditary due to protein s deficiency autosomal recessive
|
|
C566018||twinning due to superfetation
|
|
C566018||superfetation twinning
|
|
C566019||tune deafness
|
|
C566019||amusia congenital
|
|
C566019||dysmelodia
|
|
D020151||protein c deficiency
|
|
D020151||deficiencies protein c
|
|
D020151||deficiency protein c
|
|
D020151||hereditary thrombophilia due to protein c deficiency
|
|
D020151||protein c deficiencies
|
|
C563961|600316||deafness autosomal recessive 3
|
|
C563961|600316||dfnb3
|
|
C563961|600316||neurosensory nonsyndromic recessive deafness 3
|
|
C563961|600316||nsrd3
|
|
C566583|602087||arrhythmogenic right ventricular dysplasia familial 4
|
|
C566583|602087||arrhythmogenic right ventricular cardiomyopathy 4
|
|
C566583|602087||arvc4
|
|
C566583|602087||arvd4
|
|
300856||hypospadias 4 x linked susceptibility to
|
|
300856||hysp4
|
|
C566013||urate binding globulin decrease in
|
|
D020150||chorea gravidarum
|
|
D020150||chorea gravidarums
|
|
D020150||chorea pregnancy induced
|
|
D020150||choreas pregnancy induced
|
|
D020150||choreoathetoses pregnancy associated
|
|
D020150||choreoathetosis pregnancy associated
|
|
D020150||gravidarum chorea
|
|
D020150||pregnancy associated choreoathetoses
|
|
D020150||pregnancy associated choreoathetosis
|
|
D020150||pregnancy induced chorea
|
|
D020150||pregnancy induced choreas
|
|
C567344||chromosome 2q31 2 deletion syndrome
|
|
C566014||undritz anomaly
|
|
C566014||hypersegmentation of nuclei of polymorphonuclear leukocytes
|
|
C567086|611783||erythrocytosis familial 4
|
|
C567086|611783||ecyt4
|
|
C567347||thrombophilia hereditary due to protein s deficiency autosomal dominant
|
|
C567346||chromosome 1q43 q44 deletion syndrome
|
|
C567346||chromosome 1qter deletion syndrome
|
|
608236|C564269||slowed nerve conduction velocity autosomal dominant
|
|
C567739|135700||fibrosis of extraocular muscles congenital 3b
|
|
C567739|135700||blepharoptosis with absent eye movements
|
|
C567739|135700||cfeom1
|
|
C567739|135700||cfeom3b
|
|
C567739|135700||cfeom3b included
|
|
C567739|135700||feom1
|
|
C567739|135700||feom1 locus fibrosis of extraocular muscles congenital 3b included
|
|
C567739|135700||fibrosis of extraocular muscles congenital 1
|
|
C567739|135700||ophthalmoplegia congenital
|
|
601471|C536386||facial paresis hereditary congenital
|
|
601471|C536386|C563309||facial palsy congenital unilateral or bilateral
|
|
601471|C536386||facial paresis hereditary congenital 1
|
|
601471|C536386||facial paresis hereditary congenital 2
|
|
601471|C536386||hcfp1
|
|
601471|C536386||hcfp2
|
|
601471|C536386||mbs2 formerly
|
|
601471|C536386||mbs3 formerly
|
|
601471|C536386||mobius syndrome 2 formerly
|
|
601471|C536386||mobius syndrome 3 formerly
|
|
601471|C536386||moebius syndrome 2 formerly
|
|
601471|C536386||moebius syndrome 3 formerly
|
|
607450|C564400||arrhythmogenic right ventricular dysplasia familial 8
|
|
607450|C564400||arrhythmogenic right ventricular cardiomyopathy 8
|
|
607450|C564400||arvc8
|
|
607450|C564400||arvd8
|
|
D020157||amino acid transport disorders inborn
|
|
D020157||inborn transport disorders amino acid
|
|
D020157||inherited amino acid transport disorders
|
|
D020157||transport disorders amino acid inborn
|
|
C565184|610758||cerebrooculofacioskeletal syndrome 4
|
|
C565184|610758||cofs4
|
|
C580316||myofibrillar myopathy
|
|
C580316||myofibrillar myopathies
|
|
611377||bdb2
|
|
D052582||trigger finger disorder
|
|
D052582||digits trigger
|
|
D052582||digit trigger
|
|
D052582||entrapment flexor tendon
|
|
D052582||entrapments flexor tendon
|
|
D052582||finger snapping
|
|
D052582||fingers snapping
|
|
D052582||flexor tendon entrapment
|
|
D052582||flexor tendon entrapments
|
|
D052582||snapping finger
|
|
D052582||snapping fingers
|
|
D052582||tendon entrapment flexor
|
|
D052582||tendon entrapments flexor
|
|
D052582||thumbs trigger
|
|
D052582||thumb trigger
|
|
D052582||trigger digit
|
|
D052582||trigger digits
|
|
D052582||trigger thumb
|
|
D052582||trigger thumbs
|
|
D033461||hyperuricemia
|
|
D005693|230200||galactosemias
|
|
D005693|230200||classic galactosemia
|
|
D005693|230200||classic galactosemias
|
|
D005693|230200||deficiencies galactokinase
|
|
D005693|230200||deficiencies galactose 1 phosphate uridyltransferase
|
|
D005693|230200||deficiencies galactose 1 phosphate uridylyltransferase
|
|
D005693|230200||deficiencies galactose epimerase
|
|
D005693|230200||deficiencies gale
|
|
D005693|230200||deficiencies galk
|
|
D005693|230200||deficiencies galt
|
|
D005693|230200||deficiencies hereditary galactokinase
|
|
D005693|230200||deficiencies udp galactose 4 epimerase
|
|
D005693|230200||deficiency disease galactokinase
|
|
D005693|230200||deficiency disease galactose 1 phosphate uridyl transferase
|
|
D005693|230200||deficiency diseases udp galactose 4 epimerase
|
|
D005693|230200||deficiency disease udp galactose 4 epimerase
|
|
D005693|230200||deficiency disease udpglucose 4 epimerase
|
|
D005693|230200||deficiency galactokinase
|
|
D005693|230200||deficiency galactose 1 phosphate uridyltransferase
|
|
D005693|230200||deficiency galactose 1 phosphate uridylyltransferase
|
|
D005693|230200||deficiency galactose epimerase
|
|
D005693|230200||deficiency galactosemia epimerase
|
|
D005693|230200||deficiency galactosemias epimerase
|
|
D005693|230200||deficiency gale
|
|
D005693|230200||deficiency galk
|
|
D005693|230200||deficiency galt
|
|
D005693|230200||deficiency hereditary galactokinase
|
|
D005693|230200||deficiency udp galactose 4 epimerase
|
|
D005693|230200||epimerase deficiency galactosemia
|
|
D005693|230200||epimerase deficiency galactosemias
|
|
D005693|230200||galactokinase deficiencies
|
|
D005693|230200||galactokinase deficiencies hereditary
|
|
D005693|230200||galactokinase deficiency
|
|
D005693|230200||galactokinase deficiency disease
|
|
D005693|230200||galactokinase deficiency diseases
|
|
D005693|230200||galactokinase deficiency hereditary
|
|
D005693|230200||galactose 1 phosphate uridyltransferase deficiencies
|
|
D005693|230200||galactose 1 phosphate uridyltransferase deficiency
|
|
D005693|230200||galactose 1 phosphate uridyl transferase deficiency disease
|
|
D005693|230200||galactose 1 phosphate uridylyltransferase deficiencies
|
|
D005693|230200||galactose 1 phosphate uridylyltransferase deficiency
|
|
D005693|230200||galactose epimerase deficiencies
|
|
D005693|230200||galactose epimerase deficiency
|
|
D005693|230200||galactosemia
|
|
D005693|230200||galactosemia 2
|
|
D005693|230200||galactosemia 2s
|
|
D005693|230200||galactosemia 3
|
|
D005693|230200||galactosemia 3s
|
|
D005693|230200||galactosemia classic
|
|
D005693|230200||galactosemia epimerase deficiency
|
|
D005693|230200||galactosemia ii
|
|
D005693|230200||galactosemia iii
|
|
D005693|230200||galactosemia iiis
|
|
D005693|230200||galactosemias classic
|
|
D005693|230200||galactosemias epimerase deficiency
|
|
D005693|230200||gale deficiencies
|
|
D005693|230200||gale deficiency
|
|
D005693|230200||galk deficiencies
|
|
D005693|230200||galk deficiency
|
|
D005693|230200||galt deficiencies
|
|
D005693|230200||hereditary galactokinase deficiencies
|
|
D005693|230200||hereditary galactokinase deficiency
|
|
D005693|230200||udp galactose 4 epimerase deficiencies
|
|
D005693|230200||udp galactose 4 epimerase deficiency
|
|
D005693|230200||udp galactose 4 epimerase deficiency disease
|
|
D005693|230200||udp galactose 4 epimerase deficiency diseases
|
|
D005693|230200||udpglucose 4 epimerase deficiency disease
|
|
D005693|230200||udpglucose hexose 1 phosphate uridylyltransferase deficiency
|
|
D005693|230200||uridyltransferase deficiencies galactose 1 phosphate
|
|
D005693|230200||uridyltransferase deficiency galactose 1 phosphate
|
|
D005693|230200||uridylyltransferase deficiencies galactose 1 phosphate
|
|
D005693|230200||uridylyltransferase deficiency galactose 1 phosphate
|
|
D005693|230200||utp hexose 1 phosphate uridylyltransferase deficiency
|
|
D005693|230200||utp hexose 1 phosphate uridylyltransferase deficiency disease
|
|
C562657|612716||dystonia dopa responsive due to sepiapterin reductase deficiency
|
|
C562657|612716||dopa responsive dystonia due to sepiapterin reductase deficiency
|
|
C562657|612716||sepiapterin reductase deficiency
|
|
C562657|612716||spr deficiency
|
|
C566022||trochlea of the humerus aplasia of
|
|
C567353||thrombophilia hereditary due to protein c deficiency autosomal recessive
|
|
C567353|612304||proc deficiency autosomal recessive
|
|
C567353|612304||protein c deficiency autosomal recessive
|
|
C566023||down syndrome critical region
|
|
C567350||chromosome 2q32 q33 deletion syndrome
|
|
D020144||basal ganglia cerebrovascular disease
|
|
D020144||basal ganglia vascular disease
|
|
D020144||cerebrovascular disease basal ganglia
|
|
D020144||lenticulostriate diseases vascular
|
|
D020144||lenticulostriate vascular disease
|
|
D020144||lenticulostriate vascular diseases
|
|
D020144||lenticulostriate vasculopathies
|
|
D020144||lenticulostriate vasculopathy
|
|
D020144||vascular disease basal ganglia
|
|
D020144||vascular disease lenticulostriate
|
|
D020144||vascular diseases basal ganglia
|
|
D020144||vascular diseases lenticulostriate
|
|
D020144||vascular lenticulostriate diseases
|
|
D020144||vasculopathies lenticulostriate
|
|
D020144||vasculopathy lenticulostriate
|
|
C566028||triphalangeal thumb with double phalanges
|
|
D004915||leukemia erythroblastic acute
|
|
D004915||acute erythroblastic leukemia
|
|
D004915||acute erythroblastic leukemias
|
|
D004915||di guglielmo disease
|
|
D004915||di guglielmo apos s disease
|
|
D004915||di guglielmos disease
|
|
D004915||disease di guglielmo
|
|
D004915||disease di guglielmo apos s
|
|
D004915||erythremic myeloses
|
|
D004915||erythremic myelosis
|
|
D004915||erythroblastic leukemia acute
|
|
D004915||erythroblastic leukemias acute
|
|
D004915||erythroleukemia
|
|
D004915||erythroleukemias
|
|
D004915||leukemia acute erythroblastic
|
|
D004915||leukemia myeloid acute m6
|
|
D004915||leukemias acute erythroblastic
|
|
D004915||myeloid leukemia acute m6
|
|
D004915||myeloses erythremic
|
|
D004915||myelosis erythremic
|
|
D020143||gangliosidoses gm2
|
|
D020143||gangliosidose gm2
|
|
D020143||gangliosidosis gm2
|
|
D020143||gm2 gangliosidose
|
|
D020143||g m2 gangliosidoses
|
|
D020143||gm2 gangliosidoses
|
|
D020143||gm2 gangliosidosis
|
|
C566029||triosephosphate isomerase deficiency
|
|
D020141||hemostatic disorders
|
|
D020141||disorders vascular hemostatic
|
|
D020141||disorder vascular hemostatic
|
|
D020141||hemostatic disorder
|
|
D020141||hemostatic disorders vascular
|
|
D020141||hemostatic disorder vascular
|
|
D020141||vascular hemostatic disorder
|
|
D020141||vascular hemostatic disorders
|
|
D020140||lysosomal storage diseases nervous system
|
|
D020140||lysosomal enzyme disorders nervous system
|
|
D020140||nervous system lysosomal enzyme disorders
|
|
D020140||nervous system lysosomal storage diseases
|
|
C566024||transient myeloproliferative disorder of down syndrome
|
|
138900||uric acid concentration serum quantitative trait locus 1
|
|
138900||gout1
|
|
138900||gout susceptibility 1
|
|
138900||uaqtl1
|
|
C566025||leukemia megakaryoblastic of down syndrome
|
|
D020149||manganese poisoning
|
|
D020149||manganese neurotoxicity syndrome
|
|
D020149||manganese neurotoxicity syndromes
|
|
D020149||nervous system diseases manganese induced
|
|
D020149||nervous system poisoning manganese
|
|
D020149||neurotoxicity syndrome manganese
|
|
D020149||neurotoxicity syndromes manganese
|
|
D020149||poisoning manganese
|
|
D020149||syndrome manganese neurotoxicity
|
|
D020149||syndromes manganese neurotoxicity
|
|
C538101|311400||paine syndrome
|
|
C538101|311400||microcephaly with spastic diplegia
|
|
C538101|311400||microcephaly with spastic diplegia seemanova syndrome i included
|
|
C538101|311400||seemanova syndrome i
|
|
C538189|228930||fuhrmann syndrome
|
|
C538189|228930||fibular aplasia or hypoplasia femoral bowing and poly syn and oligodactyly
|
|
C562799|229050||folate malabsorption hereditary
|
|
C562799|229050||congenital folate malabsorption
|
|
C562799|229050||folic acid transport defect
|
|
C562799|229050||hereditary folate malabsorption
|
|
D020147||coagulation protein disorders
|
|
D020147||blood coagulation factor deficiencies
|
|
D020147||coagulation protein disorder
|
|
D020147||coagulation proteins disorder
|
|
D020147||coagulation proteins disorders
|
|
D020147||disorder coagulation protein
|
|
D020147||disorder coagulation proteins
|
|
D020147||disorders coagulation protein
|
|
D020147||disorders coagulation proteins
|
|
D020147||protein disorder coagulation
|
|
D020147||protein disorders coagulation
|
|
D020147||proteins disorder coagulation
|
|
D020147||proteins disorders coagulation
|
|
D020146||putaminal hemorrhage
|
|
D020146||brain hemorrhage putaminal
|
|
D020146||brain hemorrhages putaminal
|
|
D020146||hemorrhage putamen
|
|
D020146||hemorrhage putaminal
|
|
D020146||putamen hemorrhage
|
|
D020146||putaminal hematoma
|
|
C580329||opticospinal multiple sclerosis
|
|
C580329||opticospinal ms
|
|
C580329||optic spinal ms
|
|
C580329||optic spinal multiple sclerosis
|
|
D020145||basal ganglia hemorrhage
|
|
D020145||basal ganglionic hemorrhage
|
|
D020145||ganglionic hemorrhage basal
|
|
D020145||hematoma basal ganglia
|
|
D020145||hemorrhage basal ganglia
|
|
D020145||hemorrhage basal ganglionic
|
|
609048||melanoma cutaneous malignant susceptibility to 3
|
|
609048||cmm3
|
|
D051261||granulomatosis orofacial
|
|
D051261||granulomatoses orofacial
|
|
D051261||orofacial granulomatoses
|
|
D051261||orofacial granulomatosis
|
|
612692||agammaglobulinemia 6 autosomal recessive
|
|
612692||agammaglobulinemia autosomal recessive due to cd79b defect
|
|
612692||agm6
|
|
610031||polymicrogyria symmetric or asymmetric
|
|
610031||pmgysa
|
|
C567363|612286||nephrolithiasis osteoporosis hypophosphatemic 1
|
|
C567363|612286||nphlop1
|
|
C566031||triglyceride storage disease type i
|
|
C567362|612287||nephrolithiasis osteoporosis hypophosphatemic 2
|
|
C567362|612287||nphlop2
|
|
C566032||trichodysplasia xeroderma
|
|
C566034||trichoepitheliomas multiple desmoplastic
|
|
D004919||erythroplasia
|
|
D004919||erythroplasias
|
|
C567360||progeroid syndrome congenital petty type
|
|
C566030||triglyceride storage disease type ii
|
|
D020132||anticipation genetic
|
|
D020132||anticipations genetic
|
|
D020132||genetic anticipation
|
|
D020132||genetic anticipations
|
|
300831||ck syndrome
|
|
300831||mental retardation x linked with thin body habitus and cortical malformation
|
|
C567328||coloboma ocular and ichthyosis brain malformations and endocrine abnormalities
|
|
D019142||hemorrhagic fever ebola
|
|
D019142||ebola hemorrhagic fever
|
|
D019142||ebola virus disease
|
|
C567325|612389||pontocerebellar hypoplasia type 2b
|
|
300833||46 xx sex reversal 3
|
|
300833||46 xx sex reversal sox3 related chromosome xq26 deletion syndrome included
|
|
300833||chromosome xq26 duplication syndrome
|
|
300833||srxx3
|
|
C567324|612390||pontocerebellar hypoplasia type 2c
|
|
135100|D009221||myositis ossificans
|
|
135100|D009221||fibrodysplasia ossificans progressiva
|
|
135100|D009221||fop
|
|
135100|D009221||myositis ossificans progressiva
|
|
135100|D009221||progressive myositis ossificans
|
|
135100|D009221||progressive ossifying myositis
|
|
103285|C538052||propping zerres syndrome
|
|
103285|C538052||acro dermato ungual lacrimal tooth syndrome
|
|
103285|C538052||adult syndrome
|
|
103285|C538052||pigment anomaly ectrodactyly hypodontia
|
|
D054331|305700||sertoli cell only syndrome
|
|
D054331|305700||del castillo syndrome
|
|
D054331|305700||germinal cell aplasia
|
|
D054331|305700||spermatogenic failure x linked 1
|
|
D054331|305700||spgfx1
|
|
D020139||gastroschisis
|
|
D020139||congenital fissure of the abdominal cavity
|
|
D020139||gastroschises
|
|
D020138||hyperhomocysteinemias
|
|
C581628||metatropic dwarfism type ii
|
|
C581628||metatropic dwarfism type 2
|
|
C581628||metatropic dysplasia 2
|
|
C581628||metatropic dysplasia type ii
|
|
D051270||headache disorders primary
|
|
D051270||alarm clock headache
|
|
D051270||alarm clock headaches
|
|
D051270||benign cough headache
|
|
D051270||benign cough headaches
|
|
D051270||benign exertional headache
|
|
D051270||benign exertional headaches
|
|
D051270||clock headache alarm
|
|
D051270||clock headaches alarm
|
|
D051270||cough headache
|
|
D051270||cough headache benign
|
|
D051270||cough headaches benign
|
|
D051270||disorder primary headache
|
|
D051270||disorders primary headache
|
|
D051270||exertional headache benign
|
|
D051270||exertional headaches benign
|
|
D051270||headache alarm clock
|
|
D051270||headache benign cough
|
|
D051270||headache benign exertional
|
|
D051270||headache cough
|
|
D051270||headache disorder primary
|
|
D051270||headache hypnic
|
|
D051270||headache ice pick
|
|
D051270||headache primary cough
|
|
D051270||headache primary exertional
|
|
D051270||headache primary stabbing
|
|
D051270||headache primary thunderclap
|
|
D051270||headaches alarm clock
|
|
D051270||headaches benign cough
|
|
D051270||headaches benign exertional
|
|
D051270||headaches ice pick
|
|
D051270||headache stabbing
|
|
D051270||headache syndrome hypnic
|
|
D051270||headache syndromes hypnic
|
|
D051270||headache thunderclap
|
|
D051270||hypnic headache
|
|
D051270||hypnic headache syndrome
|
|
D051270||hypnic headache syndromes
|
|
D051270||ice pick headache
|
|
D051270||ice pick headaches
|
|
D051270||primary cough headache
|
|
D051270||primary exertional headache
|
|
D051270||primary headache disorder
|
|
D051270||primary headache disorders
|
|
D051270||primary stabbing headache
|
|
D051270||primary thunderclap headache
|
|
D051270||stabbing headache
|
|
D051270||thunderclap headache
|
|
235400|C538266||atypical hemolytic uremic syndrome
|
|
235400|C538266||ahus1
|
|
235400|C538266||ahus2
|
|
235400|C538266||ahus3
|
|
235400|C538266||ahus4
|
|
235400|C538266||ahus5
|
|
235400|C538266||ahus6
|
|
235400|C538266||ahus susceptibility to 1 hemolytic uremic syndrome typical included
|
|
235400|C538266||ahus susceptibility to 2
|
|
235400|C538266||ahus susceptibility to 3
|
|
235400|C538266||ahus susceptibility to 4
|
|
235400|C538266||ahus susceptibility to 5
|
|
235400|C538266||ahus susceptibility to 6
|
|
235400|C538266||hemolytic uremic syndrome atypical
|
|
235400|C538266||hemolytic uremic syndrome atypical susceptibility to 1
|
|
235400|C538266||hemolytic uremic syndrome atypical susceptibility to 2
|
|
235400|C538266||hemolytic uremic syndrome atypical susceptibility to 3
|
|
235400|C538266||hemolytic uremic syndrome atypical susceptibility to 4
|
|
235400|C538266||hemolytic uremic syndrome atypical susceptibility to 5
|
|
235400|C538266||hemolytic uremic syndrome atypical susceptibility to 6
|
|
235400|C538266||nonenteropathic hus
|
|
235400|C538266||non shiga like toxin associated hus
|
|
235400|C538266||non stx hus
|
|
251255|C567101||microcephaly with mental retardation and digital anomalies
|
|
251255|C567101||jawad syndrome
|
|
251255|C567101||jwds
|
|
251255|C567101|D011004||kelly syndrome
|
|
D007160||immunoproliferative disorders
|
|
D007160||disorder immunoproliferative
|
|
D007160||disorders immunoproliferative
|
|
D007160||immunoproliferative disorder
|
|
D051271||headache disorders secondary
|
|
D051271||analgesic overuse headache
|
|
D051271||analgesic overuse headaches
|
|
D051271||analgesic rebound headache
|
|
D051271||analgesic rebound headaches
|
|
D051271||disorder secondary headache
|
|
D051271||disorders secondary headache
|
|
D051271||headache analgesic overuse
|
|
D051271||headache analgesic rebound
|
|
D051271||headache disorder secondary
|
|
D051271||headaches analgesic overuse
|
|
D051271||headaches analgesic rebound
|
|
D051271||secondary headache disorder
|
|
D051271||secondary headache disorders
|
|
D007161||immunoproliferative small intestinal disease
|
|
D007161||alpha chain disease
|
|
D007161||alpha chain diseases
|
|
D007161||disease alpha chain
|
|
D007161||diseases alpha chain
|
|
D007161||heavy chain disease iga type
|
|
D007161||ipsid
|
|
D007161||lymphoma mediterranean
|
|
D007161||mediterranean lymphoma
|
|
C566000||glycoprotein ia deficiency
|
|
C566000||gp ia deficiency
|
|
C566006||long qt syndrome 1 2
|
|
300842||mclds mcleod phenotype
|
|
300842||neuroacanthocytosis mcleod type mcleod syndrome with chronic granulomatous disease included
|
|
C566008||vasculitis lymphocytic nodular
|
|
300845||moyamoya disease 4 with short stature hypergonadotropic hypogonadism and facial dysmorphism
|
|
300845||chromosome xq28 deletion syndrome 3 4 kb
|
|
300845||mymy4
|
|
300845||syndromic moyamoya disease
|
|
C566002||vertebral hypoplasia with lumbar kyphosis
|
|
D019150||neuroaxonal dystrophies
|
|
D019150||adult neuroaxonal dystrophy
|
|
D019150||disease seitelberger
|
|
D019150||disease seitelberger apos s
|
|
D019150||dystrophy adult neuroaxonal
|
|
D019150||dystrophy infantile neuroaxonal
|
|
D019150||dystrophy juvenile neuroaxonal
|
|
D019150||dystrophy neuroaxonal
|
|
D019150||infantile neuroaxonal dystrophy
|
|
D019150||juvenile neuroaxonal dystrophy
|
|
D019150||late infantile neuroaxonal dystrophy
|
|
D019150||nbia pla2g6 related
|
|
D019150||neuroaxonal dystrophy
|
|
D019150||neuroaxonal dystrophy adult
|
|
D019150||neuroaxonal dystrophy juvenile
|
|
D019150||neuroaxonal dystrophy late infantile
|
|
D019150||pla2g6 associated neurodegeneration
|
|
D019150||pla2g6 related nbia
|
|
D019150||seitelberger apos s disease
|
|
D019150||seitelbergers disease
|
|
C566004||venular insufficiency systemic
|
|
C565780|604387||nephronophthisis 3
|
|
C565780|604387||nephronophthisis adolescent
|
|
C565780|604387||nph3
|
|
C565780|604387||nphp3
|
|
C537252|603552||hemophagocytic lymphohistiocytosis familial 4
|
|
C537252|603552||fhl4
|
|
C537252|603552||hlh4
|
|
C537252|603552||hplh4
|
|
C567040|603585||congenital disorder of glycosylation type iif
|
|
C567040|603585||cdg2f
|
|
C567040|603585||cdgiif
|
|
C567040|603585||cdg iif
|
|
D007169||impetigo
|
|
D007169||impetigo contagiosa
|
|
D007177||inappropriate adh syndrome
|
|
D007177||adh syndrome inappropriate
|
|
D007177||antidiuretic hormone inappropriate secretion
|
|
D007177||inappropriate vasopressin secretion syndrome
|
|
D007177||schwartz bartter syndrome
|
|
D007177||siadh
|
|
D007177||syndrome inappropriate adh
|
|
D007177||syndrome of inappropriate adh siadh secretion
|
|
D007177||syndrome schwartz bartter
|
|
D007174||impulse control disorders
|
|
D007174||disorders impulse control
|
|
D007174||disorders intermittent explosive
|
|
D007174||explosive disorder intermittent
|
|
D007174||intermittent explosive disorder
|
|
D007174||intermittent explosive disorders
|
|
D007174||kleptomania
|
|
C565292|605804||dermatitis atopic 3
|
|
C565292|605804||atod3
|
|
C565292|605804||dermatitis atopic with asthma
|
|
612671||uric acid concentration serum quantitative trait locus 4
|
|
612671||gout4
|
|
612671||gout susceptibility 4
|
|
612671||uaqtl4
|
|
253260|D028921||biotinidase deficiency
|
|
253260|D028921||biotinidase deficiencies
|
|
253260|D028921||btd deficiencies
|
|
253260|D028921||btd deficiency
|
|
253260|D028921||carboxylase deficiency multiple late onset
|
|
253260|D028921||deficiencies biotinidase
|
|
253260|D028921||deficiencies btd
|
|
253260|D028921||deficiency biotinidase
|
|
253260|D028921||deficiency btd
|
|
253260|D028921||deficiency multiple carboxylase late onset
|
|
253260|D028921||late onset biotin responsive multiple carboxylase deficiency
|
|
253260|D028921||late onset multiple carboxylase deficiency
|
|
253260|D028921||multiple carboxylase deficiency late onset
|
|
D007172||erectile dysfunction
|
|
D007172||dysfunction erectile
|
|
D007172||impotence
|
|
D007172||impotence male
|
|
D007172||impotence male sexual
|
|
D007172||male impotence
|
|
D007172||male sexual impotence
|
|
D007172||sexual impotence male
|
|
C567341||thrombophilia familial due to decreased release of tissue plasminogen activator
|
|
C567341||hyperfibrinolysis familial due to increased release of tissue plasminogen activator
|
|
C566010||uterus bicornis bicollis with partial vaginal septum and unilateral hematocolpos with ipsilateral renal agenesis
|
|
C566011||urticaria familial localized heat
|
|
C566012||ureter bifid or double
|
|
600698||high mobility group at hook 2
|
|
600698||hmga2 high mobility group protein i c
|
|
600698||hmgic
|
|
600698||high mobility group protein hmgic breakpoint associated with benign lipoma
|
|
600698||babl
|
|
600698||lipo hmgic lpp fusion gene included
|
|
600698||hmgic lhfp fusion gene included
|
|
600698||hmgic rad51l1 fusion gene included
|
|
600698||hmgic hei10 fusion gene included
|
|
600698||hmgic aldh2 fusion gene included
|
|
600698||hmgic cox6c fusion gene included
|
|
D019121||burkholderia infections
|
|
D019121||burkholderia infection
|
|
D019121||infection burkholderia
|
|
D019121||infections burkholderia
|
|
C537032|245660||laryngo onycho cutaneous syndrome
|
|
C537032|245660||laryngeal and ocular granulation in indian children
|
|
C537032|245660||laryngoonychocutaneous syndrome
|
|
C537032|245660||locs
|
|
C537032|245660||logic syndrome
|
|
C567300||skin hair eye pigmentation variation in 4
|
|
C567300||shep4
|
|
C567300||skin hair eye pigmentation 4 fair dark skin
|
|
144700|D002292||carcinoma renal cell
|
|
144700|D002292||adenocarcinoma of kidney
|
|
144700|D002292||adenocarcinoma of kidney nonpapillary renal carcinoma 1 locus included
|
|
144700|D002292||adenocarcinoma renal
|
|
144700|D002292||adenocarcinoma renal cell
|
|
144700|D002292||adenocarcinomas renal cell
|
|
144700|D002292||cancer renal cell
|
|
144700|D002292||cancers renal cell
|
|
144700|D002292||carcinoma collecting duct
|
|
144700|D002292||carcinoma collecting duct kidney
|
|
144700|D002292||carcinoma hypernephroid
|
|
144700|D002292||carcinoma nephroid
|
|
144700|D002292||carcinomas collecting duct
|
|
144700|D002292||carcinomas collecting duct kidney
|
|
144700|D002292||carcinomas hypernephroid
|
|
144700|D002292||carcinomas nephroid
|
|
144700|D002292||carcinomas renal cell
|
|
144700|D002292||chromophil renal cell carcinoma
|
|
144700|D002292||chromophobe renal cell carcinoma
|
|
144700|D002292||clear cell renal carcinoma
|
|
144700|D002292||clear cell renal cell carcinoma
|
|
144700|D002292||collecting duct carcinoma
|
|
144700|D002292||collecting duct carcinoma kidney
|
|
144700|D002292||collecting duct carcinoma of the kidney
|
|
144700|D002292||collecting duct carcinomas
|
|
144700|D002292||collecting duct carcinomas kidney
|
|
144700|D002292||duct carcinoma collecting
|
|
144700|D002292||duct carcinoma collecting kidney
|
|
144700|D002292||duct carcinomas collecting
|
|
144700|D002292||duct carcinomas collecting kidney
|
|
144700|D002292||grawitz tumor
|
|
144700|D002292||hypernephroid carcinoma
|
|
144700|D002292||hypernephroid carcinomas
|
|
144700|D002292||hypernephroma
|
|
144700|D002292||hypernephromas
|
|
144700|D002292||nephroid carcinoma
|
|
144700|D002292||nephroid carcinomas
|
|
144700|D002292||nrc1 included
|
|
144700|D002292||papillary renal cell carcinoma
|
|
144700|D002292||rcc
|
|
144700|D002292||rccp1
|
|
144700|D002292||renal cell adenocarcinoma
|
|
144700|D002292||renal cell adenocarcinomas
|
|
144700|D002292||renal cell cancer
|
|
144700|D002292||renal cell cancers
|
|
144700|D002292||renal cell carcinoma
|
|
144700|D002292||renal cell carcinoma nonpapillary
|
|
144700|D002292||renal cell carcinoma papillary
|
|
144700|D002292||renal cell carcinoma papillary 1
|
|
144700|D002292||renal cell carcinomas
|
|
144700|D002292||renal collecting duct carcinoma
|
|
144700|D002292||sarcomatoid renal cell carcinoma
|
|
144700|D002292||tumor grawitz
|
|
C565100|125852||diabetes mellitus insulin dependent 2
|
|
C565100|125852||iddm2
|
|
C565100|125852||insulin dependent diabetes mellitus 2
|
|
300816||combined oxidative phosphorylation deficiency 6
|
|
300816||coxpd6
|
|
300816||encephalomyopathy mitochondrial x linked
|
|
606179|D017824||bone cysts aneurysmal
|
|
606179|D017824||aneurysmal bone cysts
|
|
606179|D017824||bone cyst aneurysmal
|
|
606179|D017824||cyst aneurysmal bone
|
|
606179|D017824||cysts aneurysmal bone
|
|
300814||nystagmus 6 congenital x linked
|
|
300814||nys6
|
|
210250|C537345||sitosterolemia
|
|
210250|C537345||macrothrombocytopenia stomatocytosis mediterranean
|
|
210250|C537345||phytosterolemia
|
|
210250|C537345||phytosterolemia macrothrombocytopenia stomatocytosis mediterranean included
|
|
210250|C537345||plant sterol storage disease
|
|
210250|C537345||pseudohomozygous familial hypercholesterolemia
|
|
210250|C537345||stsl
|
|
C567309||scoliosis arachnodactyly and blindness
|
|
C567308||c6 deficiency subtotal
|
|
C567308||complement component 6 deficiency subtotal
|
|
D009798||ocular hypertension
|
|
D009798||glaucomas suspect
|
|
D009798||glaucoma suspect
|
|
D009798||hypertension ocular
|
|
D009798||hypertensions ocular
|
|
D009798||ocular hypertensions
|
|
D009798||suspect glaucoma
|
|
D009798||suspect glaucomas
|
|
D008467||meckel diverticulum
|
|
D008467||diverticulum meckel
|
|
D008467||meckel apos s diverticulum
|
|
D021441||carcinoma pancreatic ductal
|
|
D021441||carcinoma ductal pancreatic
|
|
D021441||carcinoma pancreas duct cell
|
|
D021441||carcinomas pancreas duct cell
|
|
D021441||carcinomas pancreatic ductal
|
|
D021441||ductal carcinoma of the pancreas
|
|
D021441||ductal carcinoma pancreatic
|
|
D021441||ductal carcinomas pancreatic
|
|
D021441||duct cell carcinoma of the pancreas
|
|
D021441||duct cell carcinoma pancreas
|
|
D021441||duct cell carcinomas pancreas
|
|
D021441||pancreas duct cell carcinoma
|
|
D021441||pancreas duct cell carcinomas
|
|
D021441||pancreatic ductal carcinoma
|
|
D021441||pancreatic ductal carcinomas
|
|
D021441||pancreatic duct cell carcinoma
|
|
D008476||mediastinal cyst
|
|
D008476||cyst mediastinal
|
|
D008476||cyst pericardial
|
|
D008476||cysts mediastinal
|
|
D008476||cysts pericardial
|
|
D008476||cysts thoracic
|
|
D008476||cysts thymic
|
|
D008476||cysts tracheal
|
|
D008476||cyst thoracic
|
|
D008476||cyst thymic
|
|
D008476||cyst tracheal
|
|
D008476||mediastinal cysts
|
|
D008476||pericardial cyst
|
|
D008476||pericardial cysts
|
|
D008476||thoracic cyst
|
|
D008476||thoracic cysts
|
|
D008476||thymic cyst
|
|
D008476||thymic cysts
|
|
D008476||tracheal cyst
|
|
D008476||tracheal cysts
|
|
D010787||photosensitivity disorders
|
|
D010787||actinic dermatitides
|
|
D010787||actinic dermatitides chronic
|
|
D010787||actinic dermatitis
|
|
D010787||actinic dermatitis chronic
|
|
D010787||actinic reticuloid syndrome
|
|
D010787||actinic reticuloid syndromes
|
|
D010787||chronic actinic dermatitides
|
|
D010787||chronic actinic dermatitis
|
|
D010787||dermatitides actinic
|
|
D010787||dermatitides chronic actinic
|
|
D010787||dermatitis actinic
|
|
D010787||dermatitis chronic actinic
|
|
D010787||disorder photosensitivity
|
|
D010787||disorders photosensitivity
|
|
D010787||photodermatitides
|
|
D010787||photodermatitis
|
|
D010787||photosensitivity disorder
|
|
D010787||photosensitization
|
|
D010787||reticuloid syndrome actinic
|
|
D010787||reticuloid syndromes actinic
|
|
D010787||syndrome actinic reticuloid
|
|
D010787||syndromes actinic reticuloid
|
|
155720|C536494||uveal melanoma
|
|
155720|C536494||melanoma of the uvea
|
|
155720|C536494||melanoma uveal
|
|
155720|C536494||melanoma uveal susceptibility to 1
|
|
155720|C536494||melanoma uveal susceptibility to 2
|
|
155720|C536494||uvm1
|
|
155720|C536494||uvm2
|
|
D008471||meconium aspiration syndrome
|
|
D008471||aspiration meconium
|
|
D008471||aspiration syndrome meconium
|
|
D008471||meconium aspiration
|
|
D008471||meconium inhalation
|
|
D008471||syndrome meconium aspiration
|
|
D018208|613488||liposarcoma myxoid
|
|
D018208|613488||liposarcomas myxoid
|
|
D018208|613488||myxoid liposarcoma
|
|
D018208|613488||myxoid liposarcomas
|
|
C567738|613115||neuropathy hereditary sensory and autonomic type iib
|
|
C567738|613115||hsan2b
|
|
D051299||post dural puncture headache
|
|
D051299||headache postdural puncture
|
|
D051299||headache post dural puncture
|
|
D051299||headaches postdural puncture
|
|
D051299||headaches post dural puncture
|
|
D051299||postdural puncture headache
|
|
D051299||postdural puncture headaches
|
|
D051299||post dural puncture headaches
|
|
D051299||post lumbar puncture headache
|
|
D051298||post traumatic headache
|
|
D051298||cervicogenic headache
|
|
D051298||cervicogenic headaches
|
|
D051298||headache cervicogenic
|
|
D051298||headache post traumatic
|
|
D051298||headaches cervicogenic
|
|
D051298||headaches post traumatic
|
|
D051298||post traumatic headaches
|
|
C566506|609620||short qt syndrome 1
|
|
C566506|609620||sqt1
|
|
D019115||fasciitis necrotizing
|
|
D019115||fasciitides necrotizing
|
|
D019115||fascitides necrotizing
|
|
D019115||fascitis necrotizing
|
|
D019115||necrotizing fasciitides
|
|
D019115||necrotizing fasciitis
|
|
D019115||necrotizing fascitides
|
|
D019115||necrotizing fascitis
|
|
D014256|613229||trichotillomania
|
|
D014256|613229||trichotillomanias
|
|
D014256|613229||ttm
|
|
300635|C564469||lymphoproliferative syndrome x linked 2
|
|
300635|C564469||xiap deficiency
|
|
300635|C564469||xlp2
|
|
C566453|609706||deafness autosomal recessive 53
|
|
C566453|609706||dfnb53
|
|
C567311|612319||leukodystrophy dysmyelinating and spastic paraparesis with or without dystonia
|
|
C567314||leukodystrophy hypomyelinating 6
|
|
C567314||leukodystrophy hypomyelinating with atrophy of the basal ganglia and cerebellum
|
|
C567313||leukodystrophy hypomyelinating with hypodontia and hypogonadotropic hypogonadism
|
|
C567313||ataxia delayed dentition and hypomyelination
|
|
C567313||leukodystrophy hypomyelinating 7
|
|
C567313||leukoencephalopathy hypomyelinating with ataxia and delayed dentition
|
|
143460||5 hydroxytryptamine oxygenase regulator
|
|
143460||htor
|
|
D008479||mediastinal neoplasms
|
|
D008479||cancer mediastinal
|
|
D008479||cancer mediastinum
|
|
D008479||cancer of mediastinum
|
|
D008479||cancer of the mediastinum
|
|
D008479||cancers mediastinal
|
|
D008479||cancers mediastinum
|
|
D008479||mediastinal cancer
|
|
D008479||mediastinal cancers
|
|
D008479||mediastinal neoplasm
|
|
D008479||mediastinum cancer
|
|
D008479||mediastinum cancers
|
|
D008479||mediastinum neoplasm
|
|
D008479||mediastinum neoplasms
|
|
D008479||neoplasm mediastinal
|
|
D008479||neoplasm mediastinum
|
|
D008479||neoplasms mediastinal
|
|
D008479||neoplasms mediastinum
|
|
D008478||mediastinal emphysema
|
|
D008478||emphysema mediastinal
|
|
D008478||emphysemas mediastinal
|
|
D008478||mediastinal emphysemas
|
|
D008478||pneumomediastinum
|
|
C563417|600974||deafness autosomal recessive 7
|
|
C563417|600974||deafness autosomal recessive 11
|
|
C563417|600974||dfnb11
|
|
C563417|600974||dfnb7
|
|
D008477||mediastinal diseases
|
|
D008477||disease mediastinal
|
|
D008477||diseases mediastinal
|
|
D008477||mediastinal disease
|
|
D007153||immunologic deficiency syndromes
|
|
D007153||antibody deficiency syndrome
|
|
D007153||antibody deficiency syndromes
|
|
D007153||deficiency syndrome antibody
|
|
D007153||deficiency syndrome immunologic
|
|
D007153||deficiency syndrome immunological
|
|
D007153||deficiency syndromes antibody
|
|
D007153||deficiency syndromes immunologic
|
|
D007153||deficiency syndromes immunological
|
|
D007153||immunological deficiency syndrome
|
|
D007153||immunological deficiency syndromes
|
|
D007153||immunologic deficiency syndrome
|
|
D007153||syndrome antibody deficiency
|
|
D007153||syndrome immunological deficiency
|
|
D007153||syndrome immunologic deficiency
|
|
D007153||syndromes antibody deficiency
|
|
D007153||syndromes immunological deficiency
|
|
D007153||syndromes immunologic deficiency
|
|
D006712|236200||homocystinuria
|
|
D006712|236200||cbs deficiencies
|
|
D006712|236200||cbs deficiency
|
|
D006712|236200||cbs deficiency hyperhomocysteinemia thrombotic cbs related included
|
|
D006712|236200||cystathionine beta synthase deficiency
|
|
D006712|236200||cystathionine beta synthase deficiency disease
|
|
D006712|236200||deficiencies cbs
|
|
D006712|236200||deficiency cbs
|
|
D006712|236200||deficiency disease cystathionine beta synthase
|
|
D006712|236200||homocystinuria due to cystathionine beta synthase deficiency
|
|
D006712|236200||homocystinuria with or without response to pyridoxine
|
|
D007154||immune system diseases
|
|
D007154||disease immune
|
|
D007154||disease immune system
|
|
D007154||disease immunologic
|
|
D007154||disease immunological
|
|
D007154||diseases immune
|
|
D007154||diseases immune system
|
|
D007154||diseases immunologic
|
|
D007154||diseases immunological
|
|
D007154||diseases of immune system
|
|
D007154||disorder immune
|
|
D007154||disorders immune
|
|
D007154||immune disease
|
|
D007154||immune diseases
|
|
D007154||immune disorder
|
|
D007154||immune disorders
|
|
D007154||immune system disease
|
|
D007154||immunological disease
|
|
D007154||immunological diseases
|
|
D007154||immunologic disease
|
|
D007154||immunologic diseases
|
|
609006||deafness autosomal recessive 36 with or without vestibular involvement
|
|
609006||deafness autosomal dominant without vestibular involvement included
|
|
225100||ectopia lentis 2 isolated autosomal recessive
|
|
225100||ectol2
|
|
D008480||mediastinitis
|
|
D008480||inflammation mediastinum
|
|
D008480||inflammations mediastinum
|
|
D008480||mediastinitides
|
|
D008480||mediastinum inflammation
|
|
D008480||mediastinum inflammations
|
|
D020210||central cord syndrome
|
|
D020210||central cord injury syndrome
|
|
D020210||central spinal cord syndrome
|
|
605429||deafness nonsyndromic modifier 1
|
|
605429||dfnm1
|
|
C536992|607151||moyamoya disease 2
|
|
C536992|607151||mymy2
|
|
D020217||vertebral artery dissection
|
|
D020217||artery dissections vertebral
|
|
D020217||artery dissection vertebral
|
|
D020217||dissecting vertebral artery aneurysm
|
|
D020217||dissections vertebral artery
|
|
D020217||dissection vertebral artery
|
|
D020217||spontaneous vertebral artery dissection
|
|
D020217||traumatic vertebral artery dissection
|
|
D020217||vertebral artery dissections
|
|
D020217||vertebral artery dissection spontaneous
|
|
D020217||vertebral artery dissection traumatic
|
|
D020216||carotid cavernous sinus fistula
|
|
D020216||carotid artery cavernous sinus fistula
|
|
D020216||carotid cavernous sinus fistulas
|
|
D020216||c c fistula
|
|
D020216||c c fistulas
|
|
D020216||fistula carotid artery cavernous sinus
|
|
D020216||fistula carotid cavernous sinus
|
|
D020216||fistula c c
|
|
D020216||fistulas carotid cavernous sinus
|
|
D020216||fistulas c c
|
|
D020216||traumatic carotid cavernous sinus fistula
|
|
D007238||infarction
|
|
D007238||infarctions
|
|
D020215||carotid artery internal dissection
|
|
D020215||carotid artery dissection internal
|
|
D020215||dissection internal carotid artery
|
|
D020215||internal carotid artery dissection
|
|
D007239||infection
|
|
D007239||infections
|
|
D008569||memory disorders
|
|
D008569||age related memory disorder
|
|
D008569||age related memory disorders
|
|
D008569||cognitive retention disorder
|
|
D008569||cognitive retention disorders
|
|
D008569||deficit memory
|
|
D008569||deficits memory
|
|
D008569||memory deficit
|
|
D008569||memory deficits
|
|
D008569||memory disorder
|
|
D008569||memory disorder age related
|
|
D008569||memory disorders age related
|
|
D008569||memory disorder semantic
|
|
D008569||memory disorder spatial
|
|
D008569||memory disorders semantic
|
|
D008569||memory disorders spatial
|
|
D008569||memory loss
|
|
D008569||memory losses
|
|
D008569||retention disorder cognitive
|
|
D008569||retention disorders cognitive
|
|
D008569||semantic memory disorder
|
|
D008569||semantic memory disorders
|
|
D008569||spatial memory disorder
|
|
D008569||spatial memory disorders
|
|
D020214||cerebrovascular trauma
|
|
D020214||brain injury vascular
|
|
D020214||brain vascular injury
|
|
D020214||brain vascular trauma
|
|
D020214||injury brain vascular
|
|
D020214||injury vascular brain
|
|
D020214||trauma brain vascular
|
|
D020214||trauma cerebrovascular
|
|
D020214||vascular brain injuries
|
|
D020214||vascular brain injury
|
|
D020214||vascular injury brain
|
|
D020214||vascular trauma brain
|
|
D020214||vascular traumas brain
|
|
D020212||carotid artery injuries
|
|
D020212||artery injuries carotid
|
|
D020212||artery injury carotid
|
|
D020212||artery trauma carotid
|
|
D020212||carotid arteriopathies traumatic
|
|
D020212||carotid arteriopathy traumatic
|
|
D020212||carotid artery injury
|
|
D020212||carotid artery trauma
|
|
D020212||carotid false aneurysm
|
|
D020212||carotid false aneurysms
|
|
D020212||carotid pseudoaneurysm
|
|
D020212||false aneurysm carotid
|
|
D020212||injuries carotid artery
|
|
D020212||injury carotid artery
|
|
D020212||pseudoaneurysm carotid
|
|
D020212||trauma carotid artery
|
|
D020212||traumatic carotid arteriopathy
|
|
C564248|608389||branchiootic syndrome 3
|
|
C564248|608389||bos3
|
|
C564248|608389||bo syndrome 3
|
|
D020211||autonomic dysreflexia
|
|
D020211||autonomic dysreflexias
|
|
D020211||autonomic dysreflexia spinal
|
|
D020211||autonomic dysreflexias spinal
|
|
D020211||autonomic hyperreflexia
|
|
D020211||autonomic hyperreflexias
|
|
D020211||dysreflexia autonomic
|
|
D020211||dysreflexias autonomic
|
|
D020211||dysreflexia spinal autonomic
|
|
D020211||dysreflexias spinal autonomic
|
|
D020211||hyperreflexia autonomic
|
|
D020211||hyperreflexias autonomic
|
|
D020211||spinal autonomic dysreflexia
|
|
D020211||spinal autonomic dysreflexias
|
|
D007235||infant premature diseases
|
|
D009896||optic atrophy
|
|
D009896||atrophy optic
|
|
D008575||meniere disease
|
|
D008575||auditory vertigo
|
|
D008575||auditory vertigos
|
|
D008575||aural vertigo
|
|
D008575||disease meniere
|
|
D008575||disease m 233 ni 232 re
|
|
D008575||disease meniere apos s
|
|
D008575||disease m 233 ni 232 re apos s
|
|
D008575||diseases m 233 ni 232 re
|
|
D008575||diseases m 233 ni 232 re apos s
|
|
D008575||m 233 ni 232 re disease
|
|
D008575||m 233 ni 232 re diseases
|
|
D008575||meniere apos s disease
|
|
D008575||menieres disease
|
|
D008575||m 233 ni 232 re apos s disease
|
|
D008575||m 233 ni 232 res disease
|
|
D008575||m 233 ni 232 re apos s diseases
|
|
D008575||meniere apos s syndrome
|
|
D008575||menieres syndrome
|
|
D008575||m 233 ni 232 re apos s vertigo
|
|
D008575||m 233 ni 232 res vertigo
|
|
D008575||m 233 ni 232 re apos s vertigos
|
|
D008575||meniere syndrome
|
|
D008575||m 233 ni 232 re vertigo
|
|
D008575||otogenic vertigo
|
|
D008575||otogenic vertigos
|
|
D008575||syndrome meniere apos s
|
|
D008575||vertigo auditory
|
|
D008575||vertigo aural
|
|
D008575||vertigo m 233 ni 232 re apos s
|
|
D008575||vertigo otogenic
|
|
D008575||vertigos auditory
|
|
D008575||vertigos m 233 ni 232 re apos s
|
|
D008575||vertigos otogenic
|
|
D007244||infectious mononucleosis
|
|
D007244||fever glandular
|
|
D007244||glandular fever
|
|
D007244||mononucleosis infectious
|
|
D007241||infectious bovine rhinotracheitis
|
|
D007241||bovine rhinotracheitides infectious
|
|
D007241||bovine rhinotracheitis infectious
|
|
D007241||infectious bovine rhinotracheitides
|
|
D007241||rhinotracheitides infectious bovine
|
|
D007241||rhinotracheitis infectious bovine
|
|
300623|C564105|C580109||fragile x tremor ataxia syndrome
|
|
300623|C564105|C580109||fxtas
|
|
D000505|109200||alopecia
|
|
D000505|109200||aga1
|
|
D000505|109200||alopecia androgenetic
|
|
D000505|109200||alopecia androgenetic 1
|
|
D000505|109200||alopecia cicatrisata
|
|
D000505|109200||alopecia cicatrisatas
|
|
D000505|109200||alopecia male pattern
|
|
D000505|109200||androgenetic alopecia
|
|
D000505|109200||androgenetic alopecia aga baldness male pattern included
|
|
D000505|109200||androgenic alopecia
|
|
D000505|109200||baldness
|
|
D000505|109200||baldness male pattern
|
|
D000505|109200||cicatrisata alopecia
|
|
D000505|109200||cicatrisatas alopecia
|
|
D000505|109200||female pattern baldness
|
|
D000505|109200||male pattern alopecia
|
|
D000505|109200||male pattern baldness
|
|
D000505|109200||mpb included
|
|
D000505|109200||pattern baldness
|
|
D000505|109200||pseudopelade
|
|
C565467|243000||indifference to pain congenital autosomal recessive
|
|
C565467|243000||asymbolia for pain
|
|
C565467|243000||congenital analgesia autosomal recessive
|
|
C565467|243000||insensitivity to pain channelopathy associated
|
|
C557830||duplication 15q11 q13 syndrome
|
|
C557830||15q11 2 microdeletion
|
|
C557830||microdeletion 15q11 2
|
|
D019217||tooth attrition
|
|
D019217||attrition dental
|
|
D019217||attrition tooth
|
|
D019217||dental attrition
|
|
D019217||dental attritions
|
|
D019217||occlusal wear
|
|
D019217||occlusal wears
|
|
D019217||wear occlusal
|
|
D019217||wears occlusal
|
|
D019214||gingival overgrowth
|
|
D019214||gingival overgrowths
|
|
D019214||overgrowth gingival
|
|
D019214||overgrowths gingival
|
|
C538006|224500||dystonia musculorum deformans type 2
|
|
C538006|224500||dystonia 2 torsion autosomal recessive
|
|
C538006|224500||dystonia musculorum deformans 2
|
|
C538006|224500||dystonia torsion 2 autosomal recessive
|
|
C538006|224500||dyt2
|
|
C538006|224500||torsion dystonia 2
|
|
C538006|224500||torsion dystonia 2 autosomal recessive type
|
|
C536377|206800||anonychia congenita
|
|
C536377|206800||anonychia
|
|
C536377|206800||anonychia hyponychia congenita
|
|
C536377|206800||anonychia totalis
|
|
C536377|206800||hyponychia congenita
|
|
C536377|206800||nail disorder nonsyndromic congenital 4
|
|
C536377|206800||ndnc4
|
|
608203|C564275||neutrophil immunodeficiency syndrome
|
|
D020207||coma post head injury
|
|
D020207||coma post concussive
|
|
D020207||coma post trauma
|
|
D020207||coma post traumatic
|
|
D020207||coma post traumatic prolonged
|
|
D020207||comas post concussive
|
|
D020207||comas post head injury
|
|
D020207||comas post trauma
|
|
D020207||coma traumatic
|
|
D020207||post concussive coma
|
|
D020207||post concussive comas
|
|
D020207||post head injury coma
|
|
D020207||post head injury comas
|
|
D020207||post trauma coma
|
|
D020207||post trauma comas
|
|
D020207||post traumatic coma
|
|
D020207||traumatic coma
|
|
D020206||subarachnoid hemorrhage traumatic
|
|
D020206||hemorrhage post traumatic subarachnoid
|
|
D020206||hemorrhages post traumatic subarachnoid
|
|
D020206||hemorrhage traumatic subarachnoid
|
|
D020206||post traumatic subarachnoid hemorrhage
|
|
D020206||post traumatic subarachnoid hemorrhages
|
|
D020206||subarachnoid hemorrhage post traumatic
|
|
D020206||subarachnoid hemorrhages post traumatic
|
|
D020206||subarachnoid hemorrhages traumatic
|
|
D020206||traumatic subarachnoid hemorrhage
|
|
D020206||traumatic subarachnoid hemorrhages
|
|
D012555|181460||schistosomiasis mansoni
|
|
D012555|181460||infection schistosoma mansoni
|
|
D012555|181460||infections schistosoma mansoni
|
|
D012555|181460||intestinal schistosomiases
|
|
D012555|181460||intestinal schistosomiasis
|
|
D012555|181460||schistosoma mansoni infection
|
|
D012555|181460||schistosoma mansoni infections
|
|
D012555|181460||schistosoma mansoni infection susceptibility resistance to
|
|
D012555|181460||schistosoma mansoni intensity of infection by
|
|
D012555|181460||schistosomiases intestinal
|
|
D012555|181460||schistosomiasis intestinal
|
|
D012555|181460||sm1
|
|
D020205||skull fracture basilar
|
|
D020205||basilar skull fracture
|
|
D020205||basilar skull fractures
|
|
D020205||battle sign
|
|
D020205||battle apos s sign
|
|
D020205||battles sign
|
|
D020205||fracture basilar skull
|
|
D020205||fracture frontobasilar skull
|
|
D020205||fractures basilar skull
|
|
D020205||fractures frontobasilar skull
|
|
D020205||frontobasilar skull fracture
|
|
D020205||frontobasilar skull fractures
|
|
D020205||sign battle
|
|
D020205||sign battle apos s
|
|
D020205||skull fracture basilar childhood
|
|
D020205||skull fracture frontobasilar
|
|
D020205||skull fractures basilar
|
|
D020205||skull fractures frontobasilar
|
|
D020205||skull fracture transphenoid basilar
|
|
D007249||inflammation
|
|
D007249||inflammations
|
|
D020204||skull fracture depressed
|
|
D020204||compound depressed skull fracture
|
|
D020204||compound depressed skull fractures
|
|
D020204||depressed skull fracture
|
|
D020204||depressed skull fractures
|
|
D020204||fracture depressed skull
|
|
D020204||fractures depressed skull
|
|
D020204||skull fracture compound depressed
|
|
D020204||skull fractures compound depressed
|
|
D020204||skull fractures depressed
|
|
C567687|613237||focal segmental glomerulosclerosis 5
|
|
C567687|613237||fsgs5
|
|
C567687|613237||glomerulosclerosis focal segmental 5
|
|
D020203||brain stem hemorrhage traumatic
|
|
D020203||brainstem hematomas traumatic
|
|
D020203||brainstem hematoma traumatic
|
|
D020203||brain stem hematoma traumatic
|
|
D020203||brainstem hemorrhage post traumatic
|
|
D020203||brain stem hemorrhage post traumatic
|
|
D020203||brainstem hemorrhage traumatic
|
|
D020203||bulbar hemorrhage traumatic
|
|
D020203||hemorrhage brain stem traumatic
|
|
D020203||hemorrhage post traumatic brainstem
|
|
D020203||hemorrhage traumatic bulbar
|
|
D020203||hemorrhage traumatic medullary
|
|
D020203||medullary hemorrhage traumatic
|
|
D020203||midbrain hemorrhage traumatic
|
|
D020203||pontine hemorrhage traumatic
|
|
D020203||post traumatic brainstem hemorrhage
|
|
D020203||post traumatic brain stem hemorrhage
|
|
D020203||traumatic brainstem hematoma
|
|
D020203||traumatic brain stem hematoma
|
|
D020203||traumatic brainstem hematomas
|
|
D020203||traumatic brainstem hemorrhage
|
|
D020203||traumatic brain stem hemorrhage
|
|
D020203||traumatic bulbar hemorrhage
|
|
D020203||traumatic medullary hemorrhage
|
|
D020203||traumatic midbrain hemorrhage
|
|
D020203||traumatic pontine hemorrhage
|
|
D007247||infertility female
|
|
D007247||female infertility
|
|
D007247||female sterility
|
|
D007247||female subfertility
|
|
D007247||female sub fertility
|
|
D007247||postpartum sterility
|
|
D007247||sterility female
|
|
D007247||sterility postpartum
|
|
D007247||subfertility female
|
|
D007247||sub fertility female
|
|
D008579||meningioma
|
|
D008579||angioblastic meningioma
|
|
D008579||angioblastic meningiomas
|
|
D008579||angiomatous meningioma
|
|
D008579||angiomatous meningiomas
|
|
D008579||benign meningioma
|
|
D008579||benign meningiomas
|
|
D008579||cerebral convexity meningioma
|
|
D008579||cerebral convexity meningiomas
|
|
D008579||clear cell meningioma
|
|
D008579||clear cell meningiomas
|
|
D008579||convexity meningioma cerebral
|
|
D008579||convexity meningiomas cerebral
|
|
D008579||fibrous meningioma
|
|
D008579||fibrous meningiomas
|
|
D008579||groove meningiomas olfactory
|
|
D008579||hemangioblastic meningioma
|
|
D008579||hemangioblastic meningiomas
|
|
D008579||hemangiopericytic meningioma
|
|
D008579||hemangiopericytic meningiomas
|
|
D008579||intracranial meningioma
|
|
D008579||intracranial meningiomas
|
|
D008579||intraorbital meningioma
|
|
D008579||intraorbital meningiomas
|
|
D008579||intraventricular meningioma
|
|
D008579||intraventricular meningiomas
|
|
D008579||malignant meningioma
|
|
D008579||malignant meningiomas
|
|
D008579||meningioma angioblastic
|
|
D008579||meningioma angiomatous
|
|
D008579||meningioma benign
|
|
D008579||meningioma cerebral convexity
|
|
D008579||meningioma clear cell
|
|
D008579||meningioma fibrous
|
|
D008579||meningioma hemangioblastic
|
|
D008579||meningioma hemangiopericytic
|
|
D008579||meningioma intracranial
|
|
D008579||meningioma intraorbital
|
|
D008579||meningioma intraventricular
|
|
D008579||meningioma malignant
|
|
D008579||meningioma meningotheliomatous
|
|
D008579||meningioma microcystic
|
|
D008579||meningioma multiple
|
|
D008579||meningioma olfactory groove
|
|
D008579||meningioma papillary
|
|
D008579||meningioma parasagittal
|
|
D008579||meningioma posterior fossa
|
|
D008579||meningioma psammomatous
|
|
D008579||meningiomas
|
|
D008579||meningiomas angioblastic
|
|
D008579||meningiomas angiomatous
|
|
D008579||meningiomas benign
|
|
D008579||meningiomas cerebral convexity
|
|
D008579||meningiomas clear cell
|
|
D008579||meningioma secretory
|
|
D008579||meningiomas fibrous
|
|
D008579||meningiomas hemangioblastic
|
|
D008579||meningiomas hemangiopericytic
|
|
D008579||meningiomas intracranial
|
|
D008579||meningiomas intraorbital
|
|
D008579||meningiomas intraventricular
|
|
D008579||meningiomas malignant
|
|
D008579||meningiomas meningotheliomatous
|
|
D008579||meningiomas microcystic
|
|
D008579||meningiomas multiple
|
|
D008579||meningiomas olfactory groove
|
|
D008579||meningiomas papillary
|
|
D008579||meningiomas parasagittal
|
|
D008579||meningioma sphenoid wing
|
|
D008579||meningioma spinal
|
|
D008579||meningiomas posterior fossa
|
|
D008579||meningiomas psammomatous
|
|
D008579||meningiomas secretory
|
|
D008579||meningiomas sphenoid wing
|
|
D008579||meningiomas spinal
|
|
D008579||meningiomas transitional
|
|
D008579||meningiomas xanthomatous
|
|
D008579||meningiomatoses
|
|
D008579||meningiomatosis
|
|
D008579||meningioma transitional
|
|
D008579||meningioma xanthomatous
|
|
D008579||meningotheliomatous meningioma
|
|
D008579||meningotheliomatous meningiomas
|
|
D008579||microcystic meningioma
|
|
D008579||microcystic meningiomas
|
|
D008579||multiple meningioma
|
|
D008579||multiple meningiomas
|
|
D008579||olfactory groove meningioma
|
|
D008579||olfactory groove meningiomas
|
|
D008579||papillary meningioma
|
|
D008579||papillary meningiomas
|
|
D008579||parasagittal meningioma
|
|
D008579||parasagittal meningiomas
|
|
D008579||posterior fossa meningioma
|
|
D008579||posterior fossa meningiomas
|
|
D008579||psammomatous meningioma
|
|
D008579||psammomatous meningiomas
|
|
D008579||secretory meningioma
|
|
D008579||secretory meningiomas
|
|
D008579||sphenoid wing meningioma
|
|
D008579||sphenoid wing meningiomas
|
|
D008579||spinal meningioma
|
|
D008579||spinal meningiomas
|
|
D008579||transitional meningioma
|
|
D008579||transitional meningiomas
|
|
D008579||wing meningioma sphenoid
|
|
D008579||wing meningiomas sphenoid
|
|
D008579||xanthomatous meningioma
|
|
D008579||xanthomatous meningiomas
|
|
D020202||cerebral hemorrhage traumatic
|
|
D020202||brain hemorrhage cerebral traumatic
|
|
D020202||cerebral hematomas traumatic
|
|
D020202||cerebral hematoma traumatic
|
|
D020202||cerebral hemorrhages traumatic
|
|
D020202||cerebral intraparenchymal hematoma traumatic
|
|
D020202||cerebral intraparenchymal hemorrhage traumatic
|
|
D020202||cerebral parenchymal hemorrhage traumatic
|
|
D020202||hematomas traumatic cerebral
|
|
D020202||hematoma traumatic cerebral
|
|
D020202||hemorrhages traumatic cerebral
|
|
D020202||hemorrhages traumatic intracerebral
|
|
D020202||hemorrhage traumatic cerebral
|
|
D020202||hemorrhage traumatic intracerebral
|
|
D020202||intracerebral hemorrhages traumatic
|
|
D020202||intracerebral hemorrhage traumatic
|
|
D020202||traumatic cerebral hematoma
|
|
D020202||traumatic cerebral hematomas
|
|
D020202||traumatic cerebral hemorrhage
|
|
D020202||traumatic cerebral hemorrhages
|
|
D020202||traumatic cerebral intraparenchymal hematoma
|
|
D020202||traumatic cerebral intraparenchymal hemorrhage
|
|
D020202||traumatic cerebral parenchymal hemorrhage
|
|
D020202||traumatic intracerebral hemorrhage
|
|
D020202||traumatic intracerebral hemorrhages
|
|
D007248||infertility male
|
|
D007248||male infertility
|
|
D007248||male sterility
|
|
D007248||male subfertility
|
|
D007248||male sub fertility
|
|
D007248||sterility male
|
|
D007248||subfertility male
|
|
D007248||sub fertility male
|
|
D020201||brain hemorrhage traumatic
|
|
D020201||brain hemorrhages traumatic
|
|
D020201||cerebellar hemorrhages traumatic
|
|
D020201||cerebellar hemorrhage traumatic
|
|
D020201||hemorrhages traumatic cerebellar
|
|
D020201||hemorrhage traumatic brain
|
|
D020201||hemorrhage traumatic cerebellar
|
|
D020201||traumatic brain hemorrhage
|
|
D020201||traumatic brain hemorrhages
|
|
D020201||traumatic cerebellar hemorrhage
|
|
D020201||traumatic cerebellar hemorrhages
|
|
C567690|613227||cerebellar ataxia mental retardation and dysequilibrium syndrome 3
|
|
C567690|613227||camrq3
|
|
C567690|613227||cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3
|
|
D008577||meningeal neoplasms
|
|
D008577||benign meningeal neoplasm
|
|
D008577||benign meningeal neoplasms
|
|
D008577||cancer meningeal
|
|
D008577||cancers meningeal
|
|
D008577||intracranial meningeal neoplasm
|
|
D008577||intracranial meningeal neoplasms
|
|
D008577||leptomeningeal neoplasm
|
|
D008577||leptomeningeal neoplasms
|
|
D008577||malignant meningeal neoplasm
|
|
D008577||malignant meningeal neoplasms
|
|
D008577||meningeal cancer
|
|
D008577||meningeal cancers
|
|
D008577||meningeal neoplasm
|
|
D008577||meningeal neoplasm benign
|
|
D008577||meningeal neoplasm intracranial
|
|
D008577||meningeal neoplasm malignant
|
|
D008577||meningeal neoplasms benign
|
|
D008577||meningeal neoplasms intracranial
|
|
D008577||meningeal neoplasms malignant
|
|
D008577||meningeal neoplasm spinal
|
|
D008577||meningeal neoplasms spinal
|
|
D008577||meningeal tumor
|
|
D008577||meningeal tumors
|
|
D008577||neoplasm benign meningeal
|
|
D008577||neoplasm intracranial meningeal
|
|
D008577||neoplasm leptomeningeal
|
|
D008577||neoplasm malignant meningeal
|
|
D008577||neoplasm meningeal
|
|
D008577||neoplasms benign meningeal
|
|
D008577||neoplasms intracranial meningeal
|
|
D008577||neoplasms leptomeningeal
|
|
D008577||neoplasms malignant meningeal
|
|
D008577||neoplasms meningeal
|
|
D008577||neoplasm spinal meningeal
|
|
D008577||neoplasms spinal meningeal
|
|
D008577||spinal meningeal neoplasm
|
|
D008577||spinal meningeal neoplasms
|
|
D008577||tumor meningeal
|
|
D008577||tumors meningeal
|
|
D020200||hematoma subdural chronic
|
|
D020200||chronic subdural hematoma
|
|
D020200||chronic subdural hematomas
|
|
D020200||hematoma chronic subdural
|
|
D020200||hematomas chronic subdural
|
|
D020200||hemorrhage subdural chronic
|
|
D020200||subdural hematoma chronic
|
|
D020200||subdural hematomas chronic
|
|
D007246||infertility
|
|
D007246||reproductive sterility
|
|
D007246||sterility
|
|
D007246||sterility reproductive
|
|
D007246||subfertility
|
|
D007246||sub fertility
|
|
D022861||hermanski pudlak syndrome
|
|
D022861||hermansky pudlak syndrome
|
|
D008586||meningitis pneumococcal
|
|
D008586||experimental pneumococcal meningitides
|
|
D008586||experimental pneumococcal meningitis
|
|
D008586||meningitides streptococcus pneumoniae
|
|
D008586||meningitis experimental pneumococcal
|
|
D008586||meningitis pneumococcal experimental
|
|
D008586||meningitis pneumococcal penicillin resistant
|
|
D008586||meningitis pneumococcal recurrent
|
|
D008586||meningitis streptococcus pneumoniae
|
|
D008586||pneumococcal meningitides
|
|
D008586||pneumococcal meningitides experimental
|
|
D008586||pneumococcal meningitis
|
|
D008586||pneumococcal meningitis experimental
|
|
D008586||streptococcus pneumoniae meningitides
|
|
D008586||streptococcus pneumoniae meningitis
|
|
D008585||meningitis meningococcal
|
|
D008585||meningitis meningococcal serogroup a
|
|
D008585||meningitis meningococcal serogroup b
|
|
D008585||meningitis meningococcal serogroup c
|
|
D008585||meningitis meningococcal serogroup w135
|
|
D008585||meningitis meningococcal serogroup w 135
|
|
D008585||meningitis meningococcal serogroup y
|
|
D008585||meningitis meningococcic
|
|
D008585||meningococcal meningitis
|
|
D008585||meningococcal meningitis serogroup a
|
|
D008585||meningococcal meningitis serogroup b
|
|
D008585||meningococcal meningitis serogroup c
|
|
D008585||meningococcal meningitis serogroup w135
|
|
D008585||meningococcal meningitis serogroup w 135
|
|
D008585||meningococcal meningitis serogroup y
|
|
D008585||serogroup a meningococcal meningitis
|
|
D008585||serogroup b meningococcal meningitis
|
|
D008585||serogroup c meningococcal meningitis
|
|
D008585||serogroup w 135 meningococcal meningitis
|
|
D008585||serogroup w135 meningococcal meningitis
|
|
D008585||serogroup y meningococcal meningitis
|
|
D008584||meningitis listeria
|
|
D008584||cerebritides listeria
|
|
D008584||cerebritis listeria
|
|
D008584||listeria cerebritides
|
|
D008584||listeria cerebritis
|
|
D008584||listeria meningitides
|
|
D008584||listeria meningitis
|
|
D008584||listeria meningoencephalitides
|
|
D008584||listeria meningoencephalitis
|
|
D008584||listeria monocytogenes meningitides
|
|
D008584||listeria monocytogenes meningitis
|
|
D008584||meningitides listeria
|
|
D008584||meningitides listeria monocytogenes
|
|
D008584||meningitis listeria monocytogenes
|
|
D008584||meningoencephalitides listeria
|
|
D008584||meningoencephalitis listeria
|
|
D008583||meningitis haemophilus
|
|
D008583||haemophilus influenzae meningitis type b
|
|
D008583||haemophilus meningitides
|
|
D008583||haemophilus meningitis
|
|
D008583||haemophilus parainfluenzae meningitides
|
|
D008583||haemophilus parainfluenzae meningitis
|
|
D008583||hemophilus influenzae meningitis type b
|
|
D008583||hemophilus meningitides
|
|
D008583||hemophilus meningitis
|
|
D008583||hib meninigitis
|
|
D008583||meningitides haemophilus
|
|
D008583||meningitides haemophilus parainfluenzae
|
|
D008583||meningitides hemophilus
|
|
D008583||meningitis haemophilus influenzae type f
|
|
D008583||meningitis haemophilus parainfluenzae
|
|
D008583||meningitis hemophilus
|
|
D008583||meningitis hemophilus influenzae type b
|
|
D008583||meningitis hemophilus influenzae type f
|
|
D008583||meninigitis hib
|
|
D008583||type b haemophilus influenzae meningitis
|
|
D008583||type b hemophilus influenzae meningitis
|
|
D010899||pituitary apoplexy
|
|
D010899||apoplexy pituitary
|
|
D008582||meningitis aseptic
|
|
D008582||aseptic meningitis
|
|
C557821||orofaciodigital syndrome 11
|
|
C557821||gabrielli syndrome
|
|
C557821||ofd11
|
|
C557821||ofds xi
|
|
C557821||oral facial digital syndrome 11
|
|
C557821||oral facial digital syndrome type xi
|
|
C557821||oral facial digital syndrome with skeletal anomalies
|
|
C557821||orofaciodigital syndrome xi
|
|
D007251||influenza human
|
|
D007251||flu human
|
|
D007251||grippe
|
|
D007251||human flu
|
|
D007251||human influenza
|
|
D007251||human influenzas
|
|
D007251||influenza
|
|
D007251||influenza in human
|
|
D007251||influenza in humans
|
|
D007251||influenzas
|
|
D007251||influenzas human
|
|
D008581||meningitis
|
|
D008581||meningitides
|
|
D008581||pachymeningitides
|
|
D008581||pachymeningitis
|
|
C557820||orofaciodigital syndrome 8
|
|
C557820||oral facial digital syndrome 8
|
|
C557820||orofaciodigital syndrome viii
|
|
D020209||cranial nerve injuries
|
|
D020209||cranial nerve injury
|
|
D020209||cranial neuropathies traumatic
|
|
D020209||cranial neuropathy traumatic
|
|
D020209||injuries cranial nerve
|
|
D020209||injury cranial nerve
|
|
D020209||nerve injuries cranial
|
|
D020209||nerve injury cranial
|
|
D020209||neuropathies traumatic cranial
|
|
D020209||neuropathy traumatic cranial
|
|
D020209||traumatic cranial neuropathies
|
|
D020209||traumatic cranial neuropathy
|
|
D008580||meningism
|
|
D008580||dupre apos s syndrome
|
|
D008580||dupres syndrome
|
|
D008580||dupre syndrome
|
|
D008580||meningisms
|
|
D008580||meningismus
|
|
D008580||meningitis like reaction
|
|
D008580||meningitis like reactions
|
|
D008580||pseudomeningitides
|
|
D008580||pseudomeningitis
|
|
D008580||reaction meningitis like
|
|
D008580||reactions meningitis like
|
|
D008580||syndrome dupre
|
|
D008580||syndrome dupre apos s
|
|
D020208||brain injury chronic
|
|
D020208||brain injuries chronic
|
|
D020208||chronic brain injuries
|
|
D020208||chronic brain injury
|
|
D020208||chronic encephalopathies post concussive
|
|
D020208||chronic encephalopathy post concussive
|
|
D020208||chronic post concussive encephalopathies
|
|
D020208||chronic post concussive encephalopathy
|
|
D020208||chronic post traumatic encephalopathies
|
|
D020208||chronic post traumatic encephalopathy
|
|
D020208||chronic traumatic encephalopathy
|
|
D020208||encephalopathies chronic post concussive
|
|
D020208||encephalopathies chronic post traumatic
|
|
D020208||encephalopathies post concussive chronic
|
|
D020208||encephalopathy chronic post concussive
|
|
D020208||encephalopathy chronic post traumatic
|
|
D020208||encephalopathy chronic traumatic
|
|
D020208||encephalopathy post concussive chronic
|
|
D020208||encephalopathy post traumatic chronic
|
|
D020208||injury brain chronic
|
|
D020208||post concussive chronic encephalopathies
|
|
D020208||post concussive chronic encephalopathy
|
|
D020208||post concussive encephalopathies chronic
|
|
D020208||post concussive encephalopathy chronic
|
|
D020208||post traumatic encephalopathies chronic
|
|
D020208||post traumatic encephalopathy chronic
|
|
D020208||traumatic encephalopathies chronic
|
|
D020208||traumatic encephalopathy chronic
|
|
D019226||oral ulcer
|
|
D019226||mouth ulcer
|
|
D019226||mouth ulcers
|
|
D019226||oral ulcers
|
|
D019226||ulcer mouth
|
|
D019226||ulcer oral
|
|
D019226||ulcers mouth
|
|
D019226||ulcers oral
|
|
C567186|158330||mullerian aplasia and hyperandrogenism
|
|
C567186|158330||mullerian duct failure and hyperandrogenism
|
|
D009879||ophthalmia sympathetic
|
|
D009879||ophthalmias sympathetic
|
|
D009879||sympathetic ophthalmia
|
|
D009879||sympathetic ophthalmias
|
|
D009879||sympathetic uveitides
|
|
D009879||sympathetic uveitis
|
|
D009879||uveitides sympathetic
|
|
D009879||uveitis sympathetic
|
|
D008548||melanosis
|
|
D008548||chloasma
|
|
D008548||chloasmas
|
|
D008548||freckle
|
|
D008548||freckles
|
|
D008548||melanism
|
|
D008548||melanoses
|
|
D008548||melasma
|
|
D008548||melasmas
|
|
611131|C567005||retinitis pigmentosa 37
|
|
611131|C567005||rp37
|
|
D009878||ophthalmia neonatorum
|
|
D009877||endophthalmitis
|
|
D009877||endophthalmitides
|
|
D009877||endophthalmitides infectious
|
|
D009877||endophthalmitis infectious
|
|
D009877||infectious endophthalmitides
|
|
D009877||infectious endophthalmitis
|
|
D009877||ophthalmia
|
|
D009877||ophthalmias
|
|
D008546||melanoma experimental
|
|
D008546||b16 melanoma
|
|
D008546||b16 melanomas
|
|
D008546||cloudman s91 melanoma
|
|
D008546||experimental melanoma
|
|
D008546||experimental melanomas
|
|
D008546||harding passey melanoma
|
|
D008546||melanoma b16
|
|
D008546||melanoma cloudman s91
|
|
D008546||melanoma harding passey
|
|
D008546||melanomas b16
|
|
D008546||melanomas experimental
|
|
D008546||s91 melanoma cloudman
|
|
D008545||melanoma
|
|
D008545||malignant melanoma
|
|
D008545||malignant melanomas
|
|
D008545|155600||melanoma malignant
|
|
D008545||melanomas
|
|
D008545||melanomas malignant
|
|
263200|D017044||polycystic kidney autosomal recessive
|
|
263200|D017044||arpkd
|
|
263200|D017044||autosomal recessive polycystic kidney
|
|
263200|D017044||autosomal recessive polycystic kidney disease
|
|
263200|D017044||kidney polycystic autosomal recessive
|
|
263200|D017044||pkd3 formerly hepatic fibrosis congenital included
|
|
263200|D017044||pkhd1
|
|
263200|D017044||polycystic kidney and hepatic disease 1
|
|
263200|D017044||polycystic kidney and hepatic disease 1 autosomal recessive
|
|
263200|D017044||polycystic kidney disease autosomal recessive
|
|
263200|D017044||polycystic kidney disease infantile type 1
|
|
263200|D017044||polycystic kidney disease infantile type i
|
|
D002636|118400||cherubism
|
|
D002636|118400||crbm
|
|
D002636|118400||familial benign giant cell tumor of the jaw
|
|
D002636|118400||familial fibrous dysplasia of jaw
|
|
D002636|118400||familial multilocular cystic disease of the jaws
|
|
D007222||inert gas narcosis
|
|
D007222||depth intoxication
|
|
D007222||depth intoxications
|
|
D007222||inert gas narcoses
|
|
D007222||intoxication depth
|
|
D007222||intoxications depth
|
|
D007222||narcoses inert gas
|
|
D007222||narcoses nitrogen
|
|
D007222||narcosis inert gas
|
|
D007222||narcosis nitrogen
|
|
D007222||nitrogen narcoses
|
|
D007222||nitrogen narcosis
|
|
D010864||pilonidal sinus
|
|
D010864||cyst pilonidal
|
|
D010864||cysts pilonidal
|
|
D010864||pilonidal cyst
|
|
D010864||pilonidal cysts
|
|
D010864||sinus pilonidal
|
|
D008551||melena
|
|
D008551||melenas
|
|
C565185|610756||cerebrooculofacioskeletal syndrome 2
|
|
C565185|610756||cofs2
|
|
C562710|610549||diabetes mellitus insulin resistant with acanthosis nigricans
|
|
C562710|610549||diabetes mellitus insulin resistant with acanthosis nigricans type a
|
|
C562710|610549||insulin receptor defect in with insulin resistant diabetes mellitus and acanthosis nigricans
|
|
C562710|610549||insulin receptor defect with insulin resistant diabetes mellitus and acanthosis nigricans
|
|
C562710|610549||iran type a
|
|
C537285|601853||gomez lopez hernandez syndrome
|
|
C537285|601853||cerebellotrigeminal dermal dysplasia
|
|
C537285|601853||cerebello trigeminal dermal dysplasia
|
|
C537285|601853||glh syndrome
|
|
C535479|610158||corneal dystrophy fuchs apos endothelial 2
|
|
C535479|610158||corneal dystrophy fuchs endothelial 2
|
|
C535479|610158||corneal dystrophy fuchs apos endothelial late onset
|
|
C535479|610158||fcd1 locus
|
|
C535479|610158||fecd2
|
|
C535479|610158||fuchs apos endothelial corneal dystrophy 2
|
|
C535479|610158||late onset fuchs apos endothelial corneal dystrophy
|
|
D007228||infant nutrition disorders
|
|
D007228||infantile malnutrition
|
|
D007228||infant malnutrition
|
|
D007228||infant nutrition disorder
|
|
D007228||infant overnutrition
|
|
D007228||malnutrition infant
|
|
D007228||malnutrition infantile
|
|
D007228||malnutrition in infant
|
|
D007228||malnutrition in infants
|
|
D007228||nutrition disorder infant
|
|
D007228||nutrition disorders infant
|
|
D007228||overnutrition infant
|
|
D009889||opisthorchiasis
|
|
D009889||opisthorchiases
|
|
D009886||ophthalmoplegia
|
|
D009886||external ophthalmoplegia
|
|
D009886||external ophthalmoplegias
|
|
D009886||internal ophthalmoplegia
|
|
D009886||internal ophthalmoplegias
|
|
D009886||oculomotor paralysis
|
|
D009886||ophthalmopareses
|
|
D009886||ophthalmoparesis
|
|
D009886||ophthalmoplegia external
|
|
D009886||ophthalmoplegia internal
|
|
D009886||ophthalmoplegias
|
|
D009886||ophthalmoplegias external
|
|
D009886||ophthalmoplegias internal
|
|
D009886||paralysis oculomotor
|
|
C538339|161550||nasopharyngeal carcinoma
|
|
C538339|161550||nasopharyngeal cancer nasopharyngeal carcinoma susceptibility to 1 included
|
|
C538339|161550||nasopharyngeal carcinoma susceptibility to 2
|
|
C538339|161550|D052556|257220||npc
|
|
C538339|161550||npca
|
|
C538339|161550||npca1 included
|
|
C538339|161550||npca2
|
|
D008554||melioidosis
|
|
D008554||melioidoses
|
|
D007232||infant newborn diseases
|
|
D009894||opportunistic infections
|
|
D009894||infection opportunistic
|
|
D009894||infections opportunistic
|
|
D009894||opportunistic infection
|
|
D006849|236600||hydrocephalus
|
|
D006849|236600||aqueductal stenoses
|
|
D006849|236600||aqueductal stenosis
|
|
D006849|236600||cerebral ventriculomegalies
|
|
D006849|236600||cerebral ventriculomegalies fetal
|
|
D006849|236600||cerebral ventriculomegaly
|
|
D006849|236600||cerebral ventriculomegaly fetal
|
|
D006849|236600||communicating hydrocephalus
|
|
D006849|236600||congenital hydrocephalus
|
|
D006849|236600||fetal cerebral ventriculomegalies
|
|
D006849|236600||fetal cerebral ventriculomegaly
|
|
D006849|236600||hyc1
|
|
D006849|236600||hydrocephalus communicating
|
|
D006849|236600||hydrocephalus congenital
|
|
D006849|236600||hydrocephalus ex vacuo
|
|
D006849|236600||hydrocephalus ex vacuos
|
|
D006849|236600||hydrocephalus nonsyndromic autosomal recessive 1
|
|
D006849|236600||hydrocephalus obstructive
|
|
D006849|236600||hydrocephalus post traumatic
|
|
D006849|236600||hydrocephaly
|
|
D006849|236600||obstructive hydrocephalus
|
|
D006849|236600||post traumatic hydrocephalus
|
|
D006849|236600||stenoses aqueductal
|
|
D006849|236600||stenosis aqueductal
|
|
D006849|236600||ventriculomegalies cerebral
|
|
D006849|236600||ventriculomegalies fetal cerebral
|
|
D006849|236600||ventriculomegaly
|
|
D006849|236600||ventriculomegaly cerebral
|
|
D006849|236600||ventriculomegaly fetal cerebral
|
|
D010874||pinta
|
|
125490|D003811||dentinogenesis imperfecta
|
|
125490|D003811||dentinogenesis imperfectas
|
|
125490|D003811||dentinogenesis imperfecta shields type 2
|
|
125490|D003811||dentinogenesis imperfecta without osteogenesis imperfecta
|
|
125490|D003811||dgi1
|
|
125490|D003811||dgi ii
|
|
125490|D003811||hereditary opalescent dentin
|
|
125490|D003811||hereditary opalescent dentins
|
|
125490|D003811||imperfecta dentinogenesis
|
|
125490|D003811||imperfectas dentinogenesis
|
|
125490|D003811||opalescent dentin hereditary
|
|
125490|D003811||opalescent dentins hereditary
|
|
125490|D003811||opalescent teeth without osteogenesis imperfecta
|
|
D010871||pinealoma
|
|
D010871||mixed pineocytoma pineoblastoma
|
|
D010871||mixed pineocytoma pineoblastomas
|
|
D010871||neoplasm pineal
|
|
D010871||neoplasms pineal
|
|
D010871||pineal gland tumor
|
|
D010871||pineal gland tumors
|
|
D010871||pineal neoplasm
|
|
D010871||pineal neoplasms
|
|
D010871||pinealocytoma
|
|
D010871||pinealocytomas
|
|
D010871||pinealomas
|
|
D010871||pineal parenchymal tumor
|
|
D010871||pineal parenchymal tumors
|
|
D010871||pineal tumor
|
|
D010871||pineal tumors
|
|
D010871||pineoblastoma
|
|
D010871||pineoblastomas
|
|
D010871||pineocytoma
|
|
D010871||pineocytoma pineoblastoma mixed
|
|
D010871||pineocytoma pineoblastomas mixed
|
|
D010871||pineocytomas
|
|
D010871||tumor pineal
|
|
D010871||tumor pineal gland
|
|
D010871||tumor pineal parenchymal
|
|
D010871||tumors pineal
|
|
D010871||tumors pineal gland
|
|
D010871||tumors pineal parenchymal
|
|
C563980|605724||fanconi anemia complementation group d1
|
|
C563980|605724||fad1
|
|
C563980|605724||fancd1
|
|
C562397||hymen imperforate
|
|
D021501||flank pain
|
|
D021501||flank pain left
|
|
D021501||flank pain right
|
|
D021501||flank pains
|
|
D021501||flank pains left
|
|
D021501||flank pains right
|
|
D021501||left flank pain
|
|
D021501||left flank pains
|
|
D021501||pain flank
|
|
D021501||pain left flank
|
|
D021501||pain right flank
|
|
D021501||pains flank
|
|
D021501||pains left flank
|
|
D021501||pains right flank
|
|
D021501||right flank pain
|
|
D021501||right flank pains
|
|
C563384|601154||cardiomyopathy dilated 1e
|
|
C563384|601154||cardiomyopathy dilated with conduction defect 2
|
|
C563384|601154||cardiomyopathy dilated with conduction disorder and arrhythmia
|
|
C563384|601154||cdcd2
|
|
C563384|601154||cmd1e
|
|
106100|D054179||angioedemas hereditary
|
|
106100|D054179||angioedema hereditary
|
|
106100|D054179|D056829||angioedema hereditary type i
|
|
106100|D054179||angioneurotic edema hereditary
|
|
106100|D054179||angioneurotic edemas hereditary
|
|
106100|D054179||c1 esterase inhibitor deficiency
|
|
106100|D054179||c1 esterase inhibitor deficiency of angioedema hereditary type ii included
|
|
106100|D054179||c1 inhibitor deficiency
|
|
106100|D054179||edema hereditary angioneurotic
|
|
106100|D054179||edemas hereditary angioneurotic
|
|
106100|D054179||hae1
|
|
106100|D054179||hae2 included
|
|
106100|D054179||hane
|
|
106100|D054179||hereditary angioedema
|
|
106100|D054179||hereditary angioedemas
|
|
106100|D054179||hereditary angioneurotic edema
|
|
106100|D054179||hereditary angioneurotic edemas
|
|
C562398||madelung deformity
|
|
C562399||corneal dystrophy band shaped
|
|
C562399||band keratopathy
|
|
C536101|600462||myopathy with lactic acidosis and sideroblastic anemia
|
|
C536101|600462||mitochondrial myopathy and sideroblastic anemia
|
|
C536101|600462||mlasa
|
|
C536101|600462||mlasa1
|
|
C536101|600462||mlasa2
|
|
C536101|600462||myopathy lactic acidosis and sideroblastic anemia 1
|
|
C536101|600462||myopathy lactic acidosis and sideroblastic anemia 2
|
|
D015319|229700||fructose 1 6 diphosphatase deficiency
|
|
D015319|229700||deficiencies fructose 1 6 bisphosphatase
|
|
D015319|229700||deficiencies fructose 1 6 diphosphatase
|
|
D015319|229700||deficiencies fructose biphosphatase
|
|
D015319|229700||deficiencies fructosediphosphatase
|
|
D015319|229700||deficiencies hexosediphosphatase
|
|
D015319|229700||deficiency fructose 1 6 bisphosphatase
|
|
D015319|229700||deficiency fructose 1 6 diphosphatase
|
|
D015319|229700||deficiency fructose biphosphatase
|
|
D015319|229700||deficiency fructosediphosphatase
|
|
D015319|229700||deficiency hexosediphosphatase
|
|
D015319|229700||fructose 1 6 bisphosphatase deficiencies
|
|
D015319|229700||fructose 1 6 bisphosphatase deficiency
|
|
D015319|229700||fructose 1 6 diphosphatase deficiencies
|
|
D015319|229700||fructose biphosphatase deficiencies
|
|
D015319|229700||fructose biphosphatase deficiency
|
|
D015319|229700||fructosediphosphatase deficiencies
|
|
D015319|229700||fructosediphosphatase deficiency
|
|
D015319|229700||hexosediphosphatase deficiencies
|
|
D015319|229700||hexosediphosphatase deficiency
|
|
D009855||onchocerciasis
|
|
D009855||onchocerciases
|
|
D044225||piscirickettsiaceae infections
|
|
D044225||piscirickettsiaceae infection
|
|
D044225||piscirickettsioses
|
|
D044225||piscirickettsiosis
|
|
C537311|606937||spinocerebellar ataxia autosomal recessive 5
|
|
C537311|606937||camos
|
|
C537311|606937||cerebellar ataxia with mental retardation optic atrophy and skin abnormalities
|
|
C537311|606937||scar5
|
|
D008531||megacolon
|
|
D008531||megacolons
|
|
C567381|612255||inflammatory bowel disease 15
|
|
C567381|612255||ibd15
|
|
D010842||pica
|
|
D010842||geophagia
|
|
D010845||obesity hypoventilation syndrome
|
|
D010845||hypoventilation syndrome obesity
|
|
D010845||pickwickian syndrome
|
|
D010845||syndrome obesity hypoventilation
|
|
D010845||syndrome pickwickian
|
|
D058866||osteoporotic fractures
|
|
D058866||fracture osteoporotic
|
|
D058866||fractures osteoporotic
|
|
D058866||osteoporotic fracture
|
|
C536925|609428||tukel syndrome
|
|
C536925|609428||cfeom u
|
|
C536925|609428||congenital extraocular muscle fibrosis with ulnar hand anomalies
|
|
C536925|609428||fibrosis of extraocular muscles congenital with ulnar hand anomalies
|
|
D037081||posterior tibial tendon dysfunction
|
|
D037081||dysfunction tibialis posterior
|
|
D037081||posterior tibial tendon insufficiency
|
|
D037081||tibialis posterior dysfunction
|
|
D037081||tibial tendon dysfunction posterior
|
|
C563900|608586||keratoconus 3
|
|
C563900|608586||ktcn3
|
|
138800||goiter multinodular 1 with or without sertoli leydig cell tumors
|
|
138800|C562732||euthyroid goiter
|
|
138800||goiter nontoxic with intrathyroidal calcification
|
|
138800||mng1
|
|
138800||multinodular goiter adolescent
|
|
138800||simple goiter
|
|
C566917|611556||glycogen storage disease 0 muscle
|
|
C566917|611556||gsd 0b
|
|
C566917|611556||gsd0b
|
|
C566917|611556||muscle glycogen storage disease 0
|
|
C566917|611556||muscle glycogen synthase deficiency
|
|
D010859||pigmentation disorders
|
|
D010859||disease schamberg
|
|
D010859||disease schamberg apos s
|
|
D010859||disorder pigmentation
|
|
D010859||disorders pigmentation
|
|
D010859|300337||incontinentia pigmenti achromians
|
|
D010859||ito syndrome
|
|
D010859||pigmentation disorder
|
|
D010859||schamberg disease
|
|
D010859||schamberg apos s disease
|
|
D010859||schambergs disease
|
|
D010859||syndrome ito
|
|
D008539||meigs syndrome
|
|
D008539||meig apos s syndrome
|
|
D008539||meigs apos syndrome
|
|
D008539||meig syndrome
|
|
D009869||oophoritis
|
|
D009869||oophoritides
|
|
D008538||meige syndrome
|
|
D008538||blepharospasm oromandibular dyskinesia
|
|
D008538||blepharospasm oromandibular dyskinesias
|
|
D008538||blepharospasm oromandibular dystonia
|
|
D008538||blepharospasm oromandibular dystonias
|
|
D008538||blepharospasm oromandibular dystonia syndrome
|
|
D008538||blepharospasm oromandibular dystonia syndrome idiopathic
|
|
D008538||blepharospasm oromandibular dystonia syndromes
|
|
D008538||brueghel syndrome
|
|
D008538||dyskinesia blepharospasm oromandibular
|
|
D008538||dyskinesia idiopathic orofacial
|
|
D008538||dyskinesias blepharospasm oromandibular
|
|
D008538||dyskinesias idiopathic orofacial
|
|
D008538||dystonia blepharospasm oromandibular
|
|
D008538||dystonias blepharospasm oromandibular
|
|
D008538||dystonia syndrome blepharospasm oromandibular
|
|
D008538||dystonia syndromes blepharospasm oromandibular
|
|
D008538||idiopathic blepharospasm oromandibular dystonia syndrome
|
|
D008538||idiopathic orofacial dyskinesia
|
|
D008538||idiopathic orofacial dyskinesias
|
|
D008538||orofacial dyskinesia idiopathic
|
|
D008538||orofacial dyskinesias idiopathic
|
|
D008538||syndrome blepharospasm oromandibular dystonia
|
|
145750|D006953||hyperlipoproteinemia type iv
|
|
145750|D006953||carbohydrate inducible hyperlipemia
|
|
145750|D006953||carbohydrate inducible hyperlipemias
|
|
145750|D006953||familial hyperlipoproteinemia type 4
|
|
145750|D006953||familial hypertriglyceridemia
|
|
145750|D006953||familial type iv hyperlipoproteinemia
|
|
145750|D006953||hyperlipemia carbohydrate inducible
|
|
145750|D006953||hyperlipemias carbohydrate inducible
|
|
145750|D006953||hyperlipoproteinemias type iv
|
|
145750|D006953||hyperprebetalipoproteinemia
|
|
145750|D006953||hyper prebeta lipoproteinemia
|
|
145750|D006953||hypertriglyceridemia familial
|
|
145750|D006953||inducible hyperlipemia carbohydrate
|
|
145750|D006953||inducible hyperlipemias carbohydrate
|
|
145750|D006953||type iv hyperlipoproteinemia
|
|
145750|D006953||type iv hyperlipoproteinemias
|
|
D008532||megacolon toxic
|
|
D008532||toxic megacolon
|
|
D010850||picornaviridae infections
|
|
D010850||infection picornaviridae
|
|
D010850||infection picornavirus
|
|
D010850||infections picornaviridae
|
|
D010850||infections picornavirus
|
|
D010850||picornaviridae infection
|
|
D010850||picornavirus infection
|
|
D010850||picornavirus infections
|
|
C548086||stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features
|
|
C564688|606640||amyotrophic lateral sclerosis 3
|
|
C564688|606640||als3
|
|
D010854||piedra
|
|
D010854||black piedra
|
|
D010854||black piedras
|
|
D010854||piedra black
|
|
D010854||piedras
|
|
D010854||piedras black
|
|
D010854||piedras white
|
|
D010854||piedra white
|
|
D010854||white piedra
|
|
D010854||white piedras
|
|
C536832|610015||glutamine deficiency congenital
|
|
C536832|610015||glutamine synthase deficiency congenital systemic
|
|
C536832|610015||glutamine synthetase deficiency congenital systemic
|
|
D008556|155900||melkersson rosenthal syndrome
|
|
D008556|155900||cheilitis granulomatosa
|
|
D008556|155900||cheilitis granulomatosa facial neuropathy orofacial edema
|
|
D008556|155900||cheilitis granulomatosa orofacial edema facial neuropathy
|
|
D008556|155900||cheilitis miescher melkersson rosenthal granulomatous
|
|
D008556|155900||facial neuropathy cheilitis granulomatosa orofacial edema
|
|
D008556|155900||facial neuropathy orofacial edema cheilitis granulomatosa
|
|
D008556|155900||granulomatous cheilitis
|
|
D008556|155900||granulomatous cheilitis miescher melkersson rosenthal
|
|
D008556|155900||macrocheilia facial palsy edema
|
|
D008556|155900||melkerson rosenthal syndrome
|
|
D008556|155900||melkersson rosenthal miescher syndrome
|
|
D008556|155900||melkersson syndrome
|
|
D008556|155900||miescher melkersson rosenthal granulomatous cheilitis
|
|
D008556|155900||mros
|
|
D008556|155900||mrs
|
|
D008556|155900||orofacial edema cheilitis granulomatosa facial neuropathy
|
|
D008556|155900||orofacial edema facial neuropathy cheilitis granulomatosa
|
|
D008556|155900||rosenthal melkerson syndrome
|
|
D008556|155900||rosenthal melkersson syndrome
|
|
D008556|155900||syndrome melkerson rosenthal
|
|
606711||specific language impairment 1
|
|
606711||sli1
|
|
606711||specific language impairment quantitative trait locus on chromosome 16
|
|
D034801||mastocytoma
|
|
D034801||benign mastocytoma
|
|
D034801||extracutaneous mastocytoma
|
|
D034801||extracutaneous mastocytomas
|
|
D034801||mastocytoma benign
|
|
D034801||mastocytoma extracutaneous
|
|
D034801||mastocytomas extracutaneous
|
|
C548085||progressive transformation of germinal centers
|
|
606712||specific language impairment 2
|
|
606712||sli2
|
|
606712||specific language impairment quantitative trait locus on chromosome 19
|
|
C567548|612858||orofacial cleft 12
|
|
C567548|612858||cleft lip with or without cleft palate nonsyndromic 12
|
|
C567548|612858||ofc12
|
|
C562378||hepatic fibrosis congenital
|
|
C562379||dermatosis papulosa nigra
|
|
D009839||oligomenorrhea
|
|
D009839||oligomenorrheas
|
|
C562377||glutamate monosodium sensitivity
|
|
C562377||chinese restaurant syndrome
|
|
D009837||oligodendroglioma
|
|
D009837||adult oligodendroglioma
|
|
D009837||adult oligodendrogliomas
|
|
D009837||anaplastic oligodendroglioma
|
|
D009837||anaplastic oligodendrogliomas
|
|
D009837||childhood oligodendroglioma
|
|
D009837||childhood oligodendrogliomas
|
|
D009837||mixed oligodendroglioma astrocytoma
|
|
D009837||mixed oligodendroglioma astrocytomas
|
|
D009837||mixed oligodendroglioma ependymoma
|
|
D009837||mixed oligodendroglioma ependymomas
|
|
D009837||oligodendroblastoma
|
|
D009837||oligodendroblastomas
|
|
D009837||oligodendroglioma adult
|
|
D009837||oligodendroglioma anaplastic
|
|
D009837||oligodendroglioma astrocytoma mixed
|
|
D009837||oligodendroglioma astrocytomas mixed
|
|
D009837||oligodendroglioma childhood
|
|
D009837||oligodendroglioma ependymoma mixed
|
|
D009837||oligodendroglioma ependymomas mixed
|
|
D009837||oligodendrogliomas
|
|
D009837||oligodendrogliomas adult
|
|
D009837||oligodendrogliomas anaplastic
|
|
D009837||oligodendrogliomas childhood
|
|
D009837||oligodendrogliomas well differentiated
|
|
D009837||oligodendroglioma well differentiated
|
|
D009837||well differentiated oligodendroglioma
|
|
D009837||well differentiated oligodendrogliomas
|
|
C565287|605818||deafness autosomal recessive 27
|
|
C565287|605818||dfnb27
|
|
D056929|177200||liddle syndrome
|
|
D056929|177200||pseudoaldosteronism
|
|
D056929|177200||syndrome liddle
|
|
C566505|609621||short qt syndrome 2
|
|
C566505|609621||sqt2
|
|
211400|C567618||bronchiectasis with or without elevated sweat chloride 1
|
|
211400|C567618||besc1
|
|
211400|C567618|C567772|613071|C567813|613021||cystic fibrosis like syndrome
|
|
C557819||orofaciodigital syndrome 5
|
|
C557819||oral facial digital syndrome 5
|
|
C557819||oral facial digital syndrome type v
|
|
C557819||orofaciodigital syndrome thurston type
|
|
C557819||orofaciodigital syndrome v
|
|
C557819||polydactyly postaxial with median cleft of upper lip
|
|
C557819||thurston syndrome
|
|
C557818||orofaciodigital syndrome 9
|
|
C557818||ofd9
|
|
C557818||ofds ix
|
|
C557818||oral facial digital syndrome 9
|
|
C557818||oral facial digital syndrome type ix
|
|
C557818||oral facial digital syndrome with retinal abnormalities
|
|
C557818||orofaciodigital syndrome ix
|
|
C557818||orofaciodigital syndrome type 9
|
|
C557818||orofaciodigital syndrome with retinal abnormalities
|
|
C557817||orofaciodigital syndrome 3
|
|
C557817||brachydactyly of the hands and feet with duplication of the first toes
|
|
C557817||brachydactyly with major proximal phalangeal shortening
|
|
C557817||ofds iii
|
|
C557817||oral facial digital syndrome 3
|
|
C557817||oral facial digital syndrome type iii
|
|
C557817||orofaciodigital syndrome iii
|
|
C557817||sugarman brachydactyly
|
|
C557817||sugarman syndrome
|
|
C557815||deficiency of interleukin 1 receptor antagonist
|
|
C567642|613327||lipodystrophy congenital generalized type 4
|
|
C567642|613327||berardinelli seip congenital lipodystrophy type 4 with muscular dystrophy
|
|
C567642|613327||cgl4
|
|
C567642|613327||lipodystrophy berardinelli seip congenital type 4 with muscular dystrophy
|
|
D037061||metatarsalgia
|
|
C562384||branchial cleft anomalies
|
|
D009849||olivopontocerebellar atrophies
|
|
D009849||ataxia presenile
|
|
D009849||ataxias presenile
|
|
D009849||atrophy familial olivopontocerebellar
|
|
D009849||atrophy idiopathic olivopontocerebellar
|
|
D009849||atrophy inherited olivopontocerebellar
|
|
D009849||atrophy nonfamilial olivopontocerebellar
|
|
D009849||atrophy olivopontocerebellar
|
|
D009849||atrophy olivo ponto cerebellar
|
|
D009849||atrophy pontoolivocerebellar
|
|
D009849||degeneration olivopontocerebellar
|
|
D009849||degeneration olivo ponto cerebellar
|
|
D009849||degenerations olivopontocerebellar
|
|
D009849||degenerations olivo ponto cerebellar
|
|
D009849||dejerine thomas syndrome
|
|
D009849||familial olivopontocerebellar atrophies
|
|
D009849||familial olivopontocerebellar atrophy
|
|
D009849||idiopathic olivopontocerebellar atrophies
|
|
D009849||idiopathic olivopontocerebellar atrophy
|
|
D009849||inherited olivopontocerebellar atrophies
|
|
D009849||inherited olivopontocerebellar atrophy
|
|
D009849||nonfamilial olivopontocerebellar atrophies
|
|
D009849||nonfamilial olivopontocerebellar atrophy
|
|
D009849||olivopontocerebellar atrophies familial
|
|
D009849||olivopontocerebellar atrophies idiopathic
|
|
D009849||olivopontocerebellar atrophies inherited
|
|
D009849||olivopontocerebellar atrophies nonfamilial
|
|
D009849||olivopontocerebellar atrophy
|
|
D009849||olivo ponto cerebellar atrophy
|
|
D009849||olivopontocerebellar atrophy familial
|
|
D009849||olivopontocerebellar atrophy idiopathic
|
|
D009849||olivopontocerebellar atrophy inherited
|
|
D009849||olivopontocerebellar atrophy nonfamilial
|
|
D009849||olivopontocerebellar degeneration
|
|
D009849||olivo ponto cerebellar degeneration
|
|
D009849||olivopontocerebellar degenerations
|
|
D009849||olivo ponto cerebellar degenerations
|
|
D009849||pontoolivocerebellar atrophies
|
|
D009849||pontoolivocerebellar atrophy
|
|
D009849||presenile ataxia
|
|
D009849||presenile ataxias
|
|
D009849||syndrome dejerine thomas
|
|
C565447|245349||pyruvate dehydrogenase e3 binding protein deficiency
|
|
C565447|245349||lactic acidemia due to defect in lipoyl containing component x of the pyruvate dehydrogenase complex
|
|
C565447|245349||pdhxd
|
|
D009846||oliguria
|
|
D009846||oligurias
|
|
D009845||oligospermia
|
|
D009845||count low sperm
|
|
D009845||counts low sperm
|
|
D009845||hypospermatogenesis
|
|
D009845||low sperm count
|
|
D009845||low sperm counts
|
|
D009845||oligozoospermia
|
|
D009845||sperm count low
|
|
D009845||sperm counts low
|
|
C562875|609814||complement factor h deficiency
|
|
C562875|609814||cfhd
|
|
C562875|609814||cfh deficiency
|
|
C562875|609814||factor h deficiency
|
|
613118|D020152||antithrombin iii deficiency
|
|
613118|D020152||antithrombin 3 deficiencies
|
|
613118|D020152||antithrombin 3 deficiency
|
|
613118|D020152||antithrombin iii deficiencies
|
|
613118|D020152||at3d
|
|
613118|D020152||congenital antithrombin iii deficiency
|
|
613118|D020152||deficiencies antithrombin 3
|
|
613118|D020152||deficiencies antithrombin iii
|
|
613118|D020152||deficiency antithrombin 3
|
|
613118|D020152||deficiency antithrombin iii
|
|
613118|D020152||hereditary antithrombin deficiency
|
|
613118|D020152||thph7
|
|
613118|D020152||thrombophilia due to antithrombin iii deficiency
|
|
C566353|603629||deafness autosomal recessive 21
|
|
C566353|603629||dfnb21
|
|
D058890||granulomatous mastitis
|
|
D058890||mastitis granulomatous
|
|
C565293|605803||dermatitis atopic 2
|
|
C565293|605803||atod2
|
|
C566512|609578||cardiomyopathy familial restrictive 2
|
|
C566512|609578||rcm2
|
|
606002|C537308||spinocerebellar ataxia autosomal recessive 1
|
|
606002|C537308||aoa2
|
|
606002|C537308||ataxia ocular apraxia 2
|
|
606002|C537308||ataxia oculomotor apraxia 2
|
|
606002|C537308||ataxia with oculomotor apraxia
|
|
606002|C537308||scan2
|
|
606002|C537308||scar1
|
|
606002|C537308||spinocerebellar ataxia recessive non friedreich type 1
|
|
606002|C537308||spinocerebellar ataxia with axonal neuropathy type 2
|
|
C562393|155600||melanoma cutaneous malignant
|
|
C562393|155600||dysplastic nevus syndrome hereditary
|
|
C562393|155600||familial atypical mole malignant melanoma syndrome
|
|
C562393|155600||fammm
|
|
C562393|155600||melanoma familial
|
|
C562390||humoral hypercalcemia of malignancy
|
|
C562391||ovarian fibromata
|
|
C537396||neuropathy ataxia and retinis pigmentosa
|
|
C537396||narp syndrome
|
|
C537396||neurogenic muscle weakness ataxia and retinitis pigmentosa
|
|
C537396||neuropathy ataxia and retinitis pigmentos
|
|
C537396||neuropathy ataxia and retinitis pigmentosa
|
|
C537396||neuropathy ataxia retinitis pigmentosa syndrome
|
|
C563682||oculootofacial dysplasia
|
|
C537395||neuronal intranuclear inclusion disease
|
|
C536064||osteosclerosis with ichthyosis and premature ovarian failure
|
|
C536064||sclerosing dysplasia of bone with ichthyosis and premature ovarian failure
|
|
C536069||human spumaretrovirus infection
|
|
C536069||human spumaretroviridae infection
|
|
C537398||pili torti developmental delay neurological abnormalities
|
|
C537398||pili torti and developmental delay
|
|
C536067||hordnes engebretsen knudtson syndrome
|
|
C537399||pili torti onychodysplasia
|
|
C537399||twisted hair with nail dysplasias
|
|
C536068||hoyeraal hreidarsson syndrome
|
|
C536068||cerebellar hypoplasia with pancytopenia
|
|
D009814||oesophagostomiasis
|
|
D009814||oesophagostomiases
|
|
D001098||spider bites
|
|
D001098||arachnidism
|
|
D001098||arachnidism necrotic
|
|
D001098||bite spider
|
|
D001098||bites spider
|
|
D001098||necrotic arachnidism
|
|
D001098||spider bite
|
|
C537392||neurofibromatosis type 4 of riccardi
|
|
C537392||neurofibromatosis atypical
|
|
C537392||neurofibromatosis type iv of riccardi
|
|
C537392||neurofibromatosis variant form s of
|
|
C536061||osteopoikilosis and dacryocystitis
|
|
C536061||dacryocystitis osteopoikilosis
|
|
C536061||gunal seber basaran syndrome
|
|
D009810||odontoma
|
|
D009810||ameloblastic fibro odontoma
|
|
D009810||ameloblastic fibro odontomas
|
|
D009810||compound odontoma
|
|
D009810||compound odontomas
|
|
D009810||fibroodontoma
|
|
D009810||fibro odontoma
|
|
D009810||fibro odontoma ameloblastic
|
|
D009810||fibroodontomas
|
|
D009810||fibro odontomas
|
|
D009810||fibro odontomas ameloblastic
|
|
D009810||odontoma compound
|
|
D009810||odontomas
|
|
D009810||odontomas compound
|
|
C536062||hernandez fragoso syndrome
|
|
C536062||osteoporosis and oculocutaneous hypopigmentation syndrome
|
|
C536062||osteoporosis oculocutaneous hypopigmentation syndrome
|
|
C537390||neurofibromatosis type 5
|
|
C537390||neurofibromatosis type v
|
|
C537390||segmental neurofibromatosis
|
|
D006053|141400||goldenhar syndrome
|
|
D006053|141400||craniofacial microsomia
|
|
D006053|141400||craniofacial microsomias
|
|
D006053|141400||disease goldenhar
|
|
D006053|141400||dysostoses otomandibular
|
|
D006053|141400||dysostosis otomandibular
|
|
D006053|141400||dysplasia facioauriculovertebral
|
|
D006053|141400||dysplasia lateral facial
|
|
D006053|141400||dysplasia oculoauriculovertebral
|
|
D006053|141400||dysplasias facioauriculovertebral
|
|
D006053|141400||dysplasias lateral facial
|
|
D006053|141400||dysplasias oculoauriculovertebral
|
|
D006053|141400||facial dysplasia lateral
|
|
D006053|141400||facial dysplasias lateral
|
|
D006053|141400||facioauriculovertebral dysplasia
|
|
D006053|141400||facioauriculovertebral dysplasias
|
|
D006053|141400||facioauriculovertebral sequence
|
|
D006053|141400||facioauriculovertebral sequences
|
|
D006053|141400||fav sequence
|
|
D006053|141400||first and second branchial arch syndrome
|
|
D006053|141400||first and second pharyngeal arch syndromes
|
|
D006053|141400||goldenhar disease
|
|
D006053|141400||goldenhar gorlin syndrome
|
|
D006053|141400||goldenhar gorlin syndromes
|
|
D006053|141400||goldenhar syndrome with ipsilateral radial defect
|
|
D006053|141400||hemifacial microsomia
|
|
D006053|141400||hemifacial microsomia with radial defects
|
|
D006053|141400||hfm
|
|
D006053|141400||lateral facial dysplasia
|
|
D006053|141400||lateral facial dysplasias
|
|
D006053|141400||microsomia craniofacial
|
|
D006053|141400||microsomia hemifacial radial defects
|
|
D006053|141400||microsomias craniofacial
|
|
D006053|141400||moeschler clarren syndrome
|
|
D006053|141400||oav dysplasia
|
|
D006053|141400||oavs
|
|
D006053|141400||oavs with radial defect
|
|
D006053|141400||oculoauriculovertebral dysplasia
|
|
D006053|141400||oculoauriculovertebral dysplasias
|
|
D006053|141400||oculoauriculovertebral spectrum
|
|
D006053|141400||oculoauriculovertebral spectrums
|
|
D006053|141400||oculoauriculovertebral spectrum with radial defect
|
|
D006053|141400||oculoauriculovertebral syndrome
|
|
D006053|141400||oral mandibular auricular syndrome
|
|
D006053|141400||oral mandibular auricular syndromes
|
|
D006053|141400||otomandibular dysostoses
|
|
D006053|141400||otomandibular dysostosis
|
|
D006053|141400||syndrome goldenhar
|
|
D006053|141400||syndrome goldenhar gorlin
|
|
D006053|141400||syndrome moeschler clarren
|
|
D006053|141400||syndrome oculoauriculovertebral
|
|
D006053|141400||syndrome oral mandibular auricular
|
|
D006053|141400||syndromes goldenhar gorlin
|
|
D006053|141400||syndromes oral mandibular auricular
|
|
C537391||neurofibromatosis familial intestinal
|
|
C537391||neurofibromatosis 3b
|
|
C536060||whyte murphy fallon sly syndrome
|
|
203290|C537731||oculocutaneous albinism type 3
|
|
203290|C537731||albinism 3
|
|
203290|C537731|C537189||albinism iii
|
|
203290|C537731||albinism oculocutaneous type 3
|
|
203290|C537731|C537189||albinism oculocutaneous type iii
|
|
203290|C537731||oca3
|
|
203290|C537731|C537189||oculocutaneous albinism type iii
|
|
203290|C537731||roca
|
|
203290|C537731|C537189||rufous oculocutaneous albinism
|
|
203290|C537731|C537189||xanthism
|
|
270300|C564818||peeling skin syndrome
|
|
270300|C564818||deciduous skin
|
|
270300|C564818||keratolysis exfoliativa congenita
|
|
270300|C564818||peeling skin syndrome type b
|
|
270300|C564818|C538356|601224||pss
|
|
270300|C564818||skin peeling familial continuous generalized
|
|
C536077||hydroa vacciniforme familial
|
|
C536077||familial hydroa vacciniforme
|
|
C536074||hutterite cerebroosteonephrodysplasia syndrome
|
|
C536074||cerebroosteonephrosis syndrome
|
|
C536074||congenital shortness with mild spondylorhizomelic dwarfism
|
|
C567489|270970||spherocytosis type 3
|
|
C567489|270970||hs3
|
|
C567489|270970||sph3
|
|
C567489|270970||spherocytosis hereditary 3
|
|
C563698||mitochondrial dna depletion syndrome myopathic form
|
|
C563698||mitochondrial dna depletion myopathy autosomal recessive
|
|
114900|C562842||carcinoid tumors intestinal
|
|
611126|C567006||acyl coa dehydrogenase family member 9 deficiency of
|
|
611126|C567006||acad9 deficiency
|
|
611126|C567006||mitochondrial complex i deficiency due to acad9 deficiency
|
|
C536079||hydrolethalus syndrome
|
|
C536072||hunter mcalpine syndrome
|
|
C536072||hunter mcalpine craniosynostosis
|
|
C536072||hunter mcalpine craniosynostosis syndrome
|
|
C536071||hunter carpenter macdonald syndrome
|
|
C573012||lactic acidosis congenital infantile due to lad deficiency
|
|
C573012||dihydrolipoamide dehydrogenase deficiency
|
|
C573012||dld deficiency
|
|
C573012||lipoamide dehydrogenase deficiency lactic acidosis due to
|
|
C573012||maple syrup urine disease type iii
|
|
D025064||sex chromosome disorders
|
|
D025064||chromosome disorder sex
|
|
D025064||chromosome disorders sex
|
|
D025064||disorders sex chromosome
|
|
D025064||disorders sex chromosome abnormality
|
|
D025064||sex chromosome abnormality disorders
|
|
D025064||sex chromosome disorder
|
|
D025063||chromosome disorders
|
|
D025063||autosomal chromosome disorder
|
|
D025063||autosomal chromosome disorders
|
|
D025063||chromosomal disorder
|
|
D025063||chromosomal disorders
|
|
D025063||chromosome abnormality disorder
|
|
D025063||chromosome abnormality disorders
|
|
D025063||chromosome disorder
|
|
D025063||chromosome disorder autosomal
|
|
D025063||chromosome disorders autosomal
|
|
D025063||disorder chromosomal
|
|
D025063||disorder chromosome
|
|
D025063||disorder chromosome abnormality
|
|
D025063||disorders chromosomal
|
|
D025063||disorders chromosome
|
|
D013088||spermatocele
|
|
D013088||cyst epididymal
|
|
D013088||cysts epididymal
|
|
D013088||epididymal cyst
|
|
D013088||epididymal cysts
|
|
D013088||spermatoceles
|
|
D013086||spermatic cord torsion
|
|
D013086||spermatic cord torsions
|
|
D013086||testicular torsion
|
|
D013086||testicular torsions
|
|
D013086||torsion of testicular cord
|
|
D013086||torsion spermatic cord
|
|
D013086||torsions spermatic cord
|
|
D013086||torsions testicular
|
|
D013086||torsion testicular
|
|
C536087||ichthyosis hystrix gravior
|
|
C536087||ichthyosis lambert type
|
|
C536087||lambert type ichthyosis
|
|
C536087||porcupine man
|
|
D014390||tuberculosis meningeal
|
|
D014390||hypertrophic pachymeningitides tuberculous
|
|
D014390||hypertrophic pachymeningitis tuberculous
|
|
D014390||meningeal tuberculoses
|
|
D014390||meningeal tuberculosis
|
|
D014390||meningitides tubercular
|
|
D014390||meningitides tuberculosis
|
|
D014390||meningitides tuberculous
|
|
D014390||meningitis tubercular
|
|
D014390||meningitis tuberculosis
|
|
D014390||meningitis tuberculous
|
|
D014390||pachymeningitides tuberculous hypertrophic
|
|
D014390||pachymeningitis tuberculous hypertrophic
|
|
D014390||tb meningitides
|
|
D014390||tb meningitis
|
|
D014390||tubercular meningitides
|
|
D014390||tubercular meningitis
|
|
D014390||tuberculoses meningeal
|
|
D014390||tuberculosis meningitides
|
|
D014390||tuberculosis meningitis
|
|
D014390||tuberculous hypertrophic pachymeningitides
|
|
D014390||tuberculous hypertrophic pachymeningitis
|
|
D014390||tuberculous meningitides
|
|
D014390||tuberculous meningitis
|
|
C564991||gamma a globulin defect in assembly of
|
|
C564991||iga defect in assembly of
|
|
C564991||immunoglobulin a defect in assembly of
|
|
C563136|309541||mental retardation x linked 3
|
|
C563136|309541||methylmalonic acidemia and homocysteinemia cblx type
|
|
C563136|309541||mrx3
|
|
C564990||gastric sneezing
|
|
C564990||stomach sneeze reflex
|
|
D014394||tuberculosis osteoarticular
|
|
D014394||bone tuberculoses
|
|
D014394||bone tuberculosis
|
|
D014394||joint tuberculoses
|
|
D014394||joint tuberculosis
|
|
D014394||osteoarticular tuberculoses
|
|
D014394||osteoarticular tuberculosis
|
|
D014394||tuberculoses bone
|
|
D014394||tuberculoses joint
|
|
D014394||tuberculoses osteoarticular
|
|
D014394||tuberculosis bone
|
|
D014394||tuberculosis joint
|
|
D014393||tuberculosis oral
|
|
D014393||oral tuberculoses
|
|
D014393||oral tuberculosis
|
|
D014393||tuberculoses oral
|
|
C563664||epiphyseal dysplasia baumann type
|
|
D014392||tuberculosis ocular
|
|
D014392||ocular tuberculoses
|
|
D014392||ocular tuberculosis
|
|
D014392||tuberculoses ocular
|
|
D014391||tuberculosis miliary
|
|
D014391||miliary tuberculoses
|
|
D014391||miliary tuberculosis
|
|
D014391||tuberculoses miliary
|
|
C564999||friedreich ataxia so called with optic atrophy and sensorineural deafness
|
|
C566432|610582||diabetes mellitus transient neonatal 3
|
|
C566432|610582||tndm3 diabetes mellitus type ii autosomal dominant included
|
|
C536083||hypercholesterolemia due to arg3500 mutation of apo b 100
|
|
C536084||ichthyosis cheek eyebrow syndrome
|
|
C536084||sidransky feinstein goodman syndrome
|
|
C567407|612158||cardiomyopathy dilated 1aa
|
|
C567407|612158||cmd1aa
|
|
D001079||apudoma
|
|
D001079||apudomas
|
|
C536082||hypercalciuria childhood idiopathic
|
|
C536082||childhood idiopathic hypercalciuria
|
|
C548076||pseudohypoparathyroidism type 1c
|
|
D056266||erythro et keratodermia variabilis
|
|
D056266||erythrokeratodermia figurata variabili
|
|
D056266||erythrokeratodermia figurata variabilis
|
|
D056266||erythrokeratodermia variabili
|
|
D056266||figurata variabilis erythrokeratodermia
|
|
D056266||greither disease
|
|
D056266||mendes de costa syndrome
|
|
D056266||transgrediens et progrediens palmoplantar keratoderma
|
|
D056266||variabili erythrokeratodermia
|
|
D056266||variabilis erythrokeratodermia
|
|
D056266||variabilis erythrokeratodermia figurata
|
|
C548075||pseudohypoparathyroidism type 1b
|
|
C567485|300123||mental retardation x linked with panhypopituitarism
|
|
C567485|300123||mental retardation x linked with panhypopituitarism mental retardation x linked with isolated growth hormone deficiency
|
|
C567485|300123||mrgh included
|
|
D056267||pagetoid reticulosis
|
|
D056267||disease ketron goodman
|
|
D056267||disease woringer kolopp
|
|
D056267||ketron goodman disease
|
|
D056267||kolopp disease woringer
|
|
D056267||pagetoid reticuloses
|
|
D056267||reticuloses pagetoid
|
|
D056267||reticulosis pagetoid
|
|
D056267||woringer kolopp disease
|
|
C548077||pseudohypoparathyroidism type 2
|
|
C548077||php2
|
|
C548077||php ii
|
|
C548077||pseudohypoparathyroidism type ii
|
|
C576976||hypothyroidism congenital nongoitrous 1
|
|
C576976||hypothyroidism congenital due to tsh resistance
|
|
C576976||hypothyroidism due to unresponsiveness to thyrotropin
|
|
C576976||hypothyroidism nonautoimmune
|
|
C576976||thyroid stimulating hormone resistance to
|
|
604169||left ventricular noncompaction 1
|
|
604169||left ventricular noncompaction 1 with or without congenital heart defects
|
|
604169||lvnc1
|
|
D014387||tuberculosis laryngeal
|
|
D014387||laryngeal tuberculoses
|
|
D014387||laryngeal tuberculosis
|
|
D014387||larynx tuberculoses
|
|
D014387||larynx tuberculosis
|
|
D014387||tuberculoses laryngeal
|
|
D014387||tuberculosis of larynx
|
|
C536162|148700||keratosis palmoplantaris striata 1
|
|
C536162|148700||keratoderma palmoplantar striate form 1
|
|
C536162|148700||keratoderma palmoplantar striate form i
|
|
C536162|148700||keratosis palmoplantaris striata i
|
|
C536162|148700||kpps1
|
|
C536162|148700||palmoplantar keratoderma i striate focal or diffuse
|
|
C536162|148700||ppks1
|
|
C536162|148700||sppk1
|
|
C536162|148700||striate palmoplantar keratoderma 1
|
|
C536162|148700||striate palmoplantar keratoderma i
|
|
D014386||tuberculosis hepatic
|
|
D014386||hepatic tuberculoses
|
|
D014386||hepatic tuberculosis
|
|
D014386||tuberculoses hepatic
|
|
D014385||tuberculosis gastrointestinal
|
|
D014385||gastrointestinal tuberculosis
|
|
C548070||pontocerebellar hypoplasia type 2
|
|
D014384||tuberculosis female genital
|
|
D014384||female genital tuberculoses
|
|
D014384||female genital tuberculosis
|
|
D014384||genital tuberculoses female
|
|
D014384||genital tuberculosis female
|
|
D014384||tuberculoses female genital
|
|
C548071||megarbane jalkh syndrome
|
|
C548071||developmental delay dysmorphic features neonatal spontaneous fractures wrinkled skin and hepatic failure
|
|
D014389||tuberculosis male genital
|
|
D014389||genital tuberculoses male
|
|
D014389||genital tuberculosis male
|
|
D014389||male genital tuberculoses
|
|
D014389||male genital tuberculosis
|
|
D014389||tuberculoses male genital
|
|
D014388||tuberculosis lymph node
|
|
D014388||cervical lymphadenitis mycobacterial
|
|
D014388||cervical tuberculous lymphadenitis
|
|
D014388||lymphadenitis cervical tuberculous
|
|
D014388||lymphadenitis mycobacterial cervical
|
|
D014388||lymphadenitis tuberculous
|
|
D014388||lymph node tuberculoses
|
|
D014388||lymph node tuberculosis
|
|
D014388||mycobacterial cervical lymphadenitis
|
|
D014388||scrofula
|
|
D014388||scrofulas
|
|
D014388||tuberculoses lymph node
|
|
D014388||tuberculous lymphadenitis
|
|
D014388||tuberculous lymphadenitis cervical
|
|
C536291|609529||immunoglobulin a deficiency 2
|
|
C536291|609529||igad2
|
|
C536291|609529||iga selective deficiency of taci related
|
|
C536291|609529||immunoglobulin a selective deficiency of taci related
|
|
C536099||myokymia with neonatal epilepsy
|
|
C536099||bfnc myokymia syndrome
|
|
C536099||convulsions benign familial neonatal with myokymia
|
|
C536099||epilepsy benign neonatal with myokymia
|
|
C563670||aneurysm intracranial berry 5
|
|
D009808||odontogenic tumors
|
|
D009808||dental tissue neoplasm
|
|
D009808||dental tissue neoplasms
|
|
D009808||neoplasm dental tissue
|
|
D009808||neoplasms dental tissue
|
|
D009808||odontogenic tumor
|
|
D009808||tissue neoplasm dental
|
|
D009808||tissue neoplasms dental
|
|
D009808||tumor odontogenic
|
|
D009808||tumors odontogenic
|
|
D009807||odontogenic cysts
|
|
D009807||cyst odontogenic
|
|
D009807||cysts odontogenic
|
|
D009807||keratocyst
|
|
D009807||keratocysts
|
|
D009807||odontogenic cyst
|
|
C563674||macular degeneration age related 6
|
|
D039682||hiv associated lipodystrophy syndrome
|
|
D039682||hiv associated lipodystrophy
|
|
D039682||hiv lipodystrophy syndrome
|
|
D039682||lipodystrophy hiv associated
|
|
D039682||lipodystrophy syndrome hiv
|
|
D039682||lipodystrophy syndrome hiv associated
|
|
C536090|608931||myasthenic syndrome congenital type id
|
|
C536090|608931||myasthenic syndrome congenital associated with acetylcholine receptor deficiency
|
|
C536090|608931||myasthenic syndrome congenital postsynaptic associated with acetylcholine receptor deficiency
|
|
C537723|300260||lubs x linked mental retardation syndrome
|
|
C537723|300260||mecp2 duplication syndrome
|
|
C537723|300260||mental retardation x linked lubs type
|
|
C537723|300260||mental retardation x linked syndromic lubs type
|
|
C537723|300260||mental retardation x linked with recurrent respiratory infections
|
|
C537723|300260||mrxsl
|
|
C537723|300260||trisomy xq28
|
|
C537723|300260||xlmr syndrome lubs type
|
|
C537907|146255||barakat syndrome
|
|
C537907|146255||hdr
|
|
C537907|146255||hdrs
|
|
C537907|146255||hdr syndrome
|
|
C537907|146255||hypoparathyroidism sensorineural deafness and renal disease
|
|
C537907|146255||hypoparathyroidism sensorineural deafness and renal dysplasia syndrome
|
|
C537907|146255||nephrosis nerve deafness and hypoparathyroidism
|
|
C536094||myeloid splenomegaly
|
|
C536094||idiopathic myeloid splenomegaly
|
|
186500||syns1
|
|
186500||wl syndrome
|
|
C536092||mycobacterium tuberculosis susceptibility to infection by
|
|
103470|C537043||albinism ocular late onset sensorineural deafness
|
|
103470|C537043||albinism ocular with late onset sensorineural deafness
|
|
103470|C537043||albinism ocular with sensorineural deafness
|
|
103470|C537043||deafness and ocular albinism
|
|
103470|C537043||oasd
|
|
103470|C537043||ocular albinism with sensorineural deafness
|
|
103470|C537043||waardenburg syndrome type 2 with ocular albinism autosomal recessive
|
|
103470|C537043||waardenburg syndrome type ii with ocular albinism autosomal recessive
|
|
103470|C537043||ws2 oa
|
|
C538336|302350||nance horan syndrome
|
|
C538336|302350||cataract dental syndrome
|
|
C538336|302350||cataract x linked with hutchinsonian teeth
|
|
C538336|302350||mesiodens cataract syndrome
|
|
C538336|302350||nhs
|
|
C564605|607221||epilepsy partial with pericentral spikes
|
|
C564605|607221||epps
|
|
C564605|607221||peps
|
|
D014398||tuberculosis renal
|
|
D014398||renal tuberculoses
|
|
D014398||renal tuberculosis
|
|
D014398||tuberculoses renal
|
|
D014397||tuberculosis pulmonary
|
|
D014397||consumption pulmonary
|
|
D014397||consumptions pulmonary
|
|
D014397||phthises pulmonary
|
|
D014397||phthisis pulmonary
|
|
D014397||pulmonary consumption
|
|
D014397||pulmonary consumptions
|
|
D014397||pulmonary phthises
|
|
D014397||pulmonary phthisis
|
|
D014397||pulmonary tuberculoses
|
|
D014397||pulmonary tuberculosis
|
|
D014397||tuberculoses pulmonary
|
|
D013064||speech disorders
|
|
D013064||aprosodia
|
|
D013064||aprosodias
|
|
D013064||aprosodic speech
|
|
D013064||cluttering
|
|
D013064||clutterings
|
|
D013064||dysglossia
|
|
D013064||dysglossias
|
|
D013064||dyslalia
|
|
D013064||dyslalias
|
|
D013064||rhinolalia
|
|
D013064||rhinolalias
|
|
D013064||speech aprosodic
|
|
D013064||verbal fluency disorder
|
|
D013064||verbal fluency disorders
|
|
D014396||tuberculosis pleural
|
|
D014396||pleural tuberculoses
|
|
D014396||pleural tuberculosis
|
|
D014396||pleurisies tuberculous
|
|
D014396||pleurisy tuberculous
|
|
D014396||tuberculoses pleural
|
|
D014396||tuberculous pleurisies
|
|
D014396||tuberculous pleurisy
|
|
D014395||peritonitis tuberculous
|
|
D014395||peritoneal tuberculosis
|
|
D014395||tuberculosis peritoneal
|
|
D014395||tuberculous peritonitis
|
|
D014399||tuberculosis spinal
|
|
D014399||disease pott
|
|
D014399||disease pott apos s
|
|
D014399||pott disease
|
|
D014399||pott apos s disease
|
|
D014399||potts disease
|
|
D014399||pott apos s paraplegia
|
|
D014399||spinal tuberculoses
|
|
D014399||spinal tuberculosis
|
|
D014399||tuberculoses spinal
|
|
C564971||myopathy with giant abnormal mitochondria
|
|
C563640||lactic acidosis chronic adult form
|
|
C536021||achromatopsia 1
|
|
C536021||rod monochromacy
|
|
C536021||rod monochromatism
|
|
D005910|137800||glioma
|
|
D005910|137800||astrocytoma included
|
|
D005910|137800||ependymoma included
|
|
D005910|137800||gbm included
|
|
D005910|137800||glial cell tumor
|
|
D005910|137800||glial cell tumors
|
|
D005910|137800||glioblastoma multiforme included
|
|
D005910|137800||glioma malignant
|
|
D005910|137800||glioma mixed
|
|
D005910|137800||glioma of brain familial included
|
|
D005910|137800||gliomas
|
|
D005910|137800||gliomas malignant
|
|
D005910|137800||gliomas mixed
|
|
D005910|137800||glioma susceptibility 1
|
|
D005910|137800||glioma susceptibility 2
|
|
D005910|137800||glioma susceptibility 3
|
|
D005910|137800||glioma susceptibility 4
|
|
D005910|137800||glioma susceptibility 5
|
|
D005910|137800||glioma susceptibility 6
|
|
D005910|137800||glioma susceptibility 8
|
|
D005910|137800||glm1
|
|
D005910|137800||glm2
|
|
D005910|137800||glm3
|
|
D005910|137800||glm4
|
|
D005910|137800||glm5
|
|
D005910|137800||glm6
|
|
D005910|137800||glm8
|
|
D005910|137800||glm included
|
|
D005910|137800||malignant glioma
|
|
D005910|137800||malignant gliomas
|
|
D005910|137800||mixed glioma
|
|
D005910|137800||mixed gliomas
|
|
D005910|137800||oligodendroglioma included
|
|
D005910|137800||subependymoma included
|
|
D005910|137800||tumor glial cell
|
|
D005910|137800||tumors glial cell
|
|
C537353||metaphyseal chondrodysplasia spahr type
|
|
C537353||spahr type metaphyseal chondrodysplasia
|
|
C536022||marles greenberg persaud syndrome
|
|
C536022||manitoba oculotrichoanal syndrome
|
|
C536022||manitoba trichoanal syndrome
|
|
C536022||marles syndrome
|
|
C537350||metaphyseal acroscyphodysplasia
|
|
C537350||wedge shaped epiphyses of knees
|
|
C538682||hyperkeratosis of the palms and soles and esophageal papillomas
|
|
C538682||early onset tylosis type b
|
|
C538682||familial tylosis
|
|
C538682||focal non epidermolytic palmoplantar keratoderma
|
|
C538682||focal palmoplantar keratoderma
|
|
C538682||late onset tylosis type a
|
|
C537351||metaphyseal anadysplasia
|
|
C537351||early onset regressive form of metaphyseal dysplasia
|
|
C536020||achondroplasia and swiss type agammaglobulinemia
|
|
C536020||agammaglobulinaemia and achondroplasia
|
|
C564974||myopathy granulovacuolar lobular with electrical myotonia
|
|
C536026||marshall smith syndrome
|
|
C564973||myopathy due to malate aspartate shuttle defect
|
|
C537354||metaphyseal chondrodysplasia with cone shaped epiphyses normal hair and normal hands
|
|
C537354||cupped metaphyses and cone shaped epiphyses without alopecia or brachydactyly
|
|
C536023||maroteaux fonfria syndrome
|
|
C536023||apert syndrome with polydactyly of hands and feet
|
|
C536023||apparent apert syndrome with polydactyly
|
|
C563641||lactate dehydrogenase b deficiency
|
|
C537355||metaphyseal undermodeling spondylar dysplasia and overgrowth
|
|
C536024||marsden syndrome
|
|
C536024||dystonia familial with visual failure and striatal lucencies
|
|
C536024||leber hereditary optic neuropathy with dystonia
|
|
C564979||myasthenia congenital refractory to acetylcholinesterase inhibitors
|
|
D002388||catastrophic illness
|
|
D002388||catastrophic illnesses
|
|
D002388||illness catastrophic
|
|
D002388||illnesses catastrophic
|
|
C548006||atrial septal defect ostium primum
|
|
300582|C564479||short stature idiopathic x linked
|
|
300582|C564479||iss
|
|
C564977||myeloproliferative disease autosomal recessive
|
|
C563646||keratosis palmaris et plantaris with clinodactyly
|
|
D002389||catatonia
|
|
D002389||catatonia lethal
|
|
D002389||catatonia malignant
|
|
D002389||catatonia organic
|
|
D002389||catatonias
|
|
D002389||catatonia schizophreniform
|
|
D002389||catatonias lethal
|
|
D002389||catatonias malignant
|
|
D002389||catatonias organic
|
|
D002389||catatonias schizophreniform
|
|
D002389||catatonic disorder organic
|
|
D002389||catatonic disorders organic
|
|
D002389||lethal catatonia
|
|
D002389||lethal catatonias
|
|
D002389||malignant catatonia
|
|
D002389||malignant catatonias
|
|
D002389||organic catatonia
|
|
D002389||organic catatonias
|
|
D002389||organic catatonic disorder
|
|
D002389||organic catatonic disorders
|
|
D002389||schizophreniform catatonia
|
|
D002389||schizophreniform catatonias
|
|
C548009||atrial septal defect sinus venosus
|
|
C564976||epilepsy progressive myoclonic 2b
|
|
D002385||cataplexy
|
|
D002385||attack cataleptic
|
|
D002385||attacks cataleptic
|
|
D002385||cataleptic attack
|
|
D002385||cataleptic attacks
|
|
D002385||henneberg syndrome
|
|
D002385||status cataplexicus
|
|
D002385||syndrome henneberg
|
|
D002385||syndromes tonelessness
|
|
D002385||syndrome tonelessness
|
|
D002385||tonelessness syndrome
|
|
D002385||tonelessness syndromes
|
|
D002386||cataract
|
|
D002386||cataract membranous
|
|
D002386||cataracts
|
|
D002386||cataracts membranous
|
|
D002386||lens opacities
|
|
D002386||lens opacity
|
|
D002386||membranous cataract
|
|
D002386||membranous cataracts
|
|
D002386||opacities lens
|
|
D002386||opacity lens
|
|
D002386||pseudoaphakia
|
|
D002386||pseudoaphakias
|
|
C548012||diploid triploid mosaicism
|
|
D040701||stress disorders traumatic acute
|
|
D040701||acute stress disorder
|
|
D040701||acute stress disorders
|
|
D040701||stress disorder acute
|
|
D040701||stress disorders acute
|
|
C548011||deafness with labyrinthine aplasia microtia and microdontia lamm
|
|
C548014||gestational diabetes insipidus
|
|
C548013||dipsogenic diabetes insipidus
|
|
C548016||hypermanganesemia with dystonia polycythemia and cirrhosis
|
|
C548016||dystonia parkinsonism hypermanganesemia polycythemia and chronic liver disease
|
|
C548016||hepatic cirrhosis dystonia polycythaemia and hypermanganesaemia
|
|
C548016||hepatic cirrhosis dystonia polycythemia and hypermanganesemia
|
|
C548016||hmdpc
|
|
C548016||parkinsonism and dystonia with hypermanganesemia polycythemia and chronic liver disease
|
|
C537349||mesomelic dwarfism reinhardt pfeiffer type
|
|
C537349||hypoplasia of ulna and fibula
|
|
C537349||mesomelic dwarfism of hypoplastic ulna and fibula type
|
|
C537349||reinhardt pfeiffer mesomelic dysplasia
|
|
C537349||reinhardt pfeiffer mesomelic skeletal dysplasia
|
|
C537349||reinhardt pfeiffer syndrome
|
|
C537349||ulna and fibula hypoplasia of
|
|
C536018||achondrogenesis type 3
|
|
C536018||type 3 achondrogenesis
|
|
C536019||achondrogenesis type 4
|
|
C536019||type 4 achondrogenesis
|
|
605479||bric2
|
|
C537347||mesenteric vascular disease
|
|
C537347||acute mesenteric ischemia
|
|
C537347||chronic mesenteric ischemia
|
|
C537347||mesenteric artery ischemia
|
|
D013031||sparganosis
|
|
D013031||sparganoses
|
|
C538679||transient antero apical dyskinesia
|
|
C538678||lymphedema of the lower extremities recurrent pneumonia bronchiectasis and yellowed nails
|
|
D013035||spasm
|
|
D013035||ciliary body spasm
|
|
D013035||ciliary body spasms
|
|
D013035||generalized spasm
|
|
D013035||generalized spasms
|
|
D013035||muscle spasm
|
|
D013035||muscle spasms
|
|
D013035||muscular spasm
|
|
D013035||muscular spasms
|
|
D013035||spasm ciliary body
|
|
D013035||spasm generalized
|
|
D013035||spasm muscle
|
|
D013035||spasm muscular
|
|
D013035||spasms
|
|
D013035||spasms ciliary body
|
|
D013035||spasms generalized
|
|
D013035||spasms muscle
|
|
D013035||spasms muscular
|
|
162900|C562736||nevus epidermal
|
|
162900|C562736||nevus keratinocytic nonepidermolytic
|
|
162900|C562736||nevus keratinocytic nonepidermolytic nevus sebaceous included
|
|
D013036||spasms infantile
|
|
D013036||attack lightning
|
|
D013036||attacks lightning
|
|
D013036||attacks salaam
|
|
D013036||cryptogenic infantile spasm
|
|
D013036||cryptogenic infantile spasms
|
|
D013036||cryptogenic west syndrome
|
|
D013036||hypsarrhythmia
|
|
D013036||hypsarrhythmias
|
|
D013036||infantile spasm
|
|
D013036||infantile spasm cryptogenic
|
|
D013036||infantile spasms
|
|
D013036||infantile spasms cryptogenic
|
|
D013036||infantile spasms symptomatic
|
|
D013036||infantile spasm symptomatic
|
|
D013036||jackknife seizure
|
|
D013036||jackknife seizures
|
|
D013036||lightning attack
|
|
D013036||lightning attacks
|
|
D013036||nodding spasm
|
|
D013036||nodding spasms
|
|
D013036||salaam attacks
|
|
D013036||salaam seizures
|
|
D013036||seizure jackknife
|
|
D013036||seizures jackknife
|
|
D013036||seizures salaam
|
|
D013036||spasm cryptogenic infantile
|
|
D013036||spasm nodding
|
|
D013036||spasms cryptogenic infantile
|
|
D013036||spasms nodding
|
|
D013036||spasms symptomatic infantile
|
|
D013036||spasm symptomatic infantile
|
|
D013036||spasmus nutans
|
|
D013036||symptomatic infantile spasm
|
|
D013036||symptomatic infantile spasms
|
|
D013036||symptomatic west syndrome
|
|
D013036||syndrome cryptogenic west
|
|
D013036||syndrome symptomatic west
|
|
D013036||syndrome west
|
|
D013036||west syndrome
|
|
D013036||west syndrome cryptogenic
|
|
D013036||west syndrome symptomatic
|
|
253270|D028922||holocarboxylase synthetase deficiency
|
|
253270|D028922||carboxylase deficiency multiple neonatal form
|
|
253270|D028922||deficiencies hlcs
|
|
253270|D028922||deficiencies holocarboxylase synthetase
|
|
253270|D028922||deficiency hlcs
|
|
253270|D028922||deficiency holocarboxylase synthetase
|
|
253270|D028922||deficiency multiple carboxylase neonatal form
|
|
253270|D028922||early onset biotin responsive multiple carboxylase deficiency
|
|
253270|D028922||early onset combined carboxylase deficiency
|
|
253270|D028922||hlcs deficiencies
|
|
253270|D028922||hlcs deficiency
|
|
253270|D028922||holocarboxylase synthetase deficiencies
|
|
253270|D028922||infantile multiple carboxylase deficiency
|
|
253270|D028922||multiple carboxylase deficiency early onset
|
|
253270|D028922||multiple carboxylase deficiency neonatal form
|
|
C564982||muscular hypertonia lethal
|
|
C563651||kallmann syndrome 2 with cleft lip or palate
|
|
C537363||ichthyosiform erythroderma corneal involvement deafness
|
|
C537363||desmons syndrome
|
|
C537363||ichthyosiform erythroderma corneal involvement and deafness
|
|
C537363||keratitis ichthyosis deafness syndrome autosomal recessive
|
|
C537363||kid syndrome autosomal recessive
|
|
C536032||mastocytic enterocolitis
|
|
C563650||keratitis fugax hereditaria
|
|
C563650||keratoendotheliitis fugax hereditaria
|
|
C537364||jagell holmgren hofer syndrome
|
|
C537364||ichthyosis alopecia eclabion ectropion mental retardation
|
|
C537364||ichthyosis with alopecia eclabion ectropion and mental retardation
|
|
C536033||mastocytosis cutaneous with short stature conductive hearing loss and microtia
|
|
C564980||musk inability to smell
|
|
C537362|242860||immunodeficiency syndrome variable
|
|
C537362|242860||centromeric instability immunodeficiency syndrome
|
|
C537362||immunodeficiency centromeric instability facial anomalies syndrome
|
|
C536031||massa casaer ceulemans syndrome
|
|
C536031||arthrogryposis multiplex congenita associated with lissencephaly
|
|
C537367||mucolipidosis type 3 a
|
|
C536036||maxillonasal dysplasia binder type
|
|
C536036||binder syndrome
|
|
D014383||tuberculosis endocrine
|
|
D014383||endocrine tuberculoses
|
|
D014383||endocrine tuberculosis
|
|
D014383||tuberculoses endocrine
|
|
C564985||muscular dystrophy congenital producing arthrogryposis
|
|
D014382||tuberculosis cutaneous
|
|
D014382||cutaneous tuberculoses
|
|
D014382||cutaneous tuberculosis
|
|
D014382||scrofuloderma
|
|
D014382||scrofulodermas
|
|
D014382||skin tuberculoses
|
|
D014382||skin tuberculosis
|
|
D014382||tuberculid
|
|
D014382||tuberculids
|
|
D014382||tuberculoses cutaneous
|
|
D014382||tuberculoses skin
|
|
D014382||tuberculosis skin
|
|
C563653||kallikrein decreased urinary activity of
|
|
D014381||tuberculosis cardiovascular
|
|
D014381||cardiovascular tuberculoses
|
|
D014381||cardiovascular tuberculosis
|
|
D014381||tuberculoses cardiovascular
|
|
C564983||muscular dystrophy congenital with rapid progression
|
|
C563652||kallmann syndrome 2 with bimanual synkinesia
|
|
C536035||maternally inherited leigh syndrome
|
|
C536035||leigh disease maternally inherited
|
|
C536035||subacute necrotizing encephalomyelopathy maternally inherited
|
|
D014380||tuberculosis bovine
|
|
D014380||bovine tuberculoses
|
|
D014380||bovine tuberculosis
|
|
D014380||tuberculoses bovine
|
|
C564989||gastric volvulus intrathoracic
|
|
C563658||polyosteolysis hyperostosis syndrome
|
|
D001064||appendicitis
|
|
D001064||appendicitis perforated
|
|
D001064||appendicitis ruptured
|
|
D001064||perforated appendicitis
|
|
D001064||ruptured appendicitis
|
|
D001063||appendiceal neoplasms
|
|
D001063||appendiceal cancer
|
|
D001063||appendiceal neoplasm
|
|
D001063||appendix cancer
|
|
D001063||cancer appendiceal
|
|
D001063||cancer appendix
|
|
D001063||cancer of appendix
|
|
D001063||cancer of the appendix
|
|
D001063||neoplasm appendiceal
|
|
D001063||neoplasms appendiceal
|
|
D001068||eating disorders
|
|
D001068||appetite disorder
|
|
D001068||appetite disorders
|
|
D001068||eating disorder
|
|
182250|C537343||singleton merten syndrome
|
|
182250|C537343||merten singleton syndrome
|
|
D001072||apraxias
|
|
D001072||1 speech language disorder
|
|
D001072||1s speech language disorder
|
|
D001072||apraxia
|
|
D001072||apraxia articulatory
|
|
D001072||apraxia developmental verbal
|
|
D001072||apraxia dressing
|
|
D001072||apraxia facial oral
|
|
D001072||apraxia gestural
|
|
D001072||apraxia ideational
|
|
D001072||apraxia motor
|
|
D001072||apraxia of phonation
|
|
D001072||apraxia oral
|
|
D001072||apraxias articulatory
|
|
D001072||apraxias developmental verbal
|
|
D001072||apraxias dressing
|
|
D001072||apraxias facial oral
|
|
D001072||apraxias gestural
|
|
D001072||apraxias ideational
|
|
D001072||apraxias motor
|
|
D001072||apraxias oral
|
|
D001072||apraxias verbal
|
|
D001072||apraxia verbal
|
|
D001072||articulatory apraxia
|
|
D001072||articulatory apraxias
|
|
D001072||articulatory dyspraxia
|
|
D001072||articulatory dyspraxias
|
|
D001072||developmental verbal apraxia
|
|
D001072||developmental verbal apraxias
|
|
D001072||developmental verbal dyspraxias
|
|
D001072||disorder 1 speech language
|
|
D001072||disorder 1s speech language
|
|
D001072||dressing apraxia
|
|
D001072||dressing apraxias
|
|
D001072||dyspraxia
|
|
D001072||dyspraxia articulatory
|
|
D001072||dyspraxia developmental verbal
|
|
D001072||dyspraxia oral
|
|
D001072||dyspraxias
|
|
D001072||dyspraxias articulatory
|
|
D001072||dyspraxias developmental verbal
|
|
D001072||dyspraxias oral
|
|
D001072||dyspraxias verbal
|
|
D001072||dyspraxia verbal
|
|
D001072||facial oral apraxia
|
|
D001072||facial oral apraxias
|
|
D001072||gestural apraxia
|
|
D001072||gestural apraxias
|
|
D001072||ideational apraxia
|
|
D001072||ideational apraxias
|
|
D001072||motor apraxia
|
|
D001072||motor apraxias
|
|
D001072||oral apraxia
|
|
D001072||oral apraxias
|
|
D001072||oral dyspraxia
|
|
D001072||oral dyspraxias
|
|
D001072||phonation apraxia
|
|
D001072||phonation apraxias
|
|
D001072||speech language disorder 1s
|
|
D001072||verbal apraxia
|
|
D001072||verbal apraxia developmental
|
|
D001072||verbal apraxias
|
|
D001072||verbal apraxias developmental
|
|
D001072||verbal dyspraxia
|
|
D001072||verbal dyspraxia developmental
|
|
D001072||verbal dyspraxias
|
|
D001072||verbal dyspraxias developmental
|
|
D014376||tuberculosis
|
|
D014376||disease kochs
|
|
D014376||disease koch apos s
|
|
D014376||koch disease
|
|
D014376||koch apos s disease
|
|
D014376||kochs disease
|
|
D014376||tuberculoses
|
|
D014375||tuberculoma
|
|
D014375||tuberculomas
|
|
C537358||methylmalonic acidemia
|
|
C537358||acidemia methylmalonic
|
|
C537358||isolated methylmalonic acidemia
|
|
C537358||methylmalonic aciduria
|
|
C536027||martinez monasterio pinheiro syndrome
|
|
C536027||cleft lip palate oligodontia syndactyly hair alterations
|
|
D014379||tuberculosis avian
|
|
D014379||avian tuberculoses
|
|
D014379||avian tuberculosis
|
|
D014379||tuberculoses avian
|
|
C567436|612016||spinocerebellar ataxia autosomal recessive 9
|
|
C567436|612016||cerebellar ataxia autosomal recessive type 2
|
|
C567436|612016||coenzyme q10 deficiency primary 4
|
|
C567436|612016||coq10d4
|
|
C567436|612016||scar9
|
|
C537374||multifocal choroiditis
|
|
C536043||osteogenesis imperfecta type 2b
|
|
C536043||osteogenesis imperfecta perinatal lethal autosomal recessive
|
|
C536043||osteogenesis imperfecta type iib
|
|
C537375||multifocal fibrosclerosis
|
|
C537375||fibrosclerosis multifocal
|
|
C537375||mediastinal fibrosis familial
|
|
C537375||retroperitoneal fibrosis familial
|
|
C563719|609446||generalized epilepsy and paroxysmal dyskinesia
|
|
C563719|609446||epilepsy generalized with paroxysmal dyskinesia
|
|
C563719|609446||gepd
|
|
D001039||aphasia broca
|
|
D001039||agrammatism
|
|
D001039||anterior aphasia
|
|
D001039||anterior aphasias
|
|
D001039||aphasia anterior
|
|
D001039||aphasia ataxic
|
|
D001039||aphasia expressive
|
|
D001039||aphasia frontocortical
|
|
D001039||aphasia motor
|
|
D001039||aphasia nonfluent
|
|
D001039||aphasias anterior
|
|
D001039||aphasias ataxic
|
|
D001039||aphasias broca
|
|
D001039||aphasias frontocortical
|
|
D001039||aphasia syndromes verbal
|
|
D001039||aphasia syndrome verbal
|
|
D001039||ataxic aphasia
|
|
D001039||ataxic aphasias
|
|
D001039||broca aphasia
|
|
D001039||broca aphasias
|
|
D001039||broca dysphasia
|
|
D001039||broca apos s dysphasia
|
|
D001039||dysphasia broca
|
|
D001039||dysphasia brocas
|
|
D001039||dysphasia broca apos s
|
|
D001039||expressive aphasia
|
|
D001039||frontocortical aphasia
|
|
D001039||frontocortical aphasias
|
|
D001039||motor aphasia
|
|
D001039||nonfluent aphasia
|
|
D001039||syndromes verbal aphasia
|
|
D001039||syndrome verbal aphasia
|
|
D001039||verbal aphasia syndrome
|
|
D001039||verbal aphasia syndromes
|
|
C537372||multi centric castleman apos s disease
|
|
C537372||hhv 8 associated multicentric castleman disease
|
|
C537372||hhv8 multicentric castleman disease
|
|
C537372||idiopathic multicentric castleman apos s disease
|
|
C537372||kshv associated multicentric castleman disease
|
|
C537372||kshv muticentric castleman disease
|
|
C537372||multicentric castleman apos s disease
|
|
C537372||multicentric plasma cell variant of castleman apos s disease
|
|
C537372||plasmablastic multicentric castleman disease
|
|
C536041||osteogenesis imperfecta type 1a
|
|
C536041||osteogenesis imperfecta type 1 with dentinogenesis imperfecta
|
|
C536041||osteogenesis imperfecta type i with dentinogenesis imperfecta
|
|
C536041||osteogenesis imperfecta with opalescent teeth
|
|
C535627|140000||hand foot uterus syndrome
|
|
C535627|140000||hand foot genital syndrome
|
|
C535627|140000||hfg
|
|
C535627|140000||hfg syndrome
|
|
C535627|140000||hfu
|
|
C535627|140000||hfu syndrome
|
|
C536047||osteogenesis imperfecta type 6
|
|
C563621||lip hamartomatous
|
|
C563621||enlargement of lower lip
|
|
C563620||lipoma of the conjunctiva
|
|
C563626||leukocyte nuclear appendages hereditary prevalence of
|
|
C548029||karak syndrome
|
|
D020371|169500||adld
|
|
D020371|169500||adult pelizaeus merzbacher disease
|
|
D020371|169500||atypical pelizaeus merzbacher disease
|
|
D020371|169500||classic pelizaeus merzbacher disease
|
|
D020371|169500||cockayne pelizaeus merzbacher disease
|
|
D020371|169500||leukodystrophy hypomyelinating 1
|
|
D020371|169500||pelizaeus merzbacher disease adult
|
|
D020371|169500||pelizaeus merzbacher disease atypical
|
|
D020371|169500||pelizaeus merzbacher disease autosomal dominant or late onset type formerly
|
|
D020371|169500||pelizaeus merzbacher disease classic
|
|
D020371|169500||pelizaeus merzbacher disease transitional
|
|
D020371|169500||pelizaeus merzbacher sclerosis brain
|
|
D020371|169500||pmd
|
|
D020371|169500||sclerosis brain pelizaeus merzbacher
|
|
D020371|169500||transitional pelizaeus merzbacher disease
|
|
C563625||levator medial rectus synkinesis
|
|
C563625||oculomotor levator synkinesis
|
|
C548028||inherited peripheral neuropathy
|
|
C564955||sialidosis type i
|
|
C563624||lichen planus familial
|
|
C564954||neurologic disease infantile multisystem with osseous fragility
|
|
D003699||hepatitis d
|
|
D003699||amazon black fever
|
|
D003699||black fever amazon
|
|
D003699||delta hepatitis
|
|
D003699||delta infection
|
|
D003699||delta superinfection
|
|
D003699||delta superinfections
|
|
D003699||disease labrea
|
|
D003699||diseases labrea
|
|
D003699||fever amazon black
|
|
D003699||hepatitides delta
|
|
D003699||hepatitis delta
|
|
D003699||infection delta
|
|
D003699||infections delta
|
|
D003699||labrea disease
|
|
D003699||labrea diseases
|
|
D003699||superinfection delta
|
|
D003699||superinfections delta
|
|
D001037||aphasia
|
|
D001037||acquired aphasia
|
|
D001037||ageusic aphasia
|
|
D001037||ageusic aphasias
|
|
D001037||alogia
|
|
D001037||alogias
|
|
D001037||anepia
|
|
D001037||anepias
|
|
D001037||aphasia acquired
|
|
D001037||aphasia ageusic
|
|
D001037||aphasia auditory discriminatory
|
|
D001037||aphasia commisural
|
|
D001037||aphasia functional
|
|
D001037||aphasia global
|
|
D001037||aphasia graphomotor
|
|
D001037||aphasia intellectual
|
|
D001037||aphasia mixed
|
|
D001037||aphasia post ictal
|
|
D001037||aphasia post traumatic
|
|
D001037||aphasia progressive
|
|
D001037||aphasias ageusic
|
|
D001037||aphasias auditory discriminatory
|
|
D001037||aphasias commisural
|
|
D001037||aphasia semantic
|
|
D001037||aphasias functional
|
|
D001037||aphasias global
|
|
D001037||aphasias graphomotor
|
|
D001037||aphasias intellectual
|
|
D001037||aphasias mixed
|
|
D001037||aphasias post ictal
|
|
D001037||aphasias post traumatic
|
|
D001037||aphasias progressive
|
|
D001037||aphasias semantic
|
|
D001037||aphasias syntactical
|
|
D001037||aphasia syntactical
|
|
D001037||auditory discriminatory aphasia
|
|
D001037||auditory discriminatory aphasias
|
|
D001037||commisural aphasia
|
|
D001037||commisural aphasias
|
|
D001037||dejerine lichtheim phenomenon
|
|
D001037||discriminatory aphasia auditory
|
|
D001037||discriminatory aphasias auditory
|
|
D001037||dysphasia
|
|
D001037||dysphasia global
|
|
D001037||dysphasias global
|
|
D001037||functional aphasia
|
|
D001037||functional aphasias
|
|
D001037||global aphasia
|
|
D001037||global aphasias
|
|
D001037||global dysphasia
|
|
D001037||global dysphasias
|
|
D001037||graphomotor aphasia
|
|
D001037||graphomotor aphasias
|
|
D001037||intellectual aphasia
|
|
D001037||intellectual aphasias
|
|
D001037||lichtheim sign
|
|
D001037||lichtheim apos s sign
|
|
D001037||lichtheims sign
|
|
D001037||logagnosia
|
|
D001037||logagnosias
|
|
D001037||logamnesia
|
|
D001037||logamnesias
|
|
D001037||logasthenia
|
|
D001037||logasthenias
|
|
D001037||mixed aphasia
|
|
D001037||mixed aphasias
|
|
D001037||phenomenon dejerine lichtheim
|
|
D001037||post ictal aphasia
|
|
D001037||post ictal aphasias
|
|
D001037||post traumatic aphasia
|
|
D001037||post traumatic aphasias
|
|
D001037||progressive aphasia
|
|
D001037||progressive aphasias
|
|
D001037||semantic aphasia
|
|
D001037||semantic aphasias
|
|
D001037||sign lichtheim apos s
|
|
D001037||syntactical aphasia
|
|
D001037||syntactical aphasias
|
|
C537370||muller barth menger syndrome
|
|
C537370||cerebral malformation seizures hypertrichosis and overlapping fingers
|
|
D001036||aphakia postcataract
|
|
D001036||aphakias postcataract
|
|
D001036||postcataract aphakia
|
|
D001036||postcataract aphakias
|
|
C537371||mullerian aplasia
|
|
C537371||congenital absence of uterus and vagina
|
|
C537371||klippel feil deformity conductive deafness and absent vagina
|
|
C537371||mayer rokitansky kuster hauser syndrome type ii
|
|
C537371||mrkh type ii
|
|
C537371||mullerian duct aplasia unilateral renal agenesis and cervicothoracic somite anomalies
|
|
C537371||mullerian duct failure
|
|
C537371||murcs association
|
|
C537371||rkh syndrome
|
|
C537371||rokitansky kuster hauser syndrome
|
|
C537371||rokitansky sequence
|
|
D003693||delirium
|
|
D003693||delirium of mixed origin
|
|
D003693||deliriums subacute
|
|
D003693||delirium subacute
|
|
D003693||mixed origin delirium
|
|
D003693||mixed origin deliriums
|
|
D003693||subacute delirium
|
|
D003693||subacute deliriums
|
|
D001035||aphakia
|
|
D001035||aphakias
|
|
C548031||knobloch syndrome type iii
|
|
C567202|612690||spherocytosis type 5
|
|
C567202|612690||hs5
|
|
C567202|612690||sph5
|
|
C567202|612690||spherocytosis hereditary 5
|
|
C564251|608371||orofacial cleft 4
|
|
C564251|608371||cleft lip with or without cleft palate nonsyndromic 4
|
|
C564251|608371||ofc4
|
|
C548034||orofaciodigital syndrome 12
|
|
D002371||cat diseases
|
|
D002371||cat disease
|
|
D002371||disease cat
|
|
D002371||disease feline
|
|
D002371||diseases cat
|
|
D002371||diseases feline
|
|
D002371||feline disease
|
|
D002371||feline diseases
|
|
C548035||orofaciodigital syndrome 13
|
|
612520|C567286||diabetes mellitus insulin dependent 20
|
|
612520|C567286||iddm20
|
|
D015674||mammary neoplasms animal
|
|
D015674||animal mammary carcinoma
|
|
D015674||animal mammary carcinomas
|
|
D015674||animal mammary neoplasm
|
|
D015674||animal mammary neoplasms
|
|
D015674||carcinoma animal mammary
|
|
D015674||carcinomas animal mammary
|
|
D015674||mammary carcinoma animal
|
|
D015674||mammary carcinomas animal
|
|
D015674||mammary neoplasm
|
|
D015674||mammary neoplasm animal
|
|
D015674||mammary neoplasms
|
|
D015674||neoplasm animal mammary
|
|
D015674||neoplasm mammary
|
|
D015674||neoplasms animal mammary
|
|
D015674||neoplasms mammary
|
|
C580199||inherited thyroxine binding globulin deficiency
|
|
C580199||tbg deficiency
|
|
D015673||fatigue syndrome chronic
|
|
D015673||chronic fatigue and immune dysfunction syndrome
|
|
D015673||chronic fatigue disorder
|
|
D015673||chronic fatigue disorders
|
|
D015673||chronic fatigue fibromyalgia syndrome
|
|
D015673||chronic fatigue fibromyalgia syndromes
|
|
D015673||chronic fatigue syndrome
|
|
D015673||chronic fatigue syndromes
|
|
D015673||disorders chronic fatigue
|
|
D015673||encephalomyelitis myalgic
|
|
D015673||fatigue disorder chronic
|
|
D015673||fatigue disorders chronic
|
|
D015673||fatigue fibromyalgia syndrome chronic
|
|
D015673||fatigue fibromyalgia syndromes chronic
|
|
D015673||fatigue syndrome postviral
|
|
D015673||fatigue syndromes chronic
|
|
D015673||fatigue syndromes postviral
|
|
D015673||infectious mononucleosis like syndrome chronic
|
|
D015673||myalgic encephalomyelitis
|
|
D015673||postviral fatigue syndrome
|
|
D015673||postviral fatigue syndromes
|
|
D015673||royal free disease
|
|
D015673||syndrome chronic fatigue fibromyalgia
|
|
D015673||syndromes chronic fatigue fibromyalgia
|
|
D015673||syndromes postviral fatigue
|
|
C536039||osteogenesis imperfecta levin type
|
|
C536039|166260||gnathodiaphyseal dysplasia
|
|
C536039|166260||gnathodiaphyseal sclerosis
|
|
C536039||levin syndrome 2
|
|
C536039|166260||osteogenesis imperfecta with unusual skeletal lesions
|
|
174500|C536311||polydactyly preaxial ii
|
|
174500|C536311||polydactyly of triphalangeal thumb
|
|
174500||ppd2
|
|
174500||tpt included
|
|
174500||tpt ps syndrome included
|
|
174500||triphalangeal thumb included
|
|
174500||triphalangeal thumb polydactyly syndrome triphalangeal thumb with polysyndactyly included
|
|
174500||triphalangeal thumb polysyndactyly syndrome included
|
|
C580192||immune dysregulation polyendocrinopathy enteropathy x linked syndrome
|
|
C580192||ipex syndrome
|
|
C548030||knobloch syndrome type ii
|
|
C537385||muscular dystrophy congenital infantile with cataract and hypogonadism
|
|
C537385||familial congenital muscular dystrophy with gonadal dysgenesis
|
|
C537385||muscular dystrophy congenital with infantile cataract and hypogonadism
|
|
C536054||whyte murphy syndrome
|
|
C536054||osteopathia striata associated with familial dermopathy and white forelock
|
|
C537386||neuroaxonal dystrophy renal tubular acidosis
|
|
C537386||maccario mena weir syndrome
|
|
C536055||osteopetrosis and infantile neuroaxonal dystrophy
|
|
C536055||infantile osteopetrosis and neuronal storage disease
|
|
C536055||prenatal axonal dystrophy and osteopetrosis
|
|
C536052||osteolysis syndrome recessive
|
|
C536052||osteolysis distal with short stature mental retardation and characteristic facial appearance
|
|
D001049||apnea
|
|
D001049||apneas
|
|
C564964||leigh syndrome due to mitochondrial complex v deficiency
|
|
C563633||lattice degeneration of retina leading to retinal detachment
|
|
C537389||neurofibromatosis type 3 mixed central and peripheral
|
|
C537389||neurofibromas palmar cutaneous
|
|
C537389||neurofibromatosis type 3 riccardi type
|
|
C537389||neurofibromatosis type iii mixed central and peripheral
|
|
C537389||neurofibromatosis type iii of riccardi
|
|
C537389||neurofibromatosis type iii riccardi type
|
|
C564963||leigh syndrome due to mitochondrial complex iv deficiency
|
|
C563632||leg ulcers familial of juvenile onset
|
|
C536059|259710||osteopetrosis mild autosomal recessive form
|
|
C536059||mild autosomal recessive form of osteopetrosis
|
|
C536059|259710||osteopetrosis autosomal recessive 2
|
|
C536059|259710||osteopetrosis osteoclast poor
|
|
C564962||leigh syndrome due to mitochondrial complex iii deficiency
|
|
C537387||neurocutaneous melanosis
|
|
C537387||melanosis neurocutaneous
|
|
C537387||neurocutaneous melanosis syndrome
|
|
304150|C537860||occipital horn syndrome
|
|
304150|C537860||cutis laxa x linked
|
|
304150|C537860||cutis laxa x linked formerly
|
|
304150|C537860||eds9 formerly
|
|
304150|C537860||eds ix formerly
|
|
304150|C537860||ehlers danlos syndrome occipital horn type formerly
|
|
304150|C537860||ohs
|
|
C564961||leigh syndrome due to mitochondrial complex ii deficiency
|
|
C563630||lentiginosis centrofacial neurodysraphic
|
|
C563630||lentiginosis touraine type
|
|
C537388||neurofaciodigitorenal syndrome
|
|
C537388||freire maia pinheiro opitz syndrome
|
|
C536057||osteopetrosis lethal
|
|
C536057||autosomal malignant osteopetrosis
|
|
C536057||lethal osteopetrosis
|
|
C563637||larynx congenital partial atresia of
|
|
D001044||aphonia
|
|
D001044||absence of voice
|
|
D001044||aphonia functional
|
|
D001044||aphonia nonorganic
|
|
D001044||aphonia paralytica
|
|
D001044||aphonias functional
|
|
D001044||aphonias nonorganic
|
|
D001044||aphonia spastic
|
|
D001044||aphonias spastic
|
|
D001044||functional aphonia
|
|
D001044||functional aphonias
|
|
D001044||nonorganic aphonia
|
|
D001044||nonorganic aphonias
|
|
D001044||paralytica aphonia
|
|
D001044||spastic aphonia
|
|
D001044||spastic aphonias
|
|
D001044||voice absence
|
|
D001044||voice absences
|
|
C564967||myotonia with skeletal abnormalities and mental retardation
|
|
C563636||laryngeal web familial
|
|
C563636||glottic web congenital anterior
|
|
C563634||tooth agenesis selective 4
|
|
C563634||lateral incisors absence of
|
|
C563634||lateral incisors pegged or missing
|
|
C563634||sthag4
|
|
C563634||succedaneous teeth agenesis of
|
|
D001041||aphasia wernicke
|
|
D001041||aphasia fluent
|
|
D001041||aphasia jargon
|
|
D001041||aphasia posterior
|
|
D001041||aphasia psychosensory
|
|
D001041||aphasia receptive
|
|
D001041||aphasia sensory
|
|
D001041||aphasias jargon
|
|
D001041||aphasias posterior
|
|
D001041||aphasias psychosensory
|
|
D001041||aphasias wernicke
|
|
D001041||aphasia wernicke apos s fluent
|
|
D001041||dysphasia fluent
|
|
D001041||dysphasia receptive
|
|
D001041||dysphasia sensory
|
|
D001041||dysphasias fluent
|
|
D001041||dysphasias receptive
|
|
D001041||dysphasias sensory
|
|
D001041||dysphasia wernicke
|
|
D001041||dysphasia wernickes
|
|
D001041||dysphasia wernicke apos s
|
|
D001041||fluent aphasia
|
|
D001041||fluent aphasia wernicke
|
|
D001041||fluent aphasia wernickes
|
|
D001041||fluent aphasia wernicke apos s
|
|
D001041||fluent dysphasia
|
|
D001041||fluent dysphasias
|
|
D001041||jargon aphasia
|
|
D001041||jargon aphasias
|
|
D001041||posterior aphasia
|
|
D001041||posterior aphasias
|
|
D001041||psychosensory aphasia
|
|
D001041||psychosensory aphasias
|
|
D001041||receptive aphasia
|
|
D001041||receptive dysphasia
|
|
D001041||receptive dysphasias
|
|
D001041||sensory aphasia
|
|
D001041||sensory dysphasia
|
|
D001041||sensory dysphasias
|
|
D001041||wernicke aphasia
|
|
D001041||wernicke aphasias
|
|
D001041||wernicke dysphasia
|
|
D001041||wernicke apos s dysphasia
|
|
D001041||wernicke apos s fluent aphasia
|
|
C537381||multiple system atrophy msa with orthostatic hypotension
|
|
D002372||cat scratch disease
|
|
D002372||catscratch disease
|
|
D002372||disease catscratch
|
|
D002372||disease cat scratch
|
|
D002372||inoculation lymphoreticuloses
|
|
D002372||inoculation lymphoreticulosis
|
|
D002372||inoculative lymphoreticuloses
|
|
D002372||inoculative lymphoreticulosis
|
|
D002372||lymphoreticuloses inoculation
|
|
D002372||lymphoreticuloses inoculative
|
|
D002372||lymphoreticulosis inoculation
|
|
D002372||lymphoreticulosis inoculative
|
|
C536968|602124||torsion dystonia 7
|
|
C536968|602124||dystonia 7 torsion
|
|
C536968|602124||dyt7
|
|
C536968|602124||primary adult onset torsion dystonia
|
|
C536968|602124||torsion dystonia focal adult onset
|
|
C536968|602124||torsion dystonia focal adult onset cervical dystonia primary included
|
|
173900|D007690||polycystic kidney diseases
|
|
173900|D007690||apkd included
|
|
173900|D007690||disease polycystic kidney
|
|
173900|D007690||disease polycystic renal
|
|
173900|D007690||diseases polycystic kidney
|
|
173900|D007690||diseases polycystic renal
|
|
173900|D007690||kidney disease polycystic
|
|
173900|D007690||kidney diseases polycystic
|
|
173900|D007690||kidney polycystic
|
|
173900|D007690||kidneys polycystic
|
|
173900|D007690||pkd1
|
|
173900|D007690||polycystic kidney
|
|
173900|D007690||polycystic kidney disease
|
|
173900|D007690||polycystic kidney disease 1
|
|
173900|D007690||polycystic kidney disease adult type i apkd1 polycystic kidney disease adult included
|
|
173900|D007690||polycystic kidneys
|
|
173900|D007690||polycystic renal disease
|
|
173900|D007690||polycystic renal diseases
|
|
173900|D007690||potter type iii polycystic kidney disease included
|
|
173900|D007690||renal disease polycystic
|
|
173900|D007690||renal diseases polycystic
|
|
C563639||cutis laxa marfanoid syndrome
|
|
C563639||neonatal cutis laxa with marfanoid phenotype
|
|
D002375||catalepsy
|
|
D002375||anochlesia
|
|
D002375||anochlesias
|
|
D002375||catalepsies
|
|
D002375||cerea flexibilitas
|
|
D002375||flexibilitas cerea
|
|
D002375||flexibilities waxy
|
|
D002375||flexibility waxy
|
|
D002375||waxy flexibilities
|
|
D002375||waxy flexibility
|
|
C567060|313500||tooth agenesis selective x linked 1
|
|
C567060|313500||hypodontia oligodontia x linked 1
|
|
C567060|313500||sthagx1
|
|
306400|C564417||granulomatous disease chronic x linked
|
|
306400|C564417||cgd
|
|
306400|C564417||chronic granulomatous disease atypical
|
|
306400|C564417||chronic granulomatous disease atypical included
|
|
306400|C564417||chronic granulomatous disease x linked
|
|
306400|C564417||chronic granulomatous disease x linked cytochrome b positive granulomatous disease chronic x linked included
|
|
306400|C564417||cytochrome b negative granulomatous disease chronic x linked
|
|
306400|C564417||cytochrome b positive granulomatous disease chronic x linked
|
|
306400|C564417||granulomatous disease chronic x linked variant
|
|
306400|C564417||granulomatous disease chronic x linked variant included
|
|
C565325|605526||alzheimer disease 6
|
|
C565325|605526||ad6
|
|
C565325|605526||alzheimer disease 6 late onset
|
|
C565325|605526||alzheimer disease 6 late onset plasma beta amyloid 42 level quantitative trait locus included
|
|
606771||adiponectin serum level of quantitative trait locus 3
|
|
606771||adipqtl3
|
|
606771||caq14
|
|
606771||circulating adiponectin quantitative trait locus on chromosome 14
|
|
C548027||idiopathic juxtafoveal retinal telangiectasia
|
|
606770||adiponectin serum level of quantitative trait locus 2
|
|
606770||adipqtl2
|
|
606770||caq5
|
|
606770||circulating adiponectin quantitative trait locus on chromosome 5
|
|
D056735|601859||autoimmune lymphoproliferative syndrome
|
|
D056735|601859||alps
|
|
D056735|601859||alps1a included
|
|
D056735|601859||alps1b included
|
|
D056735|601859||alps2b
|
|
D056735|601859||autoimmune lymphoproliferative syndromes
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type 1 autosomal dominant
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type 2b
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type 2b alps2b
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type i autosomal dominant
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type i autosomal dominant autoimmune lymphoproliferative syndrome type ia included
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type i autosomal recessive included
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type ib included
|
|
D056735|601859||autoimmune lymphoproliferative syndrome type iib
|
|
D056735|601859||canale smith syndrome
|
|
D056735|601859||canale smith syndromes
|
|
D056735|601859||caspase 8 deficiencies
|
|
D056735|601859||caspase 8 deficiency
|
|
D056735|601859||ceds
|
|
D056735|601859||deficiencies caspase 8
|
|
D056735|601859||deficiency caspase 8
|
|
D056735|601859||lymphoproliferative syndrome autoimmune
|
|
D056735|601859||lymphoproliferative syndromes autoimmune
|
|
D056735|601859||syndrome autoimmune lymphoproliferative
|
|
D056735|601859||syndrome canale smith
|
|
D056735|601859||syndromes autoimmune lymphoproliferative
|
|
D056735|601859||syndromes canale smith
|
|
D014354||trypanosomiasis bovine
|
|
D014354||bovine trypanosomiases
|
|
D014354||bovine trypanosomiasis
|
|
D014354||trypanosomiases bovine
|
|
D014353||trypanosomiasis african
|
|
D014353||african sleeping sickness
|
|
D014353||african sleeping sicknesses
|
|
D014353||african trypanosomiases
|
|
D014353||african trypanosomiasis
|
|
D014353||nagana
|
|
D014353||sickness african sleeping
|
|
D014353||sicknesses african sleeping
|
|
D014353||sleeping sickness african
|
|
D014353||sleeping sicknesses african
|
|
D014353||trypanosomiases african
|
|
D014352||trypanosomiasis
|
|
D014352||trypanosomiases
|
|
D014355||chagas disease
|
|
D014355||american trypanosomiasis
|
|
D014355||chagas apos disease
|
|
D014355||disease chagas
|
|
D014355||disease chagas apos
|
|
D014355||south american trypanosomiasis
|
|
D014355||trypanosomiasis american
|
|
D014355||trypanosomiasis south american
|
|
D001139||arnold chiari malformation
|
|
D001139||arnold chiari deformity
|
|
D001139||arnold chiari malformation type 1
|
|
D001139||arnold chiari malformation type 2
|
|
D001139||arnold chiari malformation type 3
|
|
D001139||arnold chiari malformation type 4
|
|
D001139||arnold chiari malformation type i
|
|
D001139||arnold chiari malformation type ii
|
|
D001139||arnold chiari malformation type iii
|
|
D001139||arnold chiari malformation type iv
|
|
D001139||arnold chiari syndrome
|
|
D001139||chiari malformation type i
|
|
D001139||deformity arnold chiari
|
|
D001139||malformation arnold chiari
|
|
D001139||syndrome arnold chiari
|
|
D001139||type i arnold chiari malformation
|
|
D001139||type ii arnold chiari malformation
|
|
D001139||type iii arnold chiari malformation
|
|
D001139||type iv arnold chiari malformation
|
|
C537430||arima syndrome
|
|
C537430||cerebro oculo hepato renal syndrome
|
|
C537430||chorioretinal coloboma with cerebellar vermis aplasia
|
|
C537430||coloboma chorioretinal with cerebellar vermis aplasia
|
|
C537430||dekaban arima syndrome
|
|
C537430||joubert syndrome with bilateral chorioretinal coloboma
|
|
C566869|163500||night blindness congenital stationary autosomal dominant 2
|
|
C566869|163500||csnbad2
|
|
C566869|163500||night blindness congenital stationary rambusch type
|
|
C536102||myopathy congenital nonprogressive with moebius and robin sequences
|
|
C536102||carey fineman ziter syndrome
|
|
C536102||congenital nonprogressive myopathy with moebius and robin sequence
|
|
C536102||moebius sequence robin complex and hypotonia
|
|
C536102||myopathy congenital nonprogressive with moebius sequence and robin sequence
|
|
C536103||myopathy desmin storage
|
|
C536103||cardiomyopathy due to desmin defect
|
|
C536103||desmin storage myopathy
|
|
C536103||myopathy with sarcoplasmic bodies and intermediate filaments
|
|
C537431||arnold stickler bourne syndrome
|
|
C537431||corneal crystals myopathy and nephropathy
|
|
C536100||myopathic carnitine deficiency
|
|
C536100||carnitine deficiency myopathic
|
|
C563725|189800|D011225||preeclampsia eclampsia 3
|
|
C563724|189800|D011225||preeclampsia eclampsia 4
|
|
C567480|300696||myopathy x linked with postural muscle atrophy
|
|
C567480|300696||edmd6 included
|
|
C567480|300696||emery dreifuss muscular dystrophy 6 x linked included
|
|
C567480|300696||xmpma
|
|
C563885|608652||deafness autosomal dominant 47
|
|
C563885|608652||dfna47
|
|
D001134||arm injuries
|
|
D001134||arm injury
|
|
D001134||injuries arm
|
|
D001134||injury arm
|
|
C563726|189800|D011225||preeclampsia eclampsia 2
|
|
217700|C536439||corneal endothelial dystrophy type 2
|
|
217700|C536439||ched2
|
|
217700|C536439|121700||congenital hereditary endothelial dystrophy of cornea
|
|
217700|C536439||congenital hereditary endothelial dystrophy of the cornea
|
|
217700|C536439|121700||corneal dystrophy congenital hereditary endothelial
|
|
217700|C536439||corneal endothelial dystrophy 2
|
|
217700|C536439||corneal endothelial dystrophy 2 autosomal recessive
|
|
217700|C536439|121700||maumenee corneal dystrophy
|
|
D013118||spinal cord diseases
|
|
D013118||myelopathies
|
|
D013118||myelopathy
|
|
D013118||spinal cord disease
|
|
D013118||spinal cord disorder
|
|
D013118||spinal cord disorders
|
|
D013119||spinal cord injuries
|
|
D013119||contusion spinal cord
|
|
D013119||contusions spinal cord
|
|
D013119||cord contusion spinal
|
|
D013119||cord contusions spinal
|
|
D013119||cord injuries spinal
|
|
D013119||cord injury spinal
|
|
D013119||cord laceration spinal
|
|
D013119||cord lacerations spinal
|
|
D013119||cord transection spinal
|
|
D013119||cord transections spinal
|
|
D013119||cord trauma spinal
|
|
D013119||cord traumas spinal
|
|
D013119||injuries spinal cord
|
|
D013119||injury spinal cord
|
|
D013119||laceration spinal cord
|
|
D013119||lacerations spinal cord
|
|
D013119||myelopathies post traumatic
|
|
D013119||myelopathies traumatic
|
|
D013119||myelopathy post traumatic
|
|
D013119||myelopathy traumatic
|
|
D013119||post traumatic myelopathies
|
|
D013119||post traumatic myelopathy
|
|
D013119||spinal cord contusion
|
|
D013119||spinal cord contusions
|
|
D013119||spinal cord injury
|
|
D013119||spinal cord laceration
|
|
D013119||spinal cord lacerations
|
|
D013119||spinal cord transection
|
|
D013119||spinal cord transections
|
|
D013119||spinal cord trauma
|
|
D013119||spinal cord traumas
|
|
D013119||transection spinal cord
|
|
D013119||transections spinal cord
|
|
D013119||trauma spinal cord
|
|
D013119||traumas spinal cord
|
|
D013119||traumatic myelopathies
|
|
D013119||traumatic myelopathy
|
|
D013117||spinal cord compression
|
|
D013117||compression spinal cord
|
|
D013117||compressions spinal cord
|
|
D013117||compressive myelopathy
|
|
D013117||conus medullaris syndrome
|
|
D013117||conus medullaris syndromes
|
|
D013117||extramedullary spinal cord compression
|
|
D013117||myelopathy compressive
|
|
D013117||spinal cord compression extramedullary
|
|
D013117||spinal cord compressions
|
|
D013117||syndrome conus medullaris
|
|
D013117||syndromes conus medullaris
|
|
C563327|601386||deafness autosomal recessive 12
|
|
C563327|601386||dfnb12
|
|
C537426||arakawa syndrome 2
|
|
C537426||arakawa apos s syndrome 2
|
|
C537426||n5 methylhomocysteine transferase deficiency
|
|
C537426||tetrahydrofolate methyltransferase deficiency syndrome
|
|
C537427||aredyld syndrome
|
|
C537427||acral renal ectodermal dysplasia lipoatrophic diabetes
|
|
C537427||acrorenal field defect ectodermal dysplasia and lipoatrophic diabetes
|
|
C537427||aredyld
|
|
C537424||arachnodactyly ataxia cataract aminoaciduria mental retardation
|
|
D010381|169400||pelger huet anomaly
|
|
D010381|169400||anomaly pelger huet
|
|
D010381|169400||anomaly pelger hu 235 t
|
|
D010381|169400||anomaly pelger huet nuclear
|
|
D010381|169400||anomaly pelger hu 235 t nuclear
|
|
D010381|169400||anomaly pseudo pelger huet
|
|
D010381|169400||anomaly pseudo pelger hu 235 t
|
|
D010381|169400||nuclear anomaly pelger huet
|
|
D010381|169400||nuclear anomaly pelger hu 235 t
|
|
D010381|169400||ovoid neutrophil nuclei developmental delay epilepsy and skeletal abnormalities
|
|
D010381|169400||pelger hu 235 t anomaly
|
|
D010381|169400||pelger huet anomaly pseudo
|
|
D010381|169400||pelger hu 235 t anomaly pseudo
|
|
D010381|169400||pelger huet nuclear anomaly
|
|
D010381|169400||pelger hu 235 t nuclear anomaly
|
|
D010381|169400||pha
|
|
D010381|169400||pseudo pelger huet anomaly
|
|
D010381|169400||pseudo pelger hu 235 t anomaly
|
|
D010381|169400||pseudo pelger huet nuclear anomaly
|
|
D015776||keratoderma palmoplantar diffuse
|
|
D015776||syndrome thost unna
|
|
D015776||syndrome unna thost
|
|
D015776||thost unna syndrome
|
|
D015776||unna thost syndrome
|
|
C537428||arena syndrome
|
|
C537428||spastic paraplegia with iron deposits in basal ganglia
|
|
D015775||fractures stress
|
|
D015775||fatigue fracture
|
|
D015775||fatigue fractures
|
|
D015775||fracture fatigue
|
|
D015775||fracture insufficiency
|
|
D015775||fracture march
|
|
D015775||fractures fatigue
|
|
D015775||fractures insufficiency
|
|
D015775||fractures march
|
|
D015775||fracture stress
|
|
D015775||insufficiency fracture
|
|
D015775||insufficiency fractures
|
|
D015775||march fracture
|
|
D015775||march fractures
|
|
D015775||stress fracture
|
|
D015775||stress fractures
|
|
C537429||arhinia choanal atresia and microphthalmia
|
|
C537429||bosma arhinia microphthalmia syndrome
|
|
C537441||arthrogryposis and ectodermal dysplasia
|
|
C537441||alves syndrome
|
|
C537441||arthrogryposis ectodermal dysplasia other anomalies
|
|
C537441||cote adamopoulos pantelakis syndrome
|
|
C537441||todv syndrome
|
|
C537441||trichooculodermovertebral syndrome
|
|
C536110||nablus mask like facial syndrome
|
|
C562400||hyperpigmentation of eyelids
|
|
C537444||mental retardation mietens weber type
|
|
C537444||mental retardation syndrome mietens weber type
|
|
C537444||mietens weber syndrome
|
|
C536113||cerebral gigantism nevo type
|
|
C563731||cerebrorenodigital syndrome with limb malformations and triradiate acetabula
|
|
164200|C563160||oculodentodigital dysplasia
|
|
164200|C563160||oculo dento digital dysplasia
|
|
164200|C563160||oculodentodigital syndrome
|
|
164200|C563160||oculodentoosseous dysplasia
|
|
164200|C563160||oculo dento osseous dysplasia
|
|
164200|C563160||oddd
|
|
164200|C563160||odd syndrome
|
|
164200|C563160||odod
|
|
164200|C563160||osseous oculo dental dysplasia
|
|
C562401||pseudopapilledema
|
|
C537445||mental retardation smith fineman myers type
|
|
C537445||smith fineman myers syndrome
|
|
D009634|163950||noonan syndrome
|
|
D009634|163950||familial turner syndrome
|
|
D009634|163950||female pseudo turner syndrome
|
|
D009634|163950||male turner apos s syndrome
|
|
D009634|163950||male turner syndrome
|
|
D009634|163950||noonan ehmke syndrome
|
|
D009634|163950||noonan syndrome 1
|
|
D009634|163950||ns1
|
|
D009634|163950||pseudo turner syndrome female
|
|
D009634|163950||pseudo ullrich turner syndrome
|
|
D009634|163950||syndrome familial turner
|
|
D009634|163950||syndrome female pseudo turner
|
|
D009634|163950||syndrome male turner
|
|
D009634|163950||syndrome male turner apos s
|
|
D009634|163950||syndrome noonan
|
|
D009634|163950||syndrome noonan ehmke
|
|
D009634|163950||syndrome pseudo ullrich turner
|
|
D009634|163950||syndrome turner like
|
|
D009634|163950||syndrome ullrich noonan
|
|
D009634|163950||turner like syndrome
|
|
D009634|163950||turner phenotype with normal karyotype
|
|
D009634|163950||turner phenotype with normal karyotype pterygium colli syndrome included
|
|
D009634|163950||turner apos s phenotype karyotype normal
|
|
D009634|163950||turner apos s syndrome male
|
|
D009634|163950||turner syndrome familial
|
|
D009634|163950||turner syndrome male
|
|
D009634|163950||ullrich noonan syndrome
|
|
C537442||arthrogryposis epileptic seizures migrational brain disorder
|
|
C537442||arthrogryposis multiplex congenita with epileptic seizures and migrational brain disorder
|
|
C536111||partial agenesis of corpus callosum
|
|
C536112||partial atrioventricular canal
|
|
C536112||partial atrioventricular septal defects
|
|
C536112||partial common atrioventricular canal
|
|
C563736||epiphyseal dysplasia multiple with severe proximal femoral dysplasia
|
|
C562404||pulmonary arteriovenous fistulas
|
|
C563735||epiphyseal dysplasia multiple with miniepiphyses
|
|
C563734||chromosome 18 pericentric inversion
|
|
D010981|185050||platelet storage pool deficiency
|
|
D010981|185050||acquired storage pool disease
|
|
D010981|185050||deficiencies storage pool
|
|
D010981|185050||deficiency platelet storage pool
|
|
D010981|185050||deficiency storage pool
|
|
D010981|185050||familial platelet storage pool disease
|
|
D010981|185050||platelet storage pool deficiencies
|
|
D010981|185050||platelet storage pool disease
|
|
D010981|185050||storage pool deficiencies
|
|
D010981|185050||storage pool deficiency
|
|
D010981|185050||storage pool deficiency platelet
|
|
D010981|185050||storage pool platelet disease
|
|
C562408||radioulnar synostosis
|
|
D002471||cell transformation neoplastic
|
|
D002471||cell neoplastic transformation
|
|
D002471||cell neoplastic transformations
|
|
D002471||cell transformations neoplastic
|
|
D002471||neoplastic cell transformation
|
|
D002471||neoplastic cell transformations
|
|
D002471||neoplastic transformation cell
|
|
D002471||neoplastic transformations cell
|
|
D002471||transformation cell neoplastic
|
|
D002471||transformation neoplastic cell
|
|
D002471||transformations cell neoplastic
|
|
D002471||transformations neoplastic cell
|
|
D002471||transformations tumorigenic
|
|
D002471||transformation tumorigenic
|
|
D002471||tumorigenic transformation
|
|
D002471||tumorigenic transformations
|
|
D001146||arrhythmia sinus
|
|
D001146||arrhythmia sinoatrial
|
|
D001146||arrhythmias sinoatrial
|
|
D001146||arrhythmias sinus
|
|
D001146||sinoatrial arrhythmia
|
|
D001146||sinoatrial arrhythmias
|
|
D001146||sinus arrhythmia
|
|
D001146||sinus arrhythmias
|
|
D002472||cell transformation viral
|
|
D002472||cell transformations viral
|
|
D002472||transformations viral cell
|
|
D002472||transformation viral cell
|
|
D002472||viral cell transformation
|
|
D002472||viral cell transformations
|
|
C562406||bladder diverticulum
|
|
C563737||teratoid tumor atypical
|
|
613843||leber congenital amaurosis 15
|
|
613843||lca15
|
|
613843||retinitis pigmentosa juvenile tulp1 related included
|
|
D013128||spinal osteophytosis
|
|
D013128||osteophytoses spinal
|
|
D013128||osteophytosis spinal
|
|
D013128||spinal osteophytoses
|
|
D002481||cellulitis
|
|
D002481||phlegmon
|
|
D014458||ulna fractures
|
|
D014458||fractures ulna
|
|
D014458||fracture ulna
|
|
D014458||ulna fracture
|
|
173650|C536321||poikiloderma of kindler
|
|
173650|C536321||bullous acrokeratotic poikiloderma of kindler and weary
|
|
173650|C536321||congenital bullous poikiloderma
|
|
173650|C536321||kindler syndrome
|
|
173650|C536321||poikiloderma congenital with bullae weary type
|
|
173650|C536321||poikiloderma hereditary acrokeratotic
|
|
D013121||spinal curvatures
|
|
D013121||curvature spinal
|
|
D013121||curvatures spinal
|
|
D013121||spinal curvature
|
|
C536106||myostatin related muscle hypertrophy
|
|
C536106||muscle hypertrophy syndrome
|
|
C565129|123790||cutis gyrata syndrome of beare and stevenson
|
|
C565129|123790||beare stevenson cutis gyrata syndrome
|
|
C565129|123790||beare stevenson syndrome
|
|
C565129|123790||bstvs
|
|
C565129|123790||cutis gyrata syndrome of beare stevenson
|
|
C537438||arrhinia
|
|
C537438||congenital absence of the nose
|
|
C537438||nose agenesia
|
|
D013122||spinal diseases
|
|
D013122||disease spinal
|
|
D013122||diseases spinal
|
|
D013122||spinal disease
|
|
C536107||n acetyltransferase deficiency
|
|
C536107||n acetyltransferase 1 deficiency
|
|
C536107||nat1 deficiency
|
|
D015783||absent iris
|
|
D015783||congenital aniridia
|
|
D015783||irideremia
|
|
C536104|C536169|112250||myopathy limb girdle with bone fragility
|
|
D013120||spinal cord neoplasms
|
|
D013120||intradural extramedullary spinal cord neoplasms
|
|
D013120||intramedullary spinal cord neoplasms
|
|
D013120||intramedullary spinal cord neoplasms primary
|
|
D013120||neoplasm spinal cord
|
|
D013120||neoplasms spinal cord
|
|
D013120||primary intramedullary spinal cord neoplasms
|
|
D013120||primary spinal cord neoplasms intramedullary
|
|
D013120||spinal cord neoplasm
|
|
D013120||spinal cord neoplasms benign
|
|
D013120||spinal cord neoplasms intradural extramedullary
|
|
D013120||spinal cord neoplasms intramedullary
|
|
D013120||spinal cord neoplasms malignant
|
|
D013120||spinal cord neoplasms primary intramedullary
|
|
D013120||spinal cord tumor
|
|
D013120||spinal cord tumors
|
|
D013120||tumor spinal cord
|
|
D013120||tumors spinal cord
|
|
D013125||spinal neoplasms
|
|
D013125||neoplasm spinal
|
|
D013125||neoplasms spinal
|
|
D013125||spinal neoplasm
|
|
D014456||ulcer
|
|
D014456||ulcers
|
|
D015787||erythema chronicum migrans
|
|
C537439||arroyo garcia cimadevilla syndrome
|
|
C537439||bilateral anophthalmia esophageal atresia and right cryptorchidism
|
|
D013124||spinal injuries
|
|
D013124||injuries spinal
|
|
D013124||injury spinal
|
|
D013124||spinal injury
|
|
D015785||eye diseases hereditary
|
|
D015785||disease hereditary eye
|
|
D015785||diseases hereditary eye
|
|
D015785||eye disease hereditary
|
|
D015785||hereditary eye disease
|
|
D015785||hereditary eye diseases
|
|
600512||epilepsy familial temporal lobe 1
|
|
600512||adlte
|
|
600512||adpeaf
|
|
600512|C537297||epilepsy lateral temporal lobe autosomal dominant
|
|
600512|C537297||epilepsy partial with auditory features
|
|
600512||etl1
|
|
C536120||nievergelt syndrome
|
|
C536120||mesomelic dwarfism nievergelt type
|
|
C536120||mesomelic dysplasia nievergelt type
|
|
D001117||arenaviridae infections
|
|
D001117||arenaviridae infection
|
|
D001117||arenavirus infection
|
|
D001117||arenavirus infections
|
|
D001117||infection arenaviridae
|
|
D001117||infection arenavirus
|
|
D001117||infections arenaviridae
|
|
D001117||infections arenavirus
|
|
C537452||mental retardation keratoconus febrile seizures and sinoatrial block
|
|
C536121||night blindness skeletal anomalies unusual facies
|
|
C536121||hunter thomson reed syndrome
|
|
C537450||mental retardation x linked south african type
|
|
C536124||noble bass sherman syndrome
|
|
C536124||ectopia lentis chorioretinal dystrophy myopia
|
|
C536824|600975||glaucoma 3 primary infantile b
|
|
C536824|600975||glaucoma primary congenital type 3b
|
|
C536824|600975||glaucoma primary congenital type b
|
|
C536824|600975||glc3b
|
|
C536824|600975||glc3 type b
|
|
C536824|600975||primary congenital glaucoma type 3b
|
|
C537453||mental retardation macrocephaly short stature and craniofacial dysmorphism
|
|
C537453||fryns dereymaeker haegeman syndrome
|
|
C536122||night blindness congenital stationary
|
|
C536122||congenital stationary night blindness
|
|
C536122|257270||csnb1b
|
|
C536122||myopia night blindness
|
|
C536122|257270||night blindness congenital stationary complete autosomal recessive
|
|
C536122||night blindness congenital stationary type 1
|
|
C536122|257270||night blindness congenital stationary type 1b
|
|
C536122||xlcsnb
|
|
C536122||x linked congenital stationary night blindness
|
|
C536122||x linked csnb
|
|
C536123||nivelon nivelon mabille syndrome
|
|
C536123||chondrodysplasia pseudohermaphrodism syndrome
|
|
C536123||chondrodysplasia pseudohermaphroditism syndrome
|
|
C536123||pseudohermaphrodism and chondrodysplasia
|
|
D003773||dental plaque
|
|
D003773||plaque dental
|
|
C563701||omphalocele diaphragmatic hernia and radial ray defects
|
|
C563701||gershoni baruch syndrome
|
|
D001112||arcus senilis
|
|
D001112||arcus corneae
|
|
D001112||arcus corneal
|
|
D001112||corneal arcus
|
|
253000|D009085||mucopolysaccharidosis type iva
|
|
253000|D009085||mps4a morquio syndrome a
|
|
253000|D009085||mps iva
|
|
253000|D009085||morquio a disease
|
|
253000|D009085||galactosamine 6 sulfatase deficiency
|
|
253000|D009085||galns deficiency
|
|
C563704||proguanil poor metabolism of
|
|
D014428||twins conjoined
|
|
D014428||conjoined twin
|
|
D014428||conjoined twins
|
|
D014428||siamese twin
|
|
D014428||siamese twins
|
|
D014428||twin conjoined
|
|
D014428||twin siamese
|
|
D014428||twins siamese
|
|
C565162|121210||febrile convulsions familial 1
|
|
C565162|121210||1
|
|
C565162|121210||convulsions familial febrile
|
|
C565162|121210||convulsions familial febrile 1
|
|
C565162|121210||feb1
|
|
C565162|121210||febrile seizures familial 1
|
|
C565162|121210||seizures familial 1
|
|
C563708||amyotrophic lateral sclerosis chmp2b related
|
|
613825||c9d
|
|
C567484|300243||mental retardation x linked syndromic christianson type
|
|
C567484|300243||angelman like syndrome x linked
|
|
C567484|300243||christianson syndrome
|
|
C567484|300243||intellectual deficit x linked south african type
|
|
C567484|300243||mental retardation microcephaly epilepsy and ataxia syndrome
|
|
C567484|300243||mrxsch
|
|
C536176|261670||dimauro disease
|
|
C536176|261670||deficiency mutase phosphoglycerate
|
|
C536176|261670||glycogen storage disease x
|
|
C536176|261670||gsd10
|
|
C536176|261670||gsd x
|
|
C536176|261670||human muscle phosphoglycerate mutase deficiency
|
|
C536176|261670||myopathy due to phosphoglycerate mutase deficiency
|
|
C536176|261670||pgam deficiency
|
|
C536176|261670||pgamm deficiency
|
|
C536176|261670||phosphoglycerate mutase deficiency
|
|
C536176|261670||phosphoglycerate mutase muscle deficiency of
|
|
613828||generalized epilepsy with febrile seizures plus type 8
|
|
613828||gefs 8
|
|
613828||gefsp8
|
|
613828||gefs type 8
|
|
C537448||mental retardation wolff type
|
|
C537448||wolff mental retardation syndrome
|
|
C537448||wolff type mental retardation
|
|
C537448||wolff zimmermann syndrome
|
|
C537446||mental retardation spasticity ectrodactyly
|
|
C537446||ectrodactyly spastic paraplegia and mental retardation
|
|
C537446||jancar syndrome
|
|
C537446||mental retardation spasticity and transverse limb defects
|
|
C536115||nguyen syndrome
|
|
C537447||mental retardation syndrome belgian type
|
|
C537447||belgian type mental retardation syndrome
|
|
C536116||nicolaides baraitser syndrome
|
|
C536116||sparse hair and mental retardation
|
|
D014424||turner syndrome
|
|
D014424||bonnevie ullrich syndrome
|
|
D014424||gonadal dysgenesis 45 x
|
|
D014424||gonadal dysgenesis xo
|
|
D014424||monosomy x
|
|
D014424||status bonnevie ullrich
|
|
D014424||syndrome ullrich turner
|
|
D014424||turner apos s syndrome
|
|
D014424||turners syndrome
|
|
D014424||ullrich turner syndrome
|
|
D014424||xo gonadal dysgenesis
|
|
C567772|613071||bronchiectasis with or without elevated sweat chloride 3
|
|
C567772|613071||besc3
|
|
C537017|313200||bulbospinal neuronopathy x linked recessive
|
|
C537017|313200|D055534||bulbospinal muscular atrophy x linked
|
|
C537017|313200|D055534||kennedy disease
|
|
C537017|313200|D055534||kennedy spinal and bulbar muscular atrophy
|
|
C537017|313200||sbma
|
|
C537017|313200||smax1
|
|
C537017|313200|D055534||spinal and bulbar muscular atrophy x linked 1
|
|
C537017|313200||xbsn
|
|
D001129||argyria
|
|
D001129||argyrias
|
|
C537462||microphthalmia and mental deficiency
|
|
C537462||colobomatous microphthalmia
|
|
C537462||microphthalmia colobomatous
|
|
C537462||microphthalmos severe mental retardation and spastic cerebral palsy
|
|
C537462||pinsky digeorge harley syndrome
|
|
C537463||microphthalmia associated with colobomatous cyst
|
|
C537463||microphthalmos bilateral colobomatous orbital cyst
|
|
C537461||merlob grunebaum reisner syndrome
|
|
C565319|605583||deafness autosomal dominant 25
|
|
C565319|605583||dfna25
|
|
C563710||rhegmatogenous retinal detachment autosomal dominant
|
|
D003788||dental pulp diseases
|
|
D003788||dental pulp disease
|
|
D003788||disease dental pulp
|
|
D003788||diseases dental pulp
|
|
D003788||pulp disease dental
|
|
D003788||pulp diseases dental
|
|
C536135||median cleft lip corpus callosum lipoma and skin polyps
|
|
C536135||cleft median of upper lip with polyps of facial skin and nasal mucosa
|
|
C536135||pai levkoff syndrome
|
|
C536135||pai syndrome
|
|
D003789||dental pulp exposure
|
|
D003789||exposure dental pulp
|
|
D003789||pulp exposure dental
|
|
C536136||mediastinal fibrosis
|
|
C536136||fibrosing mediastinitis
|
|
C536136||idiopathic mediastinal fibrosis
|
|
C536136||sclerosing mediastinitis
|
|
C536134||medial medullary syndrome
|
|
C565326|605463||radiation sensitivity chromosome instability syndrome autosomal dominant
|
|
D003784||dental pulp calcification
|
|
D003784|125420||anomalous dysplasia of dentin
|
|
D003784||calcification dental pulp
|
|
D003784||calcifications dental pulp
|
|
D003784|125420||coronal dentin dysplasia
|
|
D003784||coronal dentin dysplasias
|
|
D003784||dental pulp calcifications
|
|
D003784||dental pulp stone
|
|
D003784||dental pulp stones
|
|
D003784||denticle
|
|
D003784||denticles
|
|
D003784||dentin anomalous dysplasia
|
|
D003784||dentin anomalous dysplasias
|
|
D003784||dentin dyspalsia shields type 2
|
|
D003784||dentin dysplasia coronal
|
|
D003784||dentin dysplasias coronal
|
|
D003784|125420||dentin dysplasia shields type ii
|
|
D003784|125420||dentin dysplasia type ii
|
|
D003784||dysplasia coronal dentin
|
|
D003784||dysplasia pulpal
|
|
D003784||dysplasias coronal dentin
|
|
D003784||dysplasias pulpal
|
|
D003784|125420||pulpal dysplasia
|
|
D003784||pulpal dysplasias
|
|
D003784||pulp calcification dental
|
|
D003784||pulp calcifications dental
|
|
D003784||pulp stone
|
|
D003784||pulp stone dental
|
|
D003784|125420||pulp stones
|
|
D003784||pulp stones dental
|
|
D003784||stone dental pulp
|
|
D003784||stone pulp
|
|
D003784||stones dental pulp
|
|
D003784||stones pulp
|
|
C563712||noncompaction of left ventricular myocardium familial isolated autosomal dominant 2
|
|
C563718||myopathy myofibrillar zasp related
|
|
C563718||mfm zasp related
|
|
C537858|136520||o apos donnell pappas syndrome
|
|
C537858|136520||foveal hypoplasia 1
|
|
C537858|136520||foveal hypoplasia and presenile cataract syndrome
|
|
C537858|136520||foveal hypoplasia congenital nystagmus corneal pannus and presenile cataracts
|
|
C537858|136520||foveal hypoplasia presenile cataract
|
|
C537858|136520||foveal hypoplasia with or without anterior segment anomalies and or cataract
|
|
C537858|136520||fvh1
|
|
D014438||typhus epidemic louse borne
|
|
D014438||brill disease
|
|
D014438||brill apos s disease
|
|
D014438||brills disease
|
|
D014438||brill zinsser disease
|
|
D014438||disease brill
|
|
D014438||disease brill apos s
|
|
D014438||disease brill zinsser
|
|
D014438||epidemic louse borne typhus
|
|
D014438||epidemic typhus
|
|
D014438||fever jail
|
|
D014438||fevers jail
|
|
D014438||jail fever
|
|
D014438||jail fevers
|
|
D014438||louse borne typhus epidemic
|
|
D014438||typhus
|
|
D014438||typhus epidemic
|
|
D015769||granuloma respiratory tract
|
|
D015769||granulomas respiratory tract
|
|
D015769||respiratory tract granuloma
|
|
D015769||respiratory tract granulomas
|
|
D014437||typhus endemic flea borne
|
|
D014437||endemic flea borne typhus
|
|
D014437||endemic typhus
|
|
D014437||flea borne typhus endemic
|
|
D014437||murine typhus
|
|
D014437||typhus endemic
|
|
D014437||typhus murine
|
|
D003790||dental pulp necrosis
|
|
D003790||autolyses dental pulp
|
|
D003790||autolysis dental pulp
|
|
D003790||dental pulp autolyses
|
|
D003790||dental pulp autolysis
|
|
D003790||dental pulp gangrene
|
|
D003790||dental pulp necroses
|
|
D003790||gangrene dental pulp
|
|
D003790||gangrene pulp
|
|
D003790||gangrenes pulp
|
|
D003790||mummification pulp
|
|
D003790||mummifications pulp
|
|
D003790||necroses dental pulp
|
|
D003790||necroses pulp
|
|
D003790||necrosis dental pulp
|
|
D003790||necrosis pulp
|
|
D003790||pulp autolyses dental
|
|
D003790||pulp autolysis dental
|
|
D003790||pulp gangrene
|
|
D003790||pulp gangrene dental
|
|
D003790||pulp gangrenes
|
|
D003790||pulp mummification
|
|
D003790||pulp mummifications
|
|
D003790||pulp necroses
|
|
D003790||pulp necroses dental
|
|
D003790||pulp necrosis
|
|
D003790||pulp necrosis dental
|
|
D013106||sphingolipidoses
|
|
D013106||sphingolipidosis
|
|
D013106||sphingolipid storage disease
|
|
D013106||sphingolipid storage diseases
|
|
D013106||storage disease sphingolipid
|
|
D013106||storage diseases sphingolipid
|
|
D017085|604131||alpha thalassemia
|
|
D017085|604131||alpha thalassemias
|
|
D017085|604131||a thalassemia
|
|
D017085|604131||disease hemoglobin h
|
|
D017085|604131||hemoglobin h disease
|
|
D017085|604131||thalassemia alpha
|
|
C536126||non functioning pancreatic endocrine tumor
|
|
C536126||non functioning endocrine pancreatic tumors
|
|
C537458||meralgia paresthetica
|
|
C537458||bernhardt roth syndrome
|
|
C537458||lateral femoral cutaneous nerve entrapment
|
|
D051303||trigeminal autonomic cephalalgias
|
|
D051303||cephalalgias trigeminal autonomic
|
|
D051303||cephalalgia trigeminal autonomic
|
|
D051303||trigeminal autonomic cephalalgia
|
|
D013103||spherocytosis hereditary
|
|
D013103||hereditary spherocytoses
|
|
D013103||spherocytoses hereditary
|
|
D014435||typhoid fever
|
|
D014435||abdominal typhus
|
|
D014435||enteric fever
|
|
D014435||enteric fevers
|
|
D014435||fever enteric
|
|
D014435||fevers enteric
|
|
D014435||fevers typhoid
|
|
D014435||fever typhoid
|
|
D014435||typhoid
|
|
D014435||typhoid fevers
|
|
D014435||typhoids
|
|
D014435||typhus abdominal
|
|
C580280||congenital methemoglobinemia
|
|
D051302||paroxysmal hemicrania
|
|
D051302||chronic paroxysmal hemicrania
|
|
D051302||chronic paroxysmal hemicranias
|
|
D051302||episodic paroxysmal hemicrania
|
|
D051302||episodic paroxysmal hemicranias
|
|
D051302||hemicrania chronic paroxysmal
|
|
D051302||hemicrania episodic paroxysmal
|
|
D051302||hemicrania paroxysmal
|
|
D051302||hemicranias chronic paroxysmal
|
|
D051302||hemicranias episodic paroxysmal
|
|
D051302||hemicranias paroxysmal
|
|
D051302||paroxysmal hemicrania chronic
|
|
D051302||paroxysmal hemicrania episodic
|
|
D051302||paroxysmal hemicranias
|
|
D051302||paroxysmal hemicranias chronic
|
|
D051302||paroxysmal hemicranias episodic
|
|
D002429||cecal diseases
|
|
D002429||cecal disease
|
|
D002429||disease cecal
|
|
D002429||diseases cecal
|
|
C567289||chromosome 2p16 1 p15 deletion syndrome
|
|
C563412|175050||juvenile polyposis with hereditary hemorrhagic telangiectasia
|
|
C563412|175050||jphht syndrome
|
|
C563412|175050||jp hht syndrome
|
|
C563412|175050||jpht
|
|
C563412|175050||jpshht
|
|
C563412|175050||jps hht
|
|
C563412|175050||juvenile polyposis hereditary hemorrhagic telangiectasia syndrome
|
|
C563412|175050||polyposis generalized juvenile with pulmonary arteriovenous malformation
|
|
C563412|175050||telangiectasia hereditary hemorrhagic with juvenile polyposis coli
|
|
D003751||dental fistula
|
|
D003751||dental fistulas
|
|
D003751||fistula dental
|
|
D003751||fistula gingival
|
|
D003751||fistulas dental
|
|
D003751||fistulas gingival
|
|
D003751||gingival fistula
|
|
D003751||gingival fistulas
|
|
D002422||causalgia
|
|
D002422||causalgia syndrome
|
|
D002422||causalgia syndromes
|
|
D002422||complex regional pain syndrome type ii
|
|
D002422||crps type ii
|
|
D002422||deafferentation pain
|
|
D002422||pain deafferentation
|
|
D002422||syndrome causalgia
|
|
D002422||syndromes causalgia
|
|
D002422||type ii complex regional pain syndrome
|
|
231050||geleophysic dysplasia 1
|
|
231050||gphysd1
|
|
D003750||dental fissures
|
|
D003750||dental fissure
|
|
D003750||fissure dental
|
|
D003750||fissures dental
|
|
D014406||tularemia
|
|
D014406||francisella tularensis infection
|
|
D014406||francisella tularensis infections
|
|
D014406||infection francisella tularensis
|
|
D014406||infections francisella tularensis
|
|
D014406||tularemias
|
|
C567291||chromosome 1q21 1 deletion syndrome 1 35 mb
|
|
C567291||1q21 1 contiguous gene deletion
|
|
C567291||1q21 1 deletion
|
|
C567291||1q21 1 microdeletion
|
|
C567291||chromosome 1q21 1 deletion syndrome
|
|
C535334|600501||abcd syndrome
|
|
C535334|600501||abcds
|
|
C535334|600501||albinism black lock cell migration disorder of the neurocytes of the gut and deafness
|
|
C567290||chromosome 1q21 1 duplication syndrome
|
|
D006509|610424||hepatitis b
|
|
D006509|610424||hbv resistance to included
|
|
D006509|610424||hbv susceptibility to hepatitis b virus resistance to included
|
|
D006509|610424||hepatitis b virus susceptibility to
|
|
C538139|222900||sucrase isomaltase deficiency congenital
|
|
C538139|222900||congenital sucrase isomaltase deficiency
|
|
C538139|222900||congenital sucrose intolerance
|
|
C538139|222900||congenital sucrose isomaltase malabsorption
|
|
C538139|222900||congenital sucrose isomaltose malabsorption
|
|
C538139|222900||csid
|
|
C538139|222900||disaccharide intolerance 1
|
|
C538139|222900||disaccharide intolerance i
|
|
C538139|222900||si deficiency
|
|
C538139|222900||sucrase isomaltase deficiency
|
|
C538139|222900||sucrose intolerance congenital
|
|
C538139|222900||sucrose isomaltase malabsorption congenital
|
|
C538139|222900||sucrose isomaltose malabsorption congenital
|
|
C567299||hepatoblastoma caused by somatic mutation
|
|
C567298||craniofaciofrontodigital syndrome
|
|
C567298||cantu craniofaciofrontodigital syndrome
|
|
D014402||tuberous sclerosis
|
|
D014402||adenoma sebaceum
|
|
D014402||bourneville disease
|
|
D014402||bourneville phacomatosis
|
|
D014402||bourneville phakomatosis
|
|
D014402||bourneville pringle disease
|
|
D014402||bourneville pringle apos s disease
|
|
D014402||bourneville pringles disease
|
|
D014402||bourneville apos s disease
|
|
D014402||bourneville apos s syndrome
|
|
D014402||bourneville syndrome
|
|
D014402||cerebral scleroses
|
|
D014402||cerebral sclerosis
|
|
D014402||disease bourneville pringle
|
|
D014402||disease bourneville pringle apos s
|
|
D014402||epiloia
|
|
D014402||phacomatosis bourneville
|
|
D014402||phakomatosis bourneville
|
|
D014402||sclerosis cerebral
|
|
D014402||sclerosis tuberosa
|
|
D014402||sclerosis tuberose
|
|
D014402||sclerosis tuberous
|
|
D014402||syndrome bourneville
|
|
D014402||syndrome bourneville apos s
|
|
D014402|C565346|191100||tuberose sclerosis
|
|
D014402|C565346|191100||tuberous sclerosis complex
|
|
D014401||tuberculosis urogenital
|
|
D014401||tuberculoses urogenital
|
|
D014401||urogenital tuberculoses
|
|
D014401||urogenital tuberculosis
|
|
D014400||tuberculosis splenic
|
|
D014400||splenic tuberculoses
|
|
D014400||splenic tuberculosis
|
|
D014400||tuberculoses splenic
|
|
C538236|201810||adrenal hyperplasia 2
|
|
C538236|201810||3 alpha beta hsd deficiency
|
|
C538236|201810||3 alpha beta hydroxysteroid dehydrogenase deficiency
|
|
C538236|201810||3 alpha beta hydroxysteroid dehydrogenase type 2 deficiency of
|
|
C538236|201810||3 beta hydroxysteroid dehydrogenase type ii deficiency of
|
|
C538236|201810||adrenal hyperplasia ii
|
|
C538236|201810||hsdb
|
|
C538236|201810||hsdb3
|
|
C537400||pilotto syndrome
|
|
C537400||cleft lip and palate congenital heart disease scoliosis short stature and mental retardation
|
|
C537401||pineal teratoma
|
|
C537401||teratoma pineal
|
|
D003769||dental occlusion traumatic
|
|
D003769||dental occlusions traumatic
|
|
D003769||occlusion dental traumatic
|
|
D003769||occlusions traumatic dental
|
|
D003769||occlusion traumatic dental
|
|
D003769||traumatic dental occlusion
|
|
D003769||traumatic dental occlusions
|
|
C565969|202700||neutropenia severe congenital autosomal dominant 1
|
|
C565969|202700||neutropenia severe congenital 1 autosomal dominant
|
|
C565969|202700||scn1
|
|
D003763||dental leakage
|
|
D003763||dental leakages
|
|
D003763||leakage dental
|
|
D003763||leakages dental
|
|
215600|C566123|C565846||cirrhosis familial
|
|
215600|C566123|C565846||cirrhosis cryptogenic included
|
|
215600|C566123|C565846||cirrhosis familial with pulmonary hypertension included
|
|
215600|C566123|C565846||cirrhosis noncryptogenic susceptibility to included
|
|
215600|C566123|C565846||copper overload cirrhosis included
|
|
215600|C566123|C565846||copper toxicosis idiopathic included
|
|
215600|C566123|C565846||endemic tyrolean infantile cirrhosis included
|
|
215600|C566123|C565846||etic included
|
|
215600|C566123|C565846||icc included
|
|
215600|C566123|C565846||ict included
|
|
215600|C566123|C565846||indian childhood cirrhosis included
|
|
215600|C566123|C565846||sen syndrome included
|
|
215600|C566123|C565846||copper toxicosis idiopathic
|
|
C537451|300148||mehmo syndrome
|
|
C537451|300148||mehmo
|
|
C537451|300148||mental retardation epileptic seizures hypogonadism and hypogenitalism microcephaly and obesity
|
|
C537451|300148||mental retardation x linked syndromic 20
|
|
C537451|300148||mental retardation x linked syndromic 25
|
|
C537451|300148||mrxs20
|
|
C537451|300148||mrxs25
|
|
C537451|300148||x linked mehmo syndrome
|
|
D005168|227500||factor vii deficiency
|
|
D005168|227500||deficiencies factor vii
|
|
D005168|227500||deficiency factor vii
|
|
D005168|227500||f7 deficiency
|
|
D005168|227500||factor vii deficiencies
|
|
D005168|227500||hypoproconvertinemia
|
|
D005168|227500||hypoproconvertinemias
|
|
D001102||arbovirus infections
|
|
D001102||arbovirus infection
|
|
D001102||infection arbovirus
|
|
D001102||infections arbovirus
|
|
D001100||arachnoiditis
|
|
D001100||arachnoiditides
|
|
D001100||arachnoid membrane inflammation
|
|
D001100||arachnoid membrane inflammations
|
|
D001100||inflammation arachnoid membrane
|
|
D001100||inflammations arachnoid membrane
|
|
C538240|104530||amelogenesis imperfecta local hypoplastic form
|
|
C538240|104530||amelogenesis imperfecta hypoplastic type
|
|
C538240|104530||hypoplastic type amelogenesis imperfecta
|
|
C538240|104530||local hypoplastic type of amelogenesis imperfecta
|
|
C538240|104530||microdontia generalized
|
|
C538240|104530||microdontia generalized included
|
|
D002430||cecal neoplasms
|
|
D002430||cancer cecal
|
|
D002430||cancer of cecum
|
|
D002430||cancer of the cecum
|
|
D002430||cecal cancer
|
|
D002430||cecal neoplasm
|
|
D002430||neoplasm cecal
|
|
D002430||neoplasms cecal
|
|
C562815|222748||dihydropyrimidinase deficiency
|
|
C562815|222748||dph deficiency
|
|
C562815|222748||dpys deficiency
|
|
C536171|222730||dicarboxylicaminoaciduria
|
|
C536171|222730||dicarboxylic aminoaciduria
|
|
C536171|222730||dicarboxylic amino aciduria
|
|
C536171|222730||dicarboxylicamino aciduria
|
|
C536171|222730||glutamate and aspartate transport defect
|
|
C536171|222730||glutamate aspartate transport defect
|
|
C536171|222730||inborn error of glutamic and aspartate transport
|
|
D015746||abdominal pain
|
|
D015746||abdominal pains
|
|
D015746||pain abdominal
|
|
D015746||pains abdominal
|
|
D015745||granuloma foreign body
|
|
D015745||foreign body granuloma
|
|
D015745||foreign body granulomas
|
|
D015745||granulomas foreign body
|
|
C566441|610125||microphthalmia syndromic 5
|
|
C566441|610125||mcops5
|
|
C566441|610125||retinal dystrophy early onset and pituitary dysfunction included
|
|
D014412||tumor virus infections
|
|
D014412||fibroma shope
|
|
D014412||infections tumor virus
|
|
D014412||infection tumor virus
|
|
D014412||papilloma shope
|
|
D014412||shope fibroma
|
|
D014412||shope papilloma
|
|
D014412||tumor virus infection
|
|
C536573|112310||boomerang dysplasia
|
|
C536573|112310||boomerang like skeletal dysplasia
|
|
C536573|112310||dwarfism with short bowed rigid limbs and characteristic facies
|
|
C536573|112310||piepkorn dysplasia
|
|
C537411||burn mckeown syndrome
|
|
C537411||bilateral choanal atresia cardiac defects deafness and dysmorphic appearance
|
|
C567268||niemann pick disease intermediate protracted neurovisceral
|
|
C537412||burnett schwartz berberian syndrome
|
|
C537412||atrophodermia reticulata
|
|
C537412||atrophodermia reticulata symmetrica faciei
|
|
C537412||atrophodermia vermiculata
|
|
C537412||folliculitis ulerythematosa
|
|
C537412||folliculitis ulerythematosa reticulata
|
|
C537412||honeycomb atrophy
|
|
C537412||keratosis pilaris
|
|
C537412||keratosis pilaris atrophicans facies
|
|
C537412||ulerythema ophryogenes
|
|
C537412||ulerythema ophryogenesis
|
|
C537412||ulerythema ophryogenes with multiple congenital anomalies
|
|
C567267||niemann pick disease intermediate with visceral involvement and rapid progression
|
|
C563110|300004||proud syndrome
|
|
C563110|300004||acc with abnormal genitalia
|
|
C563110|300004||corpus callosum agenesis of with abnormal genitalia
|
|
D003731||dental caries
|
|
D003731||caries dental
|
|
D003731||carious dentin
|
|
D003731||carious dentins
|
|
D003731||decay dental
|
|
D003731||dental decay
|
|
D003731||dental white spot
|
|
D003731||dental white spots
|
|
D003731||dentin carious
|
|
D003731||dentins carious
|
|
D003731||spots white
|
|
D003731||spot white
|
|
D003731||white spot
|
|
D003731||white spot dental
|
|
D003731||white spots
|
|
D003731||white spots dental
|
|
D015715||corneal edema
|
|
D015715||corneal edemas
|
|
D015715||edema corneal
|
|
D015715||edemas corneal
|
|
C567886|278720||xeroderma pigmentosum complementation group c
|
|
C567886|278720||xeroderma pigmentosum iii
|
|
C567886|278720||xp3
|
|
C567886|278720||xpc
|
|
C567886|278720||xpcc
|
|
C567886|278720||xp group c
|
|
C580233||lactate dehydrogenase deficiency
|
|
C580233||deficiency of lactate dehydrogenase
|
|
C580233||lactate dehydrogenase subunit deficiencies
|
|
C580233||ldh deficiency
|
|
C566947|156200||mental retardation autosomal dominant 1
|
|
C566947|156200||chromosome 2q23 1 deletion syndrome included
|
|
C566947|156200||mrd1
|
|
C567275||craniodiaphyseal dysplasia autosomal dominant
|
|
C537405||growth and mental retardation mandibulofacial dysostosis microcephaly and cleft palate
|
|
C567274||deafness congenital and onychodystrophy autosomal dominant
|
|
C567581|300807||thrombophilia x linked due to factor ix defect
|
|
C567581|300807||deep venous thrombosis protection against included
|
|
C567581|300807||thph8
|
|
C537402||pinheiro freire maia miranda syndrome
|
|
C537402||trichodermodysplasia with dental alterations
|
|
C567276||coumarin sensitivity
|
|
C537408||brunoni syndrome
|
|
C537408||mesomelia radial hypoplasia bifid thumb unusual facies
|
|
C537408||mesomelic dwarfism skeletal abnormalities and ectodermal dysplasia
|
|
C567272||epidermolysis bullosa dystrophica with subcorneal cleavage
|
|
D002418||cattle diseases
|
|
D002418||bovine disease
|
|
D002418||bovine diseases
|
|
D002418||cattle disease
|
|
D002418||disease bovine
|
|
D002418||disease cattle
|
|
D002418||diseases bovine
|
|
D002418||diseases cattle
|
|
C537422||apparent mineralocorticoid excess
|
|
C537422||cortisol 11 beta ketoreductase deficiency
|
|
D003744||dental enamel hypoplasia
|
|
D003744||ageneses enamel
|
|
D003744||agenesis enamel
|
|
D003744||enamel ageneses
|
|
D003744||enamel agenesis
|
|
D003744||enamel hypoplasia
|
|
D003744||enamel hypoplasia dental
|
|
D003744||enamel hypoplasias
|
|
D003744||enamel hypoplastic
|
|
D003744||hypomineralization molar incisor
|
|
D003744||hypoplasia dental enamel
|
|
D003744||hypoplasia enamel
|
|
D003744||hypoplasias enamel
|
|
D003744||hypoplastic enamel
|
|
D003744||molar incisor hypomineralization
|
|
C567278||holoprosencephaly 10
|
|
D003741||dental deposits
|
|
D003741||dental deposit
|
|
D003741||deposit dental
|
|
D003741||deposits dental
|
|
D003741||materia alba
|
|
C563242|261000||intrinsic factor deficiency
|
|
C563242|261000||ifd
|
|
C563242|261000||pernicious anemia congenital due to defect of intrinsic factor
|
|
153100|D008209||lymphedema
|
|
153100|D008209||congenital familial lymphedema
|
|
153100|D008209||congenital hereditary lymphedema
|
|
153100|D008209||congenital hereditary lymphedemas
|
|
153100|D008209||congenital lymphedema primary
|
|
153100|D008209||congenital lymphedemas primary
|
|
153100|D008209||early onset lymphedema
|
|
153100|D008209||early onset lymphedemas
|
|
153100|D008209||hereditary lymphedema
|
|
153100|D008209||hereditary lymphedema 1
|
|
153100|D008209||hereditary lymphedema 1s
|
|
153100|D008209||hereditary lymphedema congenital
|
|
153100|D008209||hereditary lymphedemas
|
|
153100|D008209||hereditary lymphedemas congenital
|
|
153100|D008209||hereditary lymphedema type i
|
|
153100|D008209||lmph1a
|
|
153100|D008209||lymphedema congenital hereditary
|
|
153100|D008209||lymphedema early onset
|
|
153100|D008209||lymphedema hereditary
|
|
153100|D008209||lymphedema hereditary ia
|
|
153100|D008209||lymphedema nonne milroy
|
|
153100|D008209||lymphedema primary congenital
|
|
153100|D008209||lymphedemas
|
|
153100|D008209||lymphedemas congenital hereditary
|
|
153100|D008209||lymphedemas early onset
|
|
153100|D008209||lymphedemas hereditary
|
|
153100|D008209||lymphedemas primary congenital
|
|
153100|D008209||milroy disease
|
|
153100|D008209||milroy apos s disease
|
|
153100|D008209||milroys disease
|
|
153100|D008209||nonne milroy disease
|
|
153100|D008209||nonne milroy lymphedema
|
|
153100|D008209||nonne milroy meige disease
|
|
153100|D008209||pcl
|
|
153100|D008209||primary congenital lymphedema
|
|
153100|D008209||primary congenital lymphedemas
|
|
D050010||hyperthyroxinemia familial dysalbuminemic
|
|
D050010||dysalbuminemic hyperthyroxinemia familial
|
|
D050010||familial dysalbuminemic hyperthyroxinemia
|
|
C537413||burning mouth syndrome type 3
|
|
C537413||type 3 burning mouth syndrome
|
|
C580241|150250|C537873||larsen syndrome
|
|
C536520|314390||vacterl association with hydrocephaly x linked
|
|
C536520|314390||vacterl association with hydrocephalus x linked
|
|
C536520|314390||vacterl association x linked with or without hydrocephalus
|
|
C536520|314390||vacterl h x linked
|
|
C536520|314390||vacterlx
|
|
C536520|314390||x linked vacterl h syndrome
|
|
D011218|176270||prader willi syndrome
|
|
D011218|176270||labhart willi prader fanconi syndrome
|
|
D011218|176270||labhart willi syndrome
|
|
D011218|176270||prader labhart willi syndrome
|
|
D011218|176270||prader labhart willi syndrome prader willi syndrome chromosome region included
|
|
D011218|176270||prader willi like syndrome associated with chromosome 6 included
|
|
D011218|176270||pwcr included
|
|
D011218|176270||pws
|
|
D011218|176270||royer apos s syndrome
|
|
D011218|176270||royers syndrome
|
|
D011218|176270||royer syndrome
|
|
D011218|176270||syndrome labhart willi
|
|
D011218|176270||syndrome labhart willi prader fanconi
|
|
D011218|176270||syndrome prader labhart willi
|
|
D011218|176270||syndrome prader willi
|
|
D011218|176270||syndrome royer
|
|
D011218|176270||syndrome royer apos s
|
|
D011218|176270||syndrome willi prader
|
|
D011218|176270||willi prader syndrome
|
|
C537417||butyrylcholinesterase deficiency
|
|
C537417||acylcholine acylhydrolase deficiency
|
|
C537417||apnea postanesthetic
|
|
C537417||cholinesterase 2 deficiency
|
|
C537417||pseudocholinesterase deficiency
|
|
C537417||pseudocholinesterase e1 deficiency
|
|
C537417||succinylcholine sensitivity
|
|
C537417||suxamethonium sensitivity
|
|
D051346||mobility limitation
|
|
D051346||ambulation difficulty
|
|
D051346||ambulatory difficulty
|
|
D051346||difficulty ambulation
|
|
D051346||difficulty walking
|
|
D051346||limitation mobility
|
|
D051346||mobility limitations
|
|
C537418|211750||opitz trigonocephaly syndrome
|
|
C537418|211750||trigonocephaly syndrome
|
|
D003715||dengue
|
|
D003715||classical dengue
|
|
D003715||classical dengue fever
|
|
D003715||classical dengue fevers
|
|
D003715||classical dengues
|
|
D003715||dengue classical
|
|
D003715||dengue fever
|
|
D003715||dengue fever classical
|
|
D003715||dengue fevers classical
|
|
D003715||dengues classical
|
|
D003715||fever dengue
|
|
C567249||retinitis pigmentosa 46
|
|
C567249||retinitis pigmentosa autosomal recessive idh3b related
|
|
C562593|278780||xeroderma pigmentosum complementation group g
|
|
C562593|278780||cerebrooculofacioskeletal syndrome 3 included
|
|
C562593|278780||cofs3 included
|
|
C562593|278780||xeroderma pigmentosum vii
|
|
C562593|278780||xeroderma pigmentosum vii xp7 xeroderma pigmentosum type g cockayne syndrome included
|
|
C562593|278780||xpg
|
|
C562593|278780||xpgc
|
|
C562593|278780||xpg cs included
|
|
C562593|278780||xp group g
|
|
D020295||brain stem neoplasms
|
|
D020295||brainstem neoplasm
|
|
D020295||brain stem neoplasm
|
|
D020295||brainstem neoplasm primary
|
|
D020295||brainstem neoplasms
|
|
D020295||brainstem neoplasms primary
|
|
D020295||brain stem neoplasms primary
|
|
D020295||brainstem tumor
|
|
D020295||brain stem tumor
|
|
D020295||brainstem tumors
|
|
D020295||brain stem tumors
|
|
D020295||medullary neoplasm
|
|
D020295||medullary neoplasms
|
|
D020295||medullary tumor
|
|
D020295||medullary tumors
|
|
D020295||mesencephalic neoplasm
|
|
D020295||mesencephalic neoplasms
|
|
D020295||midbrain neoplasm
|
|
D020295||midbrain neoplasms
|
|
D020295||midbrain tumor
|
|
D020295||midbrain tumors
|
|
D020295||neoplasm brainstem
|
|
D020295||neoplasm brain stem
|
|
D020295||neoplasm medullary
|
|
D020295||neoplasm mesencephalic
|
|
D020295||neoplasm midbrain
|
|
D020295||neoplasm pontine
|
|
D020295||neoplasm primary brainstem
|
|
D020295||neoplasms brainstem
|
|
D020295||neoplasms brain stem
|
|
D020295||neoplasms brainstem primary
|
|
D020295||neoplasms medullary
|
|
D020295||neoplasms mesencephalic
|
|
D020295||neoplasms midbrain
|
|
D020295||neoplasms pontine
|
|
D020295||neoplasms primary brainstem
|
|
D020295||pontine neoplasm
|
|
D020295||pontine neoplasms
|
|
D020295||pontine tumor
|
|
D020295||pontine tumors
|
|
D020295||primary brainstem neoplasm
|
|
D020295||primary brainstem neoplasms
|
|
D020295||primary brain stem neoplasms
|
|
D020295||tumor brain stem
|
|
D020295||tumor medullary
|
|
D020295||tumor midbrain
|
|
D020295||tumor pontine
|
|
D020295||tumors medullary
|
|
D020295||tumors midbrain
|
|
D020295||tumors pontine
|
|
153880|D008269||macular edema
|
|
153880|D008269||central retinal edema cystoid
|
|
153880|D008269||cymd
|
|
153880|D008269||cystoid macular dystrophy
|
|
153880|D008269||cystoid macular edema
|
|
153880|D008269||cystoid macular edema postoperative
|
|
153880|D008269||dcmd
|
|
153880|D008269||edema cystoid macular
|
|
153880|D008269||edema macular
|
|
153880|D008269||irvine gass syndrome
|
|
153880|D008269||macular dystrophy dominant cystoid
|
|
153880|D008269||macular edema cystoid
|
|
153880|D008269||mddc
|
|
153880|D008269||syndrome irvine gass
|
|
D020294||myasthenic syndromes congenital
|
|
D020294||congenital myasthenia
|
|
D020294||congenital myasthenia gravis
|
|
D020294||congenital myasthenic syndrome
|
|
D020294||congenital myasthenic syndromes
|
|
D020294||congenital myasthenic syndromes postsynaptic
|
|
D020294||congenital myasthenic syndromes presynaptic
|
|
D020294||congenital slow channel myasthenic syndromes
|
|
D020294||gravi congenital myasthenia
|
|
D020294||myasthenia gravis congenital
|
|
D020294||myasthenic syndrome congenital
|
|
D020294||myasthenic syndromes congenital slow channel
|
|
D020294||postsynaptic congenital myasthenic syndromes
|
|
D020294||presynaptic congenital myasthenic syndromes
|
|
D020294||slow channel congenital myasthenic syndromes
|
|
D020294||syndrome congenital myasthenic
|
|
D020294||syndromes congenital myasthenic
|
|
D003711||demyelinating diseases
|
|
D003711||clinically isolated cns demyelinating syndrome
|
|
D003711||clinically isolated syndrome cns demyelinating
|
|
D003711||demyelinating disease
|
|
D003711||demyelinating disorder
|
|
D003711||demyelinating disorders
|
|
D003711||demyelination
|
|
D003711||demyelinations
|
|
D020293||vasculitis central nervous system
|
|
D020293||angiitis central nervous system
|
|
D020293||angiitis cerebral
|
|
D020293||angiitis granulomatous
|
|
D020293||arteritis granulomatous
|
|
D020293||arteritis postzoster
|
|
D020293||central nervous system angiitis
|
|
D020293||central nervous system vasculitis
|
|
D020293||cerebral angiitis
|
|
D020293||cerebral vasculitis
|
|
D020293||cns vasculitis
|
|
D020293||cns vasculitis primary
|
|
D020293||cns vasculitis secondary
|
|
D020293||granulomatous angiitis
|
|
D020293||granulomatous arteritis
|
|
D020293||postzoster arteritis
|
|
D020293||primary central nervous system vasculitis
|
|
D020293||primary cns vasculitis
|
|
D020293||secondary cns vasculitis
|
|
D020293||vasculitis cerebral
|
|
D020293||vasculitis cns
|
|
D020293||vasculitis cns secondary
|
|
D020293||vasculitis primary cns
|
|
D020293||vasculitis secondary cns
|
|
310440|C564093||myopathy x linked with excessive autophagy
|
|
310440|C564093||meax
|
|
310440|C564093||xmea
|
|
605285|C535813||neuropathy hereditary motor and sensory russe type
|
|
605285|C535813||charcot marie tooth disease autosomal recessive type 4g
|
|
605285|C535813||charcot marie tooth disease type 4g
|
|
605285|C535813||charcot marie tooth neuropathy type 4g
|
|
605285|C535813||cmt4g
|
|
605285|C535813||hereditary motor and sensory neuropathy russe type
|
|
605285|C535813||hmsnr
|
|
C566695|181400||scapuloperoneal syndrome neurogenic kaeser type
|
|
C566695|181400||kaeser syndrome
|
|
C566695|181400||scapuloperoneal syndrome neurogenic type of kaeser
|
|
C566695|181400||scpnk
|
|
C566695|181400||stark kaeser syndrome
|
|
D020299||intracranial hemorrhage hypertensive
|
|
D020299||cerebral hemorrhage hypertensive
|
|
D020299||cerebral hemorrhages hypertensive
|
|
D020299||cerebral hypertensive hemorrhage
|
|
D020299||cerebral hypertensive hemorrhages
|
|
D020299||hemorrhage cerebral hypertensive
|
|
D020299||hemorrhage hypertensive cerebral
|
|
D020299||hemorrhage hypertensive intracerebral
|
|
D020299||hemorrhage hypertensive intracranial
|
|
D020299||hemorrhage intracranial hypertensive
|
|
D020299||hemorrhages cerebral hypertensive
|
|
D020299||hemorrhages hypertensive cerebral
|
|
D020299||hemorrhages hypertensive intracerebral
|
|
D020299||hemorrhages hypertensive intracranial
|
|
D020299||hemorrhages intracranial hypertensive
|
|
D020299||hypertensive cerebral hemorrhage
|
|
D020299||hypertensive cerebral hemorrhages
|
|
D020299||hypertensive hemorrhage cerebral
|
|
D020299||hypertensive hemorrhage intracranial
|
|
D020299||hypertensive hemorrhages cerebral
|
|
D020299||hypertensive hemorrhages intracranial
|
|
D020299||hypertensive intracerebral hemorrhage
|
|
D020299||hypertensive intracerebral hemorrhages
|
|
D020299||hypertensive intracranial hemorrhage
|
|
D020299||hypertensive intracranial hemorrhages
|
|
D020299||intracerebral hemorrhage hypertensive
|
|
D020299||intracerebral hemorrhages hypertensive
|
|
D020299||intracranial hemorrhages hypertensive
|
|
D020299||intracranial hypertensive hemorrhage
|
|
D020299||intracranial hypertensive hemorrhages
|
|
C565302|605727||otosclerosis 2
|
|
C565302|605727||otsc2
|
|
C537204|609307||spinocerebellar ataxia 27
|
|
C537204|609307||cerebellar ataxia autosomal dominant fgf14 related
|
|
C537204|609307||sca27
|
|
C580212||agenesis of cerebellar vermis
|
|
C580212||cerebello oculo renal syndrome
|
|
C580212||familial aplasia of the vermis
|
|
C580212||joubert bolthauser syndrome
|
|
C536527|607636||van buchem disease type 2
|
|
C536527|607636||osteosclerosis of the skull and enlarged mandible
|
|
C536527|607636||vbch2
|
|
D003719||dens in dente
|
|
D003719||dens in dentes
|
|
D003719||dente dens in
|
|
D003719||dentes dens in
|
|
D003719||in dente dens
|
|
D003719||in dentes dens
|
|
D003728||dental calculus
|
|
D003728||calculus dental
|
|
D003728||tartar
|
|
C537855|608345||nystagmus 3 congenital autosomal dominant
|
|
C537855|608345||nys3
|
|
C567258||hypoadiponectinemia
|
|
C567258||adiponectin deficiency
|
|
C537205|610246||spinocerebellar ataxia 28
|
|
C537205|610246||sca28
|
|
C562707|201400||acth deficiency isolated
|
|
C562707|201400||iad
|
|
D015701||near drowning
|
|
D015701||drowning near
|
|
D015701||drownings near
|
|
D015701||near drownings
|
|
C580224||keratitis ichthyosis deafness syndrome
|
|
C580224||keratitis ichthyosis and deafness
|
|
C566968|611307||muscular dystrophy limb girdle type 2l
|
|
C566968|611307||lgmd2l
|
|
C567264||retinitis pigmentosa 7 with bull apos s eye maculopathy
|
|
D050033|218700|C566852||thyroid dysgenesis
|
|
D050033||agenesis thyroid
|
|
D050033||dysgenesis thyroid
|
|
D050033||ectopic thyroid
|
|
D050033||ectopic thyroids
|
|
D050033||hypoplasia thyroid
|
|
D050033|218700|C566852||thyroid agenesis
|
|
D050033|218700|C566852||thyroid ectopic
|
|
D050033|218700|C566852||thyroid hypoplasia
|
|
D050033||thyroids ectopic
|
|
C567263||retinitis pigmentosa 7 digenic
|
|
D050032||postpartum thyroiditis
|
|
D050032||post partum thyroiditides
|
|
D050032||postpartum thyroiditides
|
|
D050032||post partum thyroiditis
|
|
D050032||thyroiditides postpartum
|
|
D050032||thyroiditides post partum
|
|
D050032||thyroiditis postpartum
|
|
D050032||thyroiditis post partum
|
|
D020288|260500||papilloma choroid plexus
|
|
D020288|260500||choroid plexus papilloma
|
|
D020288|260500||choroid plexus papilloma choroid plexus carcinoma included
|
|
D020288|260500||choroid plexus papillomas
|
|
D020288|260500||cpc included
|
|
D020288|260500||cpp
|
|
D020288|260500||papilloma of choroid plexus
|
|
D020288|260500||papillomas choroid plexus
|
|
C567266||deafness autosomal dominant due to mutation in myo1a
|
|
D050035||sexual infantilism
|
|
D050035||genital infantilism
|
|
D050035||infantilism genital
|
|
D050035||infantilism sexual
|
|
C537784|132900||aortic aneurysm familial thoracic 4
|
|
C537784|132900||aat4
|
|
C537784|132900||aortic aneurysm aortic dissection and patent ductus arteriosus
|
|
C537784|132900||faa4
|
|
609041|C563807||spastic paraplegia 27 autosomal recessive
|
|
609041|C563807||spg27
|
|
D020274||autoimmune diseases of the nervous system
|
|
D020274||autoimmune disease neurologic
|
|
D020274||autoimmune diseases nervous system
|
|
D020274||autoimmune diseases neurologic
|
|
D020274||autoimmune disorders nervous system
|
|
D020274||autoimmune disorders of the nervous system
|
|
D020274||autoimmune nervous system diseases
|
|
D020274||disease neurologic autoimmune
|
|
D020274||diseases neurologic autoimmune
|
|
D020274||immune diseases nervous system
|
|
D020274||immune disorders nervous system
|
|
D020274||nervous system autoimmune diseases
|
|
D020274||nervous system immune diseases
|
|
D020274||nervous system immune disorders
|
|
D020274||neurologic autoimmune disease
|
|
D020274||neurologic autoimmune diseases
|
|
C567277|601544||deafness autosomal dominant 3a
|
|
C567277|601544||dfna3a
|
|
D019283||pancreatitis acute necrotizing
|
|
D019283||acute necrotizing pancreatitis
|
|
D019283||necrotizing pancreatitis acute
|
|
C567224||chromosome 22q11 2 microduplication syndrome
|
|
C567224||22q11 2 duplication
|
|
C567224||chromosome 22q11 2 duplication syndrome
|
|
D020271||heredodegenerative disorders nervous system
|
|
D020271||degenerative disease nervous system hereditary
|
|
D020271||degenerative hereditary diseases nervous system
|
|
D020271||degenerative hereditary disorders nervous system
|
|
D020271||disease hereditary neurodegenerative
|
|
D020271||disease neurodegenerative hereditary
|
|
D020271||diseases hereditary neurodegenerative
|
|
D020271||diseases neurodegenerative hereditary
|
|
D020271||hereditary degenerative disorders nervous system
|
|
D020271||hereditary disease neurodegenerative
|
|
D020271||hereditary diseases neurodegenerative
|
|
D020271||hereditary neurodegenerative disease
|
|
D020271||hereditary neurodegenerative diseases
|
|
D020271||nervous system degenerative hereditary diseases
|
|
D020271||nervous system diseases degenerative hereditary
|
|
D020271||nervous system hereditary degenerative diseases
|
|
D020271||neurodegenerative disease hereditary
|
|
D020271||neurodegenerative diseases hereditary
|
|
D020271||neurodegenerative hereditary disease
|
|
D020271||neurodegenerative hereditary diseases
|
|
D019282||wasting syndrome
|
|
D019282||wasting disease
|
|
D019282||wasting diseases
|
|
D019282||wasting syndromes
|
|
D052537|607616||niemann pick disease type b
|
|
D052537|607616||niemann pick disease adult non neuronopathic
|
|
D052537|607616||niemann pick disease intermediate with visceral involvement and rapid progression included
|
|
D052537|607616||niemann pick disease non neuronopathic type
|
|
D052537|607616||niemann pick disease type e
|
|
D052537|607616||niemann pick disease type e included
|
|
D052537|607616||niemann pick disease type f included
|
|
D052537|607616||niemann pick disease visceral
|
|
D052537|607616||niemann pick apos s disease type b
|
|
D052537|607616||niemann pick apos s disease type e
|
|
D052537|607616||type b niemann pick disease
|
|
D020270||alcohol withdrawal seizures
|
|
D020270||alcoholic seizure
|
|
D020270||alcoholic seizures
|
|
D020270||alcohol withdrawal induced major motor seizure
|
|
D020270||alcohol withdrawal induced seizure
|
|
D020270||alcohol withdrawal induced seizures
|
|
D020270||alcohol withdrawal induced status epilepticus
|
|
D020270||alcohol withdrawal seizure
|
|
D020270||major motor seizure alcohol withdrawal induced
|
|
D020270||seizure alcoholic
|
|
D020270||seizure alcohol withdrawal
|
|
D020270||seizure alcohol withdrawal induced
|
|
D020270||seizures alcoholic
|
|
D020270||seizures alcohol withdrawal
|
|
D020270||seizures alcohol withdrawal induced
|
|
D020270||status epilepticus alcohol withdrawal induced
|
|
D020270||withdrawal induced seizure alcohol
|
|
D020270||withdrawal induced seizures alcohol
|
|
D020270||withdrawal seizure alcohol
|
|
D020270||withdrawal seizures alcohol
|
|
C565705|610199||diabetes mellitus neonatal with congenital hypothyroidism
|
|
C565705|610199||ndh syndrome
|
|
C563984|108770||atrial standstill
|
|
C563984|108770||atrial cardiomyopathy with heart block
|
|
C563984|108770||atrial standstill 1
|
|
C563984|108770||atrst1
|
|
C563984|108770||cardiomyopathy familial with conduction disturbance
|
|
C537480|254130||miyoshi myopathy
|
|
C537480|254130||miyoshi distal myopathy
|
|
C537480|254130||miyoshi muscular dystrophy 1
|
|
C537480|254130||mmd1
|
|
C537480|254130||muscular dystrophy distal late onset autosomal recessive
|
|
D020279||hereditary central nervous system demyelinating diseases
|
|
D020279||central nervous system demyelinating diseases hereditary
|
|
D020279||central nervous system demyelinating hereditary diseases
|
|
D020279||central nervous system hereditary demyelinating diseases
|
|
D020279||demyelinating central nervous system diseases hereditary
|
|
D020279||demyelinating diseases central nervous system hereditary
|
|
D020279||hereditary demyelinating diseases central nervous system
|
|
D020278||demyelinating autoimmune diseases cns
|
|
D020278||autoimmune demyelinating diseases central nervous system
|
|
D020278||autoimmune demyelinating diseases cerebral
|
|
D020278||autoimmune demyelinating diseases cns
|
|
D020278||autoimmune demyelinating diseases spinal cord
|
|
D020278||autoimmune demyelinating disorders cns
|
|
D020278||autoimmune diseases demyelinating brain
|
|
D020278||brain autoimmune demyelinating diseases
|
|
D020278||cerebral demyelinating diseases autoimmune
|
|
D020278||cns autoimmune demyelinating disorders
|
|
D020278||cns demyelinating autoimmune diseases
|
|
D020278||demyelinating autoimmune diseases brain
|
|
D020278||demyelinating autoimmune diseases central nervous system
|
|
D020278||demyelinating autoimmune diseases cerebral
|
|
D020278||demyelinating autoimmune diseases spinal cord
|
|
D020278||demyelinating autoimmune disorders cns
|
|
D020278||demyelinating disease autoimmune cns
|
|
D020278||spinal cord demyelinating autoimmune diseases
|
|
D020277||polyradiculoneuropathy chronic inflammatory demyelinating
|
|
D020277||chronic inflammatory demyelinating polyradiculoneuropathy
|
|
D020277||chronic inflammatory polyradiculoneuropathies
|
|
D020277||chronic inflammatory polyradiculoneuropathy
|
|
D020277||chronic inflammatory polyradiculopathies
|
|
D020277||chronic inflammatory polyradiculopathy
|
|
D020277||cidp
|
|
D020277||inflammatory polyradiculopathies chronic
|
|
D020277||inflammatory polyradiculopathy chronic
|
|
D020277||polyneuropathy inflammatory demyelinating chronic
|
|
D020277||polyradiculoneuropathies chronic inflammatory
|
|
D020277||polyradiculoneuropathy chronic inflammatory
|
|
D020277||polyradiculopathies chronic inflammatory
|
|
D020277||polyradiculopathy chronic inflammatory
|
|
256370||nephrotic syndrome type 4
|
|
256370||nphs4
|
|
C563923|608471||corneal dystrophy lattice type iiia
|
|
C563923|608471||cdl3a
|
|
C563923|608471||lattice corneal dystrophy type iiia
|
|
D015470|601626||leukemia myeloid acute
|
|
D015470|601626||acute myeloblastic leukemia
|
|
D015470|601626||acute myeloblastic leukemias
|
|
D015470|601626||acute myelocytic leukemia
|
|
D015470|601626||acute myelocytic leukemias
|
|
D015470|601626||acute myelogenous leukemia
|
|
D015470|601626||acute myelogenous leukemias
|
|
D015470|601626||acute myeloid leukemia
|
|
D015470|601626||acute myeloid leukemias
|
|
D015470|601626||acute myeloid leukemia with maturation
|
|
D015470|601626||acute myeloid leukemia without maturation
|
|
D015470|601626||acute nonlymphoblastic leukemia
|
|
D015470|601626||acute nonlymphoblastic leukemias
|
|
D015470|601626||acute nonlymphocytic leukemia
|
|
D015470|601626||acute nonlymphocytic leukemias
|
|
D015470|601626||aml
|
|
D015470|601626||anll
|
|
D015470|601626||leukemia acute myeloblastic
|
|
D015470|601626||leukemia acute myelocytic
|
|
D015470|601626||leukemia acute myelogenous
|
|
D015470|601626||leukemia acute myelogenous leukemia acute myeloid susceptibility to included
|
|
D015470|601626||leukemia acute myeloid
|
|
D015470|601626||leukemia acute nonlymphoblastic
|
|
D015470|601626||leukemia acute nonlymphocytic
|
|
D015470|601626||leukemia myeloblastic acute
|
|
D015470|601626||leukemia myelocytic acute
|
|
D015470|601626||leukemia myelogenous acute
|
|
D015470|601626||leukemia myeloid acute m1
|
|
D015470|601626||leukemia myeloid acute m2
|
|
D015470|601626||leukemia nonlymphoblastic acute
|
|
D015470|601626||leukemia nonlymphocytic acute
|
|
D015470|601626||leukemias acute myeloblastic
|
|
D015470|601626||leukemias acute myelocytic
|
|
D015470|601626||leukemias acute myelogenous
|
|
D015470|601626||leukemias acute myeloid
|
|
D015470|601626||leukemias acute nonlymphoblastic
|
|
D015470|601626||leukemias acute nonlymphocytic
|
|
D015470|601626||myeloblastic leukemia acute
|
|
D015470|601626||myeloblastic leukemias acute
|
|
D015470|601626||myelocytic leukemia acute
|
|
D015470|601626||myelocytic leukemias acute
|
|
D015470|601626||myelogenous leukemia acute
|
|
D015470|601626||myelogenous leukemias acute
|
|
D015470|601626||myeloid leukemia acute
|
|
D015470|601626||myeloid leukemia acute m1
|
|
D015470|601626||myeloid leukemia acute m2
|
|
D015470|601626||myeloid leukemias acute
|
|
D015470|601626||nonlymphoblastic leukemia acute
|
|
D015470|601626||nonlymphoblastic leukemias acute
|
|
D015470|601626||nonlymphocytic leukemia acute
|
|
D015470|601626||nonlymphocytic leukemias acute
|
|
312612|C564065||retinitis pigmentosa 6
|
|
312612|C564065||retinitis pigmentosa x linked recessive 6
|
|
312612|C564065||rp6
|
|
C567232||chromosome 15q26 qter deletion syndrome
|
|
C567232||drayer syndrome
|
|
D052517|272200||multiple sulfatase deficiency disease
|
|
D052517|272200||juvenile sulfatidoses
|
|
D052517|272200||juvenile sulfatidosis
|
|
D052517|272200||msd
|
|
D052517|272200||mucosulfatidosis
|
|
D052517|272200||multiple sulfatase deficiencies
|
|
D052517|272200||multiple sulfatase deficiency
|
|
D052517|272200||multiple sulphatase deficiency disease
|
|
D052517|272200||sulfatidoses juvenile
|
|
D052517|272200||sulfatidosis juvenile
|
|
D052517|272200||sulfatidosis juvenile austin type
|
|
D020265||lead poisoning nervous system adult
|
|
D020265||adult neurologic saturnism
|
|
D020265||lead induced nervous system diseases adult
|
|
D020265||lead induced polyneuropathies
|
|
D020265||lead induced polyneuropathy
|
|
D020265||lead poisoning neurologic adult
|
|
D020265||lead polyneuropathy
|
|
D020265||nervous system diseases lead induced adult
|
|
D020265||nervous system poisoning lead adult
|
|
D020265||nervous system toxicity lead adult
|
|
D020265||neurologic saturnism adult
|
|
D020265||neurotoxicity syndrome lead adult
|
|
D020265||plumbism neurologic adult
|
|
D020265||poisoning lead nervous system adult
|
|
D020265||poisoning lead neurologic adult
|
|
D020265||polyneuropathies lead induced
|
|
D020265||polyneuropathy lead
|
|
D020265||polyneuropathy lead induced
|
|
D020265||saturnism adult neurologic
|
|
D003704||dementia
|
|
D003704||amentia
|
|
D003704||amentias
|
|
D003704||dementia familial
|
|
D003704||dementias
|
|
D003704||dementias familial
|
|
D003704||dementias senile paranoid
|
|
D003704||familial dementia
|
|
D003704||familial dementias
|
|
D003704||paranoid dementia senile
|
|
D003704||paranoid dementias senile
|
|
D003704||senile paranoid dementia
|
|
D003704||senile paranoid dementias
|
|
C567239||chromosome 6pter p24 deletion syndrome
|
|
D020264||lead poisoning nervous system childhood
|
|
D020264||childhood lead encephalopathy
|
|
D020264||childhood neurologic saturnism
|
|
D020264||childhood saturine encephalopathy
|
|
D020264||encephalopathy childhood lead
|
|
D020264||encephalopathy childhood saturine
|
|
D020264||lead encephalopathy childhood
|
|
D020264||lead induced nervous system disease childhood
|
|
D020264||lead poisoning neurologic childhood
|
|
D020264||nervous system disease lead induced childhood
|
|
D020264||nervous system poisoning lead childhood
|
|
D020264||neurologic saturnism childhood
|
|
D020264||neurotoxicity syndrome lead childhood
|
|
D020264||plumbism neurologic childhood
|
|
D020264||poisoning lead nervous system childhood
|
|
D020264||poisoning lead neurologic childhood
|
|
D020264||saturine encephalopathy childhood
|
|
D020264||saturnism childhood neurologic
|
|
D020263||lead poisoning nervous system
|
|
D020263||lead induced nervous system diseases
|
|
D020263||lead neurotoxicity syndrome
|
|
D020263||lead neurotoxicity syndromes
|
|
D020263||lead poisoning neurologic
|
|
D020263||nervous system diseases lead induced
|
|
D020263||nervous system plumbism
|
|
D020263||nervous system poisoning lead
|
|
D020263||neurologic lead poisoning
|
|
D020263||neurologic plumbism
|
|
D020263||neurotoxicity syndrome lead
|
|
D020263||neurotoxicity syndromes lead
|
|
D020263||plumbism nervous system
|
|
D020263||plumbism neurologic
|
|
D020263||poisoning lead nervous system
|
|
D020263||poisoning lead neurologic
|
|
D020263||syndrome lead neurotoxicity
|
|
D020263||syndromes lead neurotoxicity
|
|
D020262||mercury poisoning nervous system
|
|
D020262||encephalopathy mercury
|
|
D020262||inorganic mercury poisoning
|
|
D020262||mad hatter disease
|
|
D020262||mad hatter diseases
|
|
D020262||mad hatter apos s disease
|
|
D020262||mad hatters disease
|
|
D020262||mercurialism nervous system
|
|
D020262||mercurialism neurologic
|
|
D020262||mercurial neuroanesthenia
|
|
D020262||mercurial psychosis
|
|
D020262||mercury encephalopathy
|
|
D020262||mercury induced nervous system diseases
|
|
D020262||mercury neurotoxicity syndrome
|
|
D020262||mercury neurotoxicity syndromes
|
|
D020262||mercury poisoning inorganic
|
|
D020262||mercury poisoning neurologic
|
|
D020262||mercury poisoning organic
|
|
D020262||mercury psychosis
|
|
D020262||minamata disease
|
|
D020262||nervous system diseases mercury induced
|
|
D020262||nervous system mercurialism
|
|
D020262||nervous system poisoning mercury
|
|
D020262||neuroanesthenia mercurial
|
|
D020262||neurologic mercurialism
|
|
D020262||neurologic mercury poisoning
|
|
D020262||neurotoxicity syndrome mercury
|
|
D020262||neurotoxicity syndromes mercury
|
|
D020262||organic mercury poisoning
|
|
D020262||poisoning inorganic mercury
|
|
D020262||poisoning mercury nervous system
|
|
D020262||poisoning mercury neurologic
|
|
D020262||poisoning neurologic mercury
|
|
D020262||poisoning organic mercury
|
|
D020262||psychosis mercurial
|
|
D020262||psychosis mercury
|
|
D020262||syndrome mercury neurotoxicity
|
|
D020262||syndromes mercury neurotoxicity
|
|
D020262||system mercurialism nervous
|
|
D020261||arsenic poisoning
|
|
D020261||arsenical neurotoxicity syndrome
|
|
D020261||arsenical neurotoxicity syndromes
|
|
D020261||arsenic encephalopathies
|
|
D020261||arsenic encephalopathy
|
|
D020261||arsenic induced polyneuropathies
|
|
D020261||arsenic induced polyneuropathy
|
|
D020261||arsenic poisoning inorganic
|
|
D020261||arsenic poisoning nervous system
|
|
D020261||arsenic poisoning organic
|
|
D020261||arsenic poisonings
|
|
D020261||arsenic poisonings inorganic
|
|
D020261||arsenic poisonings organic
|
|
D020261||encephalopathies arsenic
|
|
D020261||encephalopathy arsenic
|
|
D020261||inorganic arsenic poisoning
|
|
D020261||inorganic arsenic poisonings
|
|
D020261||nervous system organic arsenic poisoning
|
|
D020261||nervous system poisoning arsenic
|
|
D020261||neurotoxicity syndrome arsenical
|
|
D020261||neurotoxicity syndromes arsenical
|
|
D020261||organic arsenic poisoning
|
|
D020261||organic arsenic poisoning nervous system
|
|
D020261||organic arsenic poisonings
|
|
D020261||poisoning arsenic
|
|
D020261||poisoning arsenic nervous system
|
|
D020261||poisoning inorganic arsenic
|
|
D020261||poisoning organic arsenic
|
|
D020261||poisonings arsenic
|
|
D020261||poisonings inorganic arsenic
|
|
D020261||poisonings organic arsenic
|
|
D020261||polyneuropathy arsenic induced
|
|
D020261||syndrome arsenical neurotoxicity
|
|
D020261||syndromes arsenical neurotoxicity
|
|
D020260||heavy metal poisoning nervous system
|
|
D020260||poisoning heavy metals nervous system
|
|
C563673|610370||diarrhea 4 malabsorptive congenital
|
|
C563673|610370||diar4
|
|
C563673|610370||enteric anendocrinosis
|
|
D049068||plagiocephaly nonsynostotic
|
|
D049068||deformational plagiocephalies
|
|
D049068||deformational plagiocephaly
|
|
D049068||nonsynostotic plagiocephaly
|
|
D049068||plagiocephalies deformational
|
|
D049068||plagiocephalies positional
|
|
D049068||plagiocephaly deformational
|
|
D049068||plagiocephaly positional
|
|
D049068||positional plagiocephalies
|
|
D049068||positional plagiocephaly
|
|
D019292||skull base neoplasms
|
|
D019292||neoplasm skull base
|
|
D019292||neoplasms skull base
|
|
D019292||skull base neoplasm
|
|
C535761|256300||nephrosis congenital
|
|
C535761|256300||cnf
|
|
C535761|256300||congenital nephrotic syndrome 1
|
|
C535761|256300||congenital nephrotic syndrome finnish type
|
|
C535761|256300||finnish congenital nephrosis
|
|
C535761|256300||nephrosis 1 congenital finnish type
|
|
C535761|256300||nephrotic syndrome congenital
|
|
C535761|256300||nephrotic syndrome idiopathic
|
|
C535761|256300||nephrotic syndrome type 1
|
|
C535761|256300||nphs1
|
|
D062025||organophosphate poisoning
|
|
D062025||organophosphate poisonings
|
|
D062025||organophosphorus poisoning
|
|
D062025||organothiophosphate poisoning
|
|
D062025||organothiophosphate poisonings
|
|
D062025||organothiophosphonate poisoning
|
|
D062025||organothiophosphonate poisonings
|
|
D062025||poisoning organophosphate
|
|
D062025||poisoning organothiophosphate
|
|
D062025||poisoning organothiophosphonate
|
|
D062025||poisonings organophosphate
|
|
D062025||poisonings organothiophosphate
|
|
D062025||poisonings organothiophosphonate
|
|
D016112|146700||ichthyosis vulgaris
|
|
D016112|146700||dominant ichthyosis vulgaris
|
|
D016112|146700||ichthyosis simplex
|
|
D016112|146700||ichthyosis simplices
|
|
D016112|146700||ichthyosis vulgaris dominant
|
|
D062026||alice in wonderland syndrome
|
|
D020269||alcoholic neuropathy
|
|
D020269||alcoholic axonal neuropathies
|
|
D020269||alcoholic axonal neuropathy
|
|
D020269||alcoholic neuropathies
|
|
D020269||alcoholic polyneuritides
|
|
D020269||alcoholic polyneuritis
|
|
D020269||alcoholic polyneuropathies
|
|
D020269||alcoholic polyneuropathy
|
|
D020269||alcohol induced peripheral neuropathies
|
|
D020269||alcohol induced peripheral neuropathy
|
|
D020269||alcohol induced polyneuropathies
|
|
D020269||alcohol induced polyneuropathy
|
|
D020269||alcohol related autonomic polyneuropathies
|
|
D020269||alcohol related autonomic polyneuropathy
|
|
D020269||alcohol related polyneuropathies
|
|
D020269||alcohol related polyneuropathy
|
|
D020269||autonomic polyneuropathies alcohol related
|
|
D020269||autonomic polyneuropathy alcohol related
|
|
D020269||axonal neuropathies alcoholic
|
|
D020269||axonal neuropathy alcoholic
|
|
D020269||neuropathies alcoholic
|
|
D020269||neuropathies alcoholic axonal
|
|
D020269||neuropathies alcohol induced peripheral
|
|
D020269||neuropathy alcoholic
|
|
D020269||neuropathy alcoholic axonal
|
|
D020269||neuropathy alcohol induced peripheral
|
|
D020269||peripheral neuropathies alcohol induced
|
|
D020269||peripheral neuropathy alcohol induced
|
|
D020269||polyneuritides alcoholic
|
|
D020269||polyneuritis alcoholic
|
|
D020269||polyneuropathies alcoholic
|
|
D020269||polyneuropathies alcohol induced
|
|
D020269||polyneuropathies alcohol related
|
|
D020269||polyneuropathies alcohol related autonomic
|
|
D020269||polyneuropathy alcoholic
|
|
D020269||polyneuropathy alcohol induced
|
|
D020269||polyneuropathy alcohol related
|
|
D020269||polyneuropathy alcohol related autonomic
|
|
D062027||linear iga bullous dermatosis
|
|
D062027||chronic bullous disease of childhood
|
|
D062027||dermatoses linear iga
|
|
D062027||dermatoses linear iga igg
|
|
D062027||dermatosis linear iga
|
|
D062027||dermatosis linear iga igg
|
|
D062027||drug induced linear iga bullous dermatosis
|
|
D062027||drug induced linear iga dermatosis
|
|
D062027||iga dermatoses linear
|
|
D062027||iga dermatosis linear
|
|
D062027||iga igg dermatoses linear
|
|
D062027||iga igg dermatosis linear
|
|
D062027||linear iga dermatoses
|
|
D062027||linear iga dermatosis
|
|
D062027||linear iga igg bullous dermatosis
|
|
D062027||linear iga igg dermatoses
|
|
D062027||linear iga igg dermatosis
|
|
D020268||alcohol induced disorders nervous system
|
|
D020268||alcohol abuse nervous system
|
|
D020268||ethanol induced disorders nervous system
|
|
D020268||ethanol induced nervous system disorders
|
|
D020268||ethyl alcohol abuse neurologic syndromes
|
|
D020268||nervous system disorders ethanol induced
|
|
D020267||mptp poisoning
|
|
D020267||mptp induced degeneration of the striatum
|
|
D020267||mptp induced parkinsonism
|
|
D020267||mptp neurotoxicity syndrome
|
|
D020267||mptp neurotoxicity syndromes
|
|
D020267||neurotoxicity syndrome mptp
|
|
D020267||neurotoxicity syndromes mptp
|
|
D020267||parkinsonism mptp induced
|
|
D020267||poisoning 1 methyl 4 phenyl 1 2 3 6 tetrahydropyridine
|
|
D020267||poisoning mptp
|
|
C563439|600808||enuresis nocturnal 2
|
|
C563439|600808||enur2
|
|
C580205||isodicentric chromosome 15 syndrome
|
|
C580205||duplication inversion 15q11
|
|
C580205||idic 15
|
|
C580205||inv dup 15
|
|
C580205||inverted duplication 15
|
|
C580205||isodicentric chromosome 15
|
|
C580205||non distal tetrasomy 15q
|
|
C580202||intranuclear rod myopathy
|
|
C580202||intranuclear nemaline rod myopathy
|
|
C580202||nemaline myopathy with exclusively intranuclear rods
|
|
C538356|601224||potocki shaffer syndrome
|
|
C538356|601224||chromosome 11p11 2 deletion syndrome
|
|
C538356|601224||defect11 syndrome
|
|
C538356|601224||deletion of chromosome 11p11 2
|
|
C538356|601224|133701||exostoses multiple type ii
|
|
C538356|601224||p11pds
|
|
C538356|601224||proximal 11p deletion syndrome
|
|
D012512|612219||sarcoma ewing
|
|
D012512|612219||askin tumor included
|
|
D012512|612219||es
|
|
D012512|612219||ewing sarcoma
|
|
D012512|612219||ewing apos s sarcoma
|
|
D012512|612219||ewings sarcoma
|
|
D012512|612219||ewing apos s tumor
|
|
D012512|612219||ewings tumor
|
|
D012512|612219||ewing tumor
|
|
D012512|612219||neuroepithelioma peripheral included
|
|
D012512|612219||pne included
|
|
D012512|612219||sarcoma ewings
|
|
D012512|612219||sarcoma ewing apos s
|
|
D012512|612219||tumor ewing
|
|
D012512|612219||tumor ewing apos s
|
|
177000|D046351||protoporphyria erythropoietic
|
|
177000|D046351||deficiencies ferrochelatase
|
|
177000|D046351||deficiencies heme synthetase
|
|
177000|D046351||deficiency ferrochelatase
|
|
177000|D046351||deficiency heme synthetase
|
|
177000|D046351||epp
|
|
177000|D046351||erythrohepatic protoporphyria
|
|
177000|D046351||erythropoietic protoporphyria
|
|
177000|D046351||erythropoietic protoporphyrias
|
|
177000|D046351||ferrochelatase deficiencies
|
|
177000|D046351||ferrochelatase deficiency
|
|
177000|D046351||heme synthetase deficiencies
|
|
177000|D046351||heme synthetase deficiency
|
|
177000|D046351||protoporphyrias erythropoietic
|
|
177000|D046351||synthetase deficiencies heme
|
|
177000|D046351||synthetase deficiency heme
|
|
D020254||tooth ankylosis
|
|
D020254||ankyloses dental
|
|
D020254||ankyloses dentoalveolar
|
|
D020254||ankyloses tooth
|
|
D020254||ankylosis dental
|
|
D020254||ankylosis dentoalveolar
|
|
D020254||ankylosis of teeth
|
|
D020254||ankylosis tooth
|
|
D020254||dental ankyloses
|
|
D020254||dental ankylosis
|
|
D020254||dentoalveolar ankyloses
|
|
D020254||dentoalveolar ankylosis
|
|
D020254||teeth ankyloses
|
|
D020254||teeth ankylosis
|
|
D020254||tooth ankyloses
|
|
D020252||gastric antral vascular ectasia
|
|
D020252||antral vascular ectasia
|
|
D020252||antral vascular ectasias
|
|
D020252||ectasia antral vascular
|
|
D020252||ectasias antral vascular
|
|
D020252||stomachs watermelon
|
|
D020252||stomach watermelon
|
|
D020252||vascular ectasia antral
|
|
D020252||vascular ectasias antral
|
|
D020252||watermelon stomach
|
|
D020252||watermelon stomachs
|
|
D020250||postoperative nausea and vomiting
|
|
D020250||emeses postoperative
|
|
D020250||emesis postoperative
|
|
D020250||nausea and vomiting postoperative
|
|
D020250||nausea postoperative
|
|
D020250||ponv
|
|
D020250||postoperative emeses
|
|
D020250||postoperative emesis
|
|
D020250||postoperative nausea
|
|
D020250||postoperative vomiting
|
|
D020250||vomiting postoperative
|
|
D019263||dysthymic disorder
|
|
D019263||disorder dysthymic
|
|
D019263||dysthymic disorders
|
|
D020258||neurotoxicity syndromes
|
|
D020258||encephalitides toxic
|
|
D020258||encephalitis toxic
|
|
D020258||encephalopathies toxic
|
|
D020258||encephalopathy toxic
|
|
D020258||nervous system poisoning
|
|
D020258||nervous system poisonings
|
|
D020258||neurotoxic disorder
|
|
D020258||neurotoxic disorders
|
|
D020258||neurotoxicity syndrome
|
|
D020258||neurotoxin disease
|
|
D020258||neurotoxin diseases
|
|
D020258||neurotoxin disorder
|
|
D020258||neurotoxin disorders
|
|
D020258||poisoning nervous system
|
|
D020258||poisonings nervous system
|
|
D020258||syndrome neurotoxicity
|
|
D020258||syndromes neurotoxicity
|
|
D020258||toxic encephalitides
|
|
D020258||toxic encephalitis
|
|
D020258||toxic encephalopathies
|
|
D020258||toxic encephalopathy
|
|
D020257||ventricular remodeling
|
|
D020257||cardiac remodelings ventricular
|
|
D020257||cardiac remodeling ventricular
|
|
D020257||left ventricle remodeling
|
|
D020257||left ventricle remodelings
|
|
D020257||left ventricular remodeling
|
|
D020257||left ventricular remodelings
|
|
D020257||myocardial remodelings ventricular
|
|
D020257||myocardial remodeling ventricular
|
|
D020257||remodeling left ventricle
|
|
D020257||remodeling left ventricular
|
|
D020257||remodelings left ventricle
|
|
D020257||remodelings left ventricular
|
|
D020257||remodelings ventricle
|
|
D020257||remodelings ventricular
|
|
D020257||remodelings ventricular cardiac
|
|
D020257||remodelings ventricular myocardial
|
|
D020257||remodeling ventricle
|
|
D020257||remodeling ventricular
|
|
D020257||remodeling ventricular cardiac
|
|
D020257||remodeling ventricular myocardial
|
|
D020257||ventricle remodeling
|
|
D020257||ventricle remodeling left
|
|
D020257||ventricle remodelings
|
|
D020257||ventricle remodelings left
|
|
D020257||ventricular cardiac remodeling
|
|
D020257||ventricular cardiac remodelings
|
|
D020257||ventricular myocardial remodeling
|
|
D020257||ventricular myocardial remodelings
|
|
D020257||ventricular remodeling left
|
|
D020257||ventricular remodelings
|
|
D020257||ventricular remodelings left
|
|
C567209||mental retardation joint hypermobility and skin laxity with or without metabolic abnormalities
|
|
D020256||choroidal neovascularization
|
|
D020256||choroidal neovascularizations
|
|
D020256||choroid neovascularization
|
|
D020256||choroid neovascularizations
|
|
D020256||neovascularization choroid
|
|
D020256||neovascularization choroidal
|
|
D020255||vitreous detachment
|
|
D020255||detachment posterior vitreous
|
|
D020255||detachments posterior vitreous
|
|
D020255||detachments vitreous
|
|
D020255||detachment vitreous
|
|
D020255||posterior vitreous detachment
|
|
D020255||posterior vitreous detachments
|
|
D020255||vitreous detachment posterior
|
|
D020255||vitreous detachments
|
|
D020255||vitreous detachments posterior
|
|
168600||parkinson disease late onset
|
|
168600||park
|
|
168600||pd
|
|
C573023|151001||lentiginosis profusa
|
|
C573023|151001||lentiginosis diffuse
|
|
C573023|151001||lentiginosis generalized
|
|
C573023|151001||lentiginosis inherited patterned
|
|
168601||parkinson disease 1 autosomal dominant
|
|
168601||atypical parkinson disease included
|
|
168601||park1
|
|
168601||parkinson disease 1 autosomal dominant lewy body
|
|
612561|C538442||diamond blackfan anemia 6
|
|
612561||dba6
|
|
D007280||disorders of environmental origin
|
|
C543241||cardiomyopathy fatal fetal due to myocardial calcification
|
|
C543241||myocardial calcifications resulting in intrauterine fetal death
|
|
D020243||infarction anterior cerebral artery
|
|
D020243||aca infarction
|
|
D020243||aca infarctions
|
|
D020243||anterior cerebral artery infarction
|
|
D020243||anterior cerebral artery stroke
|
|
D020243||anterior cerebral artery syndrome
|
|
D020243||artery infarction heubner
|
|
D020243||artery infarction heubner apos s
|
|
D020243||heubner artery infarction
|
|
D020243||heubner apos s artery infarction
|
|
D020243||heubners artery infarction
|
|
D020243||infarction aca
|
|
D020243||infarction anterior cerebral artery circulation
|
|
D020243||infarction anterior cerebral artery distribution
|
|
D020243||infarction heubner artery
|
|
D020243||infarction heubner apos s artery
|
|
D020243||infarctions aca
|
|
D020243||stroke anterior cerebral artery
|
|
D020243||syndrome anterior cerebral artery
|
|
D020242||encephalomyelitis eastern equine
|
|
D020242||eastern equine encephalitides
|
|
D020242||eastern equine encephalitis
|
|
D020242||eastern equine encephalomyelitides
|
|
D020242||eastern equine encephalomyelitis
|
|
D020242||encephalitides eastern equine
|
|
D020242||encephalitis eastern equine
|
|
D020242||encephalomyelitides eastern equine
|
|
D020242||equine encephalitides eastern
|
|
D020242||equine encephalitis eastern
|
|
D020242||equine encephalomyelitides eastern
|
|
D020242||equine encephalomyelitis eastern
|
|
D020241||encephalomyelitis western equine
|
|
D020241||encephalitis western equine
|
|
D020241||equine encephalitis western
|
|
D020241||western equine encephalitis
|
|
D020241||western equine encephalomyelitis
|
|
C567219||deafness autosomal recessive 36 without vestibular involvement
|
|
D020240||apraxia ideomotor
|
|
D020240||apraxia classic
|
|
D020240||apraxia ideokinetic
|
|
D020240||apraxia limb kinetic
|
|
D020240||apraxias classic
|
|
D020240||apraxias ideokinetic
|
|
D020240||apraxias ideomotor
|
|
D020240||apraxias limb kinetic
|
|
D020240||apraxias transcortical
|
|
D020240||apraxia transcortical
|
|
D020240||classic apraxia
|
|
D020240||classic apraxias
|
|
D020240||dyspraxia ideomotor
|
|
D020240||dyspraxias ideomotor
|
|
D020240||ideokinetic apraxia
|
|
D020240||ideokinetic apraxias
|
|
D020240||ideomotor apraxia
|
|
D020240||ideomotor apraxias
|
|
D020240||ideomotor dyspraxia
|
|
D020240||ideomotor dyspraxias
|
|
D020240||kinetic apraxia limb
|
|
D020240||kinetic apraxias limb
|
|
D020240||limb kinetic apraxia
|
|
D020240||limb kinetic apraxias
|
|
D020240||transcortical apraxia
|
|
D020240||transcortical apraxias
|
|
C563691|609889||alpha beta t cell lymphopenia with gamma delta t cell expansion severe cytomegalovirus infection and autoimmunity
|
|
D063371||myringosclerosis
|
|
D063371||myringoscleroses
|
|
D063371||tympanoscleroses
|
|
D063371||tympanosclerosis
|
|
182920||myopathy spheroid body
|
|
C565260|606082||goiter multinodular 3
|
|
C565260|606082||mng3
|
|
118450|D016738||alagille syndrome
|
|
118450|D016738||ahd
|
|
118450|D016738||alagille apos s syndrome
|
|
118450|D016738||alagilles syndrome
|
|
118450|D016738||alagille syndrome 1
|
|
118450|D016738||alagille syndrome 2
|
|
118450|D016738||alagille watson syndrome
|
|
118450|D016738||algs
|
|
118450|D016738||algs1
|
|
118450|D016738||algs2
|
|
118450|D016738||arteriohepatic dysplasia
|
|
118450|D016738||arteriohepatic dysplasia ahd
|
|
118450|D016738||aws
|
|
118450|D016738||cardiovertebral syndrome
|
|
118450|D016738||cholestasis with peripheral pulmonary stenosis
|
|
118450|D016738||ductular hypoplasia hepatic
|
|
118450|D016738||dysplasia arteriohepatic
|
|
118450|D016738||dysplasia arteriohepatic ahd
|
|
118450|D016738||hepatic ductular hypoplasia
|
|
118450|D016738||hepatic ductular hypoplasia syndromatic
|
|
118450|D016738||hepatofacioneurocardiovertebral syndrome
|
|
118450|D016738||hypoplasia hepatic ductular
|
|
118450|D016738||paucity of interlobular bile ducts
|
|
118450|D016738||syndrome alagille
|
|
118450|D016738||syndrome alagille apos s
|
|
118450|D016738||syndrome alagille watson
|
|
118450|D016738||syndrome cardiovertebral
|
|
118450|D016738||syndrome hepatofacioneurocardiovertebral
|
|
118450|D016738||syndrome watson alagille
|
|
118450|D016738||syndrome watson miller
|
|
118450|D016738||watson alagille syndrome
|
|
118450|D016738||watson miller syndrome
|
|
D052556|257220||niemann pick disease type c
|
|
D052556|257220||neurovisceral storage disease with vertical supranuclear ophthalmoplegia
|
|
D052556|257220||neurovisceral storage disease with vertical supranuclear ophthalmoplegia niemann pick disease type d included
|
|
D052556|257220||niemann pick disease chronic neuronopathic form
|
|
D052556|257220||niemann pick disease nova scotian
|
|
D052556|257220||niemann pick disease nova scotian type included
|
|
D052556|257220||niemann pick disease subacute juvenile form
|
|
D052556|257220||niemann pick disease type c1
|
|
D052556|257220||niemann pick disease type d
|
|
D052556|257220||niemann pick disease with cholesterol esterification block
|
|
D052556|257220||niemann pick disease without sphingomyelinase deficiency
|
|
D052556|257220||niemann pick apos s disease type c
|
|
D052556|257220||niemann pick apos s disease type d
|
|
D052556|257220||nova scotia niemann pick disease type d
|
|
D052556|257220||nova scotia type d form of niemann pick disease
|
|
D052556|257220||npc1
|
|
613884||chromosome 13q14 deletion syndrome
|
|
D020246||deep vein thromboses
|
|
D020246||deep vein thrombosis
|
|
D020246||deep venous thromboses
|
|
D020246||deep venous thrombosis
|
|
D020246||phlebothromboses
|
|
D020246||phlebothrombosis
|
|
D020246||thromboses deep vein
|
|
D020246||thromboses deep venous
|
|
D020246||thromboses venous
|
|
D020246||thrombosis deep vein
|
|
D020246||thrombosis deep venous
|
|
D020246||thrombosis venous
|
|
D020246||vein thromboses deep
|
|
D020246||vein thrombosis deep
|
|
D020246||venous thromboses
|
|
D020246||venous thromboses deep
|
|
D020246||venous thrombosis deep
|
|
D020244||infarction middle cerebral artery
|
|
D020244||cerebral infarction middle cerebral artery
|
|
D020244||embolic infarction middle cerebral artery
|
|
D020244||embolus middle cerebral artery
|
|
D020244||left middle cerebral artery infarction
|
|
D020244||mca infarction
|
|
D020244||middle cerebral artery circulation infarction
|
|
D020244||middle cerebral artery embolic infarction
|
|
D020244||middle cerebral artery embolus
|
|
D020244||middle cerebral artery infarction
|
|
D020244||middle cerebral artery occlusion
|
|
D020244||middle cerebral artery stroke
|
|
D020244||middle cerebral artery syndrome
|
|
D020244||middle cerebral artery thrombosis
|
|
D020244||middle cerebral artery thrombotic infarction
|
|
D020244||occlusion middle cerebral artery
|
|
D020244||right middle cerebral artery infarction
|
|
D020244||stroke middle cerebral artery
|
|
D020244||thrombosis middle cerebral artery
|
|
D020244||thrombotic infarction middle cerebral artery
|
|
D007299||insect bites and stings
|
|
D007299||bite insect
|
|
D007299||bites insect
|
|
D007299||insect bite
|
|
D007299||insect bites
|
|
D007299||insect sting
|
|
D007299||insect stings
|
|
D007299||sting insect
|
|
D007299||stings insect
|
|
612555||breast ovarian cancer familial susceptibility to 2
|
|
612555||breast cancer familial susceptibility to 2 included
|
|
612555||brovca2
|
|
612555||ovarian cancer familial susceptibility to 2 included
|
|
C536911|155240||familial medullary thyroid carcinoma
|
|
C536911|155240||fmtc
|
|
C536911|155240||medullary thyroid cancer familial
|
|
C536911|155240||mtc
|
|
C536911|155240||mtc1
|
|
C536911|155240||thyroid cancer familial medullary
|
|
C536911|155240||thyroid carcinoma familial medullary
|
|
612551||focal segmental glomerulosclerosis 4 susceptibility to
|
|
612551||end stage renal disease nondiabetic susceptibility to included
|
|
612551||fsgs4
|
|
D050072||white heifer disease
|
|
D050072||disease white heifer
|
|
201250||amdh
|
|
C567220||kallmann syndrome 5
|
|
C538261|608583||atrial fibrillation familial 1
|
|
C538261|608583||atfb1
|
|
C538261|608583||atrial fibrillation autosomal dominant
|
|
C538261|608583||autosomal dominant atrial fibrillation
|
|
C567221||microcephaly primary autosomal recessive 5 with simplified gyral pattern
|
|
D013584|300813||sarcoma synovial
|
|
D013584|300813||sarcomas synovial
|
|
D013584|300813||synovial sarcoma
|
|
D013584|300813||synovial sarcomas
|
|
D013584|300813||synovioma
|
|
D013584|300813||synoviomas
|
|
D020232||kluver bucy syndrome
|
|
D020232||syndrome kluver bucy
|
|
D020232||temporal lobectomy behavior syndrome
|
|
155310|D007418||visceral myopathy
|
|
155310||infantile visceral myopathy
|
|
155310|C563597||megaduodenum and or megacystis
|
|
155310||mmih
|
|
155310||vscm
|
|
C566584|602086||arrhythmogenic right ventricular dysplasia familial 3
|
|
C566584|602086||arrhythmogenic right ventricular cardiomyopathy 3
|
|
C566584|602086||arvc3
|
|
C566584|602086||arvd3
|
|
D020230||serotonin syndrome
|
|
D020230||serotonin syndromes
|
|
D020230||syndrome serotonin
|
|
D020230||syndromes serotonin
|
|
D020238||prosopagnosia
|
|
D020238||acquired prosopagnosia
|
|
D020238||acquired prosopagnosias
|
|
D020238||agnosia facial recognition
|
|
D020238||agnosia for face
|
|
D020238||agnosia for faces
|
|
D020238||agnosias facial recognition
|
|
D020238||developmental prosopagnosia
|
|
D020238||developmental prosopagnosias
|
|
D020238||facial recognition agnosia
|
|
D020238||facial recognition agnosias
|
|
D020238||prosopagnosia acquired
|
|
D020238||prosopagnosia developmental
|
|
D020238||prosopagnosias
|
|
D020238||prosopagnosias acquired
|
|
D020238||prosopagnosias developmental
|
|
D020238||recognition agnosia facial
|
|
D020238||recognition agnosias facial
|
|
D020237||alexia pure
|
|
D020237||agnosias visual verbal
|
|
D020237||agnosia visual verbal
|
|
D020237||agraphia alexia without
|
|
D020237||agraphias alexia without
|
|
D020237||alexias pure
|
|
D020237||alexia syndrome without agraphia
|
|
D020237||alexia without agraphia
|
|
D020237||alexia without agraphias
|
|
D020237||blindnesses pure word
|
|
D020237||blindness pure word
|
|
D020237||pure alexia
|
|
D020237||pure alexias
|
|
D020237||pure alexia without agraphia
|
|
D020237||pure word blindness
|
|
D020237||pure word blindnesses
|
|
D020237||verbal agnosias visual
|
|
D020237||verbal agnosia visual
|
|
D020237||visual verbal agnosia
|
|
D020237||visual verbal agnosias
|
|
D020237||without agraphia alexia
|
|
D020237||without agraphias alexia
|
|
D020237||word blindnesses pure
|
|
D020237||word blindness pure
|
|
D020236||amnesia transient global
|
|
D020236||global amnesia transient
|
|
D020236||tgas transient global amnesia
|
|
D020236||tga transient global amnesia
|
|
D020236||transient global amnesia
|
|
C565557|230450||gamma glutamylcysteine synthetase deficiency hemolytic anemia due to
|
|
266140|C563004||pyropoikilocytosis hereditary
|
|
D020235||gait apraxia
|
|
D020235||apraxia bruns apos gait
|
|
D020235||apraxia frontal gait
|
|
D020235||apraxia gait
|
|
D020235||apraxia of gait
|
|
D020235||apraxias bruns apos gait
|
|
D020235||apraxias frontal gait
|
|
D020235||apraxias gait
|
|
D020235||bruns apraxia gait
|
|
D020235||bruns apos apraxia gait
|
|
D020235||bruns apos apraxia of gait
|
|
D020235||bruns gait apraxia
|
|
D020235||bruns apos gait apraxia
|
|
D020235||bruns apos gait apraxias
|
|
D020235||dyspraxia of gait
|
|
D020235||frontal gait apraxia
|
|
D020235||frontal gait apraxias
|
|
D020235||gait apraxia bruns apos
|
|
D020235||gait apraxia frontal
|
|
D020235||gait apraxias
|
|
D020235||gait apraxias bruns apos
|
|
D020235||gait apraxias frontal
|
|
D020235||gait dyspraxia
|
|
D020235||gait dyspraxias
|
|
D008589||meningococcal infections
|
|
D008589||infection meningococcal
|
|
D008589||infections meningococcal
|
|
D008589||meningococcal infection
|
|
D020234||gait ataxia
|
|
D020234||ataxia cerebellar gait
|
|
D020234||ataxia gait
|
|
D020234||ataxia of gait
|
|
D020234||ataxias cerebellar gait
|
|
D020234||ataxia sensory gait
|
|
D020234||ataxias gait
|
|
D020234||ataxias sensory gait
|
|
D020234||cerebellar gait
|
|
D020234||cerebellar gait ataxia
|
|
D020234||cerebellar gait ataxias
|
|
D020234||cerebellar gaits
|
|
D020234||gait ataxia cerebellar
|
|
D020234||gait ataxias
|
|
D020234||gait ataxias cerebellar
|
|
D020234||gait ataxia sensory
|
|
D020234||gait ataxias sensory
|
|
D020234||gait cerebellar
|
|
D020234||gaits cerebellar
|
|
D020234||sensory gait ataxia
|
|
D020234||sensory gait ataxias
|
|
D015209|613806||cholangitis sclerosing
|
|
D015209|613806||cholangiitides sclerosing
|
|
D015209|613806||cholangiitis sclerosing
|
|
D015209|613806||cholangitides primary sclerosing
|
|
D015209|613806||cholangitides sclerosing
|
|
D015209|613806||cholangitis primary sclerosing
|
|
D015209|613806||primary sclerosing cholangitides
|
|
D015209|613806||primary sclerosing cholangitis
|
|
D015209|613806||psc
|
|
D015209|613806||sclerosing cholangiitides
|
|
D015209|613806||sclerosing cholangiitis
|
|
D015209|613806||sclerosing cholangitides
|
|
D015209|613806||sclerosing cholangitides primary
|
|
D015209|613806||sclerosing cholangitis
|
|
D015209|613806||sclerosing cholangitis primary
|
|
D008588||meningocele
|
|
D008588||acquired meningocele
|
|
D008588||acquired meningoceles
|
|
D008588||herniation meningeal
|
|
D008588||herniation of meninges
|
|
D008588||herniations meningeal
|
|
D008588||meningeal herniation
|
|
D008588||meningeal herniations
|
|
D008588||meninges herniation
|
|
D008588||meninges herniations
|
|
D008588||meningocele acquired
|
|
D008588||meningocele rudimentary
|
|
D008588||meningoceles
|
|
D008588||meningoceles acquired
|
|
D008588||meningoceles rudimentary
|
|
D008588||meningoceles traumatic
|
|
D008588||meningocele traumatic
|
|
D008588||rudimentary meningocele
|
|
D008588||rudimentary meningoceles
|
|
D008588||traumatic meningocele
|
|
D008588||traumatic meningoceles
|
|
D020233||gait disorders neurologic
|
|
D020233||ambulation disorder neurologic
|
|
D020233||ambulation disorders neurologic
|
|
D020233||athetotic gait
|
|
D020233||broadened gait
|
|
D020233||charcot gait
|
|
D020233||charcot gaits
|
|
D020233||charcot apos s gait
|
|
D020233||charcots gait
|
|
D020233||drop foot gait
|
|
D020233||duck gait
|
|
D020233||festinating gait
|
|
D020233||foot gait drop
|
|
D020233||frontal gait
|
|
D020233||gait athetotic
|
|
D020233||gait broadened
|
|
D020233||gait charcot
|
|
D020233||gait charcot apos s
|
|
D020233||gait disorder neurologic
|
|
D020233||gait disorder sensorimotor
|
|
D020233||gait disorders sensorimotor
|
|
D020233||gait drop foot
|
|
D020233||gait duck
|
|
D020233||gait dysfunction neurologic
|
|
D020233||gait dysfunctions neurologic
|
|
D020233||gait festinating
|
|
D020233||gait frontal
|
|
D020233||gait hemiplegic
|
|
D020233||gait hysterical
|
|
D020233||gait reeling
|
|
D020233||gait rigid
|
|
D020233||gaits charcot
|
|
D020233||gait scissors
|
|
D020233||gait shuffling
|
|
D020233||gait spastic
|
|
D020233||gait stumbling
|
|
D020233||gait unsteady
|
|
D020233||gait widebased
|
|
D020233||hemiplegic gait
|
|
D020233||hysterical gait
|
|
D020233||locomotion disorder neurologic
|
|
D020233||locomotion disorders neurologic
|
|
D020233||marche a petit pas
|
|
D020233||neurologic ambulation disorder
|
|
D020233||neurologic ambulation disorders
|
|
D020233||neurologic gait disorder
|
|
D020233||neurologic gait disorders
|
|
D020233||neurologic gait dysfunction
|
|
D020233||neurologic gait dysfunctions
|
|
D020233||neurologic locomotion disorder
|
|
D020233||neurologic locomotion disorders
|
|
D020233||rapid fatigue of gait
|
|
D020233||reeling gait
|
|
D020233||rigid gait
|
|
D020233||scissors gait
|
|
D020233||sensorimotor gait disorder
|
|
D020233||sensorimotor gait disorders
|
|
D020233||shuffling gait
|
|
D020233||shuffling gaits
|
|
D020233||spastic gait
|
|
D020233||stumbling gait
|
|
D020233||unsteady gait
|
|
D020233||widebased gait
|
|
D008587||meningitis viral
|
|
D008587||meningitides viral
|
|
D008587||viral meningitides
|
|
D008587||viral meningitis
|
|
C567802|613055||atrial fibrillation familial 8
|
|
C567802|613055||atfb8
|
|
D008595||menorrhagia
|
|
D008595||hypermenorrhea
|
|
D008594||menopause premature
|
|
D008594||premature menopause
|
|
612542||vitamin b12 plasma level quantitative trait locus 1
|
|
612542||b12qtl1
|
|
D008591||meningomyelocele
|
|
D008591||acquired meningomyelocele
|
|
D008591||acquired meningomyeloceles
|
|
D008591||acquired myelomeningocele
|
|
D008591||acquired myelomeningoceles
|
|
D008591||meningomyelocele acquired
|
|
D008591||meningomyeloceles
|
|
D008591||meningomyeloceles acquired
|
|
D008591||myelocele
|
|
D008591||myeloceles
|
|
D008591||myelomeningocele
|
|
D008591||myelomeningocele acquired
|
|
D008591||myelomeningoceles
|
|
D008591||myelomeningoceles acquired
|
|
D008590||meningoencephalitis
|
|
D008590||cerebromeningitides
|
|
D008590||cerebromeningitis
|
|
D008590||encephalomeningitides
|
|
D008590||encephalomeningitis
|
|
D008590||meningoencephalitides
|
|
C536194|130000||ehlers danlos syndrome type 1
|
|
C536194|130000||eds1
|
|
C536194|130000||eds i
|
|
C536194|130000||ehlers danlos syndrome classic severe form
|
|
C536194|130000||ehlers danlos syndrome gravis type
|
|
C536194|130000||ehlers danlos syndrome severe classic type
|
|
C536194|130000||ehlers danlos syndrome type i
|
|
C567715|613180||polymicrogyria with optic nerve hypoplasia
|
|
C563933|600496||maturity onset diabetes of the young type 3
|
|
C563933|600496||mody3
|
|
C563933|600496||mody type 3
|
|
D020221||optic nerve injuries
|
|
D020221||avulsion optic nerve
|
|
D020221||avulsions optic nerve
|
|
D020221||contusion optic nerve
|
|
D020221||contusions optic nerve
|
|
D020221||cranial nerve ii injuries
|
|
D020221||injuries optic nerve
|
|
D020221||injury optic nerve
|
|
D020221||nerve avulsion optic
|
|
D020221||nerve avulsions optic
|
|
D020221||nerve contusion optic
|
|
D020221||nerve contusions optic
|
|
D020221||nerve injuries optic
|
|
D020221||nerve injury optic
|
|
D020221||nerve transection optic
|
|
D020221||nerve transections optic
|
|
D020221||nerve trauma optic
|
|
D020221||nerve traumas optic
|
|
D020221||neuropathies traumatic optic
|
|
D020221||neuropathy traumatic optic
|
|
D020221||optic nerve avulsion
|
|
D020221||optic nerve avulsions
|
|
D020221||optic nerve contusion
|
|
D020221||optic nerve contusions
|
|
D020221||optic nerve injury
|
|
D020221||optic nerve transection
|
|
D020221||optic nerve transections
|
|
D020221||optic nerve trauma
|
|
D020221||optic nerve traumas
|
|
D020221||optic neuropathies traumatic
|
|
D020221||optic neuropathy traumatic
|
|
D020221||second cranial nerve injuries
|
|
D020221||second cranial nerve trauma
|
|
D020221||transection optic nerve
|
|
D020221||transections optic nerve
|
|
D020221||trauma optic nerve
|
|
D020221||trauma second cranial nerve
|
|
D020221||traumas optic nerve
|
|
D020221||traumatic optic neuropathies
|
|
D020221||traumatic optic neuropathy
|
|
D020220||facial nerve injuries
|
|
D020220||avulsion facial nerve
|
|
D020220||avulsions facial nerve
|
|
D020220||cranial nerve vii injuries
|
|
D020220||facial nerve avulsion
|
|
D020220||facial nerve avulsions
|
|
D020220||facial nerve injury
|
|
D020220||facial nerve trauma
|
|
D020220||facial nerve traumas
|
|
D020220||facial neuropathies traumatic
|
|
D020220||facial neuropathy traumatic
|
|
D020220||injuries cranial nerve vii
|
|
D020220||injuries facial nerve
|
|
D020220||injuries seventh cranial nerve
|
|
D020220||injury facial nerve
|
|
D020220||nerve avulsion facial
|
|
D020220||nerve avulsions facial
|
|
D020220||nerve injuries facial
|
|
D020220||nerve injury facial
|
|
D020220||nerve trauma facial
|
|
D020220||nerve traumas facial
|
|
D020220||neuropathies traumatic facial
|
|
D020220||neuropathy traumatic facial
|
|
D020220||seventh cranial nerve injuries
|
|
D020220||trauma facial nerve
|
|
D020220||traumas facial nerve
|
|
D020220||traumatic facial neuropathies
|
|
D020220||traumatic facial neuropathy
|
|
C567924|308350||epileptic encephalopathy early infantile 1
|
|
C567924|308350||eiee1
|
|
C567924|308350||infantile epileptic dyskinetic encephalopathy
|
|
C567924|308350||infantile spasm syndrome x linked 1
|
|
C567924|308350||issx1
|
|
C567924|308350||ohtahara syndrome x linked
|
|
C567924|308350||west syndrome x linked
|
|
C567924|308350||xmesid
|
|
C538275|240300||aps1
|
|
C538275|240300||aps i
|
|
C538275|240300||autoimmune polyendocrine syndrome type 1
|
|
C538275|240300||autoimmune polyendocrine syndrome type i with or without reversible metaphyseal dysplasia
|
|
C538275|240300||autoimmune polyendocrinopathy candidiasis ectodermal dystrophy apeced
|
|
C538275|240300||autoimmune polyendocrinopathy syndrome type i autosomal dominant
|
|
C538275|240300||autoimmune polyendocrinopathy syndrome type i with reversible metaphyseal dysplasia
|
|
C538275|240300||hypoadrenocorticism with hypoparathyroidism and superficial moniliasis
|
|
C538275|240300||hypoadrenocorticism with hypoparathyroidism and superficial moniliasis autoimmune polyendocrinopathy syndrome type i autosomal dominant included
|
|
C538275|240300||pga i
|
|
C538275|240300||polyglandular deficiency syndrome persian jewish type
|
|
C538275|240300||polyglandular deficiency syndrome persian jewish type included
|
|
604116|C565827||cone rod dystrophy 3
|
|
604116|C565827||cord3
|
|
C567196|612713||kahrizi syndrome
|
|
C567196|612713||khrz
|
|
C567196|612713||mental retardation cataract coloboma and kyphosis autosomal recessive
|
|
D020227||lateral sinus thrombosis
|
|
D020227||lateral sinus thrombophlebitis
|
|
D020227||lateral sinus thromboses
|
|
D020227||phlebitis lateral sinus septic
|
|
D020227||septic phlebitis lateral sinus
|
|
D020227||sinus thromboses transverse
|
|
D020227||thrombophlebitis lateral sinus
|
|
D020227||thromboses lateral sinus
|
|
D020227||thromboses transverse sinus
|
|
D020227||thrombosis lateral sinus
|
|
D020227||thrombosis transverse sinus
|
|
D020227||transverse sinus thromboses
|
|
D020227||transverse sinus thrombosis
|
|
D020226||cavernous sinus thrombosis
|
|
D020226||cavernous sinus phlebitis septic
|
|
D020226||cavernous sinus thrombophlebitides
|
|
D020226||cavernous sinus thrombophlebitis
|
|
D020226||cavernous sinus thromboses
|
|
D020226||caverous sinus septic phlebitis
|
|
D020226||phlebitis cavernous sinus septic
|
|
D020226||septic phlebitis cavernous sinus
|
|
D020226||sinus thrombophlebitides cavernous
|
|
D020226||sinus thrombophlebitis cavernous
|
|
D020226||sinus thromboses cavernous
|
|
D020226||sinus thrombosis cavernous
|
|
D020226||thrombophlebitides cavernous sinus
|
|
D020226||thrombophlebitis cavernous sinus
|
|
D020226||thromboses cavernous sinus
|
|
D020226||thrombosis cavernous sinus
|
|
D020225||sagittal sinus thrombosis
|
|
D020225||phlebitis sagittal sinus septic
|
|
D020225||sagittal sinus septic phlebitis
|
|
D020225||sagittal sinus thrombophlebitis
|
|
D020225||sagittal sinus thromboses
|
|
D020225||septic phlebitis sagittal sinus
|
|
D020225||sinus thrombophlebitis sagittal
|
|
D020225||sinus thromboses sagittal
|
|
D020225||sinus thrombosis sagittal
|
|
D020225||thrombophlebitis sagittal sinus
|
|
D020225||thromboses sagittal sinus
|
|
D020225||thrombosis sagittal sinus
|
|
D008599||menstruation disturbances
|
|
D008599||disorder menstruation
|
|
D008599||disorders menstruation
|
|
D008599||disturbance menstruation
|
|
D008599||disturbances menstruation
|
|
D008599||hypomenorrhea
|
|
D008599||hypomenorrheas
|
|
D008599||menstruation disorder
|
|
D008599||menstruation disorders
|
|
D008599||menstruation disturbance
|
|
D008599||menstruation retrograde
|
|
D008599||menstruations retrograde
|
|
D008599||polymenorrhea
|
|
D008599||polymenorrheas
|
|
D008599||retrograde menstruation
|
|
D008599||retrograde menstruations
|
|
D020222||abducens nerve injury
|
|
D020222||abducens nerve injuries
|
|
D020222||abducens nerve trauma
|
|
D020222||abducens nerve traumas
|
|
D020222||abducens neuropathies traumatic
|
|
D020222||abducens neuropathy traumatic
|
|
D020222||cranial nerve vi injury
|
|
D020222||injuries abducens nerve
|
|
D020222||injury abducens nerve
|
|
D020222||injury cranial nerve vi
|
|
D020222||injury sixth cranial nerve
|
|
D020222||nerve injuries abducens
|
|
D020222||nerve injury abducens
|
|
D020222||nerve trauma abducens
|
|
D020222||nerve traumas abducens
|
|
D020222||sixth cranial nerve injuries
|
|
D020222||sixth cranial nerve injury
|
|
D020222||sixth nerve palsies traumatic
|
|
D020222||sixth nerve palsy traumatic
|
|
D020222||sixth nerve trauma
|
|
D020222||sixth nerve traumas
|
|
D020222||trauma abducens nerve
|
|
D020222||traumas abducens nerve
|
|
D020222||trauma sixth nerve
|
|
D020222||traumas sixth nerve
|
|
D020222||traumatic abducens neuropathies
|
|
D020222||traumatic abducens neuropathy
|
|
D020222||traumatic sixth nerve palsies
|
|
D020222||traumatic sixth nerve palsy
|
|
D050090||ovotesticular disorders of sex development
|
|
D050090|400045||46 xx gonadal dysgenesis complete sry positive
|
|
D050090||46 xx true hermaphroditism sry positive
|
|
D050090||dsd ovotesticular
|
|
D050090||dsds ovotesticular
|
|
D050090||familial true hermaphroditism
|
|
D050090||familial true hermaphroditisms
|
|
D050090||familial xx true hermaphroditism
|
|
D050090||hermaphroditism familial true
|
|
D050090||hermaphroditisms familial true
|
|
D050090||hermaphroditisms true
|
|
D050090||hermaphroditism true
|
|
D050090||ovotesticular disorder of sex development
|
|
D050090||ovotesticular dsd
|
|
D050090||ovotesticular dsds
|
|
D050090||true hermaphroditism
|
|
D050090||true hermaphroditism familial
|
|
D050090||true hermaphroditisms
|
|
D050090||true hermaphroditisms familial
|
|
D050090||xx male syndrome sry positive
|
|
613857||orofacial cleft 13
|
|
613857||ofc13
|
|
166200|D010013||osteogenesis imperfecta
|
|
166200|D010013||brittle bone disease
|
|
166200|D010013||disease lobstein
|
|
166200|D010013||disease lobstein apos s
|
|
166200|D010013||fragilitas ossium
|
|
166200|D010013||lobstein disease
|
|
166200|D010013||lobstein apos s disease
|
|
166200|D010013||lobsteins disease
|
|
166200|D010013||oi1
|
|
166200|D010013||oi type i
|
|
166200|D010013||ossiums fragilitas
|
|
166200|D010013||osteogenesis imperfecta tarda
|
|
166200|D010013||osteogenesis imperfecta tardas
|
|
166200|D010013||osteogenesis imperfecta type 1
|
|
166200|D010013||osteogenesis imperfecta type i
|
|
166200|D010013||osteogenesis imperfecta with blue sclerae
|
|
166200|D010013||osteogenesis imperfecta with blue sclerae osteopenic nonfracture syndrome included
|
|
C567144|206100||anemia hypochromic microcytic with iron overload
|
|
C567144|206100||ahmio1
|
|
C567144|206100||anemia hypochromic microcytic with iron overload 1
|
|
C567200||immunodeficiency hypogammaglobulinemia and reduced b cells
|
|
C567200||cd79b deficiency
|
|
C567200||igb deficiency
|
|
D019247||hiv wasting syndrome
|
|
D019247||aids wasting syndrome
|
|
D019247||hiv wasting disease
|
|
D019247||slim disease
|
|
D019247||wasting disease hiv
|
|
D019247||wasting syndrome aids
|
|
D019247||wasting syndrome hiv
|
|
C566578|602096||alzheimer disease 5
|
|
C566578|602096||ad5
|
|
C566578|602096||alzheimer disease familial 5
|
|
C564665|606766||azoospermia nonobstructive
|
|
C564665|606766||spermatogenic failure 3
|
|
C564665|606766||spgf3
|
|
604004|C536141||megalencephalic leukoencephalopathy with subcortical cysts
|
|
604004|C536141||infantile leukoencephalopathy and megalencephaly
|
|
604004|C536141||leukoencephalopathy with swelling and a discrepantly mild course
|
|
604004|C536141||leukoencephalopathy with swelling and cysts
|
|
604004|C536141||lvm
|
|
604004|C536141||megalencephalic leukoencephalopathy with subcortical cysts 1
|
|
604004|C536141||megalencephaly cystic leukodystrophy
|
|
604004|C536141||mlc1
|
|
604004|C536141||vacuolating leukoencephalopathy
|
|
604004|C536141||vacuolating megalencephalic leukoencephalopathy with subcortical cysts
|
|
604004|C536141||van der knaap disease
|
|
604004|C536141||van der knapp disease
|
|
604004|C536141||vl
|
|
D020331|C535807|157900||mobius syndrome
|
|
D020331||congenital oculofacial paralysis moebius
|
|
D020331||congenital ophthalmoplegia and facial paresis
|
|
D020331||m 246 bius sequence
|
|
D020331||mobius syndromes
|
|
D020331||moebius congenital oculofacial paralysis
|
|
D020331|C535807|157900||moebius sequence
|
|
D020331||moebius spectrum
|
|
D020331|C535807|157900||moebius syndrome
|
|
D020331||moebius syndromes
|
|
D020330||bell palsy
|
|
D020330||acute idiopathic facial neuropathy
|
|
D020330||acute inflammatory facial neuropathy
|
|
D020330||bell palsies
|
|
D020330||bell apos s palsies
|
|
D020330||bell apos s palsy
|
|
D020330||bells palsy
|
|
D020330||facial neuropathy idiopathic acute
|
|
D020330||facial neuropathy inflammatory acute
|
|
D020330||facial paralyses herpetic
|
|
D020330||facial paralyses idiopathic
|
|
D020330||facial paralysis herpetic
|
|
D020330||facial paralysis idiopathic
|
|
D020330||herpetic facial paralyses
|
|
D020330||herpetic facial paralysis
|
|
D020330||idiopathic acute facial neuropathy
|
|
D020330||idiopathic facial paralyses
|
|
D020330||idiopathic facial paralysis
|
|
D020330||inflammatory facial neuropathy acute
|
|
D020330||palsies bell
|
|
D020330||palsies bell apos s
|
|
D020330||palsy bell
|
|
D020330||palsy bell apos s
|
|
D020330||paralyses herpetic facial
|
|
D020330||paralyses idiopathic facial
|
|
D020330||paralysis herpetic facial
|
|
D020330||paralysis idiopathic facial
|
|
C567524||nevus flammeus of nape of neck
|
|
C567524||erythema nuchae
|
|
C567524||unna nevus
|
|
C536150|132800||keratoacanthoma familial
|
|
C536150|132800||epithelioma self healing squamous 1
|
|
C536150|132800||ess1 formerly
|
|
C536150|132800||ferguson smith type epithelioma
|
|
C536150|132800||msse
|
|
C536150|132800||multiple self healing squamous epithelioma
|
|
C536150|132800||multiple self healing squamous epithelioma susceptibility to
|
|
D020339||optic nerve glioma
|
|
D020339||adult optic nerve glioma
|
|
D020339||astrocytoma malignant optic nerve
|
|
D020339||childhood optic nerve glioma
|
|
D020339||glioma optic
|
|
D020339||glioma optic nerve
|
|
D020339||glioma optic nerve adult
|
|
D020339||glioma optic nerve childhood
|
|
D020339||gliomas optic
|
|
D020339||gliomas optic nerve
|
|
D020339||malignant astrocytoma optic nerve
|
|
D020339||malignant optic nerve astrocytoma
|
|
D020339||optic glioma
|
|
D020339||optic gliomas
|
|
D020339||optic nerve glioma adult
|
|
D020339||optic nerve glioma childhood
|
|
D020339||optic nerve gliomas
|
|
D020339||optic nerve malignant astrocytoma
|
|
D020338||vestibular neuronitis
|
|
D020338||acute peripheral vestibulopathies
|
|
D020338||acute peripheral vestibulopathy
|
|
D020338||acute vestibular neuritides
|
|
D020338||acute vestibular neuritis
|
|
D020338||epidemic neurolabyrinthitides
|
|
D020338||epidemic neurolabyrinthitis
|
|
D020338||episodic recurrent vertigo
|
|
D020338||episodic recurrent vertigos
|
|
D020338||inflammations vestibular nerve
|
|
D020338||inflammation vestibular nerve
|
|
D020338||nerve inflammations vestibular
|
|
D020338||nerve inflammation vestibular
|
|
D020338||nerve neuritides vestibular
|
|
D020338||nerve neuritis vestibular
|
|
D020338||neuritides acute vestibular
|
|
D020338||neuritides recurrent vestibular
|
|
D020338||neuritides subacute vestibular
|
|
D020338||neuritides vestibular
|
|
D020338||neuritides vestibular nerve
|
|
D020338||neuritis acute vestibular
|
|
D020338||neuritis recurrent vestibular
|
|
D020338||neuritis subacute vestibular
|
|
D020338||neuritis vestibular
|
|
D020338||neuritis vestibular nerve
|
|
D020338||neurolabyrinthitides epidemic
|
|
D020338||neurolabyrinthitis epidemic
|
|
D020338||neuronitides vestibular
|
|
D020338||neuronitis vestibular
|
|
D020338||neuropathies vestibular
|
|
D020338||neuropathy vestibular
|
|
D020338||peripheral vestibulopathies acute
|
|
D020338||peripheral vestibulopathy acute
|
|
D020338||recurrent vertigo episodic
|
|
D020338||recurrent vertigos episodic
|
|
D020338||recurrent vestibular neuritides
|
|
D020338||recurrent vestibular neuritis
|
|
D020338||recurrent vestibulopathies
|
|
D020338||recurrent vestibulopathy
|
|
D020338||subacute vestibular neuritides
|
|
D020338||subacute vestibular neuritis
|
|
D020338||vertigo episodic recurrent
|
|
D020338||vertigos episodic recurrent
|
|
D020338||vestibular nerve inflammation
|
|
D020338||vestibular nerve inflammations
|
|
D020338||vestibular nerve neuritides
|
|
D020338||vestibular nerve neuritis
|
|
D020338||vestibular neuritides
|
|
D020338||vestibular neuritides acute
|
|
D020338||vestibular neuritides recurrent
|
|
D020338||vestibular neuritides subacute
|
|
D020338||vestibular neuritis
|
|
D020338||vestibular neuritis acute
|
|
D020338||vestibular neuritis recurrent
|
|
D020338||vestibular neuritis subacute
|
|
D020338||vestibular neuronitides
|
|
D020338||vestibular neuropathies
|
|
D020338||vestibular neuropathy
|
|
D020338||vestibulopathies acute peripheral
|
|
D020338||vestibulopathies recurrent
|
|
D020338||vestibulopathy acute peripheral
|
|
D020338||vestibulopathy recurrent
|
|
D006029||glycosuria
|
|
D020336||paraparesis spastic
|
|
D020336||lower extremity weakness spastic
|
|
D020336||parapareses spastic
|
|
D020336||spastic lower extremity weakness
|
|
D020336||spastic parapareses
|
|
D020336||spastic paraparesis
|
|
D020335||paraparesis
|
|
D020335||cerebral paraparesis
|
|
D020335||chronic progressive paraparesis
|
|
D020335||hypotonic paraparesis
|
|
D020335||parapareses
|
|
D020335||paraparesis cerebral
|
|
D020335||paraparesis chronic progressive
|
|
D020335||paraparesis hypotonic
|
|
D020335||paraparesis spinal
|
|
D020335||progressive paraparesis chronic
|
|
D020335||spinal paraparesis
|
|
C567528||encephalocardiomyopathy mitochondrial neonatal due to atp synthase deficiency
|
|
D020333||tolosa hunt syndrome
|
|
D019339||nevus flammeus
|
|
D019339||port wine stains
|
|
D019339||stain port wine
|
|
D019339||stains port wine
|
|
C563444|600792||deafness autosomal recessive 5
|
|
C563444|600792||dfnb5
|
|
C563444|600792||neurosensory nonsyndromic recessive deafness 5
|
|
C563444|600792||nsrd5
|
|
C536360|608542||aneurysm intracranial berry 2
|
|
C536360|608542||anib2
|
|
D019337||hematologic neoplasms
|
|
D019337||hematological malignancies
|
|
D019337||hematological malignancy
|
|
D019337||hematological neoplasm
|
|
D019337||hematological neoplasms
|
|
D019337||hematologic malignancies
|
|
D019337||hematologic malignancy
|
|
D019337||hematologic neoplasm
|
|
D019337||hematopoietic malignancies
|
|
D019337||hematopoietic malignancy
|
|
D019337||hematopoietic neoplasm
|
|
D019337||hematopoietic neoplasms
|
|
D019337||malignancies hematologic
|
|
D019337||malignancies hematological
|
|
D019337||malignancies hematopoietic
|
|
D019337||malignancy hematologic
|
|
D019337||malignancy hematological
|
|
D019337||malignancy hematopoietic
|
|
D019337||neoplasm hematologic
|
|
D019337||neoplasm hematological
|
|
D019337||neoplasm hematopoietic
|
|
D019337||neoplasms hematologic
|
|
D019337||neoplasms hematological
|
|
D019337||neoplasms hematopoietic
|
|
194071|C536853||familial wilms tumor 2
|
|
194071|C536853||wilms tumor 2
|
|
194071|C536853||wt2
|
|
C566431|610599||retinitis pigmentosa 36
|
|
C566431|610599||rp36
|
|
C566204||brachydactyly long thumb type
|
|
C567535||megalencephaly
|
|
C566206||brachmann de lange like facial changes with microcephaly metatarsus adductus and developmental delay
|
|
D019351||rubulavirus infections
|
|
D019351||infection rubulavirus
|
|
D019351||infections rubulavirus
|
|
D019351||rubulavirus infection
|
|
D019350||astroviridae infections
|
|
D019350||astroviridae infection
|
|
D019350||infection astroviridae
|
|
D019350||infections astroviridae
|
|
C567533||anemia nonspherocytic hemolytic due to g6pd deficiency
|
|
D020324||amnesia anterograde
|
|
D020324||amnesia post ictal
|
|
D020324||amnesias anterograde
|
|
D020324||amnesias post ictal
|
|
D020324||anterograde amnesia
|
|
D020324||anterograde amnesias
|
|
D020324||anterograde memory loss
|
|
D020324||anterograde memory losses
|
|
D020324||losses post ictal memory
|
|
D020324||loss post ictal memory
|
|
D020324||memory loss anterograde
|
|
D020324||memory losses anterograde
|
|
D020324||memory losses post ictal
|
|
D020324||memory loss post ictal
|
|
D020324||post ictal amnesia
|
|
D020324||post ictal amnesias
|
|
D020324||post ictal memory loss
|
|
D020324||post ictal memory losses
|
|
D020323||tics
|
|
D020323||chorea habit
|
|
D020323||choreas habit
|
|
D020323||gestural tic
|
|
D020323||gestural tics
|
|
D020323||habit chorea
|
|
D020323||habit choreas
|
|
D020323||habit spasm
|
|
D020323||habit spasms
|
|
D020323||habituation spasm
|
|
D020323||habituation spasms
|
|
D020323||motor tic
|
|
D020323||motor tics
|
|
D020323||spasm habit
|
|
D020323||spasm habituation
|
|
D020323||spasms habit
|
|
D020323||spasms habituation
|
|
D020323||tic
|
|
D020323||tic gestural
|
|
D020323||tic motor
|
|
D020323||tics gestural
|
|
D020323||tics motor
|
|
D020323||tics transient
|
|
D020323||tics vocal
|
|
D020323||tic transient
|
|
D020323||tic vocal
|
|
D020323||transient tic
|
|
D020323||transient tics
|
|
D020323||vocal tic
|
|
D020323||vocal tics
|
|
D006044||goiter nodular
|
|
D006044||goiters nodular
|
|
D006044||nodular goiter
|
|
D006044||nodular goiters
|
|
D006045||goiter substernal
|
|
D006045||goiter intrathoracic
|
|
D006045||goiters intrathoracic
|
|
D006045||goiters substernal
|
|
D006045||intrathoracic goiter
|
|
D006045||intrathoracic goiters
|
|
D006045||substernal goiter
|
|
D006045||substernal goiters
|
|
C567406|612161||aneurysm intracranial berry 7
|
|
C567406|612161||anib7
|
|
D056730|180860||silver russell syndrome
|
|
D056730|180860||dwarfism silver russell
|
|
D056730|180860||russell silver syndrome
|
|
D056730|180860||silver russell dwarfism
|
|
D056730|180860||syndrome russell silver
|
|
D056730|180860||syndrome silver russell
|
|
D006042||goiter
|
|
D006042||goiters
|
|
D006043||goiter endemic
|
|
D006043||endemic goiter
|
|
D006043||endemic goiters
|
|
D006043||goiters endemic
|
|
192200|D014648||varicose veins
|
|
192200|D014648||varices
|
|
192200|D014648||varicose vein
|
|
192200|D014648||varix
|
|
192200|D014648||veins varicose
|
|
192200|D014648||vein varicose
|
|
C536339|175900||porokeratosis disseminated superficial actinic 1
|
|
C536339|175900||dsap
|
|
C536339|175900||dsap1
|
|
C536339|175900||porok3
|
|
C536339|175900||porokeratosis 3 disseminated superficial actinic type
|
|
C580500||trisomy 18
|
|
C580500||complete trisomy 18 syndrome
|
|
C580500||edwards syndrome
|
|
C580500||trisomy 18 syndrome
|
|
C580500||trisomy e syndrome
|
|
D020329||essential tremor
|
|
D020329||benign essential tremor
|
|
D020329||benign essential tremors
|
|
D020329||essential tremor benign
|
|
D020329||essential tremors
|
|
D020329||essential tremors benign
|
|
D020329||familial tremor
|
|
D020329||familial tremors
|
|
D020329||hereditary essential tremor
|
|
D020329||tremor benign essential
|
|
D020329||tremor essential
|
|
D020329||tremor familial
|
|
D020329||tremors benign essential
|
|
D020329||tremors essential
|
|
D020329||tremors familial
|
|
C562769|274700||thyroid dyshormonogenesis 3
|
|
C562769|274700||hypothyroidism congenital due to dyshormonogenesis 3
|
|
C562769|274700||tdh3
|
|
C562769|274700||thyroid hormonogenesis genetic defect in 3
|
|
607965||systemic lupus erythematosus with nephritis susceptibility to 1
|
|
607965||slen1
|
|
D019349||roseolovirus infections
|
|
D019349||infection roseolovirus
|
|
D019349||infections roseolovirus
|
|
D019349||roseolovirus infection
|
|
606353|C536416||primary lateral sclerosis juvenile
|
|
606353|C536416||juvenile primary lateral sclerosis
|
|
606353|C536416||plsj
|
|
606353|C536416||pls juvenile
|
|
257980|C537742||odontoonychodermal dysplasia
|
|
257980|C537742||oodd
|
|
D006467|306700||hemophilia a
|
|
D006467|306700||as autosomal hemophilia
|
|
D006467|306700||autosomal hemophilia a
|
|
D006467|306700||autosomal hemophilia as
|
|
D006467|306700||classic hemophilia
|
|
D006467|306700||classic hemophilias
|
|
D006467|306700||congenital hemophilia a
|
|
D006467|306700||congenital hemophilia as
|
|
D006467|306700||deficiency factor viii
|
|
D006467|306700||factor 8 deficiency congenital
|
|
D006467|306700||factor viii deficiency
|
|
D006467|306700||factor viii deficiency congenital
|
|
D006467|306700||haemophilia
|
|
D006467|306700||hema
|
|
D006467|306700||hemophilia
|
|
D006467|306700||hemophilia a autosomal
|
|
D006467|306700||hemophilia a congenital
|
|
D006467|306700||hemophilia as
|
|
D006467|306700||hemophilia as autosomal
|
|
D006467|306700||hemophilia as congenital
|
|
D006467|306700||hemophilia classic
|
|
D006467|306700||hemophilias classic
|
|
C566210||rh null disease amorph type
|
|
607967||systemic lupus erythematosus with nephritis susceptibility to 3
|
|
607967||slen3
|
|
607966||systemic lupus erythematosus with nephritis susceptibility to 2
|
|
607966||slen2
|
|
D019320||embolism paradoxical
|
|
D019320||crossed embolism
|
|
D019320||crossed embolisms
|
|
D019320||embolism crossed
|
|
D019320||embolisms crossed
|
|
D019320||embolisms paradoxical
|
|
D019320||paradoxical embolism
|
|
D019320||paradoxical embolisms
|
|
C567503||mesomelic dysplasia camera type
|
|
C535741|603147||congenital disorder of glycosylation type 1c
|
|
C535741|603147||carbohydrate deficient glycoprotein syndrome type i with deficient glycosylation of dolichol linked oligosaccharide formerly
|
|
C535741|603147||carbohydrate deficient glycoprotein syndrome type v
|
|
C535741|603147||carbohydrate deficient glycoprotein syndrome type v formerly
|
|
C535741|603147||cdg1c
|
|
C535741|603147||cdgic
|
|
C535741|603147||cdg ic
|
|
C535741|603147||cdgs5 formerly
|
|
C535741|603147||congenital disorder of glycosylation type ic
|
|
607949||mycobacterium tuberculosis susceptibility to 1
|
|
607949||mtbs1
|
|
607948||mycobacterium tuberculosis susceptibility to
|
|
607948||mycobacterium tuberculosis protection against included
|
|
C566600|601952||keratosis linearis with ichthyosis congenita and sclerosing keratoderma
|
|
C566600|601952||klick syndrome
|
|
D006008||glycogen storage disease
|
|
D006008||disease glycogen storage
|
|
D006008||diseases glycogen storage
|
|
D006008||glycogenoses
|
|
D006008||glycogenosis
|
|
D006008||glycogen storage diseases
|
|
D006008||storage disease glycogen
|
|
D006008||storage diseases glycogen
|
|
C567469|300717||myopathy reducing body x linked early onset severe
|
|
D020315||latex hypersensitivity
|
|
D020315||allergies latex
|
|
D020315||allergies rubber
|
|
D020315||allergies rubber latex
|
|
D020315||allergy latex
|
|
D020315||allergy rubber
|
|
D020315||allergy rubber latex
|
|
D020315||hypersensitivities latex
|
|
D020315||hypersensitivity latex
|
|
D020315||latex allergies
|
|
D020315||latex allergy
|
|
D020315||latex hypersensitivities
|
|
D020315||natural rubber latex allergy
|
|
D020315||rubber allergies
|
|
D020315||rubber allergy
|
|
D020315||rubber latex allergies
|
|
D020315||rubber latex allergy
|
|
D020314||central nervous system fungal infections
|
|
D020314||central nervous system mycoses
|
|
D020314||fungal infections central nervous system
|
|
D020314||infections fungal central nervous system
|
|
D020314||mycoses central nervous system
|
|
D009999||ossification heterotopic
|
|
D009999||ectopic ossification
|
|
D009999||heterotopic ossification
|
|
D009999||ossification ectopic
|
|
D009999||ossification pathologic
|
|
D009999||ossification pathological
|
|
D009999||pathological ossification
|
|
D009999||pathologic ossification
|
|
D007333||insulin resistance
|
|
D007333||insulin sensitivity
|
|
D007333||resistance insulin
|
|
D007333||sensitivity insulin
|
|
C567036|604625||tooth agenesis selective 3
|
|
C567036|604625||hypodontia oligodontia 3
|
|
C567036|604625||sthag3
|
|
D008664||metal metabolism inborn errors
|
|
D008664||metal metabolism inborn error
|
|
D056828|610618||hereditary angioedema type iii
|
|
D056828|610618||angioedema estrogen sensitive hereditary
|
|
D056828|610618||angioedema hereditary type iii
|
|
D056828|610618||angioedemas estrogen sensitive hereditary
|
|
D056828|610618||angioneurotic edema hereditary with normal c1 inhibitor concentration and function
|
|
D056828|610618||estrogen related hae
|
|
D056828|610618||estrogen related haes
|
|
D056828|610618||estrogen sensitive hae
|
|
D056828|610618||estrogen sensitive haes
|
|
D056828|610618||estrogen sensitive hereditary angioedema
|
|
D056828|610618||estrogen sensitive hereditary angioedemas
|
|
D056828|610618||hae3
|
|
D056828|610618||hae estrogen related
|
|
D056828|610618||hae estrogen sensitive
|
|
D056828|610618||hae iii
|
|
D056828|610618||haes estrogen related
|
|
D056828|610618||haes estrogen sensitive
|
|
D056828|610618||hae with normal c1 inhibitor concentration and function
|
|
D056828|610618||hereditary angioedema estrogen sensitive
|
|
D056828|610618||hereditary angioedemas estrogen sensitive
|
|
D056828|610618||hereditary angioedema with normal c1 inhibitor activity
|
|
C567201|612691||polymicrogyria bilateral occipital
|
|
D010985||platybasia
|
|
D010985||basilar impression
|
|
D010985||basilar impressions
|
|
D010985||impression basilar
|
|
D010985||impressions basilar
|
|
D010985||platybasias
|
|
C566398|603218||huntington disease like 1
|
|
C566398|603218||hdl1
|
|
C566398|603218||hln1
|
|
C566398|603218||huntington like neurodegenerative disorder 1
|
|
C566398|603218||huntington like neurodegenerative disorder autosomal dominant
|
|
C566398|603218||prion disease early onset with prominent psychiatric features
|
|
C563065|302000||bullous dystrophy hereditary macular type
|
|
C563065|302000||ebm
|
|
C563065|302000||epidermolysis bullosa macular type
|
|
D058968||pythiosis
|
|
607039|C564633||deafness autosomal recessive 22
|
|
607039|C564633||dfnb22
|
|
D019318||porcine reproductive and respiratory syndrome
|
|
D019318||blue eared pig disease
|
|
D019318||mystery swine disease
|
|
D019318||pig disease blue eared
|
|
D019318||porcine epidemic abortion and respiratory syndrome
|
|
D019318||prrs
|
|
D019318||swine disease mystery
|
|
D019318||swine infertility and respiratory syndrome
|
|
D019315||retrobulbar hemorrhage
|
|
D019315||hemorrhage retrobulbar
|
|
D019315||retrobulbar hemorrhages
|
|
D056304||genu valgum
|
|
D056304||genu valga
|
|
D056304||genu valgas
|
|
D056304||genu valgums
|
|
D056304||knees knock
|
|
D056304||knock knee
|
|
D056304||knock knees
|
|
D056304||valga genu
|
|
D056304||valgas genu
|
|
C535413|606595||charcot marie tooth disease type 2f
|
|
C535413|606595||charcot marie tooth disease axonal type 2f
|
|
C535413|606595||charcot marie tooth disease neuronal type 2f
|
|
C535413|606595||charcot marie tooth neuropathy type 2f
|
|
C535413|606595||cmt2f
|
|
C535413|606595||cmt 2f
|
|
D056305||genu varum
|
|
D056305||bow leg
|
|
D056305||bow legs
|
|
D056305||genu varus
|
|
D056305||leg bow
|
|
D056305||legs bow
|
|
C567516||temple baraitser syndrome
|
|
C567516||mental retardation severe and absent nails of hallux and pollex
|
|
C536078|307000||hydrocephalus x linked
|
|
C536078|307000||aqueductal stenosis x linked
|
|
C536078|307000||aqueductal stenosis x linked xlas hydrocephalus x linked with congenital idiopathic intestinal pseudoobstruction included
|
|
C536078|307000||hsas
|
|
C536078|307000||hsas1
|
|
C536078|307000||hycx
|
|
C536078|307000||hydrocephalus due to congenital stenosis of aqueduct of sylvius
|
|
C567511||chromosome 22q11 2 deletion syndrome distal
|
|
C567511||distal chromosome 22q11 2 deletion syndrome
|
|
D020306||tuberculosis central nervous system
|
|
D020306||central nervous system tuberculosis
|
|
D008679||metaplasia
|
|
D006015||glycogen storage disease type viii
|
|
D006015||glycogenosis 8
|
|
C567518||bestrophinopathy
|
|
D020301||vasospasm intracranial
|
|
D020301||angiospasm cerebral
|
|
D020301||angiospasm intracranial
|
|
D020301||angiospasms cerebral
|
|
D020301||angiospasms intracranial
|
|
D020301||artery spasm cerebral
|
|
D020301||artery spasms cerebral
|
|
D020301||cerebral angiospasm
|
|
D020301||cerebral angiospasms
|
|
D020301||cerebral artery spasm
|
|
D020301||cerebral artery spasms
|
|
D020301||cerebral vasospasm
|
|
D020301||cerebral vasospasms
|
|
D020301||cerebrovascular spasm
|
|
D020301||cerebrovascular spasms
|
|
D020301||intracranial angiospasm
|
|
D020301||intracranial angiospasms
|
|
D020301||intracranial vascular spasm
|
|
D020301||intracranial vascular spasms
|
|
D020301||intracranial vasospasm
|
|
D020301||intracranial vasospasms
|
|
D020301||spasm cerebral artery
|
|
D020301||spasm cerebrovascular
|
|
D020301||spasm intracranial vascular
|
|
D020301||spasms cerebral artery
|
|
D020301||spasms cerebrovascular
|
|
D020301||spasms intracranial vascular
|
|
D020301||vascular spasm intracranial
|
|
D020301||vascular spasms intracranial
|
|
D020301||vasospasm cerebral
|
|
D020301||vasospasms cerebral
|
|
D020301||vasospasms intracranial
|
|
C567517||sex reversal female with dysgenesis of kidneys adrenals and lungs
|
|
D020300||intracranial hemorrhages
|
|
D020300||brain hemorrhage
|
|
D020300||brain hemorrhages
|
|
D020300||hemorrhage brain
|
|
D020300||hemorrhage intracranial
|
|
D020300||hemorrhage posterior fossa
|
|
D020300||hemorrhages brain
|
|
D020300||hemorrhages intracranial
|
|
D020300||hemorrhages posterior fossa
|
|
D020300||intracranial hemorrhage
|
|
D020300||posterior fossa hemorrhage
|
|
D020300||posterior fossa hemorrhages
|
|
C567519||tremor hereditary essential and idiopathic normal pressure hydrocephalus
|
|
C567519||etinph
|
|
D010996||pleural effusion
|
|
D010996||effusion pleural
|
|
D010996||effusions pleural
|
|
D010996||pleural effusions
|
|
C538351|609285||nemaline myopathy 4
|
|
C538351|609285||capm2 included
|
|
C538351|609285||cap myopathy 2 included
|
|
C538351|609285||cap myopathy tpm2 related
|
|
C538351|609285||nem4
|
|
C538351|609285||nemaline myopathy caused by mutation in the tropomyosin 2 gene
|
|
D010995||pleural diseases
|
|
D010995||disease pleural
|
|
D010995||diseases pleural
|
|
D010995||pleural disease
|
|
D010998||pleurisy
|
|
D010998||pleurisies
|
|
D010998||pleuritides
|
|
D010998||pleuritis
|
|
D010997||pleural neoplasms
|
|
D010997||neoplasm pleural
|
|
D010997||neoplasms pleural
|
|
D010997||pleural neoplasm
|
|
609029|C535733||emanuel syndrome
|
|
609029|C535733|613700||22 syndrome
|
|
609029|C535733||der 22 syndrome due to 3 1 meiotic disjunction events
|
|
609029|C535733||supernumary der 22 syndrome
|
|
609029|C535733||supernumary der 22 t 11 22 syndrome
|
|
609029|C535733||supernumary derivative 22 chromosome syndrome
|
|
609029|C535733||supernumerary der 22 syndrome
|
|
609029|C535733||supernumerary der 22 t 11
|
|
609029|C535733||supernumerary der 22 t 11 22 syndrome
|
|
606612||muscular dystrophy dystroglycanopathy congenital with or without mental retardation type b 5
|
|
606612||mdc1c
|
|
606612||mddgb5
|
|
606612|C564691||muscular dystrophy congenital 1c
|
|
606612||muscular dystrophy congenital fkrp related
|
|
C531598||familial acanthosis nigricans
|
|
C562647|146300||hypophosphatasia adult
|
|
C562647|146300||hypophosphatasia mild
|
|
C562647|146300||hypophosphatasia mild odontohypophosphatasia included
|
|
C531599||achondroplastic dwarfism
|
|
606613||high density lipoprotein cholesterol level quantitative trait locus 1
|
|
606613||hdlc1
|
|
606613||hdlcq1
|
|
D044342||malnutrition
|
|
D044342||nutritional deficiencies
|
|
D044342||nutritional deficiency
|
|
D044342||undernutrition
|
|
D044343||overnutrition
|
|
D007319||sleep initiation and maintenance disorders
|
|
D007319||awakening early
|
|
D007319||chronic insomnia
|
|
D007319||dims disorders of initiating and maintaining sleep
|
|
D007319||disorders of initiating and maintaining sleep
|
|
D007319||dysfunction sleep initiation
|
|
D007319||dysfunctions sleep initiation
|
|
D007319||early awakening
|
|
D007319||insomnia
|
|
D007319||insomnia chronic
|
|
D007319||insomnia disorder
|
|
D007319||insomnia disorders
|
|
D007319||insomnia nonorganic
|
|
D007319||insomnia primary
|
|
D007319||insomnia psychophysiological
|
|
D007319||insomnia rebound
|
|
D007319||insomnias
|
|
D007319||insomnia secondary
|
|
D007319||insomnia transient
|
|
D007319||nonorganic insomnia
|
|
D007319||primary insomnia
|
|
D007319||psychophysiological insomnia
|
|
D007319||rebound insomnia
|
|
D007319||secondary insomnia
|
|
D007319||sleep initiation dysfunction
|
|
D007319||sleep initiation dysfunctions
|
|
D007319||sleeplessness
|
|
D007319||transient insomnia
|
|
D008649||mesonephroma
|
|
D008649||mesonephromas
|
|
D009976||orthomyxoviridae infections
|
|
D009976||infection orthomyxoviridae
|
|
D009976||infection orthomyxovirus
|
|
D009976||infections orthomyxoviridae
|
|
D009976||infections orthomyxovirus
|
|
D009976||orthomyxoviridae infection
|
|
D009976||orthomyxovirus infection
|
|
D009976||orthomyxovirus infections
|
|
D008644||mesial movement of teeth
|
|
D008644||mesial drift of teeth
|
|
D008644||mesial migration of teeth
|
|
D008644||teeth mesial drift
|
|
D008644||teeth mesial migration
|
|
D008644||teeth mesial movement
|
|
C563579|157170||holoprosencephaly 2
|
|
C563579|157170||hpe2
|
|
253601|C535899||limb girdle muscular dystrophy type 2b
|
|
253601|C535899||lgmd2b
|
|
253601|C535899||lgmd3
|
|
253601|C535899||muscular dystrophy limb girdle type 2b
|
|
253601|C535899||muscular dystrophy limb girdle type 3
|
|
D015451|109543||leukemia lymphocytic chronic b cell
|
|
D015451|109543||b cell chronic lymphocytic leukemia
|
|
D015451|109543||b cell leukemia chronic
|
|
D015451|109543||b cell leukemias chronic
|
|
D015451|109543||b cell malignancy low grade
|
|
D015451|109543||bcll
|
|
D015451|109543||b lymphocytic leukemia chronic
|
|
D015451|109543||b lymphocytic leukemias chronic
|
|
D015451|109543||chronic b cell leukemia
|
|
D015451|109543||chronic b cell leukemias
|
|
D015451|109543||chronic b lymphocytic leukemia
|
|
D015451|109543||chronic b lymphocytic leukemias
|
|
D015451|109543||chronic lymphoblastic leukemia
|
|
D015451|109543||chronic lymphoblastic leukemias
|
|
D015451|109543||chronic lymphocytic leukemia
|
|
D015451|109543||chronic lymphocytic leukemias
|
|
D015451|109543||cll
|
|
D015451|109543||cll lymphoplasmacytoid lymphoma
|
|
D015451|109543||cll lymphoplasmacytoid lymphomas
|
|
D015451|109543||clls1
|
|
D015451|109543||clls2
|
|
D015451|109543||clls3
|
|
D015451|109543||clls4
|
|
D015451|109543||clls5
|
|
D015451|109543||dbm
|
|
D015451|109543||diffuse well differentiated lymphocytic lymphoma
|
|
D015451|109543||disrupted in b cell malignancy
|
|
D015451|109543||leukemia b cell chronic
|
|
D015451|109543||leukemia chronic b cell
|
|
D015451|109543||leukemia chronic b lymphocytic
|
|
D015451|109543||leukemia chronic lymphatic
|
|
D015451|109543||leukemia chronic lymphocytic
|
|
D015451|109543||leukemia chronic lymphocytic b cell
|
|
D015451|109543||leukemia chronic lymphocytic susceptibility to 1
|
|
D015451|109543||leukemia chronic lymphocytic susceptibility to 2
|
|
D015451|109543||leukemia chronic lymphocytic susceptibility to 3
|
|
D015451|109543||leukemia chronic lymphocytic susceptibility to 4
|
|
D015451|109543||leukemia chronic lymphocytic susceptibility to 5
|
|
D015451|109543||leukemia lymphoblastic chronic
|
|
D015451|109543||leukemia lymphocytic chronic
|
|
D015451|109543||leukemias chronic b cell
|
|
D015451|109543||leukemias chronic b lymphocytic
|
|
D015451|109543||leukemias chronic lymphoblastic
|
|
D015451|109543||lymphoblastic leukemia chronic
|
|
D015451|109543||lymphoblastic leukemias chronic
|
|
D015451|109543||lymphocytic leukemia chronic
|
|
D015451|109543||lymphocytic leukemia chronic b cell
|
|
D015451|109543||lymphocytic leukemias chronic
|
|
D015451|109543||lymphocytic lymphoma
|
|
D015451|109543||lymphocytic lymphoma diffuse well differentiated
|
|
D015451|109543||lymphocytic lymphomas
|
|
D015451|109543||lymphocytic lymphoma small
|
|
D015451|109543||lymphocytic lymphomas small
|
|
D015451|109543||lymphocytic lymphomas well differentiated
|
|
D015451|109543||lymphocytic lymphoma well differentiated
|
|
D015451|109543||lymphoma cll lymphoplasmacytoid
|
|
D015451|109543||lymphoma lymphocytic
|
|
D015451|109543||lymphoma lymphocytic diffuse well differentiated
|
|
D015451|109543||lymphoma lymphocytic well differentiated
|
|
D015451|109543||lymphoma lymphoplasmacytoid cll
|
|
D015451|109543||lymphomas cll lymphoplasmacytoid
|
|
D015451|109543||lymphomas lymphocytic
|
|
D015451|109543||lymphoma small cell
|
|
D015451|109543||lymphoma small lymphocytic
|
|
D015451|109543||lymphoma small lymphocytic plasmacytoid
|
|
D015451|109543||lymphomas small cell
|
|
D015451|109543||lymphomas small lymphocytic
|
|
D015451|109543||lymphomas well differentiated lymphocytic
|
|
D015451|109543||lymphoma well differentiated lymphocytic
|
|
D015451|109543||lymphoplasmacytoid lymphoma cll
|
|
D015451|109543||lymphoplasmacytoid lymphomas cll
|
|
D015451|109543||small cell lymphoma
|
|
D015451|109543||small cell lymphomas
|
|
D015451|109543||small lymphocytic lymphoma
|
|
D015451|109543||small lymphocytic lymphomas
|
|
D015451|109543||well differentiated lymphocytic lymphoma
|
|
D015451|109543||well differentiated lymphocytic lymphomas
|
|
C537923|300321||opitz kaveggia syndrome
|
|
C537923|300321||fgs
|
|
C537923|300321||fgs1
|
|
C537923|300321||fgs2
|
|
C537923|300321||fgs3
|
|
C537923|300321||fgs4
|
|
C537923|300321||fg syndrome
|
|
C537923|300321||fg syndrome 1
|
|
C537923|300321||fg syndrome 2
|
|
C537923|300321||fg syndrome 3
|
|
C537923|300321||fg syndrome 4
|
|
C537923|300321||keller syndrome
|
|
C537923|300321||mental retardation large head imperforate anus congenital hypotonia and partial agenesis of corpus callosum
|
|
C537923|300321||mental retardation large head imperforate anus congenital hypotonia and partial agenesis of the corpus callosum
|
|
C537923|300321||mental retardation x linked cask related
|
|
C537923|300321||mental retardation x linked with nystagmus
|
|
C537923|300321||mental retardation x linked with or without nystagmus included
|
|
C537923|300321||oks
|
|
C567067|300653||phosphoglycerate kinase 1 deficiency
|
|
C567067|300653||pgk1 deficiency
|
|
C567067|300653||pgk deficiency
|
|
C567067|300653||phosphoglycerate kinase deficiency
|
|
C536789|603116||craniosynostosis anal anomalies and porokeratosis
|
|
C536789|603116|208250|C537560||cap syndrome
|
|
C536789|603116||cdags syndrome
|
|
C564658|606787||peripheral arterial occlusive disease 1
|
|
C564658|606787||paod1
|
|
D019310||pseudolymphoma
|
|
D019310||hyperplasia reactive lymphoid
|
|
D019310||hyperplasias reactive lymphoid
|
|
D019310||lymphocytoma
|
|
D019310||lymphocytomas
|
|
D019310||lymphoid hyperplasia reactive
|
|
D019310||lymphoid hyperplasias reactive
|
|
D019310||pseudolymphomas
|
|
D019310||reactive lymphoid hyperplasia
|
|
D019310||reactive lymphoid hyperplasias
|
|
C566487|610006||2 methylbutyryl coa dehydrogenase deficiency
|
|
C566487|610006||2 mbcd deficiency
|
|
C566487|610006||2 methylbutyryl coenzyme a dehydrogenase deficiency
|
|
C566487|610006||2 methylbutyryl glycinuria
|
|
C566487|610006||sbcadd
|
|
C566487|610006||short branched chain acyl coa dehydrogenase deficiency
|
|
D008659||metabolic diseases
|
|
D008659||disease metabolic
|
|
D008659||diseases metabolic
|
|
D008659||metabolic disease
|
|
D008659||thesaurismoses
|
|
D008659||thesaurismosis
|
|
D008654||mesothelioma
|
|
D008654||mesotheliomas
|
|
D007331||insulin coma
|
|
D007331||coma insulin
|
|
D007331||insulin shock
|
|
D007331||shock insulin
|
|
D008661||metabolism inborn errors
|
|
D008661||error inborn metabolism
|
|
D008661||errors inborn metabolism
|
|
D008661||errors metabolism inborn
|
|
D008661||errors metabolisms inborn
|
|
D008661||inborn errors metabolism
|
|
D008661||inborn errors metabolisms
|
|
D008661||inborn errors of metabolism
|
|
D008661||inborn metabolism error
|
|
D008661||inborn metabolism errors
|
|
D008661||metabolism error inborn
|
|
D008661||metabolism errors inborn
|
|
D008661||metabolism inborn error
|
|
D008661||metabolisms inborn errors
|
|
150800||hlrcc
|
|
150800||lrcc
|
|
150800||mcl
|
|
150800||mcul1
|
|
150800||multiple cutaneous and uterine leiomyomata 1 with or without renal cell carcinoma
|
|
D055008||anthracosis
|
|
D055008||anthracoses
|
|
D055008||black lung
|
|
D055008||black lung disease
|
|
D055008||black lung diseases
|
|
D055008||black lungs
|
|
D055008||coal miner lung
|
|
D055008||coal miner apos s lung
|
|
D055008||coal miners lung
|
|
D055008||coal miner apos s lungs
|
|
D055008||coalworker pneumoconiosis
|
|
D055008||coal worker pneumoconiosis
|
|
D055008||coalworker apos s pneumoconioses
|
|
D055008||coal worker apos s pneumoconioses
|
|
D055008||coalworker apos s pneumoconiosis
|
|
D055008||coalworkers pneumoconiosis
|
|
D055008||coal worker apos s pneumoconiosis
|
|
D055008||coal workers pneumoconiosis
|
|
D055008||lung black
|
|
D055008||lungs black
|
|
D055008||miner apos s lung coal
|
|
D055008||miner apos s lungs coal
|
|
D055008||pneumoconioses coalworker apos s
|
|
D055008||pneumoconioses coal worker apos s
|
|
D055008||pneumoconiosis coal worker
|
|
D055008||pneumoconiosis coalworker apos s
|
|
D055008||pneumoconiosis coal workers
|
|
D055008||pneumoconiosis coal worker apos s
|
|
D005878|143500||gilbert disease
|
|
D005878|143500||arias type hyperbilirubinemia
|
|
D005878|143500||arias type hyperbilirubinemias
|
|
D005878|143500||constitutional liver dysfunction
|
|
D005878|143500||disease gilbert
|
|
D005878|143500||disease gilbert apos s
|
|
D005878|143500||familial nonhemolytic jaundice
|
|
D005878|143500||gilbert lereboullet syndrome
|
|
D005878|143500||gilbert apos s disease
|
|
D005878|143500||gilberts disease
|
|
D005878|143500||gilbert apos s syndrome
|
|
D005878|143500||gilberts syndrome
|
|
D005878|143500||gilbert syndrome
|
|
D005878|143500||hblrg
|
|
D005878|143500||hyperbilirubinemia 1
|
|
D005878|143500||hyperbilirubinemia 1s
|
|
D005878|143500||hyperbilirubinemia arias type
|
|
D005878|143500||hyperbilirubinemia gilbert type
|
|
D005878|143500||hyperbilirubinemia i
|
|
D005878|143500||hyperbilirubinemias arias type
|
|
D005878|143500||meulengracht syndrome
|
|
D005878|143500||syndrome gilbert
|
|
D005878|143500||syndrome gilbert apos s
|
|
D005878|143500||unconjugated benign bilirubinemia
|
|
D055009||spondylosis
|
|
D055009||cervical spondylosis
|
|
D055009||lumbarsacral spondylosis
|
|
D055009||spondylosis cervical
|
|
D055009||spondylosis deformans
|
|
D055009||spondylosis lumbarsacral
|
|
D055009||spondylosis thoracic
|
|
D055009||thoracic spondylosis
|
|
608446|D009203||myocardial infarction
|
|
608446|D009203||infarction myocardial
|
|
608446|D009203||infarctions myocardial
|
|
608446|D009203||infarct myocardial
|
|
608446|D009203||infarcts myocardial
|
|
608446|D009203||mci1 included
|
|
608446|D009203||mci2
|
|
608446|D009203||myocardial infarct
|
|
608446|D009203||myocardial infarction protection against included
|
|
608446|D009203||myocardial infarctions
|
|
608446|D009203||myocardial infarction susceptibility to
|
|
608446|D009203||myocardial infarction susceptibility to 1 included
|
|
608446|D009203||myocardial infarction susceptibility to 2
|
|
608446|D009203||myocardial infarcts
|
|
D057667||conducted energy weapon injuries
|
|
D057667||injuries stun gun
|
|
D057667||injuries taser
|
|
D057667||injury stun gun
|
|
D057667||injury taser
|
|
D057667||stun gun injuries
|
|
D057667||stun gun injury
|
|
D057667||taser injuries
|
|
D057667||taser injury
|
|
C565201|610321||prostate cancer hereditary 7
|
|
C565201|610321||hpc7
|
|
C565201|610321||prostate cancer aggressiveness
|
|
C537998|224410||dyssegmental dysplasia
|
|
C537998|224410||anisospondylic camptomicromelic dwarfism
|
|
C537998|224410||anisospondylic camptomicromelic dwarfism silverman handmaker type
|
|
C537998|224410||ddsh
|
|
C537998|224410||dyssegmental dwarfism
|
|
C537998|224410||dyssegmental dwarfism silverman handmaker type
|
|
C537998|224410||dyssegmental dysplasia silverman handmaker type
|
|
D009959||oropharyngeal neoplasms
|
|
D009959||cancer of oropharnyx
|
|
D009959||cancer of the oropharynx
|
|
D009959||cancer oropharyngeal
|
|
D009959||cancer oropharynx
|
|
D009959||cancers oropharyngeal
|
|
D009959||cancers oropharynx
|
|
D009959||neoplasm oropharyngeal
|
|
D009959||neoplasm oropharynx
|
|
D009959||neoplasms oropharyngeal
|
|
D009959||neoplasms oropharynx
|
|
D009959||oropharnyx cancer
|
|
D009959||oropharnyx cancers
|
|
D009959||oropharyngeal cancer
|
|
D009959||oropharyngeal cancers
|
|
D009959||oropharyngeal neoplasm
|
|
D009959||oropharynx cancer
|
|
D009959||oropharynx cancers
|
|
D009959||oropharynx neoplasm
|
|
D009959||oropharynx neoplasms
|
|
C537312|608029||spinocerebellar ataxia autosomal recessive 6
|
|
C537312|608029||cerebellar ataxia infantile nonprogressive autosomal recessive
|
|
C537312|608029||norwegian infantile onset ataxia
|
|
C537312|608029||scar6
|
|
D009958||orofaciodigital syndromes
|
|
D009958||dysplasia linguofacialis
|
|
D009958||gorlin psaume syndrome
|
|
D009958||mohr syndrome
|
|
D009958||oral facial digital syndrome
|
|
D009958||oral facial digital syndrome type ii
|
|
D009958||orodigitofacial dysostosis
|
|
D009958||orodigitofacial syndrome
|
|
D009958||orofaciodigital syndrome
|
|
D009958||oro facio digital syndrome
|
|
D009958||orofaciodigital syndrome ii
|
|
D009958||orofaciodigital syndrome iis
|
|
D009958||orofaciodigital syndrome is
|
|
D009958||syndrome gorlin psaume
|
|
D009958||syndrome mohr
|
|
D009958||syndrome orofaciodigital
|
|
D009958||syndromes orofaciodigital
|
|
D009957||oroantral fistula
|
|
D009957||fistula oroantral
|
|
D009957||fistulas oroantral
|
|
D009957||oroantral fistulas
|
|
D009956||psittacosis
|
|
D009956||ornithoses
|
|
D009956||ornithosis
|
|
D009956||psittacoses
|
|
C535956|131750||epidermolysis bullosa dystrophica pasini type
|
|
C535956|131750||albopapuloid dominant dystrophic eb
|
|
C535956|131750||albopapuloid dominant dystrophic epidermolysis bullosa ebdd epidermolysis bullosa dystrophica with subcorneal cleavage included
|
|
C535956|131750||ddeb
|
|
C535956|131750||dystrophic epidermolysis bullosa autosomal dominant
|
|
C535956|131750||ebdct
|
|
C535956|131750||ebdsc included
|
|
C535956|131750||epidermolysis bullosa dystrophica autosomal dominant
|
|
C535956|131750|226600|D016108||epidermolysis bullosa dystrophica cockayne touraine type
|
|
D008630||mercury poisoning
|
|
D008630||mercury poisonings
|
|
D008630||poisoning mercury
|
|
D008630||poisonings mercury
|
|
D055013||osteoarthritis spine
|
|
D055013||lumbar osteoarthritis
|
|
D055013||osteoarthritis lumbar
|
|
D055013||osteoarthritis spinal
|
|
D055013||spinal osteoarthritis
|
|
D055013||spine osteoarthritis
|
|
150270|C562861||laryngeal adductor paralysis
|
|
150270|C562861||lap
|
|
150270|C562861||vocal cord dysfunction adductor type
|
|
D055010||posterior cervical sympathetic syndrome
|
|
D055010||barre lieou syndrome
|
|
D055010||syndrome barre lieou
|
|
D055010||syndrome of barre lieou
|
|
C563983|600165||nanophthalmos 1
|
|
C563983|600165||microphthalmos simple autosomal dominant
|
|
C563983|600165||nanophthalmia 1
|
|
C563983|600165||nanophthalmos autosomal dominant
|
|
C563983|600165||nanophthalmos with high hyperopia and angle closure glaucoma
|
|
C563983|600165||nno1
|
|
C538068|229800||fructosuria
|
|
C538068|229800||essential benign fructosuria
|
|
C538068|229800||fructosuria essential
|
|
C538068|229800||hepatic fructokinase deficiency
|
|
C538068|229800||ketohexokinase deficiency
|
|
D008639||mesenteric cyst
|
|
D008639||cyst mesenteric
|
|
D008639||cysts mesenteric
|
|
D008639||mesenteric cysts
|
|
D012174|268000||retinitis pigmentosa
|
|
D012174|268000||cone rod degeneration
|
|
D012174|268000||cone rod degenerations
|
|
D012174|268000||cone rod dystrophies
|
|
D012174|268000||cone rod dystrophies retinal
|
|
D012174|268000|120970||cone rod dystrophy
|
|
D012174|268000|120970||cone rod dystrophy 2
|
|
D012174|268000||cone rod dystrophy retinal
|
|
D012174|268000||cone rod retinal dystrophies
|
|
D012174|268000|120970||cone rod retinal dystrophy
|
|
D012174|268000||degeneration cone rod
|
|
D012174|268000||degenerations cone rod
|
|
D012174|268000||degenerations tapetoretinal
|
|
D012174|268000||degeneration tapetoretinal
|
|
D012174|268000||dystrophies cone rod
|
|
D012174|268000||dystrophies cone rod retinal
|
|
D012174|268000||dystrophies retinal cone rod
|
|
D012174|268000||dystrophies rod cone
|
|
D012174|268000||dystrophy cone rod
|
|
D012174|268000||dystrophy cone rod retinal
|
|
D012174|268000||dystrophy retinal cone rod
|
|
D012174|268000||dystrophy rod cone
|
|
D012174|268000||pigmentary retinopathies
|
|
D012174|268000||pigmentary retinopathy
|
|
D012174|268000||retinal cone rod dystrophies
|
|
D012174|268000|120970||retinal cone rod dystrophy
|
|
D012174|268000||retinal dystrophies cone rod
|
|
D012174|268000||retinal dystrophy cone rod
|
|
D012174|268000||retinitis pigmentosa 22
|
|
D012174|268000||retinitis pigmentosa 23
|
|
D012174|268000||retinitis pigmentosa 24
|
|
D012174|268000||retinitis pigmentosa 28
|
|
D012174|268000||retinopathies pigmentary
|
|
D012174|268000||retinopathy pigmentary
|
|
D012174|268000||rod cone dystrophies
|
|
D012174|268000||rod cone dystrophy
|
|
D012174|268000||rp
|
|
D012174|268000||rp22
|
|
D012174|268000||rp23
|
|
D012174|268000||rp24
|
|
D012174|268000||rp28
|
|
D012174|268000||tapetoretinal degeneration
|
|
D012174|268000||tapetoretinal degenerations
|
|
D008637||mesenchymoma
|
|
D008637||mesenchymomas
|
|
C536028|212720||martsolf syndrome
|
|
C536028|212720||cataract mental retardation hypogonadism
|
|
D008641||mesenteric vascular occlusion
|
|
D008641||mesenteric vascular occlusions
|
|
D008641||occlusion mesenteric vascular
|
|
D008641||occlusions mesenteric vascular
|
|
D008641||vascular occlusion mesenteric
|
|
D008641||vascular occlusions mesenteric
|
|
133020|D004916||erythromelalgia
|
|
133020|D004916||erythermalgia
|
|
133020|D004916||erythermalgia primary
|
|
133020|D004916||erythermalgias
|
|
133020|D004916||erythermalgias primary
|
|
133020|D004916||erythromelalgia familial
|
|
133020|D004916||erythromelalgia familial neuropathy small fiber included
|
|
133020|D004916||erythromelalgia primary
|
|
133020|D004916||erythromelalgias
|
|
133020|D004916||familial erythromelalgia
|
|
133020|D004916||primary erythermalgia
|
|
133020|D004916||primary erythermalgias
|
|
133020|D004916||primary erythromelalgia
|
|
133020|D004916||sfnp included
|
|
133020|D004916||small fiber neuropathy
|
|
133020|D004916||small nerve fiber neuropathy
|
|
D008640||mesenteric lymphadenitis
|
|
D008640||lymphadenitides mesenteric
|
|
D008640||lymphadenitis mesenteric
|
|
D008640||mesenteric lymphadenitides
|
|
D010954||plasmacytoma
|
|
D010954||plasma cell tumor
|
|
D010954||plasma cell tumors
|
|
D010954||plasmacytomas
|
|
D010954||plasmocytoma
|
|
D010954||plasmocytomas
|
|
D010954||tumor plasma cell
|
|
D010954||tumors plasma cell
|
|
217400|C535473||corneal dystrophy and perceptive deafness
|
|
217400|C535473||cdpd
|
|
217400|C535473||cdpd1
|
|
217400|C535473||congenital corneal dystrophy progressive sensorineural deafness
|
|
217400|C535473||corneal dystrophy and sensorineural deafness
|
|
217400|C535473||harboyan syndrome
|
|
C567437|612015||congenital disorder of glycosylation type in
|
|
C567437|612015||cdg1n
|
|
C567437|612015||cdgin
|
|
C567437|612015||cdg in
|
|
D008607||intellectual disability
|
|
D008607||deficiencies mental
|
|
D008607||deficiency mental
|
|
D008607||disabilities intellectual
|
|
D008607||disability intellectual
|
|
D008607||idiocy
|
|
D008607||intellectual disabilities
|
|
D008607||mental deficiencies
|
|
D008607||mental deficiency
|
|
D008607||mental retardation
|
|
D008607||mental retardation psychosocial
|
|
D008607||mental retardations psychosocial
|
|
D008607||psychosocial mental retardation
|
|
D008607||psychosocial mental retardations
|
|
D008607||retardation mental
|
|
D008607||retardation psychosocial mental
|
|
D008607||retardations psychosocial mental
|
|
C563958|600320||diabetes mellitus insulin dependent 5
|
|
C563958|600320||iddm5
|
|
C563958|600320||insulin dependent diabetes mellitus 5
|
|
D010927||placental insufficiency
|
|
D010927||insufficiency placental
|
|
176807|D011471||prostatic neoplasms
|
|
176807|D011471||cancer of prostate
|
|
176807|D011471||cancer of the prostate
|
|
176807|D011471||cancer prostate
|
|
176807|D011471||cancer prostatic
|
|
176807|D011471||cancers prostate
|
|
176807|D011471||cancers prostatic
|
|
176807|D011471||hpcqtl19
|
|
176807|D011471||neoplasm prostate
|
|
176807|D011471||neoplasm prostatic
|
|
176807|D011471||neoplasms prostate
|
|
176807|D011471||neoplasms prostatic
|
|
176807|D011471||prostate cancer
|
|
176807|D011471||prostate cancer aggressiveness quantitative trait locus on chromosome 19
|
|
176807|D011471||prostate cancers
|
|
176807|D011471||prostate neoplasm
|
|
176807|D011471||prostate neoplasms
|
|
176807|D011471||prostatic cancer
|
|
176807|D011471||prostatic cancers
|
|
176807|D011471||prostatic neoplasm
|
|
200150|D054546||neuroacanthocytosis
|
|
200150|D054546||acanthocytoses chorea
|
|
200150|D054546||acanthocytosis chorea
|
|
200150|D054546||acanthocytosis with neurologic disorder
|
|
200150|D054546||chac
|
|
200150|D054546||chorea acanthocytoses
|
|
200150|D054546||chorea acanthocytosis
|
|
200150|D054546||chorea acanthocytosis syndrome
|
|
200150|D054546||chorea acanthocytosis syndromes
|
|
200150|D054546||choreoacanthocytoses
|
|
200150|D054546||choreoacanthocytosis
|
|
200150|D054546||levine critchley syndrome
|
|
C567502|611890||lethal arthrogryposis with anterior horn cell disease
|
|
C567502|611890||laahd
|
|
D056364||colloid cysts
|
|
D056364||colloid cyst
|
|
D056364||cyst colloid
|
|
D056364||cysts colloid
|
|
D055034||osteochondrosis
|
|
D055034||koehler disease
|
|
D055034||koehler apos s disease
|
|
D055034||koehlers disease
|
|
D055034||navicular osteochondroses
|
|
D055034||navicular osteochondrosis
|
|
D055034||osgood schlatter disease
|
|
D055034||osteochondroses
|
|
D055034||osteochondroses navicular
|
|
D055034||osteochondrosis navicular
|
|
D055035||osteochondroses spinal
|
|
D055035||osteochondrosis of spine
|
|
D055035||osteochondrosis spinal
|
|
D055035||spinal osteochondroses
|
|
D055035||spine osteochondroses
|
|
D055035||spine osteochondrosis
|
|
D010921||placenta accreta
|
|
D010921||accreta placenta
|
|
D010921||increta placenta
|
|
D010921||percreta placenta
|
|
D010921||placenta increta
|
|
D010921||placenta percreta
|
|
D010923||placenta previa
|
|
D010923||placenta praevia
|
|
D055031||primary graft dysfunction
|
|
D055031||dysfunction primary graft
|
|
D055031||graft dysfunction primary
|
|
D010922||placenta diseases
|
|
D010922||disease placenta
|
|
D010922||disease placental
|
|
D010922||diseases placenta
|
|
D010922||diseases placental
|
|
D010922||disorder placenta
|
|
D010922||disorders placenta
|
|
D010922||placenta disease
|
|
D010922||placenta disorder
|
|
D010922||placenta disorders
|
|
D010922||placental disease
|
|
D010922||placental diseases
|
|
C567643|613325||rhabdoid tumor predisposition syndrome 2
|
|
C567643|613325||rtps2
|
|
C567450|611953||macular degeneration age related 11
|
|
C567450|611953||armd11
|
|
270450|C564816||insulin like growth factor i resistance to
|
|
270450|C564816||igf i resistance
|
|
270450|C564816||igf i resistance insulin like growth factor i resistance to due to increased binding protein included
|
|
270450|C564816||somatomedin c resistance to
|
|
270450|C564816||somatomedin end organ insensitivity to
|
|
606799|D020521||stroke
|
|
606799|D020521||acute cerebrovascular accident
|
|
606799|D020521||acute cerebrovascular accidents
|
|
606799|D020521||acute stroke
|
|
606799|D020521||acute strokes
|
|
606799|D020521||apoplexy
|
|
606799|D020521||apoplexy cerebrovascular
|
|
606799|D020521||brain vascular accident
|
|
606799|D020521||brain vascular accidents
|
|
606799|D020521||cerebral stroke
|
|
606799|D020521||cerebral strokes
|
|
606799|D020521||cerebrovascular accident acute
|
|
606799|D020521||cerebrovascular accidents
|
|
606799|D020521||cerebrovascular accidents acute
|
|
606799|D020521||cerebrovascular apoplexy
|
|
606799|D020521||cerebrovascular stroke
|
|
606799|D020521||cerebrovascular strokes
|
|
606799|D020521||cva cerebrovascular accident
|
|
606799|D020521||cvas cerebrovascular accident
|
|
606799|D020521||strk1
|
|
606799|D020521||stroke acute
|
|
606799|D020521||stroke cerebral
|
|
606799|D020521||stroke cerebrovascular
|
|
606799|D020521||strokes
|
|
606799|D020521||strokes acute
|
|
606799|D020521||strokes cerebral
|
|
606799|D020521||strokes cerebrovascular
|
|
606799|D020521||stroke susceptibility to 1
|
|
606799|D020521||vascular accident brain
|
|
606799|D020521||vascular accidents brain
|
|
D010939||plant poisoning
|
|
D010939||plant poisonings
|
|
D010939||poisoning plant
|
|
D010939||poisonings plant
|
|
C566970|611291||severe combined immunodeficiency with microcephaly growth retardation and sensitivity to ionizing radiation
|
|
C566970|611291||nhej1 syndrome
|
|
C566970|611291||nhej1 syndrome severe combined immunodeficiency with sensitivity to ionizing radiation due to nhej1 deficiency included
|
|
C566970|611291||scid autosomal recessive t cell negative b cell negative nk cell positive and sensitivity to ionizing radiation due to nhej1 deficiency
|
|
C566970|611291||scid autosomal recessive t cell negative b cell negative nk cell positive and sensitivity to ionizing radiation due to nhej1 deficiency included
|
|
C566970|611291||scid autosomal recessive t cell negative b cell negative nk cell positive with microcephaly growth retardation and sensitivity to ionizing radiation
|
|
C566970|611291||severe combined immunodeficiency with sensitivity to ionizing radiation due to nhej1 deficiency
|
|
D010930||plague
|
|
D010930||black death
|
|
D010930||black deaths
|
|
D010930||black plague
|
|
D010930||black plagues
|
|
D010930||bubonic plague
|
|
D010930||death black
|
|
D010930||deaths black
|
|
D010930||meningeal plague
|
|
D010930||meningeal plagues
|
|
D010930||plague black
|
|
D010930||plague bubonic
|
|
D010930||plague meningeal
|
|
D010930||plague pneumonic
|
|
D010930||plague pulmonic
|
|
D010930||plagues black
|
|
D010930||plague septicemic
|
|
D010930||plagues meningeal
|
|
D010930||plagues pneumonic
|
|
D010930||plagues pulmonic
|
|
D010930||plagues septicemic
|
|
D010930||pneumonic plague
|
|
D010930||pneumonic plagues
|
|
D010930||pulmonic plague
|
|
D010930||pulmonic plagues
|
|
D010930||septicemic plague
|
|
D010930||septicemic plagues
|
|
D009771|164230||obsessive compulsive disorder
|
|
D009771|164230||anankastic personalities
|
|
D009771|164230||anankastic personality
|
|
D009771|164230||disorder obsessive compulsive
|
|
D009771|164230||disorders obsessive compulsive
|
|
D009771|164230||neuroses obsessive compulsive
|
|
D009771|164230||neurosis obsessive compulsive
|
|
D009771|164230||obsessive compulsive disorders
|
|
D009771|164230||obsessive compulsive neuroses
|
|
D009771|164230||obsessive compulsive neurosis
|
|
D009771|164230||ocd
|
|
D009771|164230||personalities anankastic
|
|
D009771|164230||personality anankastic
|
|
D013180||sprains and strains
|
|
D013180||sprain
|
|
D013180||sprains
|
|
D013180||strain
|
|
D013180||strains
|
|
D013180||strains and sprains
|
|
D009918||orbital neoplasms
|
|
D009918||neoplasm orbital
|
|
D009918||neoplasms orbital
|
|
D009918||orbital neoplasm
|
|
D009917||orbital fractures
|
|
D009917||blow out fracture
|
|
D009917||blow out fractures
|
|
D009917||fracture blow out
|
|
D009917||fracture orbital
|
|
D009917||fractures blow out
|
|
D009917||fractures orbital
|
|
D009917||orbital fracture
|
|
D009916||orbital diseases
|
|
D009916||disease orbital
|
|
D009916||diseases orbital
|
|
D009916||orbital disease
|
|
D013182||sprue tropical
|
|
D013182||idiopathic tropical malabsorption syndrome
|
|
D013182||tropical sprue
|
|
D001198||ascaridiasis
|
|
D001198||ascaridiases
|
|
D009914||oral submucous fibrosis
|
|
D009914||fibroses oral submucous
|
|
D009914||fibrosis oral submucous
|
|
D009914||oral submucous fibroses
|
|
D009914||submucous fibroses oral
|
|
D009914||submucous fibrosis oral
|
|
D001196||ascariasis
|
|
D001196||ascariases
|
|
D009912||oral manifestations
|
|
D009912||manifestation oral
|
|
D009912||manifestations oral
|
|
D009912||oral manifestation
|
|
C536450|310490||cowchock syndrome
|
|
C536450|310490||charcot marie tooth disease with deafness and mental retardation
|
|
C536450|310490||charcot marie tooth disease x linked recessive 4
|
|
C536450|310490||cmtx4
|
|
C536450|310490||cowck
|
|
C536450|310490||nadmr
|
|
C536450|310490||namsd
|
|
C536450|310490||neuropathy axonal motor sensory with deafness and mental retardation
|
|
D001195||asbestosis
|
|
D001195||asbestoses
|
|
D001195||idiopathic interstitial pneumonitis from asbestos exposure
|
|
D001195||pulmonary fibrosis from asbestos exposure
|
|
C538388|307150||hypertrichosis congenital generalized x linked
|
|
C538388|307150||cgh
|
|
C538388|307150||chromosome xq27 1 interchromosomal insertion syndrome
|
|
C538388|307150||hcg
|
|
C538388|307150||htc2
|
|
C538388|307150||hypertrichosis congenital generalized
|
|
C538388|307150||macias flores garcia cruz rivera syndrome
|
|
C536065|311300||oto palato digital syndrome type 1
|
|
C536065|311300||frontootopalatodigital osteodysplasia included
|
|
C536065|311300||opd1
|
|
C536065|311300||opd i syndrome
|
|
C536065|311300||opd syndrome 1 otopalatodigital spectrum disorder included
|
|
C536065|311300||opd syndrome type 1
|
|
C536065|311300||otopalatodigital syndrome type 1
|
|
C536065|311300||otopalatodigital syndrome type i
|
|
C536065|311300||taybi syndrome
|
|
D006958|114000||hyperostosis cortical congenital
|
|
D006958|114000||caffey de toni silvermann syndrome
|
|
D006958|114000||caffey disease
|
|
D006958|114000||caffey apos s disease familial
|
|
D006958|114000||congenital cortical hyperostoses
|
|
D006958|114000||congenital cortical hyperostosis
|
|
D006958|114000||congenital hyperostoses cortical
|
|
D006958|114000||congenital hyperostosis cortical
|
|
D006958|114000||cortical congenital hyperostoses
|
|
D006958|114000||cortical congenital hyperostosis
|
|
D006958|114000||cortical hyperostoses congenital
|
|
D006958|114000||cortical hyperostoses infantile
|
|
D006958|114000||cortical hyperostosis congenital
|
|
D006958|114000||cortical hyperostosis infantile
|
|
D006958|114000||disease caffey
|
|
D006958|114000||disease familial caffey apos s
|
|
D006958|114000||familial caffey disease
|
|
D006958|114000||familial caffey apos s disease
|
|
D006958|114000||familial caffeys disease
|
|
D006958|114000||familial infantile cortical hyperostosis
|
|
D006958|114000||hyperostoses congenital cortical
|
|
D006958|114000||hyperostoses cortical congenital
|
|
D006958|114000||hyperostoses infantile cortical
|
|
D006958|114000||hyperostosis congenital cortical
|
|
D006958|114000||hyperostosis infantile cortical
|
|
D006958|114000||infantile cortical hyperostoses
|
|
D006958|114000||infantile cortical hyperostosis
|
|
D006958|114000||infantile cortical hyperostosis prenatal cortical hyperostosis lethal included
|
|
D006958|114000||syndrome caffey de toni silvermann
|
|
605376||heterotaxy visceral 2 autosomal
|
|
605376||htx
|
|
605376||htx2
|
|
D010900||pituitary diseases
|
|
D010900||adenohypophyseal disease
|
|
D010900||adenohypophyseal diseases
|
|
D010900||anterior pituitary disease
|
|
D010900||anterior pituitary diseases
|
|
D010900||disease adenohypophyseal
|
|
D010900||disease anterior pituitary
|
|
D010900||disease neurohypophyseal
|
|
D010900||disease pituitary
|
|
D010900||disease pituitary gland
|
|
D010900||disease posterior pituitary
|
|
D010900||diseases adenohypophyseal
|
|
D010900||diseases anterior pituitary
|
|
D010900||diseases neurohypophyseal
|
|
D010900||diseases pituitary
|
|
D010900||diseases pituitary gland
|
|
D010900||diseases posterior pituitary
|
|
D010900||disorder hypophyseal
|
|
D010900||disorder pituitary
|
|
D010900||disorders hypophyseal
|
|
D010900||disorders pituitary
|
|
D010900||hypophyseal disorder
|
|
D010900||hypophyseal disorders
|
|
D010900||neurohypophyseal disease
|
|
D010900||neurohypophyseal diseases
|
|
D010900||pituitary disease
|
|
D010900||pituitary disease anterior
|
|
D010900||pituitary disease posterior
|
|
D010900||pituitary diseases anterior
|
|
D010900||pituitary diseases posterior
|
|
D010900||pituitary disorder
|
|
D010900||pituitary disorders
|
|
D010900||pituitary gland disease
|
|
D010900||pituitary gland diseases
|
|
D010900||posterior pituitary disease
|
|
D010900||posterior pituitary diseases
|
|
C538613|312000||panhypopituitarism x linked
|
|
C538613|312000||phpx
|
|
C538613|312000||pituitary dwarfism iv formerly
|
|
C564515|300433||mental retardation x linked 81
|
|
C564515|300433||mrx81
|
|
D013174||sporotrichosis
|
|
D013174||sporotrichoses
|
|
C566576|602099||amyotrophic lateral sclerosis 5
|
|
C566576|602099||als5
|
|
C566551|602429||glaucoma 1 open angle d
|
|
C566551|602429|C566383|603383||glaucoma primary open angle adult onset
|
|
C566551|602429||glc1d
|
|
D010916||pityriasis rubra pilaris
|
|
D010915||pityriasis
|
|
D010915||pityriases
|
|
D009920||orchitis
|
|
D009920||orchitides
|
|
202300|C565972||adrenocortical carcinoma hereditary
|
|
202300|C565972||adcc
|
|
202300|C565972||adrenocortical carcinoma pediatric included
|
|
C562865|612356||heparin cofactor ii deficiency
|
|
C562865|612356||hcf2 deficiency
|
|
C562865|612356||hcf ii deficiency
|
|
C562865|612356||thph10
|
|
C562865|612356||thrombophilia due to heparin cofactor ii deficiency
|
|
C562865|612356||thrombophilia susceptibility to due to heparin cofactor ii deficiency
|
|
C567410|600625||orofacial cleft 11
|
|
C567410|600625||chcl included
|
|
C567410|600625||cleft lip with or without cleft palate nonsyndromic 11
|
|
C567410|600625||cleft lip with or without cleft palate nonsyndromic 11 cleft lip congenital healed included
|
|
C567410|600625||congenital healed cleft lip included
|
|
C567410|600625||ofc11
|
|
D010911||pituitary neoplasms
|
|
D010911||adenoma pituitary
|
|
D010911||adenomas pituitary
|
|
D010911||cancer of pituitary
|
|
D010911||cancer of the pituitary
|
|
D010911||cancer pituitary
|
|
D010911||cancers pituitary
|
|
D010911||carcinoma pituitary
|
|
D010911||carcinomas pituitary
|
|
D010911||neoplasm pituitary
|
|
D010911||neoplasms pituitary
|
|
D010911||pituitary adenoma
|
|
D010911||pituitary adenomas
|
|
D010911||pituitary cancer
|
|
D010911||pituitary cancers
|
|
D010911||pituitary carcinoma
|
|
D010911||pituitary carcinomas
|
|
D010911||pituitary neoplasm
|
|
D010911||pituitary tumor
|
|
D010911||pituitary tumors
|
|
D010911||tumor pituitary
|
|
D010911||tumors pituitary
|
|
C536384||faces syndrome
|
|
C562672||hyperglycinemia transient neonatal
|
|
C536385||facial ectodermal dysplasia
|
|
C536385||bitemporal forceps marks syndrome
|
|
C536385||focal facial dermal dysplasia type 2
|
|
C536385||focal facial dermal dysplasia type ii
|
|
C536385||setleis syndrome
|
|
D052801||male urogenital diseases
|
|
D052801||genitourinary disease male
|
|
D052801||genitourinary diseases male
|
|
D052801||male genitourinary disease
|
|
D052801||male genitourinary diseases
|
|
D052801||male urogenital disease
|
|
D052801||urogenital disease male
|
|
D052801||urogenital diseases male
|
|
C562670||glucoglycinuria
|
|
C536383||eyebrows duplication of with stretchable skin and syndactyly
|
|
C536388||faciocardiorenal syndrome
|
|
C536388||eastman bixler syndrome
|
|
D013161||splenic rupture
|
|
D013161||rupture splenic
|
|
D013161||ruptures splenic
|
|
D013161||splenic ruptures
|
|
C536389||faciomandibular myoclonus nocturnal
|
|
C536389||nocturnal facio mandibular myoclonus
|
|
C562674||hyperleucine isoleucinemia
|
|
C536387||facio thoraco genital syndrome
|
|
C536387||congenital anomalies involving mainly the face thorax and genitalia
|
|
C536387||faciothoracogenital syndrome
|
|
D013160||splenic neoplasms
|
|
D013160||cancer of spleen
|
|
D013160||cancer of the spleen
|
|
D013160||cancer spleen
|
|
D013160||cancer splenic
|
|
D013160||cancers spleen
|
|
D013160||cancers splenic
|
|
D013160||neoplasm spleen
|
|
D013160||neoplasm splenic
|
|
D013160||neoplasms spleen
|
|
D013160||neoplasms splenic
|
|
D013160||spleen cancer
|
|
D013160||spleen cancers
|
|
D013160||spleen neoplasm
|
|
D013160||spleen neoplasms
|
|
D013160||splenic cancer
|
|
D013160||splenic cancers
|
|
D013160||splenic neoplasm
|
|
D001176||arthrogryposis
|
|
D001176||amyoplasia congenita
|
|
D001176||arthrogryposes
|
|
D001176||arthrogryposes congenital multiple
|
|
D001176||arthrogryposis congenital multiple
|
|
D001176||arthrogryposis multiplex congenita
|
|
D001176||arthrogryposis multiplex congenita amc
|
|
D001176||arthrogryposis multiplex congenitas
|
|
D001176||arthrogryposis multiplex congenitas amc
|
|
D001176||arthromyodysplasia congenital
|
|
D001176||arthromyodysplasias congenital
|
|
D001176||congenita arthrogryposis multiplex
|
|
D001176||congenita arthrogryposis multiplex amc
|
|
D001176||congenital arthromyodysplasia
|
|
D001176||congenital arthromyodysplasias
|
|
D001176||congenital multiple arthrogryposes
|
|
D001176||congenital multiple arthrogryposis
|
|
D001176||congenitas arthrogryposis multiplex
|
|
D001176||congenitas arthrogryposis multiplex amc
|
|
D001176||fibrous ankylosis of multiple joints
|
|
D001176||guerin stern syndrome
|
|
D001176||gu 233 rin stern syndrome
|
|
D001176||multiple arthrogryposes congenital
|
|
D001176||multiple arthrogryposis congenital
|
|
D001176||multiplex congenita arthrogryposis
|
|
D001176||multiplex congenita arthrogryposis amc
|
|
D001176||multiplex congenitas arthrogryposis
|
|
D001176||multiplex congenitas arthrogryposis amc
|
|
D001176||myodystrophia fetalis deformans
|
|
D001176||otto syndrome
|
|
D001176||rocher sheldon syndrome
|
|
D001176||rossi syndrome
|
|
D001176||syndrome guerin stern
|
|
D001176||syndrome gu 233 rin stern
|
|
D001176||syndrome otto
|
|
D001176||syndrome rocher sheldon
|
|
D001176||syndrome rossi
|
|
C562678||acetyl coa carboxylase deficiency
|
|
C562678||acaca deficiency
|
|
D013009|613938||somnambulism
|
|
D013009|613938||nocturnal wandering
|
|
D013009|613938||parasomnia sleep terrors type included
|
|
D013009|613938||parasomnia sleepwalking type
|
|
D013009|613938||psmnst included
|
|
D013009|613938||psmnsw
|
|
D013009|613938||sleepwalking
|
|
D013009|613938||sleep walking
|
|
D013009|613938||sleep walking disorder
|
|
D013009|613938||sleep walking disorders
|
|
D013009|613938||wandering nocturnal
|
|
C536380||evan apos s syndrome
|
|
C536380||autoimmune hemolytic anemia and autoimmune thrombocytopenia
|
|
C536380||evan syndrome
|
|
D012507|181000||sarcoidosis
|
|
D012507|181000||besnier boeck disease
|
|
D012507|181000||besnier boeck schaumann syndrome
|
|
D012507|181000||boeck disease
|
|
D012507|181000||boeck sarcoid
|
|
D012507|181000||boeck apos s disease
|
|
D012507|181000||boecks disease
|
|
D012507|181000||boeck apos s sarcoid
|
|
D012507|181000||boecks sarcoid
|
|
D012507|181000||disease schaumann
|
|
D012507|181000||sarcoid boeck apos s
|
|
D012507|181000||sarcoidoses
|
|
D012507|181000||sarcoidosis susceptibility to 1
|
|
D012507|181000||sarcoidosis susceptibility to 2
|
|
D012507|181000||sarcoidosis susceptibility to 3
|
|
D012507|181000||schaumann disease
|
|
D012507|181000||schaumann apos s syndrome
|
|
D012507|181000||schaumann apos s syndromes
|
|
D012507|181000||schaumann syndrome
|
|
D012507|181000||ss1
|
|
D012507|181000||ss2
|
|
D012507|181000||ss3
|
|
D012507|181000||syndrome besnier boeck schaumann
|
|
D012507|181000||syndrome schaumann
|
|
D012507|181000||syndrome schaumann apos s
|
|
D001177||arthropathy neurogenic
|
|
D001177||arthropathies neurogenic
|
|
D001177||charcot joint
|
|
D001177||charcot apos s joint
|
|
D001177||charcots joint
|
|
D001177||joint charcot apos s
|
|
D001177||neurogenic arthropathies
|
|
D001177||neurogenic arthropathy
|
|
D001183||arthus reaction
|
|
D001183||arthus phenomenon
|
|
D001183||phenomenon arthus
|
|
D001183||reaction arthus
|
|
C536352|193220||vitreoretinochoroidopathy
|
|
C536352|193220||advirc
|
|
C536352|193220||autosomal dominant vitreoretinochoroidopathy
|
|
C536352|193220||microcornea rod cone dystrophy cataract and posterior staphyloma
|
|
C536352|193220||mrcs included
|
|
C536352|193220||vitreoretinochoroidopathy autosomal dominant
|
|
C536352|193220||vitreoretinochoroidopathy autosomal dominant with nanophthalmos
|
|
C536352|193220||vitreoretinochoroidopathy autosomal dominant with nanophthalmos microcornea rod cone dystrophy cataract and posterior staphyloma included
|
|
C536352|193220||vitreoretinochoroidopathy dominant
|
|
C536352|193220||vitreoretinochoroidopathy with microcornea glaucoma and cataract
|
|
C536352|193220||vrcp
|
|
C567429|612069||amyotrophic lateral sclerosis 10
|
|
C567429|612069||amyotrophic lateral sclerosis 10 with or without frontotemporal dementia als10 frontotemporal lobar degeneration with tdp43 inclusions tardbp related
|
|
C567429|612069||frontotemporal dementia with tdp43 inclusions tardbp related included
|
|
C567429|612069||ftld tdp tardbp related included
|
|
606689||glaucoma 1 open angle b
|
|
606689||glc1b
|
|
D018296|132600||pilomatrixoma
|
|
D018296|132600||benign pilomatricoma
|
|
D018296|132600||benign pilomatrixoma
|
|
D018296|132600||calcifying epithelioma of malherbe
|
|
D018296|132600||epithelioma calcificans of malherbe
|
|
D018296|132600||malherbe calcifying epithelioma
|
|
D018296|132600||pilomatricoma
|
|
D018296|132600||pilomatricoma benign
|
|
D018296|132600||pilomatrixoma benign
|
|
D018296|132600||ptr
|
|
C536379||anonychia onychodystrophy with brachydactyly type b and ectrodactyly
|
|
C536379||kumar levick syndrome
|
|
D013158||splenic diseases
|
|
D013158||disease splenic
|
|
D013158||diseases splenic
|
|
D013158||splenic disease
|
|
C535686|600332||rippling muscle disease 1
|
|
C535686|600332||rippling muscle disease
|
|
C535686|600332||rippling muscle disease 2
|
|
C535686|600332||rippling muscle disease 2 included
|
|
C535686|600332||rmd
|
|
C535686|600332||rmd1
|
|
C535686|600332||rmd2 included
|
|
D013159||splenic infarction
|
|
D013159||infarction splenic
|
|
D013159||infarctions splenic
|
|
D013159||infarct of the spleen
|
|
D013159||infarct splenic
|
|
D013159||infarcts splenic
|
|
D013159||splenic infarctions
|
|
D013159||splenic infarcts
|
|
C562682||methionine malabsorption syndrome
|
|
C562682||oasthouse urine disease
|
|
C562682||smith strang disease
|
|
C536395||neonatal herpes
|
|
C536395||neonatal herpes simplex virus infection
|
|
C536396||neonatal ovarian cyst
|
|
C536396||fetal ovarian cyst
|
|
C536393||fairbank disease
|
|
C536393||dysplasia epiphysealis multiplex
|
|
C536393||epiphyseal dysplasia fairbank type
|
|
C536393||epiphyseal dysplasia ribbing type
|
|
C536393||fairbank multiple epiphyseal dysplasia
|
|
C536399||nephroblastomatosis fetal ascites macrosomia and wilms tumor
|
|
C536399||perlman syndrome
|
|
C536399||renal hamartomas nephroblastomatosis and fetal gigantism
|
|
609026|C563812||cataract age related cortical 1
|
|
609026|C563812||arcc1
|
|
609026|C563812||cataract 28
|
|
609026|C563812||ctrct28
|
|
C562684||hyper beta alaninemia
|
|
C562684||hyperalaninemia
|
|
C536397||neonatal systemic lupus erythematosus
|
|
C536397||neonatal lupus
|
|
C536397||neonatal lupus syndrome
|
|
D055091||bronchomalacia
|
|
D055091||bronchi chondromalacia
|
|
D055091||bronchi chondromalacias
|
|
D055091||bronchomalacias
|
|
D055091||chondromalacia of bronchi
|
|
D009902||optic neuritis
|
|
D009902||anterior optic neuritides
|
|
D009902||anterior optic neuritis
|
|
D009902||neuritides anterior optic
|
|
D009902||neuritides optic
|
|
D009902||neuritides posterior optic
|
|
D009902||neuritides retrobulbar
|
|
D009902||neuritis anterior optic
|
|
D009902||neuritis optic
|
|
D009902||neuritis posterior optic
|
|
D009902||neuritis retrobulbar
|
|
D009902||neuropapillitides
|
|
D009902||neuropapillitis
|
|
D009902||optic neuritides
|
|
D009902||optic neuritides anterior
|
|
D009902||optic neuritides posterior
|
|
D009902||optic neuritis anterior
|
|
D009902||optic neuritis posterior
|
|
D009902||posterior optic neuritides
|
|
D009902||posterior optic neuritis
|
|
D009902||retrobulbar neuritides
|
|
D009902||retrobulbar neuritis
|
|
D055092||laryngomalacia
|
|
D055092||chondromalacia of larynx
|
|
D055092||laryngomalacias
|
|
D055092||larynx chondromalacia
|
|
D055092||larynx chondromalacias
|
|
D009901||optic nerve diseases
|
|
D009901||cranial nerve ii diseases
|
|
D009901||cranial nerve ii disorder
|
|
D009901||disk disorder optic
|
|
D009901||disk disorders optic
|
|
D009901||foster kennedy syndrome
|
|
D009901||lesion neural optical
|
|
D009901||lesions neural optical
|
|
D009901||neural optical lesion
|
|
D009901||neural optical lesions
|
|
D009901||neuropathies optic
|
|
D009901||neuropathy optic
|
|
D009901||optic disk disorder
|
|
D009901||optic disk disorders
|
|
D009901||optic nerve disease
|
|
D009901||optic neuropathies
|
|
D009901||optic neuropathy
|
|
D009901||second cranial nerve diseases
|
|
D009901||syndrome foster kennedy
|
|
D055093||periodontal atrophy
|
|
D055093||atrophy of periodontium
|
|
D055093||gingivo osseous atrophies
|
|
D055093||gingivo osseous atrophy
|
|
D055093||periodontal atrophies
|
|
D055093||periodontium atrophies
|
|
D055093||periodontium atrophy
|
|
D001184||articulation disorders
|
|
D001184||articulation disorder
|
|
D001184||articulation disorder developmental
|
|
D001184||articulation disorders developmental
|
|
D001184||articulation disorder speech
|
|
D001184||articulation disorders speech
|
|
D001184||articulations unintelligible
|
|
D001184||articulation unintelligible
|
|
D001184||developmental articulation disorder
|
|
D001184||developmental articulation disorders
|
|
D001184||disarticulation disorder
|
|
D001184||disarticulation disorders
|
|
D001184||disorder disarticulation
|
|
D001184||disorders disarticulation
|
|
D001184||impairment phonological
|
|
D001184||impairment phonology
|
|
D001184||impairments phonological
|
|
D001184||impairments phonology
|
|
D001184||misarticulation
|
|
D001184||phonological impairment
|
|
D001184||phonological impairments
|
|
D001184||phonology impairment
|
|
D001184||phonology impairments
|
|
D001184||speech articulation disorder
|
|
D001184||speech articulation disorders
|
|
D001184||unintelligible articulation
|
|
D001184||unintelligible articulations
|
|
C562689|277440|C562794||rickets hereditary vitamin d resistant
|
|
C562689|277440|C562794||generalized resistance to 1 25 dihydroxyvitamin d
|
|
C562689|277440|C562794||hypocalcemic vitamin d resistant rickets
|
|
C562689|277440|C562794||vitamin d resistant rickets with end organ unresponsiveness to 1 25 dihydroxycholecalciferol
|
|
C536392||factor 8 deficiency acquired
|
|
C536392||factor viii deficiency acquired
|
|
C536392||hemophilia a acquired
|
|
D055090||tracheomalacia
|
|
D055090||chondromalacia of trachea
|
|
D055090||trachea chondromalacia
|
|
D055090||trachea chondromalacias
|
|
D055090||tracheomalacias
|
|
D055089||tracheobronchomalacia
|
|
D055089||chondromalacia of trachea and bronchi
|
|
D055089||syndrome williams campbell
|
|
D055089||tracheobronchomalacias
|
|
D055089||williams campbell syndrome
|
|
C565289|605809||myasthenia familial infantile 1
|
|
C565289|605809||cms1a1
|
|
C565289|605809||cms ia1
|
|
C565289|605809||congenital myasthenic syndrome type ia1
|
|
C565289|605809||fim1
|
|
607417|C564404||mental retardation autosomal recessive 2
|
|
607417|C564404||mental retardation autosomal recessive 2a
|
|
607417|C564404||mrt2
|
|
607417|C564404||mrt2a
|
|
D013166||spondylitis
|
|
D013166||spondylitides
|
|
D014496||urachal cyst
|
|
D014496||cysts umbilical
|
|
D014496||cysts urachal
|
|
D014496||cyst umbilical
|
|
D014496||cyst urachal
|
|
D014496||umbilical cyst
|
|
D014496||umbilical cysts
|
|
D014496||urachal cysts
|
|
D013163||splenomegaly
|
|
D013163||enlarged spleen
|
|
D013163||spleen enlarged
|
|
C537559|123150||jackson weiss syndrome
|
|
C537559|123150||acrocephalosyndactyly jackson weiss type
|
|
C537559|123150||craniosynostosis midfacial hypoplasia and foot abnormalities
|
|
C537559|123150||enlarged great toes and craniofacial abnormalities
|
|
C537559|123150||jws
|
|
D013169||spondylolysis
|
|
D013169||spondylolyses
|
|
D013168||spondylolisthesis
|
|
D013168||spondylistheses
|
|
D013168||spondylisthesis
|
|
D013168||spondylolistheses
|
|
D001159||arterio arterial fistula
|
|
D001159||arterio arterial fistulas
|
|
D001159||fistula arterio arterial
|
|
D001159||fistulas arterio arterial
|
|
C562654||hypokalemia familial
|
|
C562654||gullner syndrome
|
|
C562654||hypokalemic alkalosis familial with specific renal tubulopathy
|
|
C562651||ethanolaminosis
|
|
C562651||ethanolamine kinase deficiency
|
|
C563982||hyperparathyroidism primary caused by water clear cell hyperplasia
|
|
D003103|120200||coloboma
|
|
D003103|120200||coi
|
|
D003103|120200||coloboma ocular
|
|
D003103|120200||coloboma of iris choroid and retina
|
|
D003103|120200||colobomas
|
|
D003103|120200||coloboma uveoretinal
|
|
D003103|120200||ocular coloboma
|
|
D003103|120200||uveoretinal coloboma
|
|
C562658||tryptophanuria with dwarfism
|
|
149200|C537210||knuckle pads leuconychia and sensorineural deafness
|
|
149200|C537210||bart pumphrey syndrome
|
|
149200|C537210||knuckle pads leukonychia and sensorineural deafness
|
|
149200|C537210||knuckle pads leukonychia deafness and keratosis palmoplantaris
|
|
C559045||recurrent spontaneous hypothermia with hypoplasia of the corpus callosum
|
|
D001157||arterial occlusive diseases
|
|
D001157||arterial obstructive disease
|
|
D001157||arterial obstructive diseases
|
|
D001157||arterial occlusive disease
|
|
D001157||disease arterial obstructive
|
|
D001157||disease arterial occlusive
|
|
D001157||diseases arterial obstructive
|
|
D001157||diseases arterial occlusive
|
|
D001157||obstructive disease arterial
|
|
D001157||obstructive diseases arterial
|
|
D001157||occlusive disease arterial
|
|
D001157||occlusive diseases arterial
|
|
C562659||tyrosinosis
|
|
D002485||cementoma
|
|
D002485||cementomas
|
|
D001161||arteriosclerosis
|
|
D001161||arterioscleroses
|
|
C563730|609352||epidermolysis bullosa simplex with migratory circinate erythema
|
|
607921|C564310||retinitis pigmentosa 30
|
|
607921|C564310||macular degeneration included
|
|
607921|C564310||rp30
|
|
D013130||spinal stenosis
|
|
D013130||spinal stenoses
|
|
D013130||stenoses spinal
|
|
D013130||stenosis spinal
|
|
D015792||retinal dysplasia
|
|
D015792||dysplasia retinal
|
|
D015792||dysplasias retinal
|
|
D015792||retinal dysplasias
|
|
C563990||cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
|
|
C563990||carasil
|
|
C563990||cerebrovascular disease with thin skin alopecia and disc disease
|
|
C563990||familial young adult onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension
|
|
C563990||maeda syndrome
|
|
C563990||nemoto disease
|
|
C563990||subcortical vascular encephalopathy progressive
|
|
612783|C557827||immune dysfunction with t cell inactivation due to calcium entry defect 2
|
|
612783|C557827||imd10
|
|
612783|C557827||immunodeficiency 10
|
|
612783|C557827||stim1 deficiency
|
|
C563994||atrioventricular septal defect with blepharophimosis and anal and radial defects
|
|
C562662||brown oculocutaneous albinism
|
|
C562662||albinism brown oculocutaneous
|
|
C562663||bads syndrome
|
|
C562663||black locks with albinism and deafness syndrome
|
|
D001165||arteriovenous malformations
|
|
D001165||arteriovenous malformation
|
|
D001165||malformation arteriovenous
|
|
D001165||malformations arteriovenous
|
|
C567847|612949||hypomyelination global cerebral
|
|
C567847|612949||agc1 deficiency
|
|
C567847|612949||aspartate glutamate carrier 1 deficiency
|
|
D001164||arteriovenous fistula
|
|
D001164||aneurysm arteriovenous
|
|
D001164||arteriovenous aneurysm
|
|
D001164||arteriovenous fistulas
|
|
D001164||fistula arteriovenous
|
|
D001164||fistulas arteriovenous
|
|
C562669||hydroxyprolinemia
|
|
C562669||4 hydroxy l proline oxidase deficiency
|
|
D014890|608710||wegener granulomatosis
|
|
D014890|608710||granulomatosis wegener
|
|
D014890|608710||granulomatosis wegener apos s
|
|
D014890|608710||granulomatosis with polyangitis
|
|
D014890|608710||wegener apos s granulomatosis
|
|
D014890|608710||wg
|
|
C563997||dysphasia familial developmental
|
|
D001162||arteriosclerosis obliterans
|
|
D001162||obliterans arteriosclerosis
|
|
C564538|300301||ectodermal dysplasia anhidrotic with immunodeficiency osteopetrosis and lymphedema
|
|
C564538|300301||oledaid
|
|
D001169||arthritis experimental
|
|
D001169||adjuvant arthritis
|
|
D001169||arthritides collagen
|
|
D001169||arthritis adjuvant
|
|
D001169||arthritis adjuvant induced
|
|
D001169||arthritis collagen
|
|
D001169||arthritis collagen induced
|
|
D001169||collagen arthritides
|
|
D001169||collagen arthritis
|
|
D001169||collagen induced arthritides
|
|
D001169||collagen induced arthritis
|
|
D002493||central nervous system diseases
|
|
D002493||central nervous system disorders
|
|
D002493||cns disease
|
|
D002493||cns diseases
|
|
176780|D056887||pelvic organ prolapse
|
|
176780|D056887||organ prolapse pelvic
|
|
176780|D056887||organ prolapses pelvic
|
|
176780|D056887||pelvic organ prolapses
|
|
176780|D056887||pelvic organ prolapse susceptibility to
|
|
176780|D056887||pelvic organ prolapse susceptibility to 2
|
|
176780|D056887||prolapse of vagina and rectum
|
|
176780|D056887||prolapse pelvic organ
|
|
176780|D056887||prolapses pelvic organ
|
|
176780|D056887||prolapses urogenital
|
|
176780|D056887||prolapses vaginal vault
|
|
176780|D056887||prolapse urogenital
|
|
176780|D056887||prolapse vaginal vault
|
|
176780|D056887||pvop1 included
|
|
176780|D056887||pvop2
|
|
176780|D056887|D012005||rectal prolapse
|
|
176780|D056887||urogenital prolapse
|
|
176780|D056887||urogenital prolapses
|
|
176780|D056887||vaginal prolapse pelvic organ prolapse susceptibility to 1 included
|
|
176780|D056887||vaginal vault prolapse
|
|
176780|D056887||vaginal vault prolapses
|
|
176780|D056887||vault prolapses vaginal
|
|
176780|D056887||vault prolapse vaginal
|
|
D001168||arthritis
|
|
D001168||arthritides
|
|
D001168||polyarthritides
|
|
D001168||polyarthritis
|
|
D002494||central nervous system infections
|
|
D002494||central nervous system infection
|
|
D002494||infections central nervous system
|
|
275120||thyrotropin releasing hormone deficiency
|
|
275120||hypothalamic hypothyroidism
|
|
275120||trh deficiency
|
|
D001167||arteritis
|
|
D001167||arterial inflammation
|
|
D001167||arteritides
|
|
D001167||inflammation arterial
|
|
C564727|300030||deafness x linked 3
|
|
C564727|300030||deafness x linked 4 congenital sensorineural
|
|
C564727|300030||dfn4
|
|
C564727|300030||dfnx3
|
|
114580|C567779||candidiasis familial 1
|
|
114580|C567779||candf1
|
|
114580|C567779||candidiasis familial chronic mucocutaneous autosomal dominant with or without thyroid disease
|
|
114580|C567779||cmct
|
|
D064807||anticholinergic syndrome
|
|
D064807||anticholinergic syndrome central
|
|
D064807||anticholinergic syndrome peripheral
|
|
D064807||anticholinergic syndromes
|
|
D064807||anticholinergic syndromes central
|
|
D064807||anticholinergic syndromes peripheral
|
|
D064807||central anticholinergic syndrome
|
|
D064807||central anticholinergic syndromes
|
|
D064807||peripheral anticholinergic syndrome
|
|
D064807||peripheral anticholinergic syndromes
|
|
D064807||syndrome anticholinergic
|
|
D064807||syndrome central anticholinergic
|
|
D064807||syndrome peripheral anticholinergic
|
|
D064807||syndromes anticholinergic
|
|
D064807||syndromes central anticholinergic
|
|
D064807||syndromes peripheral anticholinergic
|
|
D001171||arthritis juvenile
|
|
D001171||arthritis juvenile chronic
|
|
D001171||arthritis juvenile enthesitis related
|
|
D001171||arthritis juvenile idiopathic
|
|
D001171||arthritis juvenile psoriatic
|
|
D001171||arthritis juvenile rheumatoid
|
|
D001171||arthritis juvenile systemic
|
|
D001171||chronic arthritis juvenile
|
|
D001171||enthesitis related arthritis juvenile
|
|
D001171||idiopathic arthritis juvenile
|
|
D001171||juvenile arthritis
|
|
D001171||juvenile chronic arthritis
|
|
D001171||juvenile enthesitis related arthritis
|
|
D001171||juvenile idiopathic arthritis
|
|
D001171||juvenile oligoarthritis
|
|
D001171||juvenile onset still disease
|
|
D001171||juvenile onset stills disease
|
|
D001171||juvenile onset still apos s disease
|
|
D001171||juvenile psoriatic arthritis
|
|
D001171||juvenile rheumatoid arthritis
|
|
D001171||juvenile systemic arthritis
|
|
D001171||oligoarthritis juvenile
|
|
D001171||polyarthritis juvenile rheumatoid factor negative
|
|
D001171||polyarthritis juvenile rheumatoid factor positive
|
|
D001171||psoriatic arthritis juvenile
|
|
D001171||rheumatoid arthritis juvenile
|
|
D001171||still disease juvenile onset
|
|
D001171||still apos s disease juvenile onset
|
|
D001171||stills disease juvenile onset
|
|
D001171||systemic arthritis juvenile
|
|
D064806||dysbiosis
|
|
D064806||disbacterioses
|
|
D064806||disbacteriosis
|
|
D064806||disbioses
|
|
D064806||disbiosis
|
|
D064806||dysbacterioses
|
|
D064806||dysbacteriosis
|
|
D064806||dysbioses
|
|
D064806||dys symbioses
|
|
D064806||dys symbiosis
|
|
C566138|118210||charcot marie tooth disease axonal type 2a1
|
|
C566138|118210||charcot marie tooth disease axonal autosomal dominant type 2a1
|
|
C566138|118210||charcot marie tooth disease neuronal type 2a1
|
|
C566138|118210||charcot marie tooth neuropathy type 2a1
|
|
C566138|118210||cmt2a1
|
|
C566138|118210||hereditary motor and sensory neuropathy iia1
|
|
C566138|118210||hmsn2a1
|
|
C566138|118210||hmsn iia1
|
|
D001170||arthritis infectious
|
|
D001170||arthritides bacterial
|
|
D001170||arthritides infectious
|
|
D001170||arthritides septic
|
|
D001170||arthritides suppurative
|
|
D001170||arthritides viral
|
|
D001170||arthritis bacterial
|
|
D001170||arthritis septic
|
|
D001170||arthritis suppurative
|
|
D001170||arthritis viral
|
|
D001170||bacterial arthritides
|
|
D001170||bacterial arthritis
|
|
D001170||infectious arthritides
|
|
D001170||infectious arthritis
|
|
D001170||septic arthritides
|
|
D001170||septic arthritis
|
|
D001170||suppurative arthritides
|
|
D001170||suppurative arthritis
|
|
D001170||viral arthritides
|
|
D001170||viral arthritis
|
|
D014474||unconsciousness
|
|
D014474||consciousness loss of
|
|
D014474||loss of consciousness
|
|
D014474||state unconscious
|
|
D014474||unconscious state
|
|
D014474||unconscious states
|
|
D013145||spirochaetales infections
|
|
D013145||infection spirochaetales
|
|
D013145||infection spirochete
|
|
D013145||infections spirochaetales
|
|
D013145||infections spirochete
|
|
D013145||spirochaetales infection
|
|
D013145||spirochete infection
|
|
D013145||spirochete infections
|
|
606657||glaucoma normal tension susceptibility to
|
|
606657||glaucoma normal pressure susceptibility to
|
|
606657||npg
|
|
606657||ntg
|
|
C536461||waaler aarskog syndrome
|
|
C537792||axial osteosclerosis
|
|
C537792||osteomesopyknosis
|
|
C537793||ayazi syndrome
|
|
C537793||choroideremia deafness obesity
|
|
C537793||choroideremia obesity and congenital deafness
|
|
C537793||choroideremia with deafness and obesity
|
|
D001259||ataxia
|
|
D001259||appendicular ataxia
|
|
D001259||appendicular ataxias
|
|
D001259||ataxia appendicular
|
|
D001259||ataxia limb
|
|
D001259||ataxia motor
|
|
D001259||ataxias
|
|
D001259||ataxias appendicular
|
|
D001259||ataxia sensory
|
|
D001259||ataxias limb
|
|
D001259||ataxias motor
|
|
D001259||ataxias sensory
|
|
D001259||ataxias truncal
|
|
D001259||ataxia truncal
|
|
D001259||ataxy
|
|
D001259||coordination impairment
|
|
D001259||coordination impairments
|
|
D001259||coordination lack
|
|
D001259||dyscoordination
|
|
D001259||dyssynergia
|
|
D001259||impairment coordination
|
|
D001259||impairments coordination
|
|
D001259||incoordination
|
|
D001259||incoordinations
|
|
D001259||lack of coordination
|
|
D001259||limb ataxia
|
|
D001259||limb ataxias
|
|
D001259||motor ataxia
|
|
D001259||motor ataxias
|
|
D001259||rubral tremor
|
|
D001259||rubral tremors
|
|
D001259||sensory ataxia
|
|
D001259||sensory ataxias
|
|
D001259||tremor rubral
|
|
D001259||tremors rubral
|
|
D001259||truncal ataxia
|
|
D001259||truncal ataxias
|
|
C537790||axial mesodermal dysplasia spectrum
|
|
C537790||russell weaver bull syndrome
|
|
C537791||axial osteomalacia
|
|
C537791||atypical osteomalacia involving the axial skeleton
|
|
C537796||bagatelle cassidy syndrome
|
|
C537796||macrocephaly hypertelorism short limbs hearing loss and developmental delay
|
|
C537796||macrocephaly short limbs deafness
|
|
D014570||urologic diseases
|
|
D014570||diseases urinary tract
|
|
D014570||diseases urologic
|
|
D014570||diseases urological
|
|
D014570||disease urinary tract
|
|
D014570||disease urologic
|
|
D014570||disease urological
|
|
D014570||urinary tract disease
|
|
D014570||urinary tract diseases
|
|
D014570||urological disease
|
|
D014570||urological diseases
|
|
D014570||urologic disease
|
|
C562753||nasal bones absence of
|
|
C562753||nasal cartilages agenesis of
|
|
C537797||bahemuka brown syndrome
|
|
C537797||spastic paraplegia facial cutaneous lesions
|
|
C537794||baby rattle pelvic dysplasia
|
|
C562751||epistaxis hereditary
|
|
C537795||baetz greenwalt syndrome
|
|
C537795||hypoplastic right sided heart complex
|
|
C562757||ciliary discoordination due to random ciliary orientation
|
|
C562757||rutland ciliary disorientation syndrome
|
|
D001251||astigmatism
|
|
D001250||asthma exercise induced
|
|
D001250||asthmas exercise induced
|
|
D001250||bronchospasm exercise induced
|
|
D001250||bronchospasms exercise induced
|
|
D001250||exercise induced asthma
|
|
D001250||exercise induced asthmas
|
|
D001250||exercise induced bronchospasm
|
|
D001250||exercise induced bronchospasms
|
|
D002581||uterine cervical incompetence
|
|
D002581||cervical incompetence uterine
|
|
D002581||cervices incompetent
|
|
D002581||cervix incompetence
|
|
D002581||cervix incompetent
|
|
D002581||incompetence cervix
|
|
D002581||incompetence uterine cervical
|
|
D002581||incompetent cervices
|
|
D002581||incompetent cervix
|
|
613730||hemorrhagic destruction of the brain subependymal calcification and cataracts
|
|
613730||hdbscc
|
|
D001254||astrocytoma
|
|
D001254||anaplastic astrocytoma
|
|
D001254||anaplastic astrocytomas
|
|
D001254||astrocytic glioma
|
|
D001254||astrocytic gliomas
|
|
D001254||astrocytoma anaplastic
|
|
D001254||astrocytoma cerebral
|
|
D001254||astrocytoma childhood cerebral
|
|
D001254||astrocytoma fibrillary
|
|
D001254||astrocytoma gemistocytic
|
|
D001254||astrocytoma grade i
|
|
D001254||astrocytoma grade ii
|
|
D001254||astrocytoma grade iii
|
|
D001254||astrocytoma intracranial
|
|
D001254||astrocytoma juvenile pilocytic
|
|
D001254||astrocytoma pilocytic
|
|
D001254||astrocytoma protoplasmic
|
|
D001254||astrocytomas
|
|
D001254||astrocytomas anaplastic
|
|
D001254||astrocytomas cerebral
|
|
D001254||astrocytomas childhood cerebral
|
|
D001254||astrocytomas fibrillary
|
|
D001254||astrocytomas gemistocytic
|
|
D001254||astrocytomas grade i
|
|
D001254||astrocytomas grade ii
|
|
D001254||astrocytomas grade iii
|
|
D001254||astrocytomas intracranial
|
|
D001254||astrocytomas juvenile pilocytic
|
|
D001254||astrocytomas pilocytic
|
|
D001254||astrocytomas protoplasmic
|
|
D001254||astrocytoma subependymal giant cell
|
|
D001254||astroglioma
|
|
D001254||astrogliomas
|
|
D001254||cerebral astrocytoma
|
|
D001254||cerebral astrocytoma childhood
|
|
D001254||cerebral astrocytomas
|
|
D001254||cerebral astrocytomas childhood
|
|
D001254||childhood cerebral astrocytoma
|
|
D001254||childhood cerebral astrocytomas
|
|
D001254||fibrillary astrocytoma
|
|
D001254||fibrillary astrocytomas
|
|
D001254||gemistocytic astrocytoma
|
|
D001254||gemistocytic astrocytomas
|
|
D001254||glioma astrocytic
|
|
D001254||gliomas astrocytic
|
|
D001254||grade i astrocytoma
|
|
D001254||grade i astrocytomas
|
|
D001254||grade ii astrocytoma
|
|
D001254||grade ii astrocytomas
|
|
D001254||grade iii astrocytoma
|
|
D001254||grade iii astrocytomas
|
|
D001254||intracranial astrocytoma
|
|
D001254||intracranial astrocytomas
|
|
D001254||juvenile pilocytic astrocytoma
|
|
D001254||juvenile pilocytic astrocytomas
|
|
D001254||mixed oligoastrocytoma
|
|
D001254||mixed oligoastrocytomas
|
|
D001254||oligoastrocytoma mixed
|
|
D001254||oligoastrocytomas mixed
|
|
D001254||pilocytic astrocytoma
|
|
D001254||pilocytic astrocytoma juvenile
|
|
D001254||pilocytic astrocytomas
|
|
D001254||pilocytic astrocytomas juvenile
|
|
D001254||protoplasmic astrocytoma
|
|
D001254||protoplasmic astrocytomas
|
|
D001254||subependymal giant cell astrocytoma
|
|
C565772|604432||spinocerebellar ataxia 11
|
|
C565772|604432||sca11
|
|
C562759||bundle branch block familial isolated complete right
|
|
613723||muscular dystrophy limb girdle type 2q
|
|
613723||lgmd2q
|
|
613724||leukoencephalopathy with dystonia and motor neuropathy
|
|
613724||sterol carrier protein 2 deficiency
|
|
D002590||cestode infections
|
|
D002590||bertielliases
|
|
D002590||bertielliasis
|
|
D002590||cenuriases
|
|
D002590||cenuriasis
|
|
D002590||cestode infection
|
|
D002590||coenuriases
|
|
D002590||coenuriasis
|
|
D002590||dipylidiases
|
|
D002590||dipylidiasis
|
|
D002590||infection cestode
|
|
D002590||infections cestode
|
|
D002590||infections tapeworm
|
|
D002590||infection tapeworm
|
|
D002590||raillietiniases
|
|
D002590||raillietiniasis
|
|
D002590||tapeworm infection
|
|
D002590||tapeworm infections
|
|
613729||chromosome 7q11 23 deletion syndrome distal 1 2 mb
|
|
613729||distal chromosome 7q11 23 deletion syndrome
|
|
D013231||steatitis
|
|
D013231||steatitides
|
|
C537789||axenfeld rieger anomaly with cardiac defects and sensorineural hearing loss
|
|
C537789||axenfeld rieger anomaly with atrial septal defect and sensorineural hearing loss
|
|
C563834|608907||alzheimer disease 9
|
|
C563834|608907||ad9
|
|
C563834|608907||alzheimer disease 9 late onset
|
|
233300||ovarian dysgenesis 1
|
|
233300||odg1
|
|
233300||ovarian dysgenesis hypergonadotropic autosomal recessive
|
|
233300||ovarian dysgenesis hypergonadotropic with normal karyotype
|
|
233300||ovarian failure hypergonadotropic
|
|
233300||xxgd
|
|
233300||xx gonadal dysgenesis
|
|
C537787||aphalangia syndactyly microcephaly
|
|
608244|C564268||otosclerosis 3
|
|
608244|C564268||otsc3
|
|
C537788||aplasia cutis congenita intestinal lymphangiectasia
|
|
C537788||acc with intestinal lymphangiectasia
|
|
C537788||aplasia cutis congenita with intestinal lymphangiectasia
|
|
D014565||urogenital neoplasms
|
|
D014565||cancer genitourinary
|
|
D014565||cancer genito urinary
|
|
D014565||cancers genitourinary
|
|
D014565||cancers genito urinary
|
|
D014565||cancers urogenital
|
|
D014565||cancer urogenital
|
|
D014565||genito urinary cancer
|
|
D014565||genitourinary cancer
|
|
D014565||genito urinary cancers
|
|
D014565||genitourinary cancers
|
|
D014565||genito urinary neoplasm
|
|
D014565||genitourinary neoplasm
|
|
D014565||genito urinary neoplasms
|
|
D014565||genitourinary neoplasms
|
|
D014565||neoplasm genitourinary
|
|
D014565||neoplasm genito urinary
|
|
D014565||neoplasms genitourinary
|
|
D014565||neoplasms genito urinary
|
|
D014565||neoplasms urogenital
|
|
D014565||neoplasm urogenital
|
|
D014565||urogenital cancer
|
|
D014565||urogenital cancers
|
|
D014565||urogenital neoplasm
|
|
C537786|610256||aphakia congenital primary
|
|
C537786|610256||congenital primary aphakia
|
|
D014564||urogenital abnormalities
|
|
D014564||abnormalities genitourinary
|
|
D014564||abnormalities urogenital
|
|
D014564||abnormality genitourinary
|
|
D014564||abnormality urogenital
|
|
D014564||genitourinary abnormalities
|
|
D014564||genitourinary abnormality
|
|
D014564||urogenital abnormality
|
|
C536472||upington disease
|
|
C536472||familial dyschondroplasia
|
|
C536472||perthes like hip disease enchondromata and ecchondromata
|
|
C562760||capillary malformations congenital 1
|
|
C536473||upton young syndrome
|
|
C536473||mental retardation and multiple nevi
|
|
C536473||severe developmental delay and multiple strawberry naevi
|
|
C536470||uniparental disomy of chromosome 2
|
|
C536470||uniparental disomy of 2
|
|
C536471||uniparental disomy paternal chromosome 14
|
|
C536471||paternal uniparental disomy 14
|
|
155600||melanoma cutaneous malignant susceptibility to 1
|
|
155600||cmm
|
|
155600||cmm1
|
|
155600||dns
|
|
155600||mlm
|
|
C536476||urban schosser spohn syndrome
|
|
C536476||hereditary mucoepithelial dysplasia
|
|
C536476||mucoepithelial dysplasia hereditary
|
|
D014581||urticaria
|
|
D014581||hives
|
|
D014581||urticarias
|
|
609069|C563796||diabetes mellitus permanent neonatal with cerebellar agenesis
|
|
609069|C563796||paca
|
|
609069|C563796||pancreatic and cerebellar agenesis
|
|
C536477||urethral obstruction sequence
|
|
C536477||early urethral obstruction sequence
|
|
C566460|609646||deafness autosomal recessive 42
|
|
C566460|609646||dfnb42
|
|
C562761||splenoportal vascular anomalies
|
|
C536474||urachal adenocarcinoma
|
|
C536474||adenocarcinoma of the urachus
|
|
155601||melanoma cutaneous malignant susceptibility to 2
|
|
155601||cmm2
|
|
C536475||urachal cancer
|
|
C536475||urachal carcinoma
|
|
D001264||athetosis
|
|
D001264||athetoid movement
|
|
D001264||athetoid movements
|
|
D001264||athetoses
|
|
D001264||disease hammond
|
|
D001264||disease hammond apos s
|
|
D001264||diseases hammond
|
|
D001264||diseases hammond apos s
|
|
D001264||hammond disease
|
|
D001264||hammond diseases
|
|
D001264||hammond apos s disease
|
|
D001264||hammonds disease
|
|
D001264||hammond apos s diseases
|
|
D001264||movement athetoid
|
|
D001264||movements athetoid
|
|
C564246|608394||deafness autosomal dominant 43
|
|
C564246|608394||dfna43
|
|
C562768||hypothyroidism autoimmune
|
|
C536928|276300||turcot syndrome
|
|
C536928|276300||brain tumor polyposis syndrome 1
|
|
C536928|276300||btp1 syndrome
|
|
C536928|276300||btps1
|
|
C536928|276300||childhood cancer syndrome
|
|
C536928|276300||cmmrds
|
|
C536928|276300||cns tumors with familial polyposis of the colon
|
|
C536928|276300||constitutional mismatch repair deficiency syndrome
|
|
C536928|276300||mismatch repair cancer syndrome
|
|
C536928|276300||mismatch repair deficiency
|
|
C536928|276300||mmrcs
|
|
C536928|276300||mmr deficiency
|
|
C562765||esophageal ring lower
|
|
D002598||chagas cardiomyopathy
|
|
D002598||cardiomyopathy chagas
|
|
D002598||cardiomyopathy chagas apos
|
|
D002598||cardiovascular trypanosomiasis
|
|
D002598||chagas apos cardiomyopathy
|
|
D002598||myocarditis chagas
|
|
D002598||trypanosomiasis cardiovascular
|
|
D001261||pulmonary atelectasis
|
|
D001261||atelectases
|
|
D001261||atelectases compression
|
|
D001261||atelectases compression pulmonary
|
|
D001261||atelectases congestive
|
|
D001261||atelectases congestive pulmonary
|
|
D001261||atelectases contraction pulmonary
|
|
D001261||atelectases postoperative pulmonary
|
|
D001261||atelectases pulmonary
|
|
D001261||atelectases resorption
|
|
D001261||atelectases resorption pulmonary
|
|
D001261||atelectasis
|
|
D001261||atelectasis compression
|
|
D001261||atelectasis compression pulmonary
|
|
D001261||atelectasis congestive
|
|
D001261||atelectasis congestive pulmonary
|
|
D001261||atelectasis contraction pulmonary
|
|
D001261||atelectasis postoperative pulmonary
|
|
D001261||atelectasis pulmonary
|
|
D001261||atelectasis resorption
|
|
D001261||atelectasis resorption pulmonary
|
|
D001261||collapse lung
|
|
D001261||compression atelectases
|
|
D001261||compression atelectasis
|
|
D001261||compression pulmonary atelectases
|
|
D001261||compression pulmonary atelectasis
|
|
D001261||congestive atelectases
|
|
D001261||congestive atelectasis
|
|
D001261||congestive pulmonary atelectases
|
|
D001261||congestive pulmonary atelectasis
|
|
D001261||contraction pulmonary atelectases
|
|
D001261||contraction pulmonary atelectasis
|
|
D001261||lung collapse
|
|
D001261||postoperative pulmonary atelectases
|
|
D001261||postoperative pulmonary atelectasis
|
|
D001261||pulmonary atelectases
|
|
D001261||pulmonary atelectases compression
|
|
D001261||pulmonary atelectases congestive
|
|
D001261||pulmonary atelectases contraction
|
|
D001261||pulmonary atelectases postoperative
|
|
D001261||pulmonary atelectases resorption
|
|
D001261||pulmonary atelectasis compression
|
|
D001261||pulmonary atelectasis congestive
|
|
D001261||pulmonary atelectasis contraction
|
|
D001261||pulmonary atelectasis postoperative
|
|
D001261||pulmonary atelectasis resorption
|
|
D001261||resorption atelectases
|
|
D001261||resorption atelectasis
|
|
D001261||resorption pulmonary atelectases
|
|
D001261||resorption pulmonary atelectasis
|
|
613720||epileptic encephalopathy early infantile 7
|
|
613720||eiee7
|
|
613721||epileptic encephalopathy early infantile 11
|
|
613721||eiee11
|
|
D001265||athletic injuries
|
|
D001265||athletic injury
|
|
D001265||injuries athletic
|
|
D001265||injuries sports
|
|
D001265||injury athletic
|
|
D001265||injury sports
|
|
D001265||sports injuries
|
|
D001265||sports injury
|
|
613722||epileptic encephalopathy early infantile 12
|
|
613722||eiee12
|
|
D064706||vocal cord dysfunction
|
|
D064706||dysfunctions vocal cord
|
|
D064706||dysfunction vocal cord
|
|
D064706||exercise induced vocal cord dysfunction
|
|
D064706||paradoxical vocal fold motion
|
|
D064706||paradoxical vocal fold motion disorder
|
|
D064706||vocal cord dysfunctions
|
|
613717||treacher collins syndrome 2
|
|
613717||tcs2
|
|
613718||deafness autosomal recessive 74
|
|
613718||dfnb74
|
|
120970||cord
|
|
120970||cord2
|
|
120970||crd
|
|
120970||crd2
|
|
120970||rcrd2
|
|
C536469||uniparental disomy of 13
|
|
C536469||maternal uniparental disomy of chromosome 13
|
|
C536469||paternal uniparental disomy 13
|
|
C536469||paternal uniparental disomy of chromosome 13
|
|
C536469||uniparental disomy of chromosome 13
|
|
C536467||waardenburg syndrome type 4
|
|
C536467||hirschsprung disease with pigmentary anomaly
|
|
C536467|277580||shah waardenburg syndrome
|
|
C536467||waardenburg hirschsprung disease
|
|
C536467|277580||waardenburg shah syndrome
|
|
C536467|277580||waardenburg syndrome type 4a
|
|
C536467|277580||waardenburg syndrome type iva
|
|
C536467|277580||waardenburg syndrome with hirschsprung disease type 4a
|
|
C537798||fetal trimethadione syndrome
|
|
C537798||trimethadione embryopathy
|
|
C536468||uniparental disomy of 11
|
|
C536468||paternal uniparental disomy for chromosome 11 type
|
|
C536468||uniparental disomy of chromosome 11
|
|
D014571||urologic neoplasms
|
|
D014571||cancer of the urinary tract
|
|
D014571||cancer of urinary tract
|
|
D014571||cancers urinary tract
|
|
D014571||cancers urologic
|
|
D014571||cancers urological
|
|
D014571||cancer urinary tract
|
|
D014571||cancer urologic
|
|
D014571||cancer urological
|
|
D014571||neoplasms urinary tract
|
|
D014571||neoplasms urologic
|
|
D014571||neoplasms urological
|
|
D014571||neoplasm urinary tract
|
|
D014571||neoplasm urologic
|
|
D014571||neoplasm urological
|
|
D014571||tract neoplasms urinary
|
|
D014571||tract neoplasm urinary
|
|
D014571||urinary tract cancer
|
|
D014571||urinary tract cancers
|
|
D014571||urinary tract neoplasm
|
|
D014571||urinary tract neoplasms
|
|
D014571||urological cancer
|
|
D014571||urological cancers
|
|
D014571||urological neoplasm
|
|
D014571||urological neoplasms
|
|
D014571||urologic cancer
|
|
D014571||urologic cancers
|
|
D014571||urologic neoplasm
|
|
C536168|148210||keratitis ichthyosis and deafness kid syndrome
|
|
C536168|148210||keratitis ichthyosis deafness syndrome autosomal dominant
|
|
C536168|148210||kid syndrome
|
|
C536168|148210||kid syndrome autosomal dominant
|
|
C566579|602093||cone dystrophy 3
|
|
C566579|602093||cod3
|
|
C566579|602093||cone rod dystrophy 14
|
|
C566579|602093||cord14
|
|
C566579|602093||cord14 included
|
|
C566579|602093||retinal cone dystrophy
|
|
C566579|602093||retinal cone dystrophy cone rod dystrophy 14 included
|
|
C536483||uropathy distal obstructive polydactyly
|
|
D001238||asphyxia neonatorum
|
|
D001237||asphyxia
|
|
D001237||asphyxias
|
|
D001237||suffocation
|
|
D001237||suffocations
|
|
C536481||urogenital adysplasia
|
|
C562730||adenocarcinoma of esophagus
|
|
C562731||teratoma ovarian
|
|
C562731||dermoid cyst ovarian
|
|
C565706|610198||3 methylglutaconic aciduria type v
|
|
C565706|610198||cardiomyopathy dilated with ataxia
|
|
C565706|610198||dcma
|
|
C565706|610198||mga5
|
|
C565706|610198||mga type v
|
|
C565706|610198||mgca5
|
|
C562738||histiocytosis familial lipochrome
|
|
C562739||cloacogenic carcinoma
|
|
D002561||cerebrovascular disorders
|
|
D002561||brain vascular disorder
|
|
D002561||brain vascular disorders
|
|
D002561||cerebrovascular disorder
|
|
D002561||cerebrovascular insufficiencies
|
|
D002561||cerebrovascular insufficiency
|
|
D002561||cerebrovascular occlusion
|
|
D002561||cerebrovascular occlusions
|
|
D002561||insufficiencies cerebrovascular
|
|
D002561||insufficiency cerebrovascular
|
|
D002561||intracranial vascular disease
|
|
D002561||intracranial vascular diseases
|
|
D002561||intracranial vascular disorder
|
|
D002561||intracranial vascular disorders
|
|
D002561||occlusion cerebrovascular
|
|
D002561||occlusions cerebrovascular
|
|
D002561||vascular disease intracranial
|
|
D002561||vascular diseases intracranial
|
|
D002561||vascular disorder brain
|
|
D002561||vascular disorder intracranial
|
|
D002561||vascular disorders brain
|
|
D002561||vascular disorders intracranial
|
|
C563750|609283||progressive external ophthalmoplegia with mitochondrial dna deletions autosomal dominant 2
|
|
C563750|609283||peoa2
|
|
C563750|609283||progressive external ophthalmoplegia autosomal dominant 2
|
|
C562737||connective tissue nevus
|
|
D013217||starvation
|
|
D013217||famine
|
|
D013217||famines
|
|
D013217||starvations
|
|
D014549||urinary incontinence
|
|
D014549||incontinence urinary
|
|
613702||klippel feil syndrome 3 autosomal dominant
|
|
613702||kfs3
|
|
D014548||urinary fistula
|
|
D014548||fistulas urinary
|
|
D014548||fistula urinary
|
|
D014548||urinary fistulas
|
|
613703||microphthalmia isolated with coloboma 6
|
|
613703||mcopcb6
|
|
D015878||mydriasis
|
|
613704||microphthalmia isolated 7
|
|
613704||mcop7
|
|
D015877||miosis
|
|
D015877||constricted pupil
|
|
D015877||constricted pupils
|
|
D015877||mioses
|
|
D015877||mioses persistent
|
|
D015877||mioses pupillary
|
|
D015877||miosis persistent
|
|
D015877||miosis pupillary
|
|
D015877||persistent mioses
|
|
D015877||persistent miosis
|
|
D015877||pupil constricted
|
|
D015877||pupillary mioses
|
|
D015877||pupillary miosis
|
|
D015877||pupils constricted
|
|
D015877||pupil small
|
|
D015877||pupils small
|
|
D015877||small pupil
|
|
D015877||small pupils
|
|
613706||noonan syndrome 7
|
|
613706||ns7
|
|
613707||leopard syndrome 3
|
|
D005173|612416||factor xi deficiency
|
|
D005173|612416||deficiencies factor xi
|
|
D005173|612416||deficiency factor xi
|
|
D005173|612416||f11 deficiency
|
|
D005173|612416||factor xi deficiencies
|
|
D005173|612416||hemophilia c
|
|
D005173|612416||plasma thromboplastin antecedent deficiency
|
|
D005173|612416||pta deficiency
|
|
D005173|612416||rosenthal apos s syndrome
|
|
D005173|612416||rosenthals syndrome
|
|
D005173|612416||rosenthal apos s syndromes
|
|
D005173|612416||rosenthal syndrome
|
|
D005173|612416||rosenthal syndromes
|
|
D005173|612416||syndrome rosenthal
|
|
D005173|612416||syndrome rosenthal apos s
|
|
C536478||urioste martinez frias syndrome
|
|
C536478||urioste syndrome
|
|
D014545||urinary calculi
|
|
D014545||calculi urinary
|
|
D014545||calculus urinary
|
|
D014545||stones urinary
|
|
D014545||stones urinary tract
|
|
D014545||stone urinary
|
|
D014545||stone urinary tract
|
|
D014545||urinary calculus
|
|
D014545||urinary stone
|
|
D014545||urinary stones
|
|
D014545||urinary tract stone
|
|
D014545||urinary tract stones
|
|
D015875||anisocoria
|
|
D015875||anisocoria physiologic
|
|
D015875||inequality pupillary size
|
|
D015875||physiologic anisocoria
|
|
D015875||pupil diameter unequal
|
|
D015875||pupillary size inequality
|
|
C566504|609622||short qt syndrome 3
|
|
C566504|609622||sqt3
|
|
C563354|601316||deafness autosomal dominant 10
|
|
C563354|601316||dfna10
|
|
C567032|610992||phosphoserine aminotransferase deficiency
|
|
C567032|610992||psatd
|
|
C567032|610992||psat deficiency
|
|
C536495||vacterl association
|
|
C536495||vactel association
|
|
C536495||vacterl syndrome
|
|
C536495||vertebral anal tracheoesophageal esophageal radial anomalies
|
|
D001248||asthenopia
|
|
D001248||eye fatigue
|
|
D001248||eyestrain
|
|
D001248||fatigue eye
|
|
D001248||fatigue visual
|
|
D001248||visual fatigue
|
|
C538138|307030||hyperglycerolemia
|
|
C538138|307030||gk1 deficiency
|
|
C538138|307030||gkd
|
|
C538138|307030||gk deficiency
|
|
C538138|307030||glycerol kinase deficiency
|
|
D001247||asthenia
|
|
D001247||asthenias
|
|
C562741||adamantinoma of long bones
|
|
D002578||uterine cervical dysplasia
|
|
D002578||cervical dysplasia uterine
|
|
D002578||cervix dysplasia
|
|
D002578||dysplasia cervix
|
|
D002578||dysplasia uterine cervical
|
|
C562742||blepharochalasis and double lip
|
|
C562742||ascher syndrome
|
|
D002579||uterine cervical erosion
|
|
D002579||cervical erosion uterine
|
|
D002579||cervix erosion
|
|
D002579||cervix erosion uterine
|
|
D002579||erosion cervix
|
|
D002579||erosion uterine cervical
|
|
D002579||erosion uterine cervix
|
|
D002579||uterine cervix erosion
|
|
C536499||tetra amelia with pulmonary hypoplasia
|
|
C536499||absence of upper and lower limbs with pulmonary hypoplasia
|
|
C536499||syndrome of tetraamelia with pulmonary hypoplasia
|
|
C567640|613329||plasminogen activator inhibitor 1 deficiency
|
|
C567640|613329||hyperfibrinolysis due to pai1 deficiency
|
|
C536496||tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities
|
|
C536496||absence of all four limbs with ectodermal dysplasia and lacrimal duct abnormalities
|
|
C536496||tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities
|
|
C562740||hemangiopericytoma malignant
|
|
C536497||x linked tetra amelia
|
|
C536497||tetra amelia x linked
|
|
D002575||uterine cervicitis
|
|
D002575||cervicitides
|
|
D002575||cervicitides uterine
|
|
D002575||cervicitis
|
|
D002575||cervicitis uterine
|
|
D002575||uterine cervicitides
|
|
D002577||uterine cervical diseases
|
|
D002577||cervical diseases uterine
|
|
D002577||cervical disease uterine
|
|
D002577||cervix disease
|
|
D002577||cervix diseases
|
|
D002577||disease cervix
|
|
D002577||diseases cervix
|
|
D002577||diseases uterine cervical
|
|
D002577||disease uterine cervical
|
|
D002577||uterine cervical disease
|
|
C536491||usher syndrome type 2b
|
|
C537316|301840||spinocerebellar ataxia x linked 4
|
|
C537316|301840||ataxia dementia syndrome x linked
|
|
C537316|301840||scax4
|
|
C565607|224750||schopf schulz passarge syndrome
|
|
C565607|224750||eccrine tumors with ectodermal dysplasia
|
|
C565607|224750||keratosis palmoplantaris with cystic eyelids hypodontia and hypotrichosis
|
|
C565607|224750||ssps
|
|
D002573||cervical rib syndrome
|
|
D002573||anomalous cervical rib syndrome
|
|
D002573||cervical rib cervical band syndrome
|
|
D002573||cervical rib syndromes
|
|
D002573||naffziger apos s syndrome
|
|
D002573||naffziger apos s syndromes
|
|
D002573||naffziger syndrome
|
|
D002573||naffziger syndromes
|
|
D002573||syndrome cervical rib
|
|
D002573||syndrome cervical rib cervical band
|
|
D002573||syndrome naffziger
|
|
D002573||syndrome naffziger apos s
|
|
D002573||syndromes cervical rib
|
|
D002573||syndromes naffziger
|
|
D002573||syndromes naffziger apos s
|
|
613700||supernumerary der 22 t 8
|
|
D064726||triple negative breast neoplasms
|
|
D064726||breast cancers triple negative
|
|
D064726||breast cancer triple negative
|
|
D064726||breast neoplasms triple negative
|
|
D064726||breast neoplasm triple negative
|
|
D064726||er negative pr negative her2 negative breast cancer
|
|
D064726||er negative pr negative her2 negative breast neoplasms
|
|
D064726||triple negative breast cancer
|
|
D064726||triple negative breast cancers
|
|
D064726||triple negative breast neoplasm
|
|
C537207|156550||kniest dysplasia
|
|
C537207|156550||kniest chondrodystrophy
|
|
C537207|156550||kniest syndrome
|
|
C537207|156550||swiss cheese cartilage dysplasia
|
|
D013226||status epilepticus
|
|
D013226||absence status
|
|
D013226||complex partial status epilepticus
|
|
D013226||electrographic status epilepticus
|
|
D013226||generalized convulsive status epilepticus
|
|
D013226||generalized status epilepticus
|
|
D013226||grand mal status epilepticus
|
|
D013226||non convulsive status epilepticus
|
|
D013226||petit mal status
|
|
D013226||simple partial status epilepticus
|
|
D013226||status absence
|
|
D013226||status epilepticus complex partial
|
|
D013226||status epilepticus electrographic
|
|
D013226||status epilepticus generalized
|
|
D013226||status epilepticus generalized convulsive
|
|
D013226||status epilepticus grand mal
|
|
D013226||status epilepticus non convulsive
|
|
D013226||status epilepticus simple partial
|
|
D013226||status epilepticus subclinical
|
|
D013226||status petit mal
|
|
D013226||subclinical status epilepticus
|
|
C536289|300584||immunodeficiency without anhidrotic ectodermal dysplasia
|
|
C536289|300584||immunodeficiency isolated
|
|
C536289|300584||immunodeficiency pure
|
|
C566618|601815||phosphoglycerate dehydrogenase deficiency
|
|
C566618|601815||phgdh deficiency
|
|
D014552||urinary tract infections
|
|
D014552||infections urinary tract
|
|
D014552||infection urinary tract
|
|
D014552||tract infections urinary
|
|
D014552||tract infection urinary
|
|
D014552||urinary tract infection
|
|
D015882||retinal necrosis syndrome acute
|
|
D015882||acute retinal necroses
|
|
D015882||acute retinal necrosis
|
|
D015882||necroses acute retinal
|
|
D015882||necrosis acute retinal
|
|
D015882||retinal necroses acute
|
|
D015882||retinal necrosis acute
|
|
D014550||urinary incontinence stress
|
|
D014550||incontinence urinary stress
|
|
D014550||stress incontinence urinary
|
|
D014550||urinary stress incontinence
|
|
D013224||status asthmaticus
|
|
D013224||asthmatic crises
|
|
D013224||asthmatic crisis
|
|
D013224||asthmatic shock
|
|
D013224||asthmatic shocks
|
|
D013224||asthmaticus status
|
|
D013224||crises asthmatic
|
|
D013224||crisis asthmatic
|
|
D013224||shock asthmatic
|
|
D013224||shocks asthmatic
|
|
C567750|613105||choroidal dystrophy central areolar 2
|
|
C567750|613105||cacd2
|
|
C567750|613105||central areolar choroidal dystrophy 2
|
|
C567750|613105||macular dystrophy progressive
|
|
D014555||urination disorders
|
|
D014555||disorders urination
|
|
D014555||disorder urination
|
|
D014555||urination disorder
|
|
D002549||diffuse cerebral sclerosis of schilder
|
|
D002549||alper disease
|
|
D002549||alper apos s disease
|
|
D002549||alpers disease
|
|
D002549||alpers apos disease
|
|
D002549||alper apos s syndrome
|
|
D002549||alpers apos syndrome
|
|
D002549||alper syndrome
|
|
D002549||balo concentric sclerosis
|
|
D002549||balo apos s concentric sclerosis
|
|
D002549||cerebral sclerosis diffuse
|
|
D002549||concentric sclerosis balo
|
|
D002549||concentric sclerosis balo apos s
|
|
D002549||diffuse cerebral scleroses
|
|
D002549||diffuse cerebral sclerosis
|
|
D002549||diffuse scleroses myelinoclastic
|
|
D002549||diffuse sclerosis myelinoclastic
|
|
D002549||disease alpers apos
|
|
D002549||disease schilder
|
|
D002549||disease schilder apos s
|
|
D002549||encephalitis periaxialis
|
|
D002549||encephalitis periaxialis concentrica
|
|
D002549||encephalitis periaxialis diffusa
|
|
D002549||myelinoclastic diffuse scleroses
|
|
D002549||myelinoclastic diffuse sclerosis
|
|
D002549||poliodystrophia cerebri
|
|
D002549||progressive neuronal degeneration of childhood with liver disease
|
|
D002549||progressive sclerosing poliodystrophies
|
|
D002549||progressive sclerosing poliodystrophy
|
|
D002549||schilder disease
|
|
D002549||schilder apos s disease
|
|
D002549||schilders disease
|
|
D002549||scleroses balo apos s concentric
|
|
D002549||scleroses myelinoclastic diffuse
|
|
D002549||sclerosis diffuse cerebral
|
|
D002549||sclerosis myelinoclastic diffuse
|
|
D002549||sudanophilic cerebral sclerosis
|
|
D002549||syndrome alpers
|
|
D002549||syndrome alpers huttenlocher
|
|
D051437||renal insufficiency
|
|
D051437||failure kidney
|
|
D051437||failure renal
|
|
D051437||failures kidney
|
|
D051437||failures renal
|
|
D051437||insufficiency kidney
|
|
D051437||kidney failure
|
|
D051437||kidney failures
|
|
D051437||kidney insufficiencies
|
|
D051437||kidney insufficiency
|
|
D051437||renal failure
|
|
D051437||renal failures
|
|
D051437||renal insufficiencies
|
|
612563|C567253||diamond blackfan anemia 8
|
|
612563|C567253||dba8
|
|
D002545||brain ischemia
|
|
D002545||brain ischemias
|
|
D002545||cerebral ischemia
|
|
D002545||cerebral ischemias
|
|
D002545||encephalopathy ischemic
|
|
D002545||ischemia brain
|
|
D002545||ischemia cerebral
|
|
D002545||ischemias cerebral
|
|
D002545||ischemic encephalopathies
|
|
D002545||ischemic encephalopathy
|
|
C536421||prinzmetal apos s variant angina
|
|
D003876||atopic dermatitides
|
|
D003876||atopic dermatitis
|
|
D003876||atopic eczema
|
|
D003876||atopic neurodermatitides
|
|
D003876||atopic neurodermatitis
|
|
D003876||dermatitides atopic
|
|
D003876||disseminated neurodermatitides
|
|
D003876||disseminated neurodermatitis
|
|
D003876||eczema atopic
|
|
D003876||eczema infantile
|
|
D003876||infantile eczema
|
|
D003876||neurodermatitides atopic
|
|
D003876||neurodermatitides disseminated
|
|
D003876||neurodermatitis atopic
|
|
D003876||neurodermatitis disseminated
|
|
C537752||onychotrichodysplasia and neutropenia
|
|
C537752||onychotrichodysplasia chronic neutropenia and mental retardation syndrome
|
|
D002546||ischemic attack transient
|
|
D002546||anterior circulation transient ischemic attack
|
|
D002546||attacks transient ischemic
|
|
D002546||attack transient ischemic
|
|
D002546||brainstem ischemias transient
|
|
D002546||brainstem ischemia transient
|
|
D002546||brain stem ischemia transient
|
|
D002546||brainstem transient ischemic attack
|
|
D002546||brain stem transient ischemic attack
|
|
D002546||brain tia
|
|
D002546||carotid circulation transient ischemic attack
|
|
D002546||cerebral ischemias transient
|
|
D002546||cerebral ischemia transient
|
|
D002546||crescendo transient ischemic attacks
|
|
D002546||ischemias transient brainstem
|
|
D002546||ischemias transient cerebral
|
|
D002546||ischemia transient brainstem
|
|
D002546||ischemia transient cerebral
|
|
D002546||ischemic attacks transient
|
|
D002546||posterior circulation transient ischemic attack
|
|
D002546||tia brain
|
|
D002546||tias transient ischemic attack
|
|
D002546||tia transient ischemic attack
|
|
D002546||transient brainstem ischemia
|
|
D002546||transient cerebral ischemia
|
|
D002546||transient cerebral ischemias
|
|
D002546||transient ischemic attack
|
|
D002546||transient ischemic attack anterior circulation
|
|
D002546||transient ischemic attack brainstem
|
|
D002546||transient ischemic attack brain stem
|
|
D002546||transient ischemic attack carotid circulation
|
|
D002546||transient ischemic attack posterior circulation
|
|
D002546||transient ischemic attacks
|
|
D002546||transient ischemic attacks crescendo
|
|
D002546||transient ischemic attack vertebrobasilar circulation
|
|
D002546||vertebrobasilar circulation transient ischemic attack
|
|
C536422||progeria short stature pigmented nevi
|
|
C536422||mulvihill smith syndrome
|
|
C536422||progeroid short stature with pigmented nevi
|
|
D003877||dermatitis contact
|
|
D003877||contact dermatitides
|
|
D003877||contact dermatitis
|
|
D003877||contact eczema
|
|
D003877||contact hypersensitivities
|
|
D003877||contact hypersensitivity
|
|
D003877||contact sensitivities
|
|
D003877||contact sensitivity
|
|
D003877||dermatitides contact
|
|
D003877||dermatitis venenata
|
|
D003877||eczema contact
|
|
D003877||hypersensitivities contact
|
|
D003877||hypersensitivity contact
|
|
D003877||sensitivities contact
|
|
D003877||sensitivity contact
|
|
D002547||cerebral palsy
|
|
D002547||athetoid cerebral palsy
|
|
D002547||atonic cerebral palsy
|
|
D002547||cerebral palsies athetoid
|
|
D002547||cerebral palsies dyskinetic
|
|
D002547||cerebral palsies dystonic rigid
|
|
D002547||cerebral palsies monoplegic
|
|
D002547||cerebral palsy athetoid
|
|
D002547||cerebral palsy atonic
|
|
D002547||cerebral palsy congenital
|
|
D002547||cerebral palsy diplegic infantile
|
|
D002547||cerebral palsy dyskinetic
|
|
D002547||cerebral palsy dystonic rigid
|
|
D002547||cerebral palsy hypotonic
|
|
D002547||cerebral palsy mixed
|
|
D002547||cerebral palsy monoplegic
|
|
D002547||cerebral palsy monoplegic infantile
|
|
D002547||cerebral palsy quadriplegic infantile
|
|
D002547||cerebral palsy rolandic type
|
|
D002547||cerebral palsy spastic
|
|
D002547||congenital cerebral palsy
|
|
D002547||cp cerebral palsy
|
|
D002547||diplegia spastic
|
|
D002547||diplegias spastic
|
|
D002547||diplegic infantile cerebral palsy
|
|
D002547||dyskinetic cerebral palsy
|
|
D002547||dystonic rigid cerebral palsies
|
|
D002547||dystonic rigid cerebral palsy
|
|
D002547||hypotonic cerebral palsies
|
|
D002547||hypotonic cerebral palsy
|
|
D002547||infantile cerebral palsy diplegic
|
|
D002547||infantile cerebral palsy monoplegic
|
|
D002547||infantile cerebral palsy quadriplegic
|
|
D002547||little disease
|
|
D002547||little apos s disease
|
|
D002547||mixed cerebral palsies
|
|
D002547||mixed cerebral palsy
|
|
D002547||monoplegic cerebral palsies
|
|
D002547||monoplegic cerebral palsy
|
|
D002547||monoplegic infantile cerebral palsy
|
|
D002547||quadriplegic infantile cerebral palsy
|
|
D002547||rolandic type cerebral palsy
|
|
D002547||spastic cerebral palsies
|
|
D002547||spastic cerebral palsy
|
|
D002547||spastic diplegia
|
|
D002547||spastic diplegias
|
|
C537750||oncocytoma renal
|
|
C537750||renal oncocytoma
|
|
C567098|613608||epilepsy familial adult myoclonic 3
|
|
C567098|613608||cortical myoclonic tremor with epilepsy familial 3
|
|
C567098|613608||fame3
|
|
C567098|613608||fcmte3
|
|
C537934|603358||finnish lethal neonatal metabolic syndrome
|
|
C537934|603358||fellman syndrome
|
|
C537934|603358||finnish lactic acidosis with hepatic hemosiderosis
|
|
C537934|603358||flnms
|
|
C537934|603358||gracile syndrome
|
|
C537934|603358||growth retardation amino aciduria cholestasis iron overload lactic acidosis and early death
|
|
C537934|603358||lactic acidosis finnish with hepatic hemosiderosis
|
|
C536420||primrose syndrome
|
|
C537751||oncogenic osteomalacia
|
|
D003872||dermatitis
|
|
D003872||dermatitides
|
|
D002542||intracranial embolism and thrombosis
|
|
D002542||brain embolism and thrombosis
|
|
D002542||cerebral embolism and thrombosis
|
|
D002542||embolism and thrombosis brain
|
|
D003873||dermatitis exfoliative
|
|
D003873||dermatitides exfoliative
|
|
D003873||dermatitis exfoliativa
|
|
D003873||erythroderma
|
|
D003873||erythrodermas
|
|
D003873||exfoliative dermatitides
|
|
D003873||exfoliative dermatitis
|
|
D002543||cerebral hemorrhage
|
|
D002543||brain hemorrhage cerebral
|
|
D002543||brain hemorrhages cerebral
|
|
D002543||cerebral brain hemorrhage
|
|
D002543||cerebral brain hemorrhages
|
|
D002543||cerebral hemorrhages
|
|
D002543||cerebral parenchymal hemorrhage
|
|
D002543||cerebral parenchymal hemorrhages
|
|
D002543||cerebrum hemorrhage
|
|
D002543||cerebrum hemorrhages
|
|
D002543||hemorrhage cerebral
|
|
D002543||hemorrhage cerebral brain
|
|
D002543||hemorrhage cerebral parenchymal
|
|
D002543||hemorrhage cerebrum
|
|
D002543||hemorrhage intracerebral
|
|
D002543||hemorrhages cerebral
|
|
D002543||hemorrhages cerebral brain
|
|
D002543||hemorrhages cerebral parenchymal
|
|
D002543||hemorrhages cerebrum
|
|
D002543||hemorrhages intracerebral
|
|
D002543||intracerebral hemorrhage
|
|
D002543||intracerebral hemorrhages
|
|
D002543||parenchymal hemorrhage cerebral
|
|
D002543||parenchymal hemorrhages cerebral
|
|
D003874||dermatitis herpetiformis
|
|
D003874||disease duhring
|
|
D003874||disease duhring apos s
|
|
D003874||duhring disease
|
|
D003874||duhring apos s disease
|
|
D003874||duhrings disease
|
|
C562711||adrenocortical hypofunction chronic primary congenital
|
|
C562711||addison disease congenital
|
|
D064752||atrial remodeling
|
|
D064752||atrium remodeling
|
|
D064752||cardiac remodeling atrial
|
|
D064752||electrical remodeling
|
|
D064752||myocardial remodeling atrial
|
|
D064752||remodeling atrial
|
|
D064752||remodeling atrial cardiac
|
|
D064752||remodeling atrial myocardial
|
|
D064752||remodeling atrium
|
|
D064752||remodeling electrical
|
|
D003875||drug eruptions
|
|
D003875||dermatitis adverse drug reaction
|
|
D003875||dermatitis medicamentosa
|
|
D003875||drug eruption
|
|
D003875||drug eruption maculopapular
|
|
D003875||drug eruptions maculopapular
|
|
D003875||drug reaction morbilliform
|
|
D003875||drug reactions morbilliform
|
|
D003875||eruption drug
|
|
D003875||eruption maculopapular drug
|
|
D003875||eruptions drug
|
|
D003875||eruptions maculopapular drug
|
|
D003875||exanthem maculopapular
|
|
D003875||exanthem morbilliform
|
|
D003875||exanthems maculopapular
|
|
D003875||exanthems morbilliform
|
|
D003875||maculopapular drug eruption
|
|
D003875||maculopapular drug eruptions
|
|
D003875||maculopapular exanthem
|
|
D003875||maculopapular exanthems
|
|
D003875||morbilliform drug reaction
|
|
D003875||morbilliform drug reactions
|
|
D003875||morbilliform exanthem
|
|
D003875||morbilliform exanthems
|
|
D003875||reaction morbilliform drug
|
|
D003875||reactions morbilliform drug
|
|
C562716||delta beta thalassemia
|
|
C562717||rh deficiency syndrome
|
|
C531816|102700||severe combined immunodeficiency due to adenosine deaminase deficiency
|
|
C531816|102700||ada deficiency
|
|
C531816|102700||ada scid
|
|
C531816|102700||adenosine deaminase deficiency
|
|
C531816|102700||adenosine deaminase deficiency partial
|
|
C531816|102700||adenosine deaminase deficiency partial included
|
|
C531816|102700||adenosine deaminase deficient severe combined immunodeficiency
|
|
C531816|102700||adenosine deaminase deficient severe combined immunodeficiency disease
|
|
C531816|102700||agammaglobulinemia swiss type
|
|
C531816|102700||bubble boy disease
|
|
C531816|102700||delayed late onset adenosine deaminase deficiency
|
|
C531816|102700||partial ada deficiency
|
|
C531816|102700||partial ada deficiency included
|
|
C531816|102700||partial adenosine deaminase deficiency
|
|
C531816|102700||scid1
|
|
C531816|102700||scid due to ada deficiency
|
|
C531816|102700||scid due to ada deficiency delayed onset
|
|
C531816|102700||scid due to ada deficiency early onset
|
|
C531816|102700||scid due to ada deficiency early onset scid due to ada deficiency delayed onset included
|
|
C531816|102700||scid due to ada deficiency late onset
|
|
C531816|102700||scid due to ada deficiency late onset included
|
|
C531816|102700||severe combined immunodeficiency alymphocytotic type
|
|
C531816|102700||severe combined immunodeficiency autosomal recessive t cell negative b cell negative nk cell negative due to adenosine deaminase deficiency
|
|
D063425||binge drinking
|
|
D063425||drinking binge
|
|
C538278|176305||preaxial deficiency postaxial polydactyly and hypospadias
|
|
C538278|176305||autosomal dominant preaxial deficiency postaxial polydactyly and hypospadias
|
|
C538278|176305||guttmacher syndrome
|
|
607523|C564384||toenail dystrophy isolated
|
|
607523|C564384||nail disorder nonsyndromic congenital 8
|
|
607523|C564384||ndnc8
|
|
D015858||anisometropia
|
|
D014526||urethritis
|
|
D014526||urethritides
|
|
D014525||urethral stricture
|
|
D014525||anterior urethral stricture
|
|
D014525||anterior urethral strictures
|
|
D014525||posterior urethral stricture
|
|
D014525||posterior urethral strictures
|
|
D014525||stenoses urethral
|
|
D014525||stenosis urethral
|
|
D014525||strictures urethral
|
|
D014525||stricture urethral
|
|
D014525||urethral stenoses
|
|
D014525||urethral stenosis
|
|
D014525||urethral stricture anterior
|
|
D014525||urethral stricture posterior
|
|
D014525||urethral strictures
|
|
D014525||urethral strictures anterior
|
|
D014525||urethral strictures posterior
|
|
C536589|104290||alternating hemiplegia of childhood
|
|
C536589|104290||ahc1
|
|
C536589|104290||alternating hemiplegia
|
|
C536589|104290||alternating hemiplegia of childhood 1
|
|
C536589|104290||alternating hemiplegia syndrome
|
|
D014524||urethral obstruction
|
|
D014524||obstructions urethral
|
|
D014524||obstruction urethral
|
|
D014524||urethral obstructions
|
|
C537745||olivopontocerebellar hypoplasia fetal onset
|
|
C537745||pontocerebellar hypoplasia type 5
|
|
C567768|613077||progressive external ophthalmoplegia with mitochondrial dna deletions autosomal dominant 5
|
|
C567768|613077||peoa5
|
|
C567768|613077||progressive external ophthalmoplegia autosomal dominant 5
|
|
C536413||primary granulocytic sarcoma
|
|
C536418||primary orthostatic tremor
|
|
C536418||orthostatic tremor primary
|
|
C536418||shaky leg syndrome
|
|
C537749||onat syndrome
|
|
C537749||subaortic stenosis short stature syndrome
|
|
D014523||urethral neoplasms
|
|
D014523||cancer of the urethra
|
|
D014523||cancer of urethra
|
|
D014523||cancers urethra
|
|
D014523||cancers urethral
|
|
D014523||cancer urethra
|
|
D014523||cancer urethral
|
|
D014523||neoplasms urethra
|
|
D014523||neoplasms urethral
|
|
D014523||neoplasm urethra
|
|
D014523||neoplasm urethral
|
|
D014523||urethra cancer
|
|
D014523||urethra cancers
|
|
D014523||urethral cancer
|
|
D014523||urethral cancers
|
|
D014523||urethral neoplasm
|
|
D014523||urethra neoplasm
|
|
D014523||urethra neoplasms
|
|
D051436||renal insufficiency chronic
|
|
D051436||chronic kidney disease
|
|
D051436||chronic kidney diseases
|
|
D051436||chronic kidney insufficiencies
|
|
D051436||chronic kidney insufficiency
|
|
D051436||chronic renal disease
|
|
D051436||chronic renal diseases
|
|
D051436||chronic renal insufficiencies
|
|
D051436||chronic renal insufficiency
|
|
D051436||disease chronic kidney
|
|
D051436||disease chronic renal
|
|
D051436||diseases chronic kidney
|
|
D051436||diseases chronic renal
|
|
D051436||kidney disease chronic
|
|
D051436||kidney diseases chronic
|
|
D051436||kidney insufficiencies chronic
|
|
D051436||kidney insufficiency chronic
|
|
D051436||renal disease chronic
|
|
D051436||renal diseases chronic
|
|
D051436||renal insufficiencies chronic
|
|
D014522||urethral diseases
|
|
D014522||diseases urethral
|
|
D014522||disease urethral
|
|
D014522||urethral disease
|
|
C538659|176200||porphyria south african type
|
|
C538659|176200||ppox deficiency variegate porphyria homozygous variant
|
|
C538659|176200||vp
|
|
C537747||omphalocele cleft palate syndrome lethal
|
|
C537747||cleft palate omphalocele syndrome lethal
|
|
C537747||lethal omphalocele cleft palate syndrome
|
|
C536417||primary malignant melanoma of the cervix
|
|
C536417||primary malignant melanoma of the cervix uteri
|
|
C536417||primary malignant melanoma of the uterine cervix
|
|
C536417||radiation induced malignant melanoma of the cervix
|
|
C537748||omphalocele exstrophy imperforate anus
|
|
C537748||oeis complex
|
|
C537748||omphalocele exstrophy imperforate anus spinal defects
|
|
C537748||omphalocele exstrophy of the cloaca imperforate anus and spinal defects
|
|
D001228||aspergillosis
|
|
D001228||aspergilloses
|
|
C566121|119530||orofacial cleft 1
|
|
C566121|119530||cleft lip palate nonsyndromic
|
|
C566121|119530||cleft lip with or without cleft palate nonsyndromic 1
|
|
C566121|119530||orofacial cleft nonsyndromic
|
|
C563557|158901||facioscapulohumeral muscular dystrophy 1b
|
|
C563557|158901||facioscapulohumeral muscular dystrophy 2
|
|
C563557|158901||facioscapulohumeral muscular dystrophy 2 digenic
|
|
C563557|158901||fshd1b
|
|
C563557|158901||fshd2
|
|
C563557|158901||fshd2 digenic
|
|
C563557|158901||fshmd1b
|
|
C563557|158901||muscular dystrophy facioscapulohumeral type 1b
|
|
C563557|158901||muscular dystrophy facioscapulohumeral type 2
|
|
C537760||renoprival hypertension
|
|
C567791|613068||neurodegeneration due to cerebral folate transport deficiency
|
|
C536432||cochleosaccular degeneration of the inner ear and progressive cataracts
|
|
C536432||cochleosaccular degeneration
|
|
C536432||cochleosaccular degeneration of the inner ear with progressive cataracts
|
|
C537763||chromosome 6 ring syndrome
|
|
C537763||ring 6 chromosome
|
|
C537763||ring chromosome 6 syndrome
|
|
C537764||chromosome 6 deletion 6q13 q15
|
|
C537764||deletion 6q13 q15
|
|
C537764||monosomy 6q13 q15
|
|
D002558||cerebrospinal fluid otorrhea
|
|
D002558||cerebrospinal fluid otorrhea post traumatic
|
|
D002558||cerebrospinal fluid otorrheas
|
|
D002558||cerebrospinal fluid otorrhea spontaneous
|
|
D002558||cerebrospinal fluid otorrhea traumatic
|
|
D002558||cerebrospinal otorrhea
|
|
D002558||otorrhea cerebrospinal
|
|
D002558||otorrhea cerebrospinal fluid
|
|
D002558||otorrhea cerebrospinal fluid post traumatic
|
|
D002558||otorrhea cerebrospinal fluid spontaneous
|
|
D002558||otorrhea cerebrospinal fluid traumatic
|
|
D002558||otorrhea post traumatic cerebrospinal fluid
|
|
D002558||otorrhea spontaneous cerebrospinal fluid
|
|
D002558||otorrhea traumatic cerebrospinal fluid
|
|
D002558||post traumatic cerebrospinal fluid otorrhea
|
|
D002558||post traumatic otorrhea cerebrospinal fluid
|
|
D002558||spontaneous cerebrospinal fluid otorrhea
|
|
D002558||spontaneous otorrhea cerebrospinal fluid
|
|
D002558||traumatic cerebrospinal fluid otorrhea
|
|
D002558||traumatic otorrhea cerebrospinal fluid
|
|
D001229||aspergillosis allergic bronchopulmonary
|
|
D001229||allergic aspergilloses bronchopulmonary
|
|
D001229||allergic aspergillosis bronchopulmonary
|
|
D001229||allergic bronchopulmonary aspergilloses
|
|
D001229||allergic bronchopulmonary aspergillosis
|
|
D001229||aspergilloses allergic bronchopulmonary
|
|
D001229||aspergilloses bronchopulmonary allergic
|
|
D001229||aspergillosis bronchopulmonary allergic
|
|
D001229||bronchopulmonary allergic aspergilloses
|
|
D001229||bronchopulmonary allergic aspergillosis
|
|
D001229||bronchopulmonary aspergilloses allergic
|
|
D001229||bronchopulmonary aspergillosis allergic
|
|
D002559||cerebrospinal fluid rhinorrhea
|
|
D002559||cerebrospinal fluid rhinorrhea post traumatic
|
|
D002559||cerebrospinal fluid rhinorrheas
|
|
D002559||cerebrospinal fluid rhinorrhea spontaneous
|
|
D002559||cerebrospinal fluid rhinorrhea traumatic
|
|
D002559||cerebrospinal rhinorrhea
|
|
D002559||cerebrospinal rhinorrheas
|
|
D002559||post traumatic cerebrospinal fluid rhinorrhea
|
|
D002559||post traumatic rhinorrhea cerebrospinal fluid
|
|
D002559||rhinorrhea cerebrospinal
|
|
D002559||rhinorrhea cerebrospinal fluid
|
|
D002559||rhinorrhea cerebrospinal fluid post traumatic
|
|
D002559||rhinorrhea cerebrospinal fluid spontaneous
|
|
D002559||rhinorrhea cerebrospinal fluid traumatic
|
|
D002559||rhinorrhea post traumatic cerebrospinal fluid
|
|
D002559||rhinorrheas cerebrospinal
|
|
D002559||rhinorrheas cerebrospinal fluid
|
|
D002559||rhinorrhea spontaneous cerebrospinal fluid
|
|
D002559||rhinorrhea traumatic cerebrospinal fluid
|
|
D002559||spontaneous cerebrospinal fluid rhinorrhea
|
|
D002559||spontaneous rhinorrhea cerebrospinal fluid
|
|
D002559||traumatic cerebrospinal fluid rhinorrhea
|
|
D002559||traumatic rhinorrhea cerebrospinal fluid
|
|
C537762||chromosome 5 uniparental disomy
|
|
C537762||mosaic trisomy of chromosome 5
|
|
C537762||uniparental disomy of 5
|
|
C562723||hyperheparinemia
|
|
C562724||dysprothrombinemia
|
|
D003884||dermoid cyst
|
|
D003884||cyst dermoid
|
|
D003884||cysts dermoid
|
|
D003884||dermoid
|
|
D003884||dermoid cysts
|
|
D003884||dermoids
|
|
D004374|607411||ductus arteriosus patent
|
|
D004374|607411||patency of the ductus arteriosus
|
|
D004374|607411||patent ductus arteriosus
|
|
D004374|607411||patent ductus arteriosus familial
|
|
D004374|607411||pda
|
|
D004374|607411||pda1
|
|
C562721||lazy leukocyte syndrome
|
|
C562727||dysfibrinogenemia congenital
|
|
258660||nonarteritic anterior ischemic optic neuropathy susceptibility to
|
|
258660||naion susceptibility to
|
|
258660||optic neuropathy anterior ischemic susceptibility to
|
|
160150||myopathy centronuclear 1
|
|
160150||cnm1
|
|
160150|C563544||myopathy centronuclear autosomal dominant
|
|
160150|C563544||myotubular myopathy autosomal dominant
|
|
D003881||dermatomycoses
|
|
D003881||dermatomycosis
|
|
D003881||fungal skin disease
|
|
D003881||fungal skin diseases
|
|
D003881||skin disease fungal
|
|
D003881||skin diseases fungal
|
|
225060|C536726||zlotogora ogur syndrome
|
|
225060|C536726||autosomal recessive ectodermal dysplasia
|
|
225060|C536726||bustos simosa pinto cisternas syndrome
|
|
225060|C536726||cleft lip palate ectodermal dysplasia syndrome
|
|
225060|C536726||cleft lip with or without cleft palate nonsyndromic 7 included
|
|
225060|C536726||clped1
|
|
225060|C536726||ectodermal dysplasia cleft lip and palate mental retardation and syndactyly
|
|
225060|C536726||ectodermal dysplasia cleft lip and palate mental retardation and syndactyly orofacial cleft 7 included
|
|
225060|C536726||ectodermal dysplasia margarita island type
|
|
225060|C536726||ectodermal dysplasia type 4
|
|
225060|C536726||ed4
|
|
225060|C536726||ofc7 included
|
|
D002551||cerebral ventricle neoplasms
|
|
D002551||brain ventricular neoplasm
|
|
D002551||brain ventricular neoplasms
|
|
D002551||brain ventricular tumor
|
|
D002551||brain ventricular tumors
|
|
D002551||cerebral ventricle neoplasm
|
|
D002551||cerebral ventricle tumor
|
|
D002551||cerebral ventricle tumors
|
|
D002551||cerebroventricular neoplasm
|
|
D002551||cerebroventricular neoplasms
|
|
D002551||intraventricular neoplasm
|
|
D002551||intraventricular neoplasms
|
|
D002551||neoplasm brain ventricular
|
|
D002551||neoplasm cerebral ventricle
|
|
D002551||neoplasm cerebroventricular
|
|
D002551||neoplasm intraventricular
|
|
D002551||neoplasms brain ventricular
|
|
D002551||neoplasms cerebral ventricle
|
|
D002551||neoplasms cerebroventricular
|
|
D002551||neoplasms intraventricular
|
|
D002551||neoplasms ventricular brain
|
|
D002551||tumor brain ventricular
|
|
D002551||tumor cerebral ventricle
|
|
D002551||tumors brain ventricular
|
|
D002551||tumors cerebral ventricle
|
|
D002551||ventricle tumor cerebral
|
|
D002551||ventricle tumors cerebral
|
|
D002551||ventricular neoplasm brain
|
|
D002551||ventricular neoplasms brain
|
|
D002551||ventricular tumor brain
|
|
D002551||ventricular tumors brain
|
|
D003882||dermatomyositis
|
|
D003882||adult type dermatomyositides
|
|
D003882||adult type dermatomyositis
|
|
D003882||childhood type dermatomyositides
|
|
D003882||childhood type dermatomyositis
|
|
D003882||dermatomyositides
|
|
D003882||dermatomyositides adult type
|
|
D003882||dermatomyositides childhood type
|
|
D003882||dermatomyositis adult type
|
|
D003882||dermatomyositis childhood type
|
|
D003882||dermatopolymyositides
|
|
D003882||dermatopolymyositis
|
|
D003882||polymyositis dermatomyositides
|
|
D003882||polymyositis dermatomyositis
|
|
D013206||staphylococcal scalded skin syndrome
|
|
D013206||disease ritter
|
|
D013206||disease ritter apos s
|
|
D013206||ritter disease
|
|
D013206||ritter apos s disease
|
|
D013206||ritters disease
|
|
D013206||scalded skin syndromes staphylococcal
|
|
D013206||scalded skin syndrome staphylococcal
|
|
D013206||staphylococcal scalded skin syndromes
|
|
D013206||syndromes staphylococcal scalded skin
|
|
D013206||syndrome staphylococcal scalded skin
|
|
D013207||staphylococcal skin infections
|
|
D013207||diseases staphylococcal skin
|
|
D013207||disease staphylococcal skin
|
|
D013207||infections staphylococcal skin
|
|
D013207||infection staphylococcal skin
|
|
D013207||skin diseases staphylococcal
|
|
D013207||skin disease staphylococcal
|
|
D013207||skin infections staphylococcal
|
|
D013207||skin infection staphylococcal
|
|
D013207||skin staphylococcal disease
|
|
D013207||skin staphylococcal diseases
|
|
D013207||skin staphylococcal infection
|
|
D013207||skin staphylococcal infections
|
|
D013207||staphylococcal disease skin
|
|
D013207||staphylococcal diseases skin
|
|
D013207||staphylococcal infection skin
|
|
D013207||staphylococcal infections skin
|
|
D013207||staphylococcal skin disease
|
|
D013207||staphylococcal skin diseases
|
|
D013207||staphylococcal skin infection
|
|
D015868||pars planitis
|
|
D015868||planitis pars
|
|
243500|C538167||acidemia isovaleric
|
|
243500|C538167||isovaleric acid coa dehydrogenase deficiency
|
|
243500|C538167||isovaleric acidemia
|
|
243500|C538167||isovaleryl coa carboxylase deficiency
|
|
243500|C538167||isovaleryl coa dehydrogenase deficiency
|
|
243500|C538167||iva
|
|
243500|C538167||ivd deficiency
|
|
C562729||esophageal squamous cell carcinoma
|
|
D015867||uveitis intermediate
|
|
D015867||chronic cyclitis
|
|
D015867||cyclitis chronic
|
|
D015867||intermediate uveitis
|
|
D064749||retrocaval ureter
|
|
D064749||circumcaval ureter
|
|
D064749||ureter circumcaval
|
|
D064749||ureter retrocaval
|
|
D015866||uveitis posterior
|
|
D015866||posterior uveitis
|
|
C564566|300210||mental retardation x linked 58
|
|
C564566|300210||mrx58
|
|
D015861||retinal neovascularization
|
|
D015861||neovascularization retinal
|
|
611010|C567028||fibromatosis gingival 4
|
|
611010|C567028||fibromatosis gingival hereditary 4
|
|
611010|C567028||ggf4
|
|
611010|C567028||gingf4
|
|
611010|C567028||hgf4
|
|
C536423||progeroid syndrome neonatal
|
|
C536423||neonatal progeroid syndrome
|
|
C536423||wiedemann rautenstrauch syndrome
|
|
C537754||renal dysplasia limb defects syndrome
|
|
C537754||renal dysplasia mesomelia and radiohumeral fusion
|
|
C537754||ulbright hodes syndrome
|
|
C537755||renal dysplasia diffuse cystic
|
|
C537755||diffuse cystic renal dysplasia
|
|
D013202||staphylococcal food poisoning
|
|
D013202||food poisonings staphylococcal
|
|
D013202||food poisoning staphylococcal
|
|
D013202||poisonings staphylococcal food
|
|
D013202||poisoning staphylococcal food
|
|
D013202||staphylococcal food poisonings
|
|
C536429||cloverleaf skull micromelia thoracic dysplasia
|
|
C536429||micromelic bone dysplasia with cloverleaf skull
|
|
C563776|609197||glucocorticoid deficiency 3
|
|
C563776|609197||familial glucocorticoid deficiency 3
|
|
C563776|609197||fgd3
|
|
C563776|609197||gccd2 formerly
|
|
C563776|609197||gccd3
|
|
C563776|609197||glucocorticoid deficiency 2 formerly
|
|
D013203||staphylococcal infections
|
|
D013203||infections staphylococcal
|
|
D013203||infection staphylococcal
|
|
D013203||staphylococcal infection
|
|
D015864||panuveitis
|
|
C567765|613086||glaucoma 3 primary congenital d
|
|
C567765|613086||glc3d
|
|
C536427||cleft palate midfacial hypoplasia triangular facies and sensorineural hearing loss
|
|
C536427||unusual triangular facies associated with cleft palate malocclusion midfacial hypoplasia and sensorineural hearing loss
|
|
D015863||iridocyclitis
|
|
D015863||cyclitides heterochromic
|
|
D015863||cyclitis heterochromic
|
|
D015863||heterochromic cyclitides
|
|
D015863||heterochromic cyclitis
|
|
D015863||iridocyclitides
|
|
D052776||female urogenital diseases
|
|
D052776||female genitourinary disease
|
|
D052776||female genitourinary diseases
|
|
D052776||female urogenital disease
|
|
D052776||genitourinary disease female
|
|
D052776||genitourinary diseases female
|
|
D052776||urogenital disease female
|
|
D052776||urogenital diseases female
|
|
C536428||cleidorhizomelic syndrome
|
|
C536428||cleido rhizomelic syndrome
|
|
C536428||rhizomelic shortness with clavicular defect
|
|
C536428||wallis zieff goldblatt syndrome
|
|
149730|C538132||lacrimoauriculodentodigital syndrome
|
|
149730|C538132||ladd
|
|
149730|C538132||levy hollister syndrome
|
|
C537759||renal tubular acidosis distal type 3
|
|
C537759||bicarbonate wasting rta
|
|
C537759||renal tubular acidosis iii
|
|
C537759||rta bicarbonate wasting type
|
|
C537759||rta dislocation type
|
|
D015862||choroid diseases
|
|
D015862||choroidal disease
|
|
D015862||choroidal diseases
|
|
D015862||choroid disease
|
|
D015862||disease choroid
|
|
D015862||disease choroidal
|
|
D015862||diseases choroid
|
|
D015862||diseases choroidal
|
|
D002527||myoclonic cerebellar dyssynergia
|
|
D002527||ataxia dentate cerebellar
|
|
D002527||ataxias dentate cerebellar
|
|
D002527||atrophies dentate cerebellar
|
|
D002527||atrophy dentate cerebellar
|
|
D002527||cerebellar ataxias dentate
|
|
D002527||cerebellar atrophy dentate
|
|
D002527||cerebellar dyssynergia
|
|
D002527||cerebellar dyssynergia myoclonic
|
|
D002527||cerebellar dyssynergias
|
|
D002527||cerebellar dyssynergias myoclonic
|
|
D002527||cerebelloparenchymal disorder v
|
|
D002527||dentate cerebellar ataxia
|
|
D002527||dentate cerebellar ataxias
|
|
D002527||dentate cerebellar atrophies
|
|
D002527||dentate cerebellar atrophy
|
|
D002527||dentate nucleus syndrome ramsay hunt
|
|
D002527||dyssynergia cerebellar
|
|
D002527||dyssynergia cerebellaris myoclonica
|
|
D002527||dyssynergia cerebellaris myoclonica of hunt
|
|
D002527||dyssynergia cerebellaris progressiva
|
|
D002527||dyssynergia myoclonic cerebellar
|
|
D002527||dyssynergias cerebellar
|
|
D002527||dyssynergias myoclonic cerebellar
|
|
D002527||myoclonic cerebellar dyssynergias
|
|
D002527||ramsay hunt cerebellar syndrome
|
|
D002527||ramsay hunt dentate syndrome
|
|
D002527||spinodentate atrophy
|
|
C537770||anorchia
|
|
C537770||absence of testes
|
|
C537770||anorchia familial
|
|
C537770||congenital absence of testes
|
|
C537770||empty scrotum
|
|
C537770||testicular regression embryonic
|
|
C537770||testicular regression syndrome
|
|
C537770||vanishing testes
|
|
C537770||xy gonadal agenesis syndrome
|
|
C537770||xy gonadal dysgenesis syndrome
|
|
D002528||cerebellar neoplasms
|
|
D002528||benign cerebellar neoplasm
|
|
D002528||benign cerebellar neoplasms
|
|
D002528||cancer cerebellar
|
|
D002528||cerebellar cancer
|
|
D002528||cerebellar cancers
|
|
D002528||cerebellar neoplasm
|
|
D002528||cerebellar neoplasm benign
|
|
D002528||cerebellar neoplasm malignant
|
|
D002528||cerebellar neoplasm primary
|
|
D002528||cerebellar neoplasms benign
|
|
D002528||cerebellar neoplasms malignant
|
|
D002528||cerebellar neoplasms primary
|
|
D002528||cerebellar tumor
|
|
D002528||cerebellar tumors
|
|
D002528||cerebellum primary neoplasm
|
|
D002528||cerebellum primary neoplasms
|
|
D002528||malignant cerebellar neoplasm
|
|
D002528||malignant cerebellar neoplasms
|
|
D002528||neoplasm benign cerebellar
|
|
D002528||neoplasm cerebellar
|
|
D002528||neoplasm cerebellum primary
|
|
D002528||neoplasm malignant cerebellar
|
|
D002528||neoplasms cerebellar
|
|
D002528||neoplasms cerebellar benign
|
|
D002528||neoplasms cerebellar malignant
|
|
D002528||neoplasms cerebellar primary
|
|
D002528||primary cerebellar neoplasm
|
|
D002528||primary cerebellar neoplasms
|
|
D002528||primary neoplasm cerebellum
|
|
D002528||primary neoplasms cerebellum
|
|
D002528||tumor cerebellar
|
|
C536440||corneal hypesthesia familial
|
|
C536440||trigeminal anesthesia familial
|
|
D003859||dependent personality disorder
|
|
D003859||dependent personality disorders
|
|
D003859||disorder dependent personality
|
|
D003859||passive dependent personality
|
|
D003859||personality disorder dependent
|
|
D003859||personality passive dependent
|
|
C537771||anorectal atresia
|
|
C537771||anorectal malformation
|
|
C537771||anorectal stenosis
|
|
C566419|602966||orofacial cleft 2
|
|
C566419|602966||cleft lip with or without cleft palate nonsyndromic 2
|
|
C566419|602966||ofc2
|
|
189800|D011225||pre eclampsia
|
|
189800|D011225||edema proteinuria hypertension gestosis
|
|
189800|D011225||eph complex
|
|
189800|D011225||eph gestosis
|
|
189800|D011225||eph toxemia
|
|
189800|D011225||eph toxemias
|
|
189800|D011225||gestosis edema proteinuria hypertension
|
|
189800|D011225||gestosis eph
|
|
189800|D011225||gestosis hypertension edema proteinuria
|
|
189800|D011225||gestosis proteinuria edema hypertension
|
|
189800|D011225||hellp included
|
|
189800|D011225||hemolysis elevated liver enzymes and low platelet count included
|
|
189800|D011225||hypertension edema proteinuria gestosis
|
|
189800|D011225||pee
|
|
189800|D011225||pee1
|
|
189800|D011225||pee2
|
|
189800|D011225||pee3
|
|
189800|D011225||pee4
|
|
189800|D011225||preeclampsia
|
|
189800|D011225||preeclampsia eclampsia 1
|
|
189800|D011225||preg1
|
|
189800|D011225||pregnancy toxemia
|
|
189800|D011225||pregnancy toxemias
|
|
189800|D011225||proteinuria edema hypertension gestosis
|
|
189800|D011225||toxemia eph
|
|
189800|D011225||toxemia of pregnancy
|
|
189800|D011225||toxemia of pregnancy hypertension pregnancy induced included
|
|
189800|D011225||toxemia pregnancy
|
|
189800|D011225||toxemias eph
|
|
189800|D011225||toxemias pregnancy
|
|
C566299||alzheimer disease early onset with cerebral amyloid angiopathy
|
|
C566495|609965||deafness autosomal dominant 53
|
|
C566495|609965||dfna53
|
|
D002524||cerebellar ataxia
|
|
D002524||adiadochokineses
|
|
D002524||adiadochokinesis
|
|
D002524||ataxia cerebellar
|
|
D002524||ataxias cerebellar
|
|
D002524||cerebellar ataxias
|
|
D002524||cerebellar dysmetria
|
|
D002524||cerebellar dysmetrias
|
|
D002524||cerebellar hemiataxia
|
|
D002524||cerebellar hemiataxias
|
|
D002524||cerebellar incoordination
|
|
D002524||cerebellar incoordinations
|
|
D002524||dysmetria
|
|
D002524||dysmetria cerebellar
|
|
D002524||dysmetrias
|
|
D002524||dysmetrias cerebellar
|
|
D002524||hemiataxia cerebellar
|
|
D002524||hemiataxias cerebellar
|
|
D002524||hypermetria
|
|
D002524||hypermetrias
|
|
D002524||incoordination cerebellar
|
|
D002524||incoordinations cerebellar
|
|
C536444||corneodermatoosseous syndrome
|
|
C536444||cdo syndrome
|
|
C536444||corneal dystrophy epithelial and short stature
|
|
C536444||corneal dystrophy epithelial with skin and skeletal changes
|
|
C537772||anotia
|
|
C537772||microtia
|
|
D002526||cerebellar diseases
|
|
D002526||cerebellar disease
|
|
D002526||cerebellar disorder
|
|
D002526||cerebellar disorders
|
|
D002526||cerebellar dysfunction
|
|
D002526||cerebellar dysfunctions
|
|
D002526||cerebellar syndrome
|
|
D002526||cerebellar syndromes
|
|
D002526||cerebellum disease
|
|
D002526||cerebellum diseases
|
|
D002526||disease cerebellar
|
|
D002526||disease cerebellum
|
|
D002526||disorder cerebellar
|
|
D002526||dysfunction cerebellar
|
|
D002526||syndrome cerebellar
|
|
C537773||ansell bywaters elderking syndrome
|
|
257850|C567605||oculodentodigital dysplasia autosomal recessive
|
|
257850|C567605||oculodentoosseous dysplasia autosomal recessive
|
|
257850|C567605||oddd autosomal recessive
|
|
257850|C567605||odod autosomal recessive
|
|
605355|C538397||nemaline myopathy 5
|
|
605355|C538397||amish nemaline myopathy
|
|
605355|C538397||anm
|
|
605355|C538397||nem5
|
|
605355|C538397||nemaline myopathy amish type
|
|
605355|C538397||nemaline myopathy caused by mutation in the troponin t1 gene
|
|
C549759||phyllodes tumor of the prostate
|
|
C549759||malignant phyllodes tumor of prostate
|
|
D015835||ocular motility disorders
|
|
D015835||brown apos s tendon sheath syndrome
|
|
D015835||brown tendon sheath syndrome
|
|
D015835||conjugate gaze spasm
|
|
D015835||conjugate gaze spasms
|
|
D015835||convergence excess
|
|
D015835||convergence excesses
|
|
D015835||convergence insufficiencies
|
|
D015835||convergence insufficiency
|
|
D015835||cyclophoria
|
|
D015835||cyclophorias
|
|
D015835||deficiencies smooth pursuit
|
|
D015835||deficiency smooth pursuit
|
|
D015835||deviation skew
|
|
D015835||deviations skew
|
|
D015835||dyskinesia paroxysmal ocular
|
|
D015835||dyskinesias paroxysmal ocular
|
|
D015835||excess convergence
|
|
D015835||eye motility disorder
|
|
D015835||eye motility disorders
|
|
D015835||eye movement disorder
|
|
D015835||eye movement disorders
|
|
D015835||gaze spasms conjugate
|
|
D015835||insufficiencies convergence
|
|
D015835||insufficiency convergence
|
|
D015835||internuclear ophthalmoplegia
|
|
D015835||internuclear ophthalmoplegias
|
|
D015835||ocular dyskinesia paroxysmal
|
|
D015835||ocular dyskinesias paroxysmal
|
|
D015835||ocular motility disorder
|
|
D015835||ocular torticollis
|
|
D015835||ophthalmoplegia internuclear
|
|
D015835||ophthalmoplegias internuclear
|
|
D015835||opsoclonus
|
|
D015835||parinaud apos s syndrome
|
|
D015835||parinauds syndrome
|
|
D015835||parinaud syndrome
|
|
D015835||paroxysmal ocular dyskinesia
|
|
D015835||paroxysmal ocular dyskinesias
|
|
D015835||pseudoophthalmoplegia
|
|
D015835||pseudoophthalmoplegias
|
|
D015835||pursuit deficiencies smooth
|
|
D015835||pursuit deficiency smooth
|
|
D015835||skew deviation
|
|
D015835||skew deviations
|
|
D015835||smooth pursuit deficiencies
|
|
D015835||smooth pursuit deficiency
|
|
D015835||spasm of conjugate gaze
|
|
D015835||syndrome brown apos s tendon sheath
|
|
D015835||syndrome parinaud
|
|
D015835||syndrome parinaud apos s
|
|
D015835||tendon sheath syndrome of brown
|
|
D015834||cochlear diseases
|
|
D015834||cochlear disease
|
|
D015834||disease cochlear
|
|
D015834||diseases cochlear
|
|
607341|C537067||focal cortical dysplasia of taylor
|
|
607341|C537067||cdt
|
|
607341|C537067||cdtbc included
|
|
607341|C537067||cdtd included
|
|
607341|C537067||cortical dysplasia of taylor
|
|
607341|C537067||cortical dysplasia of taylor dysplasia only included
|
|
607341|C537067||cortical dysplasia of taylor with balloon cells
|
|
607341|C537067||cortical dysplasia of taylor with balloon cells included
|
|
607341|C537067||cortical dysplasia of taylor without balloon cells included
|
|
607341|C537067||fcdt
|
|
607341|C537067||focal cortical dysplasia of taylor type iia
|
|
607341|C537067||focal cortical dysplasia of taylor type iib
|
|
607341|C537067||focal cortical dysplasia of taylor type iib included
|
|
607341|C537067||focal cortical dysplasia type 2
|
|
607341|C537067||focal cortical dysplasia type ii
|
|
607341|C537067||focal cortical dysplasia type ii focal cortical dysplasia of taylor type iia included
|
|
D015838||chondromatosis synovial
|
|
D015838||chondromatoses synovial
|
|
D015838||chondrometaplasias synovial
|
|
D015838||chondrometaplasia synovial
|
|
D015838||henderson jones syndrome
|
|
D015838||osteochondromatoses synovial
|
|
D015838||osteochondromatosis synovial
|
|
D015838||reichel apos s syndrome
|
|
D015838||reichels syndrome
|
|
D015838||reichel syndrome
|
|
D015838||syndrome henderson jones
|
|
D015838||syndrome reichel apos s
|
|
D015838||synovial chondromatoses
|
|
D015838||synovial chondromatosis
|
|
D015838||synovial chondrometaplasia
|
|
D015838||synovial chondrometaplasias
|
|
D015838||synovial osteochondromatoses
|
|
D015838||synovial osteochondromatosis
|
|
D007898|608207||leishmaniasis visceral
|
|
D007898|608207||black fever
|
|
D007898|608207||fever black
|
|
D007898|608207||kala azar
|
|
D007898|608207||kala azar susceptibility to 1
|
|
D007898|608207||kaza1
|
|
D007898|608207||leishmaniasis visceral susceptibility to 1
|
|
D007898|608207||visceral leishmaniasis
|
|
D015837||vestibular diseases
|
|
D015837||diseases vestibular
|
|
D015837||disease vestibular
|
|
D015837||vestibular disease
|
|
C536436||coffin siris syndrome
|
|
C536436||fifth digit syndrome
|
|
C537767||anophthalmia plus syndrome
|
|
C537767||fryns anophthalmia syndrome
|
|
C537767||fryns microphthalmia syndrome
|
|
C537767||microphthalmia with facial clefting
|
|
C536434||codas syndrome
|
|
C536434||cerebral ocular dental auricular and skeletal syndrome
|
|
C536434||cerebral ocular dental auricular skeletal anomalies syndrome
|
|
C537765||chromosome 6 monosomy 6p23
|
|
C537765||deletion 6p23
|
|
C537765||monosomy 6p23
|
|
C536435||coffin syndrome 1
|
|
C536435||dwarfism lean spastic type
|
|
C536435||lean spastic dwarfism
|
|
C537766||anonychia onychodystrophy with hypoplasia or absence of distal phalanges
|
|
C537766||anonychia and absence hypoplasia of distal phalanges
|
|
C537766||cooks syndrome
|
|
D015831||osteochondroma
|
|
D015831||cartilaginous exostoses
|
|
D015831||cartilaginous exostosis
|
|
D015831||chondrosteoma
|
|
D015831||chondrosteomas
|
|
D015831||exostoses cartilaginous
|
|
D015831||exostoses osteocartilaginous
|
|
D015831||exostosis cartilaginous
|
|
D015831||exostosis osteocartilaginous
|
|
D015831||osteocartilaginous exostoses
|
|
D015831||osteocartilaginous exostosis
|
|
D015831||osteochondromas
|
|
C537769||anophthalmos with limb anomalies
|
|
C537769||anophthalmia syndactyly
|
|
C537769||anophthalmia waardenburg syndrome
|
|
C537769||anophthalmos syndactyly
|
|
C537769||microphthalmia with limb anomalies
|
|
C537769||ophthalmoacromelic syndrome
|
|
C537769||waardenburg anophthalmia syndrome
|
|
D001206||ascorbic acid deficiency
|
|
D001206||ascorbic acid deficiencies
|
|
D001206||deficiencies ascorbic acid
|
|
D001206||deficiencies vitamin c
|
|
D001206||deficiency ascorbic acid
|
|
D001206||deficiency vitamin c
|
|
D001206||vitamin c deficiencies
|
|
D001206||vitamin c deficiency
|
|
D002539||cerebral arterial diseases
|
|
D002539||arterial disease cerebral
|
|
D002539||arterial diseases cerebral
|
|
D002539||artery disease cerebral
|
|
D002539||artery diseases cerebral
|
|
D002539||cerebral arterial disease
|
|
D002539||cerebral artery disease
|
|
D002539||cerebral artery diseases
|
|
D002539||disease cerebral arterial
|
|
D002539||disease cerebral artery
|
|
D002539||diseases cerebral arterial
|
|
D002539||diseases cerebral artery
|
|
612372|C567531||major affective disorder 9
|
|
612372|C567531||mafd9
|
|
C537782||aorta pulmonary artery fistula
|
|
C537782||aorto pulmonary artery fistula
|
|
C537782||aortopulmonary fistula
|
|
300643|C564467||rolandic epilepsy mental retardation and speech dyspraxia x linked
|
|
300643|C564467||resdx
|
|
D002534||hypoxia brain
|
|
D002534||anoxia brain
|
|
D002534||anoxia cerebral
|
|
D002534||anoxic brain damage
|
|
D002534||anoxic encephalopathies
|
|
D002534||anoxic encephalopathy
|
|
D002534||brain anoxia
|
|
D002534||brain damage anoxic
|
|
D002534||brain damage hypoxic
|
|
D002534||brain hypoxia
|
|
D002534||cerebral anoxia
|
|
D002534||cerebral hypoxia
|
|
D002534||damage anoxic brain
|
|
D002534||damage hypoxic brain
|
|
D002534||encephalopathies anoxic
|
|
D002534||encephalopathies hypoxic
|
|
D002534||encephalopathy anoxic
|
|
D002534||encephalopathy hypoxic
|
|
D002534||hypoxia cerebral
|
|
D002534||hypoxic brain damage
|
|
D002534||hypoxic encephalopathies
|
|
D002534||hypoxic encephalopathy
|
|
C537785||aortic arch anomaly with peculiar facies and mental retardation
|
|
C536455||craniofacial dyssynostosis
|
|
C536455||craniofacial dyssynostosis and short stature
|
|
C536455||craniofacial dyssynostosis with short stature
|
|
C536455||craniosynostosis craniofacial dysostosis syndrome
|
|
D003866||depressive disorder
|
|
D003866||depression endogenous
|
|
D003866||depression neurotic
|
|
D003866||depressions endogenous
|
|
D003866||depressions neurotic
|
|
D003866||depressions unipolar
|
|
D003866||depression unipolar
|
|
D003866||depressive disorders
|
|
D003866||depressive neuroses
|
|
D003866||depressive neurosis
|
|
D003866||depressive syndrome
|
|
D003866||depressive syndromes
|
|
D003866||disorder depressive
|
|
D003866||disorders depressive
|
|
D003866||endogenous depression
|
|
D003866||endogenous depressions
|
|
D003866||melancholia
|
|
D003866||melancholias
|
|
D003866||neuroses depressive
|
|
D003866||neurosis depressive
|
|
D003866||neurotic depression
|
|
D003866||neurotic depressions
|
|
D003866||syndrome depressive
|
|
D003866||syndromes depressive
|
|
D003866||unipolar depression
|
|
D003866||unipolar depressions
|
|
C536452||crane heise syndrome
|
|
C536452||cleft lip palate agenesis of clavicles and cervical vertebrae and talipes equinovarus
|
|
C537783||loeys dietz syndrome type 2b
|
|
D002537||intracranial arteriosclerosis
|
|
D002537||arterioscleroses cerebral
|
|
D002537||arterioscleroses intracranial
|
|
D002537||arteriosclerosis cerebral
|
|
D002537||arteriosclerosis intracranial
|
|
D002537||atheroscleroses cerebral
|
|
D002537||atheroscleroses intracranial
|
|
D002537||atherosclerosis cerebral
|
|
D002537||atherosclerosis intracranial
|
|
D002537||cerebral arterioscleroses
|
|
D002537||cerebral arteriosclerosis
|
|
D002537||cerebral atheroscleroses
|
|
D002537||cerebral atherosclerosis
|
|
D002537||intracranial arterioscleroses
|
|
D002537||intracranial atheroscleroses
|
|
D002537||intracranial atherosclerosis
|
|
C562701||fleck retina of kandori
|
|
D002532||intracranial aneurysm
|
|
D002532||aneurysm anterior cerebral artery
|
|
D002532||aneurysm anterior communicating artery
|
|
D002532||aneurysm basilar artery
|
|
D002532||aneurysm berry
|
|
D002532||aneurysm brain
|
|
D002532||aneurysm cerebral
|
|
D002532||aneurysm giant intracranial
|
|
D002532||aneurysm intracranial
|
|
D002532||aneurysm intracranial mycotic
|
|
D002532||aneurysm middle cerebral artery
|
|
D002532||aneurysm posterior cerebral artery
|
|
D002532||aneurysm posterior communicating artery
|
|
D002532||aneurysms basilar artery
|
|
D002532||aneurysms berry
|
|
D002532||aneurysms brain
|
|
D002532||aneurysms cerebral
|
|
D002532||aneurysms giant intracranial
|
|
D002532||aneurysms intracranial
|
|
D002532||aneurysms intracranial mycotic
|
|
D002532||anterior cerebral artery aneurysm
|
|
D002532||anterior communicating artery aneurysm
|
|
D002532||artery aneurysm basilar
|
|
D002532||artery aneurysms basilar
|
|
D002532||basilar artery aneurysm
|
|
D002532||basilar artery aneurysms
|
|
D002532||berry aneurysm
|
|
D002532||berry aneurysms
|
|
D002532||brain aneurysm
|
|
D002532||brain aneurysms
|
|
D002532||cerebral aneurysm
|
|
D002532||cerebral aneurysms
|
|
D002532||giant intracranial aneurysm
|
|
D002532||giant intracranial aneurysms
|
|
D002532||intracranial aneurysm giant
|
|
D002532||intracranial aneurysms
|
|
D002532||intracranial aneurysms giant
|
|
D002532||intracranial mycotic aneurysm
|
|
D002532||intracranial mycotic aneurysms
|
|
D002532||middle cerebral artery aneurysm
|
|
D002532||mycotic aneurysm intracranial
|
|
D002532||mycotic aneurysms intracranial
|
|
D002532||posterior cerebral artery aneurysm
|
|
D002532||posterior communicating artery aneurysm
|
|
C562700||pupillary membrane persistence of
|
|
C562705||pituitary dwarfism with large sella turcica
|
|
C536486|276904||usher syndrome type 1c
|
|
C536486|276904||ush1c
|
|
C536486|276904||usher syndrome acadian variety
|
|
C536486|276904|C564753||usher syndrome type i acadian variety
|
|
C536486|276904|C564753||usher syndrome type ic
|
|
D001201||ascites
|
|
D055673|200990||acrocallosal syndrome
|
|
D055673|200990||acls
|
|
D055673|200990||acrocallosal syndromes
|
|
D055673|200990||hallux duplication postaxial polydactyly and absence of corpus callosum
|
|
D055673|200990||jbts12 included
|
|
D055673|200990||joubert syndrome 12 15 digenic included
|
|
D055673|200990||schinzel acrocallosal syndrome joubert syndrome 12 included
|
|
D055673|200990||syndrome acrocallosal
|
|
D055673|200990||syndromes acrocallosal
|
|
C562709||insulin receptor defect in
|
|
D014516||ureteral neoplasms
|
|
D014516||cancer of the ureter
|
|
D014516||cancer of ureter
|
|
D014516||cancers ureteral
|
|
D014516||cancer ureteral
|
|
D014516||neoplasms of ureter
|
|
D014516||neoplasms ureteral
|
|
D014516||neoplasm ureteral
|
|
D014516||ureteral cancer
|
|
D014516||ureteral cancers
|
|
D014516||ureteral neoplasm
|
|
D014516||ureter cancer
|
|
D014516||ureter cancer of
|
|
D014516||ureter cancers
|
|
D014516||ureter neoplasm
|
|
D014516||ureter neoplasms
|
|
D062108||may thurner syndrome
|
|
D062108||cockett syndrome
|
|
D062108||compression syndrome iliocaval
|
|
D062108||compression syndromes iliocaval
|
|
D062108||iliac vein compression syndrome
|
|
D062108||iliocaval compression syndrome
|
|
D062108||iliocaval compression syndromes
|
|
D062108||syndrome cockett
|
|
D062108||syndrome iliocaval compression
|
|
D062108||syndrome may thurner
|
|
D062108||syndromes iliocaval compression
|
|
D014515||ureteral diseases
|
|
D014515||diseases ureteral
|
|
D014515||disease ureteral
|
|
D014515||ureteral disease
|
|
D015845||tonic pupil
|
|
D015845||adie pupil
|
|
D015845||adie apos s pupil
|
|
D015845||adies pupil
|
|
D015845||myotonic pupil
|
|
D015845||myotonic pupils
|
|
D015845||neuropathic tonic pupil
|
|
D015845||neuropathic tonic pupils
|
|
D015845||pupil adie
|
|
D015845||pupil adie apos s
|
|
D015845||pupil local tonic
|
|
D015845||pupillotonia
|
|
D015845||pupillotonias
|
|
D015845||pupil myotonic
|
|
D015845||pupil neuropathic tonic
|
|
D015845||pupils adie apos s
|
|
D015845||pupils local tonic
|
|
D015845||pupils myotonic
|
|
D015845||pupils neuropathic tonic
|
|
D015845||pupils tonic
|
|
D015845||pupil tonic
|
|
D015845||tonic pupil local
|
|
D015845||tonic pupil neuropathic
|
|
D015845||tonic pupils
|
|
D015845||tonic pupils local
|
|
D015845||tonic pupils neuropathic
|
|
D014514||ureteral calculi
|
|
D014514||calculi ureteral
|
|
D014514||calculus ureteral
|
|
D014514||ureteral calculus
|
|
C562708||prolactin deficiency isolated
|
|
D007625|530000||kearns sayre syndrome
|
|
D007625|530000||chronic progressive external ophthalmoplegia with myopathy
|
|
D007625|530000||cpeo with myopathies
|
|
D007625|530000||cpeo with myopathy
|
|
D007625|530000||cpeo with ragged red fibers
|
|
D007625|530000||cytopathy kearn sayre mitochondrial
|
|
D007625|530000||kearn sayre mitochondrial cytopathy
|
|
D007625|530000||kearns sayre mitochondrial cytopathy
|
|
D007625|530000||kearns sayre shy daroff syndrome
|
|
D007625|530000||kearns syndrome
|
|
D007625|530000||kearns apos syndrome
|
|
D007625|530000||kearn syndrome
|
|
D007625|530000||kss
|
|
D007625|530000|C540770||mitochondrial cytopathy
|
|
D007625|530000||mitochondrial cytopathy kearn sayre
|
|
D007625|530000||myopathies cpeo with
|
|
D007625|530000||myopathy cpeo with
|
|
D007625|530000||oculocraniosomatic syndrome
|
|
D007625|530000||oculocraniosomatic syndromes
|
|
D007625|530000||ophthalmoplegia pigmentary degeneration of retina and cardiomyopathy
|
|
D007625|530000||ophthalmoplegia plus syndrome
|
|
D007625|530000||ophthalmoplegia plus syndromes
|
|
D007625|530000||ophthalmoplegia progressive external with ragged red fibers
|
|
D007625|530000||sayre syndrome kearns
|
|
D007625|530000||syndrome kearns
|
|
D007625|530000||syndrome kearns apos
|
|
D007625|530000||syndrome kearns sayre
|
|
D007625|530000||syndrome kearns sayre shy daroff
|
|
D007625|530000||syndrome oculocraniosomatic
|
|
D007625|530000||syndrome ophthalmoplegia plus
|
|
C566882|265120||surfactant metabolism dysfunction pulmonary 1
|
|
C566882|265120||interstitial lung disease due to surfactant protein b deficiency
|
|
C566882|265120||interstitial lung disease nonspecific due to surfactant protein b deficiency
|
|
C566882|265120||pulmonary alveolar proteinosis congenital 1
|
|
C566882|265120||smdp1
|
|
C548420||vascular compression of the duodenum
|
|
D014518||ureterocele
|
|
D014518||ureteroceles
|
|
D014517||ureteral obstruction
|
|
D014517||obstructions ureteral
|
|
D014517||obstruction ureteral
|
|
D014517||ureteral obstructions
|
|
C537778||antisynthetase syndrome
|
|
C536448||costocoracoid ligament congenitally short
|
|
C536448||congenital shortness of the costocoracoid ligament
|
|
C537779||antithrombin deficiency type 2
|
|
C536445||coronal synostosis syndactyly and jejunal atresia
|
|
C537776||anterior spinal artery stroke
|
|
D014511||uremia
|
|
D014511||uremias
|
|
C536449||cote katsantoni syndrome
|
|
D015841||enophthalmos
|
|
D052798||balanitis xerotica obliterans
|
|
D052798||kraurosis penis
|
|
D015840||oculomotor nerve diseases
|
|
D015840||cranial nerve iii diseases
|
|
D015840||nerve disease oculomotor
|
|
D015840||nerve diseases oculomotor
|
|
D015840||nerve disorder oculomotor
|
|
D015840||nerve disorders oculomotor
|
|
D015840||nerve palsies oculomotor
|
|
D015840||nerve palsy oculomotor
|
|
D015840||nerve paralyses oculomotor
|
|
D015840||nerve paralysis oculomotor
|
|
D015840||neuropathies oculomotor
|
|
D015840||neuropathy oculomotor
|
|
D015840||oculomotor nerve disease
|
|
D015840||oculomotor nerve disorder
|
|
D015840||oculomotor nerve disorders
|
|
D015840||oculomotor nerve palsies
|
|
D015840||oculomotor nerve palsy
|
|
D015840||oculomotor nerve paralyses
|
|
D015840||oculomotor nerve paralysis
|
|
D015840||oculomotor neuropathies
|
|
D015840||oculomotor neuropathy
|
|
D015840||palsies oculomotor nerve
|
|
D015840||palsies partial third nerve
|
|
D015840||palsies third nerve
|
|
D015840||palsies total third nerve
|
|
D015840||palsy oculomotor nerve
|
|
D015840||palsy partial third nerve
|
|
D015840||palsy third nerve
|
|
D015840||palsy total third nerve
|
|
D015840||paralyses oculomotor nerve
|
|
D015840||paralyses third nerve
|
|
D015840||paralysis oculomotor nerve
|
|
D015840||paralysis third nerve
|
|
D015840||partial third nerve palsies
|
|
D015840||partial third nerve palsy
|
|
D015840||third cranial nerve diseases
|
|
D015840||third nerve palsies
|
|
D015840||third nerve palsies partial
|
|
D015840||third nerve palsies total
|
|
D015840||third nerve palsy
|
|
D015840||third nerve palsy partial
|
|
D015840||third nerve palsy total
|
|
D015840||third nerve paralyses
|
|
D015840||third nerve paralysis
|
|
D015840||total third nerve palsies
|
|
D015840||total third nerve palsy
|
|
300630||mental retardation x linked syndromic fried type
|
|
300630||mental retardation x linked syndromic 21
|
|
300630||mrx59
|
|
300630||mrxs21
|
|
300630||mrxsf
|
|
C566277||anonychia ectrodactyly
|
|
C566278||anonychia with flexural pigmentation
|
|
C535749|608540||congenital disorder of glycosylation type 1k
|
|
C535749|608540||cdg1k
|
|
C535749|608540||cdgik
|
|
C535749|608540||cdg ik
|
|
C535749|608540||congenital disorder of glycosylation type ik
|
|
D064793||teratogenesis
|
|
C563326|601388||diabetes mellitus insulin dependent 12
|
|
C563326|601388||iddm12
|
|
C563326|601388||insulin dependent diabetes mellitus 12
|
|
D063466||respiratory aspiration of gastric contents
|
|
C567473|300710||alopecia androgenetic 2
|
|
C567473|300710||aga2
|
|
D015819||substance abuse intravenous
|
|
D015819||drug abuse intravenous
|
|
D015819||drug abuse parenteral
|
|
D015819||intravenous drug abuse
|
|
D015819||intravenous substance abuse
|
|
D015819||parenteral drug abuse
|
|
143400|C537373||multicystic renal dysplasia bilateral
|
|
143400|C537373||hydronephrosis due to pujo
|
|
143400|C537373||mcrd
|
|
143400|C537373||mrd
|
|
143400|C537373||pelvi ureteric junction obstruction
|
|
143400|C537373||pelviureteric junction obstruction
|
|
143400|C537373||pujo
|
|
609049|C537185||pierson syndrome
|
|
609049|C537185||microcoria and congenital nephrotic syndrome
|
|
609049|C537185||microcoria congenital nephrotic syndrome
|
|
609049|C537185||nephrotic syndrome congenital with ocular abnormalities and congenital myasthenic syndrome
|
|
C563476|167320||inclusion body myopathy with early onset paget disease and frontotemporal dementia
|
|
C563476|167320||ibmpfd
|
|
C563476|167320||ibmpfd1
|
|
C563476|167320||inclusion body myopathy with early onset paget disease of bone and or frontotemporal dementia
|
|
C563476|167320||inclusion body myopathy with early onset paget disease with or without frontotemporal dementia 1
|
|
C563476|167320||inclusion body myopathy with paget disease of bone and or frontotemporal dementia
|
|
C563476|167320||lower motor neuron degeneration with paget like bone disease
|
|
C563476|167320||msp1
|
|
C563476|167320||multisystem proteinopathy 1
|
|
C563476|167320||muscular dystrophy limb girdle with paget disease of bone
|
|
C563476|167320||pagetoid amyotrophic lateral sclerosis
|
|
C563476|167320||pagetoid neuroskeletal syndrome
|
|
D015814||ocular hypotension
|
|
D015814||hypotension ocular
|
|
D015814||hypotony ocular
|
|
D015814||ocular hypotony
|
|
C537707||kallikrein hypertension
|
|
C537707||kallikrein attenuated hypertension
|
|
D015812||glaucoma angle closure
|
|
D015812||angle closure glaucoma
|
|
D015812||angle closure glaucomas
|
|
D015812||closed angle glaucoma
|
|
D015812||closed angle glaucomas
|
|
D015812||glaucoma closed angle
|
|
D015812||glaucoma narrow angle
|
|
D015812||glaucomas angle closure
|
|
D015812||glaucomas closed angle
|
|
D015812||glaucomas narrow angle
|
|
D015812||glaucomas uncompensated
|
|
D015812||glaucomas uncompensative
|
|
D015812||glaucoma uncompensated
|
|
D015812||glaucoma uncompensative
|
|
D015812||narrow angle glaucoma
|
|
D015812||narrow angle glaucomas
|
|
D015812||uncompensated glaucoma
|
|
D015812||uncompensated glaucomas
|
|
D015812||uncompensative glaucoma
|
|
D015812||uncompensative glaucomas
|
|
C537708||kifafa seizure disorder
|
|
C537708||complex familial seizure disorder
|
|
C537708||vitsala
|
|
D015811||iris neoplasms
|
|
D015811||iris neoplasm
|
|
D015811||neoplasm iris
|
|
D015811||neoplasms iris
|
|
D015818||eye infections bacterial
|
|
D015818||bacterial eye infection
|
|
D015818||bacterial eye infections
|
|
D015818||bacterial ocular infection
|
|
D015818||bacterial ocular infections
|
|
D015818||eye infection bacterial
|
|
D015818||infection bacterial eye
|
|
D015818||infection bacterial ocular
|
|
D015818||infections bacterial eye
|
|
D015818||infections bacterial ocular
|
|
D015818||ocular infection bacterial
|
|
D015818||ocular infections bacterial
|
|
D015817||eye infections
|
|
D015817||eye infection
|
|
D015817||infection eye
|
|
D015817||infection ocular
|
|
D015817||infections eye
|
|
D015817||infections ocular
|
|
D015817||ocular infection
|
|
D015817||ocular infections
|
|
D007706|309400||menkes kinky hair syndrome
|
|
D007706|309400||congenital hypocupremia
|
|
D007706|309400||congenital hypocupremias
|
|
D007706|309400||copper transport disease
|
|
D007706|309400||diseases kinky hair
|
|
D007706|309400||diseases menkes apos
|
|
D007706|309400||diseases steely hair
|
|
D007706|309400||disease steely hair
|
|
D007706|309400||hair diseases kinky
|
|
D007706|309400||hair diseases steely
|
|
D007706|309400||hypocupremia congenital
|
|
D007706|309400||hypocupremias congenital
|
|
D007706|309400||kinky hair disease
|
|
D007706|309400||kinky hair diseases
|
|
D007706|309400||kinky hair syndrome
|
|
D007706|309400||menkea syndrome
|
|
D007706|309400||menkea syndromes
|
|
D007706|309400||menkes disease
|
|
D007706|309400||menkes apos disease
|
|
D007706|309400||menkes apos diseases
|
|
D007706|309400||menkes syndrome
|
|
D007706|309400||mk
|
|
D007706|309400||mnk
|
|
D007706|309400||steely hair disease
|
|
D007706|309400||steely hair diseases
|
|
D007706|309400||steely hair syndrome
|
|
D007706|309400||steely hair syndromes
|
|
D007706|309400||syndrome menkea
|
|
D007706|309400||syndromes menkea
|
|
D007706|309400||syndromes steely hair
|
|
D007706|309400||syndrome steely hair
|
|
D007706|309400||x linked copper deficiency
|
|
C537701|239000||hyperostosis corticalis deformans juvenilis
|
|
C537701||chronic congenital idiopathic hyperphosphatasemia
|
|
C537701||familial idiopathic hyperphosphatasemia
|
|
C537701||familial osteoectasia
|
|
C537701|239000||hyperphosphatasemia chronic congenital idiopathic
|
|
C537701||hyperphosphatasemia with bone disease
|
|
C537701|239000||hyperphosphatasia familial idiopathic
|
|
C537701||idiopathic hyperphosphatasia
|
|
C537701|239000||juvenile paget disease
|
|
C537701||juvenile paget apos s disease
|
|
C537701||osteochalasia desmalis familiaris
|
|
C537701|239000||osteoectasia familial
|
|
C537701||osteoectasia with hyperphosphatasia
|
|
C535755|266265||congenital disorder of glycosylation type 2c
|
|
C535755|266265||cdg2c
|
|
C535755|266265||cdgiic
|
|
C535755|266265||cdg iic
|
|
C535755|266265||congenital disorder of glycosylation type iic
|
|
C535755|266265||lad2
|
|
C535755|266265||leukocyte adhesion deficiency type 2
|
|
C535755|266265||leukocyte adhesion deficiency type ii
|
|
C535755|266265||rambam hasharon syndrome
|
|
C535755|266265|C535289|129400||rhs
|
|
D051474||neuralgia postherpetic
|
|
D051474||postherpetic neuralgia
|
|
C537700||juvenile osteoporosis
|
|
C537700||childhood onset primary osteoporosis
|
|
C537700||idiopathic juvenile osteoporosis
|
|
C537700||juvenile primary osteoporosis
|
|
C537700||osteoporosis juvenile
|
|
C566287||anal sphincter myopathy internal
|
|
C566287||proctalgia fugax due to anal sphincter myopathy
|
|
C566280||aniridia microcornea and spontaneously reabsorbed cataract
|
|
C566281||aniridia and absent patella
|
|
C537703||juvenile systemic scleroderma
|
|
C566282||spinal arterial venous malformations with cutaneous hemangiomas
|
|
C566283||hemangiomatosis disseminated
|
|
C566288||frontotemporal dementia with motor neuron disease
|
|
C537720||macrodactyly of the hand
|
|
C537720||megalodactylism of the hand
|
|
C537720||megalodactyly of the hand
|
|
C537718||volcke soekarman syndrome
|
|
D015823||acanthamoeba keratitis
|
|
D015823||acanthamoeba keratitides
|
|
D015823||keratitides acanthamoeba
|
|
D015823||keratitis acanthamoeba
|
|
C536842|133100||polycythemia primary familial and congenital
|
|
C536842|133100||benign familial polycythemia
|
|
C536842|133100||congenital erythrocytosis
|
|
C536842|133100||ecyt1
|
|
C536842|133100||erythrocytosis autosomal dominant benign
|
|
C536842|133100||erythrocytosis familial 1
|
|
C536842|133100||familial erythrocytosis
|
|
C536842|133100||familial erythrocytosis 1
|
|
C536842|133100||familial polycythemia
|
|
C536842|133100||hereditary erythrocytosis
|
|
C536842|133100||pfcp
|
|
C536842|133100||primary familial polycythemia
|
|
C537719||macrodactyly of the foot
|
|
C537719||megalodactylism of the foot
|
|
C537719||megalodactyly of the foot
|
|
C566290||amyotrophic lateral sclerosis autosomal recessive
|
|
D015822||eye infections parasitic
|
|
D015822||eye infection parasitic
|
|
D015822||infection parasitic eye
|
|
D015822||infection parasitic ocular
|
|
D015822||infections parasitic eye
|
|
D015822||infections parasitic ocular
|
|
D015822||ocular infection parasitic
|
|
D015822||ocular infections parasitic
|
|
D015822||parasitic eye infection
|
|
D015822||parasitic eye infections
|
|
D015822||parasitic ocular infection
|
|
D015822||parasitic ocular infections
|
|
D015829||uveitis suppurative
|
|
D015829||suppurative uveitides
|
|
D015829||suppurative uveitis
|
|
D015829||uveitides suppurative
|
|
D015828||eye infections viral
|
|
D015828||eye infection viral
|
|
D015828||infections viral eye
|
|
D015828||infections viral ocular
|
|
D015828||infection viral eye
|
|
D015828||infection viral ocular
|
|
D015828||ocular infections viral
|
|
D015828||ocular infection viral
|
|
D015828||viral eye infection
|
|
D015828||viral eye infections
|
|
D015828||viral ocular infection
|
|
D015828||viral ocular infections
|
|
D015827||onchocerciasis ocular
|
|
D015827||blindness river
|
|
D015827||ocular onchocerciases
|
|
D015827||ocular onchocerciasis
|
|
D015827||onchocerciases ocular
|
|
D015827||river blindness
|
|
C566295||amastia bilateral with ureteral triplication and dysmorphism
|
|
C537713||lynch lee murday syndrome
|
|
C537713||caudal appendage short terminal phalanges deafness cryptorchidism and mental retardation
|
|
425500|C564029||hairy ears y linked
|
|
425500|C564029||hypertrichosis pinnae auris y linked
|
|
C537711||lymphedema microcephaly and chorioretinopathy syndrome
|
|
C537711||chorioretinal dysplasia microcephaly mental retardation syndrome
|
|
C537711||lymphedema and retinal folds with microcephaly and microphthalmos
|
|
C537711||lymphedema microcephaly chorioretinopathy syndrome
|
|
C537711||microcephaly lymphedema chorioretinal dysplasia
|
|
C537711||microcephaly lymphedema chorioretinal dysplasia syndrome
|
|
C566298||alzheimer disease familial 1
|
|
C537716||macrocephaly mesodermal hamartoma spectrum
|
|
C537716||elattoproteus syndrome
|
|
C537716||gigantism partial of hands and feet nevi hemihypertrophy and macrocephaly
|
|
C537716||hemihypertrophy and macrocephaly
|
|
C537716||partial gigantism of hands and feet nevi hemihypertrophy macrocephaly
|
|
C566291||amyotrophic lateral sclerosis sporadic
|
|
D015821||eye infections fungal
|
|
D015821||eye infection fungal
|
|
D015821||fungal eye infection
|
|
D015821||fungal eye infections
|
|
D015821||fungal ocular infection
|
|
D015821||fungal ocular infections
|
|
D015821||infection fungal eye
|
|
D015821||infection fungal ocular
|
|
D015821||infection ocular mycotic
|
|
D015821||infections fungal eye
|
|
D015821||infections fungal ocular
|
|
D015821||infections ocular mycotic
|
|
D015821||mycoses ocular
|
|
D015821||mycosis ocular
|
|
D015821||mycotic infection ocular
|
|
D015821||mycotic infections ocular
|
|
D015821||ocular infection fungal
|
|
D015821||ocular infections fungal
|
|
D015821||ocular mycoses
|
|
D015821||ocular mycosis
|
|
D015821||ocular mycotic infection
|
|
D015821||ocular mycotic infections
|
|
D015821||oculomycoses
|
|
D015821||oculomycosis
|
|
C537717||macrocephaly benign familial
|
|
C537717||benign familial macrocephaly
|
|
C537717||benign familial megalencephaly
|
|
C537717||cole hughes syndrome
|
|
C566292||amyotrophic dystonic paraplegia
|
|
C537714||macdermot winter syndrome
|
|
C537714||prominent glabella microcephaly hypogenitalism
|
|
605259|C537195||spinocerebellar ataxia 13
|
|
605259|C537195||autosomal dominant cerebellar ataxia with mental retardation
|
|
605259|C537195||cerebellar ataxia autosomal dominant with mental retardation
|
|
605259|C537195||sca13
|
|
C537715||macleod fraser syndrome
|
|
C566294||amelia and terminal transverse hemimelia
|
|
D017681|607685||hypereosinophilic syndrome
|
|
D017681|607685||endocarditis loeffler
|
|
D017681|607685||endocarditis loefflers
|
|
D017681|607685||endocarditis loeffler apos s
|
|
D017681|607685||eosinophilic leukemia
|
|
D017681|607685||eosinophilic leukemias
|
|
D017681|607685||hes
|
|
D017681|607685||hypereosinophilic syndrome idiopathic
|
|
D017681|607685||hypereosinophilic syndromes
|
|
D017681|607685||hypereosinophilic syndromes idiopathic
|
|
D017681|607685||idiopathic hypereosinophilic syndrome
|
|
D017681|607685||idiopathic hypereosinophilic syndromes
|
|
D017681|607685||leukemia eosinophilic
|
|
D017681|607685||leukemias eosinophilic
|
|
D017681|607685||loeffler endocarditis
|
|
D017681|607685||loeffler apos s endocarditis
|
|
D017681|607685||loefflers endocarditis
|
|
D017681|607685||syndrome hypereosinophilic
|
|
D017681|607685||syndrome idiopathic hypereosinophilic
|
|
D017681|607685||syndromes hypereosinophilic
|
|
D017681|607685||syndromes idiopathic hypereosinophilic
|
|
C566255||cardiomyopathy right ventricular dilated
|
|
C567586||mental retardation x linked syndromic zdhhc9 related
|
|
C566256||arrhenoblastoma thyroid adenoma
|
|
D020391||muscular dystrophy facioscapulohumeral
|
|
D020391||atrophies facioscapulohumeral
|
|
D020391||atrophy facioscapulohumeral
|
|
D020391||dystrophies facioscapulohumeral muscular
|
|
D020391||dystrophies landouzy dejerine
|
|
D020391||dystrophy facioscapulohumeral muscular
|
|
D020391||dystrophy landouzy dejerine
|
|
D020391||facioscapulohumeral atrophies
|
|
D020391||facioscapulohumeral atrophy
|
|
D020391||facio scapulo humeral dystrophy
|
|
D020391||facioscapulohumeral muscular dystrophies
|
|
D020391||facioscapulohumeral type progressive muscular dystrophy
|
|
D020391||facioscapuloperoneal muscular dystrophy
|
|
D020391||fsh muscular dystrophy
|
|
D020391||landouzy dejerine dystrophies
|
|
D020391||landouzy dejerine dystrophy
|
|
D020391||muscular dystrophies facioscapulohumeral
|
|
D020391||muscular dystrophy landouzy dejerine
|
|
D020391||progressive muscular dystrophy facioscapulohumeral type
|
|
613790||complement component 8 deficiency type i
|
|
613790||c8ag deficiency
|
|
613790||c8 alpha gamma deficiency
|
|
613790||c8d1
|
|
613790||c8 deficiency type i
|
|
C566258||arms malformation of
|
|
C536081|236800||hydroxykynureninuria
|
|
C536081|236800||kynureninase deficiency
|
|
C536081|236800||xanthurenic aciduria
|
|
613792||chromosome 3pter p25 deletion syndrome
|
|
613792||3p syndrome
|
|
D063485||acanthocheilonemiasis
|
|
D063485||acanthocheilonemiases
|
|
C564174|143850||orthostatic hypotensive disorder streeten type
|
|
C564174|143850||hyperbradykininism
|
|
C564174|143850||ohds
|
|
C564174|143850||orthostatic hypotensive disorder
|
|
612459||body mass index quantitative trait locus 13
|
|
612459||bmiq13
|
|
D006099||granuloma
|
|
D006099||granulomas
|
|
613789||complement component 8 deficiency type ii
|
|
613789||c8b deficiency
|
|
613789||c8 beta deficiency
|
|
613789||c8d2
|
|
613789||c8 deficiency type ii
|
|
613789||complement component 8b deficiency
|
|
C536652|260800||pentosuria
|
|
C536652|260800||l xylulose reductase deficiency
|
|
C536652|260800||l xylulosuria
|
|
C536652|260800||pntsu
|
|
C536652|260800||xylitol dehydrogenase deficiency
|
|
144750|C536748||worth syndrome
|
|
144750|C536748||benign hyperostosis corticalis generalisata
|
|
144750|C536748||endosteal hyperostosis autosomal dominant
|
|
144750|C536748||endosteal hyperostosis worth type
|
|
144750|C536748||hyperostosis corticalis generalisata benign form of worth with torus palatinus
|
|
144750|C536748||hyperostosis corticalis generalisata congenita
|
|
144750|C536748||osteosclerosis autosomal dominant
|
|
144750|C536748||osteosclerosis autosomal dominant worth type with torus palatinus
|
|
300843|C564092||bornholm eye disease
|
|
300843|C564092||bed
|
|
300843|C564092||myopia high with nonprogressive cone dysfunction
|
|
612460||body mass index quantitative trait locus 14
|
|
612460||bmiq14
|
|
C566262||familial hyperbeta and prebetalipoproteinemia
|
|
C565798|604302||rheumatoid arthritis systemic juvenile
|
|
C565798|604302||systemic juvenile rheumatoid arthritis
|
|
C567593||primary ovarian insufficiency fragile x associated
|
|
C567593||fragile x premature ovarian failure
|
|
C580551||y chromosome infertility
|
|
C580551||y chromosome related azoospermia
|
|
C566263||hyperlipemia with familial hypercholesterolemic xanthomatosis
|
|
C567596||mineralocorticoid deficiency isolated
|
|
C537721||macroepiphyseal dysplasia mcalister coe type
|
|
C537721||macroepiphyseal dysplasia with osteoporosis wrinkled skin and aged appearance
|
|
C537721||mcalister coe whyte syndrome
|
|
C566264||broad betalipoproteinemia
|
|
C537722||macrogyria pseudobulbar palsy and mental retardation
|
|
C537722||kuzniecky andermann syndrome
|
|
C566265||floating betalipoproteinemia
|
|
C567582|300804||joubert syndrome 10
|
|
C567582|300804||jbts10
|
|
C537725||lung agenesis
|
|
C537725||congenital lung agenesis
|
|
C537725||pulmonary agenesis
|
|
C537725||unilateral lobar pulmonary agenesis
|
|
C537725||unilateral lung agenesis
|
|
C566260||apolipoprotein e deficiency or defect of
|
|
C567591||emery dreifuss muscular dystrophy 6 x linked
|
|
C567591||emery dreifuss muscular dystrophy 6
|
|
C537726||lutz richner landolt syndrome
|
|
C537726||biliary malformation with renal tubular insufficiency
|
|
C537726||cholestatic jaundice and renal tubular insufficiency
|
|
C537726||renal tubular insufficiency cholestatic jaundice and multiple congenital anomalies
|
|
C566261||dysbetalipoproteinemia due to defect in apolipoprotein e d
|
|
D020386||isaacs syndrome
|
|
D020386||acquired neuromyotonia
|
|
D020386||continuous muscle activity syndrome
|
|
D020386||continuous myokymia
|
|
D020386||continuous myokymias
|
|
D020386||gamstorp wohlfart syndrome
|
|
D020386||gamstorp wohlfart syndromes
|
|
D020386||isaacs mertens syndrome
|
|
D020386||isaacs pseudomyotonia syndrome
|
|
D020386||isaacs apos syndrome
|
|
D020386||isaac syndrome
|
|
D020386||myokymia continuous
|
|
D020386||myokymia myotonia muscle wasting and hyperhidrosis
|
|
D020386||myokymias continuous
|
|
D020386||neuromyotonia
|
|
D020386||neuromyotonia acquired
|
|
D020386||pseudomyotonia
|
|
D020386||pseudomyotonia syndrome of isaacs
|
|
D020386||quantal squander
|
|
D020386||syndrome of continuous muscle activity
|
|
D020386||syndromes gamstorp wohlfart
|
|
D020386||syndromes isaacs mertens
|
|
D018088||tuberculosis multidrug resistant
|
|
D018088||drug resistant tuberculosis
|
|
D018088||mdr tuberculosis
|
|
D018088||multidrug resistant tuberculosis
|
|
D018088||multi drug resistant tuberculosis
|
|
D018088||tuberculosis drug resistant
|
|
D018088||tuberculosis mdr
|
|
D018088||tuberculosis multi drug resistant
|
|
D020385||myokymia
|
|
D020385||chorea fibrillary
|
|
D020385||chorea morvan
|
|
D020385||chorea morvan apos s
|
|
D020385||chorea morvan apos s fibrillary
|
|
D020385||choreas fibrillary
|
|
D020385||choreas morvan
|
|
D020385||choreas morvan apos s
|
|
D020385||fibrillary chorea
|
|
D020385||fibrillary chorea morvan apos s
|
|
D020385||fibrillary choreas
|
|
D020385||generalized myokymia
|
|
D020385||generalized myokymias
|
|
D020385||kymatism
|
|
D020385||kymatisms
|
|
D020385||morvan chorea
|
|
D020385||morvan choreas
|
|
D020385||morvan fibrillary chorea
|
|
D020385||morvan apos s chorea
|
|
D020385||morvans chorea
|
|
D020385||morvan apos s choreas
|
|
D020385||morvan apos s fibrillary chorea
|
|
D020385||morvans fibrillary chorea
|
|
D020385||myokymia generalized
|
|
D020385||myokymias
|
|
D020385||myokymias generalized
|
|
C562509|119500||popliteal pterygium syndrome
|
|
C562509|119500||cleft lip palate paramedian mucous cysts of the lower lip popliteal pterygium digital and genital anomalies
|
|
C562509|119500||faciogenitopopliteal syndrome
|
|
C562509|119500||facio genito popliteal syndrome
|
|
C562509|119500||pps
|
|
C536410||neural tube defects x linked
|
|
C536410||anencephaly spina bifida
|
|
C537741||odontomicronychial dysplasia
|
|
C567597||46 xx gonadal dysgenesis partial or complete autosomal
|
|
C567597||xx male syndrome sry negative
|
|
C566267||hypobetalipoproteinemia familial
|
|
C566267||acanthocytosis with hypobetalipoproteinemia
|
|
C566267||hypobetalipoproteinemia familial 1
|
|
C566267||hypobetalipoproteinemia normotriglyceridemic
|
|
180849|D012415||rubinstein taybi syndrome
|
|
180849|D012415||broad thumb hallux syndrome
|
|
180849|D012415||broad thumb hallux syndromes
|
|
180849|D012415||broad thumbs and great toes characteristic facies and mental retardation
|
|
180849|D012415||rsts1
|
|
180849|D012415||rsts2
|
|
180849|D012415||rubinstein syndrome
|
|
180849|D012415||rubinstein taybi syndrome 1
|
|
180849|D012415||rubinstein taybi syndrome 2
|
|
180849|D012415||syndrome broad thumb hallux
|
|
180849|D012415||syndrome rubinstein
|
|
180849|D012415||syndrome rubinstein taybi
|
|
180849|D012415||syndromes broad thumb hallux
|
|
C565723|609757||williams beuren region duplication syndrome
|
|
C565723|609757||chromosome 7q11 23 duplication syndrome
|
|
C565723|609757||chromosome 7q11 23 triplication syndrome included
|
|
C565723|609757||somerville van der aa syndrome wbs triplication syndrome included
|
|
C565723|609757||wbs duplication syndrome
|
|
C537740||odontoma dysphagia syndrome
|
|
C537740||boder syndrome
|
|
C537740||odontomatosis multiple odontomas with dysphagia
|
|
D049188||prenatal injuries
|
|
D049188||injuries prenatal
|
|
D049188||injury prenatal
|
|
D049188||prenatal injury
|
|
C565046|132450||epiphyseal dysplasia multiple with myopia and conductive deafness
|
|
C565046|132450||edmmd
|
|
C565775|604401||arrhythmogenic right ventricular dysplasia familial 6
|
|
C565775|604401||arrhythmogenic right ventricular cardiomyopathy 6
|
|
C565775|604401||arvc6
|
|
C565775|604401||arvd6
|
|
C563753|609270||spinocerebellar ataxia autosomal recessive 7
|
|
C563753|609270||scar7
|
|
613779||c3d
|
|
D015807||eye injuries penetrating
|
|
D015807||eye injury penetrating
|
|
D015807||injuries penetrating eye
|
|
D015807||injury penetrating eye
|
|
D015807||penetrating eye injuries
|
|
D015807||penetrating eye injury
|
|
D050171||dyslipidemias
|
|
D050171||dyslipidemia
|
|
D050171||dyslipoproteinemia
|
|
D050171||dyslipoproteinemias
|
|
D050174||genetic diseases y linked
|
|
D050174||diseases y linked genetic
|
|
D050174||disease y linked genetic
|
|
D050174||genetic diseases y chromosome linked
|
|
D050174||genetic disease y linked
|
|
D050174||y linked genetic disease
|
|
D050174||y linked genetic diseases
|
|
C536403||nephrotic syndrome ocular anomalies
|
|
C536403||familial infantile nephrotic syndrome with ocular abnormalities
|
|
C536403||glastre cochat bouvier syndrome
|
|
C566273||alpha 1 antitrypsin deficiency autosomal recessive
|
|
C566273|D019896|613490||alpha 1 antitrypsin deficiency
|
|
C566273||alpha 1 protease inhibitor deficiency
|
|
C566273||alpha 1 related emphysema
|
|
C566273||genetic emphysema
|
|
C566273||hereditary pulmonary emphysema
|
|
C566273||inherited emphysema
|
|
C563311|601457||severe combined immunodeficiency autosomal recessive t cell negative b cell negative nk cell positive
|
|
C563311|601457||scid t cell negative b cell negative nk cell positive
|
|
D020191|125370||myoclonic epilepsies progressive
|
|
D020191|125370|254900||action myoclonus renal failure syndrome
|
|
D020191|125370||ataxia chorea seizures and dementia
|
|
D020191|125370||atrophies dentatorubral pallidoluysian
|
|
D020191|125370||atrophy dentatorubral pallidoluysian
|
|
D020191|125370||atypical inclusion body disease
|
|
D020191|125370||atypical inclusion body diseases
|
|
D020191|125370||biotin responsive encephalopathies
|
|
D020191|125370||biotin responsive encephalopathy
|
|
D020191|125370||dentatorubral pallidoluysian atrophies
|
|
D020191|125370||dentatorubral pallidoluysian atrophy
|
|
D020191|125370||disease atypical inclusion body
|
|
D020191|125370||disease naito oyanagi
|
|
D020191|125370||diseases atypical inclusion body
|
|
D020191|125370||diseases naito oyanagi
|
|
D020191|125370||drpla
|
|
D020191|125370||encephalopathies biotin responsive
|
|
D020191|125370||encephalopathy biotin responsive
|
|
D020191|125370||epilepsies progressive myoclonic
|
|
D020191|125370||epilepsies progressive myoclonus
|
|
D020191|125370||epilepsy progressive myoclonic
|
|
D020191|125370||epilepsy progressive myoclonus
|
|
D020191|125370||familial progressive myoclonic epilepsy
|
|
D020191|125370||haw river syndrome
|
|
D020191|125370||haw river syndromes
|
|
D020191|125370||hrs
|
|
D020191|125370||inclusion body disease atypical
|
|
D020191|125370||inclusion body diseases atypical
|
|
D020191|125370||may white syndrome
|
|
D020191|125370||myoclonic epilepsy progressive
|
|
D020191|125370|C538427||myoclonic epilepsy with choreoathetosis
|
|
D020191|125370||myoclonus epilepsies progressive
|
|
D020191|125370|254900||myoclonus nephropathy syndrome
|
|
D020191|125370||myoclonus nephropathy syndromes
|
|
D020191|125370||naito oyanagi disease
|
|
D020191|125370||naito oyanagi diseases
|
|
D020191|125370||nod
|
|
D020191|125370||oyanagi disease naito
|
|
D020191|125370||progressive myoclonic epilepsies
|
|
D020191|125370||progressive myoclonus epilepsies
|
|
D020191|125370||progressive myoclonus epilepsy
|
|
D020191|125370||river syndrome haw
|
|
D020191|125370||river syndromes haw
|
|
D020191|125370||syndrome haw river
|
|
D020191|125370||syndrome myoclonus nephropathy
|
|
D020191|125370||syndromes haw river
|
|
D020191|125370||syndromes myoclonus nephropathy
|
|
C536401||nephropathy deafness hyperparathyroidism
|
|
C536401||nephropathy deafness and hyperparathyroidism
|
|
C537732||oculodental syndrome rutherfurd syndrome
|
|
C537732||corneal dystrophy with gum hypertrophy
|
|
C537732||gingival hypertrophy corneal dystrophy
|
|
C537732||gingival hypertrophy with corneal dystrophy
|
|
C537732||rutherfurd syndrome
|
|
C566275||antibody deficiency due to defect in cd19
|
|
D018232|268220||rhabdomyosarcoma alveolar
|
|
D018232|268220||alveolar rhabdomyosarcoma
|
|
D018232|268220||alveolar rhabdomyosarcomas
|
|
D018232|268220||rhabdomyosarcoma 2
|
|
D018232|268220||rhabdomyosarcomas alveolar
|
|
D018232|268220||rms2
|
|
D018232|268220||rmsa
|
|
C536402||nephrosis deafness urinary tract digital malformation
|
|
C536402||nephrosis with deafness and urinary tract and digital malformations
|
|
C537733||oculodentoosseous dysplasia recessive
|
|
D050177||overweight
|
|
C536407||neuhauser eichner opitz syndrome
|
|
C536407||encephalopathy recurrent of childhood
|
|
C537738||oculopalatoskeletal syndrome
|
|
C537738||craniosynostosis with lid anomalies
|
|
C537738||michels syndrome
|
|
C536408||neural crest tumor
|
|
C536408||neural crest derived tumors
|
|
C537739||oculorenocerebellar syndrome
|
|
C566270||apolipoprotein c iii deficiency
|
|
C536405||neu laxova syndrome
|
|
C537736||oculomaxillofacial dysostosis
|
|
C537736||oblique facial clefts
|
|
C537736||oculomaxillofacial dysplasia with oblique facial clefts
|
|
C537736||richieri costa gorlin syndrome
|
|
C566271||aortic arch interruption facial palsy and retinal coloboma
|
|
C536406||neuhauser daly magnelli syndrome
|
|
C536406||essential tremors nystagmus and duodenal ulceration
|
|
C536406||tremor nystagmus and duodenal ulcer
|
|
C536406||tremor nystagmus duodenal ulcer
|
|
C536406||tremors nystagmus and duodenal ulcers
|
|
C537737||oculomelic amyoplasia
|
|
C537737||arthrogryposis distal type 5
|
|
C537737||arthrogryposis distal type iib
|
|
C537737||arthrogryposis with oculomotor limitation and electroretinal abnormalities
|
|
C566272||townes brocks branchiootorenal like syndrome
|
|
C566237||atrial tachyarrhythmia with short pr interval
|
|
C567568||hypoglossia isolated
|
|
C566238||atrial septal defect with atrioventricular conduction defects
|
|
C566238||asd with atrioventricular conduction defects
|
|
D012618|269600||sea blue histiocyte syndrome
|
|
D012618|269600||disease sea blue histiocyte
|
|
D012618|269600||diseases sea blue histiocyte
|
|
D012618|269600||histiocyte disease sea blue
|
|
D012618|269600||histiocyte diseases sea blue
|
|
D012618|269600||histiocyte syndrome sea blue
|
|
D012618|269600||histiocyte syndromes sea blue
|
|
D012618|269600||histiocytoses sea blue
|
|
D012618|269600||histiocytosis sea blue
|
|
D012618|269600||sea blue histiocyte disease
|
|
D012618|269600||sea blue histiocyte diseases
|
|
D012618|269600||sea blue histiocyte syndromes
|
|
D012618|269600||sea blue histiocytoses
|
|
D012618|269600||sea blue histiocytosis
|
|
D012618|269600||syndrome sea blue histiocyte
|
|
D012618|269600||syndromes sea blue histiocyte
|
|
C566233||azotemia familial
|
|
D020370||osteoarthritis knee
|
|
D020370||knee osteoarthritides
|
|
D020370||knee osteoarthritis
|
|
D020370||knee osteoarthritis of
|
|
D020370||knees osteoarthritis of
|
|
D020370||osteoarthritides knee
|
|
D020370||osteoarthritis of knees
|
|
C566415|603034||endplate acetylcholinesterase deficiency
|
|
C566415|603034||cms1c
|
|
C566415|603034||cms ic
|
|
C566415|603034||congenital myasthenic syndrome type ic
|
|
C566415|603034||ead
|
|
C566415|603034||engel congenital myasthenic syndrome
|
|
C566415|603034||myasthenic syndrome congenital engel type
|
|
C566234||axenfeld rieger anomaly with partially absent eye muscles distinctive face hydrocephaly and skeletal abnormalities
|
|
C566234||de hauwere syndrome
|
|
C566234||iris dysplasia with ocular hypertelorism psychomotor retardation and sensorineural deafness
|
|
C567567||hypoglossia with situs inversus
|
|
C566235||aurocephalosyndactyly
|
|
C566235||auralcephalosyndactyly
|
|
C567566||hypotonia seizures and precocious puberty
|
|
C563561|158590||neuropathy distal hereditary motor type iia
|
|
C563561|158590||charcot marie tooth disease spinal iia
|
|
C563561|158590||dhmn2a
|
|
C563561|158590||hmn2a
|
|
C563561|158590||hmn iia
|
|
C563561|158590||neuronopathy distal hereditary motor type iia
|
|
C563561|158590||spinal muscular atrophy distal adult autosomal dominant iia
|
|
551000||mitochondrial myopathy lethal infantile
|
|
551000||limm
|
|
613776||chromosome 17p13 1 deletion syndrome
|
|
D006069||gonorrhea
|
|
D006069||gonorrheas
|
|
C580539||x linked infantile nystagmus
|
|
C580539||congenital motor nystagmus
|
|
C580539||frmd7 related infantile nystagmus
|
|
C580539||idiopathic infantile nystagmus
|
|
C580539|C537853|310700||nys1
|
|
C580539||x linked congenital nystagmus
|
|
C580539||x linked idiopathic infantile nystagmus
|
|
D006073||gout
|
|
D006073||gouts
|
|
C567459|611907||episodic ataxia type 7
|
|
C567459|611907||ea7
|
|
C580533||x linked chondrodysplasia punctata 1
|
|
C580533||arylsulfatase e deficiency
|
|
C580533||chondrodysplasia punctata 1 x linked
|
|
C580533||x linked recessive chondrodysplasia punctata 1
|
|
C566240||atrial septal defect primum type
|
|
C567571||vitamin d dependent rickets type 2b with normal vitamin d receptor
|
|
C567571||vddr2b
|
|
C566241||atrial septal defect secundum type
|
|
C567574||46 xy gonadal dysgenesis complete sry related
|
|
C567574||gonadal dysgenesis xy female type
|
|
C536293|213300||joubert syndrome 1
|
|
C536293|213300||cerebellar vermis agenesis
|
|
C536293|213300||cerebellooculorenal syndrome 1
|
|
C536293|213300||cerebelloparenchymal disorder 4
|
|
C536293|213300||cerebelloparenchymal disorder iv
|
|
C536293|213300||cors1
|
|
C536293|213300||cpd4
|
|
C536293|213300||jbts
|
|
C536293|213300||jbts1
|
|
C536293|213300||joubert boltshauser syndrome
|
|
C536293|213300||joubert syndrome
|
|
C567570||mitchell riley syndrome
|
|
270550|C536787||spastic ataxia charlevoix saguenay type
|
|
270550|C536787||arsacs
|
|
270550|C536787||autosomal recessive spastic ataxia of charlevoix saguenay
|
|
270550|C536787||charlevoix saguenay spastic ataxia
|
|
270550|C536787||sacs
|
|
270550|C536787||spastic ataxia 6 autosomal recessive
|
|
270550|C536787||spastic ataxia of charlevoix saguenay
|
|
270550|C536787||spax6
|
|
D020364||paraneoplastic polyneuropathy
|
|
D020364||neuropathies paraneoplastic
|
|
D020364||neuropathies paraneoplastic peripheral
|
|
D020364||neuropathy paraneoplastic
|
|
D020364||neuropathy paraneoplastic peripheral
|
|
D020364||paraneoplastic neuropathies
|
|
D020364||paraneoplastic neuropathy
|
|
D020364||paraneoplastic peripheral neuropathies
|
|
D020364||paraneoplastic peripheral neuropathy
|
|
D020364||paraneoplastic polyneuropathies
|
|
D020364||peripheral neuropathies paraneoplastic
|
|
D020364||peripheral neuropathy paraneoplastic
|
|
D020364||polyneuropathies paraneoplastic
|
|
D020364||polyneuropathy paraneoplastic
|
|
D003803||dentigerous cyst
|
|
D003803||cyst dentigerous
|
|
D003803||cysts dentigerous
|
|
D003803||dentigerous cysts
|
|
C566248||asymmetric short stature syndrome
|
|
D020363||limbic encephalitis
|
|
D020363||encephalitides paraneoplastic limbic
|
|
D020363||encephalitis limbic
|
|
D020363||encephalitis paraneoplastic limbic
|
|
D020363||limbic encephalitis paraneoplastic
|
|
D020363||paraneoplastic limbic encephalitis
|
|
C567579||glycogen storage disease type ixa2
|
|
C567579||gsd9a2
|
|
C567579||gsd ixa2
|
|
D020362||paraneoplastic cerebellar degeneration
|
|
D020362||anti yo associated paraneoplastic cerebellar degeneration
|
|
D020362||cerebellar degeneration paraneoplastic
|
|
D020362||cerebellar syndrome paraneoplastic
|
|
D020362||cerebellar syndromes paraneoplastic
|
|
D020362||degeneration paraneoplastic cerebellar
|
|
D020362||paraneoplastic cerebellar degeneration anti yo associated
|
|
D020362||paraneoplastic cerebellar syndrome
|
|
D020362||paraneoplastic cerebellar syndromes
|
|
D003805||dentin dysplasia
|
|
D003805||dentin dysplasias
|
|
D003805||dysplasia dentin
|
|
D003805||dysplasias dentin
|
|
D020361||paraneoplastic syndromes nervous system
|
|
D020361||autonomic dysfunction paraneoplastic
|
|
D020361||autonomic dysfunctions paraneoplastic
|
|
D020361||encephalomyelitis paraneoplastic
|
|
D020361||nervous system paraneoplastic syndromes
|
|
D020361||neurologic syndrome paraneoplastic
|
|
D020361||neurologic syndromes paraneoplastic
|
|
D020361||paraneoplastic autonomic dysfunction
|
|
D020361||paraneoplastic autonomic dysfunctions
|
|
D020361||paraneoplastic encephalomyelitides
|
|
D020361||paraneoplastic encephalomyelitis
|
|
D020361||paraneoplastic neurologic syndrome
|
|
D020361||paraneoplastic neurologic syndromes
|
|
D020361||syndrome paraneoplastic neurologic
|
|
D020361||syndromes paraneoplastic neurologic
|
|
C567576||rett syndrome atypical
|
|
C567575||46 xy true hermaphroditism sry related
|
|
C566245||external auditory canal bilateral atresia of with congenital vertical talus
|
|
C566245||atresia of external auditory canal and conduction deafness
|
|
C567578||frontootopalatodigital osteodysplasia
|
|
C566246||ataxia with fasciculations
|
|
C567577||otopalatodigital spectrum disorder
|
|
C566247||ataxia spastic with congenital miosis
|
|
C566247||miosis congenital with spastic ataxia
|
|
192605|C536334||ventricular tachycardia familial
|
|
192605|C536334||ventricular tachycardia familial polymorphic
|
|
C565593|225790||encephaloclastic proliferative vasculopathy
|
|
C565593|225790||epv
|
|
C565593|225790||hydranencephaly fowler type
|
|
C565593|225790||hydrocephaly hydranencephaly due to cerebral vasculopathy
|
|
C565593|225790||proliferative vasculopathy and hydranencephaly hydrocephaly syndrome
|
|
C565593|225790||pvhh
|
|
D045602||steatorrhea
|
|
607078|C535505||epiphyseal dysplasia multiple 5
|
|
607078|C535505||bhmed
|
|
607078|C535505||edm5
|
|
607078|C535505||microepiphyseal dysplasia bilateral hereditary
|
|
607078|C535505||multiple epiphyseal dysplasia 5
|
|
607078|C535505||multiple epiphyseal dysplasia matn3 related
|
|
C562687|222700||lysinuric protein intolerance
|
|
C562687|222700||dibasic amino aciduria ii
|
|
C562687|222700||hyperdibasic aminoaciduria
|
|
C562687|222700||lpi
|
|
C562687|222700||lpi lysinuric protein intolerance
|
|
127750|D020961||lewy body disease
|
|
127750|D020961||cortical lewy body disease
|
|
127750|D020961||dementia lewy body
|
|
127750|D020961||diffuse lewy body disease
|
|
127750|D020961||diffuse lewy body disease diffuse lewy body disease with gaze palsy included
|
|
127750|D020961||dlb
|
|
127750|D020961||lewy body dementia
|
|
127750|D020961||lewy body disease cortical
|
|
127750|D020961||lewy body disease diffuse
|
|
127750|D020961||lewy body type senile dementia
|
|
127750|D020961||lewy body variant of alzheimer disease included
|
|
C567833|612989||optic atrophy 7
|
|
C567833|612989||opa7
|
|
D006086||graft vs host disease
|
|
D006086||disease graft versus host
|
|
D006086||disease graft vs host
|
|
D006086||disease homologous wasting
|
|
D006086||disease runt
|
|
D006086||diseases graft versus host
|
|
D006086||diseases graft vs host
|
|
D006086||graft versus host disease
|
|
D006086||graft versus host diseases
|
|
D006086||graft vs host diseases
|
|
D006086||homologous wasting disease
|
|
D006086||runt disease
|
|
612433||deafness autosomal recessive 45
|
|
612433||dfnb45
|
|
612431||deafness autosomal dominant 27
|
|
612431||dfna27
|
|
D006083||graft occlusion vascular
|
|
D006083||graft restenoses vascular
|
|
D006083||graft restenosis vascular
|
|
D006083||occlusion vascular graft
|
|
D006083||restenosis vascular graft
|
|
D006083||vascular graft occlusion
|
|
D006083||vascular graft restenosis
|
|
C537564|156400||jansen type metaphyseal chondrodysplasia
|
|
C537564|156400||metaphyseal chondrodysplasia jansen type
|
|
C537564|156400||metaphyseal chondrodysplasia murk jansen type
|
|
C537564|156400||murk jansen type metaphyseal chondrodysplasia
|
|
C567583||mental retardation x linked znf711 related
|
|
C567583||mental retardation x linked 97
|
|
C567585||chromosome xp11 23 p11 22 duplication syndrome
|
|
C566253||arteritis familial granulomatous with juvenile polyarthritis
|
|
C567584||mental retardation x linked syp related
|
|
C567584||mrxsyp
|
|
C566646|601650||paragangliomas 2
|
|
C566646|601650||glomus tumors familial 2
|
|
C566646|601650||pgl2
|
|
D003807||dentin sensitivity
|
|
D003807||dentine hypersensitivities
|
|
D003807||dentine hypersensitivity
|
|
D003807||dentine sensitivities
|
|
D003807||dentine sensitivity
|
|
D003807||dentin hypersensitivities
|
|
D003807||dentin hypersensitivity
|
|
D003807||dentin sensitivities
|
|
D003807||hypersensitivities dentin
|
|
D003807||hypersensitivities dentine
|
|
D003807||hypersensitivity dentin
|
|
D003807||hypersensitivity dentine
|
|
D003807||sensitivities dentin
|
|
D003807||sensitivities dentine
|
|
D003807||sensitivity dentin
|
|
D003807||sensitivity dentine
|
|
D018058||tympanic membrane perforation
|
|
D018058||eardrum perforation
|
|
D018058||membrane perforation tympanic
|
|
D018058||membrane rupture tympanic
|
|
D018058||perforation eardrum
|
|
D018058||rupture tympanic membrane
|
|
D018058||tympanic membrane rupture
|
|
253800||muscular dystrophy dystroglycanopathy congenital with brain and eye anomalies type a 4
|
|
253800||fcmd
|
|
253800|D058494|236670||fukuyama congenital muscular dystrophy
|
|
253800||mddga4
|
|
253800||walker warburg syndrome or muscle eye brain disease fktn related
|
|
D003809||dentin secondary
|
|
D003809||dentins secondary
|
|
D003809||secondary dentin
|
|
D003809||secondary dentins
|
|
C536096|159900||myoclonic dystonia
|
|
C536096|159900||alcohol responsive dystonia
|
|
C536096|159900||dystonia 11
|
|
C536096|159900||dystonia alcohol responsive
|
|
C536096|159900||dyt11
|
|
C536096|159900||hereditary essential myoclonus
|
|
C536096|159900||myoclonus dystonia
|
|
C536096|159900||myoclonus dystonia syndrome
|
|
C536096|159900||myoclonus hereditary essential
|
|
C567580||chromosome xq28 duplication syndrome
|
|
C567580||gdi1 duplication syndrome
|
|
C566250||aryl hydrocarbon hydroxylase inducibility
|
|
C566250||ahh inducibility
|
|
C567547||corneal dystrophy subepithelial mucinous
|
|
C567547||subepithelial mucinous corneal dystrophy
|
|
C567546||corneal dystrophy posterior amorphous
|
|
C567546||posterior amorphous corneal dystrophy
|
|
611247|C567073||major affective disorder 4
|
|
611247|C567073||mafd4
|
|
143465|D001289||attention deficit disorder with hyperactivity
|
|
143465|D001289||adhd
|
|
143465|D001289||adhd1
|
|
143465|D001289||adhd2
|
|
143465|D001289||adhd3
|
|
143465|D001289||adhd4
|
|
143465|D001289||adhd5
|
|
143465|D001289||adhd6
|
|
143465|D001289||adhd7
|
|
143465|D001289||attention deficit disorder
|
|
143465|D001289||attention deficit disorders
|
|
143465|D001289||attention deficit disorders with hyperactivity
|
|
143465|D001289||attention deficit hyperactivity disorder
|
|
143465|D001289||attention deficit hyperactivity disorders
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 1
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 2
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 3
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 4
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 5
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 6
|
|
143465|D001289||attention deficit hyperactivity disorder susceptibility to 7
|
|
143465|D001289||brain dysfunction minimal
|
|
143465|D001289||deficit disorder attention
|
|
143465|D001289||deficit disorders attention
|
|
143465|D001289||deficit hyperactivity disorder attention
|
|
143465|D001289||deficit hyperactivity disorders attention
|
|
143465|D001289||digit span quantitative trait locus
|
|
143465|D001289||disorder attention deficit
|
|
143465|D001289||disorder attention deficit hyperactivity
|
|
143465|D001289||disorders attention deficit
|
|
143465|D001289||disorders attention deficit hyperactivity
|
|
143465|D001289||dysfunction minimal brain
|
|
143465|D001289||hyperactivity of childhood
|
|
143465|D001289||hyperkinetic syndrome
|
|
143465|D001289||minimal brain dysfunction
|
|
143465|D001289||motor timing quantitative trait locus
|
|
143465|D001289||syndromes hyperkinetic
|
|
C536328|600273||polycystic kidneys severe infantile with tuberous sclerosis
|
|
C536328|600273||chromosome 16p13 3 deletion syndrome distal
|
|
C536328|600273||pkdts
|
|
C536328|600273||polycystic kidney disease infantile severe with tuberous sclerosis
|
|
C536328|600273||tuberous sclerosis polycystic kidney disease contiguous gene syndrome
|
|
C567545||metaphyseal anadysplasia 1
|
|
C567545||mandp1
|
|
C567544||sensorineural deafness with mild renal dysfunction
|
|
C566214||adult i blood group with congenital cataract
|
|
C566214||adult i blood group phenotype
|
|
C566214||adult i blood group without congenital cataract
|
|
215400|D002817||chordoma
|
|
215400|D002817||chdm
|
|
215400|D002817||chordomas
|
|
215400|D002817||chordoma susceptibility to
|
|
D007383||intermittent claudication
|
|
D007383||claudication intermittent
|
|
D058926||intraoperative awareness
|
|
D058926||anesthesia awareness
|
|
D058926||anesthesia awareness during
|
|
D058926||awareness anesthesia
|
|
D058926||awareness during anesthesia
|
|
D058926||awareness intraoperative
|
|
D058926||during anesthesia awareness
|
|
601776||ehlers danlos syndrome musculocontractural type 1
|
|
601776||adducted thumb clubfoot and progressive joint and skin laxity syndrome
|
|
601776||atcs
|
|
601776||dundar syndrome
|
|
601776||edsmc
|
|
601776||edsmc1
|
|
D058923||medial tibial stress syndrome
|
|
D058923||medial tibial stress syndrome mtss
|
|
D058923||shin splint
|
|
D058923||shin splints
|
|
D058922||inflammatory breast neoplasms
|
|
D058922||breast cancer inflammatory
|
|
D058922||breast cancers inflammatory
|
|
D058922||breast carcinoma inflammatory
|
|
D058922||breast carcinomas inflammatory
|
|
D058922||breast neoplasm inflammatory
|
|
D058922||breast neoplasms inflammatory
|
|
D058922||cancer inflammatory breast
|
|
D058922||cancers inflammatory breast
|
|
D058922||carcinoma inflammatory breast
|
|
D058922||carcinomas inflammatory breast
|
|
D058922||inflammatory breast cancer
|
|
D058922||inflammatory breast cancer ibc
|
|
D058922||inflammatory breast cancers
|
|
D058922||inflammatory breast carcinoma
|
|
D058922||inflammatory breast carcinomas
|
|
D058922||inflammatory breast neoplasm
|
|
D058922||neoplasm inflammatory breast
|
|
D058922||neoplasms inflammatory breast
|
|
C566226||basilar impression primary
|
|
C567557||cardiac conduction defect nonspecific
|
|
C566228||banki syndrome
|
|
C566222||bpes with duane retraction syndrome
|
|
C566222||bpes type i autosomal recessive
|
|
C566222||bpes without ovarian failure
|
|
C566222||bpes with ovarian failure
|
|
C567553||keratosis follicularis spinulosa decalvans autosomal dominant
|
|
C566223||blepharochalasis superior
|
|
D020347||lithiasis
|
|
D020347||calculoses
|
|
D020347||calculosis
|
|
D020347||lithiases
|
|
226600|D016108||epidermolysis bullosa dystrophica
|
|
226600|D016108||bullosa dystrophica epidermolysis
|
|
226600|D016108||bullosa dystrophicas epidermolysis
|
|
226600|D016108||bullosa dystrophic epidermolysis
|
|
226600|D016108||bullosas dystrophic epidermolysis
|
|
226600|D016108||cockayne touraine disease
|
|
226600|D016108||cockayne touraine type epidermolysis bullosa
|
|
226600|D016108||dystrophica epidermolysis bullosa
|
|
226600|D016108||dystrophicas epidermolysis bullosa
|
|
226600|D016108||dystrophic epidermolysis bullosa
|
|
226600|D016108||dystrophic epidermolysis bullosa autosomal recessive
|
|
226600|D016108||dystrophic epidermolysis bullosas
|
|
226600|D016108||epidermolysis bullosa dystrophic
|
|
226600|D016108||epidermolysis bullosa dystrophica autosomal recessive
|
|
226600|D016108||epidermolysis bullosa dystrophica dominant
|
|
226600|D016108||epidermolysis bullosa dystrophica hallopeau siemens type
|
|
226600|D016108||epidermolysis bullosa dystrophica hallopeau siemens type ebr1 epidermolysis bullosa dystrophica autosomal recessive localisata variant included
|
|
226600|D016108||epidermolysis bullosa dystrophica inversa autosomal recessive included
|
|
226600|D016108||epidermolysis bullosa dystrophica recessive
|
|
226600|D016108||epidermolysis bullosa dystrophicas
|
|
226600|D016108||epidermolysis bullosas dystrophic
|
|
226600|D016108||hallopeau siemens disease
|
|
226600|D016108||rdeb
|
|
D006059||gonadal dysgenesis
|
|
D006059||dysgenesis gonadal
|
|
D006059||gonadal agenesis
|
|
D020345||enterocolitis necrotizing
|
|
D020345||necrotizing enterocolitis
|
|
D006058||gonadal disorders
|
|
D006058||disorder gonadal
|
|
D006058||disorders gonadal
|
|
D006058||gonadal disorder
|
|
D020343||hypertensive encephalopathy
|
|
D020343||encephalopathy hypertensive
|
|
D006060||gonadal dysgenesis mixed
|
|
D006060||mixed gonadal dysgenesis
|
|
D006061||gonadal dysgenesis 46 xy
|
|
D006061||46 xy complete gonadal dysgenesis
|
|
D006061||46 xy gonadal dysgenesis
|
|
D006061||46 xy gonadal sex reversal
|
|
D006061||complete gonadal dysgenesis 46 xy
|
|
D006061||pure gonadal dysgenesis 46 xy
|
|
D006061||sex reversal gonadal 46 xy
|
|
D006061||swyer syndrome
|
|
D006061||syndrome swyer
|
|
D006061||xy pure gonadal dysgenesis
|
|
C565710|610187||diaphragmatic hernia 3
|
|
C565710|610187||dih3
|
|
C566230||ovalocytosis malaysian melanesian filipino type
|
|
C566231||elliptocytosis 4
|
|
600430|C538317||brachydactyly mental retardation syndrome
|
|
600430||albright hereditary osteodystrophy like syndrome chromosome 2q37 deletion syndrome included
|
|
600430||bdmr
|
|
D019462||syncope vasovagal
|
|
D019462||cerebral syncope
|
|
D019462||cerebral syncopes
|
|
D019462||faint neurally mediated
|
|
D019462||faints neurally mediated
|
|
D019462||malignant neurocardiogenic syncope
|
|
D019462||malignant neurocardiogenic syncopes
|
|
D019462||neurally mediated faint
|
|
D019462||neurally mediated faints
|
|
D019462||neurocardiogenic syncope
|
|
D019462||neurocardiogenic syncope malignant
|
|
D019462||neurocardiogenic syncopes
|
|
D019462||neurocardiogenic syncopes malignant
|
|
D019462||neurogenic syncope
|
|
D019462||neurogenic syncopes
|
|
D019462||supine syncope
|
|
D019462||supine syncopes
|
|
D019462||syncope cerebral
|
|
D019462||syncope malignant neurocardiogenic
|
|
D019462||syncope neurocardiogenic
|
|
D019462||syncope neurogenic
|
|
D019462||syncopes cerebral
|
|
D019462||syncopes malignant neurocardiogenic
|
|
D019462||syncopes neurocardiogenic
|
|
D019462||syncopes neurogenic
|
|
D019462||syncopes supine
|
|
D019462||syncope supine
|
|
D019462||syncopes vasodepressor
|
|
D019462||syncopes vasovagal
|
|
D019462||syncope vasodepressor
|
|
D019462||syncope vasovagal neurally mediated
|
|
D019462||vasodepressor syncope
|
|
D019462||vasodepressor syncopes
|
|
D019462||vasovagal syncope
|
|
D019462||vasovagal syncopes
|
|
183600|C567893||split hand foot deformity 1
|
|
183600|C567893||ecd
|
|
183600|C567893|C574275||ectrodactyly
|
|
183600|C567893||shfd1
|
|
183600|C567893||shfm1
|
|
183600|C567893||shsf1
|
|
183600|C567893|C574275||split hand deformity
|
|
183600|C567893||split hand foot malformation 1
|
|
183600|C567893||split hand foot malformation 1 with or without deafness
|
|
D019465||craniofacial abnormalities
|
|
D019465||abnormalities craniofacial
|
|
D019465||abnormality craniofacial
|
|
D019465||craniofacial abnormality
|
|
607004|C564635||brachydactyly type a1 b
|
|
607004|C564635||bda1b
|
|
C567402||diastasis recti and weakness of the linea alba
|
|
C567401||cerebroretinal microangiopathy with calcifications and cysts
|
|
C567401||coats plus syndrome
|
|
C567401||labrune syndrome
|
|
C567401||leukoencephalopathy brain calcifications and cysts
|
|
268310|C535863||robinow syndrome autosomal recessive
|
|
268310|C535863||costovertebral segmentation defect with mesomelia formerly
|
|
268310|C535863||covesdem syndrome formerly robinow syndrome autosomal recessive with aplasia hypoplasia of phalanges and metacarpals metatarsals included
|
|
268310|C535863||robinow syndrome autosomal recessive with brachy syn polydactyly included
|
|
268310|C535863||rrs
|
|
D021782||multicystic dysplastic kidney
|
|
D021782||bilateral multicystic dysplastic kidneys
|
|
D021782||dysplasia multicystic kidney
|
|
D021782||dysplasia multicystic renal
|
|
D021782||dysplasias multicystic kidney
|
|
D021782||dysplasias multicystic renal
|
|
D021782||kidney dysplasia multicystic
|
|
D021782||kidney dysplasias multicystic
|
|
D021782||multicystic dysplastic kidneys
|
|
D021782||multicystic kidney
|
|
D021782||multicystic kidney dysplasia
|
|
D021782||multicystic kidney dysplasias
|
|
D021782||multicystic kidneys
|
|
D021782||multicystic renal dysplasia
|
|
D021782||multicystic renal dysplasias
|
|
D021782||renal dysplasia multicystic
|
|
D021782||renal dysplasias multicystic
|
|
D021782||unilateral multicystic dysplastic kidney
|
|
C567409||usher syndrome type id f
|
|
252500||icd
|
|
252500||ml ii
|
|
252500||ml ii alpha beta
|
|
C538116|306955||heterotaxy visceral x linked
|
|
C538116|306955||chtd1 included
|
|
C538116|306955||dextrocardia with other cardiac malformations
|
|
C538116|306955||heterotaxy visceral 1 x linked
|
|
C538116|306955|270100||heterotaxy visceral 5 autosomal
|
|
C538116|306955||htx1
|
|
C538116|306955||laterality x linked
|
|
C538116|306955||situs inversus complex cardiac defects and splenic defects x linked
|
|
C538116|306955||situs inversus complex cardiac defects and splenic defects x linked congenital heart defects multiple types 1 x linked included
|
|
C538116|306955||visceral heterotaxia
|
|
D007589|243700||autosomal dominant hies
|
|
D007589|243700||autosomal dominant hiess
|
|
D007589|243700||autosomal recessive hies
|
|
D007589|243700||autosomal recessive hiess
|
|
D007589|243700||buckley syndrome
|
|
D007589|243700||buckley syndromes
|
|
D007589|243700||hies autosomal recessive
|
|
D007589|243700||hiess autosomal dominant
|
|
D007589|243700||hiess autosomal recessive
|
|
D007589|243700||hie syndrome
|
|
D007589|243700||hie syndromes
|
|
D007589|243700||hyper ige recurrent infection syndrome autosomal recessive
|
|
D007589|243700||hyper ige syndrome
|
|
D007589|243700||hyper ige syndrome autosomal recessive
|
|
D007589|243700||hyper ige syndromes
|
|
D007589|243700||hyperimmunoglobulinemia e syndrome
|
|
D007589|243700||hyperimmunoglobulinemia e syndromes
|
|
D007589|243700||hyperimmunoglobulin e recurrent infection syndrome
|
|
D007589|243700||hyper immunoglobulin e syndrome autosomal dominant
|
|
D007589|243700||hyper immunoglobulin e syndrome autosomal recessive
|
|
D007589|243700||job buckley syndrome
|
|
D007589|243700||job buckley syndromes
|
|
D007589|243700||job apos s syndrome
|
|
D007589|243700||jobs syndrome
|
|
D007589|243700||job syndromes
|
|
D007589|243700||syndrome buckley
|
|
D007589|243700||syndrome hie
|
|
D007589|243700||syndrome hyper ige
|
|
D007589|243700||syndrome hyperimmunoglobulinemia e
|
|
D007589|243700||syndrome job
|
|
D007589|243700||syndrome job buckley
|
|
D007589|243700||syndrome job apos s
|
|
D007589|243700||syndromes buckley
|
|
D007589|243700||syndromes hie
|
|
D007589|243700||syndromes hyperimmunoglobulinemia e
|
|
D007589|243700||syndromes job
|
|
D007589|243700||syndromes job buckley
|
|
C563695|609573||photoparoxysmal response 3
|
|
C563695|609573||photoparoxysmal response with or without myoclonic epilepsy
|
|
C563695|609573||ppr3
|
|
D018126||odontodysplasia
|
|
D018126||dysplasia odontogenic
|
|
D018126||dysplasias odontogenic
|
|
D018126||ghost teeth
|
|
D018126||ghost tooth
|
|
D018126||odontodysplasias
|
|
D018126||odontogenesis imperfecta
|
|
D018126||odontogenic dysplasia
|
|
D018126||odontogenic dysplasias
|
|
D018126||teeth ghost
|
|
D018126||tooth ghost
|
|
D019457||chromosome breakage
|
|
D019457||breakage chromosomal
|
|
D019457||breakage chromosome
|
|
D019457||breakages chromosomal
|
|
D019457||breakages chromosome
|
|
D019457||break chromosomal
|
|
D019457||break chromosome
|
|
D019457||breaks chromosomal
|
|
D019457||breaks chromosome
|
|
D019457||chromosomal break
|
|
D019457||chromosomal breakage
|
|
D019457||chromosomal breakages
|
|
D019457||chromosomal breaks
|
|
D019457||chromosome break
|
|
D019457||chromosome breakages
|
|
D019457||chromosome breaks
|
|
C537768|601186||anophthalmia with pulmonary hypoplasia
|
|
C537768|601186||anophthalmia clinical with mild facial dysmorphism and variable malformations of the lung heart and diaphragm
|
|
C537768|601186||anophthalmia microphthalmia and pulmonary hypoplasia
|
|
C537768|601186||matthew wood syndrome
|
|
C537768|601186||mcopcb8 included
|
|
C537768|601186||mcops9
|
|
C537768|601186||microphthalmia syndromic 9
|
|
C537768|601186||pulmonary agenesis microphthalmia and diaphragmatic defect
|
|
C537768|601186||pulmonary agenesis microphthalmia and diaphragmatic defect pmd microphthalmia isolated with coloboma 8 included
|
|
C537768|601186||spear syndrome
|
|
C567412||paroxysmal exertion induced dyskinesia and hemolytic anemia
|
|
C537004|220111||leigh syndrome french canadian type
|
|
C537004|220111||cox deficiency french canadian type
|
|
C537004|220111||cox deficiency saguenay lac saint jean type
|
|
C537004|220111||cytochrome c oxidase deficiency french canadian type
|
|
C537004|220111||leigh syndrome saguenay lac saint jean type
|
|
C537004|220111||lsfc
|
|
D020447||parasomnias
|
|
D020447||benign neonatal sleep myoclonus
|
|
D020447||drunkennesses sleep
|
|
D020447||drunkenness sleep
|
|
D020447||myoclonus benign neonatal sleep
|
|
D020447||neonatal sleep myoclonus benign
|
|
D020447||parasomnia
|
|
D020447||paroxysm sleep sensory
|
|
D020447||paroxysms sleep sensory
|
|
D020447||sensory paroxysm sleep
|
|
D020447||sensory paroxysms sleep
|
|
D020447||sleep drunkenness
|
|
D020447||sleep drunkennesses
|
|
D020447||sleep related abnormal swallowing syndrome
|
|
D020447||sleep sensory paroxysm
|
|
D020447||sleep sensory paroxysms
|
|
C567476|300706||mental retardation x linked syndromic turner type
|
|
C567476|300706||mental retardation and macrocephaly syndrome
|
|
C567476|300706||mrxst
|
|
C567476|300706||mrxs turner
|
|
C536042|166210||osteogenesis imperfecta type 2a
|
|
C536042|166210||oi2
|
|
C536042|166210||oic
|
|
C536042|166210||oi type ii
|
|
C536042|166210||osteogenesis imperfecta congenita
|
|
C536042|166210||osteogenesis imperfecta congenita perinatal lethal form
|
|
C536042|166210||osteogenesis imperfecta type ii
|
|
C536042|166210||osteogenesis imperfecta type iia
|
|
C536042|166210||vrolik disease
|
|
C536042|166210||vrolik type of osteogenesis imperfecta
|
|
C563794|609115||limb girdle muscular dystrophy type 1g
|
|
C563794|609115||lgmd1g
|
|
607624|C537302||griscelli syndrome type 2
|
|
607624|C537302||albinism partial with immunodeficiency
|
|
607624|C537302||griscelli syndrome with hemophagocytic syndrome
|
|
607624|C537302||gs2
|
|
607624|C537302||paid syndrome
|
|
607624|C537302||partial albinism and immunodeficiency
|
|
607624|C537302||partial albinism and immunodeficiency syndrome
|
|
C567420||deafness unilateral with delayed endolymphatic hydrops
|
|
D020430||cubital tunnel syndrome
|
|
D020430||cubital tunnel syndromes
|
|
D020430||syndrome cubital tunnel
|
|
D020430||syndromes cubital tunnel
|
|
D020430||tunnel syndrome cubital
|
|
D020430||tunnel syndromes cubital
|
|
D020430||ulnar nerve compression cubital tunnel
|
|
D020430||ulnar nerve entrapment elbow
|
|
C538564|603554||reticuloendotheliosis familial with eosinophilia
|
|
C538564|603554||severe combined immunodeficiency with hypereosinophilia
|
|
604250|C537248||hemochromatosis type 3
|
|
604250|C537248||hemochromatosis due to defect in transferrin receptor 2
|
|
604250|C537248||hfe3
|
|
D020437||hypoglossal nerve diseases
|
|
D020437||cranial nerve xii diseases
|
|
D020437||cranial nerve xii disorders
|
|
D020437||hypoglossal nerve disease
|
|
D020437||hypoglossal nerve palsies
|
|
D020437||hypoglossal nerve palsy
|
|
D020437||hypoglossal neuralgia
|
|
D020437||hypoglossal neuralgias
|
|
D020437||hypoglossal neuropathies
|
|
D020437||hypoglossal neuropathy
|
|
D020437||neuralgia hypoglossal
|
|
D020437||neuralgias hypoglossal
|
|
D020437||neuropathies hypoglossal
|
|
D020437||neuropathy hypoglossal
|
|
D020437||palsies hypoglossal nerve
|
|
D020437||palsy hypoglossal nerve
|
|
D020437||twelfth cranial nerve diseases
|
|
D020437||twelfth cranial nerve disorder
|
|
D020436||accessory nerve diseases
|
|
D020436||accessory nerve disease
|
|
D020436||cranial nerve eleven diseases
|
|
D020436||cranial nerve eleven disorders
|
|
D020436||cranial nerve xi diseases
|
|
D020436||eleventh cranial nerve disease
|
|
D020436||spinal accessory nerve diseases
|
|
D020435||glossopharyngeal nerve diseases
|
|
D020435||cranial nerve ix diseases
|
|
D020435||cranial nerve ix disorders
|
|
D020435||glossopharyngeal motor neuropathies
|
|
D020435||glossopharyngeal motor neuropathy
|
|
D020435||glossopharyngeal nerve disease
|
|
D020435||glossopharyngeal nerve sensory neuropathy
|
|
D020435||glossopharyngeal nerve taste disorder
|
|
D020435||glossopharyngeal neuralgia
|
|
D020435||glossopharyngeal neuralgias
|
|
D020435||motor neuropathies glossopharyngeal
|
|
D020435||motor neuropathy glossopharyngeal
|
|
D020435||neuralgia glossopharyngeal
|
|
D020435||neuralgias glossopharyngeal
|
|
D020435||ninth cranial nerve diseases
|
|
D020435||sensory neuropathy glossopharyngeal nerve
|
|
D020435||taste disorder glossopharyngeal nerve
|
|
D020434||abducens nerve diseases
|
|
D020434||6th nerve palsies
|
|
D020434||6th nerve palsy
|
|
D020434||abducens nerve disease
|
|
D020434||abducens nerve palsies
|
|
D020434||abducens nerve palsy
|
|
D020434||abducens palsy childhood benign recurrent
|
|
D020434||benign recurrent abducens palsy children
|
|
D020434||benign recurrent abducens palsy of childhood
|
|
D020434||cranial nerve vi diseases
|
|
D020434||cranial nerve vi palsy
|
|
D020434||lateral rectus palsies
|
|
D020434||lateral rectus palsy
|
|
D020434||nerve palsies 6th
|
|
D020434||nerve palsies vi
|
|
D020434||nerve palsy 6th
|
|
D020434||nerve palsy vi
|
|
D020434||palsies 6th nerve
|
|
D020434||palsies abducens nerve
|
|
D020434||palsies lateral rectus
|
|
D020434||palsies sixth nerve
|
|
D020434||palsies vi nerve
|
|
D020434||palsy 6th nerve
|
|
D020434||palsy abducens nerve
|
|
D020434||palsy lateral rectus
|
|
D020434||palsy sixth nerve
|
|
D020434||palsy vi nerve
|
|
D020434||sixth cranial nerve diseases
|
|
D020434||sixth cranial nerve disorders
|
|
D020434||sixth cranial nerve palsy
|
|
D020434||sixth nerve palsies
|
|
D020434||sixth nerve palsy
|
|
D020434||vi nerve palsy
|
|
D020434||vith cranial nerve diseases
|
|
D020433||trigeminal nerve diseases
|
|
D020433||cranial nerve v diseases
|
|
D020433||fifth cranial nerve diseases
|
|
D020433||idiopathic trigeminal neuropathies
|
|
D020433||idiopathic trigeminal neuropathy
|
|
D020433||neuropathies idiopathic trigeminal
|
|
D020433||neuropathies trigeminal
|
|
D020433||neuropathy idiopathic trigeminal
|
|
D020433||neuropathy trigeminal
|
|
D020433||raeder paratrigeminal syndrome
|
|
D020433||syndrome raeder paratrigeminal
|
|
D020433||trigeminal nerve disease
|
|
D020433||trigeminal nerve disorder
|
|
D020433||trigeminal nerve disorders
|
|
D020433||trigeminal neuropathies
|
|
D020433||trigeminal neuropathies idiopathic
|
|
D020433||trigeminal neuropathy
|
|
D020433||trigeminal neuropathy idiopathic
|
|
D020432||trochlear nerve diseases
|
|
D020432||cranial nerve iv diseases
|
|
D020432||fourth cranial nerve diseases
|
|
D020432||fourth cranial nerve palsy
|
|
D020432||fourth nerve palsies
|
|
D020432||fourth nerve palsy
|
|
D020432||myokymias superior oblique
|
|
D020432||myokymia superior oblique
|
|
D020432||neurogenic superior oblique palsy
|
|
D020432||neuropathies trochlear
|
|
D020432||neuropathy trochlear
|
|
D020432||palsies fourth nerve
|
|
D020432||palsies trochlear nerve
|
|
D020432||palsy fourth nerve
|
|
D020432||palsy trochlear nerve
|
|
D020432||superior oblique myokymia
|
|
D020432||superior oblique myokymias
|
|
D020432||superior oblique palsy neurogenic
|
|
D020432||trochlear nerve disease
|
|
D020432||trochlear nerve disorder
|
|
D020432||trochlear nerve disorders
|
|
D020432||trochlear nerve palsies
|
|
D020432||trochlear nerve palsy
|
|
D020432||trochlear neuropathies
|
|
D020432||trochlear neuropathy
|
|
D020431||olfactory nerve diseases
|
|
D020431||cranial nerve i diseases
|
|
D020431||cranial nerve i disorders
|
|
D020431||first cranial nerve diseases
|
|
D020431||olfactory nerve disease
|
|
D006130||growth disorders
|
|
D006130||disorder growth
|
|
D006130||growth disorder
|
|
C536049|610915||osteogenesis imperfecta type viii
|
|
C536049|610915||oi8
|
|
C536049|610915||oi type viii
|
|
607836||autoimmune disease susceptibility to 1
|
|
607836||ais1
|
|
607836||autoimmune disease susceptibility locus chromosome 1p related
|
|
607836||vamas2
|
|
607836||vitiligo associated multiple autoimmune disease susceptibility 2
|
|
C567378|612261||inflammatory bowel disease 17
|
|
C567378|612261||ibd17
|
|
D020427||peroneal neuropathies
|
|
D020427||common peroneal neuropathies
|
|
D020427||common peroneal neuropathy
|
|
D020427||deep peroneal neuropathies
|
|
D020427||deep peroneal neuropathy
|
|
D020427||external popliteal neuropathies
|
|
D020427||external popliteal neuropathy
|
|
D020427||fibular nerve disease
|
|
D020427||fibular nerve diseases
|
|
D020427||fibular neuropathies
|
|
D020427||fibular neuropathy
|
|
D020427||lateral popliteal neuropathies
|
|
D020427||lateral popliteal neuropathy
|
|
D020427||nerve disease fibular
|
|
D020427||nerve disease peroneal
|
|
D020427||nerve diseases fibular
|
|
D020427||nerve diseases peroneal
|
|
D020427||nerve paralyses peroneal
|
|
D020427||nerve paralysis peroneal
|
|
D020427||neuropathies common peroneal
|
|
D020427||neuropathies deep peroneal
|
|
D020427||neuropathies external popliteal
|
|
D020427||neuropathies fibular
|
|
D020427||neuropathies lateral popliteal
|
|
D020427||neuropathies peroneal
|
|
D020427||neuropathies superficial peroneal
|
|
D020427||neuropathy common peroneal
|
|
D020427||neuropathy deep peroneal
|
|
D020427||neuropathy external popliteal
|
|
D020427||neuropathy fibular
|
|
D020427||neuropathy lateral popliteal
|
|
D020427||neuropathy peroneal
|
|
D020427||neuropathy superficial peroneal
|
|
D020427||paralyses peroneal nerve
|
|
D020427||paralysis peroneal nerve
|
|
D020427||peroneal nerve disease
|
|
D020427||peroneal nerve diseases
|
|
D020427||peroneal nerve paralyses
|
|
D020427||peroneal nerve paralysis
|
|
D020427||peroneal neuropathies common
|
|
D020427||peroneal neuropathies deep
|
|
D020427||peroneal neuropathies superficial
|
|
D020427||peroneal neuropathy
|
|
D020427||peroneal neuropathy common
|
|
D020427||peroneal neuropathy deep
|
|
D020427||peroneal neuropathy superficial
|
|
D020427||popliteal neuropathies external
|
|
D020427||popliteal neuropathies lateral
|
|
D020427||popliteal neuropathy external
|
|
D020427||popliteal neuropathy lateral
|
|
D020427||superficial peroneal neuropathies
|
|
D020427||superficial peroneal neuropathy
|
|
D020426||sciatic neuropathy
|
|
D020426||lesion of sciatic nerve
|
|
D020426||nerve disease sciatic
|
|
D020426||nerve diseases sciatic
|
|
D020426||nerve lesion sciatic
|
|
D020426||nerve lesions sciatic
|
|
D020426||nerve palsies sciatic
|
|
D020426||nerve palsy sciatic
|
|
D020426||neuralgia neuritides sciatic nerve
|
|
D020426||neuralgia neuritis sciatic nerve
|
|
D020426||neuritides sciatic
|
|
D020426||neuritis sciatic
|
|
D020426||neuropathies sciatic
|
|
D020426||neuropathy sciatic
|
|
D020426||palsies sciatic nerve
|
|
D020426||palsy sciatic nerve
|
|
D020426||sciatic nerve disease
|
|
D020426||sciatic nerve diseases
|
|
D020426||sciatic nerve lesion
|
|
D020426||sciatic nerve lesions
|
|
D020426||sciatic nerve neuralgia neuritides
|
|
D020426||sciatic nerve neuralgia neuritis
|
|
D020426||sciatic nerve palsies
|
|
D020426||sciatic nerve palsy
|
|
D020426||sciatic neuritides
|
|
D020426||sciatic neuritis
|
|
D020426||sciatic neuropathies
|
|
D020425||radial neuropathy
|
|
D020425||crutch palsies
|
|
D020425||crutch palsy
|
|
D020425||lesion radial nerve
|
|
D020425||lesions radial nerve
|
|
D020425||lesion superficial radial nerve
|
|
D020425||nerve disease radial
|
|
D020425||nerve diseases radial
|
|
D020425||nerve lesion radial
|
|
D020425||nerve lesions radial
|
|
D020425||neuropathies radial
|
|
D020425||neuropathy radial
|
|
D020425||palsies crutch
|
|
D020425||palsy crutch
|
|
D020425||radial nerve disease
|
|
D020425||radial nerve diseases
|
|
D020425||radial nerve lesion
|
|
D020425||radial nerve lesions
|
|
D020425||radial neuropathies
|
|
D020425||saturday night palsies
|
|
D020425||saturday night palsy
|
|
D020425||superficial radial nerve lesion
|
|
D020424||ulnar neuropathies
|
|
D020424||nerve diseases ulnar
|
|
D020424||nerve disease ulnar
|
|
D020424||nerve palsies ulnar
|
|
D020424||nerve palsy ulnar
|
|
D020424||neuritides ulnar
|
|
D020424||neuritis ulnar
|
|
D020424||neuropathies ulnar
|
|
D020424||neuropathy ulnar
|
|
D020424||palsies ulnar nerve
|
|
D020424||palsy ulnar nerve
|
|
D020424||ulnar nerve disease
|
|
D020424||ulnar nerve diseases
|
|
D020424||ulnar nerve palsies
|
|
D020424||ulnar nerve palsy
|
|
D020424||ulnar neuritides
|
|
D020424||ulnar neuritis
|
|
D020424||ulnar neuropathy
|
|
D020423||median neuropathy
|
|
D020423||distal medial neuropathies
|
|
D020423||distal medial neuropathy
|
|
D020423||medial neuropathies distal
|
|
D020423||medial neuropathy distal
|
|
D020423||median nerve disease
|
|
D020423||median nerve diseases
|
|
D020423||median nerve neuralgia
|
|
D020423||median nerve neuralgias
|
|
D020423||median neuropathies
|
|
D020423||median neuropathies proximal
|
|
D020423||median neuropathy proximal
|
|
D020423||nerve disease median
|
|
D020423||nerve diseases median
|
|
D020423||neuralgia median nerve
|
|
D020423||neuralgias median nerve
|
|
D020423||neuropathies distal medial
|
|
D020423||neuropathies median
|
|
D020423||neuropathies proximal median
|
|
D020423||neuropathy distal medial
|
|
D020423||neuropathy median
|
|
D020423||neuropathy proximal median
|
|
D020423||proximal median neuropathies
|
|
D020423||proximal median neuropathy
|
|
D020422||mononeuropathies
|
|
D020422||mononeuritides
|
|
D020422||mononeuritis
|
|
D020422||mononeuritis multiplex
|
|
D020422||mononeuropathy
|
|
D020422||mononeuropathy multiplex
|
|
D020422||mononeuropathy multiplex syndrome
|
|
D020422||mononeuropathy multiplex syndromes
|
|
D020422||syndrome mononeuropathy multiplex
|
|
D020422||syndromes mononeuropathy multiplex
|
|
C563739|609313||erythrokeratodermia variabilis 3
|
|
C563739|609313||ekv3
|
|
C563739|609313||erythrokeratodermia variabilis kamouraska type
|
|
C563739|609313||mednik
|
|
C563739|609313||mental retardation enteropathy deafness peripheral neuropathy ichthyosis and keratoderma
|
|
D020421||vagus nerve diseases
|
|
D020421||cranial nerve x diseases
|
|
D020421||disorder pneumogastric nerve
|
|
D020421||disorders pneumogastric nerve
|
|
D020421||motor disorder vagus nerve
|
|
D020421||neuropathies vagus
|
|
D020421||neuropathy vagus
|
|
D020421||pneumogastric nerve disorder
|
|
D020421||pneumogastric nerve disorders
|
|
D020421||sensory disorder vagus nerve
|
|
D020421||tenth cranial nerve diseases
|
|
D020421||vagus nerve disease
|
|
D020421||vagus nerve disorder
|
|
D020421||vagus nerve disorders
|
|
D020421||vagus nerve motor disorder
|
|
D020421||vagus nerve sensory disorder
|
|
D020421||vagus neuropathies
|
|
D020421||vagus neuropathy
|
|
D008796||metrorrhagia
|
|
D008796||bleeding between periods
|
|
D008796||bleeding breakthrough
|
|
D008796||breakthrough bleeding
|
|
D008796||dysfunctional uterine bleeding
|
|
D008796||dysfunctional uterine bleedings
|
|
D008796||intermenstrual bleeding
|
|
D008796||spotting
|
|
D008796||uterine bleeding dysfunctional
|
|
604271|C565805||short stature idiopathic autosomal
|
|
604271|C565805||growth hormone deficiency isolated partial
|
|
604271|C565805||growth hormone insensitivity to partial
|
|
604271|C565805||partial ighd growth hormone insensitivity to partial included
|
|
D020429||tibial neuropathy
|
|
D020429||internal popliteal neuropathies
|
|
D020429||internal popliteal neuropathy
|
|
D020429||lateral plantar neuropathies
|
|
D020429||lateral plantar neuropathy
|
|
D020429||medial plantar nerve disease
|
|
D020429||medial plantar neuropathies
|
|
D020429||medial plantar neuropathy
|
|
D020429||medial popliteal neuropathies
|
|
D020429||medial popliteal neuropathy
|
|
D020429||nerve diseases tibial
|
|
D020429||nerve disease tibial
|
|
D020429||neuropathies internal popliteal
|
|
D020429||neuropathies lateral plantar
|
|
D020429||neuropathies medial plantar
|
|
D020429||neuropathies medial popliteal
|
|
D020429||neuropathies posterior tibial
|
|
D020429||neuropathies tibial
|
|
D020429||neuropathy internal popliteal
|
|
D020429||neuropathy lateral plantar
|
|
D020429||neuropathy medial plantar
|
|
D020429||neuropathy medial popliteal
|
|
D020429||neuropathy posterior tibial
|
|
D020429||neuropathy post traumatic tibial
|
|
D020429||neuropathy tibial
|
|
D020429||plantar neuropathy lateral
|
|
D020429||plantar neuropathy medial
|
|
D020429||popliteal neuropathies internal
|
|
D020429||popliteal neuropathies medial
|
|
D020429||popliteal neuropathy internal
|
|
D020429||popliteal neuropathy medial
|
|
D020429||posterior tibial nerve diseases
|
|
D020429||posterior tibial neuropathies
|
|
D020429||posterior tibial neuropathy
|
|
D020429||post traumatic tibial neuropathies
|
|
D020429||post traumatic tibial neuropathy
|
|
D020429||tibial nerve disease
|
|
D020429||tibial nerve diseases
|
|
D020429||tibial neuropathies
|
|
D020429||tibial neuropathies posterior
|
|
D020429||tibial neuropathies post traumatic
|
|
D020429||tibial neuropathy posterior
|
|
D020429||tibial neuropathy post traumatic
|
|
D020428||femoral neuropathy
|
|
D020428||femoral mononeuropathies
|
|
D020428||femoral mononeuropathy
|
|
D020428||femoral nerve disease
|
|
D020428||femoral nerve diseases
|
|
D020428||femoral neuritis
|
|
D020428||femoral neuropathies
|
|
D020428||mononeuropathies femoral
|
|
D020428||mononeuropathy femoral
|
|
D020428||nerve disease femoral
|
|
D020428||nerve diseases femoral
|
|
D020428||neuropathies femoral
|
|
D020428||neuropathy femoral
|
|
D019449||pouchitis
|
|
D019449||ileitis pouch
|
|
D019449||pouch ileitis
|
|
C566443|610102||complement component 7 deficiency
|
|
C566443|610102||c7d
|
|
C566443|610102||c7 deficiency
|
|
D010235|168000||paraganglioma
|
|
D010235|168000||cbt1
|
|
D010235|168000||gangliocytic paraganglioma
|
|
D010235|168000||gangliocytic paragangliomas
|
|
D010235|168000||paraganglioma gangliocytic
|
|
D010235|168000||paragangliomas
|
|
D010235|168000||paragangliomas 1
|
|
D010235|168000||paragangliomas familial 1
|
|
D010235|168000||paragangliomas familial nonchromaffin 1 paragangliomas with sensorineural hearing loss included
|
|
D010235|168000||paragangliomas gangliocytic
|
|
D010235|168000||paragangliomata
|
|
D010235|168000||pgl
|
|
D010235|168000||pgl1
|
|
C567714|613192||mental retardation autosomal recessive 13
|
|
C567714|613192||mrt13
|
|
D057768||infantile apparent life threatening event
|
|
D057768||idiopathic apparent life threatening event
|
|
D019446||endotoxemia
|
|
D019446||endotoxemias
|
|
D057767||kashin beck disease
|
|
D057767||disease kashin beck
|
|
C536677|193230||snowflake vitreoretinal degeneration
|
|
C536677|193230||snowflake degeneration in hereditary vitreoretinal degeneration
|
|
C536677|193230||svd
|
|
C536677|193230||vitreoretinal degeneration snowflake type
|
|
D006105||granulomatous disease chronic
|
|
D006105||autosomal recessive chronic granulomatous disease
|
|
D006105||chronic granulomatous disease
|
|
D006105||chronic granulomatous diseases
|
|
D006105||disease chronic granulomatous
|
|
D006105||diseases chronic granulomatous
|
|
D006105||granulomatous diseases chronic
|
|
D006105||x linked chronic granulomatous disease
|
|
D006106||granulosa cell tumor
|
|
D006106||cancer granulosa cell
|
|
D006106||cancer of granulosa cells
|
|
D006106||cancers granulosa cell
|
|
D006106||cell cancer granulosa
|
|
D006106||cell cancers granulosa
|
|
D006106||cells cancer granulosa
|
|
D006106||cells cancers granulosa
|
|
D006106||granulosa cell cancer
|
|
D006106||granulosa cell cancers
|
|
D006106||granulosa cells cancer
|
|
D006106||granulosa cells cancers
|
|
D006106||granulosa cell tumors
|
|
D006106||tumor granulosa cell
|
|
D006106||tumors granulosa cell
|
|
D006103||granuloma lethal midline
|
|
D006103||granuloma gangraenescens
|
|
D006103||granulomas lethal midline
|
|
D006103||lethal midline granuloma
|
|
D006103||lethal midline granulomas
|
|
D006103||midline granuloma lethal
|
|
D006103||midline granulomas lethal
|
|
D006103||polymorphic reticuloses
|
|
D006103||polymorphic reticulosis
|
|
D006103||reticuloses polymorphic
|
|
D006103||reticulosis polymorphic
|
|
D006104||granuloma plasma cell
|
|
D006104||granulomas plasma cell
|
|
D006104||inflammatory pseudotumor
|
|
D006104||inflammatory pseudotumors
|
|
D006104||plasma cell granuloma
|
|
D006104||plasma cell granulomas
|
|
D006104||pseudotumor inflammatory
|
|
D006104||pseudotumors inflammatory
|
|
D006101||granuloma giant cell
|
|
D006101||epulides giant cell
|
|
D006101||epulis giant cell
|
|
D006101||giant cell epulides
|
|
D006101||giant cell epulis
|
|
D006101||giant cell granuloma
|
|
D006101||giant cell granulomas
|
|
D006101||granuloma giant cell reparative
|
|
D006101||granulomas giant cell
|
|
D006101||peripheral giant cell granuloma
|
|
C536880|604320||spinal muscular atrophy with respiratory distress 1
|
|
C536880|604320||autosomal recessive distal spinal muscular atrophy 1
|
|
C536880|604320||dhmn6
|
|
C536880|604320||diaphragmatic spinal muscular atrophy
|
|
C536880|604320||distal hereditary motor neuronopathy type vi
|
|
C536880|604320||distal spinal muscular atrophy type 1
|
|
C536880|604320||dsma1
|
|
C536880|604320||hmn6
|
|
C536880|604320||hmnvi
|
|
C536880|604320||hmn vi
|
|
C536880|604320||neuronopathy distal hereditary motor type vi
|
|
C536880|604320||neuronopathy severe infantile axonal with respiratory failure
|
|
C536880|604320||severe infantile axonal neuropathy with respiratory failure
|
|
C536880|604320||sianrf
|
|
C536880|604320||smard1
|
|
C536880|604320||spinal muscular atrophy diaphragmatic
|
|
C536880|604320||spinal muscular atrophy distal autosomal recessive 1
|
|
C536880|604320||spinal muscular atrophy with respiratory distress
|
|
C536880|604320||spinal muscular atrophy with respiratory distress type 1
|
|
D006102||granuloma laryngeal
|
|
D006102||granuloma of larynx
|
|
D006102||granulomas laryngeal
|
|
D006102||laryngeal granuloma
|
|
D006102||laryngeal granulomas
|
|
D006102||larynx granuloma
|
|
D006102||larynx granulomas
|
|
D055111||failed back surgery syndrome
|
|
D057772||vascular system injuries
|
|
D057772||injuries vascular
|
|
D057772||injuries vascular system
|
|
D057772||injury vascular
|
|
D057772||injury vascular system
|
|
D057772||system injuries vascular
|
|
D057772||system injury vascular
|
|
D057772||vascular injuries
|
|
D057772||vascular injury
|
|
D057772||vascular system injury
|
|
D055112||pyometra
|
|
D055112||pyometras
|
|
D055113||chronic periodontitis
|
|
D055113||adult periodontitides
|
|
D055113||adult periodontitis
|
|
D055113||chronic periodontitides
|
|
D055113||periodontitides adult
|
|
D055113||periodontitides chronic
|
|
D055113||periodontitis adult
|
|
D055113||periodontitis chronic
|
|
D057774||post exercise hypotension
|
|
D057774||hypotension postexercise
|
|
D057774||hypotension post exercise
|
|
D057774||hypotensions postexercise
|
|
D057774||hypotensions post exercise
|
|
D057774||postexercise hypotension
|
|
D057774||postexercise hypotensions
|
|
D057774||post exercise hypotensions
|
|
C537991|605589||charcot marie tooth disease type 2b2
|
|
C537991|605589||arcmt2b
|
|
C537991|605589||charcot marie tooth disease axonal autosomal recessive b2
|
|
C537991|605589||charcot marie tooth disease axonal autosomal recessive type 2b2
|
|
C537991|605589||charcot marie tooth disease axonal autosomal recessive type b2
|
|
C537991|605589||charcot marie tooth disease axonal type 2b2
|
|
C537991|605589||charcot marie tooth disease neuronal type 2b2
|
|
C537991|605589||charcot marie tooth neuropathy type 2b2
|
|
C537991|605589||cmt2b2
|
|
C537991|605589||cmt 2b2
|
|
D020417||nystagmus congenital
|
|
D020417||congenital nystagmus
|
|
C536631|609241||schindler disease type i
|
|
C536631|609241||alpha galactosidase b deficiency
|
|
C536631|609241||alpha galnac deficiency schindler type
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency adult onset
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency type 1
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency type 2
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency type i
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency type ii
|
|
C536631|609241||alpha n acetylgalactosaminidase deficiency type iii
|
|
C536631|609241||alpha naga deficiency
|
|
C536631|609241||angiokeratoma corporis diffusum glycopeptiduria
|
|
C536631|609241||galb deficiency
|
|
C536631|609241||kanzaki disease
|
|
C536631|609241||lysosomal glycoaminoacid storage disease angiokeratoma corporis diffusum
|
|
C536631|609241||naga deficiency
|
|
C536631|609241||naga deficiency type 2
|
|
C536631|609241||naga deficiency type i
|
|
C536631|609241||naga deficiency type i alpha n acetylgalactosaminidase deficiency type iii included
|
|
C536631|609241||naga deficiency type ii
|
|
C536631|609241||naga deficiency type iii
|
|
C536631|609241||naga deficiency type iii included
|
|
C536631|609241||neuroaxonal dystrophy schindler type
|
|
C536631|609241||neuronal axonal dystrophy schindler type
|
|
C536631|609241||schindler disease
|
|
C536631|609241||schindler disease type 1
|
|
C536631|609241||schindler disease type 2
|
|
C536631|609241||schindler disease type ii
|
|
C536631|609241||schindler disease type iii
|
|
C536631|609241||schindler disease type iii included
|
|
607765|C535442||bile acid synthesis defect congenital 1
|
|
607765|C535442||3 beta hydroxy delta 5 c27 steroid oxidoreductase deficiency
|
|
607765|C535442||3 beta hydroxy delta 5 c27 steroid oxidoreductase deficiency of
|
|
607765|C535442||cbas1
|
|
607765|C535442||cholestasis progressive familial intrahepatic 4
|
|
607765|C535442||congenital bile acid synthesis defect type 1 cbas1
|
|
607765|C535442||progressive familial intrahepatic cholestasis 4
|
|
184840|C537494||stickler syndrome type 3
|
|
184840|C537494||stickler syndrome nonocular type
|
|
184840|C537494||stickler syndrome type iii
|
|
184840|C537494||stl3
|
|
C564701|606528||homozygous 11p15 p14 deletion syndrome
|
|
C564701|606528||hyperinsulinism infantile with enteropathy and deafness
|
|
118800|C537181||paroxysmal nonkinesigenic dyskinesia
|
|
118800|C537181||choreoathetosis familial paroxysmal
|
|
118800|C537181||choreoathetosis nonkinesigenic
|
|
118800|C537181||dystonia 8
|
|
118800|C537181||dyt8
|
|
118800|C537181||familial paroxysmal choreoathetosis
|
|
118800|C537181||familial paroxysmal nonkinesigenic dyskinesia
|
|
118800|C537181||fpd1
|
|
118800|C537181||mount reback syndrome
|
|
118800|C537181||nonkinesigenic choreoathetosis
|
|
118800|C537181||paroxysmal dystonic choreoathetosis
|
|
118800|C537181||paroxysmal nonkinesigenic dyskinesia 1
|
|
118800|C537181||pdc
|
|
118800|C537181||pnkd1
|
|
D007446||chromosome inversion
|
|
D007446||chromosomal inversion
|
|
D007446||chromosomal inversions
|
|
D007446||chromosome inversions
|
|
D007446||inversion chromosomal
|
|
D007446||inversion chromosome
|
|
D007446||inversions chromosomal
|
|
D007446||inversions chromosome
|
|
D007443||intussusception
|
|
D007443||intestinal invagination
|
|
D007443||intestinal invaginations
|
|
D007443||intussusceptions
|
|
D007443||intususception
|
|
D007443||intususceptions
|
|
D007443||invagination intestinal
|
|
D007443||invaginations intestinal
|
|
C564643|606943||usher syndrome type ig
|
|
C564643|606943||ush1g
|
|
C565217|610227||seborrhea like dermatitis with psoriasiform elements
|
|
166260||gdd
|
|
C564570|300194||alport syndrome mental retardation midface hypoplasia and elliptocytosis
|
|
C564570|300194||amme complex
|
|
C564570|300194||ats mr
|
|
C564570|300194||chromosome xq22 3 telomeric deletion syndrome
|
|
611064||asthma related traits susceptibility to 5
|
|
611064||asrt5
|
|
612390||pch2c
|
|
C563671|610381||cone rod dystrophy 11
|
|
C563671|610381||cord11
|
|
C567679|613266||waardenburg syndrome type 4c
|
|
C567679|613266||waardenburg syndrome type ivc
|
|
C567679|613266||waardenburg syndrome with hirschsprung disease type 4c
|
|
C567679|613266||waardenburg syndrome with hirschsprung disease type 4c waardenburg syndrome type ivc
|
|
C567679|613266||ws4c
|
|
C564599|607259||spastic paraplegia 7 autosomal recessive
|
|
C564599|607259||spg7
|
|
D007418||intestinal pseudo obstruction
|
|
D007418||chronic idiopathic intestinal pseudo obstruction
|
|
D007418||congenital short bowel syndrome
|
|
D007418||enteric neuropathy
|
|
D007418||idiopathic intestinal pseudo obstruction
|
|
D007418||idiopathic intestinal pseudo obstructions
|
|
D007418||ileus paralytic
|
|
D007418||intestinal pseudoobstruction
|
|
D007418||intestinal pseudo obstruction idiopathic
|
|
D007418||intestinal pseudoobstructions
|
|
D007418||intestinal pseudo obstructions
|
|
D007418||intestinal pseudo obstructions idiopathic
|
|
D007418||myopathies visceral
|
|
D007418||myopathy visceral
|
|
D007418||paralytic ileus
|
|
D007418||pseudointestinal obstruction syndrome
|
|
D007418||pseudo obstruction idiopathic intestinal
|
|
D007418||pseudoobstruction intestinal
|
|
D007418||pseudo obstruction intestinal
|
|
D007418||pseudo obstructions idiopathic intestinal
|
|
D007418||pseudoobstructions intestinal
|
|
D007418||pseudo obstructions intestinal
|
|
D007418||pseudoobstructive syndrome
|
|
D007418||visceral myopathies
|
|
D044483||intestinal polyposis
|
|
D044483||cronkhite canada syndrome
|
|
D044483||polyposis intestinal
|
|
D044483||polyposis skin pigmentation alopecia and fingernail changes
|
|
277610|C535776||pierre robin syndrome with fetal chondrodysplasia
|
|
277610|C535776||heterozygous osmed
|
|
277610|C535776||heterozygous otospondylomegaepiphyseal dysplasia
|
|
277610|C535776||weissenbacher zweymuller syndrome
|
|
277610|C535776||weissenbacher zweym 252 ller syndrome
|
|
277610|C535776||wzs
|
|
D004421|612067||dystonia
|
|
D004421|612067||diurnal dystonia
|
|
D004421|612067|C567430||dystonia 16
|
|
D004421|612067||dystonia diurnal
|
|
D004421|612067||dystonia limb
|
|
D004421|612067||dystonia muscle
|
|
D004421|612067||dystonia paroxysmal
|
|
D004421|612067|C567430||dyt16
|
|
D004421|612067||limb dystonia
|
|
D004421|612067||muscle dystonia
|
|
D004421|612067||paroxysmal dystonia
|
|
D007416||intestinal perforation
|
|
D007416||intestinal perforations
|
|
D007416||perforation intestinal
|
|
D007416||perforations intestinal
|
|
D007417||intestinal polyps
|
|
D007417||intestinal polyp
|
|
D007417||polyp intestinal
|
|
D007417||polyps intestinal
|
|
D007414||intestinal neoplasms
|
|
D007414||cancer intestinal
|
|
D007414||cancer intestines
|
|
D007414||cancer of intestines
|
|
D007414||cancer of the intestines
|
|
D007414||cancers intestinal
|
|
D007414||cancers intestines
|
|
D007414||intestinal cancer
|
|
D007414||intestinal cancers
|
|
D007414||intestinal neoplasm
|
|
D007414||intestines cancer
|
|
D007414||intestines cancers
|
|
D007414||intestines neoplasm
|
|
D007414||intestines neoplasms
|
|
D007414||neoplasm intestinal
|
|
D007414||neoplasm intestines
|
|
D007414||neoplasms intestinal
|
|
D007414||neoplasms intestines
|
|
D007415||intestinal obstruction
|
|
D007415||intestinal obstructions
|
|
D007415||obstruction intestinal
|
|
D007412||intestinal fistula
|
|
D007412||cholecystoduodenal fistula
|
|
D007412||colovesical fistula
|
|
D007412||enterocutaneous fistula
|
|
D007412||fistula cholecystoduodenal
|
|
D007412||fistula colovesical
|
|
D007412||fistula enterocutaneous
|
|
D007412||fistula intestinal
|
|
C536480|236730||urofacial syndrome
|
|
C536480|236730||facial palsy partial with urinary abnormalities
|
|
C536480|236730||hydronephrosis inverted smile
|
|
C536480|236730||hydronephrosis with peculiar facial expression
|
|
C536480|236730||inverted smile and occult neuropathic bladder
|
|
C536480|236730||inverted smile neurogenic bladder
|
|
C536480|236730||ochoa syndrome
|
|
C536480|236730||partial facial palsy with urinary abnormalities
|
|
C536480|236730||ufs
|
|
C536480|236730||ufs1
|
|
C536480|236730||urofacial ochoa apos s syndrome
|
|
C536480|236730||urofacial syndrome 1
|
|
D007410||intestinal diseases
|
|
D007410||disease intestinal
|
|
D007410||diseases intestinal
|
|
D007410||intestinal disease
|
|
D007411||intestinal diseases parasitic
|
|
D007411||disease parasitic intestinal
|
|
D007411||diseases parasitic intestinal
|
|
D007411||intestinal disease parasitic
|
|
D007411||parasitic intestinal disease
|
|
D007411||parasitic intestinal diseases
|
|
612389||pch2b
|
|
D052536|257200||niemann pick disease type a
|
|
D052536|257200||cholesterol lipidoses neuronal
|
|
D052536|257200||cholesterol lipidosis neuronal
|
|
D052536|257200||classical niemann pick disease
|
|
D052536|257200||deficiencies sphingomyelinase
|
|
D052536|257200||deficiency sphingomyelinase
|
|
D052536|257200||lipidoses neuronal cholesterol
|
|
D052536|257200||lipidoses sphingomyelin
|
|
D052536|257200||lipidoses sphingomyelin cholesterol
|
|
D052536|257200||lipidosis neuronal cholesterol
|
|
D052536|257200||lipidosis sphingomyelin
|
|
D052536|257200||lipidosis sphingomyelin cholesterol
|
|
D052536|257200||neuronal cholesterol lipidoses
|
|
D052536|257200||neuronal cholesterol lipidosis
|
|
D052536|257200||niemann pick disease acute neuronopathic form
|
|
D052536|257200||niemann pick disease acute neurovisceral form
|
|
D052536|257200||niemann pick disease classical
|
|
D052536|257200||niemann pick disease neuronopathic type
|
|
D052536|257200||niemann pick apos s disease type a
|
|
D052536|257200||ophthalmoplegias supraoptic vertical
|
|
D052536|257200||ophthalmoplegia supraoptic vertical
|
|
D052536|257200||sphingomyelinase deficiencies
|
|
D052536|257200||sphingomyelinase deficiency
|
|
D052536|257200||sphingomyelinase deficiency disease
|
|
D052536|257200||sphingomyelinase deficiency diseases
|
|
D052536|257200||sphingomyelinase deficiency niemann pick disease intermediate protracted neurovisceral included
|
|
D052536|257200||sphingomyelin cholesterol lipidoses
|
|
D052536|257200||sphingomyelin cholesterol lipidosis
|
|
D052536|257200||sphingomyelin lipidoses
|
|
D052536|257200||sphingomyelin lipidosis
|
|
D052536|257200||supraoptic vertical ophthalmoplegia
|
|
D052536|257200||supraoptic vertical ophthalmoplegias
|
|
D052536|257200||type a niemann pick disease
|
|
D052536|257200||vertical ophthalmoplegias supraoptic
|
|
D052536|257200||vertical ophthalmoplegia supraoptic
|
|
D057792||mirizzi syndrome
|
|
D057792||mirizzi apos s syndrome
|
|
D057792||mirizzis syndrome
|
|
D057792||syndrome mirizzi
|
|
D057792||syndrome mirizzi apos s
|
|
193300|D006623||von hippel lindau disease
|
|
193300|D006623||angiomatoses familial cerebelloretinal
|
|
193300|D006623||angiomatoses familial cerebello retinal
|
|
193300|D006623||angiomatosis familial cerebelloretinal
|
|
193300|D006623||angiomatosis familial cerebello retinal
|
|
193300|D006623||angiomatosis retinae
|
|
193300|D006623||cerebelloretinal angiomatoses familial
|
|
193300|D006623||cerebello retinal angiomatoses familial
|
|
193300|D006623||cerebelloretinal angiomatosis familial
|
|
193300|D006623||cerebello retinal angiomatosis familial
|
|
193300|D006623||familial cerebelloretinal angiomatoses
|
|
193300|D006623||familial cerebello retinal angiomatoses
|
|
193300|D006623||familial cerebelloretinal angiomatosis
|
|
193300|D006623||familial cerebello retinal angiomatosis
|
|
193300|D006623||hippel lindau disease
|
|
193300|D006623||lindau disease
|
|
193300|D006623||lindau apos s disease
|
|
193300|D006623||lindaus disease
|
|
193300|D006623||lindau apos s diseases
|
|
193300|D006623||retinae angiomatosis
|
|
193300|D006623||syndromes vhl
|
|
193300|D006623||syndrome vhl
|
|
193300|D006623||syndrome von hippel lindau
|
|
193300|D006623||vhl
|
|
193300|D006623||vhl syndrome
|
|
193300|D006623||vhl syndromes
|
|
193300|D006623||von hippel lindau syndrome
|
|
193300|D006623||von hippel lindau syndrome modifiers of included
|
|
C537663|301845||bazex dupre christol syndrome
|
|
C537663|301845||bazex syndrome
|
|
C537663|301845||bdcs
|
|
C537663|301845||bzx
|
|
C537663|301845||follicular atrophoderma and basal cell carcinomas
|
|
C537663|301845||follicular atrophoderma basal cell carcinoma syndrome
|
|
C537663|301845||follicular atrophoderma basocellular proliferations hypotrichosis syndrome
|
|
C567854|612943||retinitis pigmentosa 42
|
|
C567854|612943||rp42
|
|
607459|C537583||sensory ataxic neuropathy dysarthria and ophthalmoparesis
|
|
607459|C537583||scae included
|
|
607459|C537583||sensory ataxic neuropathy with mitochondrial dna deletions autosomal recessive spinocerebellar ataxia with epilepsy included
|
|
251200||microcephaly 1 primary autosomal recessive
|
|
251200||mcph1
|
|
251200||pcc syndrome
|
|
278700|D014983||xeroderma pigmentosum
|
|
278700|D014983||kaposi disease
|
|
278700|D014983||kaposi apos s disease
|
|
278700|D014983||kaposis disease
|
|
278700|D014983||xeroderma pigmentosum complementation group a
|
|
278700|D014983||xeroderma pigmentosum i
|
|
278700|D014983||xp1
|
|
278700|D014983||xpa
|
|
278700|D014983||xp group a
|
|
D006100||granuloma inguinale
|
|
D006100||donovanosis
|
|
D006100||granuloma venereum
|
|
D007431||intraoperative complications
|
|
D007431||complication intraoperative
|
|
D007431||complication peroperative
|
|
D007431||complications intraoperative
|
|
D007431||complications peroperative
|
|
D007431||injuries surgical
|
|
D007431||injury surgical
|
|
D007431||intraoperative complication
|
|
D007431||peroperative complication
|
|
D007431||peroperative complications
|
|
D007431||surgical injuries
|
|
D007431||surgical injury
|
|
612379||congenital disorder of glycosylation type iq
|
|
612379||cdg1q
|
|
612379||cdgiq
|
|
612379||cdg iq
|
|
612379||coloboma ocular with ichthyosis brain malformations and endocrine abnormalities
|
|
611046||mycobacterium tuberculosis susceptibility to 2
|
|
611046||mtbs2
|
|
611040||microphthalmia isolated 5
|
|
611040||mcop5
|
|
611040|C567024||microphthalmia posterior with retinitis pigmentosa foveoschisis and optic disc drusen
|
|
C535716|601455||neuropathy hereditary motor and sensory lom type
|
|
C535716|601455||charcot marie tooth disease demyelinating autosomal recessive type 4d
|
|
C535716|601455||charcot marie tooth disease type 4d
|
|
C535716|601455||charcot marie tooth neuropathy type 4d
|
|
C535716|601455||cmt4d
|
|
C535716|601455||hereditary motor and sensory neuropathy lom type
|
|
C535716|601455||hmsn4d
|
|
C535716|601455||hmsnl
|
|
D043171||chromosomal instability
|
|
D043171||chromosomal instabilities
|
|
D043171||chromosomal stabilities
|
|
D043171||chromosomal stability
|
|
D043171||chromosome instabilities
|
|
D043171||chromosome instability
|
|
D043171||chromosome stabilities
|
|
D043171||chromosome stability
|
|
D043171||instabilities chromosomal
|
|
D043171||instabilities chromosome
|
|
D043171||instability chromosomal
|
|
D043171||instability chromosome
|
|
D043171||stabilities chromosomal
|
|
D043171||stabilities chromosome
|
|
D043171||stability chromosomal
|
|
D043171||stability chromosome
|
|
C564640|606966||nephronophthisis 4
|
|
C564640|606966||nephronophthisis 4 juvenile
|
|
C564640|606966||nphp4
|
|
C563884|608653||deafness autosomal recessive 32
|
|
C563884|608653||dfnb32
|
|
D055154||dysphonia
|
|
D055154||dysphonia hyperkinetic
|
|
D055154||dysphonia organic tremor
|
|
D055154||dysphonia spastic
|
|
D055154||hyperkinetic dysphonia
|
|
D055154||neurologic adducter spastic dysphonia
|
|
D055154||organic tremor dysphonia
|
|
D055154||phonation disorder
|
|
D055154||phonation disorders
|
|
D055154||spastic dysphonia
|
|
D055154||spastic dysphonia neurologic adducter
|
|
D056486||drug induced liver injury
|
|
D056486||acute liver injury drug induced
|
|
D056486||disease drug induced liver
|
|
D056486||diseases drug induced liver
|
|
D056486||drug induced acute liver injury
|
|
D056486||drug induced hepatitides
|
|
D056486||drug induced hepatitis
|
|
D056486||drug induced liver disease
|
|
D056486||drug induced liver diseases
|
|
D056486||drug induced liver injuries
|
|
D056486||hepatitides drug induced
|
|
D056486||hepatitides toxic
|
|
D056486||hepatitis drug induced
|
|
D056486||hepatitis toxic
|
|
D056486||injuries drug induced liver
|
|
D056486||injury drug induced liver
|
|
D056486||liver disease drug induced
|
|
D056486||liver diseases drug induced
|
|
D056486||liver injuries drug induced
|
|
D056486||liver injury drug induced
|
|
D056486||liver injury drug induced acute
|
|
D056486||toxic hepatitides
|
|
D056486||toxic hepatitis
|
|
D056487||drug induced liver injury chronic
|
|
D056487||chronic drug induced liver injury
|
|
D056487||hepatitis chronic drug induced
|
|
D056487||hepatitis chronic drug related
|
|
D056487||liver injury drug induced chronic
|
|
C538064|305620||frontometaphyseal dysplasia
|
|
D007409||intestinal atresia
|
|
D007409||apple peel intestinal atresia
|
|
D007409||apple peel intestinal atresias
|
|
D007409||apple peel small bowel syndrome
|
|
D007409||apple peel syndrome
|
|
D007409||apple peel syndromes
|
|
D007409||atresia apple peel intestinal
|
|
D007409||atresia congenital intestinal
|
|
D007409||atresia intestinal
|
|
D007409||atresia jejunal
|
|
D007409||atresias apple peel intestinal
|
|
D007409||atresias congenital intestinal
|
|
D007409||congenital intestinal atresia
|
|
D007409||congenital intestinal atresias
|
|
D007409||familial apple peel jejunal atresia
|
|
D007409||intestinal atresia apple peel
|
|
D007409||intestinal atresia congenital
|
|
D007409||intestinal atresias apple peel
|
|
D007409||intestinal atresias congenital
|
|
D007409||jejunal atresia
|
|
D043183||irritable bowel syndrome
|
|
D043183||colitides mucous
|
|
D043183||colitis mucous
|
|
D043183||colon irritable
|
|
D043183||irritable bowel syndromes
|
|
D043183||irritable colon
|
|
D043183||mucous colitides
|
|
D043183||mucous colitis
|
|
D043183||syndrome irritable bowel
|
|
D043183||syndromes irritable bowel
|
|
D007405||intervertebral disc displacement
|
|
D007405||disc displacement intervertebral
|
|
D007405||disc displacements intervertebral
|
|
D007405||disc herniated
|
|
D007405||disc prolapsed
|
|
D007405||discs herniated
|
|
D007405||disc slipped
|
|
D007405||discs prolapsed
|
|
D007405||discs slipped
|
|
D007405||disk displacement intervertebral
|
|
D007405||disk displacements intervertebral
|
|
D007405||disk herniated
|
|
D007405||disk prolapse
|
|
D007405||disk prolapsed
|
|
D007405||disk prolapses
|
|
D007405||disks herniated
|
|
D007405||disk slipped
|
|
D007405||disks prolapsed
|
|
D007405||disks slipped
|
|
D007405||displacement intervertebral disc
|
|
D007405||displacement intervertebral disk
|
|
D007405||displacements intervertebral disc
|
|
D007405||displacements intervertebral disk
|
|
D007405||herniated disc
|
|
D007405||herniated discs
|
|
D007405||herniated disk
|
|
D007405||herniated disks
|
|
D007405||intervertebral disc displacements
|
|
D007405||intervertebral disk displacement
|
|
D007405||intervertebral disk displacements
|
|
D007405||prolapsed disc
|
|
D007405||prolapsed discs
|
|
D007405||prolapsed disk
|
|
D007405||prolapsed disks
|
|
D007405||prolapse disk
|
|
D007405||prolapses disk
|
|
D007405||slipped disc
|
|
D007405||slipped discs
|
|
D007405||slipped disk
|
|
D007405||slipped disks
|
|
C566021|613254||tuberous sclerosis 2
|
|
C566021|613254||tsc2
|
|
C566021|613254||tsc2 angiomyolipomas renal modifier of included
|
|
D007402||intertrigo
|
|
C564299|608036||diabetes mellitus noninsulin dependent type 4
|
|
C564299|608036||diabetes mellitus noninsulin dependent 4
|
|
C564299|608036||niddm4
|
|
C564299|608036||noninsulin dependent diabetes mellitus 4
|
|
C565375|252011||mitochondrial complex ii deficiency
|
|
C565375|252011||succinate coq reductase deficiency
|
|
C565698|610220||deafness autosomal recessive 59
|
|
C565698|610220||dfnb59
|
|
C536316|609796||peeling skin syndrome acral type
|
|
C536316|609796||acral peeling skin syndrome
|
|
C536316|609796||apss
|
|
C536316|609796||peeling skin syndrome type a
|
|
C537979|613108||candf4
|
|
C537979|613108||candidiasis familial 4
|
|
C537979|613108||candidiasis familial chronic mucocutaneous
|
|
C537979|613108||candidiasis familial type 4
|
|
C537979|613108||familial chronic mucocutaneous candidiasis
|
|
C562573||cyclopia
|
|
D008708||methemoglobinemia
|
|
D008708||methemoglobinemias
|
|
C562577||cirrhosis cryptogenic
|
|
C563421|600965||deafness autosomal dominant 6
|
|
C563421|600965||deafness autosomal dominant 14
|
|
C563421|600965||deafness autosomal dominant 38
|
|
C563421|600965||dfna14
|
|
C563421|600965||dfna38
|
|
C563421|600965||dfna6
|
|
C562574||visceral myopathy familial
|
|
C536294|608091||joubert syndrome 2
|
|
C536294|608091||cerebellooculorenal syndrome 2
|
|
C536294|608091||cors2
|
|
C536294|608091||jbts2
|
|
194050|D018980||williams syndrome
|
|
194050|D018980||aortic stenoses hypercalcemia supravalvar
|
|
194050|D018980||aortic stenosis hypercalcemia supravalvar
|
|
194050|D018980||beuren syndrome
|
|
194050|D018980||chromosome 7q11 23 deletion syndrome
|
|
194050|D018980||chromosome 7q11 23 deletion syndrome 1 5 to 1 8 mb
|
|
194050|D018980||contiguous gene syndrome williams
|
|
194050|D018980||hypercalcemia supravalvar aortic stenoses
|
|
194050|D018980||hypercalcemia supravalvar aortic stenosis
|
|
194050|D018980||stenoses hypercalcemia supravalvar aortic
|
|
194050|D018980||stenosis hypercalcemia supravalvar aortic
|
|
194050|D018980||supravalvar aortic stenosis syndrome
|
|
194050|D018980||syndrome beuren
|
|
194050|D018980||syndrome williams
|
|
194050|D018980||syndrome williams beuren
|
|
194050|D018980||wbs
|
|
194050|D018980||williams beuren syndrome
|
|
194050|D018980||williams contiguous gene syndrome
|
|
194050|D018980||wms
|
|
194050|D018980||ws
|
|
C567327|612380||inflammatory bowel disease 22
|
|
C567327|612380||ibd22
|
|
D040921||stress disorders traumatic
|
|
D040921||stress disorder traumatic
|
|
D040921||traumatic stress disorder
|
|
D040921||traumatic stress disorders
|
|
C566881|267450||respiratory distress syndrome in premature infants
|
|
C566881|267450||hyaline membrane disease formerly
|
|
C566881|267450||rds of prematurity
|
|
C567817|613007||biliary cirrhosis primary 2
|
|
C567817|613007||pbc2
|
|
D005764|109350||gastroesophageal reflux
|
|
D005764|109350||acid reflux gastric
|
|
D005764|109350||esophageal reflux
|
|
D005764|109350||gastric acid reflux
|
|
D005764|109350||gastric acid reflux disease
|
|
D005764|109350||gastro esophageal reflux
|
|
D005764|109350||gastroesophageal reflux disease
|
|
D005764|109350||gastroesophageal reflux pediatric
|
|
D005764|109350||gastro oesophageal reflux
|
|
D005764|109350||ger
|
|
D005764|109350||gerd
|
|
D005764|109350||reflux gastric acid
|
|
D005764|109350||reflux gastroesophageal
|
|
D005764|109350||reflux gastro esophageal
|
|
D005764|109350||reflux gastro oesophageal
|
|
C562580||cirrhosis familial with pulmonary hypertension
|
|
C562580||indian childhood cirrhosis
|
|
142690|C538118||hidradenitis suppurativa familial
|
|
142690|C538118||acne inversa familial
|
|
142690|C538118||acne inversa familial 1
|
|
142690|C538118||acne inversa familial 2
|
|
142690|C538118||acne inversa familial 3
|
|
142690|C538118||acninv1
|
|
142690|C538118||acninv2
|
|
142690|C538118||acninv3
|
|
C562581||hypercalcemia idiopathic of infancy
|
|
D055191||delayed emergence from anesthesia
|
|
D055191||awakening post anesthesia delayed
|
|
D055191||awakenings post anesthesia delayed
|
|
D055191||delayed awakening from anesthesia
|
|
D055191||delayed awakening post anesthesia
|
|
D055191||delayed awakening post procedural
|
|
D055191||delayed awakenings post anesthesia
|
|
D055191||delayed awakenings post procedural
|
|
D055191||delayed recovery from anesthesia
|
|
D055191||delayed regaining of consciousness
|
|
D055191||delayed return of consciousness
|
|
D055191||post anesthesia delayed awakening
|
|
D055191||post anesthesia delayed awakenings
|
|
D055191||post procedural delayed awakening
|
|
D055191||post procedural delayed awakenings
|
|
C562589||orotic aciduria ii
|
|
C562589||omp decarboxylase deficiency
|
|
C562589||orotidylic decarboxylase deficiency
|
|
C535581|605676||cardiomyopathy dilated with woolly hair and keratoderma
|
|
C535581|605676||carvajal syndrome
|
|
C535581|605676||dcwhk
|
|
C535581|605676||epidermolytic palmoplantar keratoderma woolly hair and dilated cardiomyopathy
|
|
C535581|605676||palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair
|
|
C565449|245340||erythrocyte lactate transporter defect
|
|
C565449|245340||lactate transporter defect myopathy due to
|
|
C536051|259600||osteolysis hereditary multicentric
|
|
C536051|259600||al aqeel sewairi syndrome
|
|
C536051|259600||hereditary multicentric osteolysis
|
|
C536051|259600||mona
|
|
C536051|259600||multicentric osteolysis nodulosis and arthropathy
|
|
C536051|259600||nao syndrome
|
|
C536051|259600||nodulosis arthropathy osteolysis syndrome
|
|
C536051|259600||torg osteolysis syndrome
|
|
C536051|259600||torg syndrome
|
|
C536051|259600||torg winchester syndrome
|
|
C536051|259600||torg winchester syndrome formerly
|
|
C565057|130700||emphysema hereditary pulmonary
|
|
606579||vitiligo associated multiple autoimmune disease susceptibility 1
|
|
606579||slev1
|
|
606579||systemic lupus erythematosus vitiligo related
|
|
606579||vamas1
|
|
606579|D014820||vitiligo
|
|
606579||vtlg
|
|
D029242|308905||optic atrophy hereditary leber
|
|
D029242|308905||disease leber apos s
|
|
D029242|308905||diseases leber apos s
|
|
D029242|308905||hereditary optic neuroretinopathies
|
|
D029242|308905||hereditary optic neuroretinopathy
|
|
D029242|308905||leber disease
|
|
D029242|308905||leber hereditary optic atrophy
|
|
D029242|308905||leber hereditary optic neuropathy
|
|
D029242|308905||leber hereditary optic neuropathy modifier of
|
|
D029242|308905||leber optic atrophy
|
|
D029242|308905||leber optic atrophy and dystonia
|
|
D029242|308905||leber optic atrophy susceptibility to
|
|
D029242|308905||leber optic neuropathy
|
|
D029242|308905||leber apos s disease
|
|
D029242|308905||lebers disease
|
|
D029242|308905||leber apos s diseases
|
|
D029242|308905||leber apos s hereditary optic atrophy
|
|
D029242|308905||leber apos s hereditary optic neuropathy
|
|
D029242|308905||leber apos s optic atrophy
|
|
D029242|308905||leber apos s optic neuropathy
|
|
D029242|308905||lebers optic neuropathy
|
|
D029242|308905||lhon
|
|
D029242|308905||lhon modifier of
|
|
D029242|308905||loas
|
|
D029242|308905||neuropathy leber apos s optic
|
|
D029242|308905||neuroretinopathies hereditary optic
|
|
D029242|308905||neuroretinopathy hereditary optic
|
|
D029242|308905||optic atrophy leber
|
|
D029242|308905||optic atrophy leber hereditary
|
|
D029242|308905||optic atrophy leber type
|
|
D029242|308905||optic neuropathy leber apos s
|
|
D029242|308905||optic neuroretinopathies hereditary
|
|
D029242|308905||optic neuroretinopathy hereditary
|
|
C536263||radial ray hypoplasia choanal atresia
|
|
C536263||radial ray hypoplasia with choanal atresia
|
|
C537594||shapiro syndrome
|
|
C537594||shapiro apos s syndrome
|
|
C536264||radiation induced angiosarcoma of the breast
|
|
C536264||post irradiation angiosarcoma of the breast
|
|
C537595||sharma kapoor ramji syndrome
|
|
C535601|300018||dosage sensitive sex reversal
|
|
C535601|300018||46 xy sex reversal 2
|
|
C535601|300018||46 xy sex reversal dax1 related
|
|
C535601|300018||srxy2
|
|
C563880||robin sequence with distinctive facial appearance and brachydactyly
|
|
C536261||radial defect robin sequence
|
|
C536261||bilateral radial defects club foot deformity micrognathia and cleft palate
|
|
C536261||bruce winship syndrome
|
|
C565079|127550||dyskeratosis congenita autosomal dominant
|
|
C565079|127550||dkca1
|
|
C565079|127550||dyskeratosis congenita autosomal dominant 1
|
|
C565079|127550||dyskeratosis congenita scoggins type
|
|
C536262||radial hypoplasia triphalangeal thumbs and hypospadias
|
|
C536262||radial hypoplasia triphalangeal thumbs hypospadias and maxillary diastema
|
|
C536262||radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema
|
|
C536262||schmitt gillenwater kelly syndrome
|
|
C537593||severe infantile axonal neuropathy
|
|
C536267||radio renal syndrome
|
|
D013282||stomatitis denture
|
|
D013282||denture stomatitides
|
|
D013282||denture stomatitis
|
|
D013282||stomatitides denture
|
|
C537598||short limb dwarfism al gazali type
|
|
C537598||lethal neonatal short limb dwarfism
|
|
C537598||lethal short limb skeletal dysplasia al gazali type
|
|
C536268||radio ulnar synostosis type 1
|
|
C536268||congenital radio ulnar synostosis
|
|
D013283||stomatitis herpetic
|
|
D013283||gingivostomatitides herpetic
|
|
D013283||gingivostomatitis herpetic
|
|
D013283||herpes simplex oral
|
|
D013283||herpetic gingivostomatitides
|
|
D013283||herpetic gingivostomatitis
|
|
D013283||herpetic stomatitides
|
|
D013283||herpetic stomatitis
|
|
D013283||oral herpes simplex
|
|
D013283||simplex oral herpes
|
|
D013283||stomatitides herpetic
|
|
C537599||short rib polydactyly syndrome beemer type
|
|
C537599||beemer langer syndrome
|
|
C537599||short rib polydactyly syndrome type 4
|
|
C537599||short rib polydactyly syndrome type iv
|
|
C537599||short rib syndrome beemer type
|
|
C537599||srps iv
|
|
C537599||srps type 4
|
|
C536265||radiation induced brachial plexopathy
|
|
C536265||radiation induced brachial neuritis
|
|
C536265||radiation injury to the brachial plexus
|
|
D013280||stomatitis
|
|
D013280||mucositides oral
|
|
D013280||mucositis oral
|
|
D013280||oral mucositides
|
|
D013280||oral mucositis
|
|
D013280||oromucositides
|
|
D013280||oromucositis
|
|
D013280||stomatitides
|
|
D013281||stomatitis aphthous
|
|
D013281||aphthae
|
|
D013281||aphthous stomatitides
|
|
D013281||aphthous stomatitis
|
|
D013281||aphthous ulcer
|
|
D013281||aphthous ulcers
|
|
D013281||canker sore
|
|
D013281||canker sores
|
|
D013281||periadenitis mucosa necrotica recurrens
|
|
D013281||sore canker
|
|
D013281||sores canker
|
|
D013281||stomatitides aphthous
|
|
D013281||ulcer aphthous
|
|
D013281||ulcers aphthous
|
|
C537597||short limb dwarf lethal colavita kozlowski type
|
|
C537597||colavita kozlowski syndrome
|
|
C562559||prognathism mandibular
|
|
C562559||habsburg jaw
|
|
C562559||hapsburg jaw
|
|
C562557||polythelia familial
|
|
C562557||accessory nipples
|
|
C562557||nipples supernumerary
|
|
C562557||polymastia
|
|
C537590||severe combined immunodeficiency atypical
|
|
C537590||scid atypical
|
|
C536260||quebec platelet disorder
|
|
C536260||factor v quebec
|
|
D020190|254770||myoclonic epilepsy juvenile
|
|
D020190|254770||adolescent myoclonic epilepsies
|
|
D020190|254770||adolescent myoclonic epilepsy
|
|
D020190|254770||eca4 included
|
|
D020190|254770||eig13
|
|
D020190|254770||eig7
|
|
D020190|254770||ejm
|
|
D020190|254770||ejm1 included
|
|
D020190|254770||ejm2 included
|
|
D020190|254770||ejm3
|
|
D020190|254770||ejm4
|
|
D020190|254770||ejm5
|
|
D020190|254770||ejm5 included
|
|
D020190|254770||epilepsies adolescent myoclonic
|
|
D020190|254770||epilepsies juvenile myoclonic
|
|
D020190|254770||epilepsy adolescent myoclonic
|
|
D020190|254770||epilepsy childhood absence susceptibility to 4 included
|
|
D020190|254770||epilepsy idiopathic generalized susceptibility to 13
|
|
D020190|254770||epilepsy idiopathic generalized susceptibility to 7
|
|
D020190|254770||epilepsy juvenile myoclonic
|
|
D020190|254770||epilepsy juvenile myoclonic susceptibility to 5 included
|
|
D020190|254770||epilepsy myoclonic juvenile
|
|
D020190|254770||impulsive petit mal epilepsy
|
|
D020190|254770||impulsive petit mal janz
|
|
D020190|254770||janz impulsive petit mal
|
|
D020190|254770||janz juvenile myoclonic epilepsy
|
|
D020190|254770||janz syndrome
|
|
D020190|254770||janz syndrome myoclonic epilepsy juvenile susceptibility to 1 included
|
|
D020190|254770||jme
|
|
D020190|254770||jme juvenile myoclonic epilepsy
|
|
D020190|254770||jmes juvenile myoclonic epilepsy
|
|
D020190|254770||juvenile myoclonic epilepsies
|
|
D020190|254770||juvenile myoclonic epilepsy
|
|
D020190|254770||juvenile myoclonic epilepsy of janz
|
|
D020190|254770||myoclonic epilepsies adolescent
|
|
D020190|254770||myoclonic epilepsies juvenile
|
|
D020190|254770||myoclonic epilepsy adolescent
|
|
D020190|254770||myoclonic epilepsy juvenile 1
|
|
D020190|254770||myoclonic epilepsy juvenile 2 included
|
|
D020190|254770||myoclonic epilepsy juvenile susceptibility to 3
|
|
D020190|254770||myoclonic epilepsy juvenile susceptibility to 4
|
|
D020190|254770||petit mal impulsive
|
|
D020190|254770||petit mal impulsive janz
|
|
D020190|254770||petit mals impulsive
|
|
D020190|254770||syndrome janz
|
|
C537928|609955||fibromatosis gingival 3
|
|
C537928|609955||fibromatosis gingival hereditary 3
|
|
C537928|609955||ggf3
|
|
C537928|609955||gingf3
|
|
C537928|609955||hgf3
|
|
D013275||stomach rupture
|
|
D013275||gastric rupture
|
|
D013275||gastric ruptures
|
|
D013275||rupture gastric
|
|
D013275||ruptures gastric
|
|
D013275||ruptures stomach
|
|
D013275||rupture stomach
|
|
D013275||stomach ruptures
|
|
D013276||stomach ulcer
|
|
D013276||gastric ulcer
|
|
D013276||gastric ulcers
|
|
D013276||stomach ulcers
|
|
D013276||ulcer gastric
|
|
D013276||ulcers gastric
|
|
D013276||ulcers stomach
|
|
D013276||ulcer stomach
|
|
D013273||diverticulum stomach
|
|
D013273||diverticula gastric
|
|
D013273||diverticula stomach
|
|
D013273||diverticulum gastric
|
|
D013273||gastric diverticula
|
|
D013273||gastric diverticulum
|
|
D013273||stomach diverticula
|
|
D013273||stomach diverticulum
|
|
C536259||qazi markouizos syndrome
|
|
C536259||dysharmonic skeletal maturation muscular fibre disproportion
|
|
C536259||puertorican infant hypotonia syndrome
|
|
C536259||puerto rican infant hypotonia syndrome
|
|
C536196|130020||ehlers danlos syndrome type 3
|
|
C536196|130020||benign hypermobility syndrome
|
|
C536196|130020||eds3
|
|
C536196|130020||eds iii
|
|
C536196|130020||ehlers danlos syndrome hypermobility type
|
|
C536196|130020||ehlers danlos syndrome type iii
|
|
D013277||stomach volvulus
|
|
D013277||gastric volvulus
|
|
D013277||volvulus gastric
|
|
D013277||volvulus stomach
|
|
C562561||pyloric atresia
|
|
C536274||ichthyosis mental retardation dwarfism and renal impairment
|
|
C562562||colonic atresia
|
|
D013290||streptococcal infections
|
|
D013290||infections streptococcal
|
|
D013290||infection streptococcal
|
|
D013290||streptococcal infection
|
|
C536272||ichthyosis tapered fingers midline groove up
|
|
C536272||oral and digital anomalies with ichthyosis
|
|
C536272||unusual facies digital abnormalities and ichthyosis
|
|
C536273||autosomal recessive ichthyosis with hypotrichosis
|
|
C562565||uterine anomalies
|
|
C563896||midface hypoplasia obesity developmental delay and neonatal hypotonia
|
|
C563693|609886||glomerulocystic kidney disease with hyperuricemia and isosthenuria
|
|
C562563||microcolon
|
|
C536276||idiopathic basal ganglia calcification childhood onset
|
|
C536276||basal ganglia calcification idiopathic childhood onset
|
|
C536276||bilateral striopallidodentate calcinosis childhood onset
|
|
C536276||cerebral calcification nonarteriosclerotic childhood onset idiopathic
|
|
C536276||cerebral calcification nonarteriosclerotic idiopathic childhood onset
|
|
C536276||ibgc childhood onset
|
|
C536276||striopallidodentate calcinosis bilateral childhood onset
|
|
C563665|610773||mitochondrial phosphate carrier deficiency
|
|
C563665|610773||mpcd
|
|
C562564||gallbladder agenesis of
|
|
C535311|258501||costeff optic atrophy syndrome
|
|
C535311|258501||3 methylglutaconic aciduria type iii
|
|
C535311|258501||costeff syndrome
|
|
C535311|258501||iraqi jewish optic atrophy plus
|
|
C535311|258501||iraqi jewish apos optic atrophy plus apos
|
|
C535311|258501||mga3
|
|
C535311|258501||mga type iii
|
|
C535311|258501||mgca3
|
|
C535311|258501||opa3 autosomal recessive
|
|
C535311|258501||optic atrophy 3 autosomal recessive
|
|
C535311|258501||optic atrophy infantile with chorea and spastic paraplegia
|
|
C535311|258501||optic atrophy plus syndrome
|
|
609033|C536343||posterior column ataxia with retinitis pigmentosa
|
|
609033|C536343||axpc1
|
|
609033|C536343||pcarp
|
|
C562568||cerebellar hypoplasia
|
|
C536270||radioulnar synostosis retinal pigment abnormalities
|
|
D049913|219090||acth secreting pituitary adenoma
|
|
D049913|219090||acth producing pituitary adenoma
|
|
D049913|219090||acth producing pituitary adenomas
|
|
D049913|219090||acth secreting pituitary adenomas
|
|
D049913|219090||adenoma corticotroph
|
|
D049913|219090||adenomas corticotroph
|
|
D049913|219090||corticotroph adenoma
|
|
D049913|219090||corticotroph adenomas
|
|
D049913|219090||corticotropin secreting adenoma pituitary
|
|
D049913|219090||corticotropin secreting adenomas pituitary
|
|
D049913|219090||pituitary adenoma acth producing
|
|
D049913|219090||pituitary adenoma acth secreting
|
|
D049913|219090||pituitary adenomas acth producing
|
|
D049913|219090||pituitary adenomas acth secreting
|
|
D049913|219090||pituitary corticotropin secreting adenoma
|
|
D049913|219090||pituitary corticotropin secreting adenomas
|
|
C566875|300055||mental retardation x linked syndromic 13
|
|
C566875|300055|C564724||mental retardation with psychosis pyramidal signs and macroorchidism
|
|
C566875|300055||mrx16
|
|
C566875|300055||mrx79
|
|
C566875|300055||mrxs13
|
|
C566875|300055||ppmx
|
|
C536269||radio ulnar synostosis type 2
|
|
C565719|610143||deafness autosomal recessive 62
|
|
C565719|610143||dfnb62
|
|
C562386|145500||hypertension essential
|
|
C562386|145500||eht
|
|
C562386|145500||hypertension essential body mass related
|
|
C562386|145500||hypertension essential kidney function related
|
|
C562386|145500||hypertension essential susceptibility to 1
|
|
C562386|145500||hypertension essential susceptibility to 2
|
|
C562386|145500||hypertension essential susceptibility to 3
|
|
C562386|145500||hypertension essential susceptibility to 4
|
|
C562386|145500||hypertension essential susceptibility to 5
|
|
C562386|145500||hypertension essential susceptibility to 6
|
|
C562386|145500||hypertension essential susceptibility to 7
|
|
C562386|145500||hypertension essential susceptibility to 8
|
|
C562386|145500||hyt1
|
|
C562386|145500||hyt2
|
|
C562386|145500||hyt3
|
|
C562386|145500||hyt4
|
|
C562386|145500||hyt5
|
|
C562386|145500||hyt6
|
|
C562386|145500||hyt7
|
|
C562386|145500||hyt8
|
|
C567355|612300||cd59 deficiency
|
|
C567355|612300||hacd59
|
|
C567355|612300||hemolytic anemia cd59 mediated with or without immune mediated polyneuropathy
|
|
C536286||immotile cilia syndrome due to defective radial spokes
|
|
C536286||ciliary dyskinesia with defective radial spokes
|
|
C536286||cilia with defective radial spokes
|
|
C536283||idiopathic subglottic tracheal stenosis
|
|
C536284||iida kannari syndrome
|
|
C536284||craniosynostosis with joint contractures ear deformity cleft palate scoliosis and other features
|
|
D014592||uterine hemorrhage
|
|
D014592||bleedings vaginal
|
|
D014592||bleeding uterine
|
|
D014592||bleeding vaginal
|
|
D014592||hemorrhage uterine
|
|
D014592||uterine bleeding
|
|
D014592||uterine bleedings
|
|
D014592||uterine hemorrhages
|
|
D014592||vaginal bleeding
|
|
D014592||vaginal bleedings
|
|
D014591||uterine diseases
|
|
D014591||disease endometrial
|
|
D014591||diseases endometrial
|
|
D014591||diseases uterine
|
|
D014591||disease uterine
|
|
D014591||endometrial disease
|
|
D014591||endometrial diseases
|
|
D014591||uterine disease
|
|
C536287||immotile cilia syndrome due to excessively long cilia
|
|
C536287||ciliary dyskinesia with excessively long cilia
|
|
C536288||thymic aplasia
|
|
C536288||immune defect due to absence of thymus
|
|
C536288||nezelof syndrome
|
|
219100||cutis laxa autosomal recessive type ia
|
|
219100||arcl1
|
|
219100||arcl1a
|
|
219100|C562628||cutis laxa autosomal recessive
|
|
D025242||spondylarthropathies
|
|
D025242||spondylarthropathy
|
|
D025242||spondylitis marie strumpell
|
|
D025242||spondyloarthropathies
|
|
D025242||spondyloarthropathy
|
|
D025242||syndrome bechterew
|
|
D025241||spondylarthritis
|
|
D025241||arthritis spinal
|
|
D025241||spinal arthritides
|
|
D025241||spinal arthritis
|
|
D025241||spondylarthritides
|
|
C536281||idiopathic pulmonary hemosiderosis
|
|
C536281||alveolar hypoventilation syndrome
|
|
C536281||hemosiderosis pulmonary with deficiency of gamma a globulin
|
|
C536281||pulmonary hemosiderosis
|
|
C536282||pulmonary arterial hypertension
|
|
C536282||familial primary pulmonary hypertension
|
|
C536282||idiopathic pulmonary arterial hypertension
|
|
C536282||idiopathic pulmonary hypertension
|
|
C536282||pph1 with hht
|
|
C536282||primary pulmonary hypertension
|
|
C536282||pulmonary hypertension primary 1 with hereditary hemorrhagic telangiectasia
|
|
C536282||pulmonary hypertension primary dexfenfluramine associated
|
|
C536282||pulmonary hypertension primary fenfluramine associated
|
|
C566533|602499||macrophthalmia colobomatous with microcornea
|
|
C566533|602499||macom
|
|
C562538||cerebrocostomandibular syndrome
|
|
C562538||ccm syndrome
|
|
C562538||cerebrocostomandibular like syndrome
|
|
C562538||rib gap defects with micrognathia
|
|
D001282||atrial flutter
|
|
D001282||atrial flutters
|
|
D001282||auricular flutter
|
|
D001282||auricular flutters
|
|
D001282||flutter atrial
|
|
D001282||flutter auricular
|
|
D001282||flutters atrial
|
|
D001282||flutters auricular
|
|
D001281||atrial fibrillation
|
|
D001281||atrial fibrillations
|
|
D001281||auricular fibrillation
|
|
D001281||auricular fibrillations
|
|
D001281||familial atrial fibrillation
|
|
D001281||fibrillation atrial
|
|
D001281||fibrillation auricular
|
|
D001281||fibrillations atrial
|
|
D001281||fibrillations auricular
|
|
C535919|302800||charcot marie tooth disease x linked 1
|
|
C535919|302800||charcot marie tooth disease x linked dominant 1
|
|
C535919|302800||charcot marie tooth neuropathy x linked 1
|
|
C535919|302800||charcot marie tooth peroneal muscular atrophy x linked
|
|
C535919|302800||cmt2 formerly
|
|
C535919|302800||cmtx
|
|
C535919|302800||cmtx1
|
|
C535919|302800||cmtx 1
|
|
C535919|302800||hereditary motor and sensory neuropathy x linked
|
|
C535919|302800||hmsn x linked
|
|
131100|D018761||multiple endocrine neoplasia type 1
|
|
131100|D018761||mea 1
|
|
131100|D018761||mea i
|
|
131100|D018761||men1
|
|
131100|D018761||men 1
|
|
131100|D018761||men i
|
|
131100|D018761||multiple endocrine neoplasia type i
|
|
131100|D018761||multiple endocrine neoplasms type 1
|
|
131100|D018761||neoplasia multiple endocrine type 1
|
|
131100|D018761||neoplasms multiple endocrine type 1
|
|
131100|D018761||neoplasms multiple endocrine type i
|
|
131100|D018761||wermer syndrome
|
|
131100|D018761||wermer syndrome men1 somatic mutations included
|
|
C562681|250850||methionine adenosyltransferase deficiency
|
|
C562681|250850||hypermethioninemia isolated persistent
|
|
C562681|250850||mat i iii deficiency
|
|
607876||adcme
|
|
607876||cortical myoclonic tremor with epilepsy familial 2
|
|
607876||fcmte2
|
|
D014582||urticaria pigmentosa
|
|
D014582||cutaneous mastocytoses maculopapular
|
|
D014582||cutaneous mastocytosis maculopapular
|
|
D014582||maculopapular cutaneous mastocytoses
|
|
D014582||maculopapular cutaneous mastocytosis
|
|
C567930|613096||spastic paraplegia 36 autosomal dominant
|
|
C567930|613096||spg36
|
|
C563703|609535||drug metabolism poor cyp2c19 related
|
|
C563703|609535||clopidogrel poor metabolism of included
|
|
C563703|609535||mephenytoin poor metabolism of included
|
|
C563703|609535||opremazole poor metabolism of included
|
|
C563703|609535||proguanil poor metabolism of included
|
|
C563871||microcephaly primary autosomal recessive 5
|
|
C563870||neuropathy hereditary sensory and autonomic adult onset with anosmia
|
|
D052958||tarlov cysts
|
|
D052958||cyst perineural
|
|
D052958||cyst perineurial
|
|
D052958||cyst sacral perineural
|
|
D052958||cysts perineural
|
|
D052958||cysts perineurial
|
|
D052958||cysts sacral perineural
|
|
D052958||cysts sacral tarlov
|
|
D052958||cysts tarlov
|
|
D052958||perineural cyst
|
|
D052958||perineural cysts
|
|
D052958||perineurial cyst
|
|
D052958||perineurial cysts
|
|
D052958||sacral perineural cyst
|
|
D052958||sacral perineural cysts
|
|
D052958||sacral tarlov cysts
|
|
C536297||male sterility due to y chromosome deletions
|
|
C536297||partial deletion of chromosome y
|
|
C536297||partial deletion of the long arm of the y chromosome
|
|
C536297||partial deletion of y
|
|
C536297||partial deletion of y chromosome short arm
|
|
C536297||y chromosome deletions
|
|
C536297||y chromosome microdeletions
|
|
C562543||german syndrome
|
|
D013271||gastric dilatation
|
|
D013271||dilatation gastric
|
|
D013271||dilatation stomach
|
|
D013271||dilation gastric
|
|
D013271||dilation stomach
|
|
D013271||gastric dilation
|
|
D013271||stomach dilatation
|
|
D013271||stomach dilation
|
|
D013272||stomach diseases
|
|
D013272||disease gastric
|
|
D013272||diseases gastric
|
|
D013272||diseases stomach
|
|
D013272||disease stomach
|
|
D013272||gastric disease
|
|
D013272||gastric diseases
|
|
D013272||stomach disease
|
|
C536298||partial lissencephaly
|
|
C536298||focal agyria pachygyria
|
|
C536298||incomplete lissencephaly
|
|
C563774|609218||foveal hypoplasia and anterior segment dysgenesis
|
|
C563774|609218||fhonda
|
|
C563774|609218||foveal hypoplasia 2
|
|
C563774|609218||foveal hypoplasia optic nerve decussation defects and anterior segment dysgenesis without albinism
|
|
C563774|609218||foveal hypoplasia with or without optic nerve misrouting and or anterior segment dysgenesis
|
|
C563774|609218||fvh2
|
|
C536299||partington anderson syndrome
|
|
128101|C536698||whispering dysphonia hereditary
|
|
128101|C536698||dyt4
|
|
128101|C536698||hereditary whispering dysphonia
|
|
C536743|300076||woods black norbury syndrome
|
|
C536743|300076||immunoneurologic disorder x linked
|
|
C536743|300076||neonatal death immune deficiency
|
|
C536743|300076||x linked immunoneurological disorder
|
|
D009765|601665||obesity
|
|
D009765|601665||leanness included
|
|
C562548||clavicle pseudarthrosis of congenital
|
|
D001284||atrophy
|
|
D001284||atrophies
|
|
C563876||aicar transformylase inosine monophosphate cyclohydrolase deficiency
|
|
C563876|608688||aica ribosuria due to atic deficiency
|
|
C562546||megalodactyly
|
|
C562546||macrodactyly
|
|
C536292||jorgenson lenz syndrome
|
|
C536292||blepharophimosis radioulnar synostosis
|
|
C536292||mild short stature microcephaly ptosis blepharophimosis facial asymmetry and radioulnar synostosis
|
|
C536292||ptosis prognathism microcephaly radio ulnar synostosis short stature dwarfism
|
|
D049309||acanthoma
|
|
D049309||acanthoma clear cell
|
|
D049309||acanthoma degos
|
|
D049309||acanthoma pilar sheath
|
|
D049309||acanthomas
|
|
D049309||acanthomas clear cell
|
|
D049309||acanthomas pilar sheath
|
|
D049309||clear cell acanthoma
|
|
D049309||clear cell acanthomas
|
|
D049309||degos acanthoma
|
|
D049309||pilar sheath acanthoma
|
|
D049309||pilar sheath acanthomas
|
|
251290||band like calcification with simplified gyration and polymicrogyria
|
|
251290||blcpmg
|
|
C563134|302500||spinocerebellar ataxia x linked 1
|
|
C563134|302500||olivopontocerebellar atrophy x linked
|
|
C563134|302500||opcax
|
|
C563134|302500||opca x linked
|
|
C563134|302500||scax1
|
|
D064927||tick bites
|
|
D064927||bites tick
|
|
D064927||bite tick
|
|
D064927||tick bite
|
|
D014596||uterine prolapse
|
|
D014596||prolapses uterine
|
|
D014596||prolapses vaginal
|
|
D014596||prolapse uterine
|
|
D014596||prolapse vaginal
|
|
D014596||uterine prolapses
|
|
D014596||vaginal prolapse
|
|
D014596||vaginal prolapses
|
|
D014595||uterine perforation
|
|
D014595||perforations uterine
|
|
D014595||perforation uterine
|
|
D014595||uterine perforations
|
|
605201||high density lipoprotein cholesterol level quantitative trait locus 14
|
|
605201||hdlcq14
|
|
D014594||uterine neoplasms
|
|
D014594||cancer of the uterus
|
|
D014594||cancer of uterus
|
|
D014594||cancers uterine
|
|
D014594||cancers uterus
|
|
D014594||cancer uterine
|
|
D014594||cancer uterus
|
|
D014594||neoplasms uterine
|
|
D014594||neoplasms uterus
|
|
D014594||neoplasm uterine
|
|
D014594||neoplasm uterus
|
|
D014594||uterine cancer
|
|
D014594||uterine cancers
|
|
D014594||uterine neoplasm
|
|
D014594||uterus cancer
|
|
D014594||uterus cancers
|
|
D014594||uterus neoplasm
|
|
D014594||uterus neoplasms
|
|
D014593||uterine inertia
|
|
D014593||atony uterine
|
|
D014593||inertia uterine
|
|
D014593||uterine atony
|
|
C565121|124900||deafness autosomal dominant 1
|
|
C565121|124900||deafness progressive low tone
|
|
C565121|124900||dfna1
|
|
C565121|124900||hereditary low frequency hearing loss
|
|
C565121|124900||konigsmark syndrome
|
|
C565121|124900||lfhl1
|
|
D014597||uterine rupture
|
|
D014597||ruptures uterine
|
|
D014597||rupture uterine
|
|
D014597||uterine ruptures
|
|
D051516||hemospermia
|
|
D051516||hematospermia
|
|
C537671||chromosome 1 monosomy 1q32 q42
|
|
C537671||deletion 1q32 q42
|
|
C537671||monosomy 1q32 q42
|
|
132850||epstein barr virus insertion site 1 ebvs1 epstein barr virus integration site
|
|
C536341||porphyria chester type
|
|
C537672||chromosome 1 monosomy 1q4
|
|
C537672||deletion 1q4
|
|
C537672||monosomy 1q4
|
|
C537670||behrens baumann dust syndrome
|
|
C537670||oculo cerebral dysplasia
|
|
C563963||fryns macrocephaly
|
|
C563963||macrocephaly with spastic paraplegia and distinctive craniofacial appearance
|
|
C536344||vertebral fusion posterior lumbosacral blepharoptosis
|
|
C536344||congenital ptosis and posterior fusion of lumbosacral vertebrae
|
|
C536344||familial posterior lumbosacral vertebral fusion and eyelid ptosis
|
|
C536344||vertebral fusion posterior lumbosacral with blepharoptosis
|
|
C537675||gaucher like disease
|
|
C537675||pseudo gaucher disease
|
|
C537676||gay feinmesser cohen syndrome
|
|
C537676||laryngeal web congenital heart disease and low stature
|
|
C537676||subglottic bar congenital heart disease and low stature
|
|
C536342||posterior column ataxia
|
|
C536342||biemond ataxia
|
|
C565062|129900||ectrodactyly ectodermal dysplasia and cleft lip palate syndrome 1
|
|
C565062|129900||eec
|
|
C565062|129900||eec1
|
|
C565062|129900||eec syndrome 1
|
|
C563966||pick complex
|
|
C563965||peroxisome biogenesis disorder complementation group j
|
|
C536488|602097||usher syndrome type 1e
|
|
C536488|602097||ush1e
|
|
C563964||peroxisome biogenesis disorder complementation group 14
|
|
613610||cranioectodermal dysplasia 2
|
|
613610||ced2
|
|
C563969||aplasia cutis congenita with epibulbar dermoids
|
|
C563969||oculoectodermal syndrome
|
|
613611||choanal atresia and lymphedema
|
|
604278|C567038||renal tubular acidosis proximal with ocular abnormalities and mental retardation
|
|
604278|C567038||rta proximal autosomal recessive
|
|
613612||congenital disorder of glycosylation type iii
|
|
613612||cdg2i
|
|
613612||cdgiii
|
|
613612||cdg iii
|
|
C537419|605039||bohring syndrome
|
|
C537419|605039||bohring opitz syndrome
|
|
C537419|605039||bops
|
|
C537419|605039||c like syndrome
|
|
C537419|605039||opitz trigonocephaly like syndrome
|
|
D014689||venous insufficiency
|
|
D014689||insufficiencies venous
|
|
D014689||insufficiency venous
|
|
D014689||venous insufficiencies
|
|
C537682|190100||geniospasm
|
|
C537682|190100||geniospasm 1
|
|
C537682|190100||gsm1
|
|
C537682|190100||hereditary geniospasm
|
|
C537682|190100||trembling chin
|
|
613606||forsythe wakeling syndrome
|
|
613606||fws
|
|
613606||microcephaly and growth retardation with childhood onset nephrotic syndrome and thrombocytopenia
|
|
D026681||vitamin b 6 deficiency
|
|
D026681||b6 deficiencies vitamin
|
|
D026681||b6 deficiency vitamin
|
|
D026681||b6 vitamin deficiencies
|
|
D026681||b6 vitamin deficiency
|
|
D026681||deficiencies b6 vitamin
|
|
D026681||deficiencies vitamin b6
|
|
D026681||deficiency b6 vitamin
|
|
D026681||deficiency pyridoxine
|
|
D026681||deficiency vitamin b6
|
|
D026681||deficiency vitamin b 6
|
|
D026681||pyridoxine deficiency
|
|
D026681||vitamin b6 deficiencies
|
|
D026681||vitamin b6 deficiency
|
|
D026681||vitamin deficiencies b6
|
|
D026681||vitamin deficiency b6
|
|
C565757|610926||tooth agenesis selective 5
|
|
C565757|610926||he zhao deficiency
|
|
C565757|610926||hypodontia oligodontia 5
|
|
C565757|610926||sthag5
|
|
D013352||subcutaneous emphysema
|
|
D013352||emphysemas subcutaneous
|
|
D013352||emphysema subcutaneous
|
|
D013352||subcutaneous emphysemas
|
|
C537668||beemer ertbruggen syndrome
|
|
C537668||beemer lethal malformation syndrome
|
|
C536161|148600||keratosis palmoplantaris papulosa
|
|
C536161|148600||buschke fischer brauer syndrome
|
|
C536161|148600||keratoderma palmoplantar punctate type 1
|
|
C536161|148600||keratoderma palmoplantar punctate type i
|
|
C536161|148600||keratodermia palmoplantaris papulosa buschke fischer brauer type
|
|
C536161|148600||kppp1
|
|
C536161|148600||palmoplantar keratoderma punctate type i
|
|
C536161|148600||palmoplantar keratoderma punctate type ia
|
|
C536161|148600||ppkp1
|
|
C536161|148600||ppkp1a
|
|
C536161|148600||type i punctate palmoplantar keratoderma
|
|
D013353||subdural effusion
|
|
D013353||cerebrospinal fluid effusion subdural
|
|
D013353||cerebrospinal fluid leakage subdural
|
|
D013353||effusion subdural
|
|
D013353||hygroma subdural
|
|
D013353||subdural cerebrospinal fluid effusion
|
|
D013353||subdural cerebrospinal fluid leakage
|
|
D013353||subdural hygroma
|
|
C537669||behr syndrome
|
|
C537669||optic atrophy infantile hereditary behr complicated form of
|
|
C537669||optic atrophy infantile hereditary with neurologic abnormalities
|
|
D058494|236670||walker warburg syndrome
|
|
D058494|236670||alpha dystroglycanopathies
|
|
D058494|236670||cerebromuscular dystrophy fukuyama type
|
|
D058494|236670||cerebroocular dysplasia muscular dystrophy syndrome
|
|
D058494|236670||chemke syndrome
|
|
D058494|236670||cmd fukuyama
|
|
D058494|236670||cod md syndrome
|
|
D058494|236670||cod md syndromes
|
|
D058494|236670||congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies type a1
|
|
D058494|236670||disease pomt1 related muscle eye brain
|
|
D058494|236670||diseases pomt1 related muscle eye brain
|
|
D058494|236670||dystrophy fukuyama muscular
|
|
D058494|236670||fukuyama cmd
|
|
D058494|236670||fukuyama muscular dystrophy
|
|
D058494|236670||fukuyama syndrome
|
|
D058494|236670||fukuyama type congenital muscular dystrophy
|
|
D058494|236670||hard syndrome
|
|
D058494|236670||hard syndromes
|
|
D058494|236670||hydrocephalus agyria and retinal dysplasia
|
|
D058494|236670||mddga1
|
|
D058494|236670||mddga3
|
|
D058494|236670||meb muscle eye brain syndrome
|
|
D058494|236670||micropolygyria with muscular dystrophy
|
|
D058494|236670||muscle eye brain disease
|
|
D058494|236670||muscle eye brain disease pomt1 related
|
|
D058494|236670||muscle eye brain diseases
|
|
D058494|236670||muscle eye brain diseases pomt1 related
|
|
D058494|236670||muscular dystrophy congenital fukuyama type
|
|
D058494|236670||muscular dystrophy dystroglycanopathy congenital with brain and eye anomalies type a 1
|
|
D058494|236670||muscular dystrophy dystroglycanopathy congenital with brain and eye anomalies type a 3
|
|
D058494|236670||muscular dystrophy fukuyama
|
|
D058494|236670||muscular dystrophy limb girdle autosomal recessive with mental retardation
|
|
D058494|236670||pagon syndrome
|
|
D058494|236670||pagon syndromes
|
|
D058494|236670||polymicrogyria with muscular dystrophy
|
|
D058494|236670||pomt1 related muscle eye brain disease
|
|
D058494|236670||pomt1 related muscle eye brain diseases
|
|
D058494|236670||syndrome chemke
|
|
D058494|236670||syndrome cod md
|
|
D058494|236670||syndrome fukuyama
|
|
D058494|236670||syndrome hard
|
|
D058494|236670||syndrome pagon
|
|
D058494|236670||syndromes cod md
|
|
D058494|236670||syndromes hard
|
|
D058494|236670||syndromes pagon
|
|
D058494|236670||syndrome walker warburg
|
|
D058494|236670||syndrome warburg
|
|
D058494|236670||walker warburg syndrome or muscle eye brain disease pomgnt1 related
|
|
D058494|236670||walker warburg syndrome or muscle eye brain disease pomt1 related
|
|
D058494|236670||warburg syndrome
|
|
C537666||becker and duchenne dystrophies
|
|
C536336||porencephaly cerebellar hypoplasia malformations
|
|
C536336||porencephaly cerebellar hypoplasia and internal malformations
|
|
C537667||bednar apos s tumor
|
|
C537667||pigmented dermatofibrosarcoma protuberans
|
|
D014681||velopharyngeal insufficiency
|
|
D014681||inadequate velopharyngeal closure
|
|
D014681||incompetence palatopharyngeal
|
|
D014681||incompetence velopharyngeal
|
|
D014681||insufficiency velopharyngeal
|
|
D014681||palatopharyngeal incompetence
|
|
D014681||velopharyngeal closures inadequate
|
|
D014681||velopharyngeal incompetence
|
|
D013354||empyema subdural
|
|
D013354||abscess intracranial subdural
|
|
D013354||subdural empyema
|
|
D013354||subdural empyemas
|
|
D014685||venereal tumors veterinary
|
|
D014685||transmissible venereal tumor
|
|
D014685||transmissible venereal tumors
|
|
D014685||tumors transmissible venereal
|
|
D014685||tumors veterinary venereal
|
|
D014685||tumor transmissible venereal
|
|
D014685||tumor veterinary venereal
|
|
D014685||venereal tumors transmissible
|
|
D014685||venereal tumor transmissible
|
|
D014685||venereal tumor veterinary
|
|
D014685||veterinary venereal tumor
|
|
D014685||veterinary venereal tumors
|
|
D051527||odontogenic tumor squamous
|
|
D051527||odontogenic tumors squamous
|
|
D051527||squamous odontogenic tumor
|
|
D051527||squamous odontogenic tumors
|
|
D051527||tumor squamous odontogenic
|
|
D051527||tumors squamous odontogenic
|
|
D052858||cystocele
|
|
D052858||fallen urinary bladder
|
|
D052858||prolapse urinary bladder
|
|
D052858||urinary bladder prolapse
|
|
C537683||genito palato cardiac syndrome
|
|
C537683||gardner silengo wachtel syndrome
|
|
C537683||genitopalatocardiac syndrome
|
|
C537683||male pseudohermaphroditism with micrognathia cleft palate and conotruncal cardiac defect
|
|
C537680||genee wiedemann syndrome
|
|
C537680||genee wiedemann acrofacial dysostosis
|
|
C537680||miller syndrome
|
|
C537680||poads syndrome
|
|
C537680||postaxial acrofacial dysostosis
|
|
C537680||postaxial acrofacial dysostosis poads
|
|
C537680||postaxial acrofacial dysostosis poads syndrome
|
|
C537680||wildervanck smith syndrome
|
|
C536350||visceral myopathy familial external ophthalmoplegia
|
|
C536350||intestinal pseudoobstruction with external ophthalmoplegia
|
|
C536350||muscular dystrophy oculogastrointestinal
|
|
C536350||visceral myopathy familial with external ophthalmoplegia
|
|
C563974||cleidocranial dysplasia forme fruste dental anomalies only
|
|
C562642||amyloidosis primary cutaneous
|
|
C562642||primary localized cutaneous amyloidosis
|
|
C563973||hydrocephalus autosomal dominant
|
|
C536356||anemia hereditary spherocytic hemolytic
|
|
C536356||acholuric jaundice
|
|
C536356||chronic acholuric jaundice
|
|
C536356||congenital hemolytic jaundice
|
|
C536356||debrie apos s familial haemolytic disease
|
|
C536356||minkowski chauffard disease
|
|
C536356||minkowski chauffard g 228 nsslen syndrome
|
|
C536356||minkowski chauffard haemolytic jaundice
|
|
C563972||colorectal cancer hereditary nonpolyposis type 3
|
|
C563972||hnpcc3
|
|
C537684||genoa syndrome
|
|
C537684||camera lituania cohen syndrome
|
|
C537684||holoprosencephaly craniosynostosis
|
|
C537684||holoprosencephaly semilobar with craniosynostosis
|
|
C537684||semilobar holoprosencephaly and primary craniosynostosis
|
|
C563971||colorectal cancer hereditary nonpolyposis type 4
|
|
C563971||hnpcc4
|
|
C536354||vocal cord dysfunction familial
|
|
C536354||familial vocal cord dysfunction
|
|
C536354||gerhardt syndrome
|
|
C536354||laryngeal abductor paralysis
|
|
C536354||plott syndrome
|
|
C537685||genu valgum st helena familial
|
|
C537685||genu valgum hereditary pubertal
|
|
C537685||hereditary pubertal genu valgum
|
|
C537685||st helena familial genu valgum
|
|
C563978||ichthyosis exfoliativa
|
|
D000052||acanthosis nigricans
|
|
D000052||acanthosis nigrican
|
|
D000052||nigrican acanthosis
|
|
D000052||nigricans acanthosis
|
|
C562644||amyloidosis cutaneous bullous
|
|
D000051||acantholysis
|
|
D000051||acantholyses
|
|
C562645||acid phosphatase deficiency
|
|
D013369||subphrenic abscess
|
|
D013369||abscesses subdiaphragmatic
|
|
D013369||abscesses subphrenic
|
|
D013369||abscess subdiaphragmatic
|
|
D013369||abscess subphrenic
|
|
D013369||subdiaphragmatic abscess
|
|
D013369||subdiaphragmatic abscesses
|
|
D013369||subphrenic abscesses
|
|
115210|C566168||cardiomyopathy familial restrictive 1
|
|
115210|C566168||rcm
|
|
115210|C566168||rcm1
|
|
105120|C537459||meretoja syndrome
|
|
105120|C537459||amyloid cranial neuropathy with lattice corneal dystrophy
|
|
105120|C537459||amyloidosis 5
|
|
105120|C537459||amyloidosis due to mutant gelsolin
|
|
105120|C537459||amyloidosis due to mutant gelsolin cerebral amyloid angiopathy gsn related included
|
|
105120|C537459||amyloidosis finnish type
|
|
105120|C537459||amyloidosis meretoja type
|
|
105120|C537459||amyloidosis v
|
|
105120|C537459||cerebral amyloid angiopathy gsn related
|
|
105120|C537459||corneal dystrophy lattice type ii
|
|
105120|C537459||corneal dystrophy lattice type ii included
|
|
105120|C537459||familial amyloidosis finnish type
|
|
105120|C537459||finnish type amyloidosis
|
|
105120|C537459||gelsolin related amyloidosis
|
|
105120|C537459||kymenlaakso syndrome
|
|
105120|C537459||lattice corneal dystrophy associated with familial systemic amyloidosis
|
|
105120|C537459||lattice corneal dystrophy gelsolin type
|
|
105120|C537459||lattice corneal dystrophy type ii
|
|
105120|C537459||lattice corneal dystrophy type ii included
|
|
105120|C537459||lattice dystrophy of the cornea with hereditary generalized amyloidosis
|
|
105120|C537459||lcd2 included
|
|
105120|C537459||meretoja apos s syndrome
|
|
105120|C537459||meretoja type amyloidosis
|
|
C563408|601001||epidermolysis bullosa simplex autosomal recessive
|
|
C563408|601001||ebsb1
|
|
C563408|601001||epidermolysis bullosa simplex autosomal recessive 1
|
|
C536348||vibrio vulnificus infection
|
|
C537679||gemss syndrome
|
|
C537679||glaucoma ectopia microspherophakia stiff joints short stature syndrome
|
|
D013364||submandibular gland diseases
|
|
D013364||diseases submandibular gland
|
|
D013364||disease submandibular gland
|
|
D013364||gland diseases submandibular
|
|
D013364||gland disease submandibular
|
|
D013364||submandibular gland disease
|
|
C536349||viljoen kallis voges syndrome
|
|
D014694||ventricular outflow obstruction
|
|
D014694||left ventricular outflow obstruction
|
|
D014694||obstructions ventricular outflow
|
|
D014694||obstruction ventricular outflow
|
|
D014694||outflow obstruction left ventricular
|
|
D014694||outflow obstruction right ventricular
|
|
D014694||outflow obstructions ventricular
|
|
D014694||outflow obstruction ventricular
|
|
D014694||right ventricular outflow obstruction
|
|
D014694||ventricular outflow obstruction left
|
|
D014694||ventricular outflow obstruction right
|
|
D014694||ventricular outflow obstructions
|
|
D038642||shaken baby syndrome
|
|
C536346||vestibulocochlear dysfunction progressive
|
|
C536346||familial progressive vestibulo cochlear dysfunction
|
|
C536346||familial progressive vestibulocochlear dysfunction
|
|
C536346||vestibulocochlear dysfunction progressive familial
|
|
D012030||refractive errors
|
|
D012030||ametropia
|
|
D012030||ametropias
|
|
D012030||disorder refractive
|
|
D012030||disorders refractive
|
|
D012030||error refractive
|
|
D012030||errors refractive
|
|
D012030||refractive disorder
|
|
D012030||refractive disorders
|
|
D012030||refractive error
|
|
D014693||ventricular fibrillation
|
|
D014693||fibrillations ventricular
|
|
D014693||fibrillation ventricular
|
|
D014693||ventricular fibrillations
|
|
C565703|610202||cataract pulverulent juvenile onset
|
|
C565703|610202||cataract 21 multiple types
|
|
C565703|610202||cataract 21 multiple types with or without microcornea
|
|
C565703|610202||cataract congenital cerulean type 4
|
|
C565703|610202||cca4
|
|
C565703|610202||ctrct21
|
|
D013362||sublingual gland neoplasms
|
|
D013362||gland neoplasms sublingual
|
|
D013362||gland neoplasm sublingual
|
|
D013362||neoplasms sublingual gland
|
|
D013362||neoplasm sublingual gland
|
|
D013362||sublingual gland neoplasm
|
|
C536347||vibratory angioedema
|
|
C536347||angioedema vibratory
|
|
C537678||gemignani syndrome
|
|
C537678||spinocerebellar ataxia associated with localized amyotrophy of the hands sensorineural deafness and spastic paraparesis
|
|
D013365||submandibular gland neoplasms
|
|
D013365||gland neoplasms submandibular
|
|
D013365||gland neoplasm submandibular
|
|
D013365||neoplasms submandibular gland
|
|
D013365||neoplasm submandibular gland
|
|
D013365||submandibular gland neoplasm
|
|
C536362||angiofollicular ganglionic hyperplasia
|
|
C537694||jung wolff back stahl syndrome
|
|
C537694||anterior chamber cleavage disorder cerebellar hypoplasia hypothyroidism and tracheal stenosis
|
|
D000027||abortion incomplete
|
|
D000027||abortions incomplete
|
|
D000027||incomplete abortion
|
|
D000027||incomplete abortions
|
|
D001357||sarcoma avian
|
|
D001357||avian sarcoma
|
|
D001357||avian sarcomas
|
|
D001357||rous sarcoma
|
|
D001357||sarcoma rous
|
|
D001357||sarcomas avian
|
|
D000026||abortion habitual
|
|
D000026||abortion recurrent
|
|
D000026||abortions habitual
|
|
D000026||abortions recurrent
|
|
D000026||habitual abortion
|
|
D000026||habitual abortions
|
|
D000026||miscarriage recurrent
|
|
D000026||miscarriages recurrent
|
|
D000026||recurrent abortion
|
|
D000026||recurrent abortions
|
|
D000026||recurrent miscarriage
|
|
D000026||recurrent miscarriages
|
|
C536361||angel shaped phalangoepiphyseal dysplasia
|
|
C536361||angel shaped phalango epiphyseal dysplasia
|
|
C537692||judge misch wright syndrome
|
|
C537692||dry skin photophobia hyperkeratosis abnormal fingernails
|
|
C537692||keratodermia palmoplantar periorificial
|
|
C537692||palmoplantar and perioroficial keratoderma with corneal epithelial dysplasia
|
|
C563941||pectus excavatum macrocephaly short stature dysplastic nails
|
|
C563940||angiokeratoma corporis diffusum with arteriovenous fistulas
|
|
C536367||angiomatosis diffuse corticomeningeal of divry and van bogaert
|
|
C536364||angioma hereditary neurocutaneous
|
|
C536364||hereditary neurocutaneous angioma
|
|
C536365||angioma serpiginosum autosomal dominant
|
|
C536365||autosomal dominant angioma serpiginosum
|
|
C537696||juvenile gout
|
|
C537696||familial gout kidney disease
|
|
C537696||familial gouty nephropathy
|
|
C537696|162000||familial juvenile hyperuricemic nephropathy
|
|
C537696|162000||gouty nephropathy familial juvenile
|
|
C537696|162000||hyperuricemic nephropathy familial juvenile
|
|
C537696|162000||hyperuricemic nephropathy familial juvenile 1
|
|
C537696||medullary cystic kidney disease type 2
|
|
C537696|162000||nephropathy familial with gout
|
|
C537696||umod related kidney disease
|
|
C537696||uromodulin associated kidney disease
|
|
C537696||uromodulin storage disease
|
|
C563942||aphalangia partial with syndactyly and duplication of metatarsal iv
|
|
C536016|600972||achondrogenesis type 1b
|
|
C536016|600972||acg1b
|
|
C536016|600972||achondrogenesis fraccaro type
|
|
C536016|600972||achondrogenesis type ib
|
|
C536016|600972||fraccaro achondrogenesis
|
|
C563949||enteropathy familial with villous edema and immunoglobulin g2 deficiency
|
|
C563948|C538417|271150||spinal muscular atrophy type iv
|
|
C563948|C538417|271150||spinal muscular atrophy adult form
|
|
C563948|C538417|271150||spinal muscular atrophy proximal adult autosomal recessive
|
|
C564743|277410||methylmalonic aciduria and homocystinuria cbld type
|
|
C564743|277410||homocystinuria cbld type variant 1
|
|
C564743|277410||methylmalonic acidemia and homocystinuria cbld type
|
|
C564743|277410||methylmalonic acidemia and homocystinuria cbld type homocystinuria cbld type variant 1 included
|
|
C564743|277410||methylmalonic acidemia cblh type formerly
|
|
C564743|277410||methylmalonic aciduria cbld type variant 2
|
|
C564743|277410||methylmalonic aciduria cbld type variant 2 included
|
|
C564743|277410||methylmalonic aciduria cblh type formerly
|
|
C537690||juberg hayward syndrome
|
|
C537690||cleft lip palate with abnormal thumbs and microcephaly
|
|
C537690||ofds viii
|
|
C537690||oral facial digital syndrome type viii
|
|
C537690||oral facial digital syndrome with hypoplastic epiglottis
|
|
C537690||orocraniodigital syndrome
|
|
C563947||pachydermodactyly familial
|
|
607671|C564354||dystonia 13 torsion
|
|
607671|C564354||dystonia 13 torsion autosomal dominant
|
|
607671|C564354||dyt13
|
|
D001353||avian leukosis
|
|
D001353||avian leukoses
|
|
D001353||leukoses avian
|
|
D001353||leukosis avian
|
|
D000022||abortion spontaneous
|
|
D000022||abortions spontaneous
|
|
D000022||abortions tubal
|
|
D000022||abortion tubal
|
|
D000022||miscarriage
|
|
D000022||miscarriages
|
|
D000022||spontaneous abortion
|
|
D000022||spontaneous abortions
|
|
D000022||tubal abortion
|
|
D000022||tubal abortions
|
|
C536173|600231||diffuse palmoplantar keratoderma bothnian type
|
|
C536173|600231||palmoplantar keratoderma bothnian type
|
|
C536173|600231||ppkb
|
|
D012008||recurrence
|
|
D012008||recrudescence
|
|
D012008||recrudescences
|
|
D012008||recurrences
|
|
D012008||relapse
|
|
D012008||relapses
|
|
C536826|137950||glomerulopathy with fibronectin deposits
|
|
C536826|137950||fibronectin glomerulopathy
|
|
C536826|137950||gfnd1
|
|
C536826|137950||gfnd2
|
|
C536826|137950||glomerular nephritis familial with fibronectin deposits
|
|
C536826|137950||glomerulopathy with fibronectin deposits 2
|
|
D016142|236100||holoprosencephaly
|
|
D016142|236100||alobar holoprosencephalies
|
|
D016142|236100||alobar holoprosencephaly
|
|
D016142|236100||arhinencephalies
|
|
D016142|236100||arhinencephaly
|
|
D016142|236100||arhinencephaly holoprosencephaly 1 included
|
|
D016142|236100||cyclopia included
|
|
D016142|236100||demyer sequence included
|
|
D016142|236100||holoprosencephalies
|
|
D016142|236100||holoprosencephalies alobar
|
|
D016142|236100||holoprosencephalies lobar
|
|
D016142|236100||holoprosencephalies semilobar
|
|
D016142|236100||holoprosencephaly alobar
|
|
D016142|236100||holoprosencephaly familial alobar
|
|
D016142|236100||holoprosencephaly lobar
|
|
D016142|236100||holoprosencephaly semilobar
|
|
D016142|236100||hpe1 included
|
|
D016142|236100||hpec
|
|
D016142|236100||hpe familial
|
|
D016142|236100||lobar holoprosencephalies
|
|
D016142|236100||lobar holoprosencephaly
|
|
D016142|236100||semilobar holoprosencephalies
|
|
D016142|236100||semilobar holoprosencephaly
|
|
D012005||anus prolapse
|
|
D012005||anus prolapses
|
|
D012005||prolapse anus
|
|
D012005||prolapse rectal
|
|
D012005||prolapses anus
|
|
D012005||prolapses rectal
|
|
D012005||rectal prolapses
|
|
D002690||chlamydia infections
|
|
D002690||chlamydia infection
|
|
D002690||infection chlamydia
|
|
D002690||infections chlamydia
|
|
D012006||rectovaginal fistula
|
|
D012006||fistula rectovaginal
|
|
D012006||fistulas rectovaginal
|
|
D012006||rectovaginal fistulas
|
|
252010|C537475||mitochondrial complex i deficiency
|
|
252010|C537475||mitochondrial nadh dehydrogenase component of complex i deficiency of
|
|
252010|C537475||nadh coenzyme q reductase deficiency
|
|
252010|C537475||nadh q 1 oxidoreductase deficiency
|
|
C566908|611603||lissencephaly 3
|
|
C566908|611603||lis3
|
|
D013330||struma ovarii
|
|
C536359||anencephaly and spina bifida x linked
|
|
C536359||x linked anencephaly spina bifida
|
|
C567087|611777||brugada syndrome 2
|
|
C567087|611777||brgda2
|
|
C536357||anemia hypochromic microcytic
|
|
D012003||rectal fistula
|
|
D012003||anal fistula
|
|
D012003||fistula rectal
|
|
D012004||rectal neoplasms
|
|
D012004||cancer of rectum
|
|
D012004||cancer of the rectum
|
|
D012004||cancer rectal
|
|
D012004||cancer rectum
|
|
D012004||cancers rectal
|
|
D012004||cancers rectum
|
|
D012004||neoplasm rectal
|
|
D012004||neoplasm rectum
|
|
D012004||neoplasms rectal
|
|
D012004||neoplasms rectum
|
|
D012004||rectal cancer
|
|
D012004||rectal cancers
|
|
D012004||rectal neoplasm
|
|
D012004||rectal tumor
|
|
D012004||rectal tumors
|
|
D012004||rectum cancer
|
|
D012004||rectum cancers
|
|
D012004||rectum neoplasm
|
|
D012004||rectum neoplasms
|
|
D012004||tumor rectal
|
|
D012004||tumors rectal
|
|
D012001||hyperacusis
|
|
D012001||auditory hyperesthesia
|
|
D012001||auditory hyperesthesias
|
|
D012001||disturbance loudness perception
|
|
D012001||disturbances loudness perception
|
|
D012001||hyperacuses
|
|
D012001||hyperacusia
|
|
D012001||hyperacusias
|
|
D012001||hyperesthesia auditory
|
|
D012001||hyperesthesias auditory
|
|
D012001||loudness perception disturbance
|
|
D012001||loudness perception disturbances
|
|
D012001||loudness recruitment
|
|
D012001||loudness recruitments
|
|
D012001||perception disturbance loudness
|
|
D012001||perception disturbances loudness
|
|
D012001||phonophobia
|
|
D012001||phonophobias
|
|
D012001||recruitment loudness
|
|
D012002||rectal diseases
|
|
D012002||disease rectal
|
|
D012002||diseases rectal
|
|
D012002||rectal disease
|
|
D000039||peritonsillar abscess
|
|
D000039||abscesses peritonsillar
|
|
D000039||abscess peritonsillar
|
|
D000039||peritonsillar abscesses
|
|
D052878||urolithiasis
|
|
D052878||lithiasis urinary
|
|
D052878||urinary lithiasis
|
|
D000038||abscess
|
|
D000038||abscesses
|
|
C537486|605229||spastic paraplegia 14 autosomal recessive
|
|
C537486|605229||spg14
|
|
D052879||subacute combined degeneration
|
|
D052879||neuropathy subacute combined degeneration
|
|
D052879||subacute combined neuropathy degeneration
|
|
D000037||abruptio placentae
|
|
D000037||abruption placental
|
|
D000037||abruptions placental
|
|
D000037||placental abruption
|
|
D000037||placental abruptions
|
|
C567194|612715||dyschromatosis universalis hereditaria 2
|
|
C567194|612715||duh2
|
|
C563952||succinic acidemia
|
|
C563951||parotid salivary glands polycystic disease of
|
|
C536378||anonychia onychodystrophy
|
|
C536378||absent nails and dystrophic nails
|
|
C563950||band heterotopia of brain
|
|
245400||mitochondrial dna depletion syndrome 9 encephalomyopathic type with methylmalonic aciduria
|
|
245400||lactic acidosis fatal infantile formerly
|
|
245400||mtdps9
|
|
C536375||abnormal fusion of dental cementum with alveolar bone
|
|
C536375||molar i reinclusion
|
|
C536375||secondary retention of permanent molars
|
|
C566475|610444||night blindness congenital stationary autosomal dominant 3
|
|
C566475|610444||csnbad3
|
|
C566475|610444||night blindness congenital stationary nougaret type
|
|
D000031||abortion septic
|
|
D000031||abortions septic
|
|
D000031||septic abortion
|
|
D000031||septic abortions
|
|
C563954||motor neuron disease with dementia and ophthalmoplegia
|
|
D001361||avitaminosis
|
|
D001361||avitaminoses
|
|
D001361||deficiencies vitamin
|
|
D001361||deficiency vitamin
|
|
D001361||vitamin deficiencies
|
|
D001361||vitamin deficiency
|
|
D000030||abortion missed
|
|
D000030||abortions missed
|
|
D000030||missed abortion
|
|
D000030||missed abortions
|
|
C535277|606763||primary ciliary dyskinesia 2
|
|
C535277|606763||cild2
|
|
C535277|606763||ciliary dyskinesia primary 2
|
|
C535277|606763||ciliary dyskinesia primary 2 with or without situs inversus
|
|
C562628||cutis laxa autosomal recessive type i
|
|
C562629||hemolytic anemia congenital with emphysema and cutis laxa
|
|
C562629||cutis laxa emphysema and hemolytic anemia
|
|
D000034||abortion veterinary
|
|
D000034||abortions veterinary
|
|
D000034||veterinary abortion
|
|
D000034||veterinary abortions
|
|
D000033||abortion threatened
|
|
D000033||abortions threatened
|
|
D000033||threatened abortion
|
|
D000033||threatened abortions
|
|
C562627||cutis laxa autosomal dominant
|
|
D002694||chlamydiaceae infections
|
|
D002694||chlamydiaceae infection
|
|
D002694||infection chlamydiaceae
|
|
D002694||infections chlamydiaceae
|
|
D013349||subclavian steal syndrome
|
|
D013349||artery stenoses subclavian
|
|
D013349||artery stenosis subclavian
|
|
D013349||basilar steal syndrome
|
|
D013349||basilar steal syndromes
|
|
D013349||brachial basilar insufficiency syndrome
|
|
D013349||brachial basilar insufficiency syndromes
|
|
D013349||insufficiency syndrome brachial basilar
|
|
D013349||insufficiency syndromes brachial basilar
|
|
D013349||phenomenon subclavian steal
|
|
D013349||steal phenomenon subclavian
|
|
D013349||steal subclavian
|
|
D013349||steal syndrome basilar
|
|
D013349||steal syndromes basilar
|
|
D013349||steal syndromes subclavian
|
|
D013349||steal syndrome subclavian
|
|
D013349||stenoses subclavian artery
|
|
D013349||stenosis subclavian artery
|
|
D013349||subclavian artery stenoses
|
|
D013349||subclavian artery stenosis
|
|
D013349||subclavian carotid artery steal syndrome
|
|
D013349||subclavian steal
|
|
D013349||subclavian steal phenomenon
|
|
D013349||subclavian steal syndromes
|
|
D013349||syndrome brachial basilar insufficiency
|
|
D013349||syndromes brachial basilar insufficiency
|
|
D012019||reflex sympathetic dystrophy
|
|
D012019||algodystrophic syndrome
|
|
D012019||algodystrophies
|
|
D012019||algodystrophy
|
|
D012019||atrophies sudek apos s
|
|
D012019||atrophy sudek
|
|
D012019||atrophy sudek apos s
|
|
D012019||cervical sympathetic dystrophies
|
|
D012019||cervical sympathetic dystrophy
|
|
D012019||complex regional pain syndrome type i
|
|
D012019||cprs type i
|
|
D012019||cprs type is
|
|
D012019||dystrophies cervical sympathetic
|
|
D012019||dystrophies reflex sympathetic
|
|
D012019||dystrophy cervical sympathetic
|
|
D012019||dystrophy reflex sympathetic
|
|
D012019||i cprs type
|
|
D012019||is cprs type
|
|
D012019||pain syndrome type i complex regional
|
|
D012019||pain syndrome type i regional complex
|
|
D012019||reflex dystrophia sympathetic
|
|
D012019||reflex sympathetic dystrophies
|
|
D012019||reflex sympathetic dystrophy syndrome
|
|
D012019||rsd reflex sympathetic dystrophy
|
|
D012019||rsds reflex sympathetic dystrophy
|
|
D012019||shoulder hand syndrome
|
|
D012019||shoulder hand syndromes
|
|
D012019||sudek atrophy
|
|
D012019||sudek apos s atrophies
|
|
D012019||sudek apos s atrophy
|
|
D012019||sudeks atrophy
|
|
D012019||sympathetic dystrophies cervical
|
|
D012019||sympathetic dystrophies reflex
|
|
D012019||sympathetic dystrophy cervical
|
|
D012019||sympathetic dystrophy reflex
|
|
D012019||sympathetic reflex dystrophia
|
|
D012019||sympathetic reflex dystrophias
|
|
D012019||syndrome algodystrophic
|
|
D012019||syndrome reflex sympathetic dystrophy
|
|
D012019||syndrome shoulder hand
|
|
D012019||syndromes shoulder hand
|
|
D012019||type i complex regional pain syndrome
|
|
D012019||type i cprs
|
|
D012019||type is cprs
|
|
215700|D020159||citrullinemia
|
|
215700|D020159||argininosuccinate synthase deficiency disease
|
|
215700|D020159||argininosuccinate synthetase deficiencies
|
|
215700|D020159||argininosuccinate synthetase deficiency
|
|
215700|D020159||argininosuccinic acid synthase deficiency disease
|
|
215700|D020159||argininosuccinic acid synthetase deficiency
|
|
215700|D020159||argininosuccinic acid synthetase deficiency complete
|
|
215700|D020159||argininosuccinic acid synthetase deficiency disease
|
|
215700|D020159||argininosuccinic acid synthetase deficiency disease partial
|
|
215700|D020159||ass deficiencies
|
|
215700|D020159||ass deficiency
|
|
215700|D020159||citrullinemia 1
|
|
215700|D020159||citrullinemia classic
|
|
215700|D020159||citrullinemia classical
|
|
215700|D020159||citrullinemia late onset
|
|
215700|D020159||citrullinemia neonatal
|
|
215700|D020159||citrullinemias
|
|
215700|D020159||citrullinemias classic
|
|
215700|D020159||citrullinemias classical
|
|
215700|D020159||citrullinemias late onset
|
|
215700|D020159||citrullinemias neonatal
|
|
215700|D020159||citrullinemia type 1
|
|
215700|D020159||citrullinemia type i
|
|
215700|D020159||citrullinuria
|
|
215700|D020159||citrullinurias
|
|
215700|D020159||classical citrullinemia
|
|
215700|D020159||classical citrullinemias
|
|
215700|D020159||classic citrullinemia
|
|
215700|D020159||classic citrullinemias
|
|
215700|D020159||complete argininosuccinic acid synthetase deficiency disease
|
|
215700|D020159||ctln1
|
|
215700|D020159||deficiencies argininosuccinate synthetase
|
|
215700|D020159||deficiencies ass
|
|
215700|D020159||deficiency argininosuccinate synthetase
|
|
215700|D020159||deficiency argininosuccinic acid synthetase complete
|
|
215700|D020159||deficiency argininosuccinic acid synthetase partial
|
|
215700|D020159||deficiency ass
|
|
215700|D020159||deficiency disease argininosuccinate synthase
|
|
215700|D020159||deficiency disease argininosuccinic acid synthase
|
|
215700|D020159||late onset citrullinemia
|
|
215700|D020159||late onset citrullinemias
|
|
215700|D020159||neonatal citrullinemia
|
|
215700|D020159||neonatal citrullinemias
|
|
215700|D020159||partial argininosuccinic acid synthetase deficiency disease
|
|
215700|D020159||type 1 citrullinemia
|
|
C562897|267300||renal tubular acidosis distal with progressive nerve deafness
|
|
C562897|267300||renal tubular acidosis autosomal recessive with progressive nerve deafness
|
|
C562897|267300||renal tubular acidosis with progressive nerve deafness
|
|
C562897|267300||rta with progressive nerve deafness
|
|
D012010||red cell aplasia pure
|
|
D012010||aplasia erythrocyte
|
|
D012010||aplasia pure red cell
|
|
D012010||aplasias erythrocyte
|
|
D012010||aplasias pure red cell
|
|
D012010||erythrocyte aplasia
|
|
D012010||erythrocyte aplasias
|
|
D012010||pure red cell aplasia
|
|
D012010||pure red cell aplasias
|
|
D012010||red cell aplasias pure
|
|
C567877|612877||cardiomyopathy dilated 1bb
|
|
C567877|612877||cmd1bb
|
|
C563212|608611||ribose 5 phosphate isomerase deficiency
|
|
D013342||stuttering
|
|
D013342||acquired stuttering
|
|
D013342||adult stuttering
|
|
D013342||childhood stuttering
|
|
D013342||developmental stuttering
|
|
D013342||stuttering acquired
|
|
D013342||stuttering adult
|
|
D013342||stuttering childhood
|
|
D013342||stuttering developmental
|
|
C536368||angiosarcoma of the breast
|
|
C536368||breast angiosarcoma
|
|
C536369||angiostrongyliasis
|
|
C536369||abdominal angiostrongyliasis
|
|
C536369||intravitreal angiostrongyliasis
|
|
D013345||subarachnoid hemorrhage
|
|
D013345||aneurysmal subarachnoid hemorrhage
|
|
D013345||aneurysmal subarachnoid hemorrhages
|
|
D013345||hemorrhage aneurysmal subarachnoid
|
|
D013345||hemorrhage intracranial subarachnoid
|
|
D013345||hemorrhage perinatal subarachnoid
|
|
D013345||hemorrhages aneurysmal subarachnoid
|
|
D013345||hemorrhages intracranial subarachnoid
|
|
D013345||hemorrhages perinatal subarachnoid
|
|
D013345||hemorrhage spontaneous subarachnoid
|
|
D013345||hemorrhages spontaneous subarachnoid
|
|
D013345||hemorrhages subarachnoid
|
|
D013345||hemorrhage subarachnoid
|
|
D013345||intracranial subarachnoid hemorrhage
|
|
D013345||intracranial subarachnoid hemorrhages
|
|
D013345||perinatal subarachnoid hemorrhage
|
|
D013345||perinatal subarachnoid hemorrhages
|
|
D013345||sahs subarachnoid hemorrhage
|
|
D013345||sah subarachnoid hemorrhage
|
|
D013345||spontaneous subarachnoid hemorrhage
|
|
D013345||spontaneous subarachnoid hemorrhages
|
|
D013345||subarachnoid hemorrhage aneurysmal
|
|
D013345||subarachnoid hemorrhage intracranial
|
|
D013345||subarachnoid hemorrhage perinatal
|
|
D013345||subarachnoid hemorrhages
|
|
D013345||subarachnoid hemorrhages aneurysmal
|
|
D013345||subarachnoid hemorrhages intracranial
|
|
D013345||subarachnoid hemorrhages perinatal
|
|
D013345||subarachnoid hemorrhage spontaneous
|
|
D013345||subarachnoid hemorrhages spontaneous
|
|
C562790|143870||hypercalciuria absorptive 2
|
|
C562790|143870||hca2
|
|
C562790|143870||hypercalciuria familial idiopathic
|
|
D013344||subacute sclerosing panencephalitis
|
|
D013344||encephaltis inclusion body measles
|
|
D013344||inclusion body encephalitis measles
|
|
D013344||leukoencephalitides subacute sclerosing
|
|
D013344||leukoencephalitis subacute sclerosing
|
|
D013344||leukoencephalitis van bogaert
|
|
D013344||leukoencephalitis van bogaerts
|
|
D013344||leukoencephalitis van bogaert apos s
|
|
D013344||measles inclusion body encephalitis
|
|
D013344||panencephalitides subacute sclerosing
|
|
D013344||panencephalitis subacute sclerosing
|
|
D013344||sclerosing leukoencephalitides subacute
|
|
D013344||sclerosing leukoencephalitis subacute
|
|
D013344||sclerosing panencephalitides subacute
|
|
D013344||sclerosing panencephalitis subacute
|
|
D013344||sspe
|
|
D013344||subacute sclerosing leukoencephalitides
|
|
D013344||subacute sclerosing leukoencephalitis
|
|
D013344||subacute sclerosing panencephalitides
|
|
D013344||van bogaert leukoencephalitis
|
|
D013344||van bogaert apos s leukoencephalitis
|
|
D013344||van bogaerts leukoencephalitis
|
|
D000007||abdominal injuries
|
|
D000007||abdominal injury
|
|
D000007||injuries abdominal
|
|
D000007||injury abdominal
|
|
611095|C567014||mental retardation autosomal recessive 9
|
|
611095|C567014||mental retardation autosomal recessive 26
|
|
611095|C567014||mrt26
|
|
611095|C567014||mrt9
|
|
D000006||abdomen acute
|
|
D000006||abdomens acute
|
|
D000006||acute abdomen
|
|
D000006||acute abdomens
|
|
178500|D054990||idiopathic pulmonary fibrosis
|
|
178500|D054990||cryptogenic fibrosing alveolitides
|
|
178500|D054990||cryptogenic fibrosing alveolitis
|
|
178500|D054990||disease hamman rich
|
|
178500|D054990||diseases hamman rich
|
|
178500|D054990||dysplasia fibrocystic pulmonary
|
|
178500|D054990||dysplasias fibrocystic pulmonary
|
|
178500|D054990||familial idiopathic pulmonary fibrosis
|
|
178500|D054990||fibrocystic pulmonary dysplasia
|
|
178500|D054990||fibrocystic pulmonary dysplasias
|
|
178500|D054990||fibrosing alveolitides cryptogenic
|
|
178500|D054990||fibrosing alveolitis cryptogenic
|
|
178500|D054990||hamman rich disease
|
|
178500|D054990||hamman rich diseases
|
|
178500|D054990||idiopathic fibrosing alveolitis chronic form
|
|
178500|D054990||idiopathic pulmonary fibroses
|
|
178500|D054990||idiopathic pulmonary fibrosis familial
|
|
178500|D054990||interstitial pneumonias usual
|
|
178500|D054990||interstitial pneumonia usual
|
|
178500|D054990||interstitial pneumonitides usual
|
|
178500|D054990||interstitial pneumonitis usual
|
|
178500|D054990||interstitial pneumonitis usual uip hamman rich disease included
|
|
178500|D054990||ipf
|
|
178500|D054990||pneumonitides usual interstitial
|
|
178500|D054990||pneumonitis usual interstitial
|
|
178500|D054990||pulmonary dysplasia fibrocystic
|
|
178500|D054990||pulmonary dysplasias fibrocystic
|
|
178500|D054990||pulmonary fibroses idiopathic
|
|
178500|D054990||pulmonary fibrosis idiopathic
|
|
178500|D054990||usual interstitial pneumonia
|
|
178500|D054990||usual interstitial pneumonias
|
|
178500|D054990||usual interstitial pneumonitides
|
|
178500|D054990||usual interstitial pneumonitis
|
|
C566915|611561||meckel syndrome type 5
|
|
C566915|611561||mks5
|
|
C536301||parvovirus antenatal infection
|
|
C536301||maternofetal infection by parvovirus
|
|
C536301||parvovirus b19 antenatal infection
|
|
C537632||bixler christian gorlin syndrome
|
|
C537632||hmc syndrome
|
|
C537632||hypertelorism microtia facial clefting syndrome
|
|
300799||mental retardation x linked syndromic raymond type
|
|
300799||mrxsr
|
|
D000008||abdominal neoplasms
|
|
D000008||abdominal neoplasm
|
|
D000008||neoplasm abdominal
|
|
D000008||neoplasms abdominal
|
|
C537630||birdshot chorioretinopathy
|
|
C563921||congenital corneal opacities cornea guttata and corectopia
|
|
C563921||corneal opacities congenital with cornea guttata and corectopia
|
|
185900|C566096||syndactyly type i
|
|
185900|C566096||chromosome 2q35 duplication syndrome
|
|
185900|C566096||sd1
|
|
185900|C566096||sdty1
|
|
185900|C566096||zygodactyly
|
|
185900|C566096||zygodactyly craniosynostosis philadelphia type included
|
|
C563920||alopecia universalis congenita xy gonadal dysgenesis and laryngomalacia
|
|
D014647||varicose ulcer
|
|
D014647||hypertension ulcers venous
|
|
D014647||hypertension ulcer venous
|
|
D014647||stasis ulcer
|
|
D014647||stasis ulcers
|
|
D014647||stasis ulcers venous
|
|
D014647||stasis ulcer venous
|
|
D014647||ulcers stasis
|
|
D014647||ulcer stasis
|
|
D014647||ulcers varicose
|
|
D014647||ulcers venous
|
|
D014647||ulcers venous hypertension
|
|
D014647||ulcers venous stasis
|
|
D014647||ulcer varicose
|
|
D014647||ulcer venous
|
|
D014647||ulcer venous hypertension
|
|
D014647||ulcer venous stasis
|
|
D014647||varicose ulcers
|
|
D014647||venous hypertension ulcer
|
|
D014647||venous hypertension ulcers
|
|
D014647||venous stasis ulcer
|
|
D014647||venous stasis ulcers
|
|
D014647||venous ulcer
|
|
D014647||venous ulcers
|
|
D014646||varicocele
|
|
D014646||varicoceles
|
|
D052880||pyomyositis
|
|
D052880||myositis tropical
|
|
D052880||tropical myositis
|
|
D013319||strongyle infections equine
|
|
D013319||equine strongyle infection
|
|
D013319||equine strongyle infections
|
|
D013319||equine strongyloses
|
|
D013319||equine strongylosis
|
|
D013319||infection equine strongyle
|
|
D013319||infections equine strongyle
|
|
D013319||strongyle infection equine
|
|
D013319||strongyloses equine
|
|
D013319||strongylosis equine
|
|
C538617|188025||thrombocytopenia paris trousseau type
|
|
C538617|188025||chromosome 11q23 deletion syndrome
|
|
C538617|188025||tcpt
|
|
C537625||gurrieri sammito bellussi syndrome
|
|
C537625||gurrieri syndrome
|
|
C537625||skeletal dysplasia epilepsy short stature
|
|
D051556||hyperbilirubinemia neonatal
|
|
D051556||direct hyperbilirubinemia neonatal
|
|
D051556||during infancies hyperbilirubinemia
|
|
D051556||hyperbilirubinemia during infancy
|
|
D051556||hyperbilirubinemia neonatal direct
|
|
D051556||hyperbilirubinemia neonatal indirect
|
|
D051556||indirect hyperbilirubinemia neonatal
|
|
D051556||infancy hyperbilirubinemia during
|
|
D051556||neonatal direct hyperbilirubinemia
|
|
D051556||neonatal hyperbilirubinemia
|
|
D051556||neonatal indirect hyperbilirubinemia
|
|
C537628||hair defect with photosensitivity and mental retardation
|
|
C537628||calderon gonzalez cantu syndrome
|
|
C537628||kinky hair photosensitivity broken eyebrows and eyelashes and nonprogressive mental retardation
|
|
D039941||bifidobacteriales infections
|
|
D039941||bifidobacteriales infection
|
|
D039941||infection bifidobacteriales
|
|
D039941||infections bifidobacteriales
|
|
D013313||stress disorders post traumatic
|
|
D013313||acute post traumatic stress disorder
|
|
D013313||chronic post traumatic stress disorder
|
|
D013313||delayed onset post traumatic stress disorder
|
|
D013313||neuroses posttraumatic
|
|
D013313||neuroses post traumatic
|
|
D013313||posttraumatic neuroses
|
|
D013313||post traumatic neuroses
|
|
D013313||posttraumatic stress disorder
|
|
D013313||post traumatic stress disorder
|
|
D013313||posttraumatic stress disorders
|
|
D013313||post traumatic stress disorders
|
|
D013313||ptsd
|
|
D013313||stress disorder posttraumatic
|
|
D013313||stress disorder post traumatic
|
|
D013313||stress disorders posttraumatic
|
|
C537629||hair an syndrome
|
|
C537629||hyperandrogenic insulin resistant acanthosis nigricans syndrome
|
|
C537629||hyperandrogenism ha insulin resistance ir and acanthosis nigricans an
|
|
C537626||hagemoser weinstein bresnick syndrome
|
|
C537626||optic atrophy deafness and peripheral neuropathy
|
|
C537626||optic atrophy hearing loss and peripheral neuropathy
|
|
D000016||abnormalities radiation induced
|
|
D000016||abnormality radiation induced
|
|
D000016||radiation induced abnormalities
|
|
D000016||radiation induced abnormality
|
|
D049248||decapitation
|
|
D049248||decapitations
|
|
D000015||abnormalities multiple
|
|
D000015||multiple abnormalities
|
|
C536311||patterson stevenson syndrome
|
|
C536311||patterson stevenson fontaine syndrome
|
|
C536311||split foot deformity with ectrodactyly and mandibulofacial dysostosis
|
|
C536311||split foot deformity with mandibulofacial dysostosis
|
|
C536311||tpt and psd syndrome
|
|
C536311||triphalangeal thumb polydactyly syndrome
|
|
C536311||triphalangeal thumb polysyndactyly syndrome
|
|
C536311||triphalangeal thumb with polysyndactyly
|
|
C537642||chromosome 4 partial trisomy distal 4q
|
|
C537642||chromosome 4 partial trisomy 4 q25 qter
|
|
C537642||chromosome 4 partial trisomy 4 q26 or q27 qter
|
|
C537642||chromosome 4 partial trisomy 4 q31 or 32 qter
|
|
C536312||juvenile pauciarticular chronic arthritis
|
|
C536312||pauciarticular chronic arthritis
|
|
C537643||duplication 4p syndrome
|
|
C537643||chromosome 4 partial trisomy 4p
|
|
C537643||chromosome 4 trisomy 4p
|
|
C537643||duplication 4p
|
|
C537640||chromosome 4 monosomy 4q32
|
|
C537640||deletion 4q32
|
|
C537640||monosomy 4q32
|
|
C536310||patterson pseudoleprechaunism syndrome
|
|
C536310||patterson apos s leprechaunoid syndrome
|
|
C537641||chromosome 4 4q terminal deletion syndrome
|
|
C537641||chromosome 4 deletion 4q31 qter syndrome
|
|
C537641||chromosome 4 deletion 4q32 qter syndrome
|
|
C537641||chromosome 4 deletion 4q33 qter syndrome
|
|
C537641||chromosome 4 monosomy distal 4q
|
|
C537641||chromosome 4 partial monosomy of distal 4q
|
|
C563938||obesity hyperphagia and developmental delay
|
|
D000014||abnormalities drug induced
|
|
D000014||abnormality drug induced
|
|
D000014||drug induced abnormalities
|
|
D000014||drug induced abnormality
|
|
C562606||nephrosialidosis
|
|
C567383|612245||inflammatory bowel disease 14
|
|
C567383|612245||ibd14
|
|
C563937||arterial dissection with lentiginosis
|
|
D000013||congenital abnormalities
|
|
D000013||abnormalities congenital
|
|
D000013||abnormality congenital
|
|
D000013||birth defect
|
|
D000013||birth defects
|
|
D000013||congenital abnormality
|
|
D000013||congenital defect
|
|
D000013||congenital defects
|
|
D000013||defect birth
|
|
D000013||defect congenital
|
|
D000013||defects birth
|
|
D000013||defects congenital
|
|
D000013||deformities
|
|
D000013||deformity
|
|
C567380|612259||inflammatory bowel disease 16
|
|
C567380|612259||ibd16
|
|
C563936||cleft palate cardiac defect genital anomalies and ectrodactyly
|
|
C563936||acrocardiofacial syndrome
|
|
C563935||hemolytic anemia lethal congenital nonspherocytic with genital and other abnormalities
|
|
D001342||autonomic nervous system diseases
|
|
D001342||ans autonomic nervous system diseases
|
|
D001342||ans disease
|
|
D001342||ans diseases
|
|
D001342||autonomic central nervous system diseases
|
|
D001342||autonomic disease
|
|
D001342||autonomic diseases
|
|
D001342||autonomic dysfunction segmental
|
|
D001342||autonomic dysfunctions segmental
|
|
D001342||autonomic nervous system disorders
|
|
D001342||autonomic peripheral nervous system diseases
|
|
D001342||central autonomic nervous system diseases
|
|
D001342||disorders of the autonomic nervous system
|
|
D001342||nervous system diseases autonomic
|
|
D001342||nervous system diseases parasympathetic
|
|
D001342||nervous system diseases sympathetic
|
|
D001342||parasympathetic nervous system diseases
|
|
D001342||peripheral autonomic nervous system diseases
|
|
D001342||segmental autonomic dysfunction
|
|
D001342||segmental autonomic dysfunctions
|
|
D001342||sympathetic nervous system diseases
|
|
D014657||vasculitis
|
|
D014657||angiitides
|
|
D014657||angiitis
|
|
D014657||vasculitides
|
|
C563939||hirschsprung disease cardiac defects and autonomic dysfunction
|
|
C535754|608779||congenital disorder of glycosylation type 2e
|
|
C535754|608779||cdg2e
|
|
C535754|608779||cdgiie
|
|
C535754|608779||cdg iie
|
|
C535754|608779||congenital disorder of glycosylation type iie
|
|
C564253|608358||myopathy myosin storage
|
|
C564253|608358||myopathy hyaline body autosomal dominant
|
|
C567782|105210||amyloidosis hereditary transthyretin related
|
|
C567782|105210||amyloid cardiomyopathy transthyretin related included
|
|
C567782|105210||amyloid polyneuropathy familial fap amyloidosis leptomeningeal transthyretin related included
|
|
C567782|105210||hereditary amyloidosis transthyretin related
|
|
C567782|105210||transthyretin amyloidosis
|
|
C537635||partial trisomy 3q syndrome
|
|
C537635||chromosome 3 distal 3q2 trisomy
|
|
C537635||chromosome 3 trisomy 3q2
|
|
C537635||partial duplication 3q syndrome
|
|
C536305||patau syndrome
|
|
C536305||bartholin patau syndrome
|
|
C536305||chromosome 13 duplication
|
|
C536305||chromosome 13 trisomy syndrome
|
|
C536305||complete trisomy 13 syndrome
|
|
C536305||patau apos s syndrome
|
|
C536305||trisomy 13
|
|
C536305||trisomy 13 syndrome
|
|
C537636||ring chromosome 4 syndrome
|
|
C537636||ring 4 chromosome
|
|
C536302||pascual castroviejo syndrome
|
|
C536302||hemangiomas and cutaneous and intracranial vascular deformations
|
|
C536303||pashayan syndrome
|
|
C536303||blepharonasofacial malformation syndrome
|
|
C537634||chromosome 3 trisomy 3q13 2 q25
|
|
C537634||duplication 3q13 2 q25
|
|
C537634||trisomy 3q13 2 q25
|
|
C536308||patella hypoplasia mental retardation
|
|
C536308||mental retardation with patellar hypoplasia and luxation
|
|
C537639||chromosome 4q syndrome
|
|
C537639||chromosome 4 long arm deletion
|
|
C537639||chromosome 4 monosomy 4q
|
|
C537639||deletion 4q
|
|
C537639||monosomy 4q
|
|
C536306||patel bixler syndrome
|
|
C536306||alopecia dysplastic nails palmar and plantar hyperkeratosis
|
|
C536306||palmoplantar hyperkeratosis and alopecia
|
|
C537637||chromosome 4 short arm deletion
|
|
C537637||chromosome 4p deletion
|
|
C537637||deletion 4p
|
|
C537637||monosomy 4p
|
|
D014653||vascular headaches
|
|
D014653||cephalgias vascular
|
|
D014653||cephalgia vascular
|
|
D014653||headaches vascular
|
|
D014653||headache vascular
|
|
D014653||vascular cephalgia
|
|
D014653||vascular cephalgias
|
|
D014653||vascular headache
|
|
D013322||strongyloidiasis
|
|
D013322||anguilluliases
|
|
D013322||anguilluliasis
|
|
D013322||strongyloidiases
|
|
C536307||patella aplasia coxa vara tarsal synostosis
|
|
C536307||congenital coxa vara patella aplasia and tarsal synostosis
|
|
C536307||patella aplasia coxa vara and tarsal synostosis
|
|
C537638||chromosome 4 monosomy 4p14 p16
|
|
C537638||deletion 4p14 p16
|
|
C537638||monosomy 4p14 p16
|
|
C567434|612018||cataract juvenile with microcornea and glucosuria
|
|
C567434|612018||cjmg
|
|
D014652||vascular diseases
|
|
D014652||diseases vascular
|
|
D014652||disease vascular
|
|
D014652||vascular disease
|
|
C563960|600318||diabetes mellitus insulin dependent 3
|
|
C563960|600318||iddm3
|
|
C563960|600318||insulin dependent diabetes mellitus 3
|
|
C537650||chromosome 5 trisomy 5q
|
|
C537650||duplication 5q
|
|
C537650||trisomy 5q
|
|
231950|C536836||glutathionuria
|
|
231950|C536836||gamma glutamyltransferase deficiency
|
|
231950|C536836||gamma glutamyltranspeptidase deficiency
|
|
231950|C536836||ggt deficiency
|
|
231950|C536836||gtg deficiency
|
|
D002644||chickenpox
|
|
D002644||chicken pox
|
|
D002644||varicella
|
|
C566178||breast cancer familial male
|
|
C536323||pointer syndrome
|
|
C536323||skeletal abnormalities camptodactyly facial anomalies and feeding difficulties
|
|
C536320||sabinas brittle hair syndrome
|
|
C536320||brittle hair and mental deficit
|
|
C536320||sabinas syndrome
|
|
D002647||chilblains
|
|
D002647||chilblain
|
|
D002647||idiopathic pernioses
|
|
D002647||idiopathic perniosis
|
|
D002647||pernioses
|
|
D002647||pernioses idiopathic
|
|
D002647||perniosis
|
|
D002647||perniosis idiopathic
|
|
C563901||brachial palsy familial congenital
|
|
D002640||chiari frommel syndrome
|
|
D002640||disease frommel
|
|
D002640||disease frommel apos s
|
|
D002640||frommel disease
|
|
D002640||frommel apos s disease
|
|
D002640||syndrome chiari frommel
|
|
C536552|601606||trichoepithelioma multiple familial
|
|
C536552|601606||brooke fordyce trichoepitheliomas
|
|
C536552|601606||eac
|
|
C536552|601606||epithelioma adenoides cysticum of brooke
|
|
C536552|601606||epithelioma hereditary multiple benign cystic
|
|
C536552|601606||hereditary multiple benign cystic epithelioma
|
|
C536552|601606||mft1
|
|
C536552|601606||multiple familial trichoepithelioma
|
|
C536552|601606||trichoepithelioma multiple familial 1
|
|
C563905||ulnar fibular ray defect and brachydactyly
|
|
C563904||cerebrofrontofacial syndrome
|
|
D003970||diastema
|
|
D003970||diastemas
|
|
D014625||vaginal neoplasms
|
|
D014625||cancer of the vagina
|
|
D014625||cancer of vagina
|
|
D014625||cancers vagina
|
|
D014625||cancers vaginal
|
|
D014625||cancer vagina
|
|
D014625||cancer vaginal
|
|
D014625||neoplasms vagina
|
|
D014625||neoplasms vaginal
|
|
D014625||neoplasm vagina
|
|
D014625||neoplasm vaginal
|
|
D014625||vagina cancer
|
|
D014625||vagina cancers
|
|
D014625||vaginal cancer
|
|
D014625||vaginal cancers
|
|
D014625||vaginal neoplasm
|
|
D014625||vagina neoplasm
|
|
D014625||vagina neoplasms
|
|
D055947|609192||loeys dietz syndrome
|
|
D055947|609192||aat5
|
|
D055947|609192|C567156||aortic aneurysm familial thoracic 5
|
|
D055947|609192||lds1
|
|
D055947|609192||loeys dietz aortic aneurysm syndrome
|
|
D055947|609192||loeys dietz syndrome 1
|
|
D055947|609192||loeys dietz syndrome type 1a
|
|
D055947|609192||syndrome loeys dietz
|
|
C564250|608372||deafness autosomal dominant 49
|
|
C564250|608372||dfna49
|
|
D014624||vaginal fistula
|
|
D014624||fistulas vaginal
|
|
D014624||fistula vaginal
|
|
D014624||vaginal fistulas
|
|
C566180||callosities hereditary painful
|
|
C566180||callosities painful plantar
|
|
D014623||vaginal diseases
|
|
D014623||diseases vaginal
|
|
D014623||disease vaginal
|
|
D014623||vaginal disease
|
|
C580477||surfactant dysfunction
|
|
C580477||interstitial lung disease due to surfactant deficiency
|
|
C580477||pulmonary surfactant metabolism dysfunction
|
|
C580477||surfactant metabolism deficiency
|
|
D014627||vaginitis
|
|
D014627||vaginitides
|
|
C536315||pediatric ulcerative colitis
|
|
C536315||ulcerative colitis pediatric
|
|
C537646||chromosome 4 trisomy 4q25 qter
|
|
C537646||duplication 4q25 qter
|
|
C537646||trisomy 4q25 qter
|
|
C580473||succinate coa ligase deficiency
|
|
C580473||mitochondrial dna depletion encephalomyopathic form with methylmalonic aciduria
|
|
C580473||mitochondrial dna depletion syndrome encephalomyopathic form with mild methylmalonic aciduria
|
|
C580473||succinate coenzyme a ligase deficiency
|
|
C566185||heart block nonprogressive
|
|
C537647||chromosome 5 monosomy 5q35
|
|
C537647||deletion 5q35
|
|
C537647||monosomy 5q35
|
|
C566186||cardiac conduction defect nonprogressive
|
|
C536313||pavone fiumara rizzo syndrome
|
|
C536313||syndactyly type 1 with cataracts and mental retardation
|
|
C537644||chromosome 4 trisomy 4q
|
|
C537644||duplication 4q
|
|
C537644||trisomy 4q
|
|
C580471||sebocystomatosis
|
|
C566187||epidermolytic hyperkeratosis late onset
|
|
C537645||chromosome 4 trisomy 4q21
|
|
C537645||duplication 4q21
|
|
C537645||trisomy 4q21
|
|
C580472||stickler syndrome
|
|
C580472||hereditary arthro ophthalmo dystrophy
|
|
C580472||hereditary arthro ophthalmopathy
|
|
C580472||stickler dysplasia
|
|
C566188||branchial myoclonus with spastic paraparesis and cerebellar ataxia
|
|
C536319||pelizaeus merzbacher like disease autosomal recessive 2
|
|
C536319||leukodystrophy hypomyelinating 3
|
|
C536319||perinatal sudanophilic leukodystrophy
|
|
126700|C563034||basal laminar drusen
|
|
126700|C563034||drusen cuticular
|
|
126700|C563034||drusen early adult onset grouped
|
|
126700|C563034||drusen of bruch membrane
|
|
C580470||stargardt macular degeneration
|
|
C580470||stargardt disease
|
|
C566182||calcific aortic disease with immunologic abnormalities familial
|
|
C536317||peho syndrome
|
|
C536317||infantile cerebellooptic atrophy
|
|
C536317||peho like syndrome
|
|
C536317||progressive encephalopathy with edema hypsarrhythmia and optic atrophy
|
|
C537648||chromosome 5 trisomy 5p
|
|
C537648||chromosome 5 trisomy 5p complete 5p11 pter
|
|
C537648||chromosome 5 trisomy 5p partial 5p13 or 14 pter
|
|
C536318||pelizaeus merzbacher like brain sclerosis
|
|
C536318||cerebral sclerosis similar to pelizaeus merzbacher disease
|
|
C537649||chromosome 5 trisomy 5pter p13 3
|
|
C537649||duplication 5pter p13 3
|
|
C537649||trisomy 5pter p13 3
|
|
C566184||prenatal cortical hyperostosis lethal
|
|
D002659||child development disorders pervasive
|
|
D002659||autism spectrum disorder
|
|
D002659||autism spectrum disorders
|
|
D002659||development disorder pervasive
|
|
D002659||development disorders pervasive
|
|
D002659||disorder autism spectrum
|
|
D002659||disorder pervasive development
|
|
D002659||disorders autism spectrum
|
|
D002659||disorders pervasive development
|
|
D002659||pervasive child development disorders
|
|
D002659||pervasive development disorder
|
|
D002659||pervasive development disorders
|
|
D002659||spectrum disorder autism
|
|
D002659||spectrum disorders autism
|
|
C537660||basaran yilmaz syndrome
|
|
C537660||keratoderma hypotrichosis and leukonychia totalis
|
|
D029597|192500||romano ward syndrome
|
|
D029597|192500||long qt syndrome 1
|
|
D029597|192500||long qt syndrome 1 acquired susceptibility to included
|
|
D029597|192500||long qt syndrome type 1
|
|
D029597|192500||lqt1
|
|
D029597|192500||rws
|
|
D029597|192500||syndrome romano ward
|
|
D029597|192500||syndrome ward romano
|
|
D029597|192500||ventricular fibrillation with prolonged qt interval
|
|
D029597|192500||ventricular fibrillation with prolonged qt interval long qt syndrome 1 2 digenic included lqt1 2 digenic included
|
|
D029597|192500||ward romano syndrome
|
|
D029597|192500||wrs
|
|
C565346|191100||tuberous sclerosis 1
|
|
C565346|191100||tsc
|
|
C565346|191100||tsc1
|
|
C564589|607326||smith mccort dysplasia
|
|
C564589|607326||smc
|
|
C564589|607326||smc1
|
|
C564589|607326||smith mccort dysplasia 1
|
|
C537661||bassoe syndrome
|
|
C537664||bazopoulou kyrkanidou syndrome
|
|
C536334||polymorphic catecholergic ventricular tachycardia
|
|
C536334||bidirectional tachycardia induced by catecholamines
|
|
C536334||catecholamine induced polymorphic ventricular tachycardia
|
|
C536334||catecholaminergic polymorphic ventricular tachycardia
|
|
C536334||familial polymorphic ventricular tachycardia
|
|
C536334||stress induced polymorphic ventricular tachycardia
|
|
C536334||ventricular tachycardia catecholaminergic polymorphic 1
|
|
C537665||beardwell syndrome
|
|
C537665||familial ankylosing vertebral hyperostosis with tylosis
|
|
D001329||autolysis
|
|
D001329||autolyses
|
|
C536331||polydactyly myopia syndrome
|
|
C536331||czeizel brooser syndrome
|
|
C536331||polydactyly postaxial with progressive myopia
|
|
C536331||postaxial polydactyly progressive myopia syndrome
|
|
C536331||postaxial polydactyly with progressive myopia
|
|
C537662||battaglia neri syndrome
|
|
C536332||polydactyly preaxial type 1
|
|
C536332||fromont anomaly
|
|
C536332||polydactyly preaxial i
|
|
C536332||thumb polydactyly
|
|
D002658||developmental disabilities
|
|
D002658||child development deviation
|
|
D002658||child development deviations
|
|
D002658||child development disorder
|
|
D002658||child development disorders
|
|
D002658||child development disorders specific
|
|
D002658||developmental delay disorder
|
|
D002658||developmental delay disorders
|
|
D002658||developmental disability
|
|
D002658||development deviation child
|
|
D002658||development deviations child
|
|
D002658||development disorder child
|
|
D002658||development disorders child
|
|
D002658||deviation child development
|
|
D002658||disabilities developmental
|
|
D002658||disability developmental
|
|
D002653||child behavior disorders
|
|
D002653||behavior disorders child
|
|
D002653||disorders child behavior
|
|
C564543|614732||intrauterine growth retardation metaphyseal dysplasia adrenal hypoplasia congenita and genital anomalies
|
|
C564543|614732||adrenal hypoplasia cytomegalic type
|
|
C564543|614732||image syndrome
|
|
256840|C564948||neuropathy hereditary sensory with spastic paraplegia autosomal recessive
|
|
311000|C564087||ophthalmoplegia external and myopia
|
|
311000|C564087||myopia ophthalmoplegia syndrome
|
|
311000|C564087||opem
|
|
C535962|131950||epidermolysis bullosa simplex ogna type
|
|
C535962|131950||ebs og
|
|
C535962|131950||epidermolysis bullosa simplex 1
|
|
C537126|610708||optic atrophy 5
|
|
C537126|610708||opa5
|
|
D012859|270150||sjogren apos s syndrome
|
|
D012859|270150||sicca syndrome
|
|
D012859|270150||sjogrens syndrome
|
|
D012859|270150||sjogren syndrome
|
|
D012859|270150||syndrome sicca
|
|
D012859|270150||syndrome sjogren apos s
|
|
C536326||polycystic kidney disease type 1
|
|
C537657||basal ganglia calcification idiopathic 2
|
|
C536200|225320||ehlers danlos syndrome cardiac valvular form
|
|
C536200|225320||cardiac valvular form of autosomal recessive ehlers danlos syndrome
|
|
C536200|225320||cardiac valvular form of ehlers danlos syndrome
|
|
C536200|225320||ehlers danlos syndrome arthrochalasis type
|
|
C536200|225320||ehlers danlos syndrome autosomal recessive cardiac valvular form
|
|
C536324||polycystic bone disease
|
|
C537655||basal cell carcinoma infundibulocystic
|
|
C537655||basal cell carcinoma with follicular differentiation
|
|
C537655||infundibulocystic basal cell carcinoma
|
|
C537656||basal cell carcinoma multiple
|
|
C537656||multiple basal cell carcinoma
|
|
C566192||brachydactyly nystagmus cerebellar ataxia
|
|
C566193||brachydactyly type e with atrial septal defect type ii
|
|
C537659||basan syndrome
|
|
C537659||ectodermal dysplasia absent dermatoglyphics
|
|
C566194|113300||brachydactyly type e
|
|
194090|C565991||wilms tumor 3
|
|
194090|C565991||wt3
|
|
300752||protoporphyria erythropoietic x linked
|
|
300752|C567464||erythrohepatic protoporphyria x linked
|
|
300752|C567464||protoporphyria erythropoietic x linked dominant
|
|
300752||xldpp
|
|
300752||xlepp
|
|
C566156||cataract nuclear total
|
|
C567487||thrombocytopenia 3
|
|
C567487||thrombocytopenia autosomal recessive 3
|
|
613690||cardiomyopathy familial hypertrophic 7
|
|
613690||cmh7
|
|
C567307|612446||complement component 6 deficiency
|
|
C567307|612446||c6d
|
|
C567307|612446||c6 deficiency
|
|
C567307|612446||complement c6 deficiency
|
|
C567307|612446||c6 deficiency complement component 6 deficiency subtotal included
|
|
C567307|612446||c6 deficiency subtotal included
|
|
C536629|242900||schimke immunoosseous dysplasia
|
|
C536629|242900||immunoosseous dysplasia schimke type
|
|
C536629|242900||schimke immuno osseous dysplasia
|
|
C536629|242900||siod
|
|
D014604||uveal neoplasms
|
|
D014604||neoplasms uveal
|
|
D014604||neoplasm uveal
|
|
D014604||uveal neoplasm
|
|
D014603||uveal diseases
|
|
D014603||diseases uveal
|
|
D014603||disease uveal
|
|
D014603||uveal disease
|
|
C580457||spastic paraplegia type 7
|
|
C580457||hereditary spastic paraplegia paraplegin type
|
|
C580457||spastic paraplegia 7
|
|
C580458||spastic paraplegia type 8
|
|
C580458||autosomal dominant spastic paraplegia 8
|
|
C580458||hereditary spastic paraplegia 8
|
|
C580458||spastic paraplegia 8
|
|
C580458||spg 8
|
|
C580455||spastic paraplegia type 3a
|
|
C580455||spastic paraplegia 3
|
|
C580455||spastic paraplegia 3a
|
|
D014608||uveoparotid fever
|
|
D014608||fevers uveoparotid
|
|
D014608||fever uveoparotid
|
|
D014608||heerfordt syndrome
|
|
D014608||syndrome heerfordt
|
|
D014608||uveoparotid fevers
|
|
D014608||uveoparotitides
|
|
D014608||uveoparotitis
|
|
C580456||spastic paraplegia type 4
|
|
C580456||spastic paraplegia 4
|
|
D014607||uveomeningoencephalitic syndrome
|
|
D014607||disease vogt koyanagi harada
|
|
D014607||syndrome uveomeningoencephalitic
|
|
D014607||syndrome vkh
|
|
D014607||syndrome vkh vogt koyanagi harada
|
|
D014607||syndrome vogt koyanagi harada
|
|
D014607||uveomeningoencephalitides
|
|
D014607||uveomeningoencephalitis
|
|
D014607||vkh syndrome
|
|
D014607||vkh syndrome vogt koyanagi harada
|
|
D014607||vkh vogt koyanagi harada syndrome
|
|
D014607||vogt koyanagi harada disease
|
|
D014607||vogt koyanagi harada syndrome
|
|
C580453||spastic paraplegia type 11
|
|
C580453||autosomal recessive spastic paraplegia complicated with thin corpus callosum
|
|
C580453||autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
|
|
C580453||spg11 related hereditary spastic paraplegia with thin corpus callosum
|
|
D014606||uveitis anterior
|
|
D014606||anterior uveitides
|
|
D014606||anterior uveitis
|
|
D014606||uveitides anterior
|
|
612362||body mass index quantitative trait locus 12
|
|
612362||bmiq12
|
|
D014605||uveitis
|
|
D014605||uveitides
|
|
C567494||hyperphenylalaninemia non pku mild
|
|
C567491||renal tubular dysgenesis with choanal atresia and athelia
|
|
C567490||diarrhea 3 secretory sodium congenital syndromic
|
|
C566160||cataract floriform
|
|
C567493||hyperphenylalaninemia bh4 deficient due to partial pts deficiency
|
|
C566161||cataract crystalline coralliform
|
|
C566162|115700||cataract crystalline aculeiform
|
|
C566162||cataract aculeiform
|
|
D002637||chest pain
|
|
D002637||chest pains
|
|
D002637||pain chest
|
|
D002637||pains chest
|
|
D003968||diarrhea infantile
|
|
D003968||diarrheas infantile
|
|
D003968||infantile diarrhea
|
|
D003968||infantile diarrheas
|
|
D001304||auditory diseases central
|
|
D001304||auditory cortex disorder
|
|
D001304||auditory cortex disorders
|
|
D001304||auditory disease central
|
|
D001304||auditory dysfunction central
|
|
D001304||auditory pathway disorders central
|
|
D001304||central auditory disease
|
|
D001304||central auditory diseases
|
|
D001304||central auditory dysfunction
|
|
D001304||central auditory pathway disorders
|
|
D001304||cortex disorder auditory
|
|
D001304||cortex disorders auditory
|
|
D001304||dysfunction central auditory
|
|
D001304||dysfunctions central auditory
|
|
D006457|300818||hemoglobinuria paroxysmal
|
|
D006457|300818||cold paroxysmal hemoglobinuria
|
|
D006457|300818||hemoglobinuria cold paroxysmal
|
|
D006457|300818||hemoglobinuria nocturnal paroxysmal
|
|
D006457|300818||hemoglobinuria paroxysmal cold
|
|
D006457|300818||hemoglobinuria paroxysmal nocturnal
|
|
D006457|300818||marchiafava micheli syndrome
|
|
D006457|300818||nocturnal paroxysmal hemoglobinuria
|
|
D006457|300818||paroxysmal cold hemoglobinuria
|
|
D006457|300818||paroxysmal hemoglobinuria
|
|
D006457|300818||paroxysmal hemoglobinuria cold
|
|
D006457|300818||paroxysmal hemoglobinuria nocturnal
|
|
D006457|300818||paroxysmal nocturnal hemoglobinuria
|
|
D006457|300818||paroxysmal nocturnal hemoglobinuria 1
|
|
D006457|300818||pnh1
|
|
D006457|300818||syndrome marchiafava micheli
|
|
D003969||vipoma
|
|
D003969||cholera pancreatic
|
|
D003969||diarrheogenic islet cell tumor
|
|
D003969||diarrheogenic tumor
|
|
D003969||diarrheogenic tumors
|
|
D003969||pancreatic cholera
|
|
D003969||pancreatic vipoma
|
|
D003969||pancreatic vipomas
|
|
D003969||syndrome verner morrison
|
|
D003969||syndrome vipoma
|
|
D003969||tumor diarrheogenic
|
|
D003969||tumors diarrheogenic
|
|
D003969||tumors vip secreting vipoma
|
|
D003969||tumor vip secreting vipoma
|
|
D003969||vasoactive intestinal peptide producing tumor
|
|
D003969||vasoactive intestinal peptide vip tumor
|
|
D003969||verner morrison syndrome
|
|
D003969||vipoma pancreatic
|
|
D003969||vipomas
|
|
D003969||vipomas pancreatic
|
|
D003969||vipoma syndrome
|
|
D003969||vip secreting tumors vipoma
|
|
D003969||vip secreting tumor vipoma
|
|
D003969||watery diarrhea hypokalemia and achlorhydria syndrome
|
|
D003969||watery diarrhea syndrome
|
|
D003969||watery diarrhea with hypokalemic alkalosis
|
|
D003969||wdha
|
|
D003969||wdha syndrome
|
|
D003969||wdha syndromes
|
|
D003969||wdhh
|
|
C537913|609441||chondrodysplasia acromesomelic with genital anomalies
|
|
D002639||cheyne stokes respiration
|
|
D002639||respiration cheyne stokes
|
|
D001308||auditory perceptual disorders
|
|
D001308||acoustic perceptual disorder
|
|
D001308||acoustic perceptual disorders
|
|
D001308||auditory comprehension disorder
|
|
D001308||auditory comprehension disorders
|
|
D001308||auditory inattention
|
|
D001308||auditory inattentions
|
|
D001308||auditory perceptual disorder
|
|
D001308||auditory processing disorder
|
|
D001308||auditory processing disorders
|
|
D001308||comprehension disorder auditory
|
|
D001308||comprehension disorders auditory
|
|
D001308||disorder acoustic perceptual
|
|
D001308||disorder auditory comprehension
|
|
D001308||disorder auditory processing
|
|
D001308||disorder psychoacoustical
|
|
D001308||disorders acoustic perceptual
|
|
D001308||disorders auditory comprehension
|
|
D001308||disorders auditory processing
|
|
D001308||disorders psychoacoustical
|
|
D001308||inattention auditory
|
|
D001308||inattentions auditory
|
|
D001308||perceptual disorder acoustic
|
|
D001308||perceptual disorder auditory
|
|
D001308||perceptual disorders acoustic
|
|
D001308||perceptual disorders auditory
|
|
D001308||processing disorder auditory
|
|
D001308||processing disorders auditory
|
|
D001308||psychoacoustical disorder
|
|
D001308||psychoacoustical disorders
|
|
D003965||diaphragmatic eventration
|
|
D003965||diaphragm eventration
|
|
D003965||eventration diaphragmatic
|
|
D003965||eventration of diaphragm
|
|
613680||beaulieu boycott innes syndrome
|
|
613680||bbis
|
|
613680||microcephaly mental retardation and distinctive facies with cardiac and genitourinary malformations
|
|
D049288||muscular dystrophies limb girdle
|
|
D049288||limb girdle muscular dystrophies
|
|
D049288||limb girdle muscular dystrophy
|
|
D049288||limb girdle syndrome
|
|
D049288||muscular dystrophy limb girdle
|
|
D049288||myopathic limb girdle syndrome
|
|
D003967||diarrhea
|
|
D003967||diarrheas
|
|
D003963||diaper rash
|
|
D003963||diaper rashes
|
|
D003963||rash diaper
|
|
D003963||rashes diaper
|
|
613685||deafness autosomal recessive 83
|
|
613685||dfnb83
|
|
613686||spondylocostal dysostosis 4 autosomal recessive
|
|
613686||scdo4
|
|
C563723|609408||holoprosencephaly 8
|
|
C563723|609408||hpe8
|
|
612348||thrombophilia familial due to decreased release of tissue plasminogen activator thph9 hyperfibrinolysis familial due to increased release of tissue plasminogen
|
|
612348||activator included
|
|
613689||mammary digital nail syndrome
|
|
613689||mdns
|
|
613679||prothrombin deficiency congenital
|
|
613679||hypoprothrombinemia dysprothrombinemia included
|
|
D014615||vaccinia
|
|
D014615||vaccinias
|
|
C563575|157640||progressive external ophthalmoplegia with mitochondrial dna deletions autosomal dominant 1
|
|
C563575|157640||peoa1
|
|
C563575|157640||progressive external ophthalmoplegia autosomal dominant 1
|
|
611022|C567027||deafness autosomal recessive 24
|
|
611022|C567027||dfnb24
|
|
612353||porokeratosis 6 disseminated superficial actinic type
|
|
612353||dsap4
|
|
612353||porok6
|
|
167750|C536376||annular pancreas
|
|
167750|C536376||pancreas annular
|
|
C566175||carabelli anomaly of maxillary molar teeth
|
|
C566176||car factor deficiency
|
|
C563700|609549||nanophthalmos 2
|
|
C563700|609549||nanophthalmia 2
|
|
C563700|609549||nanophthalmos autosomal recessive
|
|
C563700|609549||nno2
|
|
D049292||leukoaraiosis
|
|
D049292||leukoaraioses
|
|
D049291||seroma
|
|
D049291||seromas
|
|
C566172||familial sudden death
|
|
C566173||monocyte esterase deficiency
|
|
C566173||monocyte carboxylesterase deficiency
|
|
D018198||mixed tumor malignant
|
|
D018198||malignant mixed tumor
|
|
D018198||malignant mixed tumors
|
|
D018198||mixed tumors malignant
|
|
D018198||tumor malignant mixed
|
|
D018198||tumors malignant mixed
|
|
D018197||hepatoblastoma
|
|
D018197||hepatoblastomas
|
|
D018199||mixed tumor mesodermal
|
|
D018199||mesodermal mixed tumor
|
|
D018199||mesodermal mixed tumors
|
|
D018199||mixed tumors mesodermal
|
|
D018199||tumor mesodermal mixed
|
|
D018199||tumors mesodermal mixed
|
|
D010033|166760||otitis media
|
|
D010033|166760||come rom
|
|
D010033|166760||inflammation middle ear
|
|
D010033|166760||middle ear inflammation
|
|
D010033|166760||oms
|
|
D010033|166760||otitis media chronic recurrent
|
|
D010033|166760||otitis media susceptibility to
|
|
216950||complement component c1r c1s deficiency
|
|
216950||c1r c1s deficiency
|
|
D018194||adenomyoma
|
|
D018194||adenomyomas
|
|
D018193||neoplasms complex and mixed
|
|
D018193||complex and mixed neoplasms
|
|
D002601||chancre
|
|
D002601||chancres
|
|
C537610||rhizomelic dysplasia scoliosis and retinitis pigmentosa
|
|
D018196||carcinoma adenosquamous
|
|
D018196||adenosquamous carcinoma
|
|
D018196||adenosquamous carcinomas
|
|
D018196||carcinomas adenosquamous
|
|
D002602||chancroid
|
|
D002602||chancroids
|
|
D018195||adenosarcoma
|
|
D018195||adenosarcomas
|
|
613670||mental retardation with language impairment and autistic features
|
|
C566137||charcot marie tooth disease guadalajara neuronal type
|
|
D018190||lymphatic vessel tumors
|
|
D018190||lymphatic vessel tumor
|
|
D018190||tumor lymphatic vessel
|
|
D018190||tumors lymphatic vessel
|
|
613671||mental retardation anterior maxillary protrusion and strabismus
|
|
613671||mrams
|
|
613672||spastic ataxia 4 autosomal recessive
|
|
613672||spax4
|
|
D018191||lymphangioma cystic
|
|
D018191||colli cystic hygroma
|
|
D018191||cystic hygroma
|
|
D018191||cystic hygroma colli
|
|
D018191||cystic hygromas
|
|
D018191||cystic lymphangioma
|
|
D018191||cystic lymphangiomas
|
|
D018191||hygroma
|
|
D018191||hygroma colli cystic
|
|
D018191||hygroma cystic
|
|
D018191||hygromas
|
|
D018191||hygromas cystic
|
|
D018191||lymphangiomas cystic
|
|
D003930||diabetic retinopathy
|
|
D003930||diabetic retinopathies
|
|
D003930||retinopathies diabetic
|
|
D003930||retinopathy diabetic
|
|
613674||vesicoureteral reflux 3
|
|
613674||vur3
|
|
613676||seckel syndrome 4
|
|
613676||sckl4
|
|
C580439||short qt syndrome
|
|
613668||microcephaly postnatal progressive with seizures and brain atrophy
|
|
C537609||rhizomelic dysplasia patterson lowry type
|
|
C537609||patterson lowry rhizomelic dysplasia
|
|
C537609||patterson lowry syndrome
|
|
C537602||short rib polydactyly syndrome verma naumoff type
|
|
C537602||polydactyly with neonatal chondrodystrophy type 3
|
|
C580430||salih myopathy
|
|
C580430||early onset myopathy with fatal cardiomyopathy
|
|
C580430||salih cmd
|
|
C580430||salih congenital muscular dystrophy
|
|
C537603||short stature and locking fingers
|
|
C566142||cervical hypertrichosis with underlying kyphoscoliosis
|
|
C566142||hypertrichosis posterior cervical with underlying kyphoscoliosis
|
|
C563649|148300||keratoconus 1
|
|
C563649|148300||ktcn1
|
|
C567474||mental retardation x linked syndromic 9
|
|
601696||novelty seeking personality trait
|
|
601696||risk taking behavior included
|
|
C537605||rhabdomyosarcoma of the orbit
|
|
C566140||cervical vertebral dysplasia
|
|
C535608|612952||aicardi goutieres syndrome 5
|
|
C535608|612952||ags5
|
|
C535608|612952||aicardi goutieres syndrome autosomal dominant
|
|
C537620||growth mental deficiency syndrome of myhre
|
|
C537620||laps syndrome
|
|
C537620||laryngotracheal stenosis arthropathy prognathism and short stature
|
|
C537620||myhre syndrome
|
|
C537621||grubben de cock borghgraef syndrome
|
|
D003333|122460||coronaviridae infections
|
|
D003333|122460||coronaviridae infection
|
|
D003333|122460||coronavirus 229e susceptibility
|
|
D003333|122460||cvs
|
|
D003333|122460||hcvs
|
|
D003333|122460||human coronavirus sensitivity
|
|
D003333|122460||infection coronaviridae
|
|
D003333|122460||infections coronaviridae
|
|
D002613||cheilitis
|
|
D002613||cheilitides
|
|
C566147||minicore myopathy moderate with hand involvement
|
|
C566147||multicore myopathy moderate with hand involvement
|
|
C566147||multiminicore disease moderate with hand involvement
|
|
613660||cone rod dystrophy 15
|
|
613660||cord15
|
|
613660||retinitis pigmentosa 65 included
|
|
613660||rp65 included
|
|
613661||congenital disorder of glycosylation type ip
|
|
613661||cdg1p
|
|
D008557|155950||melorheostosis
|
|
D008557|155950||mel
|
|
D008557|155950||melorheostoses
|
|
D008557|155950||melorheostosis isolated
|
|
D008557|155950||melorheostosis of leri
|
|
613662||mitochondrial dna depletion syndrome 4b mngie type
|
|
613662||mitochondrial neurogastrointestinal encephalopathy syndrome polg related
|
|
613662||mngie polg related
|
|
613662||mtdps4b
|
|
C565367|252605||mucolipidosis iii gamma
|
|
C565367|252605||ml iiic
|
|
C565367|252605||ml iii gamma
|
|
C565367|252605||mucolipidosis iiic
|
|
C565367|252605||mucolipidosis iii complementation group c
|
|
C565367|252605||mucolipidosis iii iranian variant form
|
|
C565367|252605||mucolipidosis iii variant form
|
|
D018234|606243||sarcoma alveolar soft part
|
|
D018234|606243||alveolar soft part sarcoma
|
|
D018234|606243||asps
|
|
611523|C548074||pontocerebellar hypoplasia type 6
|
|
611523|C548074||encephalopathy fatal infantile with mitochondrial respiratory chain defects
|
|
611523|C548074||pch6
|
|
612336||thrombophilia due to protein s deficiency autosomal dominant
|
|
612336||thph5
|
|
C565291|605805||dermatitis atopic 4
|
|
C565291|605805||atod4
|
|
613658||rajab syndrome
|
|
613658||developmental delay small stature microcephaly and brain calcifications
|
|
C537619||krieble bixler syndrome
|
|
C537619||autosomal dominant blepharophimosis with multiple congenital anomalies
|
|
C536045|166220||osteogenesis imperfecta type 4
|
|
C536045|166220||oi4
|
|
C536045|166220||oi type iv
|
|
C536045|166220||osteogenesis imperfecta type iv
|
|
C536045|166220||osteogenesis imperfecta with normal sclerae
|
|
607454|C537200||spinocerebellar ataxia 21
|
|
607454|C537200||sca21
|
|
C537955|115660||cerulean cataract
|
|
C537955|115660||cataract 7
|
|
C537955|115660||cataract 7 cerulean type
|
|
C537955|115660||cataract congenital blue dot type 1
|
|
C537955|115660||cataract congenital cerulean type 1
|
|
C537955|115660||cca1
|
|
C537955|115660||ctrct7
|
|
D013285|185100||strabismus
|
|
D013285|185100||comitant strabismus
|
|
D013285|185100||comitant strabismus convergent
|
|
D013285|185100||convergent comitant strabismus
|
|
D013285|185100||hypertropia
|
|
D013285|185100||hypertropias
|
|
D013285|185100||mechanical strabismus
|
|
D013285|185100||noncomitant strabismus
|
|
D013285|185100||phoria
|
|
D013285|185100||phorias
|
|
D013285|185100||squint
|
|
D013285|185100||stbms1 included
|
|
D013285|185100||strabismus comitant
|
|
D013285|185100||strabismus convergent comitant
|
|
D013285|185100||strabismus mechanical
|
|
D013285|185100||strabismus noncomitant
|
|
D013285|185100||strabismus susceptibility to
|
|
D013285|185100||strabismus susceptibility to 1 included
|
|
601682||glaucoma 1 primary open angle c
|
|
601682||glc1c
|
|
C537613||ribbing disease
|
|
C537613||diaphyseal sclerosis multiple
|
|
C537613||hereditary multiple diaphyseal sclerosis
|
|
C537613||multiple diaphyseal sclerosis
|
|
C566152||cavernous malformations of cns and retina
|
|
C537614||kozlowski warren fisher syndrome
|
|
C537614||cloverleaf skull generalised bone dysplasia
|
|
C566153||hyperkeratotic cutaneous capillary venous malformations associated with cerebral capillary malformations
|
|
C563306|601494||cardiomyopathy dilated 1d
|
|
C563306|601494||cmd1d
|
|
C563306|601494||left ventricular noncompaction 6 included
|
|
C563306|601494||lvnc6 included
|
|
C537611||rhizomelic syndrome
|
|
C537611||familial rhizomelic dysplasia
|
|
C537611||rhizomelic dysplasia familial
|
|
C567486||hypercarotenemia and vitamin a deficiency autosomal recessive
|
|
C537612||rhyns syndrome
|
|
C537612||retinitis pigmentosa hypopituitarism nephronophthisis and mild skeletal dysplasia
|
|
C537612||retinitis pigmentosa syndrome
|
|
C537705|147920||kabuki syndrome
|
|
C537705|147920||kabuk1
|
|
C537705|147920||kabuki make up syndrome
|
|
C537705|147920||kabuki makeup syndrome
|
|
C537705|147920||kabuki syndrome 1
|
|
C537705|147920||niikawa kuroki syndrome
|
|
C537618||krauss herman holmes syndrome
|
|
C537618||telecanthus hypertelorism strabismus and pes cavus syndrome
|
|
C537615||kozlowski krajewska syndrome
|
|
C537616||krasnow qazi syndrome
|
|
C537616||krasnow qazi yermakov syndrome
|
|
C566151||celiac artery stenosis from compression by median arcuate ligament of diaphragm
|
|
D018176||torovirus infections
|
|
D018176||infections torovirus
|
|
D018176||infection torovirus
|
|
D018176||torovirus infection
|
|
D018175||birnaviridae infections
|
|
D018175||birnaviridae infection
|
|
D018175||infection birnaviridae
|
|
D018175||infections birnaviridae
|
|
D003914||dextrocardia
|
|
D003914||dextrocardias
|
|
C566117||cluster headache familial
|
|
D018178||flaviviridae infections
|
|
D018178||flaviviridae infection
|
|
D018178||infection flaviviridae
|
|
D018178||infections flaviviridae
|
|
D018177||flavivirus infections
|
|
D018177||flavivirus infection
|
|
D018177||infection flavivirus
|
|
D018177||infections flavivirus
|
|
C566119||cleidocranial dysplasia forme fruste with brachydactyly
|
|
C567444||congenital heart defects x linked
|
|
C567443||ichthyosis x linked complicated
|
|
C566113||progressive encephalomyelitis with rigidity
|
|
D018174||arterivirus infections
|
|
D018174||arterivirus infection
|
|
D018174||infection arterivirus
|
|
D018174||infections arterivirus
|
|
C567446||stevenson carey syndrome
|
|
313900|C564052||thrombocytopenia 1
|
|
313900|C564052||thc
|
|
313900|C564052||thc1
|
|
313900|C564052||thrombocytopenia x linked
|
|
313900|C564052||thrombocytopenia x linked 1
|
|
313900|C564052||thrombocytopenia x linked 1 thrombocytopenia x linked intermittent included
|
|
313900|C564052||x linked thrombocytopenia
|
|
313900|C564052||xlt
|
|
D018173||circoviridae infections
|
|
D018173||circoviridae infection
|
|
D018173||circovirus infection
|
|
D018173||circovirus infections
|
|
D018173||infection circoviridae
|
|
D018173||infection circovirus
|
|
D018173||infections circoviridae
|
|
D018173||infections circovirus
|
|
C567445||hunter macdonald syndrome
|
|
C563686|609919||gallbladder disease 3
|
|
C563686|609919||gbd3
|
|
400044||46 xy sex reversal 1
|
|
400044||46 xy gonadal dysgenesis complete sry related 46 xy true hermaphroditism sry related included
|
|
400044||46 xy sex reversal sry related
|
|
400044||sex reversing locus on x formerly included srvx formerly included
|
|
400044||srxy1
|
|
400044||testis determining factor x chromosomal formerly included tdfx formerly included
|
|
400045||46 xx sex reversal 1
|
|
400045||46 xx sex reversal sry positive
|
|
400045||46 xx testicular disorder of sex development 46 xx true hermaphroditism sry positive included
|
|
400045||ovotesticular disorder of sex development included
|
|
400045||ovotesticular dsd included
|
|
400045||srxx1
|
|
400045||xx male sry positive
|
|
612319||spastic paraplegia 35 autosomal recessive
|
|
612319||fahn
|
|
612319|C580102||fatty acid hydroxylase associated neurodegeneration
|
|
612319||spg35
|
|
400043||deafness y linked 1
|
|
400043||dfny1
|
|
613646||methylmalonic aciduria due to transcobalamin receptor defect
|
|
613646||methylmalonic acidemia tcblr type
|
|
613647||spastic paraplegia 48 autosomal recessive
|
|
613647||spg48
|
|
C566825|168550||parietal foramina with cleidocranial dysplasia
|
|
C566825|168550||cleidocranial dysplasia with parietal foramina
|
|
C566825|168550||pfmccd
|
|
D006192||haemophilus infections
|
|
D006192||haemophilus infection
|
|
D006192||hemophilus infection
|
|
D006192||hemophilus infections
|
|
D006192||infection haemophilus
|
|
D006192||infection hemophilus
|
|
D006192||infections haemophilus
|
|
D006192||infections hemophilus
|
|
C564296|608088||neuropathy hereditary sensory and autonomic type i with cough and gastroesophageal reflux
|
|
C564296|608088||hsan1b
|
|
C564296|608088||hsn1b
|
|
C564296|608088||neuropathy hereditary sensory and autonomic type ib
|
|
C564296|608088||neuropathy hereditary sensory type ib
|
|
601675||trichothiodystrophy photosensitive ttdp ichthyosiform erythroderma with hair abnormality and mental and growth
|
|
601675||ibids syndrome included
|
|
601675||ichthyosis congenital with trichothiodystrophy included
|
|
601675||retardation included
|
|
601675||tay syndrome included
|
|
601675||trichothiodystrophy with congenital ichthyosis included
|
|
C536170|222600||diastrophic dysplasia
|
|
C536170|222600||dd diastrophic dysplasia broad bone platyspondylic variant included
|
|
C536170|222600||diastrophic dwarfism
|
|
C536170|222600||dtd
|
|
194200|D014927||wolff parkinson white syndrome
|
|
194200|D014927||accessory atrioventricular pathways included
|
|
194200|D014927||anomalous ventricular excitation syndrome
|
|
194200|D014927||auriculoventricular accessory pathway syndrome
|
|
194200|D014927||false bundle branch block syndrome
|
|
194200|D014927||syndrome wolff parkinson white
|
|
194200|D014927||syndrome wolf parkinson white
|
|
194200|D014927||syndrome wpw
|
|
194200|D014927||ventricular pre excitation with arrhythmia
|
|
194200|D014927||wolf parkinson white syndrome
|
|
194200|D014927||wpw syndrome
|
|
194200|D014927||wpw syndrome preexcitation syndrome included
|
|
D003919||diabetes insipidus
|
|
C566127||choreoathetosis familial inverted
|
|
C566127||infantile choreoathetosis of fisher
|
|
C563816|608996||premature ovarian failure 3
|
|
C563816|608996||pof3
|
|
D018186||pneumovirus infections
|
|
D018186||infection pneumovirus
|
|
D018186||infections pneumovirus
|
|
D018186||pneumovirus infection
|
|
D003925||diabetic angiopathies
|
|
D003925||angiopathies diabetic
|
|
D003925||angiopathy diabetic
|
|
D003925||diabetic angiopathy
|
|
D003925||diabetic microangiopathies
|
|
D003925||diabetic microangiopathy
|
|
D003925||diabetic vascular complication
|
|
D003925||diabetic vascular complications
|
|
D003925||diabetic vascular disease
|
|
D003925||diabetic vascular diseases
|
|
D003925||microangiopathies diabetic
|
|
D003925||microangiopathy diabetic
|
|
D003925||vascular complication diabetic
|
|
D003925||vascular complications diabetic
|
|
D003925||vascular disease diabetic
|
|
D003925||vascular diseases diabetic
|
|
D003926||diabetic coma
|
|
D003926||coma diabetic
|
|
D003926||comas diabetic
|
|
D003926||diabetic comas
|
|
C566478|610441||testicular microlithiasis
|
|
D018188||cardiovirus infections
|
|
D018188||cardiovirus infection
|
|
D018188||infection cardiovirus
|
|
D018188||infections cardiovirus
|
|
C536867|603563||spastic paraplegia 8 autosomal dominant
|
|
C536867|603563||spg8
|
|
D003920||diabetes mellitus
|
|
C567455||camptodactyly syndrome guadalajara type iii
|
|
180500||rgs
|
|
180500||rieg
|
|
180500||rieg1
|
|
D018182||pestivirus infections
|
|
D018182||infection pestivirus
|
|
D018182||infections pestivirus
|
|
D018182||pestivirus infection
|
|
D003921||diabetes mellitus experimental
|
|
D003921||alloxan diabetes
|
|
D003921||diabetes alloxan
|
|
D003921||diabetes streptozocin
|
|
D003921||diabetes streptozotocin
|
|
D003921||diabete streptozocin
|
|
D003921||experimental diabetes mellitus
|
|
D003921||streptozocin diabete
|
|
D003921||streptozocin diabetes
|
|
D003921||streptozotocin diabetes
|
|
C566124||choroidal osteoma bilateral
|
|
D018185||morbillivirus infections
|
|
D018185||infection morbillivirus
|
|
D018185||infections morbillivirus
|
|
D018185||morbillivirus infection
|
|
C567457||immunodeficiency gonadal dysgenesis and pulmonary fibrosis
|
|
C566125||chromate resistance
|
|
D018184||paramyxoviridae infections
|
|
D018184||infection parainfluenza virus
|
|
D018184||infection paramyxoviridae
|
|
D018184||infections parainfluenza virus
|
|
D018184||infections paramyxoviridae
|
|
D018184||parainfluenza
|
|
D018184||parainfluenza virus infection
|
|
D018184||parainfluenza virus infections
|
|
D018184||paramyxoviridae infection
|
|
D018184||virus infection parainfluenza
|
|
D018184||virus infections parainfluenza
|
|
D007863|136120||lecithin acyltransferase deficiency
|
|
D007863|136120||acyltransferase deficiencies alpha lecithin cholesterol
|
|
D007863|136120||acyltransferase deficiency alpha lecithin cholesterol
|
|
D007863|136120||acyltransferase deficiency lecithin cholesterol
|
|
D007863|136120||alpha lcat deficiency
|
|
D007863|136120||alpha lecithin cholesterol acyltransferase deficiencies
|
|
D007863|136120||alpha lecithin cholesterol acyltransferase deficiency
|
|
D007863|136120||corneal dystrophy dyslipoproteinemic
|
|
D007863|136120||deficiencies alpha lcat
|
|
D007863|136120||deficiencies alpha lecithin cholesterol acyltransferase
|
|
D007863|136120||deficiencies lcata
|
|
D007863|136120||deficiency alpha lcat
|
|
D007863|136120||deficiency alpha lecithin cholesterol acyltransferase
|
|
D007863|136120||deficiency lcat
|
|
D007863|136120||deficiency lecithin acyltransferase
|
|
D007863|136120||deficiency lecithin cholesterol acyltransferase
|
|
D007863|136120||disease fish eye
|
|
D007863|136120||dyslipoproteinemic corneal dystrophy
|
|
D007863|136120||fed
|
|
D007863|136120||fish eye disease
|
|
D007863|136120||lcata deficiencies
|
|
D007863|136120||lcata deficiency
|
|
D007863|136120||lcat deficiency
|
|
D007863|136120||lecithin cholesterol acyltransferase deficiency
|
|
D007863|136120||norum disease
|
|
D003923||diabetes mellitus lipoatrophic
|
|
D003923||diabete lipoatrophic
|
|
D003923||diabetes lipoatrophic
|
|
D003923||lipoatrophic diabete
|
|
D003923|151660|D052496||lipoatrophic diabetes
|
|
D003923||lipoatrophic diabetes mellitus
|
|
C566126||chylomicronemia familial due to circulating inhibitor of lipoprotein lipase
|
|
C566126||hyperlipoproteinemia type ic
|
|
C567635|613345||hypokalemic periodic paralysis type 2
|
|
C567635|613345||hokpp2
|
|
D045724||diverticulosis stomach
|
|
D045724||diverticulosis gastric
|
|
D045724||gastric diverticulosis
|
|
D045724||stomach diverticulosis
|
|
613640||neuropathy hereditary sensory and autonomic type ic
|
|
613640||hsan1c
|
|
613640||hsan ic
|
|
613640||hsn1c
|
|
613640||hsn ic
|
|
613640||neuropathy hereditary sensory type ic
|
|
C563662|610799||invasive pneumococcal disease recurrent isolated 1
|
|
C563662|610799||invasive pneumococcal disease protection against included
|
|
C563662|610799||ipd1
|
|
613641||charcot marie tooth disease recessive intermediate b
|
|
613641||charcot marie tooth neuropathy recessive intermediate b
|
|
613641||cmtrib
|
|
613641||ri cmtb
|
|
D045723||diverticulosis esophageal
|
|
D045723||esophageal diverticulosis
|
|
612306||thyroid stimulating hormone level quantitative trait locus 1
|
|
612306||thyrotropin quantitative trait locus 1
|
|
612306||tshqtl1
|
|
613643||parkinson disease 5 autosomal dominant
|
|
613643||park5
|
|
C567555|612840||leukocyte adhesion deficiency type iii
|
|
C567555|612840||iadd
|
|
C567555|612840||integrin activation deficiency disease
|
|
C567555|612840||lad1v
|
|
C567555|612840||lad3
|
|
C567555|612840||leukocyte adhesion deficiency 1 variant
|
|
C567555|612840||leukocyte adhesion deficiency 3
|
|
612304||thrombophilia due to protein c deficiency autosomal recessive
|
|
612304||thph4
|
|
C580424||ring chromosome 20 syndrome
|
|
C580424||r 20 syndrome
|
|
C580424||ring 20 syndrome
|
|
C580424||ring chromosome 20
|
|
C580424||ring chromosome 20 epilepsy syndrome
|
|
C580420||ren related kidney disease
|
|
C580420||familial juvenile hyperuricemic nephropathy 2
|
|
D045729||pneumonia of swine mycoplasmal
|
|
D045729||enzootic pneumonia of pigs
|
|
D045729||enzootic pneumonia of swine
|
|
D045729||mycoplasmal pneumonia of swine
|
|
D045729||mycoplasma pneumonia of pigs
|
|
D045729||mycoplasma pneumonia of swine
|
|
D045729||pneumonia of swine enzootic
|
|
D045729||swine enzootic pneumonia
|
|
D045729||swine mycoplasmal pneumonia
|
|
D045729||swine mycoplasma pneumonia
|
|
C535764|227200||eunuchoidism familial hypogonadotropic
|
|
C535764|227200||figd
|
|
C535764|227200||gonadotropin deficiency familial idiopathic
|
|
C566130||adrenal insufficiency congenital
|
|
C566131||adrenal insufficiency congenital with 46 xy sex reversal
|
|
C567464||xldpt
|
|
C566132||chlorpropamide alcohol flushing
|
|
C566132||endemic tyrolean infantile cirrhosis
|
|
C566133||chiari malformation type i with syringomyelia
|
|
C566133||cm1 with syringomyelia
|
|
D055847|609310||lynch syndrome ii
|
|
D055847|609310||coca2
|
|
D055847|609310||colon cancer familial nonpolyposis type 2
|
|
D055847|609310||colorectal cancer hereditary nonpolyposis type 2
|
|
D055847|609310||fcc2
|
|
D055847|609310||hnpcc2
|
|
D055847|609310||lynch cancer family syndrome 2
|
|
D055847|609310||lynch cancer family syndrome ii
|
|
D003928||diabetic nephropathies
|
|
D003928||diabetic glomerulosclerosis
|
|
D003928||diabetic kidney disease
|
|
D003928||diabetic kidney diseases
|
|
D003928||diabetic nephropathy
|
|
D003928||glomerulosclerosis diabetic
|
|
D003928||glomerulosclerosis nodular
|
|
D003928||intracapillary glomerulosclerosis
|
|
D003928||kidney disease diabetic
|
|
D003928||kidney diseases diabetic
|
|
D003928||kimmelstiel wilson disease
|
|
D003928||kimmelstiel wilson syndrome
|
|
D003928||nephropathies diabetic
|
|
D003928||nephropathy diabetic
|
|
D003928||nodular glomerulosclerosis
|
|
D003928||syndrome kimmelstiel wilson
|
|
C536860|607584||spastic paraplegia 24
|
|
C536860|607584||spg24
|
|
D003929||diabetic neuropathies
|
|
D003929||amyotrophies diabetic
|
|
D003929||amyotrophy diabetic
|
|
D003929||asymmetric diabetic proximal motor neuropathy
|
|
D003929||asymmetric polyneuropathies diabetic
|
|
D003929||asymmetric polyneuropathy diabetic
|
|
D003929||autonomic neuropathies diabetic
|
|
D003929||autonomic neuropathy diabetic
|
|
D003929||diabetic amyotrophies
|
|
D003929||diabetic amyotrophy
|
|
D003929||diabetic asymmetric polyneuropathies
|
|
D003929||diabetic asymmetric polyneuropathy
|
|
D003929||diabetic autonomic neuropathies
|
|
D003929||diabetic autonomic neuropathy
|
|
D003929||diabetic mononeuropathies
|
|
D003929||diabetic mononeuropathy
|
|
D003929||diabetic mononeuropathy simplex
|
|
D003929||diabetic mononeuropathy simplices
|
|
D003929||diabetic neuralgia
|
|
D003929||diabetic neuralgias
|
|
D003929||diabetic neuropathies painful
|
|
D003929||diabetic neuropathy
|
|
D003929||diabetic neuropathy painful
|
|
D003929||diabetic polyneuropathies
|
|
D003929||diabetic polyneuropathy
|
|
D003929||mononeuropathies diabetic
|
|
D003929||mononeuropathy diabetic
|
|
D003929||mononeuropathy simplex diabetic
|
|
D003929||mononeuropathy simplices diabetic
|
|
D003929||neuralgia diabetic
|
|
D003929||neuralgias diabetic
|
|
D003929||neuropathies diabetic
|
|
D003929||neuropathies diabetic autonomic
|
|
D003929||neuropathies painful diabetic
|
|
D003929||neuropathy diabetic
|
|
D003929||neuropathy diabetic autonomic
|
|
D003929||neuropathy painful diabetic
|
|
D003929||painful diabetic neuropathies
|
|
D003929||painful diabetic neuropathy
|
|
D003929||polyneuropathies diabetic
|
|
D003929||polyneuropathies diabetic asymmetric
|
|
D003929||polyneuropathy diabetic
|
|
D003929||polyneuropathy diabetic asymmetric
|
|
D003929||simplex diabetic mononeuropathy
|
|
D003929||simplices diabetic mononeuropathy
|
|
D003929||symmetric diabetic proximal motor neuropathy
|
|
181800||scoliosis idiopathic susceptibility to 1
|
|
181800||adolescent idiopathic scoliosis
|
|
181800||is1
|
|
613630||cocoon syndrome
|
|
613630||fetal encasement syndrome
|
|
227645||fanconi anemia complementation group c
|
|
227645||fa3
|
|
227645||fac
|
|
227645||facc
|
|
227645||fancc
|
|
227645||fanconi pancytopenia type 3
|
|
C567411|612132||ectodermal dysplasia anhidrotic with t cell immunodeficiency autosomal dominant
|
|
227646||fanconi anemia complementation group d2
|
|
227646||fa4
|
|
227646||facd
|
|
227646||fad2
|
|
227646||fancd
|
|
227646||fancd2
|
|
227646||fanconi anemia complementation group d
|
|
227646||fanconi pancytopenia type 4
|
|
D007499||iris diseases
|
|
D007499||disease iris
|
|
D007499||diseases iris
|
|
D007499||iris disease
|
|
D006177||gynecomastia
|
|
D006177||adolescent gynecomastia
|
|
D006177||breast enlargement male
|
|
D006177||enlargement male breast
|
|
D006177||gynecomastia adolescent
|
|
D006177||gynecomastia infant
|
|
D006177||gynecomastia newborn
|
|
D006177||infant gynecomastia
|
|
D006177||male breast enlargement
|
|
D006177||newborn gynecomastia
|
|
613625||factor v and factor viii combined deficiency of 2
|
|
613625||f5f8d2
|
|
D006175||gynatresia
|
|
D006175||asherman apos s syndrome
|
|
D006175||ashermans syndrome
|
|
D006175||asherman syndrome
|
|
D006175||gynatresias
|
|
D006175||intrauterine synechiae
|
|
D006175||syndrome asherman
|
|
D006175||syndrome asherman apos s
|
|
D006175||synechiae intrauterine
|
|
D006175||synechiae uterine
|
|
D006175||uterine synechiae
|
|
C537777|262850||anti plasmin deficiency congenital
|
|
C537777|262850||alpha 2 plasmin inhibitor deficiency
|
|
C537777|262850||antiplasmin deficiency
|
|
C537777|262850||antiplasmin deficiency congenital
|
|
C537777|262850||plasmin inhibitor deficiency
|
|
C536575|301900||borjeson forssman lehmann syndrome
|
|
C536575|301900||bfls
|
|
C536575|301900||borj
|
|
C536575|301900||borjeson syndrome
|
|
C536575|301900||mental deficiency epilepsy and endocrine disorders
|
|
C536575|301900||mental retardation epilepsy and endocrine disorders
|
|
C536575|301900||mental retardation x linked syndromic borjeson forssman lehmann type
|
|
C536575|301900||mrxsbfl
|
|
C567770|613075||macrocephaly alopecia cutis laxa and scoliosis
|
|
C567770|613075||macs syndrome
|
|
C567770|613075||tall forehead sparse hair skin hyperextensibility and scoliosis
|
|
C566100||symphalangism c s lewis type
|
|
C566100||thumbs stiff
|
|
D018149||glucose intolerance
|
|
D018149||glucose intolerances
|
|
D018149||intolerance glucose
|
|
D018149||intolerances glucose
|
|
D055577|228000||farber lipogranulomatosis
|
|
D055577|228000||ac deficiency
|
|
D055577|228000||acid ceramidase deficiencies
|
|
D055577|228000||acid ceramidase deficiency
|
|
D055577|228000||ceramidase deficiencies
|
|
D055577|228000||ceramidase deficiency
|
|
D055577|228000||ceramidase deficiency acid
|
|
D055577|228000||deficiencies ceramidase
|
|
D055577|228000||deficiencies n laurylsphingosine deacylase
|
|
D055577|228000||deficiency acid ceramidase
|
|
D055577|228000||deficiency ceramidase
|
|
D055577|228000||deficiency n laurylsphingosine deacylase
|
|
D055577|228000||disease farber apos s
|
|
D055577|228000||diseases farber apos s
|
|
D055577|228000||farber disease
|
|
D055577|228000||farber apos s disease
|
|
D055577|228000||farbers disease
|
|
D055577|228000||farber apos s diseases
|
|
D055577|228000||lipogranulomatosis farber
|
|
D055577|228000||n laurylsphingosine deacylase deficiencies
|
|
D055577|228000||n laurylsphingosine deacylase deficiency
|
|
C566105||stratton parker syndrome
|
|
C566105||growth hormone deficiency with wormian bones cardiac anomaly and brachycamptodactyly
|
|
C567439||chromosome 15q13 3 microdeletion syndrome
|
|
C567439||15q13 3 microdeletion
|
|
C567439||15q13 3 microdeletion syndrome
|
|
C567439||chromosome 15q13 3 deletion syndrome
|
|
C567439||microdeletion 15q13 3 syndrome
|
|
C566108||stormorken syndrome
|
|
C566108||thrombocytopathy asplenia and miosis
|
|
C566101||symphalangism of toes
|
|
C565691|610655||telangiectasia hereditary hemorrhagic type 4
|
|
C565691|610655||hht4
|
|
C566102||sulfhemoglobinemia congenital
|
|
600309||atrioventricular septal defect 3
|
|
600309||avsd3
|
|
C566104||striae distensae familial
|
|
125700|D020790||diabetes insipidus neurogenic
|
|
125700|D020790||cdi
|
|
125700|D020790||central diabetes insipidus
|
|
125700|D020790||diabetes insipidus central
|
|
125700|D020790||diabetes insipidus cranial type
|
|
125700|D020790||diabetes insipidus neurohypophyseal
|
|
125700|D020790||diabetes insipidus neurohypophyseal type
|
|
125700|D020790||diabetes insipidus pituitary
|
|
125700|D020790||diabetes insipidus primary central
|
|
125700|D020790||diabetes insipidus secondary to vasopressin deficiency
|
|
125700|D020790||neurogenic diabetes insipidus
|
|
125700|D020790||neurohypophyseal diabetes insipidus
|
|
125700|D020790||pituitary diabetes insipidus
|
|
125700|D020790||vasopressin defective diabetes insipidus
|
|
125700|D020790||vasopressin deficiency
|
|
C566109||storm syndrome
|
|
D045745||scleroderma limited
|
|
D045745||limited scleroderma
|
|
D045745||limited systemic scleroderma
|
|
D045745||limited systemic sclerodermas
|
|
D045745||scleroderma limited systemic
|
|
D045745||sclerodermas limited systemic
|
|
D045745||systemic scleroderma limited
|
|
D045745||systemic sclerodermas limited
|
|
D045743||scleroderma diffuse
|
|
D045743||diffuse cutaneous systemic sclerosis
|
|
D045743||diffuse scleroderma
|
|
D045743||diffuse systemic scleroses
|
|
D045743||diffuse systemic sclerosis
|
|
D045743||progressive scleroderma
|
|
D045743||progressive systemic sclerosis
|
|
D045743||scleroderma progressive
|
|
D045743||sclerodermas sudden onset
|
|
D045743||scleroderma sudden onset
|
|
D045743||scleroses diffuse systemic
|
|
D045743||sclerosis diffuse systemic
|
|
D045743||sclerosis progressive systemic
|
|
D045743||sudden onset scleroderma
|
|
D045743||sudden onset sclerodermas
|
|
D045743||systemic scleroses diffuse
|
|
D045743||systemic sclerosis diffuse
|
|
D045743||systemic sclerosis progressive
|
|
C535860|602089||hemangioma capillary infantile
|
|
C535860|602089||hci
|
|
C535860|602089||hemangioma hereditary capillary
|
|
D006188||haemonchiasis
|
|
D006188||haemonchiases
|
|
D003555|220100||cystinuria
|
|
D003555|220100||csnu
|
|
D003555|220100||csnu1 formerly
|
|
D003555|220100||csnu3 formerly
|
|
D003555|220100||cystinurias
|
|
D003555|220100||cystinuria type a b included
|
|
D003555|220100||cystinuria type b included
|
|
D003555|220100||cystinuria type i formerly
|
|
D003555|220100||cystinuria type ii formerly
|
|
D003555|220100||cystinuria type iii formerly
|
|
D003555|220100||cystinuria type non i formerly cystinuria type a included
|
|
613616||hyperoxaluria primary type iii
|
|
613616||hp3
|
|
613617||retinitis pigmentosa 58
|
|
613617||rp58
|
|
184095|C563218||spondyloepiphyseal dysplasia maroteaux type
|
|
184095||pseudo morquio syndrome type 2
|
|
184095||sed maroteaux type
|
|
C567442||rett syndrome zappella variant
|
|
C566110||stomatocytosis ii
|
|
C566111||stomatocytosis i
|
|
C566111||overhydrated hereditary stomatocytosis
|
|
C566111||potassium sodium disorder of erythrocyte
|
|
D018159||endolymphatic hydrops
|
|
D018159||hydrops endolymphatic
|
|
D019584||hot flashes
|
|
D019584||flashes hot
|
|
D018253||adenoma villous
|
|
D018253||adenomas villous
|
|
D018253||villous adenoma
|
|
D018253||villous adenomas
|
|
D018252||syringoma
|
|
D018252||syringomas
|
|
146800|D053560||ichthyosis bullosa of siemens
|
|
146800|D053560||bullous type ichthyoses
|
|
146800|D053560||bullous type ichthyosis
|
|
146800|D053560||bullous type of ichthyosis
|
|
146800|D053560||ibs ichthyosis exfoliativa included
|
|
146800|D053560||ichthyoses bullous type
|
|
146800|D053560||ichthyosis bullous type
|
|
146800|D053560||ichthyosis bullous type of siemens
|
|
146800|D053560||siemens ichthyosis bullosa
|
|
D019586||intracranial hypertension
|
|
D019586||elevated icp intracranial pressure
|
|
D019586||elevated intracranial pressure
|
|
D019586||hypertension intracranial
|
|
D019586||icp elevated intracranial pressure
|
|
D019586||icp intracranial pressure elevation
|
|
D019586||icp intracranial pressure increase
|
|
D019586||intracranial pressure elevated
|
|
D019586||intracranial pressure increase
|
|
D019586||pressure elevated intracranial
|
|
D019586||pressure increase intracranial
|
|
D018255||adenomatosis pulmonary
|
|
D018255||adenomatoses pulmonary
|
|
D018255||pulmonary adenomatoses
|
|
D018255||pulmonary adenomatosis
|
|
D006250|234500||hartnup disease
|
|
D006250|234500||amino acid transport disorder neutral
|
|
D006250|234500||hartnup disorder
|
|
D006250|234500||hnd
|
|
D006250|234500||neutral amino acid transport defect
|
|
D006250|234500||neutral amino acid transport disorder
|
|
D006250|234500||transport disorder neutral amino acid
|
|
D006250|234500||transport disorder neutral amino acids
|
|
D019585||intracranial hypotension
|
|
D019585||essential intracranial hypotension
|
|
D019585||hypotension essential intracranial
|
|
D019585||hypotension intracranial
|
|
D019585||hypotension secondary intracranial
|
|
D019585||hypotension spontaneous intracranial
|
|
D019585||intracranial hypotension essential
|
|
D019585||intracranial hypotension secondary
|
|
D019585||intracranial hypotension spontaneous
|
|
D019585||secondary intracranial hypotension
|
|
D019585||spontaneous intracranial hypotension
|
|
D018254||adenomatoid tumor
|
|
D018254||adenomatoid tumors
|
|
D018254||tumor adenomatoid
|
|
D018254||tumors adenomatoid
|
|
C567472|300711||pyloric stenosis infantile hypertrophic 4
|
|
C567472|300711||ihps4
|
|
D018251||hidrocystoma
|
|
D018251||hidrocystomas
|
|
D018250||acrospiroma
|
|
D018250||acrospiroma eccrine
|
|
D018250||acrospiromas
|
|
D018250||acrospiromas eccrine
|
|
D018250||clear cell hidradrenoma
|
|
D018250||clear cell hidradrenomas
|
|
D018250||eccrine acrospiroma
|
|
D018250||eccrine acrospiromas
|
|
D018250||hidradenoma
|
|
D018250||hidradenomas
|
|
D018250||hidradenoma solid cystic
|
|
D018250||hidradenomas solid cystic
|
|
D018250||hidradrenoma clear cell
|
|
D018250||hidradrenoma nodular
|
|
D018250||hidradrenomas clear cell
|
|
D018250||hidradrenomas nodular
|
|
D018250||nodular hidradrenoma
|
|
D018250||nodular hidradrenomas
|
|
D018250||solid cystic hidradenoma
|
|
D018250||solid cystic hidradenomas
|
|
C537129|311070||optic atrophy polyneuropathy deafness
|
|
C537129|311070||charcot marie tooth disease x linked recessive 5
|
|
C537129|311070||charcot marie tooth neuropathy x linked recessive 5
|
|
C537129|311070||cmtx5
|
|
C537129|311070||familial opticoacoustic nerve degeneration and polyneuropathy
|
|
C537129|311070||optic atrophy hearing loss and peripheral neuropathy autosomal recessive
|
|
C537129|311070||optic atrophy neural deafness and distal neurogenic amyotrophy
|
|
C537129|311070||optic atrophy polyneuropathy and deafness
|
|
C537129|311070||optic atrophy sensorineural hearing loss and polyneuropathy
|
|
C537129|311070||rosenberg chutorian syndrome
|
|
D031221||knee dislocation
|
|
D031221||dislocation knee
|
|
D031221||dislocations knee
|
|
D031221||knee dislocations
|
|
C563883|608656||prostate cancer hereditary 3
|
|
C563883|608656||hpc3
|
|
D057851||posterior capsular rupture ocular
|
|
C565789|604348||advanced sleep phase syndrome familial
|
|
C565789|604348||advanced sleep phase syndrome familial 1
|
|
C565789|604348||fasps
|
|
C565789|604348||fasps1
|
|
C535903|603543||limb mammary syndrome
|
|
C535903|603543||lms
|
|
C535903|603543||mammary hypoplasia ectrodactyly and other hand foot anomalies
|
|
C562448|608709||lipodystrophy partial acquired
|
|
C562448|608709||apld
|
|
C562448|608709||apld susceptibility to
|
|
C562448|608709||barraquer simons syndrome
|
|
C562448|608709||lipodystrophy cephalothoracic type
|
|
C562448|608709||lipodystrophy partial acquired susceptibility to
|
|
C562448|608709||lipodystrophy partial progressive
|
|
102510||acropectorovertebral dysplasia
|
|
102510||f syndrome
|
|
D018249||adenoma oxyphilic
|
|
D018249||huerthle cell tumor
|
|
D018249||hurthle cell tumor
|
|
D018249||oncocytoma
|
|
D018249||oxyphilic adenoma
|
|
C565228|609790||alzheimer disease 11
|
|
C565228|609790||ad11
|
|
C565228|609790||alzheimer disease familial 11
|
|
D018246||adrenocortical adenoma
|
|
D018246||adenoma adrenal cortical
|
|
D018246||adenoma adrenocortical
|
|
D018246||adenoma conn
|
|
D018246||adenomas adrenal cortical
|
|
D018246||adenomas adrenocortical
|
|
D018246||adenomas conn
|
|
D018246||adrenal cortical adenoma
|
|
D018246||adrenal cortical adenomas
|
|
D018246||adrenocortical adenomas
|
|
D018246||conn adenoma
|
|
D018246||conn adenomas
|
|
D018246||conn disease
|
|
D018246||conn apos s disease
|
|
D018246||conns disease
|
|
D018246||disease conn
|
|
D018246||disease conn apos s
|
|
D018245||trophoblastic tumor placental site
|
|
D018245||placental site trophoblastic tumor
|
|
D018245||placental site trophoblastic tumors
|
|
D018245||placental trophoblastic tumor
|
|
D018245||placental trophoblastic tumors
|
|
D018245||trophoblastic tumor placental
|
|
D018245||trophoblastic tumors placental
|
|
D018245||trophoblastic tumors placental site
|
|
D018245||tumor placental site trophoblastic
|
|
D018245||tumor placental trophoblastic
|
|
D018245||tumors placental site trophoblastic
|
|
D018245||tumors placental trophoblastic
|
|
D018248||adenoma liver cell
|
|
D018248||adenoma hepatocellular
|
|
D018248||adenomas hepatocellular
|
|
D018248||adenomas liver cell
|
|
D018248||benign hepatoma
|
|
D018248||benign hepatomas
|
|
D018248||hepatocellular adenoma
|
|
D018248||hepatocellular adenomas
|
|
D018248||hepatoma benign
|
|
D018248||hepatomas benign
|
|
D018248||liver cell adenoma
|
|
D018248||liver cell adenomas
|
|
D031222||patellar dislocation
|
|
D031222||dislocation patellar
|
|
D031222||dislocations patellar
|
|
D031222||patellar dislocations
|
|
D019578||multiple system atrophy
|
|
D019578||atrophies multisystem
|
|
D019578||atrophies multisystemic
|
|
D019578||atrophy multiple system
|
|
D019578||atrophy multisystem
|
|
D019578||atrophy multisystemic
|
|
D019578||multiple system atrophies
|
|
D019578||multiple system atrophy syndrome
|
|
D019578||multisystem atrophies
|
|
D019578||multisystem atrophy
|
|
D019578||multisystemic atrophies
|
|
D019578||multisystemic atrophy
|
|
D019595||severe dengue
|
|
D019595||dengue hemorrhagic fever
|
|
D019595||dengue severe
|
|
D019595||dengue shock syndrome
|
|
D019595||dengues severe
|
|
D019595||fever philippine hemorrhagic
|
|
D019595||fever singapore hemorrhagic
|
|
D019595||fever thai hemorrhagic
|
|
D019595||hemorrhagic dengue
|
|
D019595||hemorrhagic dengues
|
|
D019595||hemorrhagic fever dengue
|
|
D019595||philippine hemorrhagic fever
|
|
D019595||severe dengues
|
|
D019595||singapore hemorrhagic fever
|
|
D019595||thai hemorrhagic fever
|
|
C563161|608026||hypertensive nephropathy
|
|
C563161|608026||hnp1
|
|
D018263||adenocarcinoma follicular
|
|
D018263||adenocarcinomas follicular
|
|
D018263||carcinoma follicular thyroid
|
|
D018263||carcinomas follicular thyroid
|
|
D018263||follicular adenocarcinoma
|
|
D018263||follicular adenocarcinomas
|
|
D018263||follicular thyroid carcinoma
|
|
D018263||follicular thyroid carcinomas
|
|
D018263|188470|C572845||thyroid carcinoma follicular
|
|
D018263||thyroid carcinomas follicular
|
|
D018266||adenocarcinoma sebaceous
|
|
D018266||adenocarcinomas sebaceous
|
|
D018266||sebaceous adenocarcinoma
|
|
D018266||sebaceous adenocarcinomas
|
|
C537799|231070||gerodermia osteodysplastica
|
|
C537799|231070||geroderma osteodysplastica
|
|
C537799|231070||geroderma osteodysplastica hereditaria
|
|
C537799|231070||geroderma osteodysplasticum
|
|
C537799|231070||go
|
|
C537799|231070||walt disney dwarfism
|
|
D018265||carcinoma papillary follicular
|
|
179010||ihps
|
|
179010||ihps1
|
|
D019591||pseudophakia
|
|
D018262||adenocarcinoma clear cell
|
|
D018262||adenocarcinomas clear cell
|
|
D018262||clear cell adenocarcinoma
|
|
D018262||clear cell adenocarcinomas
|
|
102530||spermatogenic failure 6
|
|
102530||acrosome malformation of spermatozoa
|
|
102530||globozoospermia
|
|
102530||round headed spermatozoa
|
|
102530||spermatozoa round headed
|
|
102530||spgf6
|
|
D018261||mesothelioma cystic
|
|
D018261||cystic mesothelioma
|
|
D018261||cystic mesotheliomas
|
|
D018261||mesotheliomas cystic
|
|
D020567||fetal weight
|
|
D020567||body weight fetal
|
|
D020567||body weights fetal
|
|
D020567||fetal body weight
|
|
D020567||fetal body weights
|
|
D020567||fetal weights
|
|
D020567||weight fetal
|
|
D020567||weights fetal
|
|
C567479|300699||mental retardation x linked 94
|
|
C567479|300699||mental retardation x linked syndromic 29
|
|
C567479|300699||mental retardation x linked syndromic wu type
|
|
C567479|300699||mrx94
|
|
C567479|300699||mrxs29
|
|
C567479|300699||mrxsw
|
|
D045888||ganglion cysts
|
|
D045888||cyst ganglion
|
|
D045888||cyst ganglionic
|
|
D045888||cyst myxoid
|
|
D045888||cysts ganglion
|
|
D045888||cysts ganglionic
|
|
D045888||cysts myxoid
|
|
D045888||ganglion
|
|
D045888||ganglion cyst
|
|
D045888||ganglionic cyst
|
|
D045888||ganglionic cysts
|
|
D045888||ganglions
|
|
D045888||myxoid cyst
|
|
D045888||myxoid cysts
|
|
C484001||riv immunoglobulin variant protein human
|
|
C484001||protein riv human
|
|
C562719|300622||tn syndrome
|
|
C562719|300622||galactosyltransferase deficiency
|
|
C562719|300622||tn polyagglutination syndrome
|
|
C562719|300622||tnps
|
|
606003|C563207||transaldolase deficiency
|
|
162830|C563010||neutrophilia hereditary
|
|
607748|C564336||hypercholanemia familial
|
|
607748|C564336||fhca
|
|
D057868||anastomotic leak
|
|
D057868||anastomotic leakage
|
|
D057868||anastomotic leakages
|
|
D057868||anastomotic leaks
|
|
D057868||leakage anastomotic
|
|
D057868||leakages anastomotic
|
|
D057868||leak anastomotic
|
|
D057868||leaks anastomotic
|
|
607721||noonan syndrome like disorder with loose anagen hair
|
|
607721||nslh
|
|
D019588||aging premature
|
|
D019588||premature aging
|
|
C537993|601472||charcot marie tooth disease type 2d
|
|
C537993|601472||charcot marie tooth disease axonal type 2d
|
|
C537993|601472||charcot marie tooth disease neuronal type 2d
|
|
C537993|601472||charcot marie tooth neuropathy type 2d
|
|
C537993|601472||cmt2d
|
|
D018256||adenomatous polyps
|
|
D018256||adenomatous polyp
|
|
D018256||polyp adenomatous
|
|
D018256||polyps adenomatous
|
|
C565732|605019||hypobetalipoproteinemia familial 2
|
|
C565732|605019||fhbl2
|
|
C565732|605019||hypolipidemia familial combined
|
|
D057867||endoleak
|
|
D057867||endoleaks
|
|
D057867||leak perigraft
|
|
D057867||leaks perigraft
|
|
D057867||perigraft leak
|
|
D057867||perigraft leaks
|
|
D018231||leiomyomatosis
|
|
D018231||leiomyomatoses
|
|
208150|C536647||pena shokeir syndrome type 1
|
|
208150|C536647||arthrogryposis multiplex congenita pulmonary hypoplasia
|
|
208150|C536647||arthrogryposis multiplex congenita pulmonary hypoplasia cryptorchidism and unusual ophthalmological findings
|
|
208150|C536647||arthrogryposis multiplex congenita with pulmonary hypoplasia
|
|
208150|C536647||fads
|
|
208150|C536647||fetal akinesia deformation sequence
|
|
208150|C536647||fetal akinesia sequence
|
|
208150|C536647||lethal pena shokeir 1 syndrome
|
|
208150|C536647||pena shokeir syndrome type i
|
|
C563387||rhabdomyolysis cerivastatin induced
|
|
D018230||leiomyoma epithelioid
|
|
D018230||epithelioid leiomyoma
|
|
D018230||epithelioid leiomyomas
|
|
D018230||leiomyoblastoma
|
|
D018230||leiomyoblastomas
|
|
D018230||leiomyomas epithelioid
|
|
D018233||rhabdomyosarcoma embryonal
|
|
D018233||embryonal rhabdomyosarcoma
|
|
D018233||embryonal rhabdomyosarcomas
|
|
D018233||rhabdomyosarcomas embryonal
|
|
607706|C539595||charcot marie tooth disease type 4a axonal form
|
|
607706|C539595||charcot marie tooth neuropathy axonal with vocal cord paresis autosomal recessive
|
|
607706|C539595||cmt2 with vocal cord paresis autosomal recessive
|
|
D007579||jejunal diseases
|
|
D007579||disease jejunal
|
|
D007579||diseases jejunal
|
|
D007579||jejunal disease
|
|
D006950|144250||hyperlipidemia familial combined
|
|
D006950|144250||combined hyperlipidemia familial
|
|
D006950|144250||combined hyperlipidemias familial
|
|
D006950|144250||familial combined hyperlipidemia
|
|
D006950|144250||familial combined hyperlipidemias
|
|
D006950|144250||fchl
|
|
D006950|144250||hyperlipidemia multiple lipoprotein type
|
|
D006950|144250||hyperlipidemias familial combined
|
|
D006950|144250||hyperlipidemias multiple lipoprotein type
|
|
D006950|144250||lipoprotein type hyperlipidemia multiple
|
|
D006950|144250||lipoprotein type hyperlipidemias multiple
|
|
D006950|144250||multiple lipoprotein type hyperlipidemia
|
|
D006950|144250||multiple lipoprotein type hyperlipidemias
|
|
143095||cdmd
|
|
143095||hsd
|
|
D007575||jaw edentulous
|
|
D007575||edentulous jaw
|
|
D007575||edentulous jaws
|
|
D007575||jaws edentulous
|
|
D007576||jaw edentulous partially
|
|
D057873||peri implantitis
|
|
D057873||periimplantitides
|
|
D057873||peri implantitides
|
|
D057873||periimplantitis
|
|
D007580||jejunal neoplasms
|
|
D007580||cancer jejunal
|
|
D007580||cancer of jejunum
|
|
D007580||cancer of the jejunum
|
|
D007580||cancers jejunal
|
|
D007580||jejunal cancer
|
|
D007580||jejunal cancers
|
|
D007580||jejunal neoplasm
|
|
D007580||jejunum cancer
|
|
D007580||jejunum cancers
|
|
D007580||neoplasm jejunal
|
|
D007580||neoplasms jejunal
|
|
C566410|603098||deafness autosomal recessive 13
|
|
C566410|603098||dfnb13
|
|
D019559||capillary leak syndrome
|
|
D019559||capillary leak syndromes
|
|
D019559||clarkson disease
|
|
D019559||clinical capillary leak syndrome
|
|
D019559||systemic capillary leak syndrome
|
|
D018228||sarcoma small cell
|
|
D018228||cell sarcoma small
|
|
D018228||cell sarcomas small
|
|
D018228||sarcomas small cell
|
|
D018228||small cell sarcoma
|
|
D018228||small cell sarcomas
|
|
C563390||cataracts congenital with sensorineural deafness down syndrome like facial appearance short stature and mental retardation
|
|
D018227||sarcoma clear cell
|
|
D018227||clear cell sarcoma
|
|
D018227||clear cell sarcomas
|
|
D018227||melanoma malignant of soft parts
|
|
D018227||sarcomas clear cell
|
|
C565524|235000||hemihyperplasia isolated
|
|
C565524|235000||hemi 3 syndrome
|
|
C565524|235000||hemihyperplasia
|
|
C565524|235000||hemihypertrophy isolated
|
|
C565524|235000||hemihypertrophy isolated hemi 3 syndrome included
|
|
C565524|235000||hhp
|
|
C565524|235000||ih
|
|
138500||hyperglycinuria
|
|
D018229||angiomyoma
|
|
D018229||angioleiomyoma
|
|
D018229||angioleiomyomas
|
|
D018229||angiomyomas
|
|
D018229||leiomyomas vascular
|
|
D018229||leiomyoma vascular
|
|
D018229||vascular leiomyoma
|
|
D018229||vascular leiomyomas
|
|
D018224||myofibromatosis
|
|
D018224||myofibromatoses
|
|
C563394||aplasia cutis congenita high myopia and cone rod dysfunction
|
|
D018223||dermatofibrosarcoma
|
|
D018223||darier ferrand tumor
|
|
D018223||darier hoffmann tumor
|
|
D018223||dermatofibrosarcomas
|
|
D019557||dermatitis perioral
|
|
D019557||dermatitides periocular
|
|
D019557||dermatitides perioral
|
|
D019557||dermatitis periocular
|
|
D019557||periocular dermatitides
|
|
D019557||periocular dermatitis
|
|
D019557||perioral dermatitides
|
|
D019557||perioral dermatitis
|
|
D018226||fibroadenoma
|
|
D018226||fibroadenomas
|
|
C566998|611155||alzheimer disease 15
|
|
C566998|611155||ad15
|
|
C563392||rolandic epilepsy mental retardation and speech dyspraxia autosomal dominant
|
|
C563392||adresd
|
|
C563392||resdad
|
|
D018225||neoplasms fibroepithelial
|
|
D018225||fibroepithelial neoplasm
|
|
D018225||fibroepithelial neoplasms
|
|
D018225||neoplasm fibroepithelial
|
|
D018242||neuroectodermal tumors primitive
|
|
D018242||cerebral primitive neuroectodermal tumor
|
|
D018242||ependymoblastoma
|
|
D018242||ependymoblastomas
|
|
D018242||medulloepithelioma
|
|
D018242||medulloepitheliomas
|
|
D018242||neoplasm primitive neuroepithelial
|
|
D018242||neoplasms primitive neuroepithelial
|
|
D018242||neuroectodermal tumor primitive
|
|
D018242||neuroepithelial neoplasm primitive
|
|
D018242||neuroepithelial neoplasms primitive
|
|
D018242||neuroepithelial tumor primitive
|
|
D018242||neuroepithelial tumors primitive
|
|
D018242||pnet
|
|
D018242||pnets
|
|
D018242||primitive neuroectodermal tumor
|
|
D018242||primitive neuroectodermal tumors
|
|
D018242||primitive neuroepithelial neoplasm
|
|
D018242||primitive neuroepithelial neoplasms
|
|
D018242||primitive neuroepithelial tumor
|
|
D018242||primitive neuroepithelial tumors
|
|
D018242||spongioblastoma
|
|
D018242||spongioblastomas
|
|
D018242||tumor primitive neuroectodermal
|
|
D018242||tumor primitive neuroepithelial
|
|
D018242||tumors primitive neuroectodermal
|
|
D018242||tumors primitive neuroepithelial
|
|
C563398||auditory neuropathy nonsyndromic recessive
|
|
D019572||retinal neoplasms
|
|
D019572||cancer of the retina
|
|
D019572||cancer retinal
|
|
D019572||cancers retinal
|
|
D019572||neoplasm retinal
|
|
D019572||neoplasms retinal
|
|
D019572||retinal cancer
|
|
D019572||retinal cancers
|
|
D019572||retinal neoplasm
|
|
D019572||retinal tumor
|
|
D019572||retinal tumors
|
|
D019572||tumor retinal
|
|
D019572||tumors retinal
|
|
D018241||neuroectodermal tumors primitive peripheral
|
|
D018241||extracranial primitive neuroectodermal tumor
|
|
D018241||neuroectodermal neoplasm peripheral primitive
|
|
D018241||neuroectodermal tumor peripheral
|
|
D018241||neuroectodermal tumor peripheral primitive
|
|
D018241||neuroectodermal tumors peripheral
|
|
D018241||neuroepithelioma
|
|
D018241||neuroepithelioma peripheral
|
|
D018241||neuroepitheliomas
|
|
D018241||peripheral neuroectodermal tumor
|
|
D018241||peripheral neuroectodermal tumors
|
|
D018241||peripheral primitive neuroectodermal neoplasm
|
|
D018241||peripheral primitive neuroectodermal tumors
|
|
D018241||ppnet peripheral primitive neuroectodermal tumors
|
|
D018241||primitive neuroectodermal tumor extracranial
|
|
D018241||tumor peripheral neuroectodermal
|
|
D018241||tumors peripheral neuroectodermal
|
|
D019575||blindness cortical
|
|
D019575||anton babinski syndrome
|
|
D019575||anton apos s syndrome
|
|
D019575||antons syndrome
|
|
D019575||anton apos s syndrome transient
|
|
D019575||anton syndrome
|
|
D019575||blindness cortical post ictal
|
|
D019575||blindness cortical transient
|
|
D019575||blindnesses reversible cortical
|
|
D019575||blindness reversible cortical
|
|
D019575||cortical blindness
|
|
D019575||cortical blindnesses reversible
|
|
D019575||cortical blindness reversible
|
|
D019575||psychic denial of blindness
|
|
D019575||reversible cortical blindness
|
|
D019575||reversible cortical blindnesses
|
|
D019575||syndrome anton
|
|
D019575||syndrome anton babinski
|
|
D019575||syndrome anton apos s
|
|
D019575||syndrome transient anton apos s
|
|
D019575||transient anton apos s syndrome
|
|
D019575||transient antons syndrome
|
|
D019575||transient anton syndrome
|
|
C564553|300245||ptosis hereditary congenital 2
|
|
C564553|300245||ptos2
|
|
C564553|300245||ptosis x linked
|
|
C564553|300245||ptosx
|
|
D019574||optic nerve neoplasms
|
|
D019574||benign optic nerve neoplasm
|
|
D019574||benign optic nerve sheath neoplasms
|
|
D019574||benign optic nerve sheath tumors
|
|
D019574||benign optic nerve tumor
|
|
D019574||malignant optic nerve neoplasm
|
|
D019574||malignant optic nerve sheath neoplasms
|
|
D019574||malignant optic nerve sheath tumors
|
|
D019574||malignant optic nerve tumor
|
|
D019574||neoplasm benign optic nerve
|
|
D019574||neoplasm optic nerve
|
|
D019574||neoplasm optic nerve benign
|
|
D019574||neoplasms optic nerve
|
|
D019574||optic nerve neoplasm
|
|
D019574||optic nerve neoplasm benign
|
|
D019574||optic nerve sheath neoplasm
|
|
D019574||optic nerve sheath neoplasms malignant
|
|
D019574||optic nerve sheath tumors
|
|
D019574||optic nerve sheath tumors benign
|
|
D019574||optic nerve sheath tumors malignant
|
|
D019574||optic nerve tumor malignant
|
|
D019574||tumor benign optic nerve
|
|
D019574||tumor malignant optic nerve
|
|
D019574||tumor optic nerve benign
|
|
D019574||tumor optic nerve malignant
|
|
D018243||teratocarcinoma
|
|
D018243||teratocarcinomas
|
|
C563359|601283||diabetes mellitus noninsulin dependent 1
|
|
C563359|601283||niddm1
|
|
C563359|601283||noninsulin dependent diabetes mellitus 1
|
|
D049310|160500||distal myopathies
|
|
D049310|160500||als21
|
|
D049310|160500||amyotrophic lateral sclerosis 21
|
|
D049310|160500||distal 1 myopathies
|
|
D049310|160500||distal 1 myopathy
|
|
D049310|160500||distal muscular dystrophies
|
|
D049310|160500||distal muscular dystrophy
|
|
D049310|160500||distal myopathy
|
|
D049310|160500||distal myopathy 1
|
|
D049310|160500||distal myopathy 1s
|
|
D049310|160500||distal myopathy laing
|
|
D049310|160500||distal myopathy markesbery griggs type
|
|
D049310|160500||distal myopathy udd
|
|
D049310|160500||distal myopathy welander
|
|
D049310|160500||finnish markesbery muscular dystrophy
|
|
D049310|160500||laing distal myopathy
|
|
D049310|160500||laing early onset distal myopathy
|
|
D049310|160500||mpd1
|
|
D049310|160500||mpd2 formerly
|
|
D049310|160500||mpd3
|
|
D049310|160500||muscular dystrophies distal
|
|
D049310|160500||muscular dystrophies tibial
|
|
D049310|160500||muscular dystrophy distal
|
|
D049310|160500||muscular dystrophy finnish markesbery
|
|
D049310|160500||muscular dystrophy tibial
|
|
D049310|160500||muscular dystrophy udd markesbery
|
|
D049310|160500||myopathies distal
|
|
D049310|160500||myopathies distal 1
|
|
D049310|160500||myopathy 1 distal
|
|
D049310|160500||myopathy 1s distal
|
|
D049310|160500||myopathy distal
|
|
D049310|160500||myopathy distal 1
|
|
D049310|160500||myopathy distal 2 formerly
|
|
D049310|160500||myopathy distal early onset autosomal dominant
|
|
D049310|160500||myopathy laing distal
|
|
D049310|160500||myopathy late distal hereditary
|
|
D049310|160500||myopathy udd
|
|
D049310|160500||myopathy udd distal
|
|
D049310|160500||tardive tibial muscular dystrophy
|
|
D049310|160500||tibial muscular dystrophy
|
|
D049310|160500||tibial muscular dystrophy tardive
|
|
D049310|160500||tmd
|
|
D049310|160500||udd distal myopathy
|
|
D049310|160500||udd markesbery muscular dystrophy
|
|
D049310|160500||udd myopathy
|
|
D049310|160500||vcpdm formerly
|
|
D049310|160500||vocal cord and pharyngeal dysfunction with distal myopathy formerly
|
|
D019571||arrhythmogenic right ventricular dysplasia
|
|
D019571||arrhythmogenic right ventricular cardiomyopathy
|
|
D019571||arrhythmogenic right ventricular cardiomyopathy dysplasia
|
|
D019571||arrhythmogenic right ventricular dysplasia cardiomyopathy
|
|
D019571||arvd c
|
|
D019571||right ventricular dysplasia arrhythmogenic
|
|
D019571||ventricular dysplasia right arrhythmogenic
|
|
D018240||endodermal sinus tumor
|
|
D018240||endodermal sinus tumors
|
|
D018240||tumor endodermal sinus
|
|
D018240||tumors endodermal sinus
|
|
D018240||tumors yolk sac
|
|
D018240||tumor yolk sac
|
|
D018240||yolk sac tumor
|
|
D018240||yolk sac tumors
|
|
304340|C535773||mental retardation x linked syndromic 5
|
|
304340|C535773||dandy walker malformation with mental retardation basal ganglia disease and seizures
|
|
304340|C535773||mental retardation x linked with dandy walker malformation basal ganglia disease and seizures
|
|
304340|C535773||mrxs5
|
|
304340|C535773||pettigrew syndrome
|
|
304340|C535773||pgs
|
|
D006259||craniocerebral trauma
|
|
D006259||craniocerebral injuries
|
|
D006259||craniocerebral injury
|
|
D006259||craniocerebral traumas
|
|
D006259||crushing skull injuries
|
|
D006259||crushing skull injury
|
|
D006259||forehead trauma
|
|
D006259||forehead traumas
|
|
D006259||frontal region trauma
|
|
D006259||frontal region traumas
|
|
D006259||head injuries
|
|
D006259||head injuries minor
|
|
D006259||head injuries multiple
|
|
D006259||head injuries open
|
|
D006259||head injuries superficial
|
|
D006259||head injury
|
|
D006259||head injury minor
|
|
D006259||head injury multiple
|
|
D006259||head injury open
|
|
D006259||head injury superficial
|
|
D006259||head trauma
|
|
D006259||head traumas
|
|
D006259||injuries craniocerebral
|
|
D006259||injuries head
|
|
D006259||injuries minor head
|
|
D006259||injuries multiple head
|
|
D006259||injuries open head
|
|
D006259||injuries superficial head
|
|
D006259||injury craniocerebral
|
|
D006259||injury head
|
|
D006259||injury minor head
|
|
D006259||injury multiple head
|
|
D006259||injury open head
|
|
D006259||injury superficial head
|
|
D006259||minor head injuries
|
|
D006259||minor head injury
|
|
D006259||multiple head injuries
|
|
D006259||multiple head injury
|
|
D006259||occipital region trauma
|
|
D006259||occipital region traumas
|
|
D006259||occipital trauma
|
|
D006259||occipital traumas
|
|
D006259||open head injuries
|
|
D006259||open head injury
|
|
D006259||parietal region trauma
|
|
D006259||parietal region traumas
|
|
D006259||region trauma frontal
|
|
D006259||region trauma occipital
|
|
D006259||region trauma parietal
|
|
D006259||region traumas frontal
|
|
D006259||region traumas occipital
|
|
D006259||region traumas parietal
|
|
D006259||skull injuries crushing
|
|
D006259||skull injury crushing
|
|
D006259||superficial head injuries
|
|
D006259||superficial head injury
|
|
D006259||temporal region trauma
|
|
D006259||temporal region traumas
|
|
D006259||trauma craniocerebral
|
|
D006259||trauma forehead
|
|
D006259||trauma frontal region
|
|
D006259||trauma head
|
|
D006259||trauma occipital
|
|
D006259||trauma occipital region
|
|
D006259||trauma parietal region
|
|
D006259||traumas craniocerebral
|
|
D006259||traumas forehead
|
|
D006259||traumas frontal region
|
|
D006259||traumas head
|
|
D006259||traumas occipital
|
|
D006259||traumas occipital region
|
|
D006259||traumas parietal region
|
|
D006259||traumas temporal region
|
|
D006259||trauma temporal region
|
|
D006258||head and neck neoplasms
|
|
D006258||cancer of head
|
|
D006258||cancer of head and neck
|
|
D006258||cancer of neck
|
|
D006258||cancer of the head
|
|
D006258||cancer of the head and neck
|
|
D006258||cancer of the neck
|
|
D006258||head and neck cancer
|
|
D006258||head cancer
|
|
D006258||head neck neoplasms
|
|
D006258||head neoplasms
|
|
D006258||neck cancer
|
|
D006258||neck neoplasms
|
|
D006258||neoplasms head
|
|
D006258||neoplasms head and neck
|
|
D006258||neoplasms neck
|
|
D006258||neoplasms uadt
|
|
D006258||neoplasms upper aerodigestive tract
|
|
D006258||neoplasm uadt
|
|
D006258||uadt neoplasm
|
|
D006258||uadt neoplasms
|
|
D006258||upper aerodigestive tract neoplasms
|
|
D006255||rhinitis allergic seasonal
|
|
D006255||allergic rhinitides seasonal
|
|
D006255||allergic rhinitis seasonal
|
|
D006255||allergies pollen
|
|
D006255||allergy pollen
|
|
D006255||fever hay
|
|
D006255||hayfever
|
|
D006255||hay fever
|
|
D006255||pollen allergies
|
|
D006255||pollen allergy
|
|
D006255||pollinoses
|
|
D006255||pollinosis
|
|
D006255||rhinitides seasonal allergic
|
|
D006255||rhinitis seasonal allergic
|
|
D006255||seasonal allergic rhinitides
|
|
D006255||seasonal allergic rhinitis
|
|
C537596|201470||short chain acyl coa dehydrogenase deficiency
|
|
C537596|201470||acadsd
|
|
C537596|201470||acads deficiency
|
|
C537596|201470||acyl coa dehydrogenase short chain deficiency of
|
|
C537596|201470||deficiency of butyryl coa dehydrogenase
|
|
C537596|201470||lipid storage myopathy secondary to short chain acyl coa dehydrogenase deficiency
|
|
C537596|201470||scad deficiency
|
|
C537596|201470||scadh deficiency
|
|
C537596|201470||short chain acyl coenzyme a dehydrogenase deficiency
|
|
D007593||joint instability
|
|
D007593||hypermobilities joint
|
|
D007593||hypermobility joint
|
|
D007593||instabilities joint
|
|
D007593||instability joint
|
|
D007593||joint hypermobilities
|
|
D007593||joint hypermobility
|
|
D007593||joint instabilities
|
|
D007593||joint laxities
|
|
D007593||joint laxity
|
|
D007593||laxities joint
|
|
D007593||laxity joint
|
|
D057885||triploidy
|
|
D057885||triploid
|
|
D057885||triploidies
|
|
D057885||triploids
|
|
D007594||joint loose bodies
|
|
D007594||joint loose body
|
|
D007594||loose bodies joint
|
|
D007594||loose body joint
|
|
121900|C537304||groenouw type i corneal dystrophy
|
|
121900|C537304||cdgg1
|
|
121900|C537304||corneal dystrophy granular type
|
|
121900|C537304||corneal dystrophy groenouw type i
|
|
121900|C537304||corneal dystrophy punctate or nodular
|
|
121900|C537304||gcd1
|
|
121900|C537304||granular corneal dystrophy type i
|
|
D007592||joint diseases
|
|
D007592||disease joint
|
|
D007592||diseases joint
|
|
D007592||joint disease
|
|
D006261||headache
|
|
D006261||bilateral headache
|
|
D006261||bilateral headaches
|
|
D006261||cephalalgia
|
|
D006261||cephalalgias
|
|
D006261||cephalgia
|
|
D006261||cephalgias
|
|
D006261||cephalodynia
|
|
D006261||cephalodynias
|
|
D006261||cranial pain
|
|
D006261||cranial pains
|
|
D006261||generalized headache
|
|
D006261||generalized headaches
|
|
D006261||headache bilateral
|
|
D006261||headache generalized
|
|
D006261||headache ocular
|
|
D006261||headache orthostatic
|
|
D006261||headache periorbital
|
|
D006261||headache retro ocular
|
|
D006261||headaches
|
|
D006261||headaches bilateral
|
|
D006261||headaches generalized
|
|
D006261||headache sharp
|
|
D006261||headaches ocular
|
|
D006261||headaches orthostatic
|
|
D006261||headaches periorbital
|
|
D006261||headaches retro ocular
|
|
D006261||headaches sharp
|
|
D006261||headaches throbbing
|
|
D006261||headaches unilateral
|
|
D006261||headaches vertex
|
|
D006261||headache throbbing
|
|
D006261||headache unilateral
|
|
D006261||headache vertex
|
|
D006261||head pain
|
|
D006261||head pains
|
|
D006261||hemicrania
|
|
D006261||ocular headache
|
|
D006261||ocular headaches
|
|
D006261||orthostatic headache
|
|
D006261||orthostatic headaches
|
|
D006261||pain cranial
|
|
D006261||pain head
|
|
D006261||pains cranial
|
|
D006261||pains head
|
|
D006261||periorbital headache
|
|
D006261||periorbital headaches
|
|
D006261||retro ocular headache
|
|
D006261||retro ocular headaches
|
|
D006261||sharp headache
|
|
D006261||sharp headaches
|
|
D006261||throbbing headache
|
|
D006261||throbbing headaches
|
|
D006261||unilateral headache
|
|
D006261||unilateral headaches
|
|
D006261||vertex headache
|
|
D006261||vertex headaches
|
|
125310|D046589||cadasil
|
|
125310|D046589||cadasilm
|
|
125310|D046589||casil
|
|
125310|D046589||cerebral arteriopathy autosomal dominant with subcortical infarcts and leukoencephalopathy
|
|
125310|D046589||cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
|
|
125310|D046589||cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
|
|
125310|D046589||dementia hereditary multi infarct type
|
|
D018239||seminoma
|
|
D018239||seminomas
|
|
243800|C535880||johanson blizzard syndrome
|
|
243800|C535880||ectodermal dysplasia exocrine pancreatic insufficiency
|
|
243800|C535880|147791|D054868||jbs
|
|
243800|C535880||malabsorption ectodermal dysplasia nasal alar hypoplasia
|
|
243800|C535880||nasal alar hypoplasia hypothyroidism pancreatic achylia and congenital deafness
|
|
243800|C535880||nasal alar hypoplasia hypothyroidism pancreatic achylia congenital deafness
|
|
D019569||hemifacial spasm
|
|
D019569||facial spasms unilateral
|
|
D019569||facial spasm unilateral
|
|
D019569||hemifacial myokymia
|
|
D019569||hemifacial spasms
|
|
D019569||myokymia hemifacial
|
|
D019569||spasm hemifacial
|
|
D019569||spasms hemifacial
|
|
D019569||spasms unilateral facial
|
|
D019569||spasm unilateral facial
|
|
D019569||unilateral facial spasm
|
|
D019569||unilateral facial spasms
|
|
D018238||gonadoblastoma
|
|
D018238||gonadoblastomas
|
|
C566545|602459||deafness autosomal dominant 15
|
|
C566545|602459||dfna15
|
|
D018235||smooth muscle tumor
|
|
D018235||muscle tumor smooth
|
|
D018235||muscle tumors smooth
|
|
D018235||smooth muscle tumors
|
|
D018235||tumor smooth muscle
|
|
D018235||tumors smooth muscle
|
|
D057887||overbite
|
|
D057887||bite deep
|
|
D057887||bites deep
|
|
D057887||deep bite
|
|
D057887||deep bites
|
|
D057887||dental overjet
|
|
D057887||dental overjets
|
|
D057887||incisor protrusion
|
|
D057887||incisor protrusions
|
|
D057887||overbites
|
|
D057887||overjet dental
|
|
D057887||overjets dental
|
|
D057887||protrusion incisor
|
|
D057887||protrusions incisor
|
|
D019568||lung hyperlucent
|
|
D019568||hyperlucent lung
|
|
D019568||hyperlucent lungs
|
|
D019568||hyperlucent lungs unilateral
|
|
D019568||hyperlucent lung unilateral
|
|
D019568||hyperlucent thorax
|
|
D019568||lungs hyperlucent
|
|
D019568||lungs unilateral hyperlucent
|
|
D019568||lung unilateral hyperlucent
|
|
D019568||macleod syndrome
|
|
D019568||swyer james syndrome
|
|
D019568||syndrome macleod
|
|
D019568||syndrome swyer james
|
|
D019568||thorax hyperlucent
|
|
D019568||unilateral hyperlucent lung
|
|
D019568||unilateral hyperlucent lungs
|
|
D018237||germinoma
|
|
D018237||germinomas
|
|
D019567||back injuries
|
|
D019567||back injury
|
|
D019567||injuries back
|
|
D019567||injury back
|
|
D018236||carcinoma embryonal
|
|
D018236||carcinomas embryonal
|
|
D018236||embryonal carcinoma
|
|
D018236||embryonal carcinomas
|
|
D044584||carcinoma ductal
|
|
D044584||carcinomas ductal
|
|
D044584||ductal carcinoma
|
|
D044584||ductal carcinomas
|
|
C537077||febrile ulceronecrotic mucha habermann disease
|
|
C537077||ulceronecrotic mucha habermann disease
|
|
188470|C572845||thyroid cancer follicular
|
|
188470|C572845||ftc
|
|
D018211||chondrosarcoma mesenchymal
|
|
D018211||chondrosarcomas mesenchymal
|
|
D018211||mesenchymal chondrosarcoma
|
|
D018211||mesenchymal chondrosarcomas
|
|
C565725|609741||cataract congenital nuclear autosomal recessive 2
|
|
C565725|609741||cataract 22
|
|
C565725|609741||cataract 22 nuclear
|
|
C565725|609741||catcn2
|
|
C565725|609741||ctrct22
|
|
D018210||chondromatosis
|
|
D018210||chondromatoses
|
|
C537076||faye petersen ward carey syndrome
|
|
242860||immunodeficiency centromeric instability facial anomalies syndrome 1
|
|
242860||ciid
|
|
242860||icf1
|
|
242860||immune deficiency variable with centromeric instability of chromosomes 1 9 and 16
|
|
D021865||isosporiasis
|
|
D021865||isosporiases
|
|
C565199|610685||split hand foot malformation with long bone deficiency 2
|
|
C565199|610685||shfld2
|
|
C563368||craniosynostosis philadelphia type
|
|
D021866||cyclosporiasis
|
|
D021866||cyclosporiases
|
|
C564698||episodic ataxia type 4
|
|
C564698||ataxia periodic vestibulocerebellar
|
|
C564698||periodic vestibulocerebellar ataxia
|
|
D006228||hand deformities congenital
|
|
D006228||congenital hand deformities
|
|
D006228||congenital hand deformity
|
|
D006228||deformities congenital hand
|
|
D006228||deformity congenital hand
|
|
D006228||hand deformity congenital
|
|
D006229||hand dermatoses
|
|
D006229||dermatoses hand
|
|
D006229||dermatosis hand
|
|
D006229||hand dermatosis
|
|
D006226||hand deformities
|
|
D006226||deformities hand
|
|
D006226||deformity hand
|
|
D006226||hand deformity
|
|
D006227||hand deformities acquired
|
|
D006227||acquired hand deformities
|
|
D006227||acquired hand deformity
|
|
D006227||deformities acquired hand
|
|
D006227||deformity acquired hand
|
|
D006227||hand deformity acquired
|
|
C535478|136800||corneal dystrophy fuchs apos endothelial 1
|
|
C535478|136800||corneal dystrophy fuchs endothelial 1
|
|
C535478|136800||corneal dystrophy fuchs apos endothelial early onset
|
|
C535478|136800||corneal dystrophy fuchs endothelial early onset
|
|
C535478|136800||dystrophia epithelialis corneae
|
|
C535478|136800||fecd1
|
|
C535478|136800||fuchs apos dystrophy
|
|
C535478|136800||fuchs apos endothelial corneal dystrophy early onset
|
|
C537074||fara chlupackova syndrome
|
|
C537074||familial oto facio cervical dysmorphia
|
|
D006222||hamartoma
|
|
D006222||hamartomas
|
|
C537071||follicular hamartoma alopecia cystic fibrosis
|
|
C537071||congenital generalized follicular hamartoma associated with alopecia and cystic fibrosis
|
|
D003394|123500||craniofacial dysostosis
|
|
D003394|123500||cfd1
|
|
D003394|123500||craniofacial dysarthrosis
|
|
D003394|123500||craniofacial dysostoses
|
|
D003394|123500||craniofacial dysostosis crouzon
|
|
D003394|123500||craniofacial dysostosis syndrome
|
|
D003394|123500||craniofacial dysostosis type 1
|
|
D003394|123500||craniofacial dysostosis type 1 cfd1
|
|
D003394|123500||craniofacial dysostosis type i
|
|
D003394|123500||crouzon craniofacial dysostosis
|
|
D003394|123500||crouzon disease
|
|
D003394|123500||crouzon apos s disease
|
|
D003394|123500||crouzons disease
|
|
D003394|123500||crouzon syndrome
|
|
D003394|123500||disease crouzon
|
|
D003394|123500||disease crouzon apos s
|
|
D003394|123500||dysostoses craniofacial
|
|
D003394|123500||dysostosis craniofacial
|
|
D003394|123500||dysostosis crouzon craniofacial
|
|
D003394|123500||syndrome crouzon
|
|
C537072||nonpuerperal galactorrhea
|
|
C537072||ahumada del castillo syndrome
|
|
C537072||amenorrhea galactorrhea fsh decrease syndrome
|
|
C537072||amenorrhea galactorrhea nonpuerperal
|
|
C537072||amenorrhea galactorrhea syndrome
|
|
C537072||argonz ahumada del castillo syndrome
|
|
C537072||argonz del castillo syndrome
|
|
C537072||forbes albright syndrome
|
|
C537072||galactorrhea amenorrhea syndrome
|
|
C537072||galactorrhea amenorrhea without pregnancy
|
|
C537072||nonpuerperal galactorrhea amenorrhea
|
|
D006232||hand foot and mouth disease
|
|
D006232||hand foot mouth disease
|
|
D057896||striae distensae
|
|
D057896||distensae striae
|
|
D057896||marks stretch
|
|
D057896||mark stretch
|
|
D057896||stretch mark
|
|
D057896||stretch marks
|
|
D006230||hand injuries
|
|
D006230||hand injury
|
|
D006230||injuries hand
|
|
D006230||injury hand
|
|
D018209||myelolipoma
|
|
D018209||myelolipomas
|
|
C563437|600852||retinitis pigmentosa 17
|
|
C563437|600852||rp17
|
|
D057891||tetraploidy
|
|
D057891||tetraploid
|
|
D057891||tetraploidies
|
|
D057891||tetraploids
|
|
D018206||angiolipoma
|
|
D018206||angiolipomas
|
|
D018205||neoplasms adipose tissue
|
|
D018205||adipose tissue neoplasm
|
|
D018205||adipose tissue neoplasms
|
|
D018205||neoplasm adipose tissue
|
|
D018207||angiomyolipoma
|
|
D018207||angiomyolipomas
|
|
612281||ichthyosis congenital autosomal recessive 6
|
|
612281||arci6
|
|
612281||ichthyosis congenital autosomal recessive nipal4 related
|
|
D018202||pulmonary blastoma
|
|
D018202||blastoma pulmonary
|
|
D018202||blastomas pulmonary
|
|
D018202||pulmonary blastomas
|
|
C567834|612976||presbycusis 2
|
|
C567834|612976||age related hearing impairment 2
|
|
C567834|612976||arhi2
|
|
D018201||nephroma mesoblastic
|
|
D018201||congenital mesoblastic nephroma
|
|
D018201||congenital mesoblastic nephromas
|
|
D018201||mesoblastic nephroma
|
|
D018201||mesoblastic nephroma congenital
|
|
D018201||mesoblastic nephromas congenital
|
|
D018201||nephroma congenital mesoblastic
|
|
D018201||nephromas congenital mesoblastic
|
|
D018201||nephromas mesoblastic
|
|
D018204||neoplasms connective and soft tissue
|
|
D018204||connective and soft tissue neoplasms
|
|
C563370||alopecia mental retardation syndrome with convulsions and hypergonadotropic hypogonadism
|
|
D019534||shoulder impingement syndrome
|
|
D019534||impingement syndrome shoulder
|
|
D019534||impingement syndromes shoulder
|
|
D019534||impingement syndromes subacromial
|
|
D019534||impingement syndrome subacromial
|
|
D019534||shoulder impingement syndromes
|
|
D019534||subacromial impingement syndrome
|
|
D019534||subacromial impingement syndromes
|
|
D019534||syndrome shoulder impingement
|
|
D019534||syndromes shoulder impingement
|
|
D019534||syndromes subacromial impingement
|
|
D019534||syndrome subacromial impingement
|
|
D018203||sarcoma endometrial stromal
|
|
D018203||endometrial stromal sarcoma
|
|
D018203||endometrial stromal sarcomas
|
|
D018203||sarcomas endometrial stromal
|
|
D018203||stromal sarcoma endometrial
|
|
D018203||stromal sarcomas endometrial
|
|
D018220||fibroma desmoplastic
|
|
D018220||desmoplastic fibroma
|
|
D018220||desmoplastic fibromas
|
|
D018220||fibromas desmoplastic
|
|
D019553||tooth nonvital
|
|
D019553||devitalized teeth
|
|
D019553||devitalized tooth
|
|
D019553||endodontically treated teeth
|
|
D019553||endodontically treated tooth
|
|
D019553||nonvital teeth
|
|
D019553||nonvital tooth
|
|
D019553||pulpless teeth
|
|
D019553||pulpless tooth
|
|
D019553||teeth devitalized
|
|
D019553||teeth endodontically treated
|
|
D019553||teeth nonvital
|
|
D019553||teeth pulpless
|
|
D019553||tooth devitalized
|
|
D019553||tooth endodontically treated
|
|
D019553||tooth pulpless
|
|
D018222||fibromatosis aggressive
|
|
D018222||aggressive fibromatoses
|
|
D018222||aggressive fibromatosis
|
|
D018222||desmoid
|
|
D018222||desmoids
|
|
D018222||fibromatoses aggressive
|
|
C563374||hypocalcemia autosomal dominant with bartter syndrome
|
|
C537086||brachydactylous dwarfism mseleni type
|
|
C537086||brachydactylous dwarfs of mseleni
|
|
D018221||fibromatosis abdominal
|
|
D018221||abdominal fibromatoses
|
|
D018221||abdominal fibromatosis
|
|
D018221||fibromatoses abdominal
|
|
C563373||hypercalciuric hypercalcemia
|
|
C537087||brachydactyly preaxial with hallux varus and thumb abduction
|
|
C537087||christian brachydactyly
|
|
C537087||dominant preaxial brachydactyly with hallux varus and thumb abduction
|
|
C563378||muscular dystrophy congenital with severe central nervous system atrophy and absence of large myelinated fibers
|
|
D020526||brain stem infarctions
|
|
D020526||benedict syndrome
|
|
D020526||brainstem infarction
|
|
D020526||brain stem infarction
|
|
D020526||brainstem infarctions
|
|
D020526||brainstem stroke
|
|
D020526||claude syndrome
|
|
D020526||foville syndrome
|
|
D020526||infarction brainstem
|
|
D020526||infarction brain stem
|
|
D020526||infarctions brainstem
|
|
D020526||infarctions brain stem
|
|
D020526||millard gublar syndrome
|
|
D020526||stroke brainstem
|
|
D020526||syndrome millard gublar
|
|
D020526||top of the basilar syndrome
|
|
D020526||weber syndrome
|
|
C536338|175850||porokeratosis punctata palmaris et plantaris
|
|
C536338|175850||keratoderma palmoplantar punctate type ii
|
|
C536338|175850||porok2
|
|
C536338|175850||porokeratosis 2 palmar plantar and disseminated type
|
|
C536338|175850||porokeratosis palmar plantar and disseminated
|
|
C536338|175850||pppd
|
|
C536338|175850||pppd1
|
|
C537080||baritosis
|
|
C537080||deposition of barium in the lungs
|
|
C537080||inhalation of barytes
|
|
D007569||jaw abnormalities
|
|
D007569||abnormalities jaw
|
|
D007569||abnormality jaw
|
|
D007569||jaw abnormality
|
|
D020522||lymphoma mantle cell
|
|
D020522||centrocytic small cell lymphoma
|
|
D020522||centrocytic small cell lymphomas
|
|
D020522||diffuse lymphocytic lymphoma poorly differentiated
|
|
D020522||lymphocytic lymphoma diffuse poorly differentiated
|
|
D020522||lymphoma centrocytic small cell
|
|
D020522||lymphoma lymphocytic diffuse intermediate differentiated
|
|
D020522||lymphoma lymphocytic diffuse poorly differentiated
|
|
D020522||lymphoma lymphocytic intermediate
|
|
D020522||lymphoma mantle zone
|
|
D020522||lymphomas centrocytic small cell
|
|
D020522||lymphoma small cell centrocytic
|
|
D020522||lymphomas mantle cell
|
|
D020522||lymphomas mantle zone
|
|
D020522||mantle cell lymphoma
|
|
D020522||mantle cell lymphomas
|
|
D020522||mantle zone lymphoma
|
|
D020522||mantle zone lymphomas
|
|
D020522||small cell lymphoma centrocytic
|
|
D020522||small cell lymphomas centrocytic
|
|
C537084||brachioskeletogenital syndrome
|
|
D007567||jaundice neonatal
|
|
D007567||icterus gravis neonatorum
|
|
D007567||jaundice physiological neonatal
|
|
D007567||neonatal jaundice
|
|
D007567||neonatal jaundice physiological
|
|
D007567||physiological neonatal jaundice
|
|
D007567||severe jaundice in neonate
|
|
D007567||severe jaundice in newborn
|
|
C537085||brachycephalofrontonasal dysplasia
|
|
C537085||hypertelorism teebi type
|
|
C537085||teebi hypertelorism syndrome
|
|
D020520||brain infarction
|
|
D020520||anterior cerebral circulation infarction
|
|
D020520||anterior circulation brain infarction
|
|
D020520||anterior circulation infarction brain
|
|
D020520||brain infarction anterior circulation
|
|
D020520||brain infarction posterior circulation
|
|
D020520||brain infarctions
|
|
D020520||brain infarctions venous
|
|
D020520||brain infarction venous
|
|
D020520||brain venous infarction
|
|
D020520||brain venous infarctions
|
|
D020520||infarction anterior cerebral circulation
|
|
D020520||infarction anterior circulation brain
|
|
D020520||infarction brain
|
|
D020520||infarction brain anterior circulation
|
|
D020520||infarction brain posterior circulation
|
|
D020520||infarction brain venous
|
|
D020520||infarction posterior circulation brain
|
|
D020520||infarctions brain
|
|
D020520||infarctions brain venous
|
|
D020520||infarctions venous brain
|
|
D020520||infarction venous brain
|
|
D020520||posterior circulation brain infarction
|
|
D020520||posterior circulation infarction brain
|
|
D020520||venous brain infarction
|
|
D020520||venous brain infarctions
|
|
D020520||venous infarction brain
|
|
D020520||venous infarctions brain
|
|
C537082||weismann netter syndrome
|
|
C537082||anterior bowing of legs with dwarfism
|
|
C537082||bowing of legs anterior with dwarfism
|
|
C537082||toxopachyosteose diaphysaire tibio peroniere
|
|
C537082||toxopachyosteosis
|
|
C537082||toxopachyoteose diaphysaire tibio peroniere
|
|
C537082||weismann netter stuhl syndrome
|
|
D007565||jaundice
|
|
D007565||hemolytic jaundice
|
|
D007565||hemolytic jaundices
|
|
D007565||icterus
|
|
D007565||jaundice hemolytic
|
|
D007565||jaundices hemolytic
|
|
607487|C564388||cardiomyopathy dilated 1n
|
|
607487|C564388||cmd1n
|
|
C537083||boylan dew greco syndrome
|
|
C537083||congenital hypomyelination neuropathy with arthrogryposis multiplex congenita
|
|
D007573||jaw neoplasms
|
|
D007573||cancer jaw
|
|
D007573||cancer of jaw
|
|
D007573||cancer of the jaw
|
|
D007573||cancers jaw
|
|
D007573||jaw cancer
|
|
D007573||jaw cancers
|
|
D007573||jaw neoplasm
|
|
D007573||neoplasm jaw
|
|
D007573||neoplasms jaw
|
|
D007571||jaw diseases
|
|
D007571||disease jaw
|
|
D007571||diseases jaw
|
|
D007571||jaw disease
|
|
D007572||jaw fractures
|
|
D007572||fracture jaw
|
|
D007572||fractures jaw
|
|
D007572||jaw fracture
|
|
D007570||jaw cysts
|
|
D007570||cyst jaw
|
|
D007570||cysts jaw
|
|
D007570||jaw cyst
|
|
D020529||multiple sclerosis relapsing remitting
|
|
D020529||acute relapsing multiple sclerosis
|
|
D020529||multiple sclerosis acute relapsing
|
|
D020529||multiple sclerosis remitting relapsing
|
|
D020529||relapsing remitting multiple sclerosis
|
|
D020529||remitting relapsing multiple sclerosis
|
|
D020528||multiple sclerosis chronic progressive
|
|
D020528||chronic progressive multiple sclerosis
|
|
D020528||multiple sclerosis primary progressive
|
|
D020528||multiple sclerosis progressive relapsing
|
|
D020528||multiple sclerosis remittent progressive
|
|
D020528||multiple sclerosis secondary progressive
|
|
D020528||primary progressive multiple sclerosis
|
|
D020528||progressive relapsing multiple sclerosis
|
|
D020528||remittent progressive multiple sclerosis
|
|
D020528||secondary progressive multiple sclerosis
|
|
300514|C564497||fanconi anemia complementation group b
|
|
300514|C564497||fa2
|
|
300514|C564497||facb
|
|
300514|C564497||fancb
|
|
300514|C564497||fanconi pancytopenia type 2
|
|
D018217||osteosarcoma juxtacortical
|
|
D018217||juxtacortical osteosarcoma
|
|
D018217||juxtacortical osteosarcomas
|
|
D018217||osteosarcomas juxtacortical
|
|
D019547||neck pain
|
|
D019547||ache neck
|
|
D019547||aches neck
|
|
D019547||anterior cervical pain
|
|
D019547||anterior cervical pains
|
|
D019547||anterior neck pain
|
|
D019547||anterior neck pains
|
|
D019547||cervicalgia
|
|
D019547||cervicalgias
|
|
D019547||cervical pain
|
|
D019547||cervical pain anterior
|
|
D019547||cervical pain posterior
|
|
D019547||cervical pains
|
|
D019547||cervical pains anterior
|
|
D019547||cervical pains posterior
|
|
D019547||cervicodynia
|
|
D019547||cervicodynias
|
|
D019547||neckache
|
|
D019547||neck ache
|
|
D019547||neckaches
|
|
D019547||neck aches
|
|
D019547||neck pain anterior
|
|
D019547||neck pain posterior
|
|
D019547||neck pains
|
|
D019547||neck pains anterior
|
|
D019547||neck pains posterior
|
|
D019547||pain anterior cervical
|
|
D019547||pain anterior neck
|
|
D019547||pain cervical
|
|
D019547||pain neck
|
|
D019547||pain posterior cervical
|
|
D019547||pain posterior neck
|
|
D019547||pains anterior cervical
|
|
D019547||pains anterior neck
|
|
D019547||pains cervical
|
|
D019547||pains neck
|
|
D019547||pains posterior cervical
|
|
D019547||pains posterior neck
|
|
D019547||posterior cervical pain
|
|
D019547||posterior cervical pains
|
|
D019547||posterior neck pain
|
|
D019547||posterior neck pains
|
|
D005776|230800||gaucher disease
|
|
D005776|230800||acid beta glucosidase deficiency
|
|
D005776|230800||acid beta glucosidase deficiency disease
|
|
D005776|230800||acute neuronopathic gaucher disease
|
|
D005776|230800||cerebroside lipidoses glucosyl
|
|
D005776|230800||cerebroside lipidosis glucosyl
|
|
D005776|230800||cerebroside lipidosis syndrome
|
|
D005776|230800||cerebroside lipidosis syndromes
|
|
D005776|230800||chronic gaucher disease
|
|
D005776|230800||deficiencies gba
|
|
D005776|230800||deficiencies glucocerebrosidase
|
|
D005776|230800||deficiency disease glucocerebrosidase
|
|
D005776|230800||deficiency diseases glucocerebrosidase
|
|
D005776|230800||deficiency gba
|
|
D005776|230800||deficiency glucocerebrosidase
|
|
D005776|230800||disease chronic gaucher
|
|
D005776|230800||disease gaucher
|
|
D005776|230800||disease gauchers
|
|
D005776|230800||disease gaucher apos s
|
|
D005776|230800||disease glucocerebrosidase deficiency
|
|
D005776|230800||disease infantile gaucher
|
|
D005776|230800||disease juvenile gaucher
|
|
D005776|230800||disease neuronopathic gaucher
|
|
D005776|230800||disease non neuronopathic gaucher
|
|
D005776|230800||diseases gauchers
|
|
D005776|230800||diseases glucocerebrosidase deficiency
|
|
D005776|230800||gaucher disease acute neuronopathic
|
|
D005776|230800||gaucher disease acute neuronopathic type
|
|
D005776|230800||gaucher disease chronic
|
|
D005776|230800||gaucher disease chronic neuronopathic type
|
|
D005776|230800||gaucher disease infantile
|
|
D005776|230800||gaucher disease infantile cerebral
|
|
D005776|230800||gaucher disease juvenile
|
|
D005776|230800||gaucher disease juvenile and adult cerebral
|
|
D005776|230800||gaucher disease juvenile and adult cerebral gaucher disease type iiia included
|
|
D005776|230800||gaucher disease neuronopathic
|
|
D005776|230800||gaucher disease noncerebral juvenile
|
|
D005776|230800||gaucher disease non neuronopathic
|
|
D005776|230800||gaucher disease non neuronopathic form
|
|
D005776|230800||gaucher disease norrbottnian type included
|
|
D005776|230800||gaucher disease subacute neuronopathic form
|
|
D005776|230800||gaucher disease subacute neuronopathic type
|
|
D005776|230800||gaucher disease type 1
|
|
D005776|230800||gaucher disease type 2
|
|
D005776|230800||gaucher disease type 3
|
|
D005776|230800||gaucher disease type i
|
|
D005776|230800||gaucher disease type ii
|
|
D005776|230800||gaucher disease type iii
|
|
D005776|230800||gaucher disease type iiib included
|
|
D005776|230800||gaucher apos s disease
|
|
D005776|230800||gauchers disease
|
|
D005776|230800||gauchers diseases
|
|
D005776|230800||gaucher splenomegaly
|
|
D005776|230800||gaucher syndrome
|
|
D005776|230800||gba deficiencies
|
|
D005776|230800||gba deficiency
|
|
D005776|230800||gd i
|
|
D005776|230800||gd ii
|
|
D005776|230800||gd iii
|
|
D005776|230800||glucocerebrosidase deficiencies
|
|
D005776|230800||glucocerebrosidase deficiency
|
|
D005776|230800||glucocerebrosidase deficiency disease
|
|
D005776|230800||glucocerebrosidase deficiency diseases
|
|
D005776|230800||glucocerebrosidoses
|
|
D005776|230800||glucocerebrosidosis
|
|
D005776|230800||glucosylceramidase deficiency
|
|
D005776|230800||glucosylceramide beta glucosidase deficiency
|
|
D005776|230800||glucosylceramide beta glucosidase deficiency disease
|
|
D005776|230800||glucosylceramide lipidoses
|
|
D005776|230800||glucosylceramide lipidosis
|
|
D005776|230800||glucosyl cerebroside lipidoses
|
|
D005776|230800||glucosyl cerebroside lipidosis
|
|
D005776|230800||histiocytoses kerasin
|
|
D005776|230800||histiocytoses lipoid kerasin type
|
|
D005776|230800||histiocytosis kerasin
|
|
D005776|230800||histiocytosis lipoid kerasin type
|
|
D005776|230800||infantile gaucher disease
|
|
D005776|230800||juvenile gaucher disease
|
|
D005776|230800||kerasin histiocytoses
|
|
D005776|230800||kerasin histiocytosis
|
|
D005776|230800||kerasin lipoidoses
|
|
D005776|230800||kerasin lipoidosis
|
|
D005776|230800||kerasin thesaurismoses
|
|
D005776|230800||kerasin thesaurismosis
|
|
D005776|230800||lipidoses glucosylceramide
|
|
D005776|230800||lipidoses glucosyl cerebroside
|
|
D005776|230800||lipidosis glucosylceramide
|
|
D005776|230800||lipidosis glucosyl cerebroside
|
|
D005776|230800||lipidosis syndrome cerebroside
|
|
D005776|230800||lipidosis syndromes cerebroside
|
|
D005776|230800||lipoid histiocytoses kerasin type
|
|
D005776|230800||lipoid histiocytosis kerasin type
|
|
D005776|230800||lipoidoses kerasin
|
|
D005776|230800||lipoidosis kerasin
|
|
D005776|230800||neuronopathic gaucher disease
|
|
D005776|230800||non neuronopathic gaucher disease
|
|
D005776|230800||splenomegaly gaucher
|
|
D005776|230800||subacute neuronopathic gaucher disease
|
|
D005776|230800||syndrome cerebroside lipidosis
|
|
D005776|230800||syndrome gaucher
|
|
D005776|230800||syndromes cerebroside lipidosis
|
|
D005776|230800||thesaurismoses kerasin
|
|
D005776|230800||thesaurismosis kerasin
|
|
D005776|230800||type 1 gaucher disease
|
|
D005776|230800||type 2 gaucher disease
|
|
D005776|230800||type 3 gaucher disease
|
|
D018216||osteochondromatoses
|
|
D018219||histiocytoma benign fibrous
|
|
D018219||angioma sclerosing
|
|
D018219||angiomas sclerosing
|
|
D018219||benign fibrous histiocytoma
|
|
D018219||benign fibrous histiocytomas
|
|
D018219||cutaneous histiocytoma
|
|
D018219||cutaneous histiocytomas
|
|
D018219||dermatofibroma
|
|
D018219||dermatofibromas
|
|
D018219||fibrous histiocytoma
|
|
D018219||fibrous histiocytoma benign
|
|
D018219||fibrous histiocytomas
|
|
D018219||fibrous histiocytomas benign
|
|
D018219||hemangioma sclerosing
|
|
D018219||hemangiomas sclerosing
|
|
D018219||histiocytoma cutaneous
|
|
D018219||histiocytoma fibrous
|
|
D018219||histiocytomas benign fibrous
|
|
D018219||histiocytomas cutaneous
|
|
D018219||histiocytomas fibrous
|
|
D018219||sclerosing angioma
|
|
D018219||sclerosing angiomas
|
|
D018219||sclerosing hemangioma
|
|
D018219||sclerosing hemangiomas
|
|
D018218||neoplasms fibrous tissue
|
|
D018218||fibrous tissue neoplasm
|
|
D018218||fibrous tissue neoplasms
|
|
D018218||neoplasm fibrous tissue
|
|
D018213||neoplasms bone tissue
|
|
D018213||bone tissue neoplasm
|
|
D018213||bone tissue neoplasms
|
|
D018213||bony tissue neoplasm
|
|
D018213||bony tissue neoplasms
|
|
D018213||neoplasm bone tissue
|
|
D018213||neoplasm bony tissue
|
|
D018213||neoplasms bony tissue
|
|
D018213||tissue neoplasm bone
|
|
D018213||tissue neoplasm bony
|
|
D018213||tissue neoplasms bone
|
|
D018213||tissue neoplasms bony
|
|
C563383||lissencephaly type iii and bone dysplasia
|
|
D018212||giant cell tumor of bone
|
|
C563382||trisomy 18 like syndrome
|
|
D018215||osteoblastoma
|
|
D018215||giant osteoid osteoma
|
|
D018215||giant osteoid osteomas
|
|
D018215||osteoblastomas
|
|
D018215||osteoid osteoma giant
|
|
D018215||osteoid osteomas giant
|
|
D018215||osteoma giant osteoid
|
|
D018215||osteomas giant osteoid
|
|
612539|C567262||spastic paraplegia 42 autosomal dominant
|
|
612539|C567262||spg42
|
|
D018214||fibroma ossifying
|
|
D018214||fibromas ossifying
|
|
D018214||ossifying fibroma
|
|
D018214||ossifying fibromas
|
|
C563380||diaphragmatic defects limb deficiencies and ossification defects of skull
|
|
C537099||brachyolmia recessive hobaek type
|
|
C537099||brachyolmia recessive type of hobaek
|
|
C537099||brachyolmia type 1 hobaek type
|
|
C537099||spondylodysplasia with pure brachyolmia
|
|
C563342||mental retardation microcephaly epilepsy and coarse face
|
|
C563341||microcephaly congenital heart disease unilateral renal agenesis and hyposegmented lungs
|
|
C537097||brachymesophalangy 2 and 5
|
|
C537097||brachydactyly temtamy type
|
|
C537097||brachydactyly type a4
|
|
C537097||brachymesophalangy ii and v
|
|
C537097||temtamy type brachydactyly
|
|
C563817|607554||atrial fibrillation familial 3
|
|
C563817|607554||atfb3
|
|
C537098||brachyolmia
|
|
C563347||ectodermal dysplasia with natal teeth turnpenny type
|
|
C563346||martinez frias syndrome
|
|
C563346||diabetes neonatal with pancreatic hypoplasia intestinal atresia and gallbladder aplasia or hypoplasia
|
|
C563346||pancreatic hypoplasia intestinal atresia and gallbladder aplasia or hypoplasia with or without tracheoesophageal fistula
|
|
C564676||dyskinesia familial with facial myokymia
|
|
C563345||myelodysplasia immunodeficiency facial dysmorphism short stature and psychomotor delay
|
|
D006209||halitosis
|
|
D006209||halitoses
|
|
C563344||ectrodactyly of lower limbs congenital heart defect and micrognathia
|
|
C537091||brachydactyly type a5 nail dysplasia
|
|
C537091||absent middle phalanges of digits 2 5 with nail dysplasia
|
|
C537091||brachydactyly type a5 with nail dysplasia
|
|
D020514||familial hypokalemic periodic paralysis
|
|
D020514||hypokalemic periodic paralysis familial
|
|
D020514||hypokpp
|
|
D020514||hypopp
|
|
D020514||paralysis hypokalemic periodic
|
|
D020514||periodic paralysis hypokalemic
|
|
D020514||periodic paralysis hypokalemics
|
|
D020514||primary hypokalemic periodic paralysis
|
|
D020514||westphall disease
|
|
C537092||brachydactyly type a6
|
|
C537092||osebold remondini syndrome
|
|
C563349||atrophia maculosa varioliformis cutis familial
|
|
C563349||varioliform macular atrophy of the skin
|
|
C563348||spinal dysplasia anhalt type
|
|
C537090||brachydactyly type a3
|
|
C537090||brachydactyly clinodactyly
|
|
C537090||brachymesophalangy 5
|
|
C537090||brachymesophalangy v
|
|
D008865||microstomia
|
|
D008865||microstomias
|
|
D020511||neuromuscular junction diseases
|
|
D020511||neuromuscular junction disease
|
|
D020511||neuromuscular junction disorder
|
|
D020511||neuromuscular junction disorders
|
|
D020511||neuromuscular junction toxic disorders
|
|
D020511||neuromuscular transmission disorder
|
|
D020511||neuromuscular transmission disorders
|
|
D020511||toxic disorders neuromuscular junction
|
|
C563839|608890||waardenburg syndrome type 2d
|
|
C563839|608890||waardenburg syndrome type iid
|
|
C563839|608890||ws2d
|
|
277480|D056729||von willebrand disease type 3
|
|
277480|D056729||3 vwd type
|
|
277480|D056729||type 3 von willebrand apos s disease
|
|
277480|D056729||type 3 vwd
|
|
277480|D056729||von willebrand disease severe form
|
|
277480|D056729||von willebrand disease type iii
|
|
277480|D056729||vwd3
|
|
277480|D056729||vwd type 3
|
|
C537096||brachymesomelia renal syndrome
|
|
C537096||langer nishino yamaguchi syndrome
|
|
D006201||hair diseases
|
|
D006201||hair disease
|
|
C537094||brachydactyly types b and e combined
|
|
C537094||brachydactyly ballard type
|
|
C537094||brachydactyly combined b and e types
|
|
C537094||pitt williams brachydactyly
|
|
132400|C535501||epiphyseal dysplasia multiple 1
|
|
132400|C535501||edm1
|
|
132400|C535501||epiphyseal dysplasia ribbing type included
|
|
132400|C535501||multiple epiphyseal dysplasia cartilage oligomeric matrix protein related
|
|
132400|C535501||multiple epiphyseal dysplasia comp related
|
|
132400|C535501||multiple epiphyseal dysplasia comp related epiphyseal dysplasia fairbank type included
|
|
D056586||acute chest syndrome
|
|
D056586||acute chest syndromes
|
|
D056586||syndrome acute chest
|
|
D056586||syndromes acute chest
|
|
D020518||focal nodular hyperplasia
|
|
D020518||focal nodular hyperplasias
|
|
D020518||hyperplasia focal nodular
|
|
D020518||hyperplasias focal nodular
|
|
C536607|601003||brody myopathy
|
|
C536607|601003||autosomal recessive brody myopathy
|
|
C536607|601003||brody disease
|
|
D020516||brachial plexus neuropathies
|
|
D020516||brachial plexopathy
|
|
D020516||brachial plexus disease
|
|
D020516||brachial plexus diseases
|
|
D020516||brachial plexus disorder
|
|
D020516||brachial plexus disorders
|
|
D020516||brachial plexus neuropathy
|
|
D020516||dejerine klumpke palsy
|
|
D020516||erb duchenne paralyses
|
|
D020516||erb duchenne paralysis
|
|
D020516||erb palsy
|
|
D020516||erb paralyses
|
|
D020516||erb paralysis
|
|
D020516||erb apos s palsies
|
|
D020516||erb apos s palsy
|
|
D020516||erbs palsy
|
|
D020516||klumpke palsy
|
|
D020516||klumpke paralysis
|
|
D020516||klumpke apos s palsy
|
|
D020516||klumpkes palsy
|
|
D020516||lower brachial plexus neuropathy
|
|
D020516||lower brachial plexus palsy
|
|
D020516||middle brachial plexus neuropathy
|
|
D020516||neuropathies brachial plexus
|
|
D020516||neuropathy brachial plexus
|
|
D020516||palsies erb apos s
|
|
D020516||palsy dejerine klumpke
|
|
D020516||palsy erb apos s
|
|
D020516||palsy klumpke apos s
|
|
D020516||paralyses erb
|
|
D020516||paralyses erb duchenne
|
|
D020516||paralysis erb
|
|
D020516||paralysis erb duchenne
|
|
D020516||paralysis klumpke
|
|
D020516||paralysis of the lower brachial plexus
|
|
D020516||plexopathies brachial
|
|
D020516||plexopathy brachial
|
|
D020516||plexus disease brachial
|
|
D020516||plexus diseases brachial
|
|
D020516||plexus disorder brachial
|
|
D020516||plexus disorders brachial
|
|
D020516||plexus neuropathies brachial
|
|
D020516||plexus neuropathy brachial
|
|
D020516||upper brachial plexus neuropathy
|
|
612263||melanoma cutaneous malignant susceptibility to 7
|
|
612263||cmm7
|
|
C536761|300751||x linked sideroblastic anemia
|
|
C536761|300751||anemia hereditary sideroblastic
|
|
C536761|300751||anemia sex linked hypochromic sideroblastic
|
|
C536761|300751||anemia sideroblastic x linked
|
|
C536761|300751||anh1
|
|
C536761|300751||congenital sideroblastic anaemia
|
|
C536761|300751||erythroid 5 aminolevulinate synthase deficiency
|
|
C536761|300751||hereditary iron loading anemia
|
|
C536761|300751||x chromosome linked sideroblastic anemia
|
|
C536761|300751||x linked pyridoxine responsive sideroblastic anemia
|
|
C536761|300751||xlsa
|
|
D003025|119800||clubfoot
|
|
D003025|119800||ccf
|
|
D003025|119800||clubfoot congenital
|
|
D003025|119800||clubfoot congenital with or without deficiency of long bones and or mirror image polydactyly
|
|
D003025|119800||congenital talipes equinovarus
|
|
D003025|119800||equinovarus
|
|
D003025|119800||pie torcido
|
|
D003025|119800||pie torcidos
|
|
D003025|119800||talipe
|
|
D003025|119800||talipes
|
|
D003025|119800||talipes equinovarus
|
|
D003025|119800||talipes equinovarus congenital
|
|
D019512||pancreatitis alcoholic
|
|
D019512||alcoholic pancreatitis
|
|
C563977|600195||venous malformations multiple cutaneous and mucosal
|
|
C563977|600195||mucocutaneous venous malformations
|
|
C563977|600195||multiple cutaneous and mucosal venous malformations
|
|
C563977|600195||vmcm
|
|
C563977|600195||vmcm1
|
|
C537932|609524||filaminopathy autosomal dominant
|
|
C537932|609524||filamin c related myofibrillar myopathy
|
|
C537932|609524||mfm5
|
|
C537932|609524||mfm filamin c related
|
|
C537932|609524||myofibrillar myopathy filamin c related
|
|
C537932|609524||myopathy myofibrillar 5
|
|
C537932|609524||myopathy myofibrillar filamin c related
|
|
D018200||mixed tumor mullerian
|
|
D018200||mullerian mixed tumor
|
|
D018200||tumor mullerian mixed
|
|
C564689||camurati engelmann disease type ii
|
|
C563358||pulmonary arterial hypertension hereditary hemorrhagic telangiectasia related
|
|
C563358||hereditary hemorrhagic telangiectasia related pulmonary arterial hypertension
|
|
613581||retinitis pigmentosa 56
|
|
613581||maculopathy impg2 related included
|
|
613581||rp56
|
|
145700|C538389||congenital hypertrichosis lanuginosa
|
|
145700|C538389||hypertrichosis lanuginosa congenita
|
|
145700|C538389||hypertrichosis lanuginosa universalis
|
|
145700|C538389||hypertrichosis universalis
|
|
613582||retinitis pigmentosa 57
|
|
613582||rp57
|
|
D008878||middle lobe syndrome
|
|
D008878||brock apos s syndrome
|
|
D008878||brocks syndrome
|
|
D008878||brock syndrome
|
|
D008878||syndrome brock apos s
|
|
D008878||syndromes middle lobe
|
|
D006215||hallux valgus
|
|
D006215||bunion
|
|
D006215||bunions
|
|
D006215||hallux abductovalgus
|
|
D006215||metatarsus primus varus
|
|
D006215||primus varus metatarsus
|
|
D006215||varus metatarsus primus
|
|
D007644|101900||darier disease
|
|
D007644|101900||acantholytic dyskeratotic epidermal nevi
|
|
D007644|101900||acantholytic dyskeratotic epidermal nevus
|
|
D007644|101900||acrokeratosis verruciformis
|
|
D007644|101900||acrokeratosis verruciformis of hopf
|
|
D007644|101900||akv
|
|
D007644|101900||dar
|
|
D007644|101900||darier disease dd darier disease acral hemorrhagic type included
|
|
D007644|101900||darier disease segmental included
|
|
D007644|101900||darier apos s disease
|
|
D007644|101900||dariers disease
|
|
D007644|101900||darier white disease
|
|
D007644|101900||darier white diseases
|
|
D007644|101900||disease darier
|
|
D007644|101900||disease darier apos s
|
|
D007644|101900||disease darier white
|
|
D007644|101900||disease hopf
|
|
D007644|101900||diseases darier white
|
|
D007644|101900||diseases hopf
|
|
D007644|101900||hopf acrokeratosis verruciformis
|
|
D007644|101900||hopf disease
|
|
D007644|101900||hopf diseases
|
|
D007644|101900||keratosis follicularis
|
|
D007644|101900||verruciformis acrokeratosis
|
|
613587||occult macular dystrophy
|
|
613587||ocmd
|
|
613587||omd
|
|
C567796|613064||dermatitis atopic 7
|
|
C567796|613064||atod7
|
|
D006212||hallucinations
|
|
D006212||auditory hallucination
|
|
D006212||auditory hallucinations
|
|
D006212||auditory hallucinations verbal
|
|
D006212||auditory hallucination verbal
|
|
D006212||body sensation hallucination
|
|
D006212||body sensation hallucinations
|
|
D006212||dissociative hallucination
|
|
D006212||dissociative hallucinations
|
|
D006212||elementary hallucination
|
|
D006212||elementary hallucinations
|
|
D006212||gustatory hallucination
|
|
D006212||gustatory hallucinations
|
|
D006212||hallucination
|
|
D006212||hallucination auditory
|
|
D006212||hallucination dissociative
|
|
D006212||hallucination elementary
|
|
D006212||hallucination gustatory
|
|
D006212||hallucination hypnagogic
|
|
D006212||hallucination hypnapompic
|
|
D006212||hallucination kinesthetic
|
|
D006212||hallucination mood congruent
|
|
D006212||hallucination mood incongruent
|
|
D006212||hallucination of body sensation
|
|
D006212||hallucination olfactory
|
|
D006212||hallucination organic
|
|
D006212||hallucination reflex
|
|
D006212||hallucinations auditory
|
|
D006212||hallucinations dissociative
|
|
D006212||hallucinations elementary
|
|
D006212||hallucination sensory
|
|
D006212||hallucinations formed of people
|
|
D006212||hallucinations gustatory
|
|
D006212||hallucinations hypnagogic
|
|
D006212||hallucinations hypnapompic
|
|
D006212||hallucinations internal body sensation
|
|
D006212||hallucinations kinesthetic
|
|
D006212||hallucinations mood congruent
|
|
D006212||hallucinations mood incongruent
|
|
D006212||hallucinations olfactory
|
|
D006212||hallucination somatic
|
|
D006212||hallucinations organic
|
|
D006212||hallucinations reflex
|
|
D006212||hallucinations sensory
|
|
D006212||hallucinations somatic
|
|
D006212||hallucinations tactile
|
|
D006212||hallucinations verbal auditory
|
|
D006212||hallucinations visual
|
|
D006212||hallucinations visual formed
|
|
D006212||hallucinations visual unformed
|
|
D006212||hallucination tactile
|
|
D006212||hallucination verbal auditory
|
|
D006212||hallucination visual
|
|
D006212||hypnagogic hallucination
|
|
D006212||hypnagogic hallucinations
|
|
D006212||hypnapompic hallucination
|
|
D006212||hypnapompic hallucinations
|
|
D006212||kinesthetic hallucination
|
|
D006212||kinesthetic hallucinations
|
|
D006212||mood congruent hallucination
|
|
D006212||mood congruent hallucinations
|
|
D006212||mood incongruent hallucination
|
|
D006212||mood incongruent hallucinations
|
|
D006212||olfactory hallucination
|
|
D006212||olfactory hallucinations
|
|
D006212||organic hallucination
|
|
D006212||organic hallucinations
|
|
D006212||reflex hallucination
|
|
D006212||reflex hallucinations
|
|
D006212||sensory hallucination
|
|
D006212||sensory hallucinations
|
|
D006212||somatic hallucination
|
|
D006212||somatic hallucinations
|
|
D006212||tactile hallucination
|
|
D006212||tactile hallucinations
|
|
D006212||verbal auditory hallucination
|
|
D006212||verbal auditory hallucinations
|
|
D006212||visual hallucination
|
|
D006212||visual hallucinations
|
|
D008883||miliaria
|
|
D008883||heat prickly
|
|
D008883||miliaria rubra
|
|
D008883||prickly heat
|
|
D008882||mikulicz apos disease
|
|
D008882||disease mikulicz
|
|
D008882||disease mikulicz apos
|
|
D008882||mikulicz disease
|
|
D019522||vaginal discharge
|
|
D019522||discharges vaginal
|
|
D019522||discharge vaginal
|
|
D019522||vaginal discharges
|
|
C564690||noncompaction of left ventricular myocardium with congenital heart defects
|
|
C564690||left ventricular noncompaction nonisolated
|
|
C564690||left ventricular noncompaction with congenital heart defects
|
|
C535554|605552||abdominal obesity metabolic syndrome
|
|
C535554|605552||abdominal obesity metabolic syndrome 1
|
|
C535554|605552||aoms1
|
|
C535554|605552||metabolic syndrome protection against included
|
|
C535554|605552||metabolic syndrome x abdominal obesity metabolic syndrome quantitative trait locus 1 included
|
|
C538350|161800||nemaline myopathy 3
|
|
C538350|161800||myopathy actin congenital with cores
|
|
C538350|161800||myopathy actin congenital with cores included
|
|
C538350|161800||myopathy actin congenital with excess of thin myofilaments included
|
|
C538350|161800||nem3
|
|
C538350|161800||nemaline myopathy 3 with intranuclear rods
|
|
C538350|161800||nemaline myopathy 3 with intranuclear rods included
|
|
C538350|161800||nemaline myopathy caused by mutation in the alpha actin gene
|
|
C565984||short limb skeletal dysplasia with severe combined immunodeficiency
|
|
C565984||achondroplasia so called and severe combined immunodeficiency
|
|
C538364||mackay shek carr syndrome
|
|
C538364||retinal degeneration nanophthalmos glaucoma
|
|
C538364||retinal degeneration with nanophthalmos cystic macular degeneration and angle closure glaucoma
|
|
C537034||long qt syndrome type 3
|
|
C537031||littoral cell angioma of the spleen
|
|
C537031||littoral cell angioma
|
|
C538362||reticuloendotheliosis x linked
|
|
C538362||reticuloendotheliosis
|
|
C564656||digital arthropathy brachydactyly familial
|
|
C538369||retinoschisis of fovea
|
|
C538369||familial foveal retinoschisis
|
|
C538369||foveal retinoschisis
|
|
C537037||lowry maclean syndrome
|
|
C537037||mental retardation cleft palate eventration of diaphragm congenital heart defect glaucoma craniosynostosis and growth failure
|
|
D021821||communicable diseases emerging
|
|
D021821||communicable disease emerging
|
|
D021821||communicable disease reemerging
|
|
D021821||communicable disease re emerging
|
|
D021821||communicable diseases reemerging
|
|
D021821||communicable diseases re emerging
|
|
D021821||disease emerging communicable
|
|
D021821||disease emerging infectious
|
|
D021821||disease reemerging communicable
|
|
D021821||disease re emerging communicable
|
|
D021821||disease reemerging infectious
|
|
D021821||disease re emerging infectious
|
|
D021821||diseases emerging communicable
|
|
D021821||diseases emerging infectious
|
|
D021821||diseases reemerging communicable
|
|
D021821||diseases re emerging communicable
|
|
D021821||diseases reemerging infectious
|
|
D021821||diseases re emerging infectious
|
|
D021821||emerging communicable disease
|
|
D021821||emerging communicable diseases
|
|
D021821||emerging infectious disease
|
|
D021821||emerging infectious diseases
|
|
D021821||infectious disease emerging
|
|
D021821||infectious disease reemerging
|
|
D021821||infectious disease re emerging
|
|
D021821||infectious diseases emerging
|
|
D021821||infectious diseases reemerging
|
|
D021821||infectious diseases re emerging
|
|
D021821||reemerging communicable disease
|
|
D021821||re emerging communicable disease
|
|
D021821||reemerging communicable diseases
|
|
D021821||re emerging communicable diseases
|
|
D021821||reemerging infectious disease
|
|
D021821||re emerging infectious disease
|
|
D021821||reemerging infectious diseases
|
|
D021821||re emerging infectious diseases
|
|
C564655||cardioneuromyopathy with hyaline masses and nemaline rods
|
|
C537038||lowry wood syndrome
|
|
C537038||epiphyseal dysplasia microcephaly and nystagmus
|
|
C564654||cree mental retardation syndrome
|
|
C538367||mirhosseini holmes walton syndrome
|
|
C538367||retinopathy pigmentary and mental retardation
|
|
C538367||retinopathy pigmentary mental retardation
|
|
C537036||lopes gorlin syndrome
|
|
C537036||short tarsus absence of lower eyelashes
|
|
C537036||short tarsus with absence of lower eyelashes
|
|
C563675|610361||orofacial cleft 9
|
|
C563675|610361||cleft lip with or without cleft palate nonsyndromic 9
|
|
C563675|610361||ofc9
|
|
D007516||adenoma islet cell
|
|
D007516||adenomas islet cell
|
|
D007516||island cell tumor
|
|
D007516||island cell tumors
|
|
D007516||islet cell adenoma
|
|
D007516||islet cell adenomas
|
|
D007516||islet cell tumor
|
|
D007516||islet cell tumors
|
|
D007516||nesidioblastoma
|
|
D007516||tumor island cell
|
|
D007516||tumor islet cell
|
|
D007516||tumors island cell
|
|
D007516||tumors islet cell
|
|
D008844||micrognathism
|
|
D008844||micrognathisms
|
|
C564657||friedreich ataxia with retained reflexes
|
|
D007511||ischemia
|
|
D007511||ischemias
|
|
C565988||hyperzincemia and hypercalprotectinemia
|
|
C565989||xeroderma pigmentosum autosomal dominant mild
|
|
C538360||restless legs syndrome 2
|
|
C538360||autosomal dominant restless legs syndrome
|
|
C538360||restless legs syndrome autosomal dominant
|
|
C537030||lipomyelomeningocele
|
|
C537030||familial lipomyelomeningocele
|
|
C537257|235550||hepatic venoocclusive disease with immunodeficiency
|
|
C537257|235550||familial veno occlusive disease with immunodeficiency
|
|
C537257|235550||hepatic veno occlusive disease with immunodeficiency
|
|
C537257|235550||veno occlusive disease and immunodeficiency syndrome
|
|
C537257|235550||vodi
|
|
D008850||microphthalmos
|
|
D008850||microphthalmia
|
|
226650|C562639||epidermolysis bullosa junctional non herlitz type
|
|
226650|C562639||epidermolysis bullosa generalized atrophic benign gabeb epidermolysis bullosa junctional localisata variant included
|
|
226650|C562639||epidermolysis bullosa junctionalis non herlitz type
|
|
226650|C562639||epidermolysis bullosa junctional localisata variant
|
|
226650|C562639||jeb i included
|
|
226650|C562639||junctional epidermolysis bullosa inversa included
|
|
278850||46 xx sex reversal 2
|
|
278850||46 xx sex reversal partial or complete sox9 related
|
|
278850||chromosome 17q24 duplication syndrome
|
|
278850||srxx2
|
|
C565264|606056||congenital disorder of glycosylation type iib
|
|
C565264|606056||cdg2b
|
|
C565264|606056||cdgiib
|
|
C565264|606056||cdg iib
|
|
C565264|606056||glucosidase i deficiency
|
|
C538359||rds infants
|
|
C537029||lipomatous hemangiopericytoma
|
|
C537044||albinism minimal pigment type
|
|
C537044||oculocutaneous albinism minimal pigment type
|
|
C563331||aprosencephaly and cerebellar dysgenesis
|
|
C537045||albright apos s hereditary osteodystrophy
|
|
C537045||albright hereditary osteodystrophy
|
|
C564661||abducens palsy
|
|
C563330||chondrodysplasia lethal with long bone angulation and mixed bone density
|
|
C564660||momes syndrome
|
|
C564660||mental retardation obesity mandibular prognathism and eye and skin anomalies
|
|
C537048||allanson pantzar mcleod syndrome
|
|
C537048||primitive renal tubule syndrome
|
|
C537048||renotubular dysgenesis
|
|
D005633|229600||fructose intolerance
|
|
D005633|229600||aldob deficiencies
|
|
D005633|229600||aldob deficiency
|
|
D005633|229600||aldolase b deficiencies
|
|
D005633|229600||aldolase b deficiency
|
|
D005633|229600||aldolase deficiencies fructose 1 6 biphosphate
|
|
D005633|229600||aldolase deficiencies fructose 1 phosphate
|
|
D005633|229600||aldolase deficiency fructose 1 6 biphosphate
|
|
D005633|229600||aldolase deficiency fructose 1 phosphate
|
|
D005633|229600||deficiencies aldob
|
|
D005633|229600||deficiencies aldolase b
|
|
D005633|229600||deficiencies fructose 1 6 biphosphate aldolase
|
|
D005633|229600||deficiencies fructose 1 phosphate aldolase
|
|
D005633|229600||deficiency aldob
|
|
D005633|229600||deficiency aldolase b
|
|
D005633|229600||deficiency fructose 1 6 biphosphate aldolase
|
|
D005633|229600||deficiency fructose 1 phosphate aldolase
|
|
D005633|229600||fructose 1 6 biphosphate aldolase deficiencies
|
|
D005633|229600||fructose 1 6 biphosphate aldolase deficiency
|
|
D005633|229600||fructose 1 6 bisphosphate aldolase b deficiency
|
|
D005633|229600||fructose 1 phosphate aldolase deficiencies
|
|
D005633|229600||fructose 1 phosphate aldolase deficiency
|
|
D005633|229600||fructose aldolase b deficiency
|
|
D005633|229600||fructose intolerance hereditary
|
|
D005633|229600||fructose intolerances
|
|
D005633|229600||fructose intolerances hereditary
|
|
D005633|229600||fructosemia
|
|
D005633|229600||fructosemias
|
|
D005633|229600||hereditary fructose intolerance
|
|
D005633|229600||hereditary fructose intolerances
|
|
D005633|229600||intolerance fructose
|
|
D005633|229600||intolerances fructose
|
|
C537049||aloi tomasini isaia syndrome
|
|
C537049||basal cell nevus anodontia abnormal bone mineralization
|
|
C565993||vulvovaginitis allergic seminal
|
|
C537046||aldred syndrome
|
|
C537046||nonspecific mental retardation associated with retinitis pigmentosa
|
|
C537046||x linked mental handicap retinitis pigmentosa syndrome
|
|
C563333||cataract age related nuclear
|
|
C563333||nuclear sclerosis of the lens
|
|
C563339||sebaceous nevus syndrome and hemimegalencephaly
|
|
608631|D020817||asperger syndrome
|
|
608631|D020817||asperger disease
|
|
608631|D020817||asperger disorder
|
|
608631|D020817||asperger apos s disease
|
|
608631|D020817||asperger apos s disorder
|
|
608631|D020817||aspergers disorder
|
|
608631|D020817||asperger apos s syndrome
|
|
608631|D020817||aspergers syndrome
|
|
608631|D020817||asperger syndrome susceptibility to 1
|
|
608631|D020817||asperger syndrome susceptibility to 2
|
|
608631|D020817||asperger syndrome susceptibility to 3
|
|
608631|D020817||asperger syndrome susceptibility to 4
|
|
608631|D020817||aspg1
|
|
608631|D020817||aspg2
|
|
608631|D020817||aspg3
|
|
608631|D020817||aspg4
|
|
C564669||lipodystrophy with congenital cataracts and neurodegeneration
|
|
C563338||amelia autosomal recessive
|
|
611081|C567021||inflammatory bowel disease 10
|
|
611081|C567021||ibd10
|
|
C565999||platelet receptor for collagen deficiency of
|
|
C538370||retroperitoneal liposarcoma
|
|
C538370||giant pelvic retroperitoneal liposarcoma
|
|
C538370||pelvic retroperitoneal liposarcoma
|
|
610247|D057765||eosinophilic esophagitis
|
|
610247|D057765||chronic esophagitides eosinophilic
|
|
610247|D057765||chronic esophagitis eosinophilic
|
|
610247|D057765||eoe1
|
|
610247|D057765||eoe2
|
|
610247|D057765||eosinophilic chronic esophagitides
|
|
610247|D057765||eosinophilic chronic esophagitis
|
|
610247|D057765||eosinophilic esophagitides
|
|
610247|D057765||esophagitides eosinophilic
|
|
610247|D057765||esophagitides eosinophilic chronic
|
|
610247|D057765||esophagitis eosinophilic
|
|
610247|D057765||esophagitis eosinophilic 1
|
|
610247|D057765||esophagitis eosinophilic 2
|
|
610247|D057765||esophagitis eosinophilic chronic
|
|
C536961|176410||familial testotoxicosis
|
|
C536961|176410||familial gonadotrophin independent sexual precocity
|
|
C536961|176410||familial male limited precocious puberty
|
|
C536961|176410||gonadotrophin independent precocious puberty
|
|
C536961|176410||precocious pseudopuberty
|
|
C536961|176410||precocious puberty male limited
|
|
C536961|176410||pubertas praecox
|
|
C536961|176410||sexual precocity familial gonadotropin independent
|
|
C536961|176410||testotoxicosis
|
|
C536961|176410||testotoxicosis familial
|
|
C536961|176410||testotoxicosis familial leydig cell adenoma somatic with male limited precocious puberty included
|
|
C537309|271250||spinocerebellar ataxia autosomal recessive 3
|
|
C537309|271250||scabd
|
|
C537309|271250||scar3
|
|
C537309|271250||spinocerebellar ataxia with blindness and deafness
|
|
C536129|262300||achromatopsia 3
|
|
C536129|262300||achm1 formerly
|
|
C536129|262300||achm3
|
|
C536129|262300||achm 3
|
|
C536129|262300||achromatopsia with myopia
|
|
C536129|262300||pingelapese
|
|
C536129|262300||pingelapese blindness
|
|
C536129|262300||rmch1 formerly
|
|
C536129|262300||rod monochromacy 1 formerly
|
|
C536129|262300||rod monochromatism 1 formerly
|
|
C536129|262300||total colorblindness with myopia
|
|
C537039||lubani al saleh teebi syndrome
|
|
C536014|200500||acheiropodia
|
|
C536014|200500||acheiropody
|
|
C536014|200500||acheiropody brazilian type
|
|
C536014|200500||achp
|
|
C536014|200500||brazilian type acheiropody
|
|
C564679|606685||cardiomyopathy dilated 1l
|
|
C564679|606685||cmd1l
|
|
D017825|271900||canavan disease
|
|
D017825|271900||acy2 deficiency
|
|
D017825|271900||aminoacylase 2 deficiency
|
|
D017825|271900||aspa deficiency
|
|
D017825|271900||aspartoacylase deficiency
|
|
D017825|271900||asp deficiency
|
|
D017825|271900||canavan disease familial form
|
|
D017825|271900||canavan disease infantile
|
|
D017825|271900||canavan disease juvenile
|
|
D017825|271900||canavan disease neonatal
|
|
D017825|271900||canavan disease sporadic form
|
|
D017825|271900||canavan disease type i
|
|
D017825|271900||canavan disease type ii
|
|
D017825|271900||canavan disease type iii
|
|
D017825|271900||canavan van bogaert bertrand disease
|
|
D017825|271900||deficiency disease aspartoacylase
|
|
D017825|271900||disease canavan
|
|
D017825|271900||disease canavan van bogaert bertrand
|
|
D017825|271900||disease von bogaert bertrand
|
|
D017825|271900||familial form of canavan disease
|
|
D017825|271900||infantile canavan disease
|
|
D017825|271900||juvenile canavan disease
|
|
D017825|271900||leukodystrophy spongiform
|
|
D017825|271900||neonatal canavan disease
|
|
D017825|271900||spongiform leukodystrophy
|
|
D017825|271900||spongy degeneration of central nervous system
|
|
D017825|271900||spongy degeneration of infancy
|
|
D017825|271900||spongy degeneration of the brain
|
|
D017825|271900||spongy degeneration of the central nervous system
|
|
D017825|271900||spongy degeneration of white matter in infancy
|
|
D017825|271900||spongy disease of central nervous system
|
|
D017825|271900||spongy disease of white matter
|
|
D017825|271900||sporadic form of canavan disease
|
|
D017825|271900||syndrome van bogaert bertrand
|
|
D017825|271900||type i canavan disease
|
|
D017825|271900||type ii canavan disease
|
|
D017825|271900||type iii canavan disease
|
|
D017825|271900||van bogaert bertrand syndrome
|
|
D017825|271900||von bogaert bertrand disease
|
|
D012090||cumulative trauma disorders
|
|
D012090||cumulative trauma disorder
|
|
D012090||disorder cumulative trauma
|
|
D012090||disorder repetitive motion
|
|
D012090||disorders cumulative trauma
|
|
D012090||disorders repetitive motion
|
|
D012090||injuries overuse
|
|
D012090||injuries repetition strain
|
|
D012090||injuries repetitive strain
|
|
D012090||injury overuse
|
|
D012090||injury repetition strain
|
|
D012090||injury repetitive strain
|
|
D012090||motion disorder repetitive
|
|
D012090||motion disorders repetitive
|
|
D012090||overuse injuries
|
|
D012090||overuse injury
|
|
D012090||overuse syndrome
|
|
D012090||overuse syndromes
|
|
D012090||repetition strain injuries
|
|
D012090||repetition strain injury
|
|
D012090||repetitive motion disorder
|
|
D012090||repetitive motion disorders
|
|
D012090||repetitive strain injuries
|
|
D012090||repetitive strain injury
|
|
D012090||strain injuries repetition
|
|
D012090||strain injuries repetitive
|
|
D012090||strain injury repetition
|
|
D012090||strain injury repetitive
|
|
D012090||trauma disorder cumulative
|
|
D012090||trauma disorders cumulative
|
|
C566339|603720||deafness autosomal recessive 16
|
|
C566339|603720||dfnb16
|
|
C565963||alpha 2 deficient collagen disease
|
|
C565963||meigel disease
|
|
C538386||hypertelorism and tetralogy of fallot
|
|
C537056||alopecia universalis onychodystrophy vitiligo
|
|
C537056||alopecia universalis onychodystrophy and total vitiligo
|
|
C537053||alopecia hypogonadism extrapyramidal disorder
|
|
C537053||progressive extrapyramidal disorder with primary hypogonadism and alopecia
|
|
115470|C535918||schmid fraccaro syndrome
|
|
115470|C535918||cat eye syndrome
|
|
115470|C535918||ces
|
|
115470|C535918||chromosome 22 partial tetrasomy
|
|
115470|C535918||inv dup 22 q11
|
|
C537059||flat umbilicus familial
|
|
C537059||flat umbilicus autosomal dominant
|
|
C537059||umbilicus familial flat
|
|
C563301||peroxisome biogenesis disorder complementation group 4
|
|
C563301||peroxisome biogenesis disorder complementation group 6
|
|
C563301||peroxisome biogenesis disorder complementation group c
|
|
C567358|612291||joubert syndrome 8
|
|
C567358|612291||jbts8
|
|
C565960||amino aciduria with mental deficiency dwarfism muscular dystrophy osteoporosis and acidosis
|
|
C537057||alopecia epilepsy pyorrhea mental subnormality
|
|
C537057||alopecia psychomotor epilepsy pyorrhea and mental subnormality
|
|
C537057||congenital universal alopecia epilepsy mental subnormality and pyorrhea
|
|
C537057||shokeir syndrome
|
|
225000|C563117||rosselli gulienetti syndrome
|
|
C562515|308050||congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
|
C562515|308050||child syndrome
|
|
C562515|308050||ichthyosiform erythroderma unilateral with ipsilateral malformations especially absence deformity of limbs
|
|
C564631||parkinson disease 8
|
|
C537058||fitzsimmons mclachlan gilbert syndrome
|
|
C537058||mental retardation with spastic paraplegia and palmoplantar hyperkeratosis
|
|
C564638||hyperreninemic hypoaldosteronism familial 2
|
|
C563305||agammaglobulinemia non bruton type autosomal dominant
|
|
C537051||alopecia contractures dwarfism mental retardation
|
|
C537051||acd mental retardation syndrome
|
|
C537051||alopecia contractures dwarfism mental retardation syndrome
|
|
C538382|264070||hyperphenylalaninemia with primapterinuria
|
|
C538382|264070||cadh deficiency
|
|
C538382|264070||hpabh4d
|
|
C538382|264070||hyperphenylalaninemia bh4 deficient d
|
|
C538382|264070||hyperphenylalaninemia tetrahydrobiopterin deficient due to pterin 4 alpha carbinolamine dehydratase deficiency
|
|
C538382|264070||pcbd deficiency
|
|
C537052||alopecia epilepsy oligophrenia syndrome of moynahan
|
|
C537052||moynahan alopecia syndrome
|
|
C565968||alaninuria with microcephaly dwarfism enamel hypoplasia and diabetes mellitus
|
|
C565968||stimmler syndrome
|
|
C537050||alopecia congenita keratosis palmoplantaris
|
|
C537050||alopecia congenita with hyperkeratosis of the palms and soles
|
|
C537050||alopecia congenita with keratosis palmoplantaris
|
|
C564858|266200||pyruvate kinase deficiency of red cells
|
|
C564858|266200||pk deficiency
|
|
C564858|266200||pyruvate kinase deficiency
|
|
C564858|266200||pyruvate kinase deficiency of erythrocyte
|
|
D012088||reoviridae infections
|
|
D012088||infection reoviridae
|
|
D012088||infection reovirus
|
|
D012088||infections reoviridae
|
|
D012088||infections reovirus
|
|
D012088||reoviridae infection
|
|
D012088||reovirus infection
|
|
D012088||reovirus infections
|
|
145981|C537146||hypocalciuric hypercalcemia familial type 2
|
|
145981|C537146||familial benign hypercalcemia type 2
|
|
145981|C537146||familial benign hypercalcemia type ii
|
|
145981|C537146||fbh2
|
|
145981|C537146||hhc2
|
|
145981|C537146||hypercalcemia familial benign type 2
|
|
145981|C537146||hypercalcemia familial benign type ii
|
|
145981|C537146||hypocalciuric hypercalcemia familial type ii
|
|
130070|C536201||ehlers danlos syndrome progeroid form
|
|
130070|C536201||dermatan sulfate proteoglycan
|
|
130070|C536201||edsp1
|
|
130070|C536201||ehlers danlos syndrome progeroid type 1
|
|
130070|C536201||galactosyltransferase 1 deficiency
|
|
130070|C536201||galactosyltransferase i deficiency
|
|
130070|C536201||pds defective biosynthesis of
|
|
130070|C536201||progeroid variant of ehlers danlos syndrome
|
|
130070|C536201||proteodermatan sulfate defective biosynthesis of
|
|
130070|C536201||xgpt deficiency
|
|
130070|C536201||xylosylprotein 4 beta galactosyltransferase deficiency
|
|
C564641||pulmonary disease chronic obstructive severe early onset
|
|
C565973||adrenocortical carcinoma pediatric
|
|
C535544|147750||oculootoradial syndrome
|
|
C535544|147750||instituto venezolano de investigaciones cientificas syndrome
|
|
C535544|147750||ivic syndrome
|
|
C535544|147750||oors
|
|
C535544|147750||radial ray defects hearing impairment external ophthalmoplegia and thrombocytopenia
|
|
C537066||flynn aird syndrome
|
|
C538396||lambert syndrome
|
|
C538396||branchial dysplasia clubfoot inguinal hernia and biliary atresia
|
|
C537064||florid cystic endosalpingiosis of the uterus
|
|
C537064||cystic endosalpingiosis of the uterus
|
|
C565976||adrenal hypoplasia congenital with absent pituitary luteinizing hormone
|
|
C537065||flotch syndrome
|
|
C537065||friedel heid grosshans syndrome
|
|
C564645||albinism oculocutaneous type i temperature sensitive
|
|
C564645||oca1ts
|
|
108010|D002538||intracranial arteriovenous malformations
|
|
108010|D002538||arteriovenous malformation cerebral
|
|
108010|D002538||arteriovenous malformation intracranial
|
|
108010|D002538||arteriovenous malformations cerebral
|
|
108010|D002538||arteriovenous malformations intracranial
|
|
108010|D002538||arteriovenous malformations of the brain
|
|
108010|D002538||avm arteriovenous malformation intracranial
|
|
108010|D002538||bavm
|
|
108010|D002538||cerebral arteriovenous malformation
|
|
108010|D002538||cerebral arteriovenous malformations
|
|
108010|D002538||cerebral arteriovenous malformations intracranial hemorrhage in brain arteriovenous malformations susceptibility to included
|
|
108010|D002538||congenital intracranial arteriovenous malformations
|
|
108010|D002538||intracranial arteriovenous malformation
|
|
108010|D002538||intracranial arteriovenous malformation ruptured
|
|
108010|D002538||intracranial arteriovenous malformations congenital
|
|
108010|D002538||malformation cerebral arteriovenous
|
|
108010|D002538||malformation intracranial arteriovenous
|
|
108010|D002538||malformations cerebral arteriovenous
|
|
108010|D002538||malformations intracranial arteriovenous
|
|
108010|D002538||ruptured intracranial arteriovenous malformation
|
|
C565970||hypodysfibrinogenemia congenital
|
|
C565971||adrenocortical unresponsiveness to acth with postreceptor defect
|
|
C565971||familial glucocorticoid deficiency due to defect distal to acth receptor
|
|
C537068||focal facial dermal dysplasia
|
|
C537068||bitemporal aplasia cutis congenita
|
|
C537068||brauer syndrome
|
|
C537068||ffdd type 1
|
|
C537068||hereditary symmetrical aplastic nevi of temples
|
|
C540694||thrombophilia hereditary
|
|
C567520|611804||elliptocytosis 1
|
|
C567520|611804||4 1 minus trait
|
|
C567520|611804||4 1 trait
|
|
C567520|611804||el1
|
|
C567520|611804||elliptocytosis rhesus linked type
|
|
C567520|611804||protein 4 1 of erythrocyte membrane defect of
|
|
C538399||nemo mutation with immunodeficiency
|
|
C538399||nf kappa b essential modulator nemo mutation with immunodeficiency
|
|
C537069||foix chavany marie syndrome
|
|
C537069||congenital foix chavany marie syndrome
|
|
C566196|113000||brachydactyly type b1
|
|
C566196|113000||bdb
|
|
C566196|113000||bdb1
|
|
C566196|113000||brachydactyly type b
|
|
C538390||hypertrichosis anterior cervical
|
|
C538390||anterior cervical hypertrichosis
|
|
C538390||hairy throat
|
|
C538390||hairy throat syndrome
|
|
C564648||vascular malformation primary intraosseous
|
|
C564648||hemangioma intraosseous
|
|
C564648||vascular malformation osseous
|
|
C563316||deafness progressive with stapes fixation
|
|
C535602|126600||doyne honeycomb retinal dystrophy
|
|
C535602|126600||dhrd
|
|
C535602|126600||doyne honeycomb degeneration of retina
|
|
C535602|126600||doyne honeycomb degeneration of retina dhd malattia leventinese included
|
|
C535602|126600||drusen radial autosomal dominant included
|
|
C535602|126600||malattia leventinese
|
|
C535602|126600||mlvt included
|
|
D007500||iritis
|
|
D007500||iritides
|
|
C565977||hyperandrogenism nonclassic type due to 21 hydroxylase deficiency
|
|
C538394||hdl deficiency type 2
|
|
C538394||low serum hdl cholesterol
|
|
C538394||primary hypoalphalipoproteinemia
|
|
C537062||floating harbor syndrome
|
|
C537062||leisti hollander rimoin syndrome
|
|
C537062||pelletier leisti syndrome
|
|
D008831||microcephaly
|
|
D008831||microcephalies
|
|
D008831||microlissencephalies
|
|
D008831||microlissencephaly
|
|
C538393||hypertryptophanemia
|
|
C537063||florid cemento osseous dysplasia
|
|
250250|C535916||cartilage hair hypoplasia
|
|
250250|C535916||cartilage hair syndrome
|
|
250250|C535916||chh
|
|
250250|C535916||mckusick metaphyseal chondrodysplasia syndrome
|
|
250250|C535916||metaphyseal chondrodysplasia mckusick type
|
|
250250|C535916||metaphyseal chondrodysplasia recessive type
|
|
C563319|601419||myopathy myofibrillar desmin related
|
|
C563319|601419||desminopathy primary
|
|
C563319|601419||desmin related myopathy
|
|
C563319||myopathy desmin related
|
|
C538391||hypertrichosis hyperkeratosis mental retardation and distinctive facial features
|
|
C537061||flavimonas oryzihabitans bacteremia
|
|
C536183|604536||ectodermal dysplasia skin fragility syndrome
|
|
C536183|604536||mcgrath syndrome
|
|
C566493|609975||hyperinsulinemic hypoglycemia familial 4
|
|
C566493|609975||hhf4
|
|
D005175|234000||factor xii deficiency
|
|
D005175|234000||coagulation factor 12 deficiency
|
|
D005175|234000||deficiencies factor 12
|
|
D005175|234000||deficiencies factor xii
|
|
D005175|234000||deficiency factor 12
|
|
D005175|234000||deficiency factor xii
|
|
D005175|234000||deficiency hageman factor
|
|
D005175|234000||f12 deficiency
|
|
D005175|234000||factor 12 deficiencies
|
|
D005175|234000||factor 12 deficiency
|
|
D005175|234000||factor deficiency hageman
|
|
D005175|234000||factor xii deficiencies
|
|
D005175|234000||haf deficiency
|
|
D005175|234000||hageman factor deficiency
|
|
D005175|234000||hageman trait
|
|
C565940||arthrogryposis distal with mental retardation and characteristic facies
|
|
C538321||histidinuria renal tubular defect
|
|
C538321||histidinuria due to a renal tubular defect
|
|
C538321||renal histidinuria
|
|
C565941||arteriosclerosis severe juvenile
|
|
C536611|132700||familial cylindromatosis
|
|
C536611|132700||ancell spiegler cylindromas
|
|
C536611|132700||brooke spiegler syndrome
|
|
C536611|132700||brss
|
|
C536611|132700||cylindromas dermal eccrine
|
|
C536611|132700||cylindromatosis familial
|
|
C536611|132700||dermal eccrine cylindroma
|
|
C536611|132700||familial trichoepithelioma
|
|
C536611|132700|153640|C535507||sbs
|
|
C536611|132700||spiegler brooke syndrome
|
|
C536611|132700||turban tumors
|
|
C536611|132700||turban tumor syndrome
|
|
C536611|132700||apos turban tumor apos syndrome
|
|
C538325||ho kaufman mcalister syndrome
|
|
C564611||multiple congenital anomalies syndrome with cloverleaf skull
|
|
C564509|300472||corpus callosum agenesis of with mental retardation ocular coloboma and micrognathia
|
|
C564509|300472||mental retardation x linked syndromic 28
|
|
C564509|300472||mrxs28
|
|
C538323||hittner hirsch kreh syndrome
|
|
311050|C537125||optic atrophy 2
|
|
311050||opa2
|
|
311050|C537125||optic atrophy non leber type with early onset
|
|
311050|C537125||optic atrophy x linked
|
|
C565949||optic nerve hypoplasia and abnormalities of the central nervous system
|
|
C563720|609439||deafness autosomal recessive 48
|
|
C563720|609439||dfnb48
|
|
C565944||coronary sclerosis medial of infancy
|
|
C564619||cataract sutural with punctate and cerulean opacities
|
|
C565945||aplasia of extensor muscles of fingers unilateral with generalized polyneuropathy
|
|
C565947||antithrombin familial hemorrhagic diathesis due to
|
|
C563336|601363||wilms tumor 4
|
|
C563336|601363||familial wilms tumor 1
|
|
C563336|601363||fwt1
|
|
C563336|601363||wt4
|
|
C536258|608782||pyruvate dehydrogenase phosphatase deficiency
|
|
C536258|608782||lactic acidemia with pyruvate dehydrogenase phosphatase deficiency
|
|
C536258|608782||pdhpd
|
|
C538318||chromosome 2 trisomy 2p
|
|
C538318||duplication 2p
|
|
C538318||trisomy 2p
|
|
D001260|208900||ataxia telangiectasia
|
|
D001260|208900||at
|
|
D001260|208900||at1
|
|
D001260|208900||ata included
|
|
D001260|208900||ataxia telangiectasia syndrome
|
|
D001260|208900||ataxia telangiectasia variant included
|
|
D001260|208900||atc included
|
|
D001260|208900||at complementation group c included
|
|
D001260|208900||at complementation group d included
|
|
D001260|208900||at complementation group e included
|
|
D001260|208900||atd included
|
|
D001260|208900||ate included
|
|
D001260|208900||louis bar syndrome
|
|
D001260|208900||louis bar syndrome at complementation group a included
|
|
D001260|208900||syndrome ataxia telangiectasia
|
|
D001260|208900||syndrome louis bar
|
|
D001260|208900||telangiectasia cerebello oculocutaneous
|
|
C538317||chromosome 2q37 deletion syndrome
|
|
C538317||2q37 deletion syndrome
|
|
C538317||albright hereditary osteodystrophy like syndrome
|
|
C538317||chromosome 2 monosomy 2q37
|
|
C538317||deletion 2q37
|
|
C538317||monosomy 2q37
|
|
C538316||chromosome 2 monosomy 2q24
|
|
C538316||deletion 2q24
|
|
C538316||monosomy 2q24
|
|
C537495|300434||stocco dos santos syndrome
|
|
C537495|300434||mental retardation stocco dos santos type
|
|
C537495|300434||mental retardation x linked stocco dos santos type
|
|
C537495|300434||sdsx
|
|
C537495|300434||stocco dos santos x linked mental retardation syndrome
|
|
C538315||chromosome 2 monosomy 2q
|
|
C538315||deletion 2q
|
|
C538315||monosomy 2q
|
|
605462|D002280||carcinoma basal cell
|
|
605462|D002280||basal cell carcinoma
|
|
605462|D002280||basal cell carcinoma multiple included
|
|
605462|D002280||basal cell carcinoma nonsyndromic included
|
|
605462|D002280||basal cell carcinomas
|
|
605462|D002280||basal cell carcinoma susceptibility to 1
|
|
605462|D002280||basal cell carcinoma susceptibility to 2
|
|
605462|D002280||basal cell carcinoma susceptibility to 3
|
|
605462|D002280||basal cell carcinoma susceptibility to 4
|
|
605462|D002280||basal cell carcinoma susceptibility to 5
|
|
605462|D002280||basal cell carcinoma susceptibility to 6
|
|
605462|D002280||basal cell epithelioma
|
|
605462|D002280||basal cell epitheliomas
|
|
605462|D002280||bcc1
|
|
605462|D002280||bcc2
|
|
605462|D002280||bcc3
|
|
605462|D002280||bcc4
|
|
605462|D002280||bcc5
|
|
605462|D002280||bcc6
|
|
605462|D002280||carcinoma basal cell pigmented
|
|
605462|D002280||carcinomas basal cell
|
|
605462|D002280||epithelioma basal cell
|
|
605462|D002280||epitheliomas basal cell
|
|
605462|D002280||rodent ulcer
|
|
605462|D002280||rodent ulcers
|
|
605462|D002280||ulcer rodent
|
|
605462|D002280||ulcers rodent
|
|
C538319||hirschsprung disease type d brachydactyly
|
|
C538319||familial hirschsprung apos s disease and type d brachydactyly
|
|
C538319||hirschsprung disease with type d brachydactyly
|
|
C565951||angiolipomatosis familial
|
|
C565951||angiolipoma microthromboticum
|
|
C538332||naguib richieri costa syndrome
|
|
C538332||acrofrontofacionasal dysostosis 2
|
|
C538332||acrofrontofacionasal dysostosis severe
|
|
C538332||acrofrontofacionasal dysostosis with genitourinary anomalies
|
|
C538332||hypertelorism hypospadias and polysyndactyly syndrome
|
|
C538332||hypertelorism hypospadias polysyndactyly syndrome
|
|
C538332||naguib syndrome
|
|
C537000||ledderhose disease
|
|
C565952||anemia nonspherocytic hemolytic possibly due to defect in porphyrin metabolism
|
|
C537001||left sided gallbladder
|
|
C537001||gallbladder left sided
|
|
D012080||renal osteodystrophy
|
|
D012080||osteodystrophies renal
|
|
D012080||osteodystrophy renal
|
|
D012080||renal osteodystrophies
|
|
D012080||renal rickets
|
|
D012080||rickets renal
|
|
C565953||anemia nonspherocytic hemolytic associated with abnormality of red cell membrane
|
|
C538330||inclusion body myopathy autosomal dominant
|
|
C538330||inclusion body myopathy 3
|
|
C565954||anemia sideroblastic pyridoxine responsive autosomal recessive
|
|
C565954||anemia congenital sideroblastic b6 responsive
|
|
C538335||nakamura osame syndrome
|
|
C538335||spastic paraplegia mental retardation and thin corpus callosum
|
|
C538334||nakajo syndrome
|
|
C538334||nodular erythema digital changes
|
|
C538334||nodular erythema with digital changes
|
|
C564620||laryngeal atresia encephalocele and limb deformities
|
|
C537003||leichtman wood rohn syndrome
|
|
C537003||anophthalmia cleft lip palate facial anomalies and cns anomalies and hypothalamic disorder
|
|
C565959||amobarbital deficient n hydroxylation of
|
|
C564625||congenital disorder of glycosylation type iiid
|
|
C565955||amyotrophic lateral sclerosis with polyglucosan bodies
|
|
C565956||amyotrophic lateral sclerosis juvenile with dementia
|
|
C565956||als dementia complex
|
|
C536485|276900||usher syndrome type 1b
|
|
C536485|276900||retinitis pigmentosa and congenital deafness usher syndrome type ib included
|
|
C536485|276900||us1
|
|
C536485|276900||ush1
|
|
C536485|276900||ush1b included
|
|
C536485|276900||usher syndrome type ia formerly included ush1a formerly included
|
|
C536485|276900||usher syndrome type i french variety formerly included
|
|
C565958||amyloidosis of gingiva and conjunctiva with mental retardation
|
|
C565152|611489||corticosteroid binding globulin deficiency
|
|
C565152|611489||cbg deficiency
|
|
C565152|611489||transcortin deficiency
|
|
C565152|611489||transcortin deficiency corticosteroid binding globulin elevated included
|
|
C538328||holoprosencephaly recurrent infections and monocytosis
|
|
D012075||remission spontaneous
|
|
D012075||remissions spontaneous
|
|
D012075||spontaneous remission
|
|
D012075||spontaneous remissions
|
|
D012078||renal artery obstruction
|
|
D012078||obstruction renal artery
|
|
D012078||obstructions renal artery
|
|
D012078||renal artery obstructions
|
|
D012078||renal artery stenoses
|
|
D012078||renal artery stenosis
|
|
D012078||stenoses renal artery
|
|
D012078||stenosis renal artery
|
|
C538343||native american myopathy
|
|
C538343||congenital myopathy cleft palate and malignant hyperthermia
|
|
C538343||myopathy congenital with cleft palate and malignant hyperthermia
|
|
C537011||kasznica carlson coppedge syndrome
|
|
C537011||ectrodactyly spina bifida cardiopathy
|
|
C538342||nathalie syndrome
|
|
C537012||katsantoni papadakou lagoyanni syndrome
|
|
C537012||trichodermal syndrome and mental retardation
|
|
C565920||bardet biedl syndrome 11
|
|
C538341||intestinal pseudoobstruction with patent ductus arteriosus and natal teeth
|
|
C538341||natal teeth intestinal pseudoobstruction and patent ductus
|
|
C565921||bardet biedl syndrome 12
|
|
C538340||nasopharyngeal teratoma with dandy walker diaphragmatic hernia
|
|
C538340||aughton sloan milad syndrome
|
|
C537010||kashani strom utley syndrome
|
|
C537010||hypoplastic pulmonary arteries and aorta with obstructive uropathy
|
|
C537010||pulmonary aortic stenosis obstructive uropathy
|
|
607736|C535417||charcot marie tooth disease type 2j
|
|
607736|C535417||charcot marie tooth disease axonal type 2j
|
|
607736|C535417||charcot marie tooth disease type 2 with hearing loss and pupillary abnormalities
|
|
607736|C535417||charcot marie tooth neuropathy type 2j
|
|
607736|C535417||cmt2j
|
|
607736|C535417||cmt 2j
|
|
C538347||negative rheumatoid factor polyarthritis
|
|
C538347||rf ve cp
|
|
C538347||rheumatoid factor negative erosive chronic polyarthritis
|
|
C538347||rheumatoid factor negative polyarthritis
|
|
C537015||kbg syndrome
|
|
C537015||short stature characteristic facies macrodontia mental retardation and skeletal anomalies
|
|
C567699|608030||amyotrophic lateral sclerosis 6 autosomal recessive
|
|
C567699|608030||als6
|
|
C567699|608030||amyotrophic lateral sclerosis 6 autosomal recessive included
|
|
C567699|608030||amyotrophic lateral sclerosis 6 with or without frontotemporal dementia
|
|
C538345||navajo poikiloderma
|
|
C538345||navajo immune deficient poikiloderma
|
|
C537013||kaufman oculocerebrofacial syndrome
|
|
C538344||mitochondrial dna depletion syndrome 6
|
|
C538344||mpv17 associated hepatocerebral mds
|
|
C538344||mpv17 related hepatocerebral mitochondrial dna depletion syndrome
|
|
C538344||navajo familial neurogenic arthropathy
|
|
C538344||navajo neuropathy
|
|
C565926||atonic astatic syndrome of foerster
|
|
C565927||athrombia essential
|
|
C565928||atherosclerosis premature with deafness nephropathy diabetes mellitus photomyoclonus and degenerative neurologic disease
|
|
C565707|610193||arrhythmogenic right ventricular dysplasia familial 10
|
|
C565707|610193||arrhythmogenic right ventricular cardiomyopathy 10
|
|
C565707|610193||arvc10
|
|
C565707|610193||arvd10
|
|
C535845|140350||hawkinsinuria
|
|
C535845|140350||4 alpha hydroxyphenylpyruvate hydroxylase deficiency
|
|
C565923||aural atresia multiple congenital anomalies and mental retardation
|
|
D063726||delusional parasitosis
|
|
D063726||delusional parasitoses
|
|
D063726||delusional parasitoses ekbom
|
|
D063726||delusional parasitosis ekbom
|
|
D063726||delusion dermatozoic
|
|
D063726||delusion ekbom dermatozoic
|
|
D063726||delusions dermatozoic
|
|
D063726||delusions ekbom dermatozoic
|
|
D063726||delusory parasitoses
|
|
D063726||delusory parasitoses ekbom
|
|
D063726||delusory parasitosis
|
|
D063726||delusory parasitosis ekbom
|
|
D063726||dermatozoic delusion
|
|
D063726||dermatozoic delusion ekbom
|
|
D063726||dermatozoic delusions
|
|
D063726||dermatozoic delusions ekbom
|
|
D063726||ekbom delusional parasitoses
|
|
D063726||ekbom delusional parasitosis
|
|
D063726||ekbom delusory parasitoses
|
|
D063726||ekbom delusory parasitosis
|
|
D063726||ekbom dermatozoic delusion
|
|
D063726||ekbom dermatozoic delusions
|
|
D063726||ekbom psychogenic parasitoses
|
|
D063726||ekbom psychogenic parasitosis
|
|
D063726||parasitoses delusional
|
|
D063726||parasitoses delusory
|
|
D063726||parasitoses ekbom delusional
|
|
D063726||parasitoses ekbom delusory
|
|
D063726||parasitoses ekbom psychogenic
|
|
D063726||parasitoses psychogenic
|
|
D063726||parasitosis delusional
|
|
D063726||parasitosis delusory
|
|
D063726||parasitosis ekbom delusional
|
|
D063726||parasitosis ekbom delusory
|
|
D063726||parasitosis ekbom psychogenic
|
|
D063726||parasitosis psychogenic
|
|
D063726||psychogenic parasitoses
|
|
D063726||psychogenic parasitoses ekbom
|
|
D063726||psychogenic parasitosis
|
|
D063726||psychogenic parasitosis ekbom
|
|
114500|D015179||colorectal neoplasms
|
|
114500|D015179||cancer colorectal
|
|
114500|D015179||cancers colorectal
|
|
114500|D015179||carcinoma colorectal
|
|
114500|D015179||carcinomas colorectal
|
|
114500|D015179||colorectal adenoma and cancer susceptibility to
|
|
114500|D015179||colorectal cancer
|
|
114500|D015179||colorectal cancers
|
|
114500|D015179||colorectal cancer susceptibility to 1
|
|
114500|D015179||colorectal cancer susceptibility to 10
|
|
114500|D015179||colorectal cancer susceptibility to 11
|
|
114500|D015179||colorectal cancer susceptibility to 2
|
|
114500|D015179||colorectal cancer susceptibility to 3
|
|
114500|D015179||colorectal cancer susceptibility to 5
|
|
114500|D015179||colorectal cancer susceptibility to 6
|
|
114500|D015179||colorectal cancer susceptibility to 7
|
|
114500|D015179||colorectal cancer susceptibility to 8
|
|
114500|D015179||colorectal cancer susceptibility to 9
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 10
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 11
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 14q
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 16q
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 18
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 19q
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 20p
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 8q23
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 8q24
|
|
114500|D015179||colorectal cancer susceptibility to on chromosome 9
|
|
114500|D015179||colorectal carcinoma
|
|
114500|D015179||colorectal carcinomas
|
|
114500|D015179||colorectal neoplasm
|
|
114500|D015179||colorectal tumor
|
|
114500|D015179||colorectal tumors
|
|
114500|D015179||crc
|
|
114500|D015179||crcs1
|
|
114500|D015179||crcs10
|
|
114500|D015179||crcs11
|
|
114500|D015179||crcs2
|
|
114500|D015179||crcs3
|
|
114500|D015179||crcs5
|
|
114500|D015179||crcs6
|
|
114500|D015179||crcs7
|
|
114500|D015179||crcs8
|
|
114500|D015179||crcs9
|
|
114500|D015179||neoplasm colorectal
|
|
114500|D015179||neoplasms colorectal
|
|
114500|D015179||tumor colorectal
|
|
114500|D015179||tumors colorectal
|
|
C567708|613205||muscular dystrophy congenital lmna related
|
|
C567708|613205||mdcl
|
|
C537008||kapur toriello syndrome
|
|
C537008||cleft lip palate facial eye heart and intestinal anomalies
|
|
C537008||long columella with cleft lip palate and eye heart and intestinal anomalies
|
|
C538155|186300||syndactyly type v
|
|
C538155|186300||syndactyly type 5
|
|
C538155|186300||syndactyly with metacarpal and metatarsal fusion
|
|
C537009||karandikar maria kamble syndrome
|
|
C537009||cataract mental retardation anal atresia urinary defects
|
|
C537009||congenital cataract with multiple congenital anomalies in a sibship
|
|
D013375||substance withdrawal syndrome
|
|
D013375||drug withdrawal symptom
|
|
D013375||drug withdrawal symptoms
|
|
D013375||substance withdrawal syndromes
|
|
D013375||symptom drug withdrawal
|
|
D013375||symptoms drug withdrawal
|
|
D013375||symptoms withdrawal
|
|
D013375||symptom withdrawal
|
|
D013375||syndromes substance withdrawal
|
|
D013375||syndrome substance withdrawal
|
|
D013375||withdrawal symptom
|
|
D013375||withdrawal symptom drug
|
|
D013375||withdrawal symptoms
|
|
D013375||withdrawal symptoms drug
|
|
D013375||withdrawal syndromes substance
|
|
D013375||withdrawal syndrome substance
|
|
235700||hemolytic anemia nonspherocytic due to hexokinase deficiency
|
|
C538338||nasopalpebral lipoma coloboma syndrome
|
|
C538338||palpebral coloboma lipoma syndrome
|
|
C537006||leiomyoma of vulva and esophagus
|
|
C537006||esophagogastric and vulvar leiomyomatosis
|
|
C537006||leiomyomatosis esophagogastric and vulvar
|
|
C535935|602347||cholestasis progressive familial intrahepatic 3
|
|
C535935|602347||abcb4 related intrahepatic cholestasis
|
|
C535935|602347||cholestasis progressive familial intrahepatic with elevated serum gamma glutamyltransferase
|
|
C535935|602347||low gamma gt familial intrahepatic cholestasis
|
|
C535935|602347||mdr3 deficiency
|
|
C535935|602347||pfic3
|
|
C535935|602347||progressive familial intrahepatic cholestasis 3 pfic 3
|
|
C535935|602347||progressive familial intrahepatic cholestasis 3 pfic3
|
|
C535935|602347||progressive familial intrahepatic cholestasis with elevated serum gamma glutamyltransferase
|
|
C538337||nasodigitoacoustic syndrome
|
|
C538337||keipert syndrome
|
|
C537007||kaposiform hemangioendothelioma
|
|
C537007||congenital cutaneous multifocal kaposiform hemangioendothelioma
|
|
C537007||kaposiform hemangio endothelioma
|
|
C562876|212070||carboxypeptidase n deficiency
|
|
C538354||potato nose
|
|
C538354||nose anomalous shape of
|
|
C565930||ataxia telangiectasia with generalized skin pigmentation and early death
|
|
C537023||koone rizzo elias syndrome
|
|
C537023||ichthyosis mental retardation and asymptomatic spasticity
|
|
C537622|612736||guanidinoacetate methyltransferase deficiency
|
|
C537622|612736||ccds2
|
|
C537622|612736||cerebral creatine deficiency syndrome 2
|
|
C537622|612736||creatine deficiency syndrome due to gamt deficiency
|
|
C537622|612736||gamt deficiency
|
|
C538352||pellagra like syndrome
|
|
C538352||pellagra like rash with neurologic manifestations
|
|
C537020||kenny caffey syndrome
|
|
C537020||dwarfism cortical thickening of tubular bones and transient hypocalcemia
|
|
C537020||kenny caffey syndrome type 2
|
|
C537020||kenny syndrome
|
|
C565932||ataxia deafness and cardiomyopathy
|
|
C538358||powell venencie gordon syndrome
|
|
C538358||keratoderma and spastic paralysis
|
|
C538358||punctate keratoderma and spastic paralysis
|
|
C537026||lipodermatosclerosis
|
|
C537026||acute lipodermatosclerosis
|
|
D012061||relapsing fever
|
|
D012061||fever relapsing
|
|
D012061||fevers relapsing
|
|
D012061||relapsing fevers
|
|
C538357||powell chandra saal syndrome
|
|
C538357||phaver syndrome
|
|
C538357||vertebral radial congenital heart and ear defects
|
|
C537024||kosztolanyi syndrome
|
|
C537024||arachnodactyly abnormal ossification and mental retardation
|
|
C537024||syndrome of arachnodactyly disturbance of cranial ossification protruding eyes feeding difficulties and mental retardation
|
|
C537025||kotzot richter syndrome
|
|
C537025||albinism with immune and hematologic defects
|
|
C537025||oculocutaneous albinism immunodeficiency hematological disorders and minor anomalies
|
|
C563515|162820||neutrophil chemotactic response
|
|
C563515|162820||ncr
|
|
C563515|162820||neutrophil migration
|
|
C536238|303700||blue cone monochromatism
|
|
C536238|303700||bcm
|
|
C536238|303700||blue cone monochromacy
|
|
C536238|303700||cod5 included
|
|
C536238|303700||color blindness blue mono cone monochromatic type
|
|
C536238|303700||colorblindness blue mono cone monochromatic type
|
|
C536238|303700||colorblindness blue mono cone monochromatic type cbbm cone dystrophy 5 x linked included
|
|
C564609||deafness autosomal recessive
|
|
C565933||ataxia with myoclonic epilepsy and presenile dementia
|
|
277460|C535393||ataxia with vitamin e deficiency
|
|
277460|C535393||ataxia friedreich like with selective vitamin e deficiency
|
|
277460|C535393||ataxia with isolated vitamin e deficiency
|
|
277460|C535393||aved
|
|
277460|C535393||familial isolated deficiency of vitamin e
|
|
277460|C535393||familial isolated vitamin e deficiency
|
|
277460|C535393||friedreich ataxia phenotype with selective vitamin e deficiency
|
|
277460|C535393||friedreich like ataxia
|
|
277460|C535393||friedreich like ataxia with selective vitamin e deficiency
|
|
277460|C535393||ved
|
|
277460|C535393||vitamin e familial isolated deficiency of
|
|
C565934||asthma short stature and elevated iga
|
|
C564607||epilepsy intractable childhood with generalized tonic clonic seizures
|
|
C564607||icegtc
|
|
C564606||anonychia total with microcephaly
|
|
248200|C535804||stargardt disease 1
|
|
248200|C535804||ffm included
|
|
248200|C535804||fundus flavimaculatus
|
|
248200|C535804||juvenile macular degeneration
|
|
248200|C535804||macular degeneration juvenile
|
|
248200|C535804||macular dystrophy with flecks type 1
|
|
248200|C535804||macular dystrophy with flecks type 1 fundus flavimaculatus included
|
|
248200|C535804||retinal dystrophy early onset severe included
|
|
248200|C535804||stgd
|
|
248200|C535804||stgd1
|
|
260920|D054078||mevalonate kinase deficiency
|
|
260920|D054078||aciduria mevalonic
|
|
260920|D054078||hids
|
|
260920|D054078||hyper igd syndrome
|
|
260920|D054078||hyper igd syndromes
|
|
260920|D054078||hyperimmunoglobulinemia d
|
|
260920|D054078||hyperimmunoglobulinemia d and periodic fever syndrome
|
|
260920|D054078||kinase deficiencies mevalonate
|
|
260920|D054078||kinase deficiency mevalonate
|
|
260920|D054078||meva
|
|
260920|D054078||mevalonate kinase deficiencies
|
|
260920|D054078||mevalonicaciduria
|
|
260920|D054078||mevalonic aciduria
|
|
260920|D054078||mevalonicacidurias
|
|
260920|D054078||periodic fever dutch type
|
|
260920|D054078||syndrome hyper igd
|
|
606788|D000856||anorexia nervosa
|
|
606788|D000856||anon1
|
|
606788|D000856||anorexia nervosas
|
|
606788|D000856||anorexia nervosa susceptibility to 1
|
|
606788|D000856||nervosa anorexia
|
|
606788|D000856||nervosas anorexia
|
|
C537019||kennerknecht vogel syndrome
|
|
C537019||agonadism mental retardation delayed bone age
|
|
C537018||kennerknecht sorgo oberhoffer syndrome
|
|
C537018||agonadism dextrocardia diaphragmatic hernia
|
|
C537018||agonadism with multiple internal malformations
|
|
C537018||pagod syndrome
|
|
C535344|610623||cataract posterior polar 4
|
|
C535344|610623||cataract 11 multiple types
|
|
C535344|610623||cataract posterior polar 4 with microphthalmia and neurodevelopmental abnormalities
|
|
C535344|610623||cpp4 cataract 11 with microphthalmia and neurodevelopmental abnormalities included
|
|
C535344|610623||ctpp4
|
|
C535344|610623||ctrct11
|
|
C535344|610623||posterior polar cataract 4
|
|
D000169||acrodermatitis
|
|
D000169||acrodermatitides
|
|
D000169||acrodermatitis papulosa infantum
|
|
D000169||acrodermatitis papulosa infantums
|
|
D000169||acropapulo vesicular syndrome
|
|
D000169||acropapulo vesicular syndromes
|
|
D000169||childhood papular acrodermatitides
|
|
D000169||childhood papular acrodermatitis
|
|
D000169||erythemato vesiculo papulous eruptive syndrome
|
|
D000169||erythemato vesiculo papulous eruptive syndromes
|
|
D000169||gianotti crosti syndrome
|
|
D000169||infantile papular acrodermatitides
|
|
D000169||infantile papular acrodermatitis
|
|
D000169||papular acrodermatitides infantile
|
|
D000169||papular acrodermatitis infantile
|
|
D000169||papular acrodermatitis of childhood
|
|
D000169||papulovesicular acrolocated syndrome
|
|
D000169||papulovesicular acrolocated syndromes
|
|
D000169||syndrome acropapulo vesicular
|
|
D000169||syndrome erythemato vesiculo papulous eruptive
|
|
D000169||syndrome gianotti crosti
|
|
D000169||syndromes acropapulo vesicular
|
|
D000169||syndromes erythemato vesiculo papulous eruptive
|
|
D000169||syndromes papulovesicular acrolocated
|
|
C538402||aspartylglucosamidase aga deficiency
|
|
C567747|613112||macrothrombocytopenia autosomal dominant tubb1 related
|
|
C538401||arthrogryposis multiplex congenita whistling face
|
|
C538401||arthrogryposis multiplex congenita with whistling face
|
|
C538401||illium syndrome
|
|
C538401||illum syndrome
|
|
C538401||lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system
|
|
D000163||acquired immunodeficiency syndrome
|
|
D000163||acquired immune deficiency syndrome
|
|
D000163||acquired immuno deficiency syndrome
|
|
D000163||acquired immunodeficiency syndromes
|
|
D000163||acquired immuno deficiency syndromes
|
|
D000163||aids
|
|
D000163||immunodeficiency syndrome acquired
|
|
D000163||immuno deficiency syndrome acquired
|
|
D000163||immunodeficiency syndromes acquired
|
|
D000163||immuno deficiency syndromes acquired
|
|
D000163||immunologic deficiency syndrome acquired
|
|
D000163||syndrome acquired immunodeficiency
|
|
D000163||syndrome acquired immuno deficiency
|
|
D000163||syndromes acquired immunodeficiency
|
|
D000163||syndromes acquired immuno deficiency
|
|
C536750|278250||wrinkly skin syndrome
|
|
C536750|278250||wss
|
|
D013479||superior vena cava syndrome
|
|
D013479||superior vena cava obstruction
|
|
D013479||superior vena cava thrombosis
|
|
D000170||acrodynia
|
|
D000170||acrodynic erythema
|
|
D000170||childhood mercurialism chronic
|
|
D000170||childhood mercurialisms chronic
|
|
D000170||chronic childhood mercurialism
|
|
D000170||chronic childhood mercurialisms
|
|
D000170||erythema acrodynic
|
|
D000170||feer disease
|
|
D000170||feer apos s disease
|
|
D000170||feers disease
|
|
D000170||mercurialism chronic childhood
|
|
D000170||pink disease
|
|
D000170||swift disease
|
|
D000170||swift apos s disease
|
|
D000170||swifts disease
|
|
D012142||respiratory tract neoplasms
|
|
D012142||neoplasm respiratory tract
|
|
D012142||neoplasms respiratory tract
|
|
D012142||respiratory tract neoplasm
|
|
D012142||tract neoplasm respiratory
|
|
D012142||tract neoplasms respiratory
|
|
D020167|238700||hyperlysinemias
|
|
D020167|238700||alpha aminoadipic semialdehyde deficiency disease
|
|
D020167|238700||deficiencies l lysine nad oxido reductase
|
|
D020167|238700||deficiencies lysine alpha ketoglutarate reductase
|
|
D020167|238700||deficiency disease alpha aminoadipic semialdehyde
|
|
D020167|238700||deficiency disease lysine alpha ketoglutarate reductase
|
|
D020167|238700||deficiency disease saccharopine dehydrogenase
|
|
D020167|238700||deficiency l lysine nad oxido reductase
|
|
D020167|238700||deficiency lysine alpha ketoglutarate reductase
|
|
D020167|238700||familial hyperlysinemia
|
|
D020167|238700||familial hyperlysinemias
|
|
D020167|238700||hyperammonemia hyperlysinuria with
|
|
D020167|238700||hyperammonemias hyperlysinuria with
|
|
D020167|238700||hyperlysinemia
|
|
D020167|238700||hyperlysinemia familial
|
|
D020167|238700||hyperlysinemia periodic
|
|
D020167|238700||hyperlysinemias familial
|
|
D020167|238700||hyperlysinemias periodic
|
|
D020167|238700||hyperlysinemia type i
|
|
D020167|238700||hyperlysinuria with hyperammonemia
|
|
D020167|238700||hyperlysinuria with hyperammonemias
|
|
D020167|238700||l lysine nad oxido reductase deficiencies
|
|
D020167|238700||l lysine nad oxido reductase deficiency
|
|
D020167|238700||lysine alpha ketoglutarate reductase deficiencies
|
|
D020167|238700||lysine alpha ketoglutarate reductase deficiency
|
|
D020167|238700||lysine alpha ketoglutarate reductase deficiency disease
|
|
D020167|238700|C563201||lysine intolerance
|
|
D020167|238700||periodic hyperlysinemia
|
|
D020167|238700||periodic hyperlysinemias
|
|
D020167|238700||reductase deficiencies lysine alpha ketoglutarate
|
|
D020167|238700||reductase deficiency lysine alpha ketoglutarate
|
|
D020167|238700||saccharopine dehydrogenase deficiency disease
|
|
D020167|238700||with hyperammonemia hyperlysinuria
|
|
D020167|238700||with hyperammonemias hyperlysinuria
|
|
D013474||sunstroke
|
|
D013474||sun stroke
|
|
D013474||sunstrokes
|
|
D013474||sun strokes
|
|
C564559|300228||testicular germ cell tumor 1
|
|
C564559|300228||tgct1
|
|
D012140||respiratory tract diseases
|
|
D012140||disease respiratory tract
|
|
D012140||diseases respiratory tract
|
|
D012140||respiratory tract disease
|
|
D012140||tract disease respiratory
|
|
D012140||tract diseases respiratory
|
|
D013471||sunburn
|
|
D013471||sunburns
|
|
211750||c syndrome
|
|
D012141||respiratory tract infections
|
|
D012141||infection respiratory tract
|
|
D012141||infections respiratory
|
|
D012141||infections respiratory tract
|
|
D012141||infections upper respiratory
|
|
D012141||infections upper respiratory tract
|
|
D012141||respiratory infections
|
|
D012141||respiratory infection upper
|
|
D012141||respiratory tract infection
|
|
D012141||upper respiratory infections
|
|
D012141||upper respiratory tract infections
|
|
112600|C537089||brachydactyly type a2
|
|
112600|C537089||bda2
|
|
112600|C537089||brachymesophalangy 2
|
|
112600|C537089||brachymesophalangy ii
|
|
112600|C537089||mohr wriedt type brachydactyly
|
|
D013478||superior mesenteric artery syndrome
|
|
D013478||cast syndrome
|
|
D013478||duodenal compression syndrome mesenteric
|
|
D013478||mesenteric duodenal compression syndrome
|
|
D013478||syndrome cast
|
|
D013478||syndrome wilkie
|
|
D013478||wilkie syndrome
|
|
C564700||craniosynostosis syndrome autosomal recessive
|
|
D013492||suppuration
|
|
D013492||pus
|
|
C564704||charcot marie tooth neuropathy dominant intermediate b with neutropenia
|
|
D000172||acromegaly
|
|
D000172||hypersecretion syndrome somatotropin acromegaly
|
|
D000172||hypersecretion syndromes somatotropin acromegaly
|
|
D000172||inappropriate gh secretion syndrome acromegaly
|
|
D000172||inappropriate growth hormone secretion syndrome acromegaly
|
|
D000172||somatotropin hypersecretion syndrome acromegaly
|
|
D000172||somatotropin hypersecretion syndromes acromegaly
|
|
D000172||syndrome somatotropin hypersecretion acromegaly
|
|
D000172||syndromes somatotropin hypersecretion acromegaly
|
|
C535982|604498||congenital amegakaryocytic thrombocytopenia
|
|
C535982|604498||amegakaryocytic thrombocytopenia congenital
|
|
C535982|604498||camt
|
|
C564707||persistent polyclonal b cell lymphocytosis
|
|
D049328||mongolian spot
|
|
D049328||blue spot mongolian
|
|
D049328||mongolian blue spot
|
|
D049328||spot mongolian
|
|
C567478|300703||spinocerebellar ataxia x linked 5
|
|
C567478|300703||scax5
|
|
128700|C563015||preauricular fistulae congenital
|
|
128700|C563015||ear pits
|
|
128700|C563015||pafc
|
|
C536108|310465||n syndrome
|
|
C536108|310465||nsx
|
|
D000182||acth syndrome ectopic
|
|
D000182||acth syndromes ectopic
|
|
D000182||ectopic acth syndrome
|
|
D000182||ectopic acth syndromes
|
|
D000182||syndrome ectopic acth
|
|
D000182||syndromes ectopic acth
|
|
C567404|612164||epileptic encephalopathy early infantile 4
|
|
C567404|612164||eiee4
|
|
C538406||canaliculitis
|
|
C538406||keratoactinomycosis
|
|
C538405||dichuchwa
|
|
C538405||frenga
|
|
C538405||njovera
|
|
C538405||nonvenereal syphilis
|
|
300496||autism susceptibility to x linked 3
|
|
300496||autsx3
|
|
300497||asperger syndrome x linked susceptibility to 2
|
|
300497||aspgx2
|
|
300494||asperger syndrome x linked susceptibility to 1
|
|
300494||aspgx1
|
|
D051642||histiocytoma
|
|
D051642||histiocytomas
|
|
300495||autism susceptibility to x linked 2
|
|
300495||autsx2
|
|
300495||mental retardation x linked included
|
|
C538407||acute rheumatism
|
|
C538420||black hairy tongue
|
|
C538420||black tongue
|
|
C538420||lingua nigra
|
|
C538420||lingua villosa nigra
|
|
108600||spastic ataxia 1 autosomal dominant
|
|
108600||spax1
|
|
C536695|193530||weyers acrofacial dysostosis
|
|
C536695|193530||acrodental dysostosis of weyers
|
|
C536695|193530||acrofacial dysostosis of weyers
|
|
C536695|193530||curry hall syndrome
|
|
C536695|193530||wad
|
|
C536695|193530||weyers acrodental dysostosis
|
|
C538421||neurodegeneration with brain iron accumulation nbia
|
|
D000142||acidosis respiratory
|
|
D000142||acidoses respiratory
|
|
D000142||respiratory acidoses
|
|
D000142||respiratory acidosis
|
|
D000140||acidosis lactic
|
|
D000140||lactic acidosis
|
|
D001471||barrett esophagus
|
|
D001471||barrett epithelium
|
|
D001471||barrett metaplasia
|
|
D001471||barrett apos s esophagus
|
|
D001471||barretts esophagus
|
|
D001471||barrett apos s syndrome
|
|
D001471||barretts syndrome
|
|
D001471||barrett syndrome
|
|
D001471||epithelium barrett
|
|
D001471||esophagus barrett
|
|
D001471||esophagus barrett apos s
|
|
D001471||syndrome barrett
|
|
D001471||syndrome barrett apos s
|
|
C537128|165300||optic atrophy and cataract autosomal dominant
|
|
C537128|165300||opa3 autosomal dominant
|
|
C537128|165300||optic atrophy 3 autosomal dominant
|
|
C537128|165300||optic atrophy cataract and neurologic disorder
|
|
D001477||bartter syndrome
|
|
D001477||aldosteronism with hyperplasia of the adrenal cortex
|
|
D001477||bartter disease
|
|
D001477||bartter apos s disease
|
|
D001477||bartters disease
|
|
D001477||bartter apos s syndrome
|
|
D001477||bartters syndrome
|
|
D001477||juxtaglomerular hyperplasia with secondary aldosteronism
|
|
D001477||syndrome bartter
|
|
D001477||syndrome bartter apos s
|
|
D001476||bartonellaceae infections
|
|
D001476||bartonellaceae infection
|
|
D001476||infection bartonellaceae
|
|
D001476||infections bartonellaceae
|
|
D063646||carcinogenesis
|
|
D063646||carcinogeneses
|
|
D063646||oncogeneses
|
|
D063646||oncogenesis
|
|
D063646||tumorigeneses
|
|
D063646||tumorigenesis
|
|
D001474||bartonella infections
|
|
D001474||bartonella infection
|
|
D001474||bartonelloses
|
|
D001474||bartonellosis
|
|
D001474||carrion disease
|
|
D001474||carrion apos s disease
|
|
D001474||carrions disease
|
|
D001474||cat scratch fever
|
|
D001474||cat scratch fevers
|
|
D001474||disease carrion
|
|
D001474||disease carrion apos s
|
|
D001474||fever cat scratch
|
|
D001474||fever oroya
|
|
D001474||fevers cat scratch
|
|
D001474||infection bartonella
|
|
D001474||infection rochalimaea
|
|
D001474||infections bartonella
|
|
D001474||infections rochalimaea
|
|
D001474||oroya fever
|
|
D001474||rochalimaea infection
|
|
D001474||rochalimaea infections
|
|
D001474||scratch fever cat
|
|
D001474||scratch fevers cat
|
|
D001474||verruga peruana
|
|
D012128||respiratory distress syndrome adult
|
|
D012128||acute respiratory distress syndrome
|
|
D012128||adult respiratory distress syndrome
|
|
D012128||ards human
|
|
D012128||ardss human
|
|
D012128||human ards
|
|
D012128||lung shock
|
|
D012128||respiratory distress syndrome acute
|
|
D012128||shock lung
|
|
D063647||fetal alcohol spectrum disorders
|
|
D063647||alcohol related birth defects
|
|
D063647||alcohol related neurodevelopmental disorder
|
|
D063647||birth defects alcohol related
|
|
D063647||fae fetal alcohol effects
|
|
D063647||faes fetal alcohol effects
|
|
D063647||fasd
|
|
D063647||fasds
|
|
D063647||fetal alcohol syndrome
|
|
D063647||growth retardation facial abnormalities and central nervous system dysfunction
|
|
D063647||partial fetal alcohol syndrome
|
|
D063647||syndrome fetal alcohol
|
|
209500|C565924||atrichia with papular lesions
|
|
209500|C565924|612376|D015473||apl
|
|
209500|C565924||papular atrichia
|
|
D012127||respiratory distress syndrome newborn
|
|
D012127||infantile respiratory distress syndrome
|
|
D012127||neonatal respiratory distress syndrome
|
|
D012127||respiratory distress syndrome infant
|
|
D001480||basal ganglia diseases
|
|
D001480||basal ganglia disease
|
|
D001480||basal ganglia disorder
|
|
D001480||basal ganglia disorders
|
|
D001480||extrapyramidal disorder
|
|
D001480||extrapyramidal disorders
|
|
D001480||lenticulostriate disorder
|
|
D001480||lenticulostriate disorders
|
|
147791|D054868||jacobsen distal 11q deletion syndrome
|
|
147791|D054868||11q23 deletion disorder
|
|
147791|D054868||11q deletion disorder
|
|
147791|D054868||11q deletion syndrome
|
|
147791|D054868||11q terminal deletion disorder
|
|
147791|D054868||chromosome 11q deletion syndrome
|
|
147791|D054868||deletion disorder 11q
|
|
147791|D054868||deletion disorder 11q23
|
|
147791|D054868||disorder 11q23 deletion
|
|
147791|D054868||disorder 11q deletion
|
|
147791|D054868||jacobsen syndrome
|
|
147791|D054868||jacobsen thrombocytopenia
|
|
147791|D054868||paris trousseau syndrome
|
|
147791|D054868||paris trousseau thrombocytopenia
|
|
147791|D054868||partial 11q monosomy syndrome
|
|
147791|D054868||syndrome 11q deletion
|
|
147791|D054868||syndrome jacobsen
|
|
147791|D054868||syndrome paris trousseau
|
|
147791|D054868||thrombocytopenia jacobsen
|
|
147791|D054868||thrombocytopenia paris trousseau
|
|
607453|C564399||deafness autosomal dominant 44
|
|
607453|C564399||dfna44
|
|
D012120||respiration disorders
|
|
D012120||disorder respiration
|
|
D012120||disorders respiration
|
|
D012120||respiration disorder
|
|
D014782||visceral prolapse
|
|
D014782||prolapse visceral
|
|
D014782||splanchnoptosis
|
|
D014782||visceroptosis
|
|
D014786||vision disorders
|
|
D014786||blindness day
|
|
D014786||day blindness
|
|
D014786||disabilities vision
|
|
D014786||disability vision
|
|
D014786||disorders visual
|
|
D014786||disorder visual
|
|
D014786||hemeralopia
|
|
D014786||hemeralopias
|
|
D014786||impairments visual
|
|
D014786||impairment visual
|
|
D014786||macropsia
|
|
D014786||macropsias
|
|
D014786||metamorphopsia
|
|
D014786||metamorphopsias
|
|
D014786||micropsia
|
|
D014786||micropsias
|
|
D014786||vision disabilities
|
|
D014786||vision disability
|
|
D014786||vision disorder
|
|
D014786||visual disorder
|
|
D014786||visual disorders
|
|
D014786||visual impairment
|
|
D014786||visual impairments
|
|
251100|C537360||methylmalonic aciduria cbla type
|
|
251100|C537360||methylmalonic acidemia cbla type
|
|
251100|C537360||methylmalonic aciduria vitamin b12 responsive due to defect in synthesis of adenosylcobalamin cbla type
|
|
D006627|142623||hirschsprung disease
|
|
D006627|142623||aganglionic megacolon
|
|
D006627|142623||aganglionosis colonic
|
|
D006627|142623||aganglionosis rectosigmoid
|
|
D006627|142623||aganglionosis rectosigmoid colon
|
|
D006627|142623||aganglionosis total colonic
|
|
D006627|142623||colonic aganglionosis
|
|
D006627|142623||congenital intestinal aganglionosis
|
|
D006627|142623||congenital megacolon
|
|
D006627|142623||disease hirschsprung
|
|
D006627|142623||disease hirschsprung apos s
|
|
D006627|142623||hirschsprung disease susceptibility to 1
|
|
D006627|142623||hirschsprung disease susceptibility to 2
|
|
D006627|142623||hirschsprung disease susceptibility to 3
|
|
D006627|142623||hirschsprung disease susceptibility to 4
|
|
D006627|142623||hirschsprung disease susceptibility to 5
|
|
D006627|142623||hirschsprung disease susceptibility to 6
|
|
D006627|142623||hirschsprung disease susceptibility to 7
|
|
D006627|142623||hirschsprung disease susceptibility to 8
|
|
D006627|142623||hirschsprung disease susceptibility to 9
|
|
D006627|142623||hirschsprung apos s disease
|
|
D006627|142623||hirschsprungs disease
|
|
D006627|142623||hscr
|
|
D006627|142623||hscr1
|
|
D006627|142623||hscr2
|
|
D006627|142623||hscr3
|
|
D006627|142623||hscr4
|
|
D006627|142623||hscr5
|
|
D006627|142623||hscr6
|
|
D006627|142623||hscr7
|
|
D006627|142623||hscr8
|
|
D006627|142623||hscr9
|
|
D006627|142623||megacolon aganglionic
|
|
D006627|142623||megacolon congenital
|
|
D006627|142623||mgc
|
|
D006627|142623||rectosigmoid aganglionosis
|
|
D006627|142623||rectosigmoid colon aganglionosis
|
|
D006627|142623||total colonic aganglionosis
|
|
C537100||brachyphalangy polydactyly and tibial aplasia hypoplasia
|
|
C537100||brachyphalangy polydactyly and absent tibiae
|
|
C538435||lubs syndrome
|
|
C538435||pseudohermaphroditism incomplete male type i
|
|
C538435||rosewater syndrome
|
|
C538435||type i familial incomplete male pseudohermaphroditism
|
|
C537104||branchiootic syndrome
|
|
C537104||bos1
|
|
C537104||bo syndrome 1
|
|
C537104||branchiootic dysplasia
|
|
C537104||branchiootic syndrome 1
|
|
C538433||ancylostoma duodenale infection
|
|
C537101||brachytelephalangy characteristic facies kallmann
|
|
C537101||brachytelephalangy with characteristic facies and kallmann syndrome
|
|
C537101||characteristic craniofacial appearance and brachytelephalangy
|
|
256550|C537366||neuraminidase 1 deficiency
|
|
256550|C537366||cherry red spot myoclonus syndrome included
|
|
256550|C537366||ml i
|
|
256550|C537366||myoclonus cherry red spot syndrome included
|
|
256550|C537366||neu1 deficiency
|
|
256550|C537366||neu1 deficiency sialidosis type i included
|
|
256550|C537366||neu deficiency
|
|
256550|C537366||neug deficiency
|
|
256550|C537366||neuraminidase deficiency
|
|
256550|C537366||sialidase deficiency
|
|
256550|C537366||sialidoses type 2
|
|
256550|C537366||sialidosis type ii
|
|
C537102||branchial arch syndrome x linked
|
|
C537102||mandibulofacial dysostosis toriello type
|
|
D000153||acne keloid
|
|
D000153||acne keloidal
|
|
D000153||acne keloidalis
|
|
D000153||acne keloids
|
|
D000153||folliculitis keloidalis
|
|
D000153||keloid acne
|
|
D000153||keloidal acne
|
|
D000153||keloidal acnes
|
|
D000153||keloids acne
|
|
C566426|602759||prostate cancer hereditary 8
|
|
C566426|602759||hpc8
|
|
C566426|602759||pcap
|
|
C566426|602759||predisposing for prostate cancer
|
|
277580||ws4
|
|
277580||ws4a
|
|
D000152||acne vulgaris
|
|
D000152||acne
|
|
C567048|610913||surfactant metabolism dysfunction pulmonary 2
|
|
C567048|610913||desquamative interstitial pneumonitis due to surfactant protein c deficiency
|
|
C567048|610913||interstitial lung disease due to surfactant protein c deficiency
|
|
C567048|610913||pulmonary alveolar proteinosis congenital 2
|
|
C567048|610913||smdp2
|
|
D000151||acinetobacter infections
|
|
D000151||acinetobacter infection
|
|
D000151||infection acinetobacter
|
|
D000151||infection mimae
|
|
D000151||infections acinetobacter
|
|
D000151||infections mimae
|
|
D000151||mimae infection
|
|
D000151||mimae infections
|
|
C537729|606952||oculocutaneous albinism type 1b
|
|
C537729|606952||albinism oculocutaneous type ib
|
|
C537729|606952||albinism yellow mutant type
|
|
C537729|606952||oca1b
|
|
C537729|606952||oca1 ts included
|
|
C537729|606952||oculocutaneous albinism type ib
|
|
C537729|606952||yellow albinism
|
|
C537729|606952||yellow albinism albinism oculocutaneous type i temperature sensitive included
|
|
C563409|600996||arrhythmogenic right ventricular dysplasia familial 2
|
|
C563409|600996||arrhythmogenic right ventricular cardiomyopathy 2
|
|
C563409|600996||arvc2
|
|
C563409|600996||arvd2
|
|
D000160||vestibulocochlear nerve diseases
|
|
D000160||acoustic nerve disease
|
|
D000160||acoustic nerve diseases
|
|
D000160||acoustic nerve disorder
|
|
D000160||acoustic nerve disorders
|
|
D000160||cochlear nerve disease
|
|
D000160||cochlear nerve diseases
|
|
D000160||cochlear nerve disorder
|
|
D000160||cochlear nerve disorders
|
|
D000160||cochlear neuritides
|
|
D000160||cochlear neuritis
|
|
D000160||cranial nerve viii diseases
|
|
D000160||cranial nerve viii disorders
|
|
D000160||eighth cranial nerve diseases
|
|
D000160||neuritides cochlear
|
|
D000160||neuritis cochlear
|
|
D000160||vestibular nerve disease
|
|
D000160||vestibular nerve diseases
|
|
D000160||vestibular nerve disorder
|
|
D000160||vestibular nerve disorders
|
|
D000160||vestibulocochlear nerve disease
|
|
D012131||respiratory insufficiency
|
|
D012131||depressions ventilatory
|
|
D012131||respiratory depression
|
|
D012131||respiratory failure
|
|
D012131||ventilatory depression
|
|
C537534|606744||seckel syndrome 2
|
|
C537534|606744||bird headed dwarfism 2
|
|
C537534|606744||microcephalic primordial dwarfism 2
|
|
C537534|606744||sckl2
|
|
C537534|606744||seckel type dwarfism 2
|
|
D012130||respiratory hypersensitivity
|
|
D012130||hypersensitivities respiratory
|
|
D012130||hypersensitivity respiratory
|
|
D012130||respiratory hypersensitivities
|
|
D012135||respiratory sounds
|
|
D012135||breathing sound
|
|
D012135||breathing sounds
|
|
D012135||crackle
|
|
D012135||crackles
|
|
D012135||lung sound
|
|
D012135||lung sounds
|
|
D012135||pleural rub
|
|
D012135||pleural rubs
|
|
D012135||rale
|
|
D012135||rales
|
|
D012135||respiratory sound
|
|
D012135||rhonchi
|
|
D012135||rhonchus
|
|
D012135||rub pleural
|
|
D012135||sound breathing
|
|
D012135||sound lung
|
|
D012135||sound respiratory
|
|
D012135||sounds breathing
|
|
D012135||sounds lung
|
|
D012135||stridor
|
|
D012135||stridors
|
|
D012135||wheezing
|
|
D012135||wheezings
|
|
D012133||respiratory paralysis
|
|
D012133||diaphragmatic paralysis
|
|
D012133||muscle paralyses respiratory
|
|
D012133||muscle paralysis respiratory
|
|
D012133||paralysis diaphragmatic
|
|
D012133||paralysis respiratory
|
|
D012133||paralysis respiratory muscle
|
|
D012133||respiratory muscle paralysis
|
|
C538429||hypoadrenocorticism familial
|
|
C538429||adrenal aplasia
|
|
C538429||adrenal hypoplasia
|
|
C535706|608612||mandibuloacral dysplasia with type b lipodystrophy
|
|
C535706|608612||lipodystrophy type b associated with mandibuloacral dysplasia
|
|
C535706|608612||madb
|
|
D000126||achlorhydria
|
|
D000126||achylia gastrica
|
|
D000126||hypochlorhydria
|
|
C536654|261680||phosphoenolpyruvate carboxykinase deficiency
|
|
C536654|261680||pck1 deficiency cytosolic
|
|
C536654|261680||pepck deficiency cytosolic
|
|
C536654|261680||phosphoenolpyruvate carboxykinase 1 pck1 deficiency
|
|
C536654|261680||phosphoenolpyruvate carboxykinase deficiency cytosolic
|
|
C536654|261680||phosphoenolpyruvate carboxylase deficiency
|
|
C536654|261680||phosphopyruvate carboxylase deficiency
|
|
D002780||cholestasis intrahepatic
|
|
D002780||bile duct obstruction intrahepatic
|
|
D002780||biliary stases intrahepatic
|
|
D002780||biliary stasis intrahepatic
|
|
D002780||cholestases intrahepatic
|
|
D002780||intrahepatic biliary stases
|
|
D002780||intrahepatic biliary stasis
|
|
D002780||intrahepatic cholestases
|
|
D002780||intrahepatic cholestasis
|
|
C565547|231300||glaucoma 3 primary congenital a
|
|
C565547|231300||buphthalmos glaucoma primary open angle adult onset included
|
|
C565547|231300||glaucoma congenital
|
|
C565547|231300||glaucoma primary open angle juvenile onset included
|
|
C565547|231300||glc3
|
|
C565547|231300||glc3a
|
|
D002781||cholesteatoma
|
|
D002781||cholesteatomas
|
|
C564723|300066||deafness x linked 4
|
|
C564723|300066||deafness nonsyndromic sensorineural progressive 6
|
|
C564723|300066||deafness x linked 6 progressive
|
|
C564723|300066||dfn6
|
|
C564723|300066||dfnx4
|
|
D014766||viremia
|
|
D014766||viremias
|
|
D013436||sulfhemoglobinemia
|
|
D013436||sulfhemoglobinemias
|
|
C537516|601200||pleuropulmonary blastoma
|
|
C537516|601200||ppb
|
|
C537516|601200||ppb familial tumor and dysplasia syndrome
|
|
C537516|601200||ppbftds
|
|
C537241|312060||properdin deficiency x linked
|
|
C537241|312060||cfpd
|
|
C537241|312060||complement factor properdin deficiency
|
|
C537241|312060||pfd
|
|
C537241|312060||properdin deficiency type 1
|
|
C537241|312060||properdin deficiency type i
|
|
C537241|312060||properdin deficiency type iii included
|
|
C537241|312060||properdin deficiency type i properdin deficiency type ii included
|
|
C537241|312060||properdin p factor deficiency
|
|
D051677||histiocytoma malignant fibrous
|
|
D051677||fibrohistiocytic tumor malignant
|
|
D051677||fibrohistiocytic tumors malignant
|
|
D051677||fibrous histiocytoma malignant
|
|
D051677||fibrous histiocytomas malignant
|
|
D051677||histiocytomas malignant fibrous
|
|
D051677||malignant fibrohistiocytic tumor
|
|
D051677||malignant fibrohistiocytic tumors
|
|
D051677||malignant fibrous histiocytoma
|
|
D051677||malignant fibrous histiocytomas
|
|
D051677||pleomorphic malignant fibrous histiocytoma
|
|
D051677||tumor malignant fibrohistiocytic
|
|
D051677||tumors malignant fibrohistiocytic
|
|
C567210|612651||endocrine cerebroosteodysplasia
|
|
C567210|612651||eco
|
|
D000138||acidosis
|
|
D000138||acidoses
|
|
D000138||acidoses metabolic
|
|
D000138||acidosis metabolic
|
|
D000138||metabolic acidoses
|
|
D000138||metabolic acidosis
|
|
D001469||barotrauma
|
|
D001469||barotraumas
|
|
D052919|601539||refsum disease infantile
|
|
D052919|601539||adrenoleukodystrophy autosomal neonatal
|
|
D052919|601539||disease infantile refsum
|
|
D052919|601539||disease infantile refsum apos s
|
|
D052919|601539||infantile form of phytanic acid storage disease
|
|
D052919|601539||infantile phytanic acid storage disease
|
|
D052919|601539||infantile refsum disease
|
|
D052919|601539||infantile refsum apos s disease
|
|
D052919|601539||infantile refsums disease
|
|
D052919|601539||pbd1b
|
|
D052919|601539||peroxisome biogenesis disorder 1b
|
|
D052919|601539||peroxisome biogenesis disorder nald ird
|
|
D052919|601539||peroxisome biogenesis disorder neonatal adrenoleukodystrophy infantile refsum disease
|
|
D052919|601539||refsum disease infantile form
|
|
D052919|601539||refsum apos s disease infantile
|
|
D052919|601539||refsums disease infantile
|
|
D000137||acid base imbalance
|
|
D000137||acid base imbalances
|
|
D000137||imbalance acid base
|
|
D000137||imbalances acid base
|
|
C565662|219080||acth independent macronodular adrenal hyperplasia
|
|
C565662|219080||acth independent cushing syndrome
|
|
C565662|219080||acth independent macronodular adrenocortical hyperplasia
|
|
C565662|219080||adrenocorticotropic hormone independent macronodular adrenal hyperplasia
|
|
C565662|219080||aimah
|
|
C565662|219080||corticotropin independent macronodular adrenal hyperplasia
|
|
C565662|219080||cushing syndrome adrenal due to aimah
|
|
D002796||choline deficiency
|
|
D002796||choline deficiencies
|
|
D002796||deficiencies choline
|
|
D002796||deficiency choline
|
|
C566474|610445||night blindness congenital stationary autosomal dominant 1
|
|
C566474|610445||csnbad1
|
|
C566474|610445||night blindness congenital stationary rhodopsin related
|
|
D014777||virus diseases
|
|
D014777||diseases viral
|
|
D014777||diseases virus
|
|
D014777||disease viral
|
|
D014777||disease virus
|
|
D014777||viral disease
|
|
D014777||viral diseases
|
|
D014777||virus disease
|
|
D014770||virilism
|
|
D014770||androgenization
|
|
D014770||virilization
|
|
D001437||bacteriuria
|
|
D001437||bacteriurias
|
|
D002769||cholelithiasis
|
|
D002769||cholelithiases
|
|
C567645|613319||miyoshi muscular dystrophy 3
|
|
C567645|613319||miyoshi myopathy 3
|
|
C567645|613319||mmd3
|
|
D002761||cholangitis
|
|
D002761||cholangitides
|
|
C538355|610883||potocki lupski syndrome
|
|
C538355|610883||chromosome 17p11 2 duplication syndrome
|
|
C538355|610883||duplication 17p11 2 syndrome
|
|
C538355|610883||potocki lupski syndrome dup 17 p11 2p11 2
|
|
C538355|610883||ptls
|
|
D002764||cholecystitis
|
|
D002764||empyema gallbladder
|
|
D002764||empyema gall bladder
|
|
D002764||gallbladder empyema
|
|
D002764||gall bladder empyema
|
|
D002764||gallbladder inflammation
|
|
D002764||inflammation gallbladder
|
|
C563867|608747||insulin like growth factor i deficiency
|
|
C563867|608747||growth retardation with sensorineural deafness and mental retardation
|
|
C563867|608747||igf1 deficiency
|
|
259710||optb2
|
|
580000|C564013||deafness aminoglycoside induced
|
|
580000|C564013||deafness streptomycin induced
|
|
580000|C564013||streptomycin ototoxicity
|
|
D001447||balantidiasis
|
|
D001447||balantidiases
|
|
153700|D057826||vitelliform macular dystrophy
|
|
153700|D057826||adult onset foveomacular dystrophies
|
|
153700|D057826||adult onset foveomacular dystrophy
|
|
153700|D057826||adult onset vitelliform macular dystrophy
|
|
153700|D057826||aofmd
|
|
153700|D057826||avmd
|
|
153700|D057826||best disease
|
|
153700|D057826||best macular dystrophy
|
|
153700|D057826||best apos s disease
|
|
153700|D057826||best vitelliform macular dystrophy
|
|
153700|D057826|300376|D020388||bmd
|
|
153700|D057826||disease best
|
|
153700|D057826||disease best apos s
|
|
153700|D057826||dystrophies adult onset foveomacular
|
|
153700|D057826||dystrophies vitelliform macular
|
|
153700|D057826||dystrophy adult onset foveomacular
|
|
153700|D057826||dystrophy best macular
|
|
153700|D057826||dystrophy vitelliform macular
|
|
153700|D057826||foveomacular dystrophies adult onset
|
|
153700|D057826||foveomacular dystrophy adult onset
|
|
153700|D057826||foveomacular dystrophy adult onset with choroidal neovascularization
|
|
153700|D057826||juvenile onset vitelliform macular dystrophy
|
|
153700|D057826||macular degeneration polymorphic vitelline
|
|
153700|D057826||macular degeneration polymorphic vitelline best vitelliform macular dystrophy multifocal included
|
|
153700|D057826||macular dystrophies vitelliform
|
|
153700|D057826||macular dystrophy best
|
|
153700|D057826||macular dystrophy vitelliform
|
|
153700|D057826||macular dystrophy vitelliform adult onset
|
|
153700|D057826||vitelliform dystrophy
|
|
153700|D057826||vitelliform macular dystrophies
|
|
153700|D057826||vitelliform macular dystrophy adult onset
|
|
153700|D057826||vitelliform macular dystrophy early onset
|
|
153700|D057826||vitelliform macular dystrophy juvenile onset
|
|
153700|D057826||vitelliform macular dystrophy type 2
|
|
153700|D057826||vmd
|
|
D001446||balanitis
|
|
D001446||balanitides
|
|
300425||autism susceptibility to x linked 1
|
|
300425||autsx1
|
|
D001449||balkan nephropathy
|
|
D001449||balkan endemic nephropathy
|
|
D001449||danubian endemic familial nephropathy
|
|
D001449||endemic nephropathy balkan
|
|
D001449||nephropathy balkan
|
|
D001449||nephropathy balkan endemic
|
|
D002779||cholestasis
|
|
D002779||bile duct obstruction
|
|
D002779||bile duct obstructions
|
|
D002779||biliary stases
|
|
D002779||biliary stasis
|
|
D002779||cholestases
|
|
D002779||duct obstruction bile
|
|
D002779||duct obstructions bile
|
|
D002779||obstruction bile duct
|
|
D002779||obstructions bile duct
|
|
D002779||stases biliary
|
|
D002779||stasis biliary
|
|
D001442||bacteroides infections
|
|
D001442||bacteroides infection
|
|
D001442||infection bacteroides
|
|
D001442||infections bacteroides
|
|
C535959|131960||epidermolysis bullosa simplex with mottled pigmentation
|
|
C535959|131960||ebs mp
|
|
C535959|131960||speckled hyperpigmentation palmo plantar punctate keratoses and childhood blistering
|
|
C535959|131960||speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering
|
|
D002771||cholera
|
|
D002771||choleras
|
|
C565531|233710||granulomatous disease chronic autosomal recessive cytochrome b positive type ii
|
|
C565531|233710||cgd autosomal recessive cytochrome b positive type ii
|
|
C565531|233710||granulomatous disease chronic due to ncf2 deficiency
|
|
C565531|233710||ncf2 deficiency of
|
|
C565531|233710||neutrophil cytosol factor 2 deficiency of
|
|
C565531|233710||p67 phox deficiency of
|
|
D050379||arteriolosclerosis
|
|
D050379||arterioloscleroses
|
|
D001416||back pain
|
|
D001416||ache back
|
|
D001416||aches back
|
|
D001416||backache
|
|
D001416||back ache
|
|
D001416||backaches
|
|
D001416||back aches
|
|
D001416||back pains
|
|
D001416||back pain without radiation
|
|
D001416||back pain with radiation
|
|
D001416||pain back
|
|
D001416||pains back
|
|
D001416||pain syndromes vertebrogenic
|
|
D001416||pain syndrome vertebrogenic
|
|
D001416||syndromes vertebrogenic pain
|
|
D001416||syndrome vertebrogenic pain
|
|
D001416||vertebrogenic pain syndrome
|
|
D001416||vertebrogenic pain syndromes
|
|
613573||ectodermal dysplasia syndactyly syndrome 1
|
|
613573||edss1
|
|
613575||retinitis pigmentosa 55
|
|
613575||rp55
|
|
613576||ectodermal dysplasia syndactyly syndrome 2
|
|
613576||edss2
|
|
612239||scoliosis idiopathic susceptibility to 5
|
|
612239||is5
|
|
C562722|131400||eosinophilia familial
|
|
C562722|131400|C563714|609464||eos
|
|
C562722|131400||familial eosinophilia
|
|
612238||scoliosis idiopathic susceptibility to 4
|
|
612238||is4
|
|
C563443|600794||neuronopathy distal hereditary motor type v
|
|
C563443|600794||dhmn5
|
|
C563443|600794||dhmn5a
|
|
C563443|600794||dhmn v
|
|
C563443|600794||dhmn va
|
|
C563443|600794||distal hereditary motor neuronopathy type v
|
|
C563443|600794||distal hereditary motor neuropathy type v
|
|
C563443|600794||distal spinal muscular atrophy type v
|
|
C563443|600794||dsmav
|
|
C563443|600794||dsmava
|
|
C563443|600794||hmn5
|
|
C563443|600794||hmn5a
|
|
C563443|600794||hmn v
|
|
C563443|600794||hmn va
|
|
C563443|600794||neuronopathy distal hereditary motor type va
|
|
C563443|600794||neuropathy distal hereditary motor type v
|
|
C563443|600794||neuropathy distal hereditary motor type va
|
|
C563443|600794||spinal muscular atrophy distal type v
|
|
C563443|600794||spinal muscular atrophy distal type va
|
|
C563443|600794||spinal muscular atrophy distal with upper limb predominance
|
|
C565700|610213||aneurysm intracranial berry 4
|
|
C565700|610213||anib4
|
|
D050380||monckeberg medial calcific sclerosis
|
|
D050380||calcific scleroses medial
|
|
D050380||calcific sclerosis medial
|
|
D050380||medial calcific scleroses
|
|
D050380||medial calcific sclerosis
|
|
D050380||m 246 nckeberg medial calcific sclerosis
|
|
D050380||monckeberg sclerosis
|
|
D050380||m 246 nckeberg sclerosis
|
|
D050380||monckeberg apos s medial calcific sclerosis
|
|
D050380||m 246 nckeberg apos s medial calcific sclerosis
|
|
D050380||monckeberg apos s sclerosis
|
|
D050380||monckebergs sclerosis
|
|
D050380||m 246 nckeberg apos s sclerosis
|
|
D050380||m 246 nckebergs sclerosis
|
|
D050380||scleroses medial calcific
|
|
D050380||sclerosis medial calcific
|
|
D050380||sclerosis monckeberg medial calcific
|
|
D050380||sclerosis m 246 nckeberg medial calcific
|
|
D050380||sclerosis monckeberg apos s
|
|
D050380||sclerosis m 246 nckeberg apos s
|
|
D014720||vesicular exanthema of swine
|
|
D014720||swine vesicular exanthema
|
|
D014720||swine vesicular exanthemas
|
|
D048070||fetal nutrition disorders
|
|
D048070||fetal malnutrition
|
|
D048070||fetal nutrition disorder
|
|
D048070||malnutrition fetal
|
|
D048070||nutrition disorder fetal
|
|
D048070||nutrition disorders fetal
|
|
D002759||adenoma bile duct
|
|
D002759||adenomas bile duct
|
|
D002759||bile duct adenoma
|
|
D002759||bile duct adenomas
|
|
D002759||cholangioma
|
|
D002759||cholangiomas
|
|
D001424||bacterial infections
|
|
D001424||bacterial infection
|
|
D001424||infection bacterial
|
|
D001424||infections bacterial
|
|
D001423||bacterial infections and mycoses
|
|
C563551|159595||myeloproliferative syndrome transient
|
|
C563551|159595||leukemia transient
|
|
C563551|159595||mst
|
|
C563551|159595||tam
|
|
C563551|159595||transient abnormal myelopoiesis
|
|
D002754||choanal atresia
|
|
D002754||atresia choanal
|
|
D002754||atresias choanal
|
|
D002754||choanal atresias
|
|
C567197|612712||leber congenital amaurosis 13
|
|
C567197|612712||lca13
|
|
C567197|612712||retinitis pigmentosa 53 included
|
|
C567197|612712||rp53 included
|
|
613563||noonan syndrome like disorder with or without juvenile myelomonocytic leukemia
|
|
613563||cbl mutation associated syndrome
|
|
613563||cbl syndrome
|
|
613563||nsll
|
|
613558||deafness autosomal dominant 51
|
|
613558||chromosome 9q21 11 duplication syndrome
|
|
613558||dfna51
|
|
D014735||vibrio infections
|
|
D014735||infections vibrio
|
|
D014735||infection vibrio
|
|
D014735||vibrio infection
|
|
613559||combined oxidative phosphorylation deficiency 7
|
|
613559||coxpd7
|
|
C567390|612233||leukodystrophy hypomyelinating 4
|
|
C567390|612233||hld4
|
|
C567390|612233||mitchap60 disease
|
|
C567390|612233||mitochondrial hsp60 chaperonopathy
|
|
C564624|607101||deafness autosomal recessive 30
|
|
C564624|607101||dfnb30
|
|
601583||wilms tumor susceptibility to
|
|
601583||wt5
|
|
601583||wtsl
|
|
607829|C564326||mitral valve prolapse myxomatous 2
|
|
607829|C564326||mmvp2
|
|
607829|C564326||myxomatous mitral valve prolapse 2
|
|
C562692|237900||hyperbilirubinemia transient familial neonatal
|
|
C562692|237900||hblrtfn
|
|
C562692|237900||lucey driscoll syndrome breast milk jaundice included
|
|
D050398||adamantinoma
|
|
D050398||adamantinomas
|
|
C537139|600376||osler rendu weber syndrome 2
|
|
C537139|600376||telangiectasia hereditary hemorrhagic type 2
|
|
C537139|600376||telangiectasia hereditary hemorrhagic type 2 hht2 pulmonary arterial hypertension hereditary hemorrhagic telangiectasia related
|
|
254600|C562864||myeloperoxidase deficiency
|
|
254600|C562864||mpod
|
|
254600|C562864||mpo deficiency
|
|
C537652|601678||bartter syndrome antenatal type 1
|
|
C537652|601678||antenatal bartter syndrome type 1
|
|
C537652|601678||hyperprostaglandin e syndrome 1
|
|
C537652|601678||hypokalemic alkalosis with hypercalciuria antenatal
|
|
C537652|601678||hypokalemic alkalosis with hypercalciuria antenatal 1
|
|
C538655|232200||hepatorenal form of glycogen storage disease
|
|
C538655|232200||glycogen storage disease i
|
|
C538655|232200||glycogen storage disease ia
|
|
C538655|232200||glycogen storage disease type ia
|
|
C538655|232200||gsd1
|
|
C538655|232200||gsd1a
|
|
C538655|232200||gsd ia
|
|
C538655|232200||hepatorenal glycogenosis
|
|
D048089||pneumonia of calves enzootic
|
|
D048089||calf pneumonia enzootic
|
|
D048089||enzootic calf pneumonia
|
|
D048089||enzootic calf pneumonias
|
|
D048089||enzootic pneumonia of calves
|
|
D048089||pneumonia enzootic calf
|
|
D048089||pneumonias enzootic calf
|
|
613550||nephronophthisis 11
|
|
613550||nphp11
|
|
C537856|193003||nystagmus 4 congenital autosomal dominant
|
|
C537856|193003||nys4
|
|
C537856|193003||vestibulocerebellar disorder with predominant ocular signs
|
|
C535502|600204||epiphyseal dysplasia multiple 2
|
|
C535502|600204||edm2
|
|
C535502|600204||multiple epiphyseal dysplasia 2
|
|
D048090||bovine respiratory disease complex
|
|
C567206|612657||cone rod dystrophy 12
|
|
C567206|612657||cord12
|
|
257910|C564935||oculopalatocerebral syndrome
|
|
257910|C564935||oculopalatocerebral dwarfism
|
|
257910|C564935||opc dwarfism
|
|
C567070|300636||atypical mycobacteriosis familial x linked 1
|
|
C567070|300636||amcbx1
|
|
C567070|300636||atypical mycobacterial infection disseminated x linked 1
|
|
C567070|300636||atypical mycobacterial infection familial disseminated x linked 1
|
|
C567070|300636||mycobacterial disease susceptibility to x linked 1
|
|
C537568|311150||jensen syndrome
|
|
C537568|311150||nerve deafness optic nerve atrophy and dementia
|
|
C537568|311150||opticoacoustic nerve atrophy with dementia
|
|
C537568|311150||opticoacustic nerve atrophy with dementia
|
|
C537568|311150||syndrome of opticoacoustic nerve atrophy with dementia
|
|
C535857|158300||hecht syndrome
|
|
C535857|158300||arthrogryposis distal type 7
|
|
C535857|158300||da7
|
|
C535857|158300||mouth inability to open completely and short finger flexor tendons
|
|
C535857|158300||trismus pseudocamptodactyly
|
|
C535857|158300||trismus pseudocamptodactyly syndrome
|
|
C537853|310700||nystagmus 1 congenital x linked
|
|
C537853|310700||nystagmus 1 infantile x linked
|
|
C537853|310700||nystagmus congenital motor 1
|
|
C537853|310700||nystagmus infantile idiopathic formerly iin formerly nystagmus infantile periodic alternating x linked included
|
|
C537853|310700||xipan included
|
|
C537853|310700||xlpan included
|
|
D001404||babesiosis
|
|
D001404||babesia parasite infection
|
|
D001404||babesia parasite infections
|
|
D001404||babesiases
|
|
D001404||babesiasis
|
|
D001404||babesioses
|
|
D001404||babesioses human
|
|
D001404||babesiosis human
|
|
D001404||human babesioses
|
|
D001404||human babesiosis
|
|
D001404||infection babesia parasite
|
|
D001404||infections babesia parasite
|
|
D001404||piroplasmoses
|
|
D001404||piroplasmosis
|
|
D044903|256450||congenital hyperinsulinism
|
|
D044903|256450||congenital hyperinsulinisms
|
|
D044903|256450||familial hyperinsulinemic hypoglycemia 1
|
|
D044903|256450||familial hyperinsulinism
|
|
D044903|256450||familial hyperinsulinisms
|
|
D044903|256450||hhf1
|
|
D044903|256450||hhf2
|
|
D044903|256450||hyperinsulinemia hypoglycemia of infancy
|
|
D044903|256450||hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
|
|
D044903|256450||hyperinsulinemic hypoglycemia familial 1
|
|
D044903|256450||hyperinsulinemic hypoglycemia familial 2
|
|
D044903|256450||hyperinsulinemic hypoglycemia persistent
|
|
D044903|256450||hyperinsulinemic hypoglycemias persistent
|
|
D044903|256450||hyperinsulinism congenital
|
|
D044903|256450||hyperinsulinism familial
|
|
D044903|256450||hyperinsulinism neonatal
|
|
D044903|256450||hyperinsulinisms congenital
|
|
D044903|256450||hyperinsulinisms familial
|
|
D044903|256450||hyperinsulinisms neonatal
|
|
D044903|256450||hypoglycemia hyperinsulinemic of infancy
|
|
D044903|256450||hypoglycemia persistent hyperinsulinemic
|
|
D044903|256450||hypoglycemia phhi
|
|
D044903|256450||hypoglycemias persistent hyperinsulinemic
|
|
D044903|256450||hypoglycemias phhi
|
|
D044903|256450||infancy hyperinsulinemia hypoglycemia
|
|
D044903|256450||infancy hyperinsulinemia hypoglycemias
|
|
D044903|256450||neonatal hyperinsulinism
|
|
D044903|256450||neonatal hyperinsulinisms
|
|
D044903|256450||persistent hyperinsulinemia hypoglycemia of infancy
|
|
D044903|256450||persistent hyperinsulinemic hypoglycemia
|
|
D044903|256450||persistent hyperinsulinemic hypoglycemia of infancy
|
|
D044903|256450||persistent hyperinsulinemic hypoglycemias
|
|
D044903|256450||phhi
|
|
D044903|256450||phhi hypoglycemia
|
|
D044903|256450||phhi hypoglycemias
|
|
C565690|610678||combined oxidative phosphorylation deficiency 4
|
|
C565690|610678||coxpd4
|
|
D001405||reflex babinski
|
|
D001405||babinski reflex
|
|
D001405||babinski reflexes
|
|
D001405||babinski sign
|
|
D001405||babinski sign absent
|
|
D001405||babinski sign negative
|
|
D001405||babinski sign positive
|
|
D001405||babinski signs
|
|
D001405||babinski apos s reflex
|
|
D001405||babinski apos s sign
|
|
D001405||babinski apos s signs
|
|
D001405||extensor plantar reflex
|
|
D001405||extensor plantar response
|
|
D001405||extensor plantar responses
|
|
D001405||great toe paradoxical extensor reflex
|
|
D001405||paradoxical extensor reflex great toe
|
|
D001405||plantar reflex extensor
|
|
D001405||plantar response extensor
|
|
D001405||plantar responses extensor
|
|
D001405||reflex babinski apos s
|
|
D001405||reflexes babinski
|
|
D001405||reflex extensor plantar
|
|
D001405||response extensor plantar
|
|
D001405||responses extensor plantar
|
|
D001405||signs babinski apos s
|
|
C536482|191830||hereditary renal agenesis
|
|
C536482|191830||bilateral renal agenesis
|
|
C536482|191830|C563261||hereditary renal aplasia
|
|
C536482|191830||hra
|
|
C536482|191830||potter syndrome
|
|
C536482|191830|C563261||renal adysplasia
|
|
C536482|191830||renal agenesis
|
|
C536482|191830|C563261||renal aplasia
|
|
C536482|191830||renal hypodysplasia aplasia 1
|
|
C536482|191830||rhda1
|
|
C536482|191830||urogenital adysplasia hereditary
|
|
D045825||fusobacteriaceae infections
|
|
D045825||fusobacteriaceae infection
|
|
D045825||infection fusobacteriaceae
|
|
D045825||infections fusobacteriaceae
|
|
D001749|109800||urinary bladder neoplasms
|
|
D001749|109800||bladder cancer
|
|
D001749|109800||bladder cancers
|
|
D001749|109800||bladder neoplasm
|
|
D001749|109800||bladder neoplasms
|
|
D001749|109800||bladder tumor
|
|
D001749|109800||bladder tumors
|
|
D001749|109800||cancer bladder
|
|
D001749|109800||cancer of bladder
|
|
D001749|109800||cancer of the bladder
|
|
D001749|109800||cancer urinary bladder
|
|
D001749|109800||malignant tumor of urinary bladder
|
|
D001749|109800||neoplasm bladder
|
|
D001749|109800||neoplasms bladder
|
|
D001749|109800||neoplasm urinary bladder
|
|
D001749|109800||tumor bladder
|
|
D001749|109800||tumors bladder
|
|
D001749|109800||urinary bladder cancer
|
|
D001749|109800||urinary bladder neoplasm
|
|
D016889|608089||endometrial neoplasms
|
|
D016889|608089||cancer endometrial
|
|
D016889|608089||cancer endometrium
|
|
D016889|608089||cancer of endometrium
|
|
D016889|608089||cancer of the endometrium
|
|
D016889|608089||cancers endometrial
|
|
D016889|608089||cancers endometrium
|
|
D016889|608089||carcinoma endometrial
|
|
D016889|608089||carcinoma of endometrium
|
|
D016889|608089||carcinomas endometrial
|
|
D016889|608089||endometrial cancer
|
|
D016889|608089||endometrial cancers
|
|
D016889|608089||endometrial carcinoma
|
|
D016889|608089||endometrial carcinomas
|
|
D016889|608089||endometrial neoplasm
|
|
D016889|608089||endometrium cancer
|
|
D016889|608089||endometrium cancers
|
|
D016889|608089||endometrium carcinoma
|
|
D016889|608089||endometrium carcinomas
|
|
D016889|608089||neoplasm endometrial
|
|
D016889|608089||neoplasms endometrial
|
|
D045826||flavobacteriaceae infections
|
|
D045826||flavobacteriaceae infection
|
|
D045826||infection flavobacteriaceae
|
|
D045826||infections flavobacteriaceae
|
|
D045823||ileus
|
|
D014719||vesicovaginal fistula
|
|
D014719||fistulas vesicovaginal
|
|
D014719||fistula vesicovaginal
|
|
D014719||vesicovaginal fistulas
|
|
D045824||desulfovibrionaceae infections
|
|
D045824||bilophila infection
|
|
D045824||bilophila infections
|
|
D045824||desulfovibrio infection
|
|
D045824||desulfovibrio infections
|
|
D045824||desulfovibrionaceae infection
|
|
D045824||infection bilophila
|
|
D045824||infection desulfovibrio
|
|
D045824||infection desulfovibrionaceae
|
|
D045824||infection lawsonia
|
|
D045824||infections bilophila
|
|
D045824||infections desulfovibrio
|
|
D045824||infections desulfovibrionaceae
|
|
D045824||infections lawsonia
|
|
D045824||lawsonia infection
|
|
D045824||lawsonia infections
|
|
D045822||intestinal volvulus
|
|
D045822||volvulus
|
|
D045822||volvulus intestinal
|
|
D045822||volvulus intestine
|
|
C537070|229070||follicle stimulating hormone deficiency isolated
|
|
C537070|229070||isolated follicle stimulating hormone fsh deficiency
|
|
C537070|229070||isolated fsh deficiency
|
|
614869||usher syndrome type ij
|
|
614869||ush1j
|
|
C563981|600175||spinal muscular atrophy distal congenital nonprogressive
|
|
C563981|600175||spinal muscular atrophy congenital benign with contractures
|
|
C564608|607200||thyroid dyshormonogenesis 6
|
|
C564608|607200||hypothyroidism congenital due to dyshormonogenesis 6
|
|
C564608|607200||tdh6
|
|
C564608|607200||thyroid hormonogenesis genetic defect in 6
|
|
D014717||vertigo
|
|
D014717||brainstem vertigo
|
|
D014717||brain stem vertigo
|
|
D014717||brainstem vertigos
|
|
D014717||central nervous system origin vertigo
|
|
D014717||central origin vertigo
|
|
D014717||constant vertigo
|
|
D014717||essential vertigo
|
|
D014717||intermittant vertigo
|
|
D014717||paroxysmal vertigo
|
|
D014717||peripheral vertigo
|
|
D014717||positional vertigo
|
|
D014717||sensation spinning
|
|
D014717||sensations spinning
|
|
D014717||spinning sensation
|
|
D014717||spinning sensations
|
|
D014717||subjective vertigo
|
|
D014717||vertigo brainstem
|
|
D014717||vertigo brain stem
|
|
D014717||vertigo central nervous system origin
|
|
D014717||vertigo central origin
|
|
D014717||vertigo constant
|
|
D014717||vertigo essential
|
|
D014717||vertigo intermittant
|
|
D014717||vertigo paroxysmal
|
|
D014717||vertigo peripheral
|
|
D014717||vertigo positional
|
|
D014717||vertigos brainstem
|
|
D014717||vertigo subjective
|
|
D045827||cytophagaceae infections
|
|
D045827||cytophagaceae infection
|
|
D045827||flexibacteraceae infection
|
|
D045827||flexibacteraceae infections
|
|
D045827||infection cytophagaceae
|
|
D045827||infection flexibacteraceae
|
|
D045827||infections cytophagaceae
|
|
D045827||infections flexibacteraceae
|
|
D014715||vertebrobasilar insufficiency
|
|
D014715||artery insufficiencies basilar
|
|
D014715||artery insufficiencies vertebral
|
|
D014715||artery insufficiency basilar
|
|
D014715||artery insufficiency vertebral
|
|
D014715||artery ischemia basilar
|
|
D014715||artery ischemias basilar
|
|
D014715||artery ischemias vertebral
|
|
D014715||artery ischemia vertebral
|
|
D014715||artery stenoses basilar
|
|
D014715||artery stenoses vertebral
|
|
D014715||artery stenosis basilar
|
|
D014715||artery stenosis vertebral
|
|
D014715||basilar artery insufficiencies
|
|
D014715||basilar artery insufficiency
|
|
D014715||basilar artery ischemia
|
|
D014715||basilar artery ischemias
|
|
D014715||basilar artery stenoses
|
|
D014715||basilar artery stenosis
|
|
D014715||basilar insufficiencies
|
|
D014715||basilar insufficiency
|
|
D014715||dolichoectasias vertebrobasilar
|
|
D014715||dolichoectasia vertebrobasilar
|
|
D014715||insufficiencies basilar
|
|
D014715||insufficiencies basilar artery
|
|
D014715||insufficiencies vertebral artery
|
|
D014715||insufficiencies vertebrobasilar
|
|
D014715||insufficiencies vertebro basilar
|
|
D014715||insufficiency basilar
|
|
D014715||insufficiency basilar artery
|
|
D014715||insufficiency vertebral artery
|
|
D014715||insufficiency vertebrobasilar
|
|
D014715||insufficiency vertebro basilar
|
|
D014715||ischemia basilar artery
|
|
D014715||ischemias basilar artery
|
|
D014715||ischemias vertebral artery
|
|
D014715||ischemias vertebrobasilar
|
|
D014715||ischemias vertebro basilar
|
|
D014715||ischemia vertebral artery
|
|
D014715||ischemia vertebrobasilar
|
|
D014715||ischemia vertebro basilar
|
|
D014715||stenoses basilar artery
|
|
D014715||stenoses vertebral artery
|
|
D014715||stenosis basilar artery
|
|
D014715||stenosis vertebral artery
|
|
D014715||vertebral artery insufficiencies
|
|
D014715||vertebral artery insufficiency
|
|
D014715||vertebral artery ischemia
|
|
D014715||vertebral artery ischemias
|
|
D014715||vertebral artery stenoses
|
|
D014715||vertebral artery stenosis
|
|
D014715||vertebrobasilar dolichoectasia
|
|
D014715||vertebrobasilar dolichoectasias
|
|
D014715||vertebrobasilar insufficiencies
|
|
D014715||vertebro basilar insufficiencies
|
|
D014715||vertebro basilar insufficiency
|
|
D014715||vertebrobasilar ischemia
|
|
D014715||vertebro basilar ischemia
|
|
D014715||vertebrobasilar ischemias
|
|
D014715||vertebro basilar ischemias
|
|
D045828||moraxellaceae infections
|
|
D045828||infection moraxella
|
|
D045828||infection moraxellaceae
|
|
D045828||infection psychobacter
|
|
D045828||infections moraxella
|
|
D045828||infections moraxellaceae
|
|
D045828||infections psychobacter
|
|
D045828||moraxellaceae infection
|
|
D045828||moraxella infection
|
|
D045828||moraxella infections
|
|
D045828||psychobacter infection
|
|
D045828||psychobacter infections
|
|
C536587|203780||alport syndrome recessive type
|
|
C567527|225410||ehlers danlos syndrome type vii autosomal recessive
|
|
C567527|225410||dermatosparaxis
|
|
C567527|225410||eds7c
|
|
C567527|225410||eds viic
|
|
C567527|225410||ehlers danlos syndrome dermatosparaxis type
|
|
601547||cataract 3 multiple types
|
|
601547||cataract 3 multiple types with or without microcornea
|
|
601547|C563294||cataract congenital cerulean type 2
|
|
601547||cca2
|
|
601547||ctrct3
|
|
D018297||neoplasms cystic mucinous and serous
|
|
C566935|611488||macular degeneration age related 10
|
|
C566935|611488||armd10
|
|
D018299||neoplasms ductal lobular and medullary
|
|
D018299||ductal lobular and medullary neoplasms
|
|
D018298||mucoepidermoid tumor
|
|
D018298||mucoepidermoid tumors
|
|
D018298||tumor mucoepidermoid
|
|
D018298||tumors mucoepidermoid
|
|
D018293||cystadenoma serous
|
|
D018293||cystadenomas serous
|
|
D018293||serous cystadenoma
|
|
D018293||serous cystadenomas
|
|
D018292||cystadenoma papillary
|
|
D018292||cystadenomas papillary
|
|
D018292||papillary cystadenoma
|
|
D018292||papillary cystadenomas
|
|
D018295||neoplasms basal cell
|
|
D018295||basal cell cancer
|
|
D018295||basal cell cancers
|
|
D018295||basal cell neoplasm
|
|
D018295||basal cell neoplasms
|
|
D018295||cancer basal cell
|
|
D018295||cancers basal cell
|
|
D018295||cell cancer basal
|
|
D018295||cell cancers basal
|
|
D018295||cell neoplasm basal
|
|
D018295||cell neoplasms basal
|
|
D018295||neoplasm basal cell
|
|
D061085||agenesis of corpus callosum
|
|
D061085||absence of corpus callosum
|
|
D061085||ageneses corpus callosum
|
|
D061085||agenesis corpus callosum
|
|
D061085||corpus callosum absence
|
|
D061085||corpus callosum absences
|
|
D061085||corpus callosum ageneses
|
|
D061085||corpus callosum agenesis
|
|
D061085||corpus callosum agenesis of
|
|
D061085||corpus callosum dysgeneses
|
|
D061085||corpus callosum dysgenesis
|
|
D061085||corpus callosum hypogeneses
|
|
D061085||corpus callosum hypogenesis
|
|
D061085||corpus callosum malformation
|
|
D061085||dysgeneses corpus callosum
|
|
D061085||dysgenesis corpus callosum
|
|
D061085||hypogeneses corpus callosum
|
|
D061085||hypogenesis corpus callosum
|
|
D018294||neoplasms adnexal and skin appendage
|
|
D018294||adnexal and skin appendage neoplasms
|
|
278800|C535992||de sanctis cacchione syndrome
|
|
278800|C535992||desanctis cacchione syndrome
|
|
278800|C535992||xeroderma pigmentosum mental deficiency dwarfism and gonadal hypoplasia
|
|
278800|C535992||xerodermic idiocy of de sanctis and cacchione
|
|
D044504||enterocolitis neutropenic
|
|
D044504||ileocecal syndrome
|
|
D044504||neutropenic enterocolitis
|
|
D044504||syndrome ileocecal
|
|
D018291||cystadenoma mucinous
|
|
D018291||cystadenomas mucinous
|
|
D018291||mucinous cystadenoma
|
|
D018291||mucinous cystadenomas
|
|
613530||muscular dystrophy limb girdle type 1h
|
|
613530||lgmd1h
|
|
D018290||cervical intraepithelial neoplasia
|
|
D018290||cervical intraepithelial neoplasia grade iii
|
|
D018290||cervical intraepithelial neoplasm
|
|
D018290||cervical intraepithelial neoplasms
|
|
D018290||intraepithelial neoplasia cervical
|
|
D018290||intraepithelial neoplasm cervical
|
|
D018290||intraepithelial neoplasms cervical
|
|
D018290||neoplasia cervical intraepithelial
|
|
D018290||neoplasm cervical intraepithelial
|
|
D018290||neoplasms cervical intraepithelial
|
|
C567803|613038||pituitary hormone deficiency combined 1
|
|
C567803|613038||cphd1
|
|
C535731|224050||dysequilibrium syndrome
|
|
C535731|224050||autosomal recessive cerebellar ataxia with mental retardation
|
|
C535731|224050||autosomal recessive cerebellar hypoplasia with cerebral gyral simplification
|
|
C535731|224050||camrq1
|
|
C535731|224050||cerebellar ataxia and mental retardation with or without quadrupedal locomotion 1
|
|
C535731|224050||cerebellar ataxia congenital and mental retardation autosomal recessive
|
|
C535731|224050||cerebellar ataxia mental retardation and dysequilibrium syndrome 1
|
|
C535731|224050||cerebellar disorder nonprogressive with mental retardation
|
|
C535731|224050||cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion
|
|
C535731|224050||cerebellar hypoplasia vldlr associated
|
|
C535731|224050||chmrq1
|
|
C535731|224050||des
|
|
C535731|224050||des vldlr
|
|
C535731|224050||dysequilibrium syndrome vldlr
|
|
C535731|224050||vldlr associated cerebellar hypoplasia
|
|
C535731|224050||vldlrch
|
|
C535731|224050||vldlr ch
|
|
C535388|301835||arts syndrome
|
|
C535388|301835||arts
|
|
C535388|301835||ataxia deafness optic atrophy lethal
|
|
C535388|301835||ataxia fatal x linked with deafness and loss of vision
|
|
C535388|301835||mental retardation x linked syndromic 18
|
|
C535388|301835||mental retardation x linked syndromic arts type
|
|
C535388|301835||mrxs18
|
|
C535388|301835||mrxsarts
|
|
C535388|301835||x linked fatal ataxia with deafness and loss of vision
|
|
612576|C567245||split hand foot malformation with long bone deficiency 3
|
|
612576|C567245||chromosome 17p13 3 telomeric duplication syndrome
|
|
612576|C567245||shfld3
|
|
D031261||poult enteritis mortality syndrome
|
|
D031261||mortality syndrome spiking
|
|
D031261||spiking mortality syndrome
|
|
D018289||carcinoma verrucous
|
|
D018289||carcinomas verrucous
|
|
D018289||verrucous carcinoma
|
|
D018289||verrucous carcinomas
|
|
D006012|232600||glycogen storage disease type v
|
|
D006012|232600||deficiencies muscle phosphorylase
|
|
D006012|232600||deficiencies myophosphorylase
|
|
D006012|232600||deficiencies pygm
|
|
D006012|232600||deficiency muscle phosphorylase
|
|
D006012|232600||deficiency myophosphorylase
|
|
D006012|232600||deficiency pygm
|
|
D006012|232600||disease mcardle
|
|
D006012|232600||disease mcardle apos s
|
|
D006012|232600||glycogenosis 5
|
|
D006012|232600||glycogenosis 5s
|
|
D006012|232600||glycogen storage disease type 5
|
|
D006012|232600||glycogen storage disease v
|
|
D006012|232600||gsd5
|
|
D006012|232600||gsd v
|
|
D006012|232600||mcardle disease
|
|
D006012|232600||mcardle apos s disease
|
|
D006012|232600||mcardles disease
|
|
D006012|232600||mcardle syndrome
|
|
D006012|232600||mcardle syndromes
|
|
D006012|232600||mcardle type glycogen storage disease
|
|
D006012|232600||muscle glycogen phosphorylase deficiency
|
|
D006012|232600||muscle phosphorylase deficiencies
|
|
D006012|232600||muscle phosphorylase deficiency
|
|
D006012|232600||myophosphorylase deficiencies
|
|
D006012|232600||myophosphorylase deficiency
|
|
D006012|232600||phosphorylase deficiencies muscle
|
|
D006012|232600||phosphorylase deficiency muscle
|
|
D006012|232600||pygm deficiencies
|
|
D006012|232600||pygm deficiency
|
|
D006012|232600||syndrome mcardle
|
|
D006012|232600||syndromes mcardle
|
|
C536759|309555||x linked mental retardation gustavson type
|
|
C536759|309555||gust
|
|
C536759|309555||gustavson syndrome
|
|
C536759|309555||mental retardation with optic atrophy deafness and seizures
|
|
C536759|309555||mental retardation x linked severe gustavson type
|
|
C569516||trichophyton infection
|
|
C566715|180105||retinitis pigmentosa 10
|
|
C566715|180105||rp10
|
|
D017488|113800||hyperkeratosis epidermolytic
|
|
D017488|113800||bcie
|
|
D017488|113800||bie
|
|
D017488|113800||bullous congenital ichthyosiform erythroderma
|
|
D017488|113800||bullous erythroderma ichthyosiforme
|
|
D017488|113800||bullous erythroderma ichthyosiformes
|
|
D017488|113800||bullous erythroderma ichthyosiformis congenita of brocq
|
|
D017488|113800||bullous ichthyosiform erythroderma
|
|
D017488|113800||bullous ichthyosiform erythroderma congenital
|
|
D017488|113800||bullous ichthyosiform erythrodermas
|
|
D017488|113800||congenital bullous ichthyosiform erythroderma
|
|
D017488|113800||congenital ichthyosiform erythroderma bullous
|
|
D017488|113800||ehk
|
|
D017488|113800||epidermolytic hyperkeratoses
|
|
D017488|113800||epidermolytic hyperkeratosis
|
|
D017488|113800||epidermolytic ichthyosis
|
|
D017488|113800||epidermolytic ichthyosis epidermolytic hyperkeratosis late onset included
|
|
D017488|113800||erythroderma bullous ichthyosiform
|
|
D017488|113800||erythroderma ichthyosiforme bullous
|
|
D017488|113800||erythroderma ichthyosiformes bullous
|
|
D017488|113800||erythrodermas bullous ichthyosiform
|
|
D017488|113800||hyperkeratoses epidermolytic
|
|
D017488|113800||ichthyosiforme bullous erythroderma
|
|
D017488|113800||ichthyosiform erythroderma bullous
|
|
D017488|113800||ichthyosiform erythroderma bullous congenital
|
|
D017488|113800||ichthyosiform erythrodermas bullous
|
|
D017488|113800||ichthyosiformes bullous erythroderma
|
|
613517||microphthalmia isolated 6
|
|
613517||mcop6
|
|
613517||microphthalmia posterior nonsyndromic
|
|
C535349|125520||cayler cardiofacial syndrome
|
|
C535349|125520||acf
|
|
C535349|125520||asymmetric crying facies
|
|
C535349|125520||cayler apos s syndrome
|
|
C535349|125520||cayler syndrome
|
|
C535349|125520||depressor anguli oris muscle hypoplasia of
|
|
C535349|125520||facial paresis partial unilateral
|
|
C535349|125520||partial unilateral facial paralysis
|
|
C537330|260400||shwachman syndrome
|
|
C537330|260400||congenital lipomatosis of pancreas
|
|
C537330|260400||lipomatosis of pancreas congenital
|
|
C537330|260400||metaphyseal chondrodysplasia shwachman type
|
|
C537330|260400||pancreatic insufficiency and bone marrow dysfunction
|
|
C537330|260400||sds
|
|
C537330|260400||shwachman bodian diamond syndrome
|
|
C537330|260400||shwachman bodian syndrome
|
|
C537330|260400||shwachman diamond oski syndrome
|
|
C537330|260400||shwachman diamond syndrome
|
|
D018275||carcinoma lobular
|
|
D018275||carcinomas lobular
|
|
D018275||lobular carcinoma
|
|
D018275||lobular carcinomas
|
|
D018277||carcinoma mucoepidermoid
|
|
D018277||carcinomas mucoepidermoid
|
|
D018277||mucoepidermoid carcinoma
|
|
D018277||mucoepidermoid carcinomas
|
|
D018276||carcinoma medullary
|
|
D018276||carcinomas medullary
|
|
D018276||medullary carcinoma
|
|
D018276||medullary carcinomas
|
|
D018270||carcinoma ductal breast
|
|
D018270||carcinoma infiltrating duct
|
|
D018270||carcinoma invasive ductal breast
|
|
D018270||carcinoma mammary ductal
|
|
D018270||carcinomas infiltrating duct
|
|
D018270||carcinomas mammary ductal
|
|
D018270||invasive ductal carcinoma breast
|
|
D018270||mammary ductal carcinoma
|
|
D018270||mammary ductal carcinomas
|
|
611096|C567013||mental retardation autosomal recessive 10
|
|
611096|C567013||mental retardation autosomal recessive 20
|
|
611096|C567013||mrt10
|
|
611096|C567013||mrt20
|
|
D018273||carcinoma islet cell
|
|
D018273||carcinomas islet cell
|
|
D018273||islet cell carcinoma
|
|
D018273||islet cell carcinomas
|
|
D018273||islet cell tumor malignant
|
|
C564513|300436||mental retardation x linked 46
|
|
C564513|300436||mrx46
|
|
613507||glycogen storage disease xv
|
|
613507||glycogenin deficiency
|
|
613507||gsd15
|
|
613507||gsd xv
|
|
613507||gyg1 deficiency
|
|
613508||sodium serum level quantitative trait locus 1
|
|
613508||hyponatremia included
|
|
613508||ssqtl1
|
|
C537113|308940||leiomyomatosis esophageal and vulval with nephropathy
|
|
C537113|308940||alport syndrome and diffuse leiomyomatosis
|
|
C537113|308940||alport syndrome with diffuse leiomyomatosis
|
|
C537113|308940||ats dl
|
|
C537113|308940||chromosome xq22 3 centromeric deletion syndrome
|
|
C537113|308940||diffuse leiomyomatosis in alport syndrome
|
|
C537113|308940||diffuse leiomyomatosis with alport syndrome
|
|
C537113|308940||dl ats
|
|
C537113|308940||leiomyomatosis diffuse with alport syndrome
|
|
D031249||erdheim chester disease
|
|
D031249||granulomatosis lipid
|
|
D031249||lipid granulomatosis
|
|
D018268||adrenocortical carcinoma
|
|
D018268||adrenal cortical carcinoma
|
|
D018268||adrenal cortical carcinomas
|
|
D018268||adrenocortical carcinomas
|
|
D018268||carcinoma adrenal cortical
|
|
D018268||carcinoma adrenocortical
|
|
D018268||carcinomas adrenal cortical
|
|
D018268||carcinomas adrenocortical
|
|
D018267||carcinoma acinar cell
|
|
D018267||acinar carcinoma
|
|
D018267||acinar carcinomas
|
|
D018267||acinar cell adenocarcinoma
|
|
D018267||acinar cell adenocarcinomas
|
|
D018267||acinar cell carcinoma
|
|
D018267||acinar cell carcinomas
|
|
D018267||acinic cell adenocarcinoma
|
|
D018267||acinic cell adenocarcinomas
|
|
D018267||acinic cell carcinoma
|
|
D018267||acinic cell carcinomas
|
|
D018267||acinic cell tumor
|
|
D018267||acinic cell tumors
|
|
D018267||adenocarcinoma acinar cell
|
|
D018267||adenocarcinoma acinic cell
|
|
D018267||adenocarcinomas acinar cell
|
|
D018267||adenocarcinomas acinic cell
|
|
D018267||carcinoma acinar
|
|
D018267||carcinoma acinic cell
|
|
D018267||carcinomas acinar
|
|
D018267||carcinomas acinar cell
|
|
D018267||carcinomas acinic cell
|
|
D018267||serous acinar adenoma
|
|
D018267||tumor acinic cell
|
|
D018267||tumors acinic cell
|
|
D057831||lemierre syndrome
|
|
D057831||disease lemierre
|
|
D057831||disease lemierre apos s
|
|
D057831||lemierre disease
|
|
D057831||lemierre apos s disease
|
|
D057831||lemierres disease
|
|
D057831||lemierre apos s syndrome
|
|
D057831||lemierres syndrome
|
|
D057831||postanginal sepses
|
|
D057831||postanginal sepsis
|
|
D057831||sepses postanginal
|
|
D057831||sepsis postanginal
|
|
D057831||syndrome lemierre
|
|
D057831||syndrome lemierre apos s
|
|
D018269||carcinoma endometrioid
|
|
D018269||adenocarcinoma endometrioid
|
|
D018269||adenocarcinomas endometrioid
|
|
D018269||carcinomas endometrioid
|
|
D018269||endometrioid adenocarcinoma
|
|
D018269||endometrioid adenocarcinomas
|
|
D018269||endometrioid carcinoma
|
|
D018269||endometrioid carcinomas
|
|
248250|C537153||hypomagnesemia primary
|
|
248250|C537153||homg3
|
|
248250|C537153||hypomagnesemia 3 renal
|
|
248250|C537153||hypomagnesemia familial with hypercalciuria and nephrocalcinosis
|
|
248250|C537153||hypomagnesemia familial with hypercalciuria and nephrocalcinosis hypercalciuria childhood self limiting included
|
|
248250|C537153||hypomagnesemia isolated renal
|
|
248250|C537153||hypomagnesemia primary due to defect in renal tubular transport of magnesium
|
|
248250|C537153||magnesium defect in renal tubular transport of
|
|
D018286||carcinoma giant cell
|
|
D018286||carcinomas giant cell
|
|
D018286||cell carcinoma giant
|
|
D018286||cell carcinomas giant
|
|
D018286||giant cell carcinoma
|
|
D018286||giant cell carcinomas
|
|
D018285||klatskin apos s tumor
|
|
D018285||klatskins tumor
|
|
D018285||klatskin tumor
|
|
D018285||tumor klatskin apos s
|
|
157600||mirror movements 1
|
|
157600||bimanual synergia
|
|
157600||mirror movements congenital
|
|
157600||mrmv1
|
|
608423|C564242||muscular dystrophy limb girdle type 1f
|
|
608423|C564242||lgmd1f
|
|
D018287||carcinoma large cell
|
|
D018287||carcinomas large cell
|
|
D018287||cell carcinoma large
|
|
D018287||cell carcinomas large
|
|
D018287||large cell carcinoma
|
|
D018287||large cell carcinomas
|
|
601518|C537243||prostate cancer hereditary 1
|
|
601518||hpc1
|
|
601518||prca1
|
|
D018282||cystadenocarcinoma mucinous
|
|
D018282||cystadenocarcinomas mucinous
|
|
D018282||mucinous cystadenocarcinoma
|
|
D018282||mucinous cystadenocarcinomas
|
|
D018281||cholangiocarcinoma
|
|
D018281||cholangiocarcinomas
|
|
D018281||cholangiocellular carcinoma
|
|
D018284||cystadenocarcinoma serous
|
|
D018284||cystadenocarcinomas serous
|
|
D018284||serous cystadenocarcinoma
|
|
D018284||serous cystadenocarcinomas
|
|
D018283||cystadenocarcinoma papillary
|
|
D018283||cystadenocarcinomas papillary
|
|
D018283||papillary cystadenocarcinoma
|
|
D018283||papillary cystadenocarcinomas
|
|
C536642|270700||spastic paraplegia 15 autosomal recessive
|
|
C536642|270700||kjellin syndrome
|
|
C536642|270700||recessive spastic paraplegia with retinal degeneration
|
|
C536642|270700||spastic paraplegia and retinal degeneration
|
|
C536642|270700||spg15
|
|
270100||htx5
|
|
270100||siv
|
|
D018280||carcinoma skin appendage
|
|
D018280||appendage carcinoma skin
|
|
D018280||appendage carcinomas skin
|
|
D018280||carcinomas skin appendage
|
|
D018280||skin appendage carcinoma
|
|
D018280||skin appendage carcinomas
|
|
D015324|266150||pyruvate carboxylase deficiency disease
|
|
D015324|266150||ataxia with lactic acidosis 2
|
|
D015324|266150||ataxia with lactic acidosis ii
|
|
D015324|266150||ataxia with lactic acidosis type ii
|
|
D015324|266150||deficiency disease pyruvate carboxylase
|
|
D015324|266150||deficiency pyruvate carboxylase
|
|
D015324|266150||lactic acidosis with ataxia type ii
|
|
D015324|266150||pc deficiency
|
|
D015324|266150||pyruvate carboxylase deficiency
|
|
D015324|266150||type ii ataxia with lactic acidosis
|
|
D043202||steroid metabolism inborn errors
|
|
D043202||congenital errors of steroid metabolism
|
|
D043202||inborn errors of steroid metabolism
|
|
D043202||steroid metabolic diseases inborn
|
|
D043204||mineralocorticoid excess syndrome apparent
|
|
D043204||apparent mineralocorticoid excess syndrome
|
|
613502||agammaglobulinemia 4 autosomal recessive
|
|
613502||agammaglobulinemia autosomal recessive due to blnk defect
|
|
613502||agm4
|
|
C566826|168500||parietal foramina
|
|
C566826|168500||catlin marks
|
|
C566826|168500||cranium bifidum hereditary
|
|
C566826|168500||cranium bifidum hereditary parietal foramina 1 included
|
|
C566826|168500||cranium bifidum occultum
|
|
C566826|168500||enlarged parietal foramina
|
|
C566826|168500||foramina parietalia permagna
|
|
C566826|168500||fpp
|
|
C566826|168500||parietal foramina symmetric
|
|
C566826|168500||pfm
|
|
C566826|168500||pfm1 included
|
|
D003456|219050||cryptorchidism
|
|
D003456|219050||abdominal cryptorchidism
|
|
D003456|219050||bilateral cryptorchidism
|
|
D003456|219050||cryptorchidism abdominal
|
|
D003456|219050||cryptorchidism bilateral
|
|
D003456|219050||cryptorchidism inguinal
|
|
D003456|219050||cryptorchidism unilateral
|
|
D003456|219050||cryptorchidism unilateral or bilateral
|
|
D003456|219050||cryptorchism
|
|
D003456|219050||inguinal cryptorchidism
|
|
D003456|219050||testes undescended
|
|
D003456|219050||testis undescended
|
|
D003456|219050||undescended testes
|
|
D003456|219050||undescended testis
|
|
D003456|219050||unilateral cryptorchidism
|
|
D016891|600666||polycystic kidney autosomal dominant
|
|
D016891|600666||adpkd
|
|
D016891|600666||adult polycystic kidney disease
|
|
D016891|600666||adult polycystic kidney disease type 1
|
|
D016891|600666||adult polycystic kidney disease type 2
|
|
D016891|600666||apkd2
|
|
D016891|600666||apkd3
|
|
D016891|600666||autosomal dominant polycystic kidney
|
|
D016891|600666||kidney polycystic autosomal dominant
|
|
D016891|600666||pkd2
|
|
D016891|600666||pkd3
|
|
D016891|600666||polycystic kidney disease 2
|
|
D016891|600666||polycystic kidney disease 3
|
|
D016891|600666||polycystic kidney disease 3 autosomal dominant
|
|
D016891|600666||polycystic kidney disease adult
|
|
D016891|600666||polycystic kidney disease adult type 2
|
|
D016891|600666||polycystic kidney disease adult type ii
|
|
D016891|600666||polycystic kidney disease adult type iii
|
|
D016891|600666||polycystic kidney disease autosomal dominant
|
|
D016891|600666||polycystic kidney disease type 2
|
|
D016891|600666||polycystic kidney disease type 3
|
|
D016891|600666||polycystic kidney type 1 autosomal dominant disease
|
|
D016891|600666||polycystic kidney type 2 autosomal dominant disease
|
|
D018279||carcinoma signet ring cell
|
|
D018279||signet ring cell carcinoma
|
|
D018278||carcinoma neuroendocrine
|
|
D018278||carcinomas neuroendocrine
|
|
D018278||neuroendocrine carcinoma
|
|
D018278||neuroendocrine carcinomas
|
|
D017042||phenylketonuria maternal
|
|
D017042||in phenylketonuria pregnancy
|
|
D017042||in phenylketonurias pregnancy
|
|
D017042||maternal phenylalanine hydroxylase deficiency disease
|
|
D017042||maternal phenylketonuria
|
|
D017042||phenylalanine hydroxylase deficiency disease maternal
|
|
D017042||phenylketonuria pregnancy in
|
|
D017042||phenylketonurias pregnancy in
|
|
D017042||pku maternal
|
|
D017042||pregnancy in phenylketonuria
|
|
D017042||pregnancy in phenylketonurias
|
|
D017043||chalazion
|
|
D017043||chalazia
|
|
D017043||cyst meibomian
|
|
D017043||meibomian cyst
|
|
C563287||prepapillary vascular loops
|
|
C563287||preretinal vascular loops
|
|
D018376||cardiovascular abnormalities
|
|
D018376||abnormalities cardiovascular
|
|
D018376||abnormality cardiovascular
|
|
D018376||cardiovascular abnormality
|
|
D018370||leukocyte adhesion deficiency syndrome
|
|
D018370||deficiency syndrome leukocyte adhesion
|
|
D018370||deficiency syndromes leukocyte adhesion
|
|
D018370||leukocyte adhesion deficiency syndromes
|
|
D018370||syndrome leukocyte adhesion deficiency
|
|
D018370||syndromes leukocyte adhesion deficiency
|
|
600084|C564004||macrocytosis familial
|
|
D005058||eunuchism
|
|
D005058||eunuchoidism
|
|
D005058||hypogonadism male
|
|
D006396||hematemesis
|
|
D006396||hematemeses
|
|
D057971||anterior capsular rupture ocular
|
|
278000|C531854||lysosomal acid lipase deficiency
|
|
278000|C531854||acid cholesteryl ester hydrolase deficiency type 2
|
|
278000|C531854||acid lipase disease
|
|
278000|C531854||cesd
|
|
278000|C531854||cholesterol ester hydrolase deficiency
|
|
278000|C531854||cholesterol ester hydrolase deficiency wolman disease included
|
|
278000|C531854||lal deficiency
|
|
278000|C531854||lipa deficiency
|
|
D006394||hemangiosarcoma
|
|
D006394||angiosarcoma
|
|
D006394||angiosarcomas
|
|
D006394||hemangiosarcomas
|
|
D057973||dent disease
|
|
D057973||dent apos s disease
|
|
D057973||dents disease
|
|
D057973||disease dent
|
|
D057973||disease dents
|
|
D057973||disease dent apos s
|
|
D006395||hemarthrosis
|
|
D006395||hemarthroses
|
|
C565701|610212||deafness autosomal recessive 66
|
|
C565701|610212||dfnb66
|
|
D006392||hemangioma cavernous
|
|
D006392||angioma cavernous
|
|
D006392||cavernous angioma
|
|
D006392||cavernous hemangioma
|
|
D006392||cavernous hemangiomas
|
|
D006392||hemangiomas cavernous
|
|
D006392||hemangiomas strawberry
|
|
D006392||hemangioma strawberry
|
|
D006392||strawberry hemangioma
|
|
D006392||strawberry hemangiomas
|
|
D006393||hemangiopericytoma
|
|
D006393||hemangiopericytomas
|
|
D006390||hemangioendothelioma
|
|
D006390||endotheliomas vascular
|
|
D006390||endothelioma vascular
|
|
D006390||hemangio endothelioma
|
|
D006390||hemangioendotheliomas
|
|
D006390||hemangio endotheliomas
|
|
D006390||vascular endothelioma
|
|
D006390||vascular endotheliomas
|
|
D006391||hemangioma
|
|
D006391||angioma
|
|
D006391||chorangioma
|
|
D006391||chorangiomas
|
|
D006391||chorioangioma
|
|
D006391||chorioangiomas
|
|
D006391||hemangioma histiocytoid
|
|
D006391||hemangioma intramuscular
|
|
D006391||hemangiomas
|
|
D006391||hemangiomas histiocytoid
|
|
D006391||hemangiomas intramuscular
|
|
D006391||histiocytoid hemangioma
|
|
D006391||histiocytoid hemangiomas
|
|
D006391||intramuscular hemangioma
|
|
D006391||intramuscular hemangiomas
|
|
C563291||multiple epiphyseal dysplasia with robin phenotype
|
|
C563291||epiphyseal dysplasia multiple with robin phenotype
|
|
D056647||systemic vasculitis
|
|
D056647||systemic vasculitides
|
|
D056647||vasculitides systemic
|
|
D056647||vasculitis systemic
|
|
C563290||dyssegmental dysplasia with glaucoma
|
|
D056648||anti neutrophil cytoplasmic antibody associated vasculitis
|
|
D056648||anca associated vasculitide
|
|
D056648||anca associated vasculitides
|
|
D056648||anca associated vasculitis
|
|
D056648||pauci immune vasculitides
|
|
D056648||pauci immune vasculitis
|
|
D056648||vasculitide anca associated
|
|
D056648||vasculitides anca associated
|
|
D056648||vasculitides pauci immune
|
|
D056648||vasculitis anca associated
|
|
D056648||vasculitis pauci immune
|
|
D019698||hepatitis c chronic
|
|
D019698||chronic hepatitis c
|
|
D018366||vasculitis leukocytoclastic cutaneous
|
|
D018366||allergic cutaneous angiitides
|
|
D018366||allergic cutaneous angiitis
|
|
D018366||allergic cutaneous vasculitides
|
|
D018366||allergic cutaneous vasculitis
|
|
D018366||allergic vasculitides cutaneous
|
|
D018366||allergic vasculitis cutaneous
|
|
D018366||angiitides allergic cutaneous
|
|
D018366||angiitides cutaneous leukocytoclastic
|
|
D018366||angiitides hypersensitivity
|
|
D018366||angiitis allergic cutaneous
|
|
D018366||angiitis cutaneous leukocytoclastic
|
|
D018366||angiitis hypersensitivity
|
|
D018366||cutaneous allergic vasculitides
|
|
D018366||cutaneous allergic vasculitis
|
|
D018366||cutaneous angiitides allergic
|
|
D018366||cutaneous angiitis allergic
|
|
D018366||cutaneous leukocytoclastic angiitides
|
|
D018366||cutaneous leukocytoclastic angiitis
|
|
D018366||cutaneous leukocytoclastic vasculitides
|
|
D018366||cutaneous leukocytoclastic vasculitis
|
|
D018366||cutaneous vasculitides allergic
|
|
D018366||cutaneous vasculitis allergic
|
|
D018366||hypersensitivity angiitides
|
|
D018366||hypersensitivity angiitis
|
|
D018366||hypersensitivity vasculitides
|
|
D018366||hypersensitivity vasculitis
|
|
D018366||leukocytoclastic angiitides cutaneous
|
|
D018366||leukocytoclastic angiitis cutaneous
|
|
D018366||leukocytoclastic vasculitides cutaneous
|
|
D018366||leukocytoclastic vasculitis cutaneous
|
|
D018366||vasculitides allergic cutaneous
|
|
D018366||vasculitides cutaneous allergic
|
|
D018366||vasculitides cutaneous leukocytoclastic
|
|
D018366||vasculitides hypersensitivity
|
|
D018366||vasculitis allergic cutaneous
|
|
D018366||vasculitis cutaneous allergic
|
|
D018366||vasculitis cutaneous leukocytoclastic
|
|
D018366||vasculitis hypersensitivity
|
|
D017036||epilepsia partialis continua
|
|
D017036||chronic progressive epilepsia partialis continua
|
|
D017036||epilepsia partialis continua chronic progressive
|
|
D017036||epilepsies kojevnikov apos s
|
|
D017036||epilepsy kojevnikov apos s
|
|
D017036||epilepsy kojewnikov apos s
|
|
D017036||kojevnikov epilepsy
|
|
D017036||kojevnikov apos s epilepsies
|
|
D017036||kojevnikov apos s epilepsy
|
|
D017036||kojewnikov epilepsy
|
|
D017036||kojewnikov apos s epilepsy
|
|
D017036||kojewnikow apos s syndrome
|
|
D017036||kojewnikow syndrome
|
|
D017036||kozhevnikov apos s syndrome
|
|
D017036||kozhevnikov syndrome
|
|
D017036||kozhevnikow syndrome progressive variant
|
|
D017036||progressive variant of kozhevnikow syndrome
|
|
D017036||syndrome kojewnikow
|
|
D017036||syndrome kojewnikow apos s
|
|
D017036||syndrome kozhevnikov
|
|
D017036||syndrome kozhevnikov apos s
|
|
C563294||cataract congenital blue dot type 2
|
|
C563293||ectopia lentis spontaneous filtering blebs and craniofacial dysmorphism
|
|
193200||vitiligo associated multiple autoimmune disease susceptibility 6
|
|
193200||vamas6
|
|
C563760|609257||myopia 8
|
|
C563760|609257||myp8
|
|
C563296||microcephaly retinitis pigmentosa and sutural cataract
|
|
D018382||thyroid hormone resistance syndrome
|
|
D018382||generalized resistance to thyroid hormone
|
|
D018382||generalized thyroid hormone resistance
|
|
D018382||hormone resistance thyroid
|
|
D018382||refetoff dewind degroot syndrome
|
|
D018382||resistance thyroid hormone
|
|
D018382||syndrome refetoff
|
|
D018382||syndrome refetoff dewind degroot
|
|
D018382||thyroid hormone resistance
|
|
C565752|604765||cardiomyopathy dilated 1i
|
|
C565752|604765||cmd1i
|
|
C536641|162091||schwannomatosis
|
|
C536641|162091||neurilemmomatosis congenital cutaneous
|
|
C536641|162091||schwannomatosis 1
|
|
C536641|162091||swnts1
|
|
115700||cataract 4 multiple types
|
|
115700||caca
|
|
115700||cataract 4 multiple types with or without microcornea
|
|
115700||cataract nonnuclear polymorphic congenital
|
|
115700||cca3
|
|
115700||ctrct4
|
|
115700||pcc
|
|
C537617|261540||krause kivlin syndrome
|
|
C537617|261540||krause van schooneveld kivlin syndrome
|
|
C537617|261540||peters anomaly short limb dwarfism syndrome
|
|
C537617|261540||peters anomaly with short limb dwarfism
|
|
C537617|261540||peters plus syndrome
|
|
C537617|261540||peters apos plus syndrome
|
|
D005067||euthyroid sick syndromes
|
|
D005067||euthyroid sick syndrome
|
|
D005067||high t4 syndrome
|
|
D005067||high t4 syndromes
|
|
D005067||low t3 and low t4 syndrome
|
|
D005067||low t3 high t4 syndrome
|
|
D005067||low t3 low t4 syndrome
|
|
D005067||low t3 syndrome
|
|
D005067||non thyroidal illness syndrome
|
|
D005067||sick euthyroid syndrome
|
|
D005067||syndrome non thyroidal illness
|
|
D005067||syndrome sick euthyroid
|
|
D005067||syndromes non thyroidal illness
|
|
D006398||hematocele
|
|
D006398||hematoceles
|
|
D006398||hematocele scrotal
|
|
D006398||hematoceles scrotal
|
|
D006398||hematoceles testicular
|
|
D006398||hematocele testicular
|
|
D006398||scrotal hematocele
|
|
D006398||scrotal hematoceles
|
|
D006398||testicular hematocele
|
|
D006398||testicular hematoceles
|
|
153640|C535507||myh9 related disorders
|
|
153640|C535507||alport syndrome with leukocyte inclusions and macrothrombocytopenia
|
|
153640|C535507||alport syndrome with macrothrombocytopenia
|
|
153640|C535507||alport syndrome with macrothrombocytopenia formerly
|
|
153640|C535507||apsm formerly
|
|
153640|C535507||autosomal dominant myh9 spectrum disorders
|
|
153640|C535507||bdplt6
|
|
153640|C535507||bleeding disorder platelet type 6
|
|
153640|C535507||dohle leukocyte inclusions with giant platelets
|
|
153640|C535507||epstein syndrome
|
|
153640|C535507||fechtner apos s syndrome
|
|
153640|C535507||fechtner syndrome
|
|
153640|C535507||ftns
|
|
153640|C535507||macrothrombocytopathy nephritis and deafness
|
|
153640|C535507||macrothrombocytopathy nephritis deafness and leukocyte inclusions
|
|
153640|C535507||macrothrombocytopenia nephritis and deafness
|
|
153640|C535507||macrothrombocytopenia nephritis deafness and leukocyte inclusions
|
|
153640|C535507||macrothrombocytopenia with dispersed leukocytic inclusions
|
|
153640|C535507||macrothrombocytopenia with leukocyte inclusions
|
|
153640|C535507||may hegglin anomaly
|
|
153640|C535507||mha
|
|
153640|C535507||myh9 gene related autosomal macrothrombocytopenias
|
|
153640|C535507||myh9rd
|
|
153640|C535507||myh9 related disease
|
|
153640|C535507||myh9 related disorder
|
|
153640|C535507||myh9 related macrothrombocytopenias
|
|
153640|C535507||sebastian platelet syndrome
|
|
153640|C535507||sebastian syndrome
|
|
D006399||hematocolpos
|
|
227300||factor v and factor viii combined deficiency of 1
|
|
227300||f5f8d1
|
|
D056650||vulvodynia
|
|
D056650||generalized vulvodynia
|
|
D056650||generalized vulvodynias
|
|
D056650||vestibulodynia
|
|
D056650||vestibulodynias
|
|
D056650||vulvodynia generalized
|
|
D056650||vulvodynias
|
|
D056650||vulvodynias generalized
|
|
D005077||exanthema subitum
|
|
D005077||disease sixth
|
|
D005077||roseola infantum
|
|
D005077||sixth disease
|
|
D005076||exanthema
|
|
D005076||exanthem
|
|
D005076||rash
|
|
D005076||rash skin
|
|
D005076||skin rash
|
|
D056653||rheumatoid vasculitis
|
|
D056653||rheumatoid vasculitides
|
|
D056653||vasculitides rheumatoid
|
|
D056653||vasculitis rheumatoid
|
|
C566094|186000||synpolydactyly 1
|
|
C566094|186000||spd1
|
|
C566094|186000||syndactyly type ii
|
|
C566094|186000||syndactyly type ii synpolydactyly with foot anomalies included
|
|
D029021||peste des petits ruminants
|
|
D029021||pseudorinderpest
|
|
D015464|608232||leukemia myelogenous chronic bcr abl positive
|
|
D015464|608232||acml included
|
|
D015464|608232||chronic granulocytic leukemia
|
|
D015464|608232||chronic granulocytic leukemias
|
|
D015464|608232||chronic myelocytic leukemia
|
|
D015464|608232||chronic myelocytic leukemias
|
|
D015464|608232||chronic myelogenous leukemia
|
|
D015464|608232||chronic myelogenous leukemias
|
|
D015464|608232||chronic myeloid leukemia
|
|
D015464|608232||chronic myeloid leukemias
|
|
D015464|608232||cml
|
|
D015464|608232||granulocytic leukemia chronic
|
|
D015464|608232||granulocytic leukemias chronic
|
|
D015464|608232||leukemia chronic granulocytic
|
|
D015464|608232||leukemia chronic myelocytic
|
|
D015464|608232||leukemia chronic myelogenous
|
|
D015464|608232||leukemia chronic myelogenous leukemia chronic myeloid atypical included
|
|
D015464|608232||leukemia chronic myeloid
|
|
D015464|608232||leukemia granulocytic chronic
|
|
D015464|608232||leukemia myelocytic chronic
|
|
D015464|608232||leukemia myelogenous chronic
|
|
D015464|608232||leukemia myelogenous ph1 positive
|
|
D015464|608232||leukemia myeloid chronic
|
|
D015464|608232||leukemia myeloid ph1 positive
|
|
D015464|608232||leukemia myeloid philadelphia positive
|
|
D015464|608232||leukemia ph1 positive myelogenous
|
|
D015464|608232||leukemia ph1 positive myeloid
|
|
D015464|608232||leukemia philadelphia positive myeloid
|
|
D015464|608232||leukemias chronic granulocytic
|
|
D015464|608232||leukemias chronic myelocytic
|
|
D015464|608232||leukemias chronic myelogenous
|
|
D015464|608232||leukemias chronic myeloid
|
|
D015464|608232||leukemias ph1 positive myelogenous
|
|
D015464|608232||leukemias ph1 positive myeloid
|
|
D015464|608232||leukemias philadelphia positive myeloid
|
|
D015464|608232||myelocytic leukemia chronic
|
|
D015464|608232||myelocytic leukemias chronic
|
|
D015464|608232||myelogenous leukemia chronic
|
|
D015464|608232||myelogenous leukemia ph1 positive
|
|
D015464|608232||myelogenous leukemias chronic
|
|
D015464|608232||myelogenous leukemias ph1 positive
|
|
D015464|608232||myeloid leukemia chronic
|
|
D015464|608232||myeloid leukemia ph1 positive
|
|
D015464|608232||myeloid leukemia philadelphia positive
|
|
D015464|608232||myeloid leukemias chronic
|
|
D015464|608232||myeloid leukemias ph1 positive
|
|
D015464|608232||myeloid leukemias philadelphia positive
|
|
D015464|608232||ph1 positive myelogenous leukemia
|
|
D015464|608232||ph1 positive myelogenous leukemias
|
|
D015464|608232||ph1 positive myeloid leukemia
|
|
D015464|608232||ph1 positive myeloid leukemias
|
|
D015464|608232||philadelphia positive myeloid leukemia
|
|
D015464|608232||philadelphia positive myeloid leukemias
|
|
611097|C567012||mental retardation autosomal recessive 11
|
|
611097|C567012||mrt11
|
|
C564114|308930||leigh syndrome x linked
|
|
608931||cms1d
|
|
608931||cms1e included
|
|
608931||cms id myasthenic syndrome congenital with facial dysmorphism associated with acetylcholine receptor deficiency included
|
|
608931||cms ie included
|
|
608931||myasthenic syndrome congenital ie included
|
|
C538270|602483||auriculo condylar syndrome
|
|
C538270|602483||arcnd1
|
|
C538270|602483||auriculocondylar syndrome
|
|
C538270|602483||auriculocondylar syndrome 1
|
|
C538270|602483||ears prominent and constricted
|
|
C538270|602483||question mark ear
|
|
C538270|602483||question mark ears syndrome
|
|
C538270|602483||question mark ear syndrome
|
|
D018352||coronavirus infections
|
|
D018352||coronavirus infection
|
|
D018352||infection coronavirus
|
|
D018352||infections coronavirus
|
|
C565711|610170||kyphoscoliosis 1
|
|
C565711|610170||kypsc1
|
|
D018354||alphavirus infections
|
|
D018354||alphavirus infection
|
|
D018354||infection alphavirus
|
|
D018354||infections alphavirus
|
|
C564595||mammographic density
|
|
D018353||rhabdoviridae infections
|
|
D018353||infection rhabdoviridae
|
|
D018353||infections rhabdoviridae
|
|
D018353||rhabdoviridae infection
|
|
C567556|612838||brugada syndrome 5
|
|
C567556|612838||brgda5
|
|
C567556|612838||cardiac conduction defect nonspecific included
|
|
C563268||ectopia lentis with ectopia of pupil
|
|
C563268||ectopia lentis et pupillae
|
|
C562725|612423||prekallikrein deficiency
|
|
C562725|612423||fletcher factor deficiency
|
|
C562725|612423||pkk deficiency
|
|
D006374||helminthiasis animal
|
|
D006374||animal helminthiases
|
|
D006374||animal helminthiasis
|
|
D006374||helminthiases animal
|
|
D055331||adenomyoepithelioma
|
|
D055331||adenomyoepitheliomas
|
|
C566157|116300||cataract nuclear diffuse nonprogressive
|
|
C566157|116300||cataract 30
|
|
C566157|116300||cataract 30 pulverulent
|
|
C566157|116300||ctrct30
|
|
D006373||helminthiasis
|
|
D006373||helminthiases
|
|
D006373||infection nematomorpha
|
|
D006373||infections nematomorpha
|
|
D006373||nematomorpha infection
|
|
D006373||nematomorpha infections
|
|
304020||cone rod dystrophy x linked 1
|
|
304020||cod1
|
|
304020||cone dystrophy 1 x linked
|
|
D054000||nevus sebaceous of jadassohn
|
|
D054000||epidermal nevus verrucous
|
|
D054000||feuerstein mims syndrome
|
|
D054000||inflammatory linear verrucose epidermal nevus
|
|
D054000||inflammatory linear verrucous epidermal naevus
|
|
D054000||jadassohn nevus phakomatosis
|
|
D054000||jadassohn nevus sebaceus
|
|
D054000||jadassohn sebaceous nevus
|
|
D054000||linear sebaceous nevus
|
|
D054000||linear sebaceous nevus syndrome
|
|
D054000||linear verrucous epidermal nevus
|
|
D054000||nevus linear sebaceous
|
|
D054000||nevus phakomatoses organoid
|
|
D054000||nevus phakomatosis jadassohn
|
|
D054000||nevus phakomatosis organoid
|
|
D054000||nevus sebaceus of jadassohn
|
|
D054000||nevus verrucous
|
|
D054000||nevus verrucous epidermal
|
|
D054000||organoid nevus phakomatoses
|
|
D054000||organoid nevus phakomatosis
|
|
D054000||phakomatoses organoid nevus
|
|
D054000||phakomatosis jadassohn nevus
|
|
D054000||phakomatosis organoid nevus
|
|
D054000||schimmelpenning feuerstein mims syndrome
|
|
D054000||schimmelpenning syndrome
|
|
D054000||sebaceous nevus linear
|
|
D054000||sebaceous nevus of jadassohn
|
|
D054000||sebaceous nevus syndrome linear
|
|
D054000||syndrome feuerstein mims
|
|
D054000||syndrome schimmelpenning
|
|
D054000||syndrome schimmelpenning feuerstein mims
|
|
D054000||verrucous epidermal nevus
|
|
D054000||verrucous nevus
|
|
D056660||hereditary autoinflammatory diseases
|
|
D056660||autoinflammation disease hereditary
|
|
D056660||autoinflammation diseases hereditary
|
|
D056660||autoinflammatory disease hereditary
|
|
D056660||autoinflammatory diseases hereditary
|
|
D056660||disease hereditary autoinflammation
|
|
D056660||disease hereditary autoinflammatory
|
|
D056660||disease reimann periodic
|
|
D056660||diseases hereditary autoinflammation
|
|
D056660||diseases hereditary autoinflammatory
|
|
D056660||disease siegal cattan mamou
|
|
D056660||diseases reimann periodic
|
|
D056660||fever hereditary recurrent
|
|
D056660||fevers hereditary recurrent
|
|
D056660||hereditary autoinflammation disease
|
|
D056660||hereditary autoinflammation diseases
|
|
D056660||hereditary autoinflammatory disease
|
|
D056660||hereditary periodic fever syndromes
|
|
D056660||hereditary recurrent fever
|
|
D056660||hereditary recurrent fevers
|
|
D056660||periodic disease reimann
|
|
D056660||periodic diseases reimann
|
|
D056660||recurrent fever hereditary
|
|
D056660||recurrent fevers hereditary
|
|
D056660||reimann periodic disease
|
|
D056660||reimann periodic diseases
|
|
D056660||siegal cattan mamou disease
|
|
607143|C535745||congenital disorder of glycosylation type 1g
|
|
607143|C535745||cdg1g
|
|
607143|C535745||cdgig
|
|
607143|C535745||cdg ig
|
|
607143|C535745||congenital disorder of glycosylation type ig
|
|
605361|C537196||spinocerebellar ataxia 14
|
|
605361|C537196||sca14
|
|
D018344||t lymphocytopenia idiopathic cd4 positive
|
|
D018344||cd4 positive t lymphocytopenia idiopathic
|
|
D018344||cd4 t lymphocytopenia
|
|
D018344||cd4 t lymphocytopenia idiopathic
|
|
D018344||cd4 t lymphocytopenias
|
|
D018344||idiopathic cd4 positive t lymphocytopenia
|
|
D018344||idiopathic cd4 t lymphocytopenia
|
|
D018344||t lymphocytopenia cd4
|
|
D018344||t lymphocytopenia idiopathic cd4
|
|
D018344||t lymphocytopenias cd4
|
|
254900||epilepsy progressive myoclonic 4 with or without renal failure
|
|
254900||amrf
|
|
254900||epm4
|
|
D018347||hepadnaviridae infections
|
|
D018347||hepadnaviridae infection
|
|
D018347||infection hepadnaviridae
|
|
D018347||infections hepadnaviridae
|
|
C563270||macular corneal dystrophy type ii
|
|
D019694||hepatitis b chronic
|
|
D019694||chronic hepatitis b
|
|
C563277||papillary thyroid microcarcinoma
|
|
239300||hyperphosphatasia with mental retardation syndrome 1
|
|
239300||hpmrs1
|
|
239300||mabry syndrome
|
|
D019693||hepatitis autoimmune
|
|
D019693||autoimmune chronic hepatitides
|
|
D019693||autoimmune chronic hepatitis
|
|
D019693||autoimmune hepatitides
|
|
D019693||autoimmune hepatitis
|
|
D019693||chronic hepatitides autoimmune
|
|
D019693||chronic hepatitis autoimmune
|
|
D019693||hepatitides autoimmune
|
|
D019693||hepatitides autoimmune chronic
|
|
D019693||hepatitis autoimmune chronic
|
|
C563276||osteofibrous dysplasia
|
|
D018365||neoplasm residual
|
|
D018365||cancer residual
|
|
D018365||cancers residual
|
|
D018365||disease minimal residual
|
|
D018365||disease residual minimal
|
|
D018365||diseases minimal residual
|
|
D018365||diseases residual minimal
|
|
D018365||minimal disease residual
|
|
D018365||minimal diseases residual
|
|
D018365||minimal residual disease
|
|
D018365||minimal residual diseases
|
|
D018365||neoplasms residual
|
|
D018365||residual cancer
|
|
D018365||residual cancers
|
|
D018365||residual disease minimal
|
|
D018365||residual diseases minimal
|
|
D018365||residual minimal disease
|
|
D018365||residual minimal diseases
|
|
D018365||residual neoplasm
|
|
D018365||residual neoplasms
|
|
D018365||residual tumor
|
|
D018365||residual tumors
|
|
D018365||tumor residual
|
|
D018365||tumors residual
|
|
D017034||epilepsy frontal lobe
|
|
D017034||anterior fronto polar epilepsies
|
|
D017034||anterior fronto polar epilepsy
|
|
D017034||benign frontal childhood epilepsy
|
|
D017034||childhood benign frontal epilepsy
|
|
D017034||cingulate epilepsies
|
|
D017034||cingulate epilepsy
|
|
D017034||epilepsies anterior fronto polar
|
|
D017034||epilepsies cingulate
|
|
D017034||epilepsies orbito frontal
|
|
D017034||epilepsies supplementary motor
|
|
D017034||epilepsy anterior fronto polar
|
|
D017034||epilepsy benign frontal childhood
|
|
D017034||epilepsy cingulate
|
|
D017034||epilepsy opercular
|
|
D017034||epilepsy orbito frontal
|
|
D017034||epilepsy supplementary motor
|
|
D017034||frontal epilepsy benign childhood
|
|
D017034||frontal lobe epilepsies
|
|
D017034||frontal lobe epilepsy
|
|
D017034||fronto polar epilepsies anterior
|
|
D017034||fronto polar epilepsy anterior
|
|
D017034||motor epilepsies supplementary
|
|
D017034||opercular epilepsies
|
|
D017034||opercular epilepsy
|
|
D017034||orbito frontal epilepsies
|
|
D017034||orbito frontal epilepsy
|
|
D017034||supplementary motor epilepsies
|
|
D017034||supplementary motor epilepsy
|
|
612237|C563195||chondrosarcoma extraskeletal myxoid
|
|
612237|C563195||emc
|
|
D017029||epilepsy complex partial
|
|
D017029||complex partial epilepsy
|
|
D017029||complex partial seizure disorder
|
|
D017029||cryptogenic partial complex epilepsy
|
|
D017029||disorder complex partial seizures
|
|
D017029||epilepsy cryptogenic partial complex
|
|
D017029||epilepsy psychic equivalent
|
|
D017029||epilepsy psychomotor
|
|
D017029||epilepsy symptomatic partial complex
|
|
D017029||partial complex epilepsy cryptogenic
|
|
D017029||partial complex epilepsy symptomatic
|
|
D017029||partial epilepsy complex
|
|
D017029||psychic equivalent epilepsy
|
|
D017029||psychomotor epilepsy
|
|
D017029||seizure disorder complex partial
|
|
D017029||symptomatic partial complex epilepsy
|
|
C538162|608978||meacham winn culler syndrome
|
|
D019687||uterine inversion
|
|
D019687||inversion of uterus
|
|
D019687||inversion uterine
|
|
D019687||uterus inversion
|
|
C563926|608448||inflammatory bowel disease 9
|
|
C563926|608448||ibd9
|
|
D018355||rubivirus infections
|
|
D018355||infection rubivirus
|
|
D018355||infections rubivirus
|
|
D018355||rubivirus infection
|
|
D054019||immune reconstitution inflammatory syndrome
|
|
D054019||disease immune reconstitution
|
|
D054019||immune reconstitution disease
|
|
D054019||immune reconstitution syndrome
|
|
D054019||immune reconstitution syndromes
|
|
D054019||immune restoration syndrome
|
|
D054019||reconstitution disease immune
|
|
D054019||reconstitution syndrome immune
|
|
D054019||reconstitution syndromes immune
|
|
D054019||restoration syndrome immune
|
|
D054019||syndrome immune reconstitution
|
|
D054019||syndrome immune restoration
|
|
D054019||syndromes immune reconstitution
|
|
D018358||neuroendocrine tumors
|
|
D018358||neuroendocrine tumor
|
|
D018358||tumor neuroendocrine
|
|
D018358||tumors neuroendocrine
|
|
D018357||respiratory syncytial virus infections
|
|
D018357||infections respiratory syncytial virus
|
|
D018330||nevus intradermal
|
|
D018330||intradermal nevi
|
|
D018330||intradermal nevus
|
|
D018330||nevi intradermal
|
|
C538288||10p deletion syndrome partial
|
|
C538288||chromosome 10 10p partial
|
|
C538288||chromosome 10 monosomy 10p
|
|
C538288||chromosome 10 partial deletion short arm
|
|
C538288||monosomy 10p
|
|
C564574||arthrogryposis x linked type v
|
|
C538287||cataract microcornea syndrome
|
|
C538287||microcornea cataract syndrome
|
|
D018332||nevus epithelioid and spindle cell
|
|
D018332||nevus spindle cell and epithelioid
|
|
D018332||nevus spitz
|
|
D018332||spitz nevus
|
|
183840||spondyloarthropathy susceptibility to 2
|
|
183840||spda2
|
|
C538286||cataract hutterite type
|
|
D018331||nevus spindle cell
|
|
D018331||nevi spindle cell
|
|
D018331||spindle cell nevi
|
|
D018331||spindle cell nevus
|
|
D017001||tooth demineralization
|
|
D017001||demineralization tooth
|
|
D017001||hypomineralizations tooth
|
|
D017001||hypomineralization tooth
|
|
D017001||tooth hypomineralization
|
|
D017001||tooth hypomineralizations
|
|
C564572||x inactivation familial skewed 2
|
|
C563241||chronic motor tics
|
|
C563248||chondrodysplasia punctata autosomal dominant
|
|
C563248||chondrodysplasia punctata due to vitamin k deficiency
|
|
C563248||chondrodysplasia punctata due to warfarin teratogenicity
|
|
C564578||bartter syndrome type 3 with hypocalciuria
|
|
C563247||muscular dystrophy cardiac type
|
|
C538289||chromosome 10 monosomy 10q
|
|
C538289||10q deletion
|
|
C538289||deletion 10q
|
|
C538289||monosomy 10q
|
|
C538289||terminal deletion of chromosome 10q
|
|
D006349||heart valve diseases
|
|
D006349||disease heart valve
|
|
D006349||diseases heart valve
|
|
D006349||diseases valvular heart
|
|
D006349||disease valvular heart
|
|
D006349||heart diseases valvular
|
|
D006349||heart disease valvular
|
|
D006349||heart valve disease
|
|
D006349||valve disease heart
|
|
D006349||valve diseases heart
|
|
D006349||valvular heart disease
|
|
D006349||valvular heart diseases
|
|
C538280||cataract and cardiomyopathy
|
|
C538280||cardiomyopathy and cataract
|
|
C538280||sengers syndrome
|
|
C563249||carnitine acetyltransferase deficiency
|
|
D007676||kidney failure chronic
|
|
D007676||chronic kidney failure
|
|
D007676||chronic renal failure
|
|
D007676||disease end stage kidney
|
|
D007676||disease end stage renal
|
|
D007676||end stage kidney disease
|
|
D007676||end stage renal disease
|
|
D007676||end stage renal failure
|
|
D007676||esrd
|
|
D007676||kidney disease end stage
|
|
D007676||renal disease end stage
|
|
D007676||renal failure chronic
|
|
D007676||renal failure end stage
|
|
D006345||heart septal defects ventricular
|
|
D006345||defect intraventricular septal
|
|
D006345||defects intraventricular septal
|
|
D006345||defect ventricular septal
|
|
D006345||intraventricular septal defect
|
|
D006345||intraventricular septal defects
|
|
D006345||septal defect intraventricular
|
|
D006345||septal defects intraventricular
|
|
D006345||septal defects ventricular
|
|
D006345||septal defect ventricular
|
|
D006345||ventricular septal defect
|
|
D006345||ventricular septal defects
|
|
C538284||cataract congenital dominant non nuclear
|
|
C538284||autosomal dominant nonnuclear polymorphic congenital cataract
|
|
C538284||cataract nonnuclear polymorphic congenital autosomal dominant
|
|
C538284||cataract polymorphic congenital
|
|
C538283||cataract ataxia deafness
|
|
C538283||begeer syndrome
|
|
C538283||cataract ataxia deafness retardation syndrome
|
|
C538283||cataract ataxia deafness syndrome
|
|
C538283||polyneuropathy cataract deafness syndrome
|
|
D007674||kidney diseases
|
|
D007674||disease kidney
|
|
D007674||diseases kidney
|
|
D007674||kidney disease
|
|
D006343||heart septal defects
|
|
D006343||cardiac septal defects
|
|
D006343||defect heart septal
|
|
D006343||defects heart septal
|
|
D006343||heart septal defect
|
|
D006343||septal defect heart
|
|
D006343||septal defects heart
|
|
C538282||cataract anterior polar dominant
|
|
C538282||anterior polar cataracts 1
|
|
D006344||heart septal defects atrial
|
|
D006344||atrial septal defect
|
|
D006344||atrial septal defects
|
|
D006344||defect atrial septal
|
|
D006344||defects atrial septal
|
|
D006344||ostium primum persistent
|
|
D006344||ostium secundum atrial septal defect
|
|
D006344||persistent ostium primum
|
|
D006344||primum persistent ostium
|
|
D006344||septal defect atrial
|
|
D006344||septal defects atrial
|
|
C538281||cataract and congenital ichthyosis
|
|
C538281||syndromic cataract and congenital ichthyosis
|
|
D007683||kidney tubular necrosis acute
|
|
D007683||acute kidney tubular necrosis
|
|
D007683||lower nephron nephroses
|
|
D007683||lower nephron nephrosis
|
|
D007683||nephron nephroses lower
|
|
D007683||nephron nephrosis lower
|
|
D007683||nephroses lower nephron
|
|
D007683||nephrosis lower nephron
|
|
D007681||kidney papillary necrosis
|
|
D007681||necrosis kidney papillary
|
|
D007681||necrosis renal medullary
|
|
D007681||necrotizing renal papillitides
|
|
D007681||necrotizing renal papillitis
|
|
D007681||papillary necrosis kidney
|
|
D007681||papillitides necrotizing renal
|
|
D007681||renal medullary necrosis
|
|
D007681||renal papillitides necrotizing
|
|
D007681||renal papillitis necrotizing
|
|
C563337|601362||digeorge syndrome velocardiofacial syndrome complex 2
|
|
C563337|601362||dgs2
|
|
D007680||kidney neoplasms
|
|
D007680||cancer kidney
|
|
D007680||cancer of kidney
|
|
D007680||cancer of the kidney
|
|
D007680||cancer renal
|
|
D007680||cancers kidney
|
|
D007680||cancers renal
|
|
D007680||kidney cancer
|
|
D007680||kidney cancers
|
|
D007680||kidney neoplasm
|
|
D007680||neoplasm kidney
|
|
D007680||neoplasm renal
|
|
D007680||neoplasms kidney
|
|
D007680||neoplasms renal
|
|
D007680||renal cancer
|
|
D007680||renal cancers
|
|
D007680||renal neoplasm
|
|
D007680||renal neoplasms
|
|
D018327||hutchinson apos s melanotic freckle
|
|
D018327||freckle hutchinson apos s melanotic
|
|
D018327||freckle melanotic
|
|
D018327||freckles melanotic
|
|
D018327||hutchinson melanotic freckle
|
|
D018327||hutchinsons melanotic freckle
|
|
D018327||lentigo maligna
|
|
D018327||lentigo malignant
|
|
D018327||lentigos malignant
|
|
D018327||malignant lentigo
|
|
D018327||malignant lentigos
|
|
D018327||melanotic freckle
|
|
D018327||melanotic freckle hutchinson apos s
|
|
D018327||melanotic freckles
|
|
D018326||nevi and melanomas
|
|
D018326||melanomas and nevi
|
|
D018329||nevus blue
|
|
D018329||blue nevi
|
|
D018329||blue nevi cellular
|
|
D018329||blue nevus
|
|
D018329||blue nevus cellular
|
|
D018329||cellular blue nevi
|
|
D018329||cellular blue nevus
|
|
D018329||nevi blue
|
|
D018329||nevi cellular blue
|
|
D018329||nevus cellular blue
|
|
D018328||melanoma amelanotic
|
|
D018328||amelanotic melanoma
|
|
D018328||amelanotic melanomas
|
|
D018328||melanomas amelanotic
|
|
D018323||hemangioendothelioma epithelioid
|
|
D018323||epithelioid hemangioendothelioma
|
|
D018323||epithelioid hemangioendotheliomas
|
|
D018323||hemangioendotheliomas epithelioid
|
|
D018322||angiofibroma
|
|
D018322||angiofibromas
|
|
D018325||hemangioblastoma
|
|
D018325||hemangioblastoma multiple
|
|
D018325||hemangioblastomas
|
|
D018325||hemangioblastomas multiple
|
|
D018325||multiple hemangioblastoma
|
|
D018325||multiple hemangioblastomas
|
|
D018324||hemangioma capillary
|
|
D018324||capillary hemangioma
|
|
D018324||capillary hemangiomas
|
|
D018324||hemangiomas capillary
|
|
D031300||retinal vasculitis
|
|
D031300||vasculitis retinal
|
|
C563255||microspherophakia
|
|
C538299||chromosome 12 12p trisomy
|
|
C538299||duplication 12p
|
|
C538299||trisomy 12p
|
|
C563254||presenile and senile dementia
|
|
C538298||chromosome 12 ring
|
|
C538298||ring chromosome 12
|
|
C537264|601277||lamellar ichthyosis type 2
|
|
C537264|601277||arci4a
|
|
C537264|601277||ichthyosis congenita 2b
|
|
C537264|601277||ichthyosis congenita iib
|
|
C537264|601277||ichthyosis congenital autosomal recessive 4a
|
|
C537264|601277||ichthyosis lamellar 2
|
|
C537264|601277||ichthyosis lamellar 2 formerly
|
|
C537264|601277||icr2b
|
|
C537264|601277||li2 formerly
|
|
C537264|601277||type 2 lamellar ichthyosis
|
|
C538297||chromosome 11q trisomy
|
|
C538297||duplication 11q
|
|
C538297||trisomy 11q
|
|
C564583||cortical dysplasia of taylor without balloon cells
|
|
C564583||cortical dysplasia of taylor dysplasia only
|
|
C538296||chromosome 11q partial deletion
|
|
C538296||deletion 11q partial
|
|
C538296||monosomy 11q partial
|
|
613480||lymphedema hereditary ic
|
|
613480||lmph1c
|
|
C563258||islet cell adenomatosis
|
|
C538291||chromosome 10 trisomy 10pter p13
|
|
C538291||duplication 10pter p13
|
|
C538291||trisomy 10pter p13
|
|
C538290||chromosome 10 trisomy 10p
|
|
C538290||duplication 10p
|
|
C538290||trisomy 10p
|
|
613485||long qt syndrome 13
|
|
613485||lqt13
|
|
D006359||heat exhaustion
|
|
D006359||collapse heat
|
|
D006359||exhaustion heat
|
|
D006359||heat collapse
|
|
D006359||heat prostration
|
|
D006359||prostration heat
|
|
D006356||heartburn
|
|
D006356||pyroses
|
|
D006356||pyrosis
|
|
C538295||chromosome 11p partial deletion
|
|
C538295||deletion 11p 11p12
|
|
C538295||deletion 11p13
|
|
C538295||monosomy 11 p11 p12
|
|
C538295||partial deletion 11p
|
|
D020642||acatalasia
|
|
D020642||acatalasemia
|
|
D020642||acatalasemia japanese type
|
|
D020642||acatalasemia swiss type
|
|
D020642||catalase deficiencies
|
|
D020642||catalase deficiency
|
|
D020642||deficiencies catalase
|
|
D020642||deficiency catalase
|
|
D020642||disease takahara
|
|
D020642||disease takahara apos s
|
|
D020642||hypocatalasemia
|
|
D020642||hypocatalasia
|
|
D020642||japanese type acatalasemia
|
|
D020642||swiss type acatalasemia
|
|
D020642||takahara disease
|
|
D020642||takahara apos s disease
|
|
D020642||takaharas disease
|
|
D006357||heartwater disease
|
|
D006357||disease heartwater
|
|
C538294||chromosome 11 partial trisomy 11q
|
|
C538294||11q partial trisomy
|
|
C538294||chromosome 11 partial trisomy 11q13 qter
|
|
C538294||chromosome 11 partial trisomy 11q21 qter
|
|
C538294||chromosome 11 partial trisomy 11q23 qter
|
|
C538294||distal trisomy 11q
|
|
613489||congenital disorder of glycosylation type iij
|
|
613489||cdg2j
|
|
613489||cdgiij
|
|
613489||cdg iij
|
|
C538293||chromosome 11 deletion 11p
|
|
C538293||deletion 11p
|
|
C538293||monosomy 11p
|
|
C538292||chromosome 10 uniparental disomy of
|
|
C538292||mosaic trisomy 10
|
|
C538292||uniparental disomy of 10
|
|
D009800|309000||oculocerebrorenal syndrome
|
|
D009800|309000||cerebrooculorenal syndrome
|
|
D009800|309000||cerebro oculo renal syndrome
|
|
D009800|309000||deficiency phosphatidylinositol 4 5 bisphosphate 5 phosphatase
|
|
D009800|309000||dystrophy oculocerebrorenal
|
|
D009800|309000||lowe bickel syndrome
|
|
D009800|309000||lowe disease
|
|
D009800|309000||lowe oculocerebrorenal syndrome
|
|
D009800|309000||lowe syndrome
|
|
D009800|309000||lowe terrey maclachlan syndrome
|
|
D009800|309000||ocrl
|
|
D009800|309000||ocrl1
|
|
D009800|309000||oculocerebrorenal dystrophy
|
|
D009800|309000||oculocerebrorenal syndrome of lowe
|
|
D009800|309000||phosphatidylinositol 4 5 bisphosphate 5 phosphatase deficiency
|
|
D009800|309000||renal oculocerebrodystrophy
|
|
D006362||heavy chain disease
|
|
D006362||franklin disease
|
|
D006362||franklin apos s disease
|
|
D006362||franklins disease
|
|
D006362||gamma chain disease
|
|
D006362||gamma chain diseases
|
|
D006362||heavy chain diseases
|
|
D006362||mu chain disease
|
|
D006362||mu chain diseases
|
|
D007691||medullary sponge kidney
|
|
D007691||cacchi ricci disease
|
|
D007691||cacchi ricci syndrome
|
|
D007691||canalicular ectasia precalyceal
|
|
D007691||canalicular ectasias precalyceal
|
|
D007691||disease cacchi ricci
|
|
D007691||ectasia precalyceal canalicular
|
|
D007691||ectasias precalyceal canalicular
|
|
D007691||kidney sponge
|
|
D007691||kidneys sponge
|
|
D007691||medullary sponge kidneys
|
|
D007691||precalyceal canalicular ectasia
|
|
D007691||precalyceal canalicular ectasias
|
|
D007691||ricci disease cacchi
|
|
D007691||sponge kidney
|
|
D007691||sponge kidney medullary
|
|
D007691||sponge kidneys
|
|
D007691||sponge kidneys medullary
|
|
D007691||syndrome cacchi ricci
|
|
C567725|613172||cardiomyopathy dilated 1dd
|
|
C567725|613172||cmd1dd
|
|
D054039||onycholysis
|
|
D054039||onycholyses
|
|
D054039||photo onycholyses
|
|
D054039||photo onycholysis
|
|
C538235|103050||adenylosuccinate lyase deficiency
|
|
C538235|103050||adenylosuccinase deficiency
|
|
C538235|103050||adenylosuccinate lyase deficiency type 1
|
|
C538235|103050||adenylosuccinate lyase deficiency type 2
|
|
C538235|103050||adenylosuccinate lyase deficiency type 3
|
|
C538235|103050||adenylosuccinate lyase deficiency type 4
|
|
C538235|103050||adsl deficiency
|
|
C538235|103050||succinylpurinemic autism
|
|
D054038||posterior leukoencephalopathy syndrome
|
|
D054038||leukoencephalopathy syndrome posterior
|
|
D054038||leukoencephalopathy syndromes posterior
|
|
D054038||posterior reversible encephalopathy syndrome
|
|
D054038||reversible posterior leukoencephalopathy syndrome
|
|
D054038||syndrome posterior leukoencephalopathy
|
|
D054038||syndromes posterior leukoencephalopathy
|
|
600176||pachygyria with mental retardation seizures and arachnoid cysts
|
|
C563262||corneal dystrophy central type
|
|
C563262||central cloudy dystrophy of francois
|
|
D018333||odontogenic cyst calcifying
|
|
D018333||calcifying odontogenic cyst
|
|
D018333||calcifying odontogenic cysts
|
|
D018333||cyst calcifying odontogenic
|
|
D018333||cysts calcifying odontogenic
|
|
D018333||odontogenic cysts calcifying
|
|
C564591||cholesteryl ester transfer protein deficiency
|
|
C564591||cetp deficiency
|
|
C564591||hyperalphalipoproteinemia
|
|
D018335||rhabdoid tumor
|
|
D018335||rhabdoid tumors
|
|
D018335||tumor rhabdoid
|
|
D018335||tumors rhabdoid
|
|
C535289|129400||rapp hodgkin syndrome
|
|
C535289|129400||cleft lip with or without cleft palate nonsyndromic 8 included
|
|
C535289|129400||ectodermal dysplasia anhidrotic with cleft lip palate
|
|
C535289|129400||ectodermal dysplasia anhidrotic with cleft lip palate orofacial cleft 8 included
|
|
C535289|129400||ofc8 included
|
|
C563221||mydriasis congenital
|
|
D018310||sertoli leydig cell tumor
|
|
D018310||androblastoma
|
|
D018310||androblastomas
|
|
D018310||arrhenoblastoma
|
|
D018310||arrhenoblastomas
|
|
D018310||cell tumor sertoli leydig
|
|
D018310||cell tumors sertoli leydig
|
|
D018310||sertoli leydig cell tumors
|
|
D018310||tumor sertoli leydig cell
|
|
D018310||tumors sertoli leydig cell
|
|
C564557||radioulnar synostosis radial ray abnormalities and severe malformations in the male
|
|
C565881||cardiomyopathy associated with myopathy and sudden death
|
|
C565882||cardiac valvular defect developmental
|
|
613470||hemolytic anemia nonspherocytic due to glucose phosphate isomerase deficiency
|
|
C565883||cardiac septal defects with coarctation of the aorta
|
|
613471||reynolds syndrome
|
|
613471||primary biliary cirrhosis scleroderma raynaud disease and telangiectasia
|
|
C564554|300244||terminal osseous dysplasia and pigmentary defects
|
|
C564554|300244||osseous dysplasia digital with facial pigmentary defects and multiple frenula
|
|
C565884||cardiac lipidosis familial
|
|
D004535|130050||ehlers danlos syndrome
|
|
D004535|130050||cutis elastica
|
|
D004535|130050||danlos disease ehlers
|
|
D004535|130050||disease ehlers danlos
|
|
D004535|130050||eds4
|
|
D004535|130050||eds iv
|
|
D004535|130050||ehlers danlos disease
|
|
D004535|130050||ehlers danlos syndrome arterial type
|
|
D004535|130050||ehlers danlos syndrome ecchymotic type
|
|
D004535|130050||ehlers danlos syndrome sack barabas type
|
|
D004535|130050||ehlers danlos syndrome type 4 autosomal dominant
|
|
D004535|130050||ehlers danlos syndrome type iv
|
|
D004535|130050||ehlers danlos syndrome type iv autosomal dominant
|
|
D004535|130050||ehlers danlos syndrome vascular type
|
|
D004535|130050||syndrome ehlers danlos
|
|
D006327||heart block
|
|
D006327||atrioventricular dissociation
|
|
D006327||atrioventricular dissociations
|
|
D006327||auriculo ventricular dissociation
|
|
D006327||auriculo ventricular dissociations
|
|
D006327||a v dissociation
|
|
D006327||a v dissociations
|
|
D006327||block heart
|
|
D006327||blocks heart
|
|
D006327||dissociation atrioventricular
|
|
D006327||dissociation auriculo ventricular
|
|
D006327||dissociation a v
|
|
D006327||dissociations atrioventricular
|
|
D006327||dissociations auriculo ventricular
|
|
D006327||dissociations a v
|
|
D006327||heart blocks
|
|
D008989||monieziasis
|
|
D008989||monieziases
|
|
D006323||heart arrest
|
|
D006323||arrest cardiac
|
|
D006323||arrest cardiopulmonary
|
|
D006323||arrest heart
|
|
D006323||asystole
|
|
D006323||asystoles
|
|
D006323||cardiac arrest
|
|
D006323||cardiopulmonary arrest
|
|
613477||epileptic encephalopathy early infantile 5
|
|
613477||eiee5
|
|
D006322||heart aneurysm
|
|
D006322||aneurysm cardiac
|
|
D006322||aneurysm heart
|
|
D006322||aneurysms cardiac
|
|
D006322||aneurysms heart
|
|
D006322||cardiac aneurysm
|
|
D006322||cardiac aneurysms
|
|
D006322||heart aneurysms
|
|
D014898|277700||werner syndrome
|
|
D014898|277700||adult premature aging syndrome
|
|
D014898|277700||adult progeria
|
|
D014898|277700||progeria adult
|
|
D014898|277700||syndrome werner
|
|
D014898|277700||syndrome werners
|
|
D014898|277700||syndrome werner apos s
|
|
D014898|277700||werner apos s syndrome
|
|
D014898|277700||werners syndrome
|
|
D014898|277700||wrn
|
|
C536487|601067||usher syndrome type 1d
|
|
C536487|601067||ush1d
|
|
C536487|601067||ush1d f cdh23 pcdh15 digenic included
|
|
C536487|601067|C563400||usher syndrome type id
|
|
C536487|601067||usher syndrome type id f cdh23 pcdh15 digenic included
|
|
D006330||heart defects congenital
|
|
D006330||abnormalities heart
|
|
D006330||abnormality heart
|
|
D006330||congenital heart defect
|
|
D006330||congenital heart defects
|
|
D006330||defect congenital heart
|
|
D006330||defects congenital heart
|
|
D006330||heart abnormalities
|
|
D006330||heart abnormality
|
|
D006330||heart defect congenital
|
|
D006330||heart malformation of
|
|
D008992||monkey diseases
|
|
D008992||disease monkey
|
|
D008992||diseases monkey
|
|
D008992||monkey disease
|
|
D007662||ketosis
|
|
D007662||acetonemia
|
|
D007662||acetonemias
|
|
D007662||acetonuria
|
|
D007662||acetonurias
|
|
D007662||ketoacidemia
|
|
D007662||ketoacidemias
|
|
D007662||ketoacidoses
|
|
D007662||ketoacidoses metabolic
|
|
D007662||ketoacidosis
|
|
D007662||ketoacidosis metabolic
|
|
D007662||ketoaciduria
|
|
D007662||ketoacidurias
|
|
D007662||ketonemia
|
|
D007662||ketonemias
|
|
D007662||ketonuria
|
|
D007662||ketonurias
|
|
D007662||ketoses metabolic
|
|
D007662||ketosis metabolic
|
|
D007662||metabolic ketoacidoses
|
|
D007662||metabolic ketoacidosis
|
|
D007662||metabolic ketoses
|
|
D007662||metabolic ketosis
|
|
D006331||heart diseases
|
|
D006331||cardiac disease
|
|
D006331||cardiac diseases
|
|
D006331||disease cardiac
|
|
D006331||disease heart
|
|
D006331||diseases cardiac
|
|
D006331||diseases heart
|
|
D006331||heart disease
|
|
D018309||neoplasms gonadal tissue
|
|
D018309||gonadal tissue neoplasm
|
|
D018309||gonadal tissue neoplasms
|
|
D018309||neoplasm gonadal tissue
|
|
D018309||tissue neoplasm gonadal
|
|
D018309||tissue neoplasms gonadal
|
|
D055370||lung injury
|
|
D055370||chronic lung injuries
|
|
D055370||chronic lung injury
|
|
D055370||injuries lung
|
|
D055370||injuries pulmonary
|
|
D055370||injury lung
|
|
D055370||injury pulmonary
|
|
D055370||lung injuries
|
|
D055370||lung injuries chronic
|
|
D055370||lung injury chronic
|
|
D055370||pulmonary injuries
|
|
D055370||pulmonary injury
|
|
D018308||papilloma inverted
|
|
D018308||inverted papilloma
|
|
D018308||inverted papillomas
|
|
D018308||papillomas inverted
|
|
D055371||acute lung injury
|
|
D055371||acute lung injuries
|
|
D055371||lung injuries acute
|
|
D055371||lung injury acute
|
|
D019636||neurodegenerative diseases
|
|
D019636||degenerative condition neurologic
|
|
D019636||degenerative conditions neurologic
|
|
D019636||degenerative diseases central nervous system
|
|
D019636||degenerative diseases nervous system
|
|
D019636||degenerative diseases neurologic
|
|
D019636||degenerative diseases spinal cord
|
|
D019636||degenerative neurologic disease
|
|
D019636||degenerative neurologic diseases
|
|
D019636||degenerative neurologic disorder
|
|
D019636||degenerative neurologic disorders
|
|
D019636||nervous system degenerative diseases
|
|
D019636||neurodegenerative disease
|
|
D019636||neurodegenerative disorder
|
|
D019636||neurodegenerative disorders
|
|
D019636||neurologic degenerative condition
|
|
D019636||neurologic degenerative conditions
|
|
D019636||neurologic degenerative disease
|
|
D019636||neurologic degenerative diseases
|
|
D019636||neurologic disease degenerative
|
|
D019636||neurologic diseases degenerative
|
|
D019636||neurologic disorder degenerative
|
|
D019636||neurologic disorders degenerative
|
|
601495||agammaglobulinemia 1 autosomal recessive
|
|
601495||agammaglobulinemia autosomal recessive due to ighm defect
|
|
601495||agm1
|
|
D018305||ganglioneuroblastoma
|
|
D018305||ganglioneuroblastomas
|
|
D018304||esthesioneuroblastoma olfactory
|
|
D018304||aesthesioneuroblastoma
|
|
D018304||aesthesioneuroblastomas
|
|
D018304||esthesioneuroblastoma
|
|
D018304||esthesioneuroblastoma paranasal sinus nasal cavity
|
|
D018304||esthesioneuroblastomas
|
|
D018304||esthesioneuroblastomas olfactory
|
|
D018304||neuroblastoma olfactory
|
|
D018304||neuroblastomas olfactory
|
|
D018304||olfactory esthesioneuroblastoma
|
|
D018304||olfactory esthesioneuroblastomas
|
|
D018304||olfactory neuroblastoma
|
|
D018304||olfactory neuroblastomas
|
|
D018304||paranasal sinus nasal cavity esthesioneuroblastoma
|
|
D018307||neoplasms squamous cell
|
|
D018307||cancer squamous cell
|
|
D018307||cancers squamous cell
|
|
D018307||cell cancer squamous
|
|
D018307||cell cancers squamous
|
|
D018307||cell neoplasm squamous
|
|
D018307||cell neoplasms squamous
|
|
D018307||neoplasm squamous cell
|
|
D018307||squamous cell cancer
|
|
D018307||squamous cell cancers
|
|
D018307||squamous cell neoplasm
|
|
D018307||squamous cell neoplasms
|
|
300613|C564473||myopia 13
|
|
300613|C564473||myopia 13 x linked
|
|
300613|C564473||myp13
|
|
D018306||neurocytoma
|
|
D018306||central neurocytoma
|
|
D018306||central neurocytomas
|
|
D018306||neurocytoma central
|
|
D018306||neurocytomas
|
|
D018306||neurocytomas central
|
|
601499||rieg2
|
|
D018301||neoplasms mesothelial
|
|
D018301||mesothelial neoplasm
|
|
D018301||mesothelial neoplasms
|
|
D018301||neoplasm mesothelial
|
|
D018300||papilloma intraductal
|
|
D018300||intraductal papilloma
|
|
D018300||intraductal papillomas
|
|
D018300||papillomas intraductal
|
|
612376|D015473||leukemia promyelocytic acute
|
|
612376|D015473||acute promyelocytic leukemia
|
|
612376|D015473||acute promyelocytic leukemias
|
|
612376|D015473||aml m3
|
|
612376|D015473||anll m3
|
|
612376|D015473||leukemia acute promyelocytic
|
|
612376|D015473||leukemia myeloid acute m3
|
|
612376|D015473||leukemia progranulocytic
|
|
612376|D015473||m3 anll
|
|
612376|D015473||myeloid leukemia acute m3
|
|
612376|D015473||progranulocytic leukemia
|
|
612376|D015473||promyelocytic leukemia acute
|
|
D018303||ganglioglioma
|
|
D018303||benign ganglioglioma
|
|
D018303||benign gangliogliomas
|
|
D018303||ganglioglioma benign
|
|
D018303||ganglioglioma intracranial
|
|
D018303||ganglioglioma malignant
|
|
D018303||gangliogliomas
|
|
D018303||gangliogliomas benign
|
|
D018303||gangliogliomas intracranial
|
|
D018303||gangliogliomas malignant
|
|
D018303||intracranial ganglioglioma
|
|
D018303||intracranial gangliogliomas
|
|
D018303||malignant ganglioglioma
|
|
D018303||malignant gangliogliomas
|
|
D018302||neoplasms neuroepithelial
|
|
D018302||astroblastoma
|
|
D018302||astroblastomas
|
|
D018302||ependymoastrocytoma
|
|
D018302||ependymoastrocytomas
|
|
D018302||gliomatosis cerebri
|
|
D018302||neoplasm neuroepithelial
|
|
D018302||neuroepithelial neoplasm
|
|
D018302||neuroepithelial neoplasms
|
|
D018302||neuroepithelial tumor
|
|
D018302||neuroepithelial tumors
|
|
D018302||polar spongioblastoma
|
|
D018302||polar spongioblastomas
|
|
D018302||spongioblastoma polar
|
|
D018302||spongioblastomas polar
|
|
D018302||tumor neuroepithelial
|
|
D018302||tumors neuroepithelial
|
|
C563233||myelocerebellar disorder
|
|
C563233||ataxia pancytopenia syndrome
|
|
C565896||bone dysplasia lethal holmgren type
|
|
D018321||neurothekeoma
|
|
D018321||myxoma nerve sheath
|
|
D018321||myxomas nerve sheath
|
|
D018321||nerve sheath myxoma
|
|
D018321||nerve sheath myxomas
|
|
D018321||neurotheceoma
|
|
D018321||neurotheceomas
|
|
D018321||neurothecoma
|
|
D018321||neurothecomas
|
|
D018321||neurothekeomas
|
|
C564561||myotubular myopathy with abnormal genital development
|
|
C564568||adrenal hypoplasia congenital with precocious puberty
|
|
C564568||adrenal insufficiency progressive and hypogonadotropic hypogonadism
|
|
C563237||cystic disease of lung
|
|
C565893||brachymetapody anodontia hypotrichosis albinoidism
|
|
C565893||anodontia hypotrichosis syndrome
|
|
C565893||oculoosteocutaneous syndrome
|
|
C565894||brachydactyly type a2 with microcephaly
|
|
D007669||kidney calculi
|
|
D007669||calculi kidney
|
|
D007669||calculi renal
|
|
D007669||calculus kidney
|
|
D007669||calculus renal
|
|
D007669||kidney calculus
|
|
D007669||kidney stone
|
|
D007669||kidney stones
|
|
D007669||nephrolith
|
|
D007669||renal calculi
|
|
D007669||renal calculus
|
|
D007669||stone kidney
|
|
D007669||stones kidney
|
|
D006338||heart neoplasms
|
|
D006338||cancer cardiac
|
|
D006338||cancer heart
|
|
D006338||cancers cardiac
|
|
D006338||cancers heart
|
|
D006338||carcinoma cardiac
|
|
D006338||carcinomas cardiac
|
|
D006338||cardiac cancer
|
|
D006338||cardiac cancers
|
|
D006338||cardiac carcinoma
|
|
D006338||cardiac carcinomas
|
|
D006338||cardiac neoplasm
|
|
D006338||cardiac neoplasms
|
|
D006338||cardiac tumor
|
|
D006338||cardiac tumors
|
|
D006338||heart cancer
|
|
D006338||heart cancers
|
|
D006338||heart neoplasm
|
|
D006338||heart tumor
|
|
D006338||heart tumors
|
|
D006338||intracavitary tumors of the heart
|
|
D006338||myocardial tumor rhabdomyomas and fibromas
|
|
D006338||myocardial tumors rhabdomyomas and fibromas
|
|
D006338||neoplasm cardiac
|
|
D006338||neoplasm heart
|
|
D006338||neoplasms cardiac
|
|
D006338||neoplasms heart
|
|
D006338||primary cardiac tumors childhood
|
|
D006338||tumor cardiac
|
|
D006338||tumor heart
|
|
D006338||tumor myocardial rhabdomyomas and fibromas
|
|
D006338||tumors cardiac
|
|
D006338||tumors heart
|
|
D006338||tumors myocardial rhabdomyomas and fibromas
|
|
C563239||aneurysm of interventricular septum
|
|
613464||retinitis pigmentosa 51
|
|
613464||rp51
|
|
D008998||monoclonal gammopathy of undetermined significance
|
|
D008998||benign monoclonal gammapathies
|
|
D008998||benign monoclonal gammapathy
|
|
D008998||benign monoclonal gammopathies
|
|
D008998||benign monoclonal gammopathy
|
|
D008998||gammapathies benign monoclonal
|
|
D008998||gammapathy benign monoclonal
|
|
D008998||gammopathies benign monoclonal
|
|
D008998||gammopathy benign monoclonal
|
|
D008998||monoclonal gammapathies benign
|
|
D008998||monoclonal gammapathy benign
|
|
D008998||monoclonal gammapathy of undetermined significance
|
|
D008998||monoclonal gammopathies benign
|
|
D008998||monoclonal gammopathy benign
|
|
D006337||heart murmurs
|
|
D006337||cardiac murmur
|
|
D006337||cardiac murmurs
|
|
D006337||diastolic murmur
|
|
D006337||diastolic murmurs
|
|
D006337||heart murmur
|
|
D006337||innocent murmur
|
|
D006337||innocent murmurs
|
|
D006337||murmur cardiac
|
|
D006337||murmur diastolic
|
|
D006337||murmur heart
|
|
D006337||murmur innocent
|
|
D006337||murmurs cardiac
|
|
D006337||murmurs diastolic
|
|
D006337||murmurs heart
|
|
D006337||murmurs innocent
|
|
C563238|C562782|307700||parathyroid glands agenesis of
|
|
D054060||pulmonary infarction
|
|
D054060||infarction pulmonary
|
|
D054060||infarctions pulmonary
|
|
D054060||pulmonary infarctions
|
|
C566350|603649||cone rod dystrophy 7
|
|
C566350|603649||cord7
|
|
D006335||heart injuries
|
|
D006335||cardiac ruptures traumatic
|
|
D006335||cardiac rupture traumatic
|
|
D006335||heart injury
|
|
D006335||heart ruptures traumatic
|
|
D006335||heart rupture traumatic
|
|
D006335||injuries heart
|
|
D006335||injury heart
|
|
D006335||ruptures traumatic cardiac
|
|
D006335||ruptures traumatic heart
|
|
D006335||rupture traumatic cardiac
|
|
D006335||rupture traumatic heart
|
|
D006335||traumatic cardiac rupture
|
|
D006335||traumatic cardiac ruptures
|
|
D006335||traumatic heart rupture
|
|
D006335||traumatic heart ruptures
|
|
D006332||cardiomegaly
|
|
D006332||cardiac hypertrophy
|
|
D006332||enlarged heart
|
|
D006332||enlargement heart
|
|
D006332||heart enlarged
|
|
D006332||heart enlargement
|
|
D006332||heart hypertrophy
|
|
D006333||heart failure
|
|
D006333||cardiac failure
|
|
D006333||congestive heart failure
|
|
D006333||decompensation heart
|
|
D006333||heart decompensation
|
|
D006333||heart failure congestive
|
|
D006333||heart failure left sided
|
|
D006333||heart failure right sided
|
|
D006333||left sided heart failure
|
|
D006333||myocardial failure
|
|
D006333||right sided heart failure
|
|
D006341||heart rupture
|
|
D006341||cardiac free wall rupture
|
|
D006341||cardiac rupture
|
|
D006341||cardiac ruptures
|
|
D006341||free wall rupture heart
|
|
D006341||heart ruptures
|
|
D006341||ventricular free wall rupture
|
|
D007673||kidney cortex necrosis
|
|
D007673||glomerular necrosis
|
|
D007673||necrosis glomerular
|
|
D007673||necrosis kidney cortex
|
|
D007673||necrosis renal cortical
|
|
D007673||necrosis renal tubule
|
|
D007673||renal cortical necrosis
|
|
D007673||renal tubule necrosis
|
|
D006342||heart rupture post infarction
|
|
D006342||cardiac rupture post infarction
|
|
D006342||cardiac ruptures post infarction
|
|
D006342||heart ruptures post infarction
|
|
D006342||post infarction cardiac rupture
|
|
D006342||post infarction cardiac ruptures
|
|
D006342||post infarction heart rupture
|
|
D006342||post infarction heart ruptures
|
|
D006342||rupture post infarction cardiac
|
|
D006342||rupture post infarction heart
|
|
D006342||ruptures post infarction cardiac
|
|
D006342||ruptures post infarction heart
|
|
D018319||neurofibrosarcoma
|
|
D018319||neurofibrosarcomas
|
|
D018319||neurogenic sarcoma
|
|
D018319||neurogenic sarcomas
|
|
D018319||sarcoma neurogenic
|
|
D018319||sarcomas neurogenic
|
|
D018316||gliosarcoma
|
|
D018316||glioblastoma with sarcomatous component
|
|
D018316||glioma sarcomatous
|
|
D018316||gliomas sarcomatous
|
|
D018316||gliosarcomas
|
|
D018316||sarcomatous glioma
|
|
D018316||sarcomatous gliomas
|
|
214450|C537301||griscelli syndrome type 1
|
|
214450|C537301||griscelli syndrome cutaneous and neurologic type
|
|
214450|C537301||griscelli syndrome with neurologic impairment
|
|
214450|C537301||gs1
|
|
214450|C537301||partial albinism and primary neurologic disease without hemophagocytic syndrome
|
|
D018315||glioma subependymal
|
|
D018315||adult subependymal astrocytoma
|
|
D018315||adult subependymal astrocytomas
|
|
D018315||astrocytoma adult subependymal
|
|
D018315||astrocytomas adult subependymal
|
|
D018315||astrocytomas subependymal
|
|
D018315||astrocytoma subependymal
|
|
D018315||gliomas subependymal
|
|
D018315||glioses subependymal
|
|
D018315||gliosis subependymal
|
|
D018315||subependymal astrocytoma
|
|
D018315||subependymal astrocytoma adult
|
|
D018315||subependymal astrocytomas
|
|
D018315||subependymal astrocytomas adult
|
|
D018315||subependymal glioma
|
|
D018315||subependymal gliomas
|
|
D018315||subependymal glioses
|
|
D018315||subependymal gliosis
|
|
D018315||subependymoma
|
|
D018315||subependymomas
|
|
D054059||coronary occlusion
|
|
D054059||coronary occlusions
|
|
D054059||occlusion coronary
|
|
D054059||occlusions coronary
|
|
D018318||neurofibroma plexiform
|
|
D018318||elephantiasis neuromatoses
|
|
D018318||elephantiasis neuromatosis
|
|
D018318||neurofibromas plexiform
|
|
D018318||neuroma plexiform
|
|
D018318||neuromas plexiform
|
|
D018318||pachydermatocele
|
|
D018318||pachydermatoceles
|
|
D018318||plexiform neurofibroma
|
|
D018318||plexiform neurofibromas
|
|
D018318||plexiform neuroma
|
|
D018318||plexiform neuromas
|
|
D018318||tumor royale
|
|
D054058||acute coronary syndrome
|
|
D054058||acute coronary syndromes
|
|
D054058||coronary syndrome acute
|
|
D054058||coronary syndromes acute
|
|
D054058||syndrome acute coronary
|
|
D054058||syndromes acute coronary
|
|
D018317||nerve sheath neoplasms
|
|
D018317||neoplasm nerve sheath
|
|
D018317||neoplasms nerve sheath
|
|
D018317||nerve sheath neoplasm
|
|
D018317||nerve sheath tumors
|
|
D018317||nerve sheath tumors peripheral
|
|
D018317||perineurioma
|
|
D018317||perineuriomas
|
|
D018317||peripheral nerve sheath tumors
|
|
D018317||tumors of the nerve sheath
|
|
D018312||sex cord gonadal stromal tumors
|
|
D018312||gynandroblastoma
|
|
D018312||gynandroblastomas
|
|
D018312||sex cord stromal tumor
|
|
D018312||sex cord stromal tumors
|
|
D018312||tumor sex cord stromal
|
|
D018312||tumors sex cord stromal
|
|
C564571||noncompaction of left ventricular myocardium familial isolated x linked
|
|
C564571||left ventricular noncompaction isolated x linked
|
|
D018311||luteoma
|
|
D018311||gestational luteoma
|
|
D018311||gestational luteomas
|
|
D018311||luteinoma
|
|
D018311||luteoma gestational
|
|
D018311||luteoma of pregnancy
|
|
D018311||luteoma pregnancy
|
|
D018311||luteomas
|
|
D018311||luteomas gestational
|
|
D018311||luteomas pregnancy
|
|
D018311||pregnancy luteoma
|
|
D018311||pregnancy luteomas
|
|
C566489|609995||myopia 12
|
|
C566489|609995||myopia 12 autosomal dominant
|
|
C566489|609995||myp12
|
|
C536942|311900||tarp syndrome
|
|
C536942|311900||pierre robin syndrome with congenital heart malformation and clubfoot
|
|
C536942|311900||talipes equinovarus atrial septal defect robin sequence and persistence of left superior vena cava
|
|
C536942|311900||tarps
|
|
C565863||cerebrocortical degeneration of infancy
|
|
C565864||cerebral angiopathy dysphoric
|
|
C565866||cerebelloparenchymal disorder ii
|
|
C565866||cpd late onset recessive type
|
|
C538241||amelogenesis imperfecta nephrocalcinosis
|
|
C538241||absent enamel nephrocalcinosis and apparently normal calcium metabolism
|
|
C538241||amelogenesis imperfecta hypoplastic and nephrocalcinosis
|
|
C538241||amelogenesis imperfecta type ig
|
|
C538241||enamel renal syndrome
|
|
C538241||generalized enamel hypoplasia and renal dysfunction
|
|
C564535||lesch nyhan syndrome neurologic variant
|
|
C564535||hprt deficiency neurologic variant
|
|
C538248||amyloid angiopathy
|
|
C538248||amyloidosis cerebral
|
|
C538248||senile cerebral amyloid angiopathy
|
|
C563203||anodontia of permanent dentition
|
|
C563203||teeth permanent absence of
|
|
D007638||keratoconjunctivitis sicca
|
|
D007638||sicca keratoconjunctivitis
|
|
C565861||cerebrohepatorenal syndrome variant types
|
|
C565861||zellweger syndrome variant types
|
|
C564532||thrombocytosis familial x linked
|
|
D007639||keratoconjunctivitis infectious
|
|
D007639||infectious keratoconjunctivitides
|
|
D007639||infectious keratoconjunctivitis
|
|
D007639||keratoconjunctivitides infectious
|
|
C565862||cerebrofaciothoracic dysplasia
|
|
C538245||ameloonychohypohidrotic syndrome
|
|
C538245||hypocalcified hypoplastic enamel onycholysis with subungual hyperkeratosis and hypohidrosis
|
|
D007636||keratoacanthoma
|
|
D007636||keratoacanthomas
|
|
D007637||keratoconjunctivitis
|
|
D007637||keratoconjunctivitides
|
|
D007634||keratitis
|
|
D007634||keratitides
|
|
D007635||keratitis dendritic
|
|
D007635||dendritic keratitides
|
|
D007635||dendritic keratitis
|
|
D007635||furrow keratitides
|
|
D007635||furrow keratitis
|
|
D007635||keratitides dendritic
|
|
D007635||keratitides furrow
|
|
D007635||keratitis furrow
|
|
C566440|607932||microphthalmia syndromic 6
|
|
C566440|607932||anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia
|
|
C566440|607932||mcops6
|
|
C566440|607932||microphthalmia and pituitary anomalies
|
|
C566440|607932||microphthalmia with brain and digit developmental anomalies
|
|
C565867||cerebellar vermis aplasia with associated features suggesting smith lemli opitz syndrome and meckel syndrome
|
|
D054070||postthrombotic syndrome
|
|
D054070||syndrome postthrombotic
|
|
D054070||syndrome venous stasis
|
|
D054070||venous stasis syndrome
|
|
C565868||cerebellar ataxia benign with thermoanalgesia
|
|
C565868||cerebellar ataxia with loss of pain and temperature sensation
|
|
C565869||cerebellar ataxia and neurosensory deafness
|
|
D007640||keratoconus
|
|
D055397||ventilator induced lung injury
|
|
D055397||lung injuries ventilator induced
|
|
D055397||lung injury ventilator induced
|
|
D055397||ventilator induced lung injuries
|
|
D054062||deaf blind disorders
|
|
D054062||blind deaf disorder
|
|
D054062||blind deaf disorders
|
|
D054062||blindness deafness
|
|
D054062||deaf blind disorder
|
|
D054062||deaf blind disorder prelingual
|
|
D054062||deaf blind disorders prelingual
|
|
D054062||deaf blindness disorder
|
|
D054062||deaf blindness disorders
|
|
D054062||deaf blind syndrome
|
|
D054062||deaf blind syndromes
|
|
D054062||deaf mutism blind disorder
|
|
D054062||deaf mutism blind disorders
|
|
D054062||deafness blindness
|
|
D054062||deafness blindnesses prelingual
|
|
D054062||deafness blindness prelingual
|
|
D054062||disorder blind deaf
|
|
D054062||disorder deaf blind
|
|
D054062||disorder deaf blindness
|
|
D054062||disorder deaf mutism blind
|
|
D054062||disorder prelingual deaf blind
|
|
D054062||disorders blind deaf
|
|
D054062||disorders deaf blind
|
|
D054062||disorders deaf blindness
|
|
D054062||disorders deaf mutism blind
|
|
D054062||disorders prelingual deaf blind
|
|
D054062||hearing and vision loss
|
|
D054062||prelingual deaf blind disorder
|
|
D054062||prelingual deaf blind disorders
|
|
D054062||prelingual deafness blindness
|
|
D054062||prelingual deafness blindnesses
|
|
D054062||syndrome deaf blind
|
|
D054062||syndromes deaf blind
|
|
D054062||vision and hearing loss
|
|
C537456|300486||mental retardation x linked with cerebellar hypoplasia and distinctive facial appearance
|
|
C537456|300486||mental retardation x linked 60 formerly
|
|
C537456|300486||mrx60 formerly
|
|
D054061||ischemic contracture
|
|
D054061||contracture ischemic
|
|
D054061||contractures ischemic
|
|
D054061||contractures volkmann
|
|
D054061||contracture volkmann
|
|
D054061||contracture volkmann apos s ischemic
|
|
D054061||ischemic contractures
|
|
D054061||ischemic contracture volkmann apos s
|
|
D054061||volkmann contracture
|
|
D054061||volkmann contractures
|
|
D054061||volkmann ischemic contracture
|
|
D054061||volkmann apos s ischemic contracture
|
|
D054061||volkmanns ischemic contracture
|
|
D054068||livedo reticularis
|
|
D054066||leukemia large granular lymphocytic
|
|
D054066||large granular lymphocyte leukemia
|
|
D054066||leukemia lgl
|
|
D054066||leukemia lymphocytic large granular
|
|
D054066||leukemia natural killer cell large granular lymphocytic
|
|
D054066||leukemia nk lgl
|
|
D054066||leukemias lgl
|
|
D054066||leukemias nk lgl
|
|
D054066||leukemias t lgl
|
|
D054066||leukemia t cell large granular lymphocytic
|
|
D054066||leukemia t lgl
|
|
D054066||lgl leukemia
|
|
D054066||lgl leukemias
|
|
D054066||lymphoproliferative disease of granular lymphocytes
|
|
D054066||lymphoproliferative disease of large granular lymphocytes
|
|
D054066||natural killer cell large granular lymphocytic leukemia
|
|
D054066||nk cell large granular lymphocytic leukemia
|
|
D054066||nk lgl leukemia
|
|
D054066||nk lgl leukemias
|
|
D054066||t cell large granular lymphocyte leukemia
|
|
D054066||t cell large granular lymphocytic leukemia
|
|
D054066||t lgl leukemia
|
|
D054066||t lgl leukemias
|
|
C566923|611544||cataract congenital nuclear autosomal recessive 3
|
|
C566923|611544||cataract 17 multiple types
|
|
C566923|611544||catcn3
|
|
C566923|611544||ctrct17
|
|
C538238||adrenal incidentaloma
|
|
304050|D058540||aicardi syndrome
|
|
304050|D058540||agenesis of corpus callosum with chorioretinal abnormality
|
|
304050|D058540||agenesis of corpus callosum with infantile spasms and ocular abnormalities
|
|
304050|D058540||aic
|
|
304050|D058540||aicardi apos s syndrome
|
|
304050|D058540||callosal agenesis and ocular abnormalities
|
|
304050|D058540||chorioretinal anomalies with acc
|
|
304050|D058540||corpus callosum agenesis of with chorioretinal abnormality
|
|
304050|D058540||syndrome aicardi
|
|
304050|D058540||syndrome aicardi apos s
|
|
C563783|609161||striatal degeneration autosomal dominant
|
|
C563783|609161||adsd
|
|
C564542||hyper igm immunodeficiency x linked with ectodermal dysplasia hypohidrotic
|
|
C564542||xhm ed
|
|
C538255||anaplastic small cell lymphoma
|
|
C538255||small cell variant of anaplastic large cell lymphoma
|
|
C538253||amyotrophy monomelic
|
|
C538253||hirayama disease
|
|
C538253||monomelic amyotrophy
|
|
C538253||spinal muscular atrophy juvenile nonprogressive
|
|
C563324|601399||platelet disorder familial with associated myeloid malignancy
|
|
C563324|601399||fpdaml
|
|
C563324|601399||fpd aml
|
|
C563324|601399||fpdmm
|
|
C563324|601399||platelet disorder aspirin like
|
|
C563324|601399||thrombocytopenia familial with propensity to acute myelogenous leukemia
|
|
C563215||genochondromatosis
|
|
C565870||cerebellar ataxia and hypogonadotropic hypogonadism
|
|
C565870||gordon holmes syndrome
|
|
C565870||lhrh deficiency and ataxia
|
|
C565870||luteinizing hormone releasing hormone deficiency of with ataxia
|
|
C564545||androgen insensitivity syndrome due to coactivator deficiency
|
|
C564544||uruguay faciocardiomusculoskeletal syndrome
|
|
C564544||faciocardiomusculoskeletal syndrome uruguay type
|
|
C563213||myositis eosinophilic
|
|
C565872||cephalin lipidosis
|
|
D006319||hearing loss sensorineural
|
|
D006319||cochlear hearing loss
|
|
D006319||hearing loss cochlear
|
|
D006319||sensorineural hearing loss
|
|
D007647||kernicterus
|
|
D007647||bilirubin encephalopathies
|
|
D007647||bilirubin encephalopathy
|
|
D007647||encephalopathies bilirubin
|
|
D007647||encephalopathies hyperbilirubinemic
|
|
D007647||encephalopathy bilirubin
|
|
D007647||encephalopathy hyperbilirubinemic
|
|
D007647||hyperbilirubinemic encephalopathies
|
|
D007647||hyperbilirubinemic encephalopathy
|
|
C563219||fascial dystrophy congenital
|
|
D006316||hearing loss high frequency
|
|
D006316||high frequency hearing loss
|
|
C564970|255160||myopathy hyaline body autosomal recessive
|
|
C563218||brachyolmia type 2
|
|
C563218||brachyolmia maroteaux type
|
|
D006317||hearing loss noise induced
|
|
D006317||acoustic trauma
|
|
D006317||noise induced hearing loss
|
|
D006314||hearing loss conductive
|
|
D006314||conductive hearing loss
|
|
D008976||molluscum contagiosum
|
|
D006315||hearing loss functional
|
|
D006315||functional hearing loss
|
|
D006315||hearing loss nonorganic
|
|
D006315||hearing loss psychogenic
|
|
D006315||nonorganic hearing loss
|
|
D006315||psychogenic hearing loss
|
|
D006312||hearing loss bilateral
|
|
D006312||bilateral hearing loss
|
|
D006312||bilateral hearing losses
|
|
D006312||hearing losses bilateral
|
|
D006312||loss bilateral hearing
|
|
D006312||losses bilateral hearing
|
|
C538251||amyotrophic lateral sclerosis type 6
|
|
C538251||amyotrophic lateral sclerosis 6
|
|
D054081||neuronal migration disorders
|
|
D054081||disorder neuronal migration
|
|
D054081||disorders neuronal migration
|
|
D054081||migration disorder neuronal
|
|
D054081||migration disorders neuronal
|
|
D054081||neuronal migration disorder
|
|
C566958|611378||macular degeneration age related 9
|
|
C566958|611378||armd9
|
|
D006313||hearing loss central
|
|
D006313||central hearing loss
|
|
D006313||cortical deafness
|
|
D006313||deafness cortical
|
|
C538250||amyopathic dermatomyositis
|
|
C538250||idiopathic inflammatory myopathy familial
|
|
C538250||idiopathic myopathy
|
|
C538250||juvenile dermatomyositis
|
|
C538250||juvenile myositis
|
|
C538250||myopathy familial idiopathic inflammatory
|
|
D054080||vein of galen malformations
|
|
D054080||galen malformations veins
|
|
D054080||malformations vein galen
|
|
D054080||malformations veins galen
|
|
C563744|609299||prostate cancer hereditary 5
|
|
C563744|609299||hpc5
|
|
D007642||keratosis
|
|
D007642||blennorrhagica keratosis
|
|
D007642||blennorrhagicas keratosis
|
|
D007642||blennorrhagicum keratoderma
|
|
D007642||blennorrhagicums keratoderma
|
|
D007642||keratoderma blennorrhagicum
|
|
D007642||keratoderma blennorrhagicums
|
|
D007642||keratoma
|
|
D007642||keratomas
|
|
D007642||keratoses
|
|
D007642||keratosis blennorrhagica
|
|
D007642||keratosis blennorrhagicas
|
|
D006311||hearing disorders
|
|
D006311||distorted hearing
|
|
D006311||dysacusis
|
|
D006311||hearing disorder
|
|
D006311||hearing distorted
|
|
D006311||paracousis
|
|
D006311||paracusis
|
|
D004715|131200||endometriosis
|
|
D004715|131200||endo1
|
|
D004715|131200||endometrioma
|
|
D004715|131200||endometriomas
|
|
D004715|131200||endometrioses
|
|
D004715|131200||endometriosis susceptibility to 1
|
|
148370|C536155||keratolytic winter erythema
|
|
148370|C536155||erythrokeratolysis hiemalis ichthyosis
|
|
148370|C536155||kwe
|
|
148370|C536155||oudtshoorn skin
|
|
D054079||vascular malformations
|
|
D054079||malformations vascular
|
|
D054079||malformation vascular
|
|
D054079||vascular malformation
|
|
605021||myoclonic epilepsy familial infantile
|
|
605021||eim
|
|
605021||fime
|
|
607688||parkinson disease 11 autosomal dominant
|
|
607687||high density lipoprotein cholesterol level quantitative trait locus 3
|
|
607687||hdlcq3
|
|
C565841||long qt syndrome 2 3
|
|
C565842||brittle bone disorder
|
|
C538265||attenuated familial adenomatous polyposis
|
|
C538265||familial adenomatous polyposis attenuated
|
|
C565843||cleidocranial dysplasia recessive form
|
|
C565844||cleft palate deafness and oligodontia
|
|
D016715|176920||proteus syndrome
|
|
D016715|176920||elephant man disease
|
|
D016715|176920||gigantism partial of hands and feet nevi hemihypertrophy and macrocephaly elattoproteus syndrome included
|
|
D016715|176920||proteus like syndrome
|
|
D016715|176920||syndrome proteus like
|
|
D008949||adenoma pleomorphic
|
|
D008949||adenomas pleomorphic
|
|
D008949||chondroid syringoma
|
|
D008949||chondroid syringomas
|
|
D008949||mixed salivary gland tumor
|
|
D008949||pleomorphic adenoma
|
|
D008949||pleomorphic adenomas
|
|
D008949||salivary gland tumor mixed
|
|
D008949||syringoma chondroid
|
|
D008949||syringomas chondroid
|
|
C538269||aughton syndrome
|
|
C538269||dextrocardia microphthalmia cleft palate and mental retardation
|
|
C538269||dextrocardia with unusual facies and microphthalmia
|
|
C538268||auditory neuropathy
|
|
C538268||auditory dys synchrony
|
|
C538268||familial auditory neuropathy
|
|
C538268||progressive auditory neuropathy
|
|
D021922||discrete subaortic stenosis
|
|
D021922||discrete subaortic stenoses
|
|
D021922||stenoses discrete subaortic
|
|
D021922||stenosis discrete subaortic
|
|
D021922||subaortic stenoses discrete
|
|
D021922||subaortic stenosis discrete
|
|
D008947||mixed connective tissue disease
|
|
D008947||connective tissue disease mixed
|
|
D008947||mctd
|
|
D008947||sharp syndrome
|
|
D008947||syndrome sharp
|
|
D007617||kaposi varicelliform eruption
|
|
D007617||eczema herpeticum
|
|
D007617||eczema vaccinatum
|
|
D007617||eruption kaposi apos s varicelliform
|
|
D007617||eruption kaposi varicelliform
|
|
D007617||kaposi apos s varicelliform eruption
|
|
D007617||kaposis varicelliform eruption
|
|
D007617||varicelliform eruption kaposi
|
|
D007617||varicelliform eruption kaposi apos s
|
|
604290|C536004||familial apoceruloplasmin deficiency
|
|
604290|C536004||aceruloplasminemia
|
|
604290|C536004||ceruloplasmin deficiency
|
|
604290|C536004||ceruloplasmin deficiency included
|
|
604290|C536004||hemosiderosis systemic due to aceruloplasminemia included
|
|
604290|C536004||hereditary hypoceruloplasminemia
|
|
604290|C536004||hypoceruloplasminemia
|
|
604290|C536004||hypoceruloplasminemia included
|
|
D008946||mitral valve stenosis
|
|
D008946||mitral stenoses
|
|
D008946||mitral stenosis
|
|
D008946||mitral valve stenoses
|
|
D008946||stenoses mitral
|
|
D008946||stenoses mitral valve
|
|
D008946||stenosis mitral
|
|
D008946||stenosis mitral valve
|
|
D008946||valve stenoses mitral
|
|
D008946||valve stenosis mitral
|
|
D008945||mitral valve prolapse
|
|
D008945||click murmur syndrome
|
|
D008945||click murmur syndrome mitral
|
|
D008945||click murmur syndromes
|
|
D008945||click murmur syndrome systolic
|
|
D008945|157700||floppy mitral valve
|
|
D008945||floppy mitral valves
|
|
D008945||mitral click murmur syndrome
|
|
D008945||mitral valve floppy
|
|
D008945||mitral valve prolapsed
|
|
D008945||mitral valve prolapses
|
|
D008945||mitral valves floppy
|
|
D008945||mitral valves prolapsed
|
|
D008945|157700||prolapsed mitral valve
|
|
D008945||prolapsed mitral valves
|
|
D008945||prolapse mitral valve
|
|
D008945||prolapses mitral valve
|
|
D008945||syndrome click murmur
|
|
D008945||syndrome mitral click murmur
|
|
D008945||syndromes click murmur
|
|
D008945||syndrome systolic click murmur
|
|
D008945||systolic click murmur syndrome
|
|
D008945||valve prolapsed mitral
|
|
D008945||valve prolapse mitral
|
|
D008945||valve prolapses mitral
|
|
D008945||valves prolapsed mitral
|
|
D008944||mitral valve insufficiency
|
|
D008944||incompetence mitral
|
|
D008944||incompetence mitral valve
|
|
D008944||insufficiency mitral
|
|
D008944||insufficiency mitral valve
|
|
D008944||mitral incompetence
|
|
D008944||mitral insufficiency
|
|
D008944||mitral regurgitation
|
|
D008944||mitral valve incompetence
|
|
D008944||mitral valve regurgitation
|
|
D008944||regurgitation mitral
|
|
D008944||regurgitation mitral valve
|
|
D008944||valve incompetence mitral
|
|
D008944||valve insufficiency mitral
|
|
D008944||valve regurgitation mitral
|
|
D054092||foramen ovale patent
|
|
D054092||oval foramen patent
|
|
D054092||patent foramen ovale
|
|
D054092||patent oval foramen
|
|
D054091||periventricular nodular heterotopia
|
|
D054091||bilateral periventricular nodular heterotopia
|
|
D054091||familial nodular heterotopia
|
|
D054091||familial nodular heterotopias
|
|
D054091||heterotopia periventricular nodular
|
|
D054091||heterotopias familial nodular
|
|
D054091||heterotopias periventricular
|
|
D054091||heterotopias periventricular nodular
|
|
D054091||heterotopias x linked periventricular
|
|
D054091||heterotopia x linked periventricular
|
|
D054091||nodular heterotopia familial
|
|
D054091||nodular heterotopia periventricular
|
|
D054091||nodular heterotopias familial
|
|
D054091||nodular heterotopias periventricular
|
|
D054091||periventricular heterotopia
|
|
D054091||periventricular heterotopias
|
|
D054091||periventricular heterotopias x linked
|
|
D054091||periventricular heterotopia x linked
|
|
D054091||periventricular nodular heterotopias
|
|
D054091||x linked periventricular heterotopia
|
|
D054091||x linked periventricular heterotopias
|
|
C564519||brain anomalies retardation ectodermal dysplasia skeletal malformations hirschsprung disease ear eye anomalies cleft palate cryptorchidism and kidney dysplasia hypoplasia
|
|
C564519||bresek syndrome
|
|
C564519||bresheck syndrome
|
|
C565847||circumvallate placenta syndrome
|
|
C538260||atresia of small intestine
|
|
C538260||congenital atresia of the small intestine
|
|
C538260||small intestine atresia
|
|
C565848||chromosomal instability with tissue specific radiosensitivity
|
|
D054084||myocardial bridging
|
|
D054084||bridging myocardial
|
|
D054084||bridgings myocardial
|
|
D054084||myocardial bridgings
|
|
D054083||ectopia cordis
|
|
D054083||cordis ectopia
|
|
D063806||myalgia
|
|
D063806||muscle pain
|
|
D063806||muscle soreness
|
|
D063806||muscle sorenesses
|
|
D063806||muscle tenderness
|
|
D063806||pain muscle
|
|
D063806||pains muscle
|
|
D063806||soreness muscle
|
|
D063806||tenderness muscle
|
|
C564278|608180||synpolydactyly 2
|
|
C564278|608180||spd2
|
|
C564278|608180||synpolydactyly 3 3 prime 4 associated with metacarpal and metatarsal synostoses
|
|
D006009|232300||glycogen storage disease type ii
|
|
D006009|232300||acid alpha glucosidase deficiencies
|
|
D006009|232300||acid alpha glucosidase deficiency
|
|
D006009|232300||acid maltase deficiencies
|
|
D006009|232300||acid maltase deficiency
|
|
D006009|232300||acid maltase deficiency disease
|
|
D006009|232300||adult glycogen storage disease type ii
|
|
D006009|232300||alpha 1 4 glucosidase deficiencies
|
|
D006009|232300||alpha 1 4 glucosidase deficiency
|
|
D006009|232300||alpha glucosidase deficiencies
|
|
D006009|232300||alpha glucosidase deficiencies acid
|
|
D006009|232300||alpha glucosidase deficiency
|
|
D006009|232300||alpha glucosidase deficiency acid
|
|
D006009|232300||amd
|
|
D006009|232300||deficiencies acid alpha glucosidase
|
|
D006009|232300||deficiencies acid maltase
|
|
D006009|232300||deficiencies alpha 1 4 glucosidase
|
|
D006009|232300||deficiencies gaa
|
|
D006009|232300||deficiency acid alpha glucosidase
|
|
D006009|232300||deficiency acid maltase
|
|
D006009|232300||deficiency alpha 1 4 glucosidase
|
|
D006009|232300||deficiency disease acid maltase
|
|
D006009|232300||deficiency disease lysosomal alpha 1 4 glucosidase
|
|
D006009|232300||deficiency gaa
|
|
D006009|232300||deficiency of alpha glucosidase
|
|
D006009|232300||disease pompe
|
|
D006009|232300||disease pompe apos s
|
|
D006009|232300||gaa deficiencies
|
|
D006009|232300||gaa deficiency
|
|
D006009|232300||generalized glycogenoses
|
|
D006009|232300||generalized glycogenosis
|
|
D006009|232300||glycogenoses generalized
|
|
D006009|232300||glycogenosis 2
|
|
D006009|232300||glycogenosis generalized
|
|
D006009|232300||glycogenosis type ii
|
|
D006009|232300||glycogen storage disease ii
|
|
D006009|232300||glycogen storage disease type 2
|
|
D006009|232300||glycogen storage disease type ii adult
|
|
D006009|232300||glycogen storage disease type ii infantile
|
|
D006009|232300||glycogen storage disease type ii juvenile
|
|
D006009|232300||gsd2
|
|
D006009|232300||gsd2s
|
|
D006009|232300||gsd ii
|
|
D006009|232300||gsd ii acid alpha glucosidase deficiency
|
|
D006009|232300||infantile glycogen storage disease type ii
|
|
D006009|232300||juvenile glycogen storage disease type ii
|
|
D006009|232300||lysosomal alpha 1 4 glucosidase deficiency disease
|
|
D006009|232300||maltase deficiencies acid
|
|
D006009|232300||pompe disease
|
|
D006009|232300||pompe apos s disease
|
|
D006009|232300||pompes disease
|
|
D006009|232300||type ii glycogenosis
|
|
D006009|232300||type iis glycogenosis
|
|
D063807||dandruff
|
|
D063807||scurf
|
|
606346||deafness autosomal dominant 22 dfna22 deafness autosomal dominant 22 with hypertrophic cardiomyopathy
|
|
C565726|609734||proopiomelanocortin deficiency
|
|
C565726|609734||obesity early onset adrenal insufficiency and red hair
|
|
C565852||chondroitin 6 sulfaturia defective cellular immunity nephrotic syndrome
|
|
C538277||prata lib 233 ral gon 231 alves syndrome
|
|
C538277||brachydactyly scoliosis spina bifida occulta and carpal synostosis
|
|
C538277||prata liberal goncalves syndrome
|
|
C565853||chondrodysplasia punctata syndrome
|
|
C538276||prader willi habitus osteopenia and camptodactyly
|
|
C538276||urban rogers meyer syndrome
|
|
C565855||chondrodysplasia calcificans metaphysealis
|
|
C538274||autoimmune oophoritis
|
|
D007627||keloid
|
|
D007627||keloids
|
|
C565850||chorioretinal dystrophy spinocerebellar ataxia and hypogonadotropic hypogonadism
|
|
C565850||boucher neuhauser syndrome
|
|
C538279||catamenial pneumothorax
|
|
C565851||chorea benign familial
|
|
C564526||macrothrombocytopenia x linked
|
|
C564525||dyserythropoietic anemia with thrombocytopenia
|
|
C564525||dyserythropoietic anemia and thrombocytopenia
|
|
C564525||gata1 related cytopenia
|
|
C564525||gata1 related x linked cytopenia
|
|
C564525||x linked macrothrombocytopenia
|
|
C565856||cholestasis with gallstone ataxia and visual disturbance
|
|
C538273||autoimmune enteropathy
|
|
C538272||ausems wittebol post hennekam syndrome
|
|
C538272||cleft lip with progressive retinopathy
|
|
C538271||auriculoosteodysplasia
|
|
C538271||auriculo osteodysplasia
|
|
C538271||multiple osseous dysplasia characteristic ear shape and short stature
|
|
C562441|243150||intestinal atresia multiple
|
|
C562441|243150||familial intestinal polyatresia syndrome
|
|
C562441|243150||fipa
|
|
C562441|243150||minat
|
|
D054098||thrombocytopenia neonatal alloimmune
|
|
D054098||alloimmune thrombocytopenia neonatal
|
|
D054098||alloimmune thrombocytopenias neonatal
|
|
D054098||neonatal alloimmune thrombocytopenia
|
|
D054098||neonatal alloimmune thrombocytopenias
|
|
D054098||neonatal thrombocytopenia
|
|
D054098||neonatal thrombocytopenias
|
|
D054098||thrombocytopenia neonatal
|
|
D054098||thrombocytopenias neonatal
|
|
D054098||thrombocytopenias neonatal alloimmune
|
|
D005198|134600||fanconi syndrome
|
|
D005198|134600||adult fanconi syndrome
|
|
D005198|134600||bickel syndrome fanconi
|
|
D005198|134600||de toni debre fanconi syndrome
|
|
D005198|134600||diabete pseudo phlorizin
|
|
D005198|134600||diabetes pseudo phlorizin
|
|
D005198|134600||fanconi bickel syndrome
|
|
D005198|134600||fanconi bickel syndromes
|
|
D005198|134600||fanconi renotubular syndrome
|
|
D005198|134600||fanconi renotubular syndrome 1
|
|
D005198|134600||fanconi renotubular syndrome 2
|
|
D005198|134600||fanconi syndrome adult
|
|
D005198|134600||fanconi syndrome renal
|
|
D005198|134600||fanconi syndrome with intestinal malabsorption and galactose intolerance
|
|
D005198|134600||fanconi syndrome without cystinosis
|
|
D005198|134600||fanconi type glycogenosis
|
|
D005198|134600||fbs
|
|
D005198|134600||frts
|
|
D005198|134600||frts1
|
|
D005198|134600||frts2
|
|
D005198|134600||glycogenosis fanconi type
|
|
D005198|134600||hepatic glycogenosis with amino aciduria and glucosuria
|
|
D005198|134600||hepatic glycogenosis with fanconi nephropathy
|
|
D005198|134600||hepatorenal glycogenosis with renal fanconi syndrome
|
|
D005198|134600||idiopathic de toni debre fanconi syndrome
|
|
D005198|134600||lignac fanconi syndrome
|
|
D005198|134600||luder sheldon syndrome
|
|
D005198|134600||neonatal de toni debre fanconi syndrome
|
|
D005198|134600||primary toni debre fanconi syndrome
|
|
D005198|134600||proximal renal tubular dysfunction
|
|
D005198|134600||pseudo phlorizin diabete
|
|
D005198|134600||pseudo phlorizin diabetes
|
|
D005198|134600||renal fanconi syndrome
|
|
D005198|134600||renotubular syndrome fanconi
|
|
D005198|134600||rfs
|
|
D005198|134600||syndrome adult fanconi
|
|
D005198|134600||syndrome fanconi
|
|
D005198|134600||syndrome fanconi bickel
|
|
D005198|134600||syndrome fanconi renotubular
|
|
D005198|134600||syndrome lignac fanconi
|
|
D005198|134600||syndrome luder sheldon
|
|
D005198|134600||syndrome renal fanconi
|
|
D005198|134600||syndromes fanconi bickel
|
|
D005198|134600||toni debre fanconi syndrome
|
|
C538616|168300||paramyotonia congenita of von eulenburg
|
|
C538616|168300||paralysis periodica paramyotonia
|
|
C538616|168300||paralysis periodica paramyotonica
|
|
C538616|168300||paralysis periodica paramyotonica paramyotonia congenita without cold paralysis included
|
|
C538616|168300||paramyotonia congenita without cold paralysis
|
|
C538616|168300||pmc
|
|
C538616|168300||von eulenberg apos s disease
|
|
C538200||deafness autosomal dominant nonsyndromic sensorineural 3
|
|
C538200||neurosensory nonsyndromic dominant deafness 1
|
|
C565821||noncompaction of left ventricular myocardium familial isolated autosomal dominant 1
|
|
C565821||left ventricular noncompaction isolated autosomal dominant
|
|
D016506|169600||pemphigus benign familial
|
|
D016506|169600||bcpm
|
|
D016506|169600||benign chronic pemphigus
|
|
D016506|169600||benign familial pemphigus
|
|
D016506|169600||familial benign chronic pemphigus
|
|
D016506|169600||familial pemphigus benign
|
|
D016506|169600||hailey hailey disease
|
|
D016506|169600||hhd
|
|
C538204||deafness congenital onychodystrophy recessive form
|
|
C538204||deafness onycho osteodystrophy mental retardation syndrome
|
|
C538201||deafness autosomal dominant nonsyndromic sensorineural 53
|
|
D012192||retroviridae infections
|
|
D012192||infection retroviridae
|
|
D012192||infection retrovirus
|
|
D012192||infections retroviridae
|
|
D012192||infections retrovirus
|
|
D012192||retroviridae infection
|
|
D012192||retrovirus infection
|
|
D012192||retrovirus infections
|
|
C563789|609136||peripheral demyelinating neuropathy central dysmyelination waardenburg syndrome and hirschsprung disease
|
|
C563789|609136||pcwh
|
|
C563789|609136||waardenburg shah syndrome neurologic variant
|
|
D008924||mite infestations
|
|
D008924||acariasis
|
|
D008924||infestation mite
|
|
D008924||infestations mite
|
|
D008924||mange
|
|
D008924||mite infestation
|
|
C565825||cerebellar ataxia deafness and narcolepsy
|
|
608984||ataxia sensory 1 autosomal dominant
|
|
608984||adsa
|
|
608984||snax1
|
|
D024182||uniparental disomy
|
|
D024182||disomies uniparental
|
|
D024182||disomy uniparental
|
|
D024182||heterodisomies uniparental
|
|
D024182||heterodisomy uniparental
|
|
D024182||isodisomies uniparental
|
|
D024182||uniparental disomies
|
|
D024182||uniparental heterodisomies
|
|
D024182||uniparental heterodisomy
|
|
D024182||uniparental isodisomies
|
|
D024182||uniparental isodisomy
|
|
D012186||retroperitoneal neoplasms
|
|
D012186||neoplasm retroperitoneal
|
|
D012186||neoplasms retroperitoneal
|
|
D012186||retroperitoneal neoplasm
|
|
184850|D016750||stiff person syndrome
|
|
184850|D016750||congenital stiff man syndrome
|
|
184850|D016750||familial hyperekplexia
|
|
184850|D016750||hereditary hyperekplexia
|
|
184850|D016750||hyperekplexia
|
|
184850|D016750||moersch woltmann syndrome
|
|
184850|D016750||per included
|
|
184850|D016750||perm included
|
|
184850|D016750||startle syndrome
|
|
184850|D016750||stiffman syndrome
|
|
184850|D016750||stiff man syndrome
|
|
184850|D016750||stiff trunk syndrome
|
|
184850|D016750||stiff trunk syndrome progressive encephalomyelitis with rigidity included
|
|
184850|D016750||syndrome moersch woltmann
|
|
184850|D016750||syndrome stiffman
|
|
184850|D016750||syndrome stiff man
|
|
184850|D016750||syndrome stiff person
|
|
D012185||retroperitoneal fibrosis
|
|
D012185||chronic periaortitides
|
|
D012185||chronic periaortitis
|
|
D012185||disease ormond
|
|
D012185||disease ormond apos s
|
|
D012185||fibroses retroperitoneal
|
|
D012185||fibrosis inflammatory perianeurysmal
|
|
D012185||fibrosis perianeurysmal inflammatory
|
|
D012185||fibrosis retroperitoneal
|
|
D012185||idiopathic retroperitoneal fibrosis
|
|
D012185||inflammatory fibrosis perianeurysmal
|
|
D012185||inflammatory perianeurysmal fibrosis
|
|
D012185||ormond disease
|
|
D012185||ormond apos s disease
|
|
D012185||perianeurysmal fibrosis inflammatory
|
|
D012185||perianeurysmal inflammatory fibrosis
|
|
D012185||periaortitides chronic
|
|
D012185||periaortitis chronic
|
|
D012185||retroperitoneal fibroses
|
|
137750|C564234||glaucoma 1 open angle a
|
|
137750|C564234||glaucoma primary open angle juvenile onset 1
|
|
137750|C564234||glaucoma primary open angle juvenile onset 1 joag1 glaucoma 1 open angle l included
|
|
137750|C564234||glc1a
|
|
137750|C564234||glc1l included
|
|
D012188||retropneumoperitoneum
|
|
D012188||pneumoretroperitoneum
|
|
C563436|600858||cardiomyopathy familial hypertrophic 6
|
|
C563436|600858||cmh6
|
|
D050500||pancreatitis chronic
|
|
D050500||chronic pancreatitis
|
|
C536940|274000||absent radii and thrombocytopenia
|
|
C536940|274000||chromosome 1q21 1 deletion syndrome 200 kb
|
|
C536940|274000||radial aplasia amegakaryocytic thrombocytopenia
|
|
C536940|274000||radial aplasia thrombocytopenia syndrome
|
|
C536940|274000||tar
|
|
C536940|274000||tar syndrome
|
|
C536940|274000||thrombocytopenia absent radii
|
|
C536940|274000||thrombocytopenia absent radius syndrome
|
|
C565830||myasthenic syndrome due to mutation in scn4a
|
|
C538211||dens in dente and palatal invaginations
|
|
C538210||dennis fairhurst moore syndrome
|
|
C538210||hallermam streiff like syndrome
|
|
C567066|300659||mental retardation x linked 93
|
|
C567066|300659||mental retardation x linked with macrocephaly
|
|
C567066|300659||mrx93
|
|
C538213||dentin dysplasia sclerotic bones
|
|
C538213||dentin dysplasia with sclerotic bones
|
|
C538213||sclerotic bones with dentin dysplasia
|
|
C538326|300221||hodgkin disease x linked pseudoautosomal
|
|
C565834|603902||beta thalassemia dominant inclusion body type
|
|
C565834|603902||dyserythropoietic anemia congenital irish or weatherall type
|
|
C566528|602540||hid syndrome
|
|
C566528|602540||hystrix like ichthyosis with deafness
|
|
C566528|602540||ichthyosis hystrix like with deafness
|
|
C538207||deletion 6q16 q21
|
|
C538207||monosomy 6q16 q21
|
|
C538206||deal barratt dillon syndrome
|
|
C538206||fanconi syndrome ichthyosis dysmorphism jaundice and diarrhoea
|
|
C538205||deafness neurosensory autosomal recessive 47
|
|
C536993|608796||moyamoya disease 3
|
|
C536993|608796||mymy3
|
|
C538221||green sandford davison syndrome
|
|
C538220||dermatoleukodystrophy
|
|
C535382|208085||arthrogryposis renal dysfunction cholestasis syndrome
|
|
C535382|208085||arcs
|
|
C535382|208085||arcs1
|
|
C535382|208085||arcs2
|
|
C535382|208085||arc syndrome
|
|
C535382|208085||arthrogryposis multiplex congenita renal dysfunction and cholestasis
|
|
C535382|208085||arthrogryposis renal dysfunction and cholestasis
|
|
C535382|208085||arthrogryposis renal dysfunction and cholestasis 1
|
|
C535382|208085||arthrogryposis renal dysfunction and cholestasis 2
|
|
C538224||adams nance syndrome
|
|
C538224||tachycardia hypertension microphthalmos hyperglycinuria
|
|
C538223||acute zonal occult outer retinopathy
|
|
D012170||retinal vein occlusion
|
|
D012170||occlusion retinal vein
|
|
D012170||occlusions retinal vein
|
|
D012170||retinal vein occlusions
|
|
D012170||retinal vein thromboses
|
|
D012170||retinal vein thrombosis
|
|
D012170||thromboses retinal vein
|
|
D012170||thrombosis retinal vein
|
|
D012170||vein occlusion retinal
|
|
D012170||vein occlusions retinal
|
|
D012170||vein thromboses retinal
|
|
D012170||vein thrombosis retinal
|
|
C565808||generalized epilepsy with febrile seizures plus
|
|
C565801||hemosiderosis systemic due to aceruloplasminemia
|
|
D000189||actinobacillus infections
|
|
D000189||actinobacillus infection
|
|
D000189||infection actinobacillus
|
|
D000189||infections actinobacillus
|
|
C537482|604187||spastic paraplegia 10 autosomal dominant
|
|
C537482|604187||autosomal dominant spastic paraplegia
|
|
C537482|604187||spastic paraplegia 10 with or without peripheral neuropathy
|
|
C537482|604187||spg10
|
|
C565803||carney triad
|
|
C565803||gastric leiomyosarcoma pulmonary chondroma and extraadrenal paraganglioma
|
|
D000187||actinobacillosis
|
|
D000187||actinobacilloses
|
|
203655|C537055||alopecia universalis
|
|
203655|C537055||alopecia universalis congenita
|
|
203655|C537055||alunc
|
|
203655|C537055||atrichia generalized
|
|
203655|C537055||generalized atrichia
|
|
D000193||actinomycetales infections
|
|
D000193||actinomycetales infection
|
|
D000193||actinomycete infection
|
|
D000193||actinomycete infections
|
|
D000193||infection actinomycetales
|
|
D000193||infection actinomycete
|
|
D000193||infections actinomycetales
|
|
D000193||infections actinomycete
|
|
C538219||dermatofibrosarcoma protuberans
|
|
C538219||familial dermatofibrosarcoma protuberans
|
|
C538219||giant cell fibroblastoma
|
|
C538219||metastatic dermatofibrosarcoma protuberans
|
|
D012164||retinal diseases
|
|
D012164||disease retinal
|
|
D012164||diseases retinal
|
|
D012164||retinal disease
|
|
C538218||dermatitis herpetiformis familial
|
|
C538217||der kaloustian mcintosh silver syndrome
|
|
D012162||retinal degeneration
|
|
D012162||degeneration retinal
|
|
D012162||degenerations retinal
|
|
D012162||retinal degenerations
|
|
D012163||retinal detachment
|
|
D012163||detachment retinal
|
|
D012163||detachments retinal
|
|
D012163||retinal detachments
|
|
D012163||retinal pigment epithelial detachment
|
|
D012166||retinal hemorrhage
|
|
D012166||hemorrhage retinal
|
|
D012166||retinal hemorrhages
|
|
D012167||retinal perforations
|
|
D012167||break retinal
|
|
D012167||breaks retinal
|
|
D012167||dialyses retinal
|
|
D012167||hole macular
|
|
D012167||hole retinal
|
|
D012167||holes macular
|
|
D012167||holes retinal
|
|
D012167||macular hole
|
|
D012167||macular holes
|
|
D012167||perforation retinal
|
|
D012167||perforations retinal
|
|
D012167||retinal break
|
|
D012167||retinal breaks
|
|
D012167||retinal dialyse
|
|
D012167||retinal dialyses
|
|
D012167||retinal hole
|
|
D012167||retinal holes
|
|
D012167||retinal perforation
|
|
D012167||retinal tear
|
|
D012167||retinal tears
|
|
D012167||tear retinal
|
|
D012167||tears retinal
|
|
C538232||adenosarcoma of the uterus
|
|
C538232||mullerian adenosarcoma of the uterus
|
|
C538232||uterine adenosarcoma
|
|
C538231||adenocarcinoma of lung
|
|
C538231||lung adenocarcinoma
|
|
C536586|104200||alport syndrome dominant type
|
|
C536586|104200||renal failure and sensorineural hearing loss
|
|
C538230||adenocarcinoid tumor
|
|
D012183||retrograde degeneration
|
|
D012183||axonal reaction
|
|
D012183||axonal reactions
|
|
D012183||axon reaction
|
|
D012183||axon reactions
|
|
D012183||degeneration nissl
|
|
D012183||degeneration retrograde
|
|
D012183||degenerations retrograde
|
|
D012183||degenerations transneuronal retrograde
|
|
D012183||degenerations trans synaptic
|
|
D012183||degeneration transneuronal retrograde
|
|
D012183||degeneration trans synaptic
|
|
D012183||nissl degeneration
|
|
D012183||reaction axon
|
|
D012183||reaction axonal
|
|
D012183||reactions axon
|
|
D012183||reactions axonal
|
|
D012183||retrograde degenerations
|
|
D012183||retrograde degenerations transneuronal
|
|
D012183||retrograde degeneration transneuronal
|
|
D012183||transneuronal retrograde degeneration
|
|
D012183||transneuronal retrograde degenerations
|
|
D012183||trans synaptic degeneration
|
|
D012183||trans synaptic degenerations
|
|
C538234||adenosine monophosphate deaminase deficiency
|
|
C538234||myoadenylate deaminase deficiency myopathy due to
|
|
D012181||retrocochlear diseases
|
|
D012181||disease retrocochlear
|
|
D012181||diseases retrocochlear
|
|
D012181||hearing loss retrocochlear
|
|
D012181||retrocochlear disease
|
|
D012181||retrocochlear hearing loss
|
|
D000197||actinomycosis cervicofacial
|
|
D000197||actinomycoses cervicofacial
|
|
D000197||cervicofacial actinomycoses
|
|
D000197||cervicofacial actinomycosis
|
|
C537177|606693||parkinson disease 9
|
|
C537177|606693||cln12 included
|
|
C537177|606693||krs
|
|
C537177|606693||kufor rakeb syndrome
|
|
C537177|606693||pallidopyramidal degeneration with supranuclear upgaze paresis and dementia
|
|
C537177|606693||pallidopyramidal degeneration with supranuclear upgaze paresis and dementia krppd ceroid lipofuscinosis neuronal 12 included
|
|
C537177|606693||park9
|
|
C537177|606693||parkinson disease 9 autosomal recessive
|
|
D000196||actinomycosis
|
|
D000196||actinomyces infection
|
|
D000196||actinomyces infections
|
|
D000196||actinomycoses
|
|
D000196||infection actinomyces
|
|
D000196||infections actinomyces
|
|
C565817||hirschsprung disease with heart defects laryngeal anomalies and preaxial polydactyly
|
|
C564968|255600||myosclerosis autosomal recessive
|
|
C564968|255600||myopathy myosclerotic
|
|
C564968|255600||myosclerosis congenital of lowenthal
|
|
C565812||generalized epilepsy with febrile seizures plus type 5
|
|
C565812||gefsp5
|
|
C565812||gefs type 5
|
|
C565813||febrile seizures associated with afebrile seizures
|
|
C562637|226500||epidermolysis bullosa dystrophica neurotrophica
|
|
C562637|226500||ebr3
|
|
C562637|226500||epidermolysis bullosa progressiva recessive
|
|
C562637|226500||epidermolysis bullosa with congenital deafness
|
|
193235||adniv
|
|
193235||pvr
|
|
193235||vitreoretinopathy neovascular inflammatory autosomal dominant
|
|
193235||vrni
|
|
C537984|601098||charcot marie tooth disease type 1c
|
|
C537984|601098||charcot marie tooth disease demyelinating type 1c
|
|
C537984|601098||charcot marie tooth neuropathy type 1c
|
|
C537984|601098||charcot marie tooth neuropathy type 1c neuropathy hereditary motor and sensory type ic
|
|
C537984|601098||cmt1c
|
|
C537984|601098||cmt slow nerve conduction type c
|
|
C537984|601098||hmsn1c
|
|
C537984|601098||hmsnic
|
|
C537984|601098||hmsn ic
|
|
C537984|601098||neuropathy hereditary motor and sensory type ic
|
|
C536919|103500||tietz syndrome
|
|
C536919|103500||albinism and complete nerve deafness
|
|
C536919|103500||albinism deafness of tietz
|
|
C536919|103500||hypopigmentation deafness of tietz
|
|
C536919|103500||tietz albinism deafness syndrome
|
|
C564565|300211||episodic muscle weakness x linked
|
|
C564565|300211||emwx
|
|
C538229||adenoameloblastoma
|
|
C538229||adenomatoid ameloblastoma
|
|
C538229||adenomatoid odontogenic tumor
|
|
C538229||pleomorphic adenomatoid tumor
|
|
C564678|606688||spongiform encephalopathy with neuropsychiatric features
|
|
C538228||adenine phosphoribosyltransferase deficiency
|
|
C538228||2 8 dihydroxyadenine urolithiasis
|
|
C538228||2 8 dihydroxyadeninuria
|
|
C538228||aprt deficiency
|
|
C538228||dha crystalline nephropathy
|
|
C538228||urolithiasis 2 8 dihydroxyadenine
|
|
D012173||retinitis
|
|
D012173||neuroretinitis
|
|
C538104|260300||pallidopyramidal syndrome
|
|
C538104|260300||pallido pyramidal disease
|
|
C538104|260300||pallido pyramidal syndrome
|
|
C538104|260300||park15
|
|
C538104|260300||parkinson disease 15 autosomal recessive
|
|
C538104|260300||parkinson disease 15 autosomal recessive early onset
|
|
C538104|260300||parkinsonian pyramidal syndrome
|
|
C538104|260300||pkps
|
|
C566044|613765||cardiomyopathy familial hypertrophic 9
|
|
C566044|613765||cmh9
|
|
D058456|300216||retinal telangiectasis
|
|
D058456|300216||coats disease
|
|
D058456|300216||disease coats
|
|
D058456|300216||retinal telangiectases
|
|
D058456|300216||telangiectases retinal
|
|
D058456|300216||telangiectasis retinal
|
|
D012178||retinopathy of prematurity
|
|
D012178||fibroplasia retrolental
|
|
D012178||fibroplasias retrolental
|
|
D012178||prematurity retinopathies
|
|
D012178||prematurity retinopathy
|
|
D012178||retrolental fibroplasia
|
|
D012178||retrolental fibroplasias
|
|
C538376|610021||hyperinsulinemic hypoglycemia familial 7
|
|
C538376|610021||hhf7
|
|
C538376|610021||hyperinsulinemic hypoglycemia exercise induced
|
|
300519|C564495||martin probst deafness mental retardation syndrome
|
|
300519|C564495||mental retardation x linked syndromic martin probst type
|
|
300519|C564495||mrxsmp
|
|
C565904||beta aminoisobutyric acid urinary excretion of
|
|
C565904||baib urinary excretion
|
|
C565904||hyper beta aminoisobutyric aciduria
|
|
C565905||berry aneurysm cirrhosis pulmonary emphysema and cerebral calcification
|
|
C565905||cerebral aneurysm cirrhosis syndrome
|
|
311250||otc deficiency valproate sensitivity included
|
|
C565907||bcg infection generalized familial
|
|
C565902||biemond syndrome ii
|
|
D063748||bland white garland syndrome
|
|
D063748||alcapa
|
|
D063748||alcapa syndrome
|
|
D063748||alcapa syndromes
|
|
D063748||syndrome alcapa
|
|
D063748||syndrome bland white garland
|
|
D000292||pelvic inflammatory disease
|
|
D000292||adnexitis
|
|
D000292||disease inflammatory pelvic
|
|
D000292||disease pelvic inflammatory
|
|
D000292||diseases inflammatory pelvic
|
|
D000292||diseases pelvic inflammatory
|
|
D000292||inflammatory disease pelvic
|
|
D000292||inflammatory diseases pelvic
|
|
D000292||inflammatory pelvic disease
|
|
D000292||inflammatory pelvic diseases
|
|
D000292||pelvic disease inflammatory
|
|
D000292||pelvic diseases inflammatory
|
|
D000292||pelvic inflammatory diseases
|
|
C565908||bcg and salmonella infection disseminated
|
|
D000291||adnexal diseases
|
|
D000291||adnexal disease
|
|
D000291||disease adnexal
|
|
D000291||diseases adnexal
|
|
C565909||bcg infection generalized familial semibenign autosomal dominant
|
|
107320|C531622||familial antiphospholipid syndrome
|
|
107320|C531622||antiphospholipid syndrome familial
|
|
107320|C531622||lupus anticoagulant familial
|
|
226980|C536739||wolcott rallison syndrome
|
|
226980|C536739||epiphyseal dysplasia multiple with early onset diabetes mellitus
|
|
226980|C536739||iddm med syndrome
|
|
226980|C536739||med iddm syndrome
|
|
D013595||syringomyelia
|
|
D013595||hydrosyringomyelia
|
|
D013595||hydrosyringomyelias
|
|
D013595||morvan diseases
|
|
D013595||morvan apos s disease
|
|
D013595||morvans disease
|
|
D013595||morvan apos s diseases
|
|
D013595||myelosyringoses
|
|
D013595||myelosyringosis
|
|
D013595||syringomyelias
|
|
D013595||syringomyelus
|
|
D013592||syphilis latent
|
|
D013592||latent stage syphili
|
|
D013592||latent stage syphilis
|
|
D013592||latent syphilis
|
|
D013592||syphili latent stage
|
|
D013592||syphilis latent stage
|
|
C535744|609180||congenital disorder of glycosylation type 1f
|
|
C535744|609180||cdg1f
|
|
C535744|609180||cdgif
|
|
C535744|609180||cdg if
|
|
C535744|609180||congenital disorder of glycosylation type if
|
|
C562407|180920||aplasia of lacrimal and salivary glands
|
|
C562407|180920||alsg
|
|
C562407|180920||lacrimal puncta absence of included
|
|
C562407|180920||salivary glands absence of
|
|
C562407|180920||salivary glands absence of parotid aplasia or hypoplasia included
|
|
C565910||bare lymphocyte syndrome type ii complementation group a
|
|
C565910||bare lymphocyte syndrome type ii complementation group b
|
|
C565910||bare lymphocyte syndrome type ii complementation group c
|
|
C565910||bare lymphocyte syndrome type ii complementation group d
|
|
C565910||bare lymphocyte syndrome type ii complementation group e
|
|
C563657|610832||fanconi anemia complementation group n
|
|
C563657|610832||fancn
|
|
D012282||rickettsia infections
|
|
D012282||infection rickettsia
|
|
D012282||infections rickettsia
|
|
D012282||rickettsia infection
|
|
C567416|612109||oculoauricular syndrome
|
|
C567416|612109||microphthalmia microcornea anterior segment dysgenesis cataract ocular coloboma retinal pigment epithelium abnormalities rod cone dystrophy and anomalies of the external ear
|
|
C565916||bardet biedl syndrome 7
|
|
D063730||rickets hypophosphatemic
|
|
D063730||acquired vitamin d resistant rickets
|
|
D063730||hypophosphatemia vitamin d resistant rickets
|
|
D063730||hypophosphatemic ricket
|
|
D063730||hypophosphatemic rickets
|
|
D063730||ricket hypophosphatemic
|
|
D063730||rickets vitamin d resistant
|
|
C565917||bardet biedl syndrome 8
|
|
C565918||bardet biedl syndrome 9
|
|
121800|C535475||corneal dystrophy crystalline of schnyder
|
|
121800|C535475||corneal dystrophy schnyder
|
|
121800|C535475||sccd
|
|
121800|C535475||schnyder corneal dystrophy
|
|
121800|C535475||schnyder crystalline corneal dystrophy
|
|
C563697|609566||parietal foramina 3
|
|
C563697|609566||pfm3
|
|
C565919||bardet biedl syndrome 10
|
|
D000755|603903||anemia sickle cell
|
|
D000755|603903||anemias sickle cell
|
|
D000755|603903||cell disease sickle
|
|
D000755|603903||cell diseases sickle
|
|
D000755|603903||cell disorder sickle
|
|
D000755|603903||cell disorders sickle
|
|
D000755|603903||disease hemoglobin s
|
|
D000755|603903||hbs disease
|
|
D000755|603903||hemoglobin s disease
|
|
D000755|603903||hemoglobin s diseases
|
|
D000755|603903||sickle cell anemia
|
|
D000755|603903||sickle cell anemias
|
|
D000755|603903||sickle cell disease
|
|
D000755|603903||sickle cell diseases
|
|
D000755|603903||sickle cell disorder
|
|
D000755|603903||sickle cell disorders
|
|
D000755|603903||sickling disorder due to hemoglobin s
|
|
C537209|267750||knobloch syndrome
|
|
C537209|267750||kno
|
|
C537209|267750||kno1
|
|
C537209|267750||knobloch syndrome 1
|
|
C537209|267750||knobloch syndrome type i
|
|
C537209|267750||passos bueno syndrome
|
|
C537209|267750||retinal detachment and occipital encephalocele
|
|
C537209|267750||retinal detachment occipital encephalocele
|
|
D012279||rickets
|
|
D012279||rachitides
|
|
D012279||rachitis
|
|
C564602|607239||deafness autosomal recessive 33
|
|
C564602|607239||dfnb33
|
|
C563918|263400||erythrocytosis familial 2
|
|
C563918|263400||ecyt2
|
|
C563918|263400||erythrocytosis autosomal recessive benign
|
|
C563918|263400||polycythemia chuvash type
|
|
C563918|263400||polycythemia vhl dependent
|
|
C535807|157900||moebius syndrome 1
|
|
C535807|157900||mbs
|
|
C538303||chromosome 13 ring
|
|
C538303||ring chromosome 13
|
|
C538302||chromosome 12p partial deletion
|
|
C538302||12p monosomy partial
|
|
C538302||deletion 12p12 p11
|
|
C538302||deletion 12p13
|
|
C538302||monosomy 12p11
|
|
C538302||monosomy 12p13
|
|
D013580||synostosis
|
|
D013580||synostoses
|
|
C567357|612292||birk barel mental retardation dysmorphism syndrome
|
|
C567357|612292||birk barel syndrome
|
|
C567357|612292||mental retardation with hypotonia and facial dysmorphism
|
|
C538301||chromosome 12p deletion
|
|
C538301||deletion 12p
|
|
C538301||monosomy 12p
|
|
C566900|611637||primary lateral sclerosis adult 1
|
|
C566900|611637||plsa
|
|
C566900|611637||plsa1
|
|
C566900|611637||pls adult
|
|
C538300||chromosome 12 trisomy 12q
|
|
C538300||duplication 12q
|
|
C538300||trisomy 12q
|
|
309200|C564108||major affective disorder 2
|
|
309200|C564108||mafd2
|
|
309200|C564108||manic depressive illness
|
|
309200|C564108||manic depressive psychosis x linked
|
|
309200|C564108||mdi
|
|
309200|C564108||mdx
|
|
D000267||tissue adhesions
|
|
D000267||adhesions surgery induced tissue
|
|
D000267||adhesions surgical
|
|
D000267||adhesions tissue
|
|
D000267||adhesion surgery induced tissue
|
|
D000267||adhesion surgical
|
|
D000267||adhesion tissue
|
|
D000267||surgery induced tissue adhesion
|
|
D000267||surgery induced tissue adhesions
|
|
D000267||surgical adhesion
|
|
D000267||surgical adhesions
|
|
D000267||tissue adhesion
|
|
D000267||tissue adhesions surgery induced
|
|
D000267||tissue adhesion surgery induced
|
|
D063766||pediatric obesity
|
|
D063766||adolescent obesity
|
|
D063766||childhood obesity
|
|
D063766||childhood onset obesity
|
|
D063766||child obesity
|
|
D063766||obesity adolescent
|
|
D063766||obesity child
|
|
D063766||obesity childhood
|
|
D063766||obesity childhood onset
|
|
D063766||obesity in adolescence
|
|
D063766||obesity in childhood
|
|
D063766||obesity pediatric
|
|
D063766||onset obesity childhood
|
|
D000270||adie syndrome
|
|
D000270||adie apos s syndrome
|
|
D000270||holmes adie syndrome
|
|
D000270||poorly reacting pupil
|
|
D000270||poorly reacting pupils
|
|
D000270||pupil poorly reacting
|
|
D000270||pupils poorly reacting
|
|
D000270||syndrome adie
|
|
D000270||syndrome adie apos s
|
|
D000270||syndrome holmes adie
|
|
C563856|608800||sudden infant death with dysgenesis of the testes syndrome
|
|
C563856|608800||siddt
|
|
D013576||syndactyly
|
|
D013576||polysyndactyly
|
|
D013576||syndactylia
|
|
D013576||syndactylias
|
|
D013576||syndactylies
|
|
D013577||syndrome
|
|
D013577||clusters symptom
|
|
D013577||cluster symptom
|
|
D013577||symptom cluster
|
|
D013577||symptom clusters
|
|
D013577||syndromes
|
|
D013575||syncope
|
|
D013575||attack drop
|
|
D013575||cardiogenic syncope
|
|
D013575||cardiogenic syncopes
|
|
D013575||carotid sinus syncope
|
|
D013575||carotid sinus syncopes
|
|
D013575||convulsive syncope
|
|
D013575||convulsive syncopes
|
|
D013575||deglutitional syncope
|
|
D013575||deglutitional syncopes
|
|
D013575||drop attack
|
|
D013575||drop attacks
|
|
D013575||effort syncope
|
|
D013575||effort syncopes
|
|
D013575||episode syncopal
|
|
D013575||fainting
|
|
D013575||hyperventilation syncope
|
|
D013575||hyperventilation syncopes
|
|
D013575||micturition syncope
|
|
D013575||micturition syncopes
|
|
D013575||postural syncope
|
|
D013575||postural syncopes
|
|
D013575||presyncope
|
|
D013575||presyncopes
|
|
D013575||situational syncope
|
|
D013575||situational syncopes
|
|
D013575||stokes adams syncope
|
|
D013575||stokes adams syncopes
|
|
D013575||syncopal episode
|
|
D013575||syncopal episodes
|
|
D013575||syncopal vertigo
|
|
D013575||syncope cardiogenic
|
|
D013575||syncope carotid sinus
|
|
D013575||syncope convulsive
|
|
D013575||syncope deglutitional
|
|
D013575||syncope effort
|
|
D013575||syncope hyperventilation
|
|
D013575||syncope micturition
|
|
D013575||syncope postural
|
|
D013575||syncopes
|
|
D013575||syncopes cardiogenic
|
|
D013575||syncopes carotid sinus
|
|
D013575||syncopes convulsive
|
|
D013575||syncopes deglutitional
|
|
D013575||syncopes effort
|
|
D013575||syncopes hyperventilation
|
|
D013575||syncope situational
|
|
D013575||syncopes micturition
|
|
D013575||syncopes postural
|
|
D013575||syncopes situational
|
|
D013575||syncopes stokes adams
|
|
D013575||syncope stokes adams
|
|
D013575||syncopes tussive
|
|
D013575||syncope tussive
|
|
D013575||tussive syncope
|
|
D013575||tussive syncopes
|
|
D013575||vertigos syncopal
|
|
D013575||vertigo syncopal
|
|
C538310||chromosome 19 ring
|
|
C538310||ring chromosome 19
|
|
300589||nystagmus 5 congenital x linked
|
|
300589||nys5
|
|
C538314||chromosome 2 monosomy 2pter p24
|
|
C538314||deletion 2pter p24
|
|
C538314||monosomy 2pter p24
|
|
D013590||syphilis congenital
|
|
D013590||congenital syphilis
|
|
D013590||hutchinson apos s teeth
|
|
D013590||hutchinsons teeth
|
|
D013590||hutchinson teeth
|
|
D013590||teeth hutchinson apos s
|
|
C538313||chromosome 2 monosomy 2p22
|
|
C538313||deletion 2p22
|
|
C538313||monosomy 2p22
|
|
D013591||syphilis cutaneous
|
|
D013591||cutaneous syphilis
|
|
D013591||skin syphilis
|
|
D013591||syphilid
|
|
D013591||syphilids
|
|
D013591||syphilis skin
|
|
C538312||chromosome 1q duplication 1q12 q21
|
|
C538312||duplication 1q12 q21
|
|
C538311||chromosome 19 trisomy 19q
|
|
C538311||duplication 19q
|
|
C538311||trisomy 19q
|
|
D000274||adiposis dolorosa
|
|
D000274||adiposalgia
|
|
D000274||adipose tissue rheumatism
|
|
D000274||anders syndrome
|
|
D000274||dercum disease
|
|
D000274||dercum apos s disease
|
|
D000274||dercums disease
|
|
D000274||disease dercum
|
|
D000274||disease dercum apos s
|
|
D000274||lipomatosis dolorosa
|
|
D000274||morbus dercum
|
|
D000275||adjustment disorders
|
|
D000275||adjustment disorder
|
|
D000275||anniversary reaction
|
|
D000275||anniversary reactions
|
|
D000275||depression reactive
|
|
D000275||depressions reactive
|
|
D000275||disorder adjustment
|
|
D000275||disorder reactive
|
|
D000275||disorders adjustment
|
|
D000275||disorders reactive
|
|
D000275||disturbances transient situational
|
|
D000275||disturbance transient situational
|
|
D000275||reaction anniversary
|
|
D000275||reactions anniversary
|
|
D000275||reactive depression
|
|
D000275||reactive depressions
|
|
D000275||reactive disorder
|
|
D000275||reactive disorders
|
|
D000275||situational disturbances transient
|
|
D000275||situational disturbance transient
|
|
D000275||transient situational disturbance
|
|
D000275||transient situational disturbances
|
|
D013589||syphilis cardiovascular
|
|
D013589||aortitides syphilitic
|
|
D013589||aortitis syphilitic
|
|
D013589||cardiovascular syphilis
|
|
D013589||syphilitic aortitides
|
|
D013589||syphilitic aortitis
|
|
C538307||chromosome 18 trisomy 18p
|
|
C538307||duplication 18p
|
|
C538307||trisomy 18p
|
|
C538306||chromosome 18 tetrasomy 18p
|
|
C538306||18p isochromosome
|
|
C538306||18p tetrasomy
|
|
C538306||isochromosome 18p
|
|
C538306||tetrasomy 18p
|
|
C538306||tetrasomy short arm of chromosome 18
|
|
D012253||rib fractures
|
|
D012253||fracture rib
|
|
D012253||fractures rib
|
|
D012253||rib fracture
|
|
C538305||chromosome 18 deletion 18q23
|
|
C538305||deletion 18q23
|
|
C538305||monosomy 18q23
|
|
D013581||synovial cyst
|
|
D013581||cysts synovial
|
|
D013581||cyst synovial
|
|
D013581||synovial cysts
|
|
C538304||chromosome 18 ring
|
|
C538304||ring chromosome 18
|
|
D013587||syphilis
|
|
D013587||great pox
|
|
D013587||pox great
|
|
D012257||riboflavin deficiency
|
|
D012257||deficiencies riboflavin
|
|
D012257||deficiency riboflavin
|
|
D012257||riboflavin deficiencies
|
|
C538309||chromosome 18p deletion syndrome
|
|
C538309||18p deletion syndrome
|
|
C538309||18p minus syndrome
|
|
C538309||18p syndrome
|
|
C538309||del 18p syndrome
|
|
C538309||deletion 18p syndrome
|
|
D013585||synovitis
|
|
D013585||synovitides
|
|
D000757|206500||anencephaly
|
|
D000757|206500||absence of brain congenital
|
|
D000757|206500||anencephalia
|
|
D000757|206500||anencephalias
|
|
D000757|206500||anencephalies partial
|
|
D000757|206500||anencephalus
|
|
D000757|206500||anencephaly hemicranial
|
|
D000757|206500||anencephaly incomplete
|
|
D000757|206500||anencephaly partial
|
|
D000757|206500||aprosencephalies
|
|
D000757|206500||aprosencephaly
|
|
D000757|206500||brain congenital absence
|
|
D000757|206500||congenital absence of brain
|
|
D000757|206500||hemicranial anencephaly
|
|
D000757|206500||incomplete anencephaly
|
|
D000757|206500||partial anencephalies
|
|
D000757|206500||partial anencephaly
|
|
C538308||chromosome 18 trisomy 18q
|
|
C538308||duplication 18q
|
|
C538308||trisomy 18q
|
|
D013586||synovitis pigmented villonodular
|
|
D013586||pigmented villonodular synovitides
|
|
D013586||pigmented villonodular synovitis
|
|
D013586||synovitides pigmented villonodular
|
|
D013586||villonodular synovitides pigmented
|
|
D013586||villonodular synovitis pigmented
|
|
155755|C536149||melanoma astrocytoma syndrome
|
|
155755|C536149||cutaneous malignant melanoma and cerebral astrocytoma
|
|
155755|C536149||melanoma and neural system tumor syndrome
|
|
C564732|278740||xeroderma pigmentosum complementation group e
|
|
C564732|278740||xeroderma pigmentosum v
|
|
C564732|278740||xp5
|
|
C564732|278740||xpe
|
|
C564732|278740||xp group e
|
|
218800|D003414||crigler najjar syndrome
|
|
218800|D003414||crigler najar syndrome
|
|
218800|D003414||crigler najjar syndrome type 1
|
|
218800|D003414||crigler najjar syndrome type i
|
|
218800|D003414||familial nonhemolytic unconjugated hyperbilirubinemia
|
|
218800|D003414||hblrcn1
|
|
218800|D003414||hereditary unconjugated hyperbilirubinemia
|
|
218800|D003414||hyperbilirubinemia crigler najjar type i
|
|
C563523|162210||neurofibromatosis familial spinal
|
|
C563523|162210||fsnf
|
|
C563209|601492||hyaluronidase deficiency
|
|
C563209|601492||mps9
|
|
C563209|601492||mps ix
|
|
C563209|601492||mucopolysaccharidosis type ix
|
|
D006689|236000||hodgkin disease
|
|
D006689|236000||adult hodgkin lymphoma
|
|
D006689|236000||disease hodgkin
|
|
D006689|236000||disease hodgkins
|
|
D006689|236000||disease hodgkin apos s
|
|
D006689|236000||granuloma hodgkin
|
|
D006689|236000||granuloma hodgkins
|
|
D006689|236000||granuloma hodgkin apos s
|
|
D006689|236000||granuloma malignant
|
|
D006689|236000||hodgkin granuloma
|
|
D006689|236000||hodgkin lymphoma
|
|
D006689|236000||hodgkin lymphoma adult
|
|
D006689|236000||hodgkin apos s disease
|
|
D006689|236000||hodgkins disease
|
|
D006689|236000||hodgkin apos s granuloma
|
|
D006689|236000||hodgkins granuloma
|
|
D006689|236000||hodgkin apos s lymphoma
|
|
D006689|236000||hodgkins lymphoma
|
|
D006689|236000||lymphocyte depletion hodgkin apos s lymphoma
|
|
D006689|236000||lymphocyte rich classical hodgkin apos s lymphoma
|
|
D006689|236000||lymphogranuloma malignant
|
|
D006689|236000||lymphogranulomas malignant
|
|
D006689|236000||lymphoma hodgkin
|
|
D006689|236000||lymphoma hodgkin apos s
|
|
D006689|236000||malignant granuloma
|
|
D006689|236000||malignant granulomas
|
|
D006689|236000||malignant lymphogranuloma
|
|
D006689|236000||malignant lymphogranulomas
|
|
D006689|236000||mixed cellularity hodgkin apos s lymphoma
|
|
D006689|236000||nodular lymphocyte predominant hodgkin apos s lymphoma
|
|
D006689|236000||nodular sclerosing hodgkin apos s lymphoma
|
|
D012227||rhinosporidiosis
|
|
D012227||rhinosporidioses
|
|
D012226||rhinoscleroma
|
|
D012226||nasal scleroma
|
|
D012226||nasal scleromas
|
|
D012226||rhinoscleromas
|
|
D012226||scleroma nasal
|
|
D012226||scleromas nasal
|
|
C563721|609432||syndactyly mesoaxial synostotic with phalangeal reduction
|
|
C563721|609432||mssd
|
|
C563721|609432||syndactyly malik percin type
|
|
C563721|609432||syndactyly type ix
|
|
C562467|153200||lymphedema hereditary ii
|
|
C562467|153200||lymphedema late onset
|
|
C562467|153200||lymphedema praecox
|
|
C562467|153200||meige disease
|
|
C562467|153200||meige lymphedema
|
|
C567031|610997||prostate cancer hereditary 9
|
|
C567031|610997||hpc9
|
|
D012220||rhinitis
|
|
D012220||catarrh nasal
|
|
D012220||catarrhs nasal
|
|
D012220||nasal catarrh
|
|
D012220||nasal catarrhs
|
|
D012220||rhinitides
|
|
611067|C567023||spinal muscular atrophy distal autosomal recessive 4
|
|
611067|C567023||dsma4
|
|
D012223||rhinitis vasomotor
|
|
D012223||rhinitides vasomotor
|
|
D012223||vasomotor rhinitides
|
|
D012223||vasomotor rhinitis
|
|
D013554||swine erysipelas
|
|
D013554||erysipelas swine
|
|
D051799||delayed graft function
|
|
D051799||graft function delayed
|
|
D012224||rhinophyma
|
|
D012224||rhinophymas
|
|
D013555||swine vesicular disease
|
|
D013555||swine vesicular diseases
|
|
D013555||vesicular diseases swine
|
|
D013555||vesicular disease swine
|
|
D014884||waterhouse friderichsen syndrome
|
|
D014884||adrenalitides meningococcal hemorrhagic
|
|
D014884||adrenalitis meningococcal hemorrhagic
|
|
D014884||fulminant meningococcal sepsis with adrenal apoplexy
|
|
D014884||hemorrhagic adrenalitides meningococcal
|
|
D014884||hemorrhagic adrenalitis meningococcal
|
|
D014884||meningococcal hemorrhagic adrenalitides
|
|
D014884||meningococcal hemorrhagic adrenalitis
|
|
D014884||meningococcal waterhouse friderichsen syndrome
|
|
D014884||purpura fulminans waterhouse friderichsen syndrome
|
|
D014884||syndrome meningococcal waterhouse friderichsen
|
|
D014884||waterhouse friderichsen syndrome meningococcal
|
|
D014884||waterhouse friederichsen syndrome
|
|
D012221||rhinitis allergic perennial
|
|
D012221||rhinitis allergic nonseasonal
|
|
D014883||water electrolyte imbalance
|
|
D014883||imbalances water electrolyte
|
|
D014883||imbalance water electrolyte
|
|
D014883||water electrolyte imbalances
|
|
D012222||rhinitis atrophic
|
|
D012222||atrophic rhinitides
|
|
D012222||atrophic rhinitis
|
|
D012222||ozena
|
|
D012222||ozenas
|
|
D012222||rhinitides atrophic
|
|
D013553||swine diseases
|
|
D013553||diseases swine
|
|
D013553||disease swine
|
|
D013553||swine disease
|
|
C566602|601942||diabetes mellitus insulin dependent 10
|
|
C566602|601942||iddm10
|
|
C566602|601942||insulin dependent diabetes mellitus 10
|
|
D000258||adenovirus infections human
|
|
D000258||adenovirus infection human
|
|
D000258||fever pharyngo conjunctival
|
|
D000258||human adenovirus infection
|
|
D000258||human adenovirus infections
|
|
D000258||infection human adenovirus
|
|
D000258||infections human adenovirus
|
|
D000258||pharyngo conjunctival fever
|
|
D000257||adenoviridae infections
|
|
D000257||adenoviridae infection
|
|
D000257||adenovirus infection
|
|
D000257||adenovirus infections
|
|
D000257||infection adenoviridae
|
|
D000257||infection adenovirus
|
|
D000257||infections adenoviridae
|
|
D000257||infections adenovirus
|
|
312550||retinal dysplasia primary
|
|
312550||prd
|
|
D014899||wernicke encephalopathy
|
|
D014899||beriberi cerebral
|
|
D014899||cerebral beriberi
|
|
D014899||encephalopathies wernicke
|
|
D014899||encephalopathy gayet wernicke
|
|
D014899||encephalopathy wernicke
|
|
D014899||encephalopathy wernickes
|
|
D014899||encephalopathy wernicke apos s
|
|
D014899||gayet wernicke encephalopathy
|
|
D014899||wernicke disease
|
|
D014899||wernicke encephalopathies
|
|
D014899||wernicke polioencephalitis superior hemorrhagic
|
|
D014899||wernicke apos s disease
|
|
D014899||wernicke apos s encephalopathy
|
|
D014899||wernicke apos s polioencephalitis superior hemorrhagic
|
|
D014899||wernicke apos s superior hemorrhagic polioencephalitis
|
|
D014899||wernicke apos s syndrome
|
|
D014899||wernicke superior hemorrhagic polioencephalitis
|
|
D014899||wernicke syndrome
|
|
246560||chromosome 10q24 duplication syndrome
|
|
246560||shfm3
|
|
246560||shsf3
|
|
D013568||pathological conditions signs and symptoms
|
|
D013568||symptoms and general pathology
|
|
C536664|266510||peroxisome biogenesis disorders
|
|
C536664|266510||pbd3b
|
|
C536664|266510||peroxisome biogenesis disorder 3b
|
|
D014895||weil disease
|
|
D014895||disease weil
|
|
D014895||disease weil apos s
|
|
D014895||icterohemorrhagic leptospirosis
|
|
D014895||jaundice spirochetal
|
|
D014895||leptospirosis icterohemorrhagic
|
|
D014895||spirochetal jaundice
|
|
D014895||weil apos s disease
|
|
D014895||weils disease
|
|
D001478|109400||basal cell nevus syndrome
|
|
D001478|109400||bcns
|
|
D001478|109400||fifth phacomatoses
|
|
D001478|109400||fifth phacomatosis
|
|
D001478|109400||gorlin goltz syndrome
|
|
D001478|109400||gorlin syndrome
|
|
D001478|109400||multiple basal cell nevi odontogenic keratocysts and skeletal anomalies
|
|
D001478|109400||nbccs
|
|
D001478|109400||nevoid basal cell carcinoma syndrome
|
|
D001478|109400||nevus syndrome basal cell
|
|
D001478|109400||syndrome gorlin
|
|
D001478|109400||syndrome gorlin goltz
|
|
D000224||addison disease
|
|
D000224||addison apos s disease
|
|
D000224||addisons disease
|
|
D000224||adrenal insufficiency primary
|
|
D000224||adrenocortical insufficiencies primary
|
|
D000224||adrenocortical insufficiency primary
|
|
D000224||disease addison
|
|
D000224||hypoadrenalism primary
|
|
D000224||hypoadrenalisms primary
|
|
D000224||insufficiencies primary adrenocortical
|
|
D000224||insufficiency primary adrenocortical
|
|
D000224||primary adrenal insufficiency
|
|
D000224||primary adrenocortical insufficiencies
|
|
D000224||primary adrenocortical insufficiency
|
|
D000224||primary hypoadrenalism
|
|
400004|C564035||retinitis pigmentosa y linked
|
|
400004|C564035||rpy
|
|
117000|D020512||myopathy central core
|
|
117000|D020512|119600|D002973||ccd
|
|
117000|D020512||cco minicore myopathy moderate with hand involvement included
|
|
117000|D020512||central core disease
|
|
117000|D020512||central core disease of muscle
|
|
117000|D020512||central core diseases
|
|
117000|D020512||central core myopathies
|
|
117000|D020512||central core myopathy
|
|
117000|D020512||cnmdu1 included
|
|
117000|D020512||multicore myopathy moderate with hand involvement included
|
|
117000|D020512||multiminicore disease moderate with hand involvement included
|
|
117000|D020512||myopathies central core
|
|
117000|D020512||neuromuscular disease congenital with uniform type 1 fiber included
|
|
117000|D020512||shy magee syndrome
|
|
117000|D020512||syndrome shy magee
|
|
162000||fjhn
|
|
162000||hnfj
|
|
162000||hnfj1
|
|
C567809|613027||glycogen storage disease ixc
|
|
C567809|613027||gsd9c
|
|
C567809|613027||gsd ixc
|
|
D012206||rhabdomyolysis
|
|
D012206||rhabdomyolyses
|
|
D012203||rh isoimmunization
|
|
D012203||isoimmunization rh
|
|
D012203||isoimmunization rhesus
|
|
D012203||isoimmunizations rh
|
|
D012203||isoimmunizations rhesus
|
|
D012203||rhesus isoimmunization
|
|
D012203||rhesus isoimmunizations
|
|
D012203||rh isoimmunizations
|
|
D012203||rh sensitization
|
|
D012203||rh sensitizations
|
|
D012203||sensitization rh
|
|
D012203||sensitizations rh
|
|
D012207||rhabdomyoma
|
|
D012207||rhabdomyomas
|
|
D014869||water intoxication
|
|
C536458|177820||von willebrand disease platelet type
|
|
C536458|177820||bdplt3
|
|
C536458|177820||bleeding disorder platelet type 3
|
|
C536458|177820||platelet type von willebrand disease
|
|
C536458|177820||pseudo von willebrand disease
|
|
C536458|177820||vwdp
|
|
D012208||rhabdomyosarcoma
|
|
D012208||rhabdomyosarcomas
|
|
D014860||warts
|
|
D014860||verruca
|
|
D014860||verrucas
|
|
D014860||wart
|
|
D050488||hallux varus
|
|
D050488||varus hallux
|
|
C566936|611465||gallbladder disease 4
|
|
C566936|611465||gbd4
|
|
D012202||reye syndrome
|
|
D012202||adult reye apos s syndrome
|
|
D012202||adult reye syndrome
|
|
D012202||fatty liver with encephalopathy
|
|
D012202||reye johnson syndrome
|
|
D012202||reye like syndrome
|
|
D012202||reye apos s like syndrome
|
|
D012202||reye apos s syndrome
|
|
D012202||reye apos s syndrome adult
|
|
D012202||reye syndrome adult
|
|
D013530||surgical wound infection
|
|
D013530||infection postoperative wound
|
|
D013530||infections postoperative wound
|
|
D013530||infections surgical wound
|
|
D013530||infection surgical wound
|
|
D013530||postoperative wound infection
|
|
D013530||postoperative wound infections
|
|
D013530||surgical wound infections
|
|
D013530||wound infection postoperative
|
|
D013530||wound infections postoperative
|
|
D013530||wound infections surgical
|
|
D013530||wound infection surgical
|
|
D050489||bunion tailor apos s
|
|
D050489||bunionette
|
|
D050489||bunionettes
|
|
D050489||bunions tailor apos s
|
|
D050489||bunion tailors
|
|
D050489||tailor apos s bunion
|
|
D050489||tailors bunion
|
|
D050489||tailor apos s bunions
|
|
D000238||adenoma chromophobe
|
|
D000238||adenomas chromophobe
|
|
D000238||chromophobe adenoma
|
|
D000238||chromophobe adenomas
|
|
D000237||adenoma basophil
|
|
D000237||adenoma basophilic
|
|
D000237||adenomas basophil
|
|
D000237||adenomas basophilic
|
|
D000237||basophil adenoma
|
|
D000237||basophil adenomas
|
|
D000237||basophilic adenoma
|
|
D000237||basophilic adenomas
|
|
D000236||adenoma
|
|
D000236||adenoma basal cell
|
|
D000236||adenoma follicular
|
|
D000236||adenoma microcystic
|
|
D000236||adenoma monomorphic
|
|
D000236||adenoma papillary
|
|
D000236||adenomas
|
|
D000236||adenomas basal cell
|
|
D000236||adenomas follicular
|
|
D000236||adenomas microcystic
|
|
D000236||adenomas monomorphic
|
|
D000236||adenomas papillary
|
|
D000236||adenomas trabecular
|
|
D000236||adenoma trabecular
|
|
D000236||basal cell adenoma
|
|
D000236||basal cell adenomas
|
|
D000236||follicular adenoma
|
|
D000236||follicular adenomas
|
|
D000236||microcystic adenoma
|
|
D000236||microcystic adenomas
|
|
D000236||monomorphic adenoma
|
|
D000236||monomorphic adenomas
|
|
D000236||papillary adenoma
|
|
D000236||papillary adenomas
|
|
D000236||trabecular adenoma
|
|
D000236||trabecular adenomas
|
|
D000235||adenolymphoma
|
|
D000235||adenolymphomas
|
|
D000235||cystadenoma lymphomatosum papillary
|
|
D000235||papillary cystadenoma lymphomatosum
|
|
D000235||tumor warthin
|
|
D000235||warthin tumor
|
|
607432|D054082||lissencephaly
|
|
607432|D054082||agyria
|
|
607432|D054082||agyrias
|
|
607432|D054082||broad gyri of cerebrum
|
|
607432|D054082||ils
|
|
607432|D054082||large gyri of cerebrum
|
|
607432|D054082||lis1
|
|
607432|D054082||lissencephalia
|
|
607432|D054082||lissencephalias
|
|
607432|D054082||lissencephalies
|
|
607432|D054082||lissencephaly classic subcortical laminar heterotopia included
|
|
607432|D054082||macrogyria
|
|
607432|D054082||pachygyria
|
|
607432|D054082||pachygyrias
|
|
607432|D054082||subcortical band heterotopia included
|
|
C565748|604801||muscular dystrophy congenital 1b
|
|
C565748|604801||mdc1b
|
|
D000239||adenoma acidophil
|
|
D000239||acidophil adenoma
|
|
D000239||acidophil adenomas
|
|
D000239||acidophilic adenoma
|
|
D000239||acidophilic adenomas
|
|
D000239||adenoma acidophilic
|
|
D000239||adenoma eosinophil
|
|
D000239||adenoma eosinophilic
|
|
D000239||adenomas acidophil
|
|
D000239||adenomas acidophilic
|
|
D000239||adenomas eosinophil
|
|
D000239||adenomas eosinophilic
|
|
D000239||eosinophil adenoma
|
|
D000239||eosinophil adenomas
|
|
D000239||eosinophilic adenoma
|
|
D000239||eosinophilic adenomas
|
|
300672|C564064||epileptic encephalopathy early infantile 2
|
|
300672|C564064||eiee2
|
|
300672|C564064||infantile spasm syndrome x linked 2
|
|
300672|C564064||issx2
|
|
300672|C564064||rett syndrome atypical cdkl5 related
|
|
300672|C564064||rett syndrome variant with infantile spasms
|
|
D000230||adenocarcinoma
|
|
D000230||adenocarcinoma basal cell
|
|
D000230||adenocarcinoma granular cell
|
|
D000230||adenocarcinoma oxyphilic
|
|
D000230||adenocarcinomas
|
|
D000230||adenocarcinomas basal cell
|
|
D000230||adenocarcinomas granular cell
|
|
D000230||adenocarcinomas oxyphilic
|
|
D000230||adenocarcinomas tubular
|
|
D000230||adenocarcinoma tubular
|
|
D000230||adenoma malignant
|
|
D000230||adenomas malignant
|
|
D000230||basal cell adenocarcinoma
|
|
D000230||basal cell adenocarcinomas
|
|
D000230||carcinoma cribriform
|
|
D000230||carcinoma granular cell
|
|
D000230||carcinomas cribriform
|
|
D000230||carcinomas granular cell
|
|
D000230||carcinomas tubular
|
|
D000230||carcinoma tubular
|
|
D000230||cribriform carcinoma
|
|
D000230||cribriform carcinomas
|
|
D000230||granular cell adenocarcinoma
|
|
D000230||granular cell adenocarcinomas
|
|
D000230||granular cell carcinoma
|
|
D000230||granular cell carcinomas
|
|
D000230||malignant adenoma
|
|
D000230||malignant adenomas
|
|
D000230||oxyphilic adenocarcinoma
|
|
D000230||oxyphilic adenocarcinomas
|
|
D000230||tubular adenocarcinoma
|
|
D000230||tubular adenocarcinomas
|
|
D000230||tubular carcinoma
|
|
D000230||tubular carcinomas
|
|
145980|C537145||hypocalciuric hypercalcemia familial type 1
|
|
145980|C537145||familial benign hypercalcemia 1
|
|
145980|C537145||familial benign hypercalcemia type 1
|
|
145980|C537145||familial hypocalciuric hypercalcemia
|
|
145980|C537145||fbh1
|
|
145980|C537145||fhh1
|
|
145980|C537145||hhc1
|
|
145980|C537145||hypercalcemia familial benign
|
|
145980|C537145||hypercalcemia familial benign hypocalciuric hypercalcemia acquired included
|
|
145980|C537145||hypercalcemia familial benign type 1
|
|
145980|C537145||hypocalciuric hypercalcemia familial type i
|
|
D000232||adenofibroma
|
|
D000232||adenofibromas
|
|
D000232||fibroadenosis
|
|
D000231||adenocarcinoma papillary
|
|
D000231||adenocarcinomas papillary
|
|
D000231||papillary adenocarcinoma
|
|
D000231||papillary adenocarcinomas
|
|
D012216||rheumatic diseases
|
|
D012216||disease rheumatic
|
|
D012216||diseases rheumatic
|
|
D012216||enthesopathies
|
|
D012216||enthesopathy
|
|
D012216||rheumatic disease
|
|
D012216||rheumatism
|
|
D013547||sweating gustatory
|
|
D013547||auriculotemporal nerve syndrome
|
|
D013547||auriculotemporal syndrome
|
|
D013547||baillarger syndrome
|
|
D013547||frey apos s syndrome
|
|
D013547||frey syndrome
|
|
D013547||gustatory hyperhidroses
|
|
D013547||gustatory hyperhidrosis
|
|
D013547||gustatory sweating
|
|
D013547||hyperhidroses gustatory
|
|
D013547||hyperhidrosis gustatory
|
|
D013547||salivosudoriparous syndrome
|
|
D013547||salivosudoriparous syndromes
|
|
D013547||syndrome auriculotemporal
|
|
D013547||syndrome baillarger
|
|
D013547||syndrome frey
|
|
D013547||syndrome frey apos s
|
|
D013547||syndrome salivosudoriparous
|
|
D013547||syndromes salivosudoriparous
|
|
D013547||syndrome von frey
|
|
D013547||syndrome von frey apos s
|
|
D013547||von frey apos s syndrome
|
|
D013547||von freys syndrome
|
|
D013547||von frey syndrome
|
|
D012214||rheumatic heart disease
|
|
D012214||bouillaud disease
|
|
D012214||bouillaud apos s disease
|
|
D012214||bouillauds disease
|
|
D012214||disease bouillaud
|
|
D012214||disease bouillaud apos s
|
|
D012214||disease rheumatic heart
|
|
D012214||diseases rheumatic heart
|
|
D012214||heart disease rheumatic
|
|
D012214||heart diseases rheumatic
|
|
D012214||rheumatic heart diseases
|
|
D045908||monkeypox
|
|
D045908||monkey pox
|
|
D012215||rheumatic nodule
|
|
D012215||aschoff bodies
|
|
D012215||bodies aschoff
|
|
D012215||nodule rheumatic
|
|
D012215||nodules rheumatic
|
|
D012215||rheumatic nodules
|
|
D012218||rheumatoid nodule
|
|
D012218||nodule rheumatoid
|
|
D012218||nodules rheumatoid
|
|
D012218||rheumatoid nodules
|
|
D012218||rheumatoid noduloses
|
|
D012218||rheumatoid nodulosis
|
|
D013540||swayback
|
|
D013540||ataxia enzootic
|
|
D013540||ataxias enzootic
|
|
D013540||enzootic ataxia
|
|
D013540||enzootic ataxias
|
|
D013543||sweat gland diseases
|
|
D013543||diseases sweat gland
|
|
D013543||disease sweat gland
|
|
D013543||sweat gland disease
|
|
D012213||rheumatic fever
|
|
D012213||acute articular rheumatism
|
|
D012213||acute articular rheumatisms
|
|
D012213||acute rheumatic arthritides
|
|
D012213||acute rheumatic arthritis
|
|
D012213||acute rheumatic fever
|
|
D012213||acute rheumatic fevers
|
|
D012213||arthritides acute rheumatic
|
|
D012213||arthritis acute rheumatic
|
|
D012213||arthritis rheumatic acute
|
|
D012213||articular rheumatism acute
|
|
D012213||articular rheumatisms acute
|
|
D012213||fever acute rheumatic
|
|
D012213||fever rheumatic
|
|
D012213||fevers acute rheumatic
|
|
D012213||fevers rheumatic
|
|
D012213||inflammatory rheumatism
|
|
D012213||polyarthritis rheumatica
|
|
D012213||polyarthritis rheumaticas
|
|
D012213||rheumatic arthritides acute
|
|
D012213||rheumatic arthritis
|
|
D012213||rheumatic arthritis acute
|
|
D012213||rheumatic fever acute
|
|
D012213||rheumatic fevers
|
|
D012213||rheumatic fevers acute
|
|
D012213||rheumatism acute articular
|
|
D012213||rheumatism articular acute
|
|
D012213||rheumatisms acute articular
|
|
D013544||sweat gland neoplasms
|
|
D013544||neoplasms sweat gland
|
|
D013544||neoplasm sweat gland
|
|
D013544||sweat gland neoplasm
|
|
C563582|156850||microphthalmia isolated with cataract 1
|
|
C563582|156850||cataract congenital with microphthalmia
|
|
C563582|156850||catm
|
|
C563582|156850||mcopct1
|
|
C537484|604805||spastic paraplegia 12 autosomal dominant
|
|
C537484|604805||spg12
|
|
C564249|608380||retinitis pigmentosa 26
|
|
C564249|608380||rp26
|
|
D002869||chromosome aberrations
|
|
D002869||aberration chromosomal
|
|
D002869||aberration chromosome
|
|
D002869||aberration cytogenetic
|
|
D002869||aberrations chromosomal
|
|
D002869||aberrations chromosome
|
|
D002869||aberrations cytogenetic
|
|
D002869||abnormalities autosome
|
|
D002869||abnormalities chromosomal
|
|
D002869||abnormalities chromosome
|
|
D002869||abnormalities cytogenetic
|
|
D002869||abnormality autosome
|
|
D002869||abnormality chromosomal
|
|
D002869||abnormality chromosome
|
|
D002869||abnormality cytogenetic
|
|
D002869||autosome abnormalities
|
|
D002869||autosome abnormality
|
|
D002869||chromosomal aberration
|
|
D002869||chromosomal aberrations
|
|
D002869||chromosomal abnormalities
|
|
D002869||chromosomal abnormality
|
|
D002869||chromosome aberration
|
|
D002869||chromosome abnormalities
|
|
D002869||chromosome abnormality
|
|
D002869||cytogenetic aberration
|
|
D002869||cytogenetic aberrations
|
|
D002869||cytogenetic abnormalities
|
|
D002869||cytogenetic abnormality
|
|
150230|D015826||langer giedion syndrome
|
|
150230|D015826||acrodysplasia v
|
|
150230|D015826||acrodysplasia vs
|
|
150230|D015826||chromosome 8q24 1 deletion syndrome
|
|
150230|D015826||giedion langer syndrome
|
|
150230|D015826||lgs
|
|
150230|D015826||syndrome giedion langer
|
|
150230|D015826||syndrome langer giedion
|
|
150230|D015826||trichorhinophalangeal syndrome type 2
|
|
150230|D015826||trichorhinophalangeal syndrome type ii
|
|
150230|D015826||tricho rhino phalangeal syndrome type ii
|
|
150230|D015826||trichorhinophalangeal syndrome with exostoses
|
|
150230|D015826||trps2
|
|
150230|D015826||trpsii
|
|
C537300|175700||greig cephalopolysyndactyly syndrome
|
|
C537300|175700||cephalopolysyndactyly syndrome
|
|
C537300|175700||gcps
|
|
C537300|175700||greig cephalopolysyndactyly gcps syndrome
|
|
C537300|175700||greig syndrome
|
|
C537300|175700||polysyndactyly with peculiar skull shape
|
|
D000208||acute disease
|
|
D000208||acute diseases
|
|
D000208||disease acute
|
|
D000208||diseases acute
|
|
D012514|148000||sarcoma kaposi
|
|
D012514|148000||kaposi sarcoma
|
|
D012514|148000||kaposi sarcoma susceptibility to
|
|
D012514|148000||kaposi apos s sarcoma
|
|
D012514|148000||kaposis sarcoma
|
|
D012514|148000||mcd included
|
|
D012514|148000||multiple idiopathic pigmented hemangiosarcoma
|
|
D012514|148000||multiple idiopathic pigmented hemangiosarcoma susceptibility to multicentric castleman disease susceptibility to included
|
|
D012514|148000||sarcoma kaposi apos s
|
|
613451||frontonasal dysplasia 2
|
|
613451||fnd2
|
|
613453||deafness autosomal recessive 91
|
|
613453||dfnb91
|
|
D002862||chromoblastomycosis
|
|
D002862||chromoblastomycoses
|
|
D002862||chromomycoses
|
|
D002862||chromomycosis
|
|
D002862||dermatitis verrucosa
|
|
C537357|236250||methylenetetrahydrofolate reductase deficiency
|
|
C537357|236250||homocystinuria due to deficiency of n 5 10 methylenetetrahydrofolate reductase activity
|
|
C537357|236250||mthfr deficiency mthfr deficiency thermolabile type included
|
|
613454||rett syndrome congenital variant
|
|
613456||frontonasal dysplasia 3
|
|
613456||fnd3
|
|
D014846||vulvar neoplasms
|
|
D014846||cancer of the vulva
|
|
D014846||cancer of vulva
|
|
D014846||cancers vulva
|
|
D014846||cancers vulvar
|
|
D014846||cancer vulva
|
|
D014846||cancer vulvar
|
|
D014846||neoplasms vulva
|
|
D014846||neoplasms vulvar
|
|
D014846||neoplasm vulva
|
|
D014846||neoplasm vulvar
|
|
D014846||vulva cancer
|
|
D014846||vulva cancers
|
|
D014846||vulva neoplasm
|
|
D014846||vulva neoplasms
|
|
D014846||vulvar cancer
|
|
D014846||vulvar cancers
|
|
D014846||vulvar neoplasm
|
|
D014845||vulvar diseases
|
|
D014845||diseases vulvar
|
|
D014845||disease vulvar
|
|
D014845||vulvar disease
|
|
612126||glut1 deficiency syndrome 2
|
|
612126||dyt18
|
|
612126||glut1ds2
|
|
612126||paroxysmal exercise induced dyskinesia with or without epilepsy and or hemolytic anemia
|
|
612126||paroxysmal exertion induced dystonia with or without epilepsy and or hemolytic anemia
|
|
612126||ped with or without epilepsy and or hemolytic anemia
|
|
146850||immune suppression
|
|
146850||is
|
|
146850||iscw
|
|
146850||isscw
|
|
146850||streptococcal cell wall antigen suppression of immune response to
|
|
D014843||voyeurism
|
|
D014843||voyeurisms
|
|
612124||cardiomyopathy familial hypertrophic 12
|
|
612124||cmh12
|
|
D014848||vulvovaginitis
|
|
D014848||vulvovaginitides
|
|
D030401|220110||cytochrome c oxidase deficiency
|
|
D030401|220110||complex iv deficiencies
|
|
D030401|220110||complex iv deficiency
|
|
D030401|220110||cox deficiencies
|
|
D030401|220110||cox deficiency
|
|
D030401|220110||cytochrome c oxidase deficiencies
|
|
D030401|220110||cytochrome oxidase deficiencies
|
|
D030401|220110||cytochrome oxidase deficiency
|
|
D030401|220110||deficiencies complex iv
|
|
D030401|220110||deficiencies cox
|
|
D030401|220110||deficiencies cytochrome c oxidase
|
|
D030401|220110||deficiencies cytochrome oxidase
|
|
D030401|220110||deficiency complex iv
|
|
D030401|220110||deficiency cox
|
|
D030401|220110||deficiency cytochrome c oxidase
|
|
D030401|220110||deficiency cytochrome oxidase
|
|
D030401|220110||mitochondrial complex iv deficiency
|
|
D030401|220110||oxidase deficiencies cytochrome
|
|
D030401|220110||oxidase deficiencies cytochrome c
|
|
D030401|220110||oxidase deficiency cytochrome
|
|
D030401|220110||oxidase deficiency cytochrome c
|
|
D014847||vulvitis
|
|
D014847||vulvitides
|
|
C566158|116200||cataract zonular pulverulent 1
|
|
C566158|116200||cae1
|
|
C566158|116200||cataract 1 multiple types
|
|
C566158|116200||cataract 1 multiple types with or without microcornea
|
|
C566158|116200||cataract duffy linked
|
|
C566158|116200||ctrct1
|
|
C566158|116200||czp
|
|
C566158|116200||czp1
|
|
C566158|116200||pulverulent zonular cataract
|
|
D014842||von willebrand diseases
|
|
D014842||angiohemophilia
|
|
D014842||angiohemophilias
|
|
D014842||disorder von willebrand
|
|
D014842||hemophilia vascular
|
|
D014842||pseudohemophilias vascular
|
|
D014842||pseudohemophilia vascular
|
|
D014842||vascular hemophilia
|
|
D014842||vascular hemophilias
|
|
D014842||vascular pseudohemophilia
|
|
D014842||vascular pseudohemophilias
|
|
D014842||von willebrand disease
|
|
D014842||von willebrand disease recessive form
|
|
D014842||von willebrand disorder
|
|
D014842||von willebrand apos s disease
|
|
D014842||von willebrand apos s diseases
|
|
D014842||von willebrand apos s factor deficiency
|
|
D014840||vomiting anticipatory
|
|
D014840||anticipatory vomiting
|
|
C566435|610539||gaucher disease atypical due to saposin c deficiency
|
|
C537172|168400||parastremmatic dwarfism
|
|
C537172|168400||parastremmatic dysplasia
|
|
D000219||adams stokes syndrome
|
|
D000219||adam stokes attacks
|
|
D000219||attacks adam stokes
|
|
D000219||attacks stokes adams
|
|
D000219||stokes adams attacks
|
|
D000219||stokes adams syndrome
|
|
D000219||syndrome adams stokes
|
|
D000219||syndrome stokes adams
|
|
151660|D052496||lipodystrophy familial partial
|
|
151660|D052496||dunnigan syndrome
|
|
151660|D052496||familial partial lipodystrophies
|
|
151660|D052496||familial partial lipodystrophy
|
|
151660|D052496||familial partial lipodystrophy kobberling type
|
|
151660|D052496||familial partial lipodystrophy type 1
|
|
151660|D052496||familial partial lipodystrophy type 2
|
|
151660|D052496||familial partial lipodystrophy type 3
|
|
151660|D052496||fpl2
|
|
151660|D052496||fpld2
|
|
151660|D052496||fpld3
|
|
151660|D052496||koberling dunnigan syndrome
|
|
151660|D052496||lipodystrophies familial partial
|
|
151660|D052496||lipodystrophies reverse partial
|
|
151660|D052496||lipodystrophy familial of limbs and lower trunk
|
|
151660|D052496||lipodystrophy familial partial associated with pparg mutations
|
|
151660|D052496||lipodystrophy familial partial dunnigan type
|
|
151660|D052496||lipodystrophy familial partial kobberling type
|
|
151660|D052496||lipodystrophy familial partial type 1
|
|
151660|D052496||lipodystrophy familial partial type 2
|
|
151660|D052496||lipodystrophy familial partial type 3
|
|
151660|D052496||lipodystrophy reverse partial
|
|
151660|D052496||partial lipodystrophies familial
|
|
151660|D052496||partial lipodystrophies reverse
|
|
151660|D052496||partial lipodystrophy familial
|
|
151660|D052496||partial lipodystrophy reverse
|
|
151660|D052496||reverse partial lipodystrophies
|
|
151660|D052496||reverse partial lipodystrophy
|
|
151660|D052496||syndrome dunnigan
|
|
C537757|220150||renal hypouricemia
|
|
C537757|220150||dalmatian hypouricemia
|
|
C537757|220150||hypouricemia renal
|
|
C537757|220150||hypouricemia renal 1
|
|
C537757|220150||rhuc1
|
|
D019896|613490||alpha 1 antitrypsin deficiencies
|
|
D019896|613490||deficiencies alpha 1 antitrypsin
|
|
D019896|613490||deficiency alpha 1 antitrypsin
|
|
D002872||chromosome deletion
|
|
D002872||deletion chromosome
|
|
D002872||deletions chromosome
|
|
D002872||monosomies partial
|
|
D002872||monosomy partial
|
|
D002872||partial monosomies
|
|
D002872||partial monosomy
|
|
D002873||chromosome fragility
|
|
D002873||chromosomal fragility
|
|
D002873||fragility chromosomal
|
|
D002873||fragility chromosome
|
|
613443||mental retardation autosomal dominant 20
|
|
613443||mental retardation stereotypic movements epilepsy and or cerebral malformations chromosome 5q14 3 deletion syndrome included
|
|
613443||mrd20
|
|
D000210||acute phase reaction
|
|
D000210||acute phase response
|
|
D000210||acute phase state
|
|
D000210||reaction acute phase
|
|
D000210||response acute phase
|
|
D000210||state acute phase
|
|
C562429|174200||polydactyly postaxial
|
|
C562429|174200||papa
|
|
C562429|174200||papa1
|
|
C562429|174200||papb included
|
|
C562429|174200||polydactyly postaxial postaxial polydactyly type b included
|
|
C562429|174200||polydactyly postaxial type a1
|
|
C562429|174200||postaxial polydactyly type a
|
|
C562429|174200||postaxial polydactyly type b
|
|
C537380|610017||multiple synostoses syndrome 2
|
|
C537380|610017||syns2
|
|
C566619|601813||exudative vitreoretinopathy 4
|
|
C566619|601813||evr4
|
|
C567853|603513||cerebral palsy spastic quadriplegic 1
|
|
C567853|603513||cpsq1
|
|
D014855||wallerian degeneration
|
|
D014855||degeneration wallerian
|
|
C566438|610127||ceroid lipofuscinosis neuronal 10
|
|
C566438|610127||ceroid lipofuscinosis neuronal cathepsin d deficient
|
|
C566438|610127||cln10
|
|
C566438|610127||neuronal ceroid lipofuscinosis congenital
|
|
C566438|610127||neuronal ceroid lipofuscinosis due to cathepsin d deficiency
|
|
C566438|610127||neuronal ceroid lipofuscinosis due to cathepsin d deficiency neuronal ceroid lipofuscinosis congenital included
|
|
D014854||lateral medullary syndrome
|
|
D014854||dorsolateral medullary syndrome
|
|
D014854||lateral bulbar syndrome
|
|
D014854||lateral medullary syndromes
|
|
D014854||medullary syndrome dorsolateral
|
|
D014854||posterior inferior cerebellar artery syndrome
|
|
D014854||syndromes lateral medullary
|
|
D014854||syndrome vieseaux wallenberg
|
|
D014854||syndrome wallenberg
|
|
D014854||vieseaux wallenberg syndrome
|
|
D014854||wallenberg apos s syndrome
|
|
D014854||wallenbergs syndrome
|
|
D014854||wallenberg syndrome
|
|
D013529||surgical wound dehiscence
|
|
D013529||dehiscence surgical wound
|
|
D013529||wound dehiscence surgical
|
|
604060|C565828||deafness autosomal recessive 20
|
|
604060|C565828||dfnb20
|
|
C563843|608874||orofacial cleft 5
|
|
C563843|608874||cleft lip with or without cleft palate nonsyndromic 5
|
|
C563843|608874||ofc5
|
|
C535942|602082||corneal dystrophy thiel behnke type
|
|
C535942|602082||cdb2
|
|
C535942|602082||cdtb
|
|
C535942|602082||corneal dystrophy honeycomb shaped
|
|
C535942|602082||corneal dystrophy of bowman layer type ii
|
|
C535942|602082||corneal dystrophy of the bowman layer type 2
|
|
C535942|602082||tbcd
|
|
C535942|602082||thiel behnke corneal dystrophy
|
|
C537251|608898||hemophagocytic lymphohistiocytosis familial 3
|
|
C537251|608898||fhl3
|
|
C537251|608898||hlh3
|
|
C537251|608898||hplh3
|
|
253700|C535900||limb girdle muscular dystrophy type 2c
|
|
253700|C535900||adhalin deficiency secondary
|
|
253700|C535900||dmda
|
|
253700|C535900||dmda1
|
|
253700|C535900||duchenne like muscular dystrophy autosomal recessive type 1
|
|
253700|C535900||gamma sarcoglycanopathy
|
|
253700|C535900||lgmd2c
|
|
253700|C535900||limb girdle muscular dystrophy with gamma sarcoglycan deficiency
|
|
253700|C535900||maghrebian myopathy
|
|
253700|C535900||muscular dystrophy duchenne like
|
|
253700|C535900||muscular dystrophy limb girdle type 2c
|
|
253700|C535900||sarcoglycan gamma deficiency of
|
|
253700|C535900||scarmd
|
|
253700|C535900||severe childhood autosomal recessive muscular dystrophy north african type
|
|
C563323|601407||diabetes mellitus noninsulin dependent 2
|
|
C563323|601407||niddm2
|
|
C563323|601407||noninsulin dependent diabetes mellitus 2
|
|
C567468|300718||myopathy reducing body x linked childhood onset
|
|
613435||amyotrophic lateral sclerosis 12
|
|
613435||als12
|
|
D014823||vitreous hemorrhage
|
|
D014823||hemorrhage vitreous
|
|
D014823||vitreous hemorrhages
|
|
613428||retinitis pigmentosa 54
|
|
613428||rp54
|
|
C567737|613116||thrombophilia due to elevated histidine rich glycoprotein
|
|
C567737|613116||thph11
|
|
C567737|613116||thrombophilia due to elevated histidine rich glycoprotein included
|
|
C567737|613116||thrombophilia due to histidine rich glycoprotein deficiency
|
|
D014826||vocal cord paralysis
|
|
D014826||acquired vocal cord palsy
|
|
D014826||bilateral vocal cord paresis
|
|
D014826||congenital vocal cord palsy
|
|
D014826||laryngeal nerve palsy recurrent
|
|
D014826||laryngeal paralyses
|
|
D014826||laryngeal paralysis
|
|
D014826||palsies vocal cord
|
|
D014826||palsies vocal fold
|
|
D014826||palsy vocal cord
|
|
D014826||palsy vocal fold
|
|
D014826||paralyses laryngeal
|
|
D014826||paralyses vocal cord
|
|
D014826||paralysis laryngeal
|
|
D014826||paralysis unilateral vocal cord
|
|
D014826||paralysis vocal cord
|
|
D014826||paralysis vocal cord unilateral
|
|
D014826||pareses vocal cord
|
|
D014826||paresis vocal cord
|
|
D014826||partial paralysis paresis vocal cords
|
|
D014826||recurrent laryngeal nerve palsy
|
|
D014826||total vocal cord paralysis
|
|
D014826||unilateral paralysis vocal cord
|
|
D014826||unilateral vocal cord paralysis
|
|
D014826||unilateral vocal cord paresis
|
|
D014826||vocal cord palsies
|
|
D014826||vocal cord palsy
|
|
D014826||vocal cord palsy congenital
|
|
D014826||vocal cord paralyses
|
|
D014826||vocal cord paralysis unilateral
|
|
D014826||vocal cord pareses
|
|
D014826||vocal cord paresis
|
|
D014826||vocal fold palsies
|
|
D014826||vocal fold palsy
|
|
612577|C567244||amyotrophic lateral sclerosis 11
|
|
612577|C567244||als11
|
|
C562551|127600||dyskeratosis hereditary benign intraepithelial
|
|
C562551|127600||dkbi
|
|
C562551|127600||hbid
|
|
C535729|127400||dyschromatosis symmetrica hereditaria 1
|
|
C535729|127400||dsh
|
|
C535729|127400||dsh1
|
|
C535729|127400||dyschromatosis symmetrica hereditaria
|
|
C535729|127400||familial reticulate acropigmentation of dohi
|
|
C535729|127400||rad
|
|
C535729|127400||reticulate acropigmentation of dohi
|
|
C535729|127400||symmetric dyschromatosis of the extremities
|
|
D057910||implant capsular contracture
|
|
D057910||capsular contracture implant
|
|
D057910||contracture implant capsular
|
|
C536937|181450||ulnar mammary syndrome
|
|
C536937|181450||pallister ulnar mammary syndrome
|
|
C536937|181450||schinzel syndrome
|
|
C536937|181450||ulnar mammary syndrome of pallister
|
|
C536937|181450||ums
|
|
D001523||mental disorders
|
|
D001523||behavior disorders
|
|
D001523||diagnosis psychiatric
|
|
D001523||disorder mental
|
|
D001523||disorders behavior
|
|
D001523||disorders mental
|
|
D001523||mental disorder
|
|
D001523||psychiatric diagnosis
|
|
C536169|112250||diaphyseal medullary stenosis with malignant fibrous histiocytoma
|
|
C536169|112250||bdmf
|
|
C536169|112250||bone dysplasia with malignant fibrous histiocytoma
|
|
C536169|112250||bone dysplasia with medullary fibrosarcoma
|
|
C536169|112250||dmsmfh
|
|
C564953|256730||ceroid lipofuscinosis neuronal 1
|
|
C564953|256730||ceroid lipofuscinosis neuronal 1 variable age at onset
|
|
C564953|256730||ceroid lipofuscinosis neuronal 1 variable age at onset neuronal ceroid lipofuscinosis infantile included
|
|
C564953|256730||cln1
|
|
C564953|256730||incl included
|
|
C564953|256730||santavuori disease included
|
|
C564953|256730||santavuori haltia disease included
|
|
119600|D002973||cleidocranial dysplasia
|
|
119600|D002973||cleidocranial digital dysostoses
|
|
119600|D002973||cleidocranial digital dysostosis
|
|
119600|D002973||cleidocranial dysostoses
|
|
119600|D002973||cleidocranial dysostosis
|
|
119600|D002973||cleidocranial dysostosis clcd cleidocranial dysplasia forme fruste with brachydactyly included
|
|
119600|D002973||cleidocranial dysplasia forme fruste dental anomalies only included
|
|
119600|D002973||cleidocranial dysplasias
|
|
119600|D002973||dysostoses cleidocranial
|
|
119600|D002973||dysostoses cleidocranial digital
|
|
119600|D002973||dysostosis cleidocranial
|
|
119600|D002973||dysostosis cleidocranial digital
|
|
119600|D002973||dysplasia cleidocranial
|
|
119600|D002973||dysplasias cleidocranial
|
|
119600|D002973||marie sainton syndrome
|
|
119600|D002973||scheuthauer marie sainton syndrome
|
|
119600|D002973||syndrome marie sainton
|
|
119600|D002973||syndrome scheuthauer marie sainton
|
|
C563827|608932||keratoconus 2
|
|
C563827|608932||ktcn2
|
|
C566482|610042||cortical dysplasia focal epilepsy syndrome
|
|
C566482|610042||cdfe syndrome pitt hopkins like syndrome 1 included
|
|
C566482|610042||pthsl1 included
|
|
D014832||voice disorders
|
|
D014832||disturbances voice
|
|
D014832||disturbance voice
|
|
D014832||fatigues voice
|
|
D014832||fatigue voice
|
|
D014832||neurologic voice disorder
|
|
D014832||neurologic voice disorders
|
|
D014832||voice disorder
|
|
D014832||voice disorder neurologic
|
|
D014832||voice disorders neurologic
|
|
D014832||voice disturbance
|
|
D014832||voice disturbances
|
|
D014832||voice fatigue
|
|
D014832||voice fatigues
|
|
613418||bone mineral density quantitative trait locus 15
|
|
613418||bmnd15
|
|
613418||compression fracture susceptibility to
|
|
613418||metaphyseal fracture susceptibility to
|
|
613418||osteoporosis susceptibility to
|
|
D014839||vomiting
|
|
D014839||emesis
|
|
C563866|608751||cardiomyopathy familial hypertrophic 8
|
|
C563866|608751||cardiomyopathy hypertrophic mid left ventricular chamber type 1
|
|
C563866|608751||cmh8
|
|
D016649|311360||primary ovarian insufficiency
|
|
D016649|311360||fmr1 related primary ovarian insufficiency
|
|
D016649|311360||fragile x associated primary ovarian insufficiency
|
|
D016649|311360||gonadotropin resistant ovary syndrome
|
|
D016649|311360||hypergonadotropic ovarian failure x linked
|
|
D016649|311360||insufficiency primary ovarian
|
|
D016649|311360||ovarian failure premature
|
|
D016649|311360||ovarian insufficiency primary
|
|
D016649|311360||pof
|
|
D016649|311360||pof1
|
|
D016649|311360||pofx
|
|
D016649|311360||premature ovarian failure
|
|
D016649|311360||premature ovarian failure 1
|
|
D016649|311360||premature ovarian failure x linked
|
|
D016649|311360||resistant ovary syndrome
|
|
D016649|311360||x linked hypergonadotropic ovarian failure
|
|
607541|C535474||corneal dystrophy avellino type
|
|
607541|C535474||acd
|
|
607541|C535474||avellino corneal dystrophy
|
|
607541|C535474||cda
|
|
607541|C535474||cgd2
|
|
607541|C535474||combined granular lattice corneal dystrophies
|
|
607541|C535474||combined granular lattice corneal dystrophy
|
|
607541|C535474||granular and lattice corneal dystrophies
|
|
607541|C535474||granular corneal dystrophy type 2
|
|
607541|C535474||granular corneal dystrophy type ii
|
|
607541|C535474||granular lattice avellino corneal dystrophy
|
|
D057925||femoracetabular impingement
|
|
D057925||femoracetabular impingements
|
|
D057925||femoroacetabular impingement
|
|
D057925||femoro acetabular impingement
|
|
D057925||femoroacetabular impingements
|
|
D057925||femoro acetabular impingements
|
|
D057925||femoroacetabular impingement syndrome
|
|
D057925||femoroacetabular impingement syndromes
|
|
D057925||impingement femoracetabular
|
|
D057925||impingement femoroacetabular
|
|
D057925||impingement femoro acetabular
|
|
D057925||impingements femoracetabular
|
|
D057925||impingements femoroacetabular
|
|
D057925||impingements femoro acetabular
|
|
D057925||impingement syndrome femoroacetabular
|
|
D057925||impingement syndromes femoroacetabular
|
|
D057925||syndrome femoroacetabular impingement
|
|
D057925||syndromes femoroacetabular impingement
|
|
D017086||beta thalassemia
|
|
D017086||anemia cooley
|
|
D017086||anemia cooleys
|
|
D017086||anemia cooley apos s
|
|
D017086||anemia erythroblastic
|
|
D017086||anemia mediterranean
|
|
D017086||anemias erythroblastic
|
|
D017086||anemias mediterranean
|
|
D017086||beta thalassemias
|
|
D017086||beta type microcytemia
|
|
D017086||beta type microcytemias
|
|
D017086||beta type thalassemia
|
|
D017086||beta type thalassemias
|
|
D017086||cooley apos s anemia
|
|
D017086||disease hemoglobin f
|
|
D017086||erythroblastic anemia
|
|
D017086||hemoglobin f disease
|
|
D017086||intermedias thalassemia
|
|
D017086||intermedia thalassemia
|
|
D017086||majors thalassemia beta thalassemia major
|
|
D017086||major thalassemia beta thalassemia major
|
|
D017086||mediterranean anemia
|
|
D017086||mediterranean anemias
|
|
D017086||microcytemia beta type
|
|
D017086||microcytemias beta type
|
|
D017086||minors thalassemia beta thalassemia minor
|
|
D017086||minor thalassemia beta thalassemia minor
|
|
D017086||thalassemia beta
|
|
D017086||thalassemia beta type
|
|
D017086||thalassemia intermedia
|
|
D017086||thalassemia intermedias
|
|
D017086||thalassemia major
|
|
D017086||thalassemia major beta thalassemia major
|
|
D017086||thalassemia majors beta thalassemia major
|
|
D017086||thalassemia minor
|
|
D017086||thalassemia minor beta thalassemia minor
|
|
D017086||thalassemia minors beta thalassemia minor
|
|
D017086||thalassemias beta
|
|
D017086||thalassemias beta type
|
|
D017086||type microcytemia beta
|
|
D017086||type microcytemias beta
|
|
D017086||type thalassemia beta
|
|
D017086||type thalassemias beta
|
|
D002825||chorioretinitis
|
|
D002825||chorioretinitides
|
|
D017088||aids related opportunistic infections
|
|
D017088||aids related opportunistic infection
|
|
D017088||hiv related opportunistic infection
|
|
D017088||hiv related opportunistic infections
|
|
D017088||infection hiv related opportunistic
|
|
D017088||infections hiv related opportunistic
|
|
D017088||opportunistic infection aids related
|
|
D017088||opportunistic infection hiv related
|
|
D017088||opportunistic infections aids related
|
|
D017088||opportunistic infections hiv related
|
|
D002820||hydatidiform mole invasive
|
|
D002820||chorioadenoma
|
|
D002820||chorioadenomas
|
|
D002820||hydatidiform moles invasive
|
|
D002820||invasive hydatidiform mole
|
|
D002820||invasive hydatidiform moles
|
|
D002820||invasive mole
|
|
D002820||invasive moles
|
|
D002820||mole invasive
|
|
D002820||mole invasive hydatidiform
|
|
D002820||moles invasive
|
|
D002820||moles invasive hydatidiform
|
|
C563754|609266||li fraumeni syndrome 3
|
|
C563754|609266||lfs3
|
|
D002821||chorioamnionitis
|
|
D002821||amnionitides
|
|
D002821||amnionitis
|
|
D002821||chorioamnionitides
|
|
D002821||funisitides
|
|
D002821||funisitis
|
|
D002822||choriocarcinoma
|
|
D002822||choriocarcinomas
|
|
C567856|612938||growth retardation developmental delay coarse facies and early death
|
|
C567856|612938||gdfd
|
|
D014808||vitamin d deficiency
|
|
D014808||deficiencies vitamin d
|
|
D014808||deficiency vitamin d
|
|
D014808||vitamin d deficiencies
|
|
277440|C562794||vitamin d dependent rickets type 2a
|
|
277440|C562794||hvdrr
|
|
277440|C562794||pddr iia
|
|
277440|C562794||pseudovitamin d deficiency type iia
|
|
277440|C562794||rickets alopecia syndrome
|
|
277440|C562794||vddr2a
|
|
277440|C562794||vitamin d dependent rickets type 2a with or without alopecia
|
|
D014802||vitamin a deficiency
|
|
D014802||deficiencies vitamin a
|
|
D014802||deficiency vitamin a
|
|
D014802||vitamin a deficiencies
|
|
D014806||vitamin b 12 deficiency
|
|
D014806||deficiencies vitamin b12
|
|
D014806||deficiency vitamin b12
|
|
D014806||deficiency vitamin b 12
|
|
D014806||vitamin b12 deficiencies
|
|
D014806||vitamin b12 deficiency
|
|
D014804||vitamin b deficiency
|
|
D014804||deficiencies vitamin b
|
|
D014804||deficiency vitamin b
|
|
D014804||vitamin b deficiencies
|
|
D002828||choristoma
|
|
D002828||aberrant tissue
|
|
D002828||aberrant tissues
|
|
D002828||choristomas
|
|
D002828||ectopic tissue
|
|
D002828||ectopic tissues
|
|
D002828||heterotopic tissue
|
|
D002828||heterotopic tissues
|
|
D002828||tissue aberrant
|
|
D002828||tissue ectopic
|
|
D002828||tissue heterotopic
|
|
D002828||tissues aberrant
|
|
D002828||tissues ectopic
|
|
D002828||tissues heterotopic
|
|
D017098||iga deficiency
|
|
D017098||deficiencies iga
|
|
D017098||deficiency iga
|
|
D017098||iga deficiencies
|
|
D017099||igg deficiency
|
|
D017099||deficiencies igg
|
|
D017099||deficiency igg
|
|
D017099||igg deficiencies
|
|
C537884|604229||peters anomaly
|
|
601419||myopathy myofibrillar 1
|
|
601419||arrhythmogenic right ventricular cardiomyopathy 7 formerly
|
|
601419||arrhythmogenic right ventricular dysplasia familial 7 formerly
|
|
601419||arvc7 formerly
|
|
601419||arvd7 formerly
|
|
601419||cardiomyopathy dilated 1f and limb girdle muscular dystrophy type 1d formerly
|
|
601419||cardiomyopathy dilated with conduction defect and muscular dystrophy
|
|
601419||cdcd3 formerly
|
|
601419||cmd1f and lgmd1d formerly
|
|
601419||drm
|
|
601419||ibm1 formerly
|
|
601419||inclusion body myopathy 1 autosomal dominant formerly
|
|
601419||mfm1
|
|
D017093||liver failure
|
|
D017093||hepatic failure
|
|
D017094||porphyrias hepatic
|
|
D017094||hepatic porphyria
|
|
D017094||hepatic porphyrias
|
|
D017094||porphyria hepatic
|
|
D002832||choroid hemorrhage
|
|
D002832||choroidal hemorrhage
|
|
D002832||choroidal hemorrhages
|
|
D002832||hemorrhage choroid
|
|
D002832||hemorrhage choroidal
|
|
D002833||choroiditis
|
|
D002833||choroiditides
|
|
D017096||prion diseases
|
|
D017096||dementias transmissible
|
|
D017096||dementia transmissible
|
|
D017096||disorder prion induced
|
|
D017096||disorders prion induced
|
|
D017096||encephalopathies spongiform transmissible
|
|
D017096||encephalopathies transmissible spongiform
|
|
D017096||encephalopathy transmissible spongiform
|
|
D017096||human transmissible spongiform encephalopathies inherited
|
|
D017096||inherited human transmissible spongiform encephalopathies
|
|
D017096||prion associated disorders
|
|
D017096||prion disease
|
|
D017096||prion induced disorder
|
|
D017096||prion induced disorders
|
|
D017096||prion protein disease
|
|
D017096||prion protein diseases
|
|
D017096||spongiform encephalopathies transmissible
|
|
D017096||spongiform encephalopathy transmissible
|
|
D017096||transmissible dementia
|
|
D017096||transmissible dementias
|
|
D017096||transmissible spongiform encephalopathies
|
|
D017096||transmissible spongiform encephalopathy
|
|
D017091||colitis ischemic
|
|
D017091||ischemic colitis
|
|
D002830||choroid neoplasms
|
|
D002830||choroidal neoplasm
|
|
D002830||choroidal neoplasms
|
|
D002830||choroid neoplasm
|
|
D002830||neoplasm choroid
|
|
D002830||neoplasm choroidal
|
|
D002830||neoplasms choroid
|
|
D002830||neoplasms choroidal
|
|
C567426|612076||hypouricemia renal 2
|
|
C567426|612076||gout2 included
|
|
C567426|612076||gout susceptibility 2 included
|
|
C567426|612076||rhuc2
|
|
C567426|612076||uaqtl2 included
|
|
C567426|612076||uric acid concentration serum quantitative trait locus 2 included
|
|
C567233|612622||diabetes mellitus insulin dependent 23
|
|
C567233|612622||iddm23
|
|
C565776|604400||arrhythmogenic right ventricular dysplasia familial 5
|
|
C565776|604400||arrhythmogenic right ventricular cardiomyopathy 5
|
|
C565776|604400||arvc5
|
|
C565776|604400||arvd5
|
|
613402||epileptic encephalopathy early infantile 10
|
|
613402||eiee10
|
|
613402||mcsz
|
|
613402||microcephaly seizures and developmental delay
|
|
C562937|146000||hypochondroplasia
|
|
C562937|146000||hch
|
|
C562937|146000||hypochondrodysplasia
|
|
146820||immune response to synthetic polypeptide irgat
|
|
146820||igat
|
|
D014813||vitamin k deficiency
|
|
D014813||deficiencies vitamin k
|
|
D014813||deficiency vitamin k
|
|
D014813||vitamin k deficiencies
|
|
D014811||vitamin e deficiency
|
|
D014811||deficiencies vitamin e
|
|
D014811||deficiency vitamin e
|
|
D014811||vitamin e deficiencies
|
|
C537202|608703||spinocerebellar ataxia 25
|
|
C537202|608703||sca25
|
|
C537202|608703||spinocerebellar ataxia type 25
|
|
C537493|604841||stickler syndrome type 2
|
|
C537493|604841||stickler syndrome beaded vitreous type
|
|
C537493|604841||stickler syndrome type ii
|
|
C537493|604841||stickler syndrome vitreous type 2
|
|
C537493|604841||stl2
|
|
D002804||chondroblastoma
|
|
D002804||chondroblastomas
|
|
D002805||chondrocalcinosis
|
|
D002805||calcium pyrophosphate dihydrate deposition
|
|
D002805||chondrocalcinoses
|
|
D002805||pseudogout
|
|
C565322|605549||cone rod dystrophy 8
|
|
C565322|605549||cord8
|
|
C566383|603383||glaucoma 1 open angle f
|
|
C566383|603383||glc1f
|
|
270200|D016111||sjogren larsson syndrome
|
|
270200|D016111||congenital icthyosis mental retardation spasticity syndrome
|
|
270200|D016111||faldh deficiency
|
|
270200|D016111||fatty alcohol nad oxidoreductase deficiency
|
|
270200|D016111||fatty aldehyde dehydrogenase deficiency
|
|
270200|D016111||fatty aldehyde dehydrogenase deficiency disease
|
|
270200|D016111||ichthyosis oligophrenia syndrome
|
|
270200|D016111||ichthyosis spastic neurologic disorder and oligophrenia
|
|
270200|D016111||sj 246 gren larsson syndrome
|
|
270200|D016111||sls
|
|
C536119|607625||niemann pick disease type c2
|
|
C536119|607625||npc2
|
|
D005084||exhibitionism
|
|
D005084||exhibitionisms
|
|
305390||exudative vitreoretinopathy 2 x linked
|
|
305390||evr2
|
|
305390||evrx
|
|
305390||fevrx
|
|
C537833|153870||macular dystrophy concentric annular
|
|
C537833|153870||bcamd
|
|
C537833|153870||macular dystrophy benign concentric annular
|
|
C537833|153870||maculopathy bull apos s eye
|
|
C537833|153870||mcdca
|
|
D056627||peritoneal fibrosis
|
|
D056627||encapsulating peritoneal scleroses
|
|
D056627||encapsulating peritoneal sclerosis
|
|
D056627||fibroses peritoneal
|
|
D056627||fibrosing syndrome peritoneal
|
|
D056627||fibrosing syndromes peritoneal
|
|
D056627||fibrosis peritoneal
|
|
D056627||peritoneal fibroses
|
|
D056627||peritoneal fibrosing syndrome
|
|
D056627||peritoneal fibrosing syndromes
|
|
D056627||peritoneal scleroses
|
|
D056627||peritoneal scleroses encapsulating
|
|
D056627||peritoneal sclerosis
|
|
D056627||peritoneal sclerosis encapsulating
|
|
D056627||scleroses encapsulating peritoneal
|
|
D056627||scleroses peritoneal
|
|
D056627||sclerosis encapsulating peritoneal
|
|
D056627||sclerosis peritoneal
|
|
D056627||syndrome peritoneal fibrosing
|
|
D056627||syndromes peritoneal fibrosing
|
|
C567678|613267||corneal dystrophy fuchs endothelial 3
|
|
C567678|613267||fcd2 locus
|
|
C567678|613267||fecd3
|
|
D002806||chondrodysplasia punctata
|
|
D002806||chondrodysplasia punctata 2 x linked
|
|
D002806||chondrodystrophia calcificans congenita
|
|
D002806||conradi h 252 nermann happle syndrome
|
|
D002806||conradi hunermann happle syndromes
|
|
D002806||conradi h 252 nermann happle syndromes
|
|
D002806||conradi h 252 nermann syndrome
|
|
D002806||conradi h 252 nermann syndromes
|
|
D002806||dysplasia epiphysialis punctata
|
|
D002806||epiphyses stippled
|
|
D002806||hunermann conradi syndrome
|
|
D002806||stippled epiphyses
|
|
D002806||syndrome conradi hunermann
|
|
D002806||syndrome conradi h 252 nermann
|
|
D002806||syndrome conradi hunermann happle
|
|
D002806||syndrome conradi h 252 nermann happle
|
|
D002806||syndrome happle
|
|
D002806||syndrome hunermann conradi
|
|
D002806||syndromes conradi h 252 nermann
|
|
D002806||syndromes conradi hunermann happle
|
|
D002806||syndromes conradi h 252 nermann happle
|
|
D002806||x linked chondrodysplasia punctata 2
|
|
D002806||x linked dominant chondrodysplasia punctata
|
|
D031368||zoster sine herpete
|
|
D031368||zoster sine eruptione
|
|
257270|613216||csnb complete autosomal recessive
|
|
D001145|115000||arrhythmias cardiac
|
|
D001145|115000||arrhythmia
|
|
D001145|115000||arrhythmia cardiac
|
|
D001145|115000||arrythmia
|
|
D001145|115000||cardiac arrhythmia
|
|
D001145|115000||cardiac arrhythmias
|
|
D001145|115000||cardiac dysrhythmia
|
|
D001145|115000||dysrhythmia cardiac
|
|
D001145|115000|D005117||extrasystoles
|
|
D002812||chondroma
|
|
D002812||chondromas
|
|
D002812||enchondroma
|
|
D002812||enchondromas
|
|
C563177|103900||glucocorticoid remediable aldosteronism
|
|
C563177|103900||acth dependent hyperaldosteronism syndrome
|
|
C563177|103900||aldosteronism sensitive to dexamethasone
|
|
C563177|103900||fh i
|
|
C563177|103900||glucocorticoid suppressible hyperaldosteronism
|
|
C563177|103900||gra
|
|
C563177|103900||gsh
|
|
C563177|103900||hyperaldosteronism familial type i
|
|
C566913|611572||otosclerosis 7
|
|
C566913|611572||otsc7
|
|
182940|D009436||neural tube defects
|
|
182940|D009436||acrania
|
|
182940|D009436||acranias
|
|
182940|D009436||craniorachischises
|
|
182940|D009436||craniorachischisis
|
|
182940|D009436||cyst neurenteric
|
|
182940|D009436||cyst neuroenteric
|
|
182940|D009436||cysts neurenteric
|
|
182940|D009436||cysts neuroenteric
|
|
182940|D009436||defect neural tube
|
|
182940|D009436||defects neural tube
|
|
182940|D009436||developmental defects neural tube
|
|
182940|D009436||developmental neural tube defects
|
|
182940|D009436||diastematomyelia
|
|
182940|D009436||diastematomyelias
|
|
182940|D009436||dysraphism occult spinal
|
|
182940|D009436||dysraphisms occult spinal
|
|
182940|D009436||exencephalies
|
|
182940|D009436||exencephaly
|
|
182940|D009436||iniencephalies
|
|
182940|D009436||iniencephaly
|
|
182940|D009436||myelodysplasia spinal cord
|
|
182940|D009436||myelodysplasias spinal cord
|
|
182940|D009436||neural tube defect
|
|
182940|D009436||neural tube developmental defects
|
|
182940|D009436||neurenteric cyst
|
|
182940|D009436||neurenteric cysts
|
|
182940|D009436||neuroenteric cyst
|
|
182940|D009436||neuroenteric cysts
|
|
182940|D009436||ntd spina bifida included
|
|
182940|D009436||occult spinal dysraphism
|
|
182940|D009436||occult spinal dysraphisms
|
|
182940|D009436||occult spinal dysraphism sequence
|
|
182940|D009436||spinal cord myelodysplasia
|
|
182940|D009436||spinal cord myelodysplasias
|
|
182940|D009436||spinal dysraphism occult
|
|
182940|D009436||spinal dysraphisms occult
|
|
182940|D009436||tethered cord syndrome
|
|
182940|D009436||tethered cord syndromes
|
|
182940|D009436||tethered spinal cord syndrome
|
|
D005097||exostoses multiple hereditary
|
|
D005097||aclases diaphyseal
|
|
D005097||aclasis diaphyseal
|
|
D005097||bessel hagen disease
|
|
D005097||cartilaginous exostoses multiple
|
|
D005097||cartilaginous exostosis multiple
|
|
D005097||chondrodysplasia hereditary deforming
|
|
D005097||chondrodysplasias hereditary deforming
|
|
D005097||deforming chondrodysplasia hereditary
|
|
D005097||deforming chondrodysplasias hereditary
|
|
D005097||diaphyseal aclases
|
|
D005097|133700||diaphyseal aclasis
|
|
D005097||exostoses familial
|
|
D005097||exostoses hereditary multiple
|
|
D005097||exostoses multiple
|
|
D005097||exostoses multiple cartilaginous
|
|
D005097|133700||exostoses multiple type i
|
|
D005097||exostosis familial
|
|
D005097||exostosis hereditary multiple
|
|
D005097||exostosis multiple
|
|
D005097||exostosis multiple cartilaginous
|
|
D005097||familial exostoses
|
|
D005097||familial exostosis
|
|
D005097||hereditary deforming chondrodysplasia
|
|
D005097||hereditary deforming chondrodysplasias
|
|
D005097||hereditary exostoses multiple
|
|
D005097||hereditary multiple exostoses
|
|
D005097||hereditary multiple exostosis
|
|
D005097|133700||multiple cartilaginous exostoses
|
|
D005097||multiple cartilaginous exostosis
|
|
D005097||multiple exostoses
|
|
D005097||multiple exostoses hereditary
|
|
D005097||multiple exostosis
|
|
D005097||multiple exostosis hereditary
|
|
D005097||multiple hereditary exostoses
|
|
D005097||multiple osteochondroma
|
|
D005097|133700||multiple osteochondromas
|
|
D005097||multiple osteochondromatosis
|
|
D005097||osteochondroma multiple
|
|
D005097||osteochondromas multiple
|
|
D005096||exostoses
|
|
D005096||exostosis
|
|
D005099||exotropia
|
|
D005099||alternating exotropia
|
|
D005099||divergent strabismus
|
|
D005099||exodeviation
|
|
D005099||exodeviations
|
|
D005099||exophoria
|
|
D005099||exotropia alternating
|
|
D005099||exotropia monocular
|
|
D005099||exotropia primary
|
|
D005099||exotropia secondary
|
|
D005099||monocular exotropia
|
|
D005099||primary exotropia
|
|
D005099||secondary exotropia
|
|
D005099||strabismus divergent
|
|
D005094||exophthalmos
|
|
D005094||proptoses
|
|
D005094||proptosis
|
|
C567646|613318||miyoshi muscular dystrophy 2
|
|
C567646|613318||miyoshi myopathy 2
|
|
C567646|613318||mmd2
|
|
D018497||ventricular dysfunction right
|
|
D018497||dysfunction right ventricular
|
|
D018497||dysfunctions right ventricular
|
|
D018497||right ventricular dysfunction
|
|
D018497||right ventricular dysfunctions
|
|
D018497||ventricular dysfunctions right
|
|
D018496||hyperoxia
|
|
D018496||hyperoxias
|
|
C562385|206200||iron refractory iron deficiency anemia
|
|
C562385|206200||anemia hypochromic microcytic with defect in iron metabolism
|
|
C562385|206200||irida
|
|
C562385|206200||iron handling disorder hereditary
|
|
C562385|206200||pseudo iron deficiency anemia
|
|
D005177||factor xiii deficiency
|
|
D005177||deficiencies factor xiii
|
|
D005177||deficiency factor xiii
|
|
D005177||factor xiii deficiencies
|
|
300419|C563150||mental retardation x linked with or without seizures arx related
|
|
300419|C563150||mental retardation x linked 29
|
|
300419|C563150||mental retardation x linked 32
|
|
300419|C563150||mental retardation x linked 33
|
|
300419|C563150||mental retardation x linked 38
|
|
300419|C563150||mental retardation x linked 43
|
|
300419|C563150||mental retardation x linked 54
|
|
300419|C563150||mental retardation x linked 76
|
|
300419|C563150||mental retardation x linked 87
|
|
300419|C563150||mrx29
|
|
300419|C563150||mrx32
|
|
300419|C563150||mrx33
|
|
300419|C563150||mrx38
|
|
300419|C563150||mrx43
|
|
300419|C563150||mrx54
|
|
300419|C563150||mrx76
|
|
300419|C563150||mrx87
|
|
300419|C563150||mrxarx
|
|
D005185||fallopian tube neoplasms
|
|
D005185||cancer fallopian tube
|
|
D005185||cancer of the fallopian tube
|
|
D005185||cancers fallopian tube
|
|
D005185||fallopian tube cancer
|
|
D005185||fallopian tube cancers
|
|
D005185||fallopian tube neoplasm
|
|
D005185||neoplasm fallopian tube
|
|
D005185||neoplasms fallopian tube
|
|
D005184||fallopian tube diseases
|
|
D005184||disease fallopian tube
|
|
D005184||diseases fallopian tube
|
|
D005184||fallopian tube disease
|
|
D005184||obstructions tubal
|
|
D005184||obstruction tubal
|
|
D005184||tubal obstruction
|
|
D005184||tubal obstructions
|
|
D005183||failure to thrive
|
|
D005183||thrive failure to
|
|
D018488||bone demineralization pathologic
|
|
D018488||pathologic bone demineralization
|
|
C563478|166990||osteochondrodysplasia rhizomelic with callosal agenesis thrombocytopenia hydrocephalus and hypertension
|
|
D018487||ventricular dysfunction left
|
|
D018487||dysfunction left ventricular
|
|
D018487||dysfunctions left ventricular
|
|
D018487||left ventricular dysfunction
|
|
D018487||left ventricular dysfunctions
|
|
D018487||ventricular dysfunctions left
|
|
D018489||space motion sickness
|
|
D018489||adaptation syndrome space
|
|
D018489||motion sickness space
|
|
D018489||space adaptation syndrome
|
|
D018489||syndrome space adaptation
|
|
D002908||chronic disease
|
|
D002908||chronically ill
|
|
D002908||chronic diseases
|
|
D002908||chronic illness
|
|
D002908||chronic illnesses
|
|
D002908||disease chronic
|
|
D002908||diseases chronic
|
|
D002908||illness chronic
|
|
D002908||illnesses chronic
|
|
D002915||chylous ascites
|
|
D002915||ascites chylous
|
|
D002915||chyloperitoneum
|
|
D002915||chylous peritonitis
|
|
D002915||peritonitis chylous
|
|
C563362|607801||muscular dystrophy limb girdle type 1c
|
|
C563362|607801||lgmd1c
|
|
C565218|609823||deafness autosomal recessive 28
|
|
C565218|609823||dfnb28
|
|
612075||mitochondrial dna depletion syndrome 8a encephalomyopathic type with renal tubulopathy
|
|
612075||mitochondrial dna depletion syndrome encephalomyopathic with renal tubulopathy autosomal recessive mitochondrial dna depletion syndrome 8b mngie type included
|
|
612075||mitochondrial neurogastrointestinal encephalopathy syndrome rrm2b related included
|
|
612075||mngie rrm2b related included
|
|
612075||mtdp8b included
|
|
612075||mtdps8a
|
|
C565423|248190||hypomagnesemia 5 renal with ocular involvement
|
|
C565423|248190||fhhnc with severe ocular involvement
|
|
C565423|248190||homg5
|
|
C565423|248190||hypomagnesemia familial with hypercalciuria nephrocalcinosis and severe ocular involvement
|
|
C565423|248190||hypomagnesemia renal with ocular involvement
|
|
C565423|248190||macular coloboma bilateral with hypercalciuria
|
|
612073||mitochondrial dna depletion syndrome 5 encephalomyopathic with or without methylmalonic aciduria
|
|
612073||mitochondrial dna depletion syndrome encephalomyopathic form with or without methylmalonic aciduria autosomal recessive sucla2 related
|
|
612073||mtdps5
|
|
239510|C538385||hyperprolinemia type 2
|
|
239510|C538385||1 alpha pyrroline 5 carboxylate dehydrogenase deficiency
|
|
239510|C538385||1 pyrroline 5 carboxylate dehydrogenase deficiency
|
|
239510|C538385||hpii
|
|
239510|C538385||hyperprolinemia type ii
|
|
239510|C538385||type 2 hyperprolinemia
|
|
D002916||chylothorax
|
|
D054119||arachnodactyly
|
|
D054119||arachnodactylies
|
|
D017169||neoplasms post traumatic
|
|
D017169||cancer post traumatic
|
|
D017169||cancers post traumatic
|
|
D017169||malignancies post traumatic
|
|
D017169||malignancy post traumatic
|
|
D017169||neoplasm post traumatic
|
|
D017169||post traumatic cancer
|
|
D017169||post traumatic cancers
|
|
D017169||post traumatic malignancies
|
|
D017169||post traumatic malignancy
|
|
D017169||post traumatic neoplasm
|
|
D017169||post traumatic neoplasms
|
|
D020792||salivary calculi
|
|
D020792||calculi salivary
|
|
D020792||calculus salivary
|
|
D020792||salivary calculus
|
|
300376|D020388||muscular dystrophy duchenne
|
|
300376|D020388||becker muscular dystrophy
|
|
300376|D020388||becker apos s muscular dystrophy
|
|
300376|D020388||childhood muscular dystrophy pseudohypertrophic
|
|
300376|D020388||childhood pseudohypertrophic muscular dystrophy
|
|
300376|D020388||dmd
|
|
300376|D020388||duchenne and becker muscular dystrophy
|
|
300376|D020388||duchenne becker muscular dystrophy
|
|
300376|D020388||duchenne muscular dystrophy
|
|
300376|D020388||duchenne type progressive muscular dystrophy
|
|
300376|D020388||muscular dystrophy becker
|
|
300376|D020388||muscular dystrophy becker apos s
|
|
300376|D020388||muscular dystrophy becker type
|
|
300376|D020388||muscular dystrophy childhood pseudohypertrophic
|
|
300376|D020388||muscular dystrophy duchenne and becker types
|
|
300376|D020388||muscular dystrophy duchenne becker
|
|
300376|D020388||muscular dystrophy pseudohypertrophic
|
|
300376|D020388||muscular dystrophy pseudohypertrophic childhood
|
|
300376|D020388||muscular dystrophy pseudohypertrophic progressive becker type
|
|
300376|D020388||progressive muscular dystrophy duchenne type
|
|
300376|D020388||pseudohypertrophic childhood muscular dystrophy
|
|
300376|D020388||pseudohypertrophic muscular dystrophy
|
|
300376|D020388||pseudohypertrophic muscular dystrophy childhood
|
|
613390||fanconi anemia complementation group o
|
|
613390||fanco
|
|
205400|D013631||tangier disease
|
|
205400|D013631||a alphalipoprotein neuropathies
|
|
205400|D013631||a alphalipoprotein neuropathy
|
|
205400|D013631||alpha high density lipoprotein deficiency disease
|
|
205400|D013631||analphalipoproteinemia
|
|
205400|D013631||analphalipoproteinemias
|
|
205400|D013631||cholesterol thesaurismoses
|
|
205400|D013631||cholesterol thesaurismosis
|
|
205400|D013631||hdldt1
|
|
205400|D013631||high density lipoprotein deficiency tangier type
|
|
205400|D013631||high density lipoprotein deficiency type 1
|
|
205400|D013631||high density lipoprotein deficiency type i
|
|
205400|D013631||neuropathies a alphalipoprotein
|
|
205400|D013631||neuropathy a alphalipoprotein
|
|
205400|D013631||neuropathy of tangier disease
|
|
205400|D013631||tangier disease neuropathy
|
|
205400|D013631||tangier hereditary neuropathy
|
|
205400|D013631||tgd
|
|
205400|D013631||thesaurismoses cholesterol
|
|
205400|D013631||thesaurismosis cholesterol
|
|
613391||deafness autosomal recessive 84a
|
|
613391||deafness autosomal recessive 84
|
|
613391||deafness autosomal recessive 84a with vestibular dysfunction
|
|
613391||dfnb84
|
|
613391||dfnb84a
|
|
210900|D001816||bloom syndrome
|
|
210900|D001816||blm
|
|
210900|D001816||bloom apos s syndrome
|
|
210900|D001816||bloom torre machacek syndrome
|
|
210900|D001816||bs
|
|
210900|D001816||congenital telangiectatic erythema
|
|
210900|D001816||syndrome bloom
|
|
210900|D001816||syndrome bloom torre machacek
|
|
613392||deafness autosomal recessive 85
|
|
613392||dfnb85
|
|
612522|C567284||diabetes mellitus insulin dependent 22
|
|
612522|C567284||iddm22
|
|
613398||warsaw breakage syndrome
|
|
613398||wabs
|
|
C565335|605373||paragangliomas 3
|
|
C565335|605373||glomus tumors familial 3
|
|
C565335|605373||pgl3
|
|
613399||breast ovarian cancer familial susceptibility to 3
|
|
613399||breast cancer familial susceptibility to 3 included
|
|
613399||brovca3
|
|
613399||ovarian cancer familial susceptibility to 3 included
|
|
C536871|270800||spastic paraplegia type 5a recessive
|
|
C536871|270800||autosomal recessive spastic paraplegia
|
|
C536871|270800|C564811||spastic paraplegia 5a autosomal recessive
|
|
C536871|270800||spg5a
|
|
D005156||facial neuralgia
|
|
D005156||craniofacial pain syndrome
|
|
D005156||craniofacial pain syndromes
|
|
D005156||facial neuralgias
|
|
D005156||facial pain syndrome
|
|
D005156||facial pain syndromes
|
|
D005156||myofacial pain syndrome
|
|
D005156||myofacial pain syndromes
|
|
D005156||neuralgia facial
|
|
D005156||neuralgias facial
|
|
D005156||neuralgia sphenopalatine
|
|
D005156||neuralgias sphenopalatine
|
|
D005156||pain syndrome craniofacial
|
|
D005156||pain syndrome facial
|
|
D005156||pain syndrome myofacial
|
|
D005156||pain syndromes craniofacial
|
|
D005156||pain syndromes facial
|
|
D005156||pain syndromes myofacial
|
|
D005156||sphenopalatine neuralgia
|
|
D005156||sphenopalatine neuralgias
|
|
D005156||syndrome craniofacial pain
|
|
D005156||syndrome facial pain
|
|
D005156||syndrome myofacial pain
|
|
D005156||syndromes craniofacial pain
|
|
D005156||syndromes facial pain
|
|
D005156||syndromes myofacial pain
|
|
D005155||facial nerve diseases
|
|
D005155||acquired facial neuropathies
|
|
D005155||acquired facial neuropathy
|
|
D005155||cranial nerve vii diseases
|
|
D005155||cranial nerve vii disorders
|
|
D005155||disease facial nerve
|
|
D005155||diseases facial nerve
|
|
D005155||disorder facial nerve
|
|
D005155||disorders facial nerve
|
|
D005155||facial myokymia
|
|
D005155||facial myokymias
|
|
D005155||facial nerve disease
|
|
D005155||facial nerve disorder
|
|
D005155||facial nerve disorders
|
|
D005155||facial nerve motor disorders
|
|
D005155||facial nerve sensory disorders
|
|
D005155||facial neuritides
|
|
D005155||facial neuritis
|
|
D005155||facial neuropathies
|
|
D005155||facial neuropathies acquired
|
|
D005155||facial neuropathies familial
|
|
D005155||facial neuropathy
|
|
D005155||facial neuropathy acquired
|
|
D005155||facial neuropathy familial
|
|
D005155||familial facial neuropathies
|
|
D005155||familial facial neuropathy
|
|
D005155||ganglionitides geniculate
|
|
D005155||ganglionitis geniculate
|
|
D005155||geniculate ganglionitides
|
|
D005155||geniculate ganglionitis
|
|
D005155||motor disorders facial nerve
|
|
D005155||myokymia facial
|
|
D005155||myokymias facial
|
|
D005155||neuritides facial
|
|
D005155||neuritis facial
|
|
D005155||neuropathies facial
|
|
D005155||neuropathies familial facial
|
|
D005155||neuropathy facial
|
|
D005155||neuropathy familial facial
|
|
D005155||sensory disorders facial nerve
|
|
D005155||seventh cranial nerve diseases
|
|
D006486||hemosiderosis
|
|
D006486||hemosideroses
|
|
601764|D020936||epilepsy benign neonatal
|
|
601764|D020936||benign familial infantile convulsions
|
|
601764|D020936||benign familial infantile convulsions syndrome
|
|
601764|D020936||benign familial neonatal convulsions
|
|
601764|D020936||benign familial neonatal epilepsy
|
|
601764|D020936||benign familial neonatal infantile seizures
|
|
601764|D020936||benign infantile familial convulsions
|
|
601764|D020936||benign neonatal convulsion
|
|
601764|D020936||benign neonatal convulsions
|
|
601764|D020936||benign neonatal epilepsies
|
|
601764|D020936||benign neonatal epilepsy
|
|
601764|D020936||benign neonatal epilepsy nonfamilial
|
|
601764|D020936||benign neonatal infantile epilepsies
|
|
601764|D020936||benign neonatal infantile epilepsy
|
|
601764|D020936||benign neonatal non familial convulsions
|
|
601764|D020936||benign neonatal nonfamilial epilepsy
|
|
601764|D020936||benign non familial neonatal convulsions
|
|
601764|D020936||bfic1
|
|
601764|D020936||bfis1
|
|
601764|D020936||convulsion benign neonatal
|
|
601764|D020936||convulsions benign familial infantile 1
|
|
601764|D020936||convulsions benign familial neonatal
|
|
601764|D020936||convulsions benign neonatal
|
|
601764|D020936||convulsions benign neonatal familial
|
|
601764|D020936||convulsions benign neonatal non familial
|
|
601764|D020936||epilepsies benign neonatal
|
|
601764|D020936||epilepsies benign neonatal infantile
|
|
601764|D020936||epilepsy benign neonatal familial
|
|
601764|D020936||epilepsy benign neonatal infantile
|
|
601764|D020936||epilepsy benign neonatal nonfamilial
|
|
601764|D020936||epilepsy benign neonatal non familial
|
|
601764|D020936||familial benign neonatal convulsions
|
|
601764|D020936||familial benign neonatal epilepsy
|
|
601764|D020936||neonatal convulsion benign
|
|
601764|D020936||neonatal convulsions benign
|
|
601764|D020936||neonatal epilepsies benign
|
|
601764|D020936||neonatal epilepsy benign
|
|
601764|D020936||neonatal infantile epilepsies benign
|
|
601764|D020936||neonatal infantile epilepsy benign
|
|
601764|D020936||non familial benign neonatal convulsions
|
|
601764|D020936||non familial benign neonatal epilepsy
|
|
601764|D020936||seizures benign familial infantile 1
|
|
D020795||photophobia
|
|
D020795||light sensitivities
|
|
D020795||light sensitivity
|
|
D020795||photophobias
|
|
D020795||sensitivities light
|
|
D020795||sensitivity light
|
|
D005158||facial paralysis
|
|
D005158||central facial paralyses
|
|
D005158||central facial paralysis
|
|
D005158||facial palsies
|
|
D005158||facial palsy
|
|
D005158||facial palsy lower motor neuron
|
|
D005158||facial palsy upper motor neuron
|
|
D005158||facial paralyses central
|
|
D005158||facial paralyses peripheral
|
|
D005158||facial paralysis central
|
|
D005158||facial paralysis peripheral
|
|
D005158||facial paresis
|
|
D005158||hemifacial paralysis
|
|
D005158||lower motor neuron facial palsy
|
|
D005158||palsies facial
|
|
D005158||palsy facial
|
|
D005158||paralyses central facial
|
|
D005158||paralyses facial
|
|
D005158||paralyses hemifacial
|
|
D005158||paralysis central facial
|
|
D005158||paralysis facial
|
|
D005158||paralysis hemifacial
|
|
D005158||paralysis peripheral facial
|
|
D005158||pareses facial
|
|
D005158||paresis facial
|
|
D005158||peripheral facial paralysis
|
|
D005158||upper motor neuron facial palsy
|
|
D005157||facial pain
|
|
D005157||craniofacial pain
|
|
D005157||face pain
|
|
D005157||facial pain neuralgic
|
|
D005157||myofacial pain
|
|
D005157||neuralgic facial pain
|
|
D005157||orofacial pain
|
|
D005157||pain craniofacial
|
|
D005157||pain face
|
|
D005157||pain facial
|
|
D005157||pain myofacial
|
|
D005157||pain neuralgic facial
|
|
D005157||pain orofacial
|
|
D005162||factitious disorders
|
|
D005162||disorders factitious
|
|
D005162||ganser syndrome
|
|
D005162||pseudodementia
|
|
D005162||pseudopsychosis
|
|
D005162||syndrome ganser
|
|
D056784||leukoencephalopathies
|
|
D056784||cach syndrome
|
|
D056784||cach syndromes
|
|
D056784||cach vwm syndrome
|
|
D056784||cach vwm syndromes
|
|
D056784||centralis diffusa myelinosis
|
|
D056784||centralis diffusas myelinosis
|
|
D056784||childhood ataxia with central nervous system hypomyelination
|
|
D056784|C565836|603896||childhood ataxia with central nervous system hypomyelinization
|
|
D056784||childhood ataxia with diffuse central nervous system hypomyelination
|
|
D056784||cree leukoencephalopathies
|
|
D056784||cree leukoencephalopathy
|
|
D056784||diffusa myelinosis centralis
|
|
D056784||diffusas myelinosis centralis
|
|
D056784||diseases white matter
|
|
D056784||disease white matter
|
|
D056784||leukoencephalopathies cree
|
|
D056784||leukoencephalopathy
|
|
D056784||leukoencephalopathy cree
|
|
D056784|C565836|603896||leukoencephalopathy with vanishing white matter
|
|
D056784||myelinosis centralis diffusa
|
|
D056784||myelinosis centralis diffusas
|
|
D056784||syndrome cach
|
|
D056784||syndrome cach vwm
|
|
D056784||syndromes cach
|
|
D056784||syndromes cach vwm
|
|
D056784|C565836|603896||vanishing white matter leukodystrophy
|
|
D056784||white matter disease
|
|
D056784||white matter diseases
|
|
D006491||hemothorax
|
|
C565216|610234||synpolydactyly 3
|
|
C565216|610234||spd3
|
|
C536275|213600||idiopathic basal ganglia calcification 1
|
|
C536275|213600||adult onset idiopathic nonarteriosclerotic cerebral calcification
|
|
C536275|213600||basal ganglia calcification idiopathic 1
|
|
C536275|213600||basal ganglia calcification idiopathic 3 formerly
|
|
C536275|213600||bilateral striopallidodentate calcinosis
|
|
C536275|213600||bspdc
|
|
C536275|213600||cerebral calcification nonarteriosclerotic idiopathic adult onset
|
|
C536275|213600||cerebrovascular ferrocalcinosis
|
|
C536275|213600||fahr disease familial formerly
|
|
C536275|213600||familial idiopathic basal ganglia calcification
|
|
C536275|213600||ferrocalcinosis cerebrovascular
|
|
C536275|213600||fibgc
|
|
C536275|213600||ibgc1
|
|
C536275|213600||ibgc3 formerly
|
|
C536275|213600||striopallidodentate calcinosis
|
|
C536275|213600||striopallidodentate calcinosis autosomal dominant adult onset
|
|
C536275|213600||striopallidodentate calcinosis bilateral
|
|
101400|101200|D000168||saethre chotzen syndrome
|
|
101400||scs acrocephalosyndactyly type iii
|
|
101400|101200|D000168||acs3
|
|
101400|101200|D000168||acs iii
|
|
101400|101200|D000168||chotzen syndrome
|
|
101400|101200|D000168||acrocephaly skull asymmetry and mild syndactyly saethre chotzen syndrome with eyelid anomalies included
|
|
101400||blepharophimosis epicanthus inversus and ptosis 3 formerly included
|
|
101400||bpes3 formerly included
|
|
C565759|604571||bare lymphocyte syndrome type i
|
|
C565759|604571||bls type i
|
|
C565759|604571||hla class i deficiency
|
|
D018467||positive pressure respiration intrinsic
|
|
D018467||autopeep
|
|
D018467||auto peep
|
|
D018467||intrinsic peep
|
|
D018467||intrinsic positive pressure respiration
|
|
D018467||nontherapeutic positive pressure respiration
|
|
D018467||non therapeutic positive pressure respiration
|
|
D018467||occult peep
|
|
D018467||occult positive pressure respiration
|
|
D018467||peep intrinsic
|
|
D018467||peep occult
|
|
D018467||positive pressure respiration nontherapeutic
|
|
D018467||positive pressure respiration non therapeutic
|
|
D018467||positive pressure respiration occult
|
|
D018467||respiration intrinsic positive pressure
|
|
D018467||respiration nontherapeutic positive pressure
|
|
D018467||respiration non therapeutic positive pressure
|
|
D018467||respiration occult positive pressure
|
|
C562583|300323||gout hprt related
|
|
C562583|300323||hprt1 deficiency partial
|
|
C562583|300323||hprt deficiency partial
|
|
C562583|300323||hypoxanthine guanine phosphoribosyltransferase 1 deficiency partial
|
|
C562583|300323||kelley seegmiller syndrome
|
|
613382||brachydactyly type e2
|
|
613382||bde2
|
|
147050|C564133||ige responsiveness atopic
|
|
147050|C564133||atopic hypersensitivity included
|
|
147050|C564133||atopy susceptibility to included
|
|
147050|C564133||igel
|
|
147050|C564133||ige level of
|
|
147050|C564133||iger
|
|
147050|C564133||ige response underlying allergic asthma and rhinitis
|
|
147050|C564133||ige response underlying allergic asthma and rhinitis ige elevated level of included
|
|
147050|C564133||immunoglobulin e basic level of in serum
|
|
613385||autoimmune disease syndromic multisystem
|
|
D020787||central nervous system venous angioma
|
|
D020787||angioma cerebral venous
|
|
D020787||angioma intracranial venous
|
|
D020787||angiomas cerebral venous
|
|
D020787||angiomas intracranial venous
|
|
D020787||angioma venous central nervous system
|
|
D020787||cerebral venous angioma
|
|
D020787||cerebral venous angiomas
|
|
D020787||intracranial venous angioma
|
|
D020787||intracranial venous angiomas
|
|
D020787||venous angioma central nervous system
|
|
D020787||venous angioma cerebral
|
|
D020787||venous angioma intracranial
|
|
D020787||venous angiomas cerebral
|
|
D020787||venous angiomas intracranial
|
|
D020785||central nervous system vascular malformations
|
|
D020785||arteriovenous fistula dural
|
|
D020785||arteriovenous fistulas dural
|
|
D020785||brain capillary telangiectasia
|
|
D020785||brain capillary telangiectasias
|
|
D020785||brain vascular malformation
|
|
D020785||brain vascular malformations
|
|
D020785||capillary telangiectasia brain
|
|
D020785||capillary telangiectasia pontine
|
|
D020785||capillary telangiectasias brain
|
|
D020785||capillary telangiectasias pontine
|
|
D020785||central nervous system congenital vascular malformations
|
|
D020785||central nervous system vascular anomalies
|
|
D020785||cerebral embryonic artery persistent
|
|
D020785||congenital vascular malformations central nevous system
|
|
D020785||dural arteriovenous fistula
|
|
D020785||dural arteriovenous fistulas
|
|
D020785||embryonic artery persistent cerebral
|
|
D020785||malformation brain vascular
|
|
D020785||malformations brain vascular
|
|
D020785||persistent cerebral embryonic artery
|
|
D020785||pontine capillary telangiectasia
|
|
D020785||pontine capillary telangiectasias
|
|
D020785||telangiectasia brain capillary
|
|
D020785||telangiectasia pontine capillary
|
|
D020785||telangiectasias brain capillary
|
|
D020785||telangiectasias pontine capillary
|
|
D020785||vascular anomalies central nervous system
|
|
D020785||vascular malformation brain
|
|
D020785||vascular malformations brain
|
|
D020785||vascular malformations central nervous system
|
|
D020785||vascular malformations congenital nervous system
|
|
604213|C535459||chudley mccullough syndrome
|
|
604213|C535459||cmcs
|
|
604213|C535459||deafness autosomal recessive 82
|
|
604213|C535459||deafness bilateral sensorineural and hydrocephalus due to foramen of monro obstruction
|
|
604213|C535459||deafness sensorineural with partial agenesis of the corpus callosum and arachnoid cysts
|
|
604213|C535459||dfnb82
|
|
C566555|602398||desmosterolosis
|
|
D054138||sinus arrest cardiac
|
|
D054138||cardiac sinus arrest
|
|
D054138||cardiac sinus arrests
|
|
D054138||cardiac sinus pause
|
|
D054138||cardiac sinus pauses
|
|
D054138||sinus arrests cardiac
|
|
D054138||sinus pause cardiac
|
|
D054138||sinus pauses cardiac
|
|
C566766|613695||long qt syndrome 5
|
|
C566766|613695|C563614|613688||long qt syndrome 2 5 digenic included lqt2 5 digenic included
|
|
C566766|613695||long qt syndrome 5 acquired susceptibility to included
|
|
C566766|613695||lqt5
|
|
D018476||hypokinesia
|
|
D018476||antiorthostatic hypokinesia
|
|
D018476||antiorthostatic hypokinesias
|
|
D018476||bradykinesia
|
|
D018476||bradykinesias
|
|
D018476||hypodynamia
|
|
D018476||hypokinesia antiorthostatic
|
|
D018476||hypokinesias antiorthostatic
|
|
C563210|613161||beta ureidopropionase deficiency
|
|
612525|C567283||pyloric stenosis infantile hypertrophic 5
|
|
612525|C567283||ihps5
|
|
D054139||tachycardia reciprocating
|
|
D054139||reciprocal tachycardia
|
|
D054139||reciprocal tachycardias
|
|
D054139||reciprocating tachycardia
|
|
D054139||reciprocating tachycardias
|
|
D054139||tachycardia reciprocal
|
|
D054139||tachycardias reciprocal
|
|
D054139||tachycardias reciprocating
|
|
D018450||disease progression
|
|
D018450||disease exacerbation
|
|
D018450||disease progressions
|
|
D018450||progression disease
|
|
D018450||progressions disease
|
|
D017121||porphyria hepatoerythropoietic
|
|
D017121||erythrohepatic porphyria
|
|
D017121||erythrohepatic porphyrias
|
|
D017121||hepatoerythropoietic porphyria
|
|
D017121||hepatoerythropoietic porphyrias
|
|
D017121||porphyria erythrohepatic
|
|
D017121||porphyrias erythrohepatic
|
|
D017121||porphyrias hepatoerythropoietic
|
|
613370||maturity onset diabetes of the young type 10
|
|
613370||mody10
|
|
D020779||sinus pericranii
|
|
613375||maturity onset diabetes of the young type 11
|
|
613375||mody11
|
|
D006468||hemopneumothorax
|
|
613376||neuronopathy distal hereditary motor type iic
|
|
613376||dhmn2c
|
|
613376||hmn2c
|
|
613376||hmn iic
|
|
613376||neuropathy distal hereditary motor type iic
|
|
D006469||hemoptysis
|
|
D006469||hemoptyses
|
|
D005134||eye neoplasms
|
|
D005134||cancer eye
|
|
D005134||cancer of eye
|
|
D005134||cancer of the eye
|
|
D005134||cancers eye
|
|
D005134||eye cancer
|
|
D005134||eye cancers
|
|
D005134||eye neoplasm
|
|
D005134||neoplasm eye
|
|
D005134||neoplasms eye
|
|
D020773||headache disorders
|
|
D020773||cephalgia syndrome
|
|
D020773||cephalgia syndromes
|
|
D020773||chronic daily headache
|
|
D020773||chronic daily headaches
|
|
D020773||chronic headache
|
|
D020773||chronic headaches
|
|
D020773||daily headache chronic
|
|
D020773||daily headaches chronic
|
|
D020773||headache chronic
|
|
D020773||headache chronic daily
|
|
D020773||headache disorder
|
|
D020773||headache intractable
|
|
D020773||headaches chronic
|
|
D020773||headaches chronic daily
|
|
D020773||headaches intractable
|
|
D020773||headache syndrome
|
|
D020773||headache syndromes
|
|
D020773||intractable headache
|
|
D020773||intractable headaches
|
|
D020773||syndrome headache
|
|
D006465||hemoperitoneum
|
|
D006465||hemoperitoneums
|
|
D054141||ventricular flutter
|
|
D054141||ventricular flutters
|
|
D006473||postpartum hemorrhage
|
|
D006473||delayed postpartum hemorrhage
|
|
D006473||hemorrhage delayed postpartum
|
|
D006473||hemorrhage immediate postpartum
|
|
D006473||hemorrhage postpartum
|
|
D006473||immediate postpartum hemorrhage
|
|
D006473||postpartum hemorrhage delayed
|
|
D006473||postpartum hemorrhage immediate
|
|
D005141||eyelid diseases
|
|
D005141||disease eyelid
|
|
D005141||diseases eyelid
|
|
D005141||eyelid disease
|
|
D006474||hemorrhagic disorders
|
|
D006474||diatheses hemorrhagic
|
|
D006474||diathesis hemorrhagic
|
|
D006474||disorder hemorrhagic
|
|
D006474||disorders hemorrhagic
|
|
D006474||hemorrhagic diatheses
|
|
D006474||hemorrhagic diathesis
|
|
D006474||hemorrhagic disorder
|
|
D006471||gastrointestinal hemorrhage
|
|
D006471||gastrointestinal hemorrhages
|
|
D006471||hematochezia
|
|
D006471||hematochezias
|
|
D006471||hemorrhage gastrointestinal
|
|
D006472||oral hemorrhage
|
|
D006472||hemorrhage oral
|
|
D006472||oral hemorrhages
|
|
D005142||eyelid neoplasms
|
|
D005142||eyelid neoplasm
|
|
D005142||neoplasm eyelid
|
|
D005142||neoplasms eyelid
|
|
D054144||heart failure diastolic
|
|
D054144||diastolic heart failure
|
|
D054144||diastolic heart failures
|
|
D054144||heart failures diastolic
|
|
D006470||hemorrhage
|
|
D006470||bleeding
|
|
D006470||hemorrhages
|
|
D054143||heart failure systolic
|
|
D054143||heart failures systolic
|
|
D054143||systolic heart failure
|
|
D054143||systolic heart failures
|
|
D017116||low back pain
|
|
D017116||ache low back
|
|
D017116||aches low back
|
|
D017116||backache low
|
|
D017116||back ache low
|
|
D017116||backaches low
|
|
D017116||back aches low
|
|
D017116||back pain low
|
|
D017116||back pain lower
|
|
D017116||back pains low
|
|
D017116||back pains lower
|
|
D017116||low backache
|
|
D017116||low back ache
|
|
D017116||low backaches
|
|
D017116||low back aches
|
|
D017116||low back pain mechanical
|
|
D017116||low back pain posterior compartment
|
|
D017116||low back pain postural
|
|
D017116||low back pain recurrent
|
|
D017116||low back pains
|
|
D017116||lower back pain
|
|
D017116||lower back pains
|
|
D017116||lumbago
|
|
D017116||mechanical low back pain
|
|
D017116||pain low back
|
|
D017116||pain lower back
|
|
D017116||pains low back
|
|
D017116||pains lower back
|
|
D017116||postural low back pain
|
|
D017116||recurrent low back pain
|
|
D017114||liver failure acute
|
|
D017114||acute hepatic failure
|
|
D017114||acute liver failure
|
|
D017114||failure acute hepatic
|
|
D017114||failure acute liver
|
|
D017114||fulminant hepatic failure
|
|
D017114||fulminant hepatic failures
|
|
D017114||fulminant liver failure
|
|
D017114||fulminant liver failures
|
|
D017114||fulminating hepatic failure
|
|
D017114||fulminating hepatic failures
|
|
D017114||fulminating liver failure
|
|
D017114||fulminating liver failures
|
|
D017114||hepatic failure acute
|
|
D017114||hepatic failure fulminant
|
|
D017114||hepatic failure fulminating
|
|
D017114||hepatic failures fulminant
|
|
D017114||hepatic failures fulminating
|
|
D017114||liver failure fulminant
|
|
D017114||liver failure fulminating
|
|
D017114||liver failures fulminant
|
|
D017114||liver failures fulminating
|
|
D020760||spinal cord ischemia
|
|
D020760||cord ischemia spinal
|
|
D020760||cord ischemias spinal
|
|
D020760||experimental spinal cord ischemia
|
|
D020760||ischemia spinal cord
|
|
D020760||ischemias spinal cord
|
|
D020760||ischemic myelopathies
|
|
D020760||ischemic myelopathy
|
|
D020760||myelopathies ischemic
|
|
D020760||myelopathy ischemic
|
|
D020760||spinal cord ischemia experimental
|
|
D020760||spinal cord ischemias
|
|
D018461||soft tissue infections
|
|
D018461||infection soft tissue
|
|
D018461||infections soft tissue
|
|
D018461||soft tissue infection
|
|
C565278|605850||dimethylglycine dehydrogenase deficiency
|
|
C565278|605850||dmgdhd
|
|
C565278|605850||dmgdh deficiency
|
|
D018460||fractures comminuted
|
|
D018460||comminuted fracture
|
|
D018460||comminuted fractures
|
|
D018460||fracture comminuted
|
|
D020767||intracranial thrombosis
|
|
D020767||brain thromboses
|
|
D020767||brain thrombosis
|
|
D020767||brain thrombus
|
|
D020767||cerebral thromboses
|
|
D020767||cerebral thrombosis
|
|
D020767||cerebral thrombus
|
|
D020767||intracranial thromboses
|
|
D020767||intracranial thrombus
|
|
D020767||thromboses brain
|
|
D020767||thromboses cerebral
|
|
D020767||thromboses intracranial
|
|
D020767||thrombosis brain
|
|
D020767||thrombosis cerebral
|
|
D020767||thrombosis intracranial
|
|
D020767||thrombus brain
|
|
D020767||thrombus cerebral
|
|
D020767||thrombus intracranial
|
|
D005148||facial dermatoses
|
|
D005148||dermatoses facial
|
|
D005148||dermatosis facial
|
|
D005148||elastoidoses nodular
|
|
D005148||elastoidosis nodular
|
|
D005148||elastoses nodular
|
|
D005148||elastosis nodular
|
|
D005148||facial dermatosis
|
|
D005148||favre racouchot syndrome
|
|
D005148||nodular elastoidoses
|
|
D005148||nodular elastoidosis
|
|
D005148||nodular elastoses
|
|
D005148||nodular elastosis
|
|
D005148||syndrome favre racouchot
|
|
613364||spastic paraplegia 41 autosomal dominant
|
|
613364||spg41
|
|
D006479||hemorrhagic fever crimean
|
|
D006479||congo virus infection
|
|
D006479||congo virus infections
|
|
D006479||crimean hemorrhagic fever
|
|
D006479||crimean hemorrhagic fevers
|
|
D006479||fever crimean hemorrhagic
|
|
D006479||fevers crimean hemorrhagic
|
|
D006479||hemorrhagic fevers crimean
|
|
D006479||infection congo virus
|
|
D006479||infections congo virus
|
|
D020766||intracranial embolism
|
|
D020766||brain emboli
|
|
D020766||brain embolism
|
|
D020766||brain embolus
|
|
D020766||cerebral emboli
|
|
D020766||cerebral embolism
|
|
D020766||cerebral embolus
|
|
D020766||emboli brain
|
|
D020766||emboli cerebral
|
|
D020766||embolism brain
|
|
D020766||embolism cerebral
|
|
D020766||embolism intracranial
|
|
D020766||embolus brain
|
|
D020766||embolus cerebral
|
|
D020765||intracranial arterial diseases
|
|
D020765||arterial brain disease
|
|
D020765||arterial brain diseases
|
|
D020765||arterial brain disorder
|
|
D020765||arterial brain disorders
|
|
D020765||arterial disease brain
|
|
D020765||arterial disease intracranial
|
|
D020765||arterial diseases brain
|
|
D020765||arterial diseases intracranial
|
|
D020765||arterial disorder intracranial
|
|
D020765||arterial disorders intracranial
|
|
D020765||brain arterial disease
|
|
D020765||brain arterial diseases
|
|
D020765||brain diseases arterial
|
|
D020765||brain disorder arterial
|
|
D020765||brain disorders arterial
|
|
D020765||intracranial arterial disease
|
|
D020765||intracranial arterial disorder
|
|
D020765||intracranial arterial disorders
|
|
C565799|604292||ectrodactyly ectodermal dysplasia and cleft lip palate syndrome 3
|
|
C565799|604292||eec3
|
|
C565799|604292||eec syndrome 3
|
|
C565054|131440||myeloproliferative disorder chronic with eosinophilia
|
|
C565054|131440||emp
|
|
C565054|131440||eosinophils malignant proliferation of
|
|
C565054|131440||mpe
|
|
C567734|613120||brugada syndrome 7
|
|
C567734|613120||brgda7
|
|
D003616|220200||dandy walker syndrome
|
|
D003616|220200||dandy walker complex
|
|
D003616|220200|C538507||dandy walker cyst
|
|
D003616|220200||dandy walker deformity
|
|
D003616|220200||dandy walker malformation
|
|
D003616|220200||dandy walker malformation included
|
|
D003616|220200||dandy walker syndrome familial
|
|
D003616|220200||dwm included
|
|
D003616|220200||dws
|
|
D003616|220200||familial dandy walker syndrome
|
|
D003616|220200||hydrocephalus internal dandy walker type
|
|
D003616|220200||hydrocephalus noncommunicating dandy walker type
|
|
D003616|220200||luschka magendie foramina atresia
|
|
D003616|220200||malformation dandy walker
|
|
D003616|220200||syndrome dandy walker
|
|
D003616|220200||syndrome familial dandy walker
|
|
D006478||hemorrhagic fever american
|
|
D006478||american hemorrhagic fever
|
|
D006478||argentinian hemorrhagic fever
|
|
D006478||bolivian hemorrhagic fever
|
|
D006478||fever american hemorrhagic
|
|
D006478||fever argentinian hemorrhagic
|
|
D006478||fever bolivian hemorrhagic
|
|
D006478||hemorrhagic fever argentinian
|
|
D006478||hemorrhagic fever bolivian
|
|
C567931|611945||spastic paraplegia 37 autosomal dominant
|
|
C567931|611945||spg37
|
|
D020763||pathological conditions anatomical
|
|
D020763||anatomical pathological condition
|
|
D020763||anatomical pathological conditions
|
|
D020763||condition anatomical pathological
|
|
D020763||conditions anatomical pathological
|
|
D020763||pathological condition anatomical
|
|
D006475||vitamin k deficiency bleeding
|
|
D006475||hemorrhagic disease of newborn
|
|
D006475||newborn hemorrhagic disease
|
|
D006475||newborn hemorrhagic diseases
|
|
D020762||infarction posterior cerebral artery
|
|
D020762||embolic infarction posterior cerebral artery
|
|
D020762||infarction pca
|
|
D020762||pca infarction
|
|
D020762||posterior cerebral artery embolic infarction
|
|
D020762||posterior cerebral artery infarction
|
|
D020762||posterior cerebral artery stroke
|
|
D020762||posterior cerebral artery syndrome
|
|
D020762||posterior cerebral artery thrombotic infarction
|
|
D020762||stroke posterior cerebral artery
|
|
D020762||thrombotic infarction posterior cerebral artery
|
|
D005146||facial asymmetry
|
|
D005146||asymmetries facial
|
|
D005146||asymmetry facial
|
|
D005146||facial asymmetries
|
|
D006484||hemorrhoids
|
|
D006484||hemorrhoid
|
|
D005151||facial injuries
|
|
D005151||facial injury
|
|
D005151||injuries facial
|
|
D005151||injury facial
|
|
D006482||hemorrhagic fevers viral
|
|
D006482||fevers viral hemorrhagic
|
|
D006482||fever viral hemorrhagic
|
|
D006482||hemorrhagic fever viral
|
|
D006482||viral hemorrhagic fever
|
|
D006482||viral hemorrhagic fevers
|
|
D006483||hemorrhagic septicemia
|
|
D006483||bacteremia haemorrhagic
|
|
D006483||bacteremia hemorrhagic
|
|
D006483||haemorrhagic bacteremia
|
|
D006483||haemorrhagic septicaemia
|
|
D006483||haemorrhagic septicemia
|
|
D006483||hemorrhagic bacteremia
|
|
D006483||hemorrhagic septicaemia
|
|
D006483||septicaemia haemorrhagic
|
|
D006483||septicaemia hemorrhagic
|
|
D006483||septicemia haemorrhagic
|
|
D006483||septicemia hemorrhagic
|
|
D005153||facial neoplasms
|
|
D005153||facial neoplasm
|
|
D005153||neoplasm facial
|
|
D005153||neoplasms facial
|
|
C566296|613694||cardiomyopathy dilated 1u
|
|
C566296|613694||cmd1u
|
|
D006480||hemorrhagic fever with renal syndrome
|
|
D006480||epidemic hemorrhagic fever
|
|
D006480||epidemic hemorrhagic fevers
|
|
D006480||hemorrhagic fever epidemic
|
|
D006480||hemorrhagic fever korean
|
|
D006480||hemorrhagic fevers epidemic
|
|
D006480||hemorrhagic nephroso nephritides
|
|
D006480||hemorrhagic nephroso nephritis
|
|
D006480||hfrs
|
|
D006480||korean hemorrhagic fever
|
|
D006480||nephropathia epidemica
|
|
D006480||nephroso nephritides hemorrhagic
|
|
D006480||nephroso nephritis hemorrhagic
|
|
D006481||hemorrhagic fever omsk
|
|
D006481||fever omsk hemorrhagic
|
|
D006481||omsk hemorrhagic fever
|
|
D005150||facial hemiatrophy
|
|
D005150||atrophies hemifacial
|
|
D005150||atrophies progressive hemifacial
|
|
D005150||atrophy hemifacial
|
|
D005150||atrophy progressive hemifacial
|
|
D005150||atrophy romberg hemi facial
|
|
D005150||disease parry romberg
|
|
D005150||disease romberg
|
|
D005150||disease romberg apos s
|
|
D005150||facial hemiatrophies
|
|
D005150||facial hemiatrophies progressive
|
|
D005150||facial hemiatrophy of romberg
|
|
D005150||facial hemiatrophy progressive
|
|
D005150||hemiatrophies facial
|
|
D005150||hemiatrophies progressive facial
|
|
D005150||hemiatrophy facial
|
|
D005150||hemiatrophy progressive facial
|
|
D005150||hemifacial atrophies
|
|
D005150||hemifacial atrophy
|
|
D005150||hemifacial atrophy progressive
|
|
D005150||hemi facial atrophy romberg
|
|
D005150||parry romberg disease
|
|
D005150||parry romberg syndrome
|
|
D005150||progressive facial hemiatrophies
|
|
D005150||progressive facial hemiatrophy
|
|
D005150||progressive hemifacial atrophies
|
|
D005150||progressive hemifacial atrophy
|
|
D005150||romberg disease
|
|
D005150||romberg facial hemiatrophy
|
|
D005150||romberg hemi facial atrophy
|
|
D005150||romberg apos s disease
|
|
D005150||rombergs disease
|
|
D005150||syndrome parry romberg
|
|
D018459||lichen sclerosus et atrophicus
|
|
D018459||lichen scleroses
|
|
D018459||lichen sclerosis
|
|
D018459||lichen sclerosis et atrophicus
|
|
D018459||lichen sclerosus
|
|
D018459||scleroses lichen
|
|
D018459||sclerosis lichen
|
|
D018459||sclerosus lichen
|
|
D018458||persistent vegetative state
|
|
D018458||minimally conscious state
|
|
D018458||minimally conscious states
|
|
D018458||permanent vegetative state
|
|
D018458||permanent vegetative states
|
|
D018458||persistent unawareness state
|
|
D018458||persistent unawareness states
|
|
D018458||persistent vegetative states
|
|
D018458||postcomatose unawareness state
|
|
D018458||post comatose unawareness state
|
|
D018458||postcomatose unawareness states
|
|
D018458||post comatose unawareness states
|
|
D018458||post traumatic unawarenesses prolonged
|
|
D018458||post traumatic unawareness prolonged
|
|
D018458||posttraumatic unawareness state
|
|
D018458||post traumatic unawareness state
|
|
D018458||posttraumatic unawareness states
|
|
D018458||post traumatic unawareness states
|
|
D018458||post traumatic vegetative state
|
|
D018458||post traumatic vegetative states
|
|
D018458||prolonged post traumatic unawareness
|
|
D018458||prolonged post traumatic unawarenesses
|
|
D018458||pvs persistent vegetative state
|
|
D018458||pvss persistent vegetative state
|
|
D018458||state minimally conscious
|
|
D018458||state permanent vegetative
|
|
D018458||state persistent unawareness
|
|
D018458||state persistent vegetative
|
|
D018458||state postcomatose unawareness
|
|
D018458||state post comatose unawareness
|
|
D018458||state posttraumatic unawareness
|
|
D018458||state post traumatic unawareness
|
|
D018458||state post traumatic vegetative
|
|
D018458||states minimally conscious
|
|
D018458||states permanent vegetative
|
|
D018458||states persistent unawareness
|
|
D018458||states persistent vegetative
|
|
D018458||states postcomatose unawareness
|
|
D018458||states post comatose unawareness
|
|
D018458||states posttraumatic unawareness
|
|
D018458||states post traumatic unawareness
|
|
D018458||states post traumatic vegetative
|
|
D018458||states transient vegetative
|
|
D018458||states vegetative
|
|
D018458||state transient vegetative
|
|
D018458||state vegetative
|
|
D018458||transient vegetative state
|
|
D018458||transient vegetative states
|
|
D018458||unawarenesses prolonged post traumatic
|
|
D018458||unawareness prolonged post traumatic
|
|
D018458||unawareness state persistent
|
|
D018458||unawareness state postcomatose
|
|
D018458||unawareness state post comatose
|
|
D018458||unawareness state posttraumatic
|
|
D018458||unawareness state post traumatic
|
|
D018458||unawareness states persistent
|
|
D018458||unawareness states postcomatose
|
|
D018458||unawareness states post comatose
|
|
D018458||unawareness states posttraumatic
|
|
D018458||unawareness states post traumatic
|
|
D018458||vegetative state
|
|
D018458||vegetative state permanent
|
|
D018458||vegetative state persistent
|
|
D018458||vegetative state post traumatic
|
|
D018458||vegetative states
|
|
D018458||vegetative states permanent
|
|
D018458||vegetative states persistent
|
|
D018458||vegetative states post traumatic
|
|
D018458||vegetative states transient
|
|
D018458||vegetative state transient
|
|
C563307|601493||cardiomyopathy dilated 1c
|
|
C563307|601493||cardiomyopathy dilated with left ventricular noncompaction included
|
|
C563307|601493||cmd1c
|
|
C563307|601493||left ventricular noncompaction 3 included
|
|
C563307|601493||lvnc3 included
|
|
D017129||anisakiasis
|
|
D017129||anisakiases
|
|
D018455||protein s deficiency
|
|
D018455||deficiencies protein s
|
|
D018455||deficiency protein s
|
|
D018455||hereditary thrombophilia due to protein s deficiency
|
|
D018455||protein s deficiencies
|
|
D018457||placenta retained
|
|
D018457||placentas retained
|
|
D018457||retained placenta
|
|
D018457||retained placentas
|
|
C563585||metatarsus varus type i
|
|
C563583||microcephaly with chorioretinopathy autosomal dominant
|
|
C563589||mesomelic dwarfism of hypoplastic tibia and radius type
|
|
D005119||extravasation of diagnostic and therapeutic materials
|
|
D005119||contrast media extravasation
|
|
D005119||extravasation of contrast media
|
|
D005119||extravasation of diagnostic therapeutic materials
|
|
C563587||metachromatic leukodystrophy adult onset with normal arylsulfatase a
|
|
C563586||metaphyseal dysplasia with maxillary hypoplasia and brachydactyly
|
|
125420||dtdp2
|
|
D020757||amaurosis fugax
|
|
D020757||blindness monocular transient
|
|
D020757||blindness transient monocular
|
|
D020757||monocular blindness transient
|
|
D020757||transient monocular blindness
|
|
C567482|300633||hypospadias 1 x linked
|
|
C567482|300633||hysp1
|
|
613353||mononeuropathy of the median nerve mild
|
|
613353||carpal tunnel syndrome susceptibility to
|
|
613353||mnmn
|
|
D005117||cardiac complexes premature
|
|
D005117||beat premature
|
|
D005117||beats premature
|
|
D005117||cardiac complex premature
|
|
D005117||complexes premature cardiac
|
|
D005117||ectopic heartbeat
|
|
D005117||ectopic heartbeats
|
|
D005117||extrasystole
|
|
D005117||heartbeat ectopic
|
|
D005117||heartbeats ectopic
|
|
D005117||premature beat
|
|
D005117||premature beats
|
|
D005117||premature cardiac complex
|
|
D005117||premature cardiac complexes
|
|
D005117||premature cardiac complices
|
|
D007775||lactation disorders
|
|
D007775||disorder lactation
|
|
D007775||disorders lactation
|
|
D007775||hypogalactia
|
|
D007775||hypogalactias
|
|
D007775||lactation disorder
|
|
D006445||hemoglobin c disease
|
|
D006445||c disease hemoglobin
|
|
D006445||c diseases hemoglobin
|
|
D006445||hemoglobin c diseases
|
|
D020752||neurocutaneous syndromes
|
|
D020752||neurocutaneous disorder
|
|
D020752||neurocutaneous disorders
|
|
D020752||neurocutaneous syndrome
|
|
D020752||neuroectodermal dysplasia syndrome
|
|
D020752||neuroectodermal dysplasia syndromes
|
|
D020752||phacomatoses
|
|
D020752||phacomatosis
|
|
D020752||phakomatoses
|
|
D020752||phakomatosis
|
|
D020752||syndrome neurocutaneous
|
|
D020752||syndrome neuroectodermal dysplasia
|
|
D020752||syndromes neurocutaneous
|
|
D020752||syndromes neuroectodermal dysplasia
|
|
D020751||alcohol induced disorders
|
|
D020751||alcohol induced disorder
|
|
D055496||neurogenic bowel
|
|
D055496||bowel neurogenic
|
|
D055496||bowels neurogenic
|
|
D055496||neurogenic bowels
|
|
C535288|266280||rapadilino syndrome
|
|
C535288|266280||radial and patellar aplasia
|
|
C535288|266280||radial and patellar hypoplasia
|
|
D054160||systolic murmurs
|
|
D054160||ejection murmur
|
|
D054160||ejection murmurs
|
|
D054160||murmur ejection
|
|
D054160||murmurs ejection
|
|
D054160||murmurs systolic
|
|
D054160||murmurs systolic regurgitant
|
|
D054160||murmur systolic
|
|
D054160||murmur systolic regurgitant
|
|
D054160||regurgitant murmurs systolic
|
|
D054160||regurgitant murmur systolic
|
|
D054160||systolic murmur
|
|
D054160||systolic regurgitant murmur
|
|
D054160||systolic regurgitant murmurs
|
|
D006450||hemoglobin sc disease
|
|
D006450||disease hemoglobin sc
|
|
D006450||disease sc
|
|
D006450||diseases hemoglobin sc
|
|
D006450||diseases sc
|
|
D006450||hemoglobin sc diseases
|
|
D006450||sc disease
|
|
D006450||sc disease hemoglobin
|
|
D006450||sc diseases
|
|
D006450||sc diseases hemoglobin
|
|
D006450||sickle cell hemoglobin c disease
|
|
D020759||anterior spinal artery syndrome
|
|
D020759||anterior spinal artery dissection
|
|
D020759||dissection anterior spinal artery
|
|
D020759||syndrome anterior spinal artery
|
|
D020758||spinal cord vascular diseases
|
|
D020758||hematomyelia
|
|
D020758||hematomyelias
|
|
D020758||posterior spinal artery syndrome
|
|
D020758||vascular diseases spinal cord
|
|
C566801|172870||pigmented paravenous chorioretinal atrophy
|
|
C566801|172870||ppcra
|
|
C563592||membranous cranial ossification delayed
|
|
D055499||catheter related infections
|
|
D055499||catheter associated infection
|
|
D055499||catheter associated infections
|
|
D055499||catheter related infection
|
|
D055499||infection catheter associated
|
|
D055499||infection catheter related
|
|
D055499||infections catheter associated
|
|
D055499||infections catheter related
|
|
C563591||mental and growth retardation with amblyopia
|
|
D018424||cholesteatoma middle ear
|
|
D018424||aural cholesteatoma
|
|
D018424||aural cholesteatomas
|
|
D018424||cholesteatoma aural
|
|
D018424||cholesteatomas aural
|
|
D018424||cholesteatomas middle ear
|
|
D018424||middle ear cholesteatoma
|
|
D018424||middle ear cholesteatomas
|
|
C563590||meralgia paraesthetica familial
|
|
600048||breast cancer 11 22 translocation associated
|
|
600048||brcata
|
|
C567510|611868||prostate cancer hereditary 12
|
|
C567510|611868||hpc12
|
|
C563596||melanoma malignant familial intraocular
|
|
C566929|611515||febrile convulsions familial 7
|
|
C566929|611515||feb7
|
|
C566929|611515||febrile seizures familial 7
|
|
D018442||lymphoma b cell marginal zone
|
|
D018442||lymphoma malt
|
|
D018442||lymphoma mucosa associated lymphoid tissue
|
|
D018442||lymphoma of mucosa associated lymphoid tissue
|
|
D018442||lymphomas malt
|
|
D018442||malt lymphoma
|
|
D018442||malt lymphomas
|
|
D018442||marginal zone b cell lymphoma
|
|
D018442||mucosa associated lymphoid tissue lymphoma
|
|
D019773||epiretinal membrane
|
|
D019773||epiretinal membranes
|
|
D019773||membrane epiretinal
|
|
D019773||membranes epiretinal
|
|
D020513|170500||paralysis hyperkalemic periodic
|
|
D020513|170500||adynamia episodica hereditaria
|
|
D020513|170500||adynamia episodica hereditaria with or without myotonia
|
|
D020513|170500||disease gamstorp
|
|
D020513|170500||familial hyperkalemic periodic paralysis
|
|
D020513|170500||gamstorp disease
|
|
D020513|170500||gamstorp disease normokalemic periodic paralysis potassium sensitive included
|
|
D020513|170500||gamstorp episodic adynamy
|
|
D020513|170500||hyperkalemic periodic paralysis
|
|
D020513|170500||hyperkalemic periodic paralysis familial
|
|
D020513|170500||hyperkalemic periodic paralysis type 2
|
|
D020513|170500||hyperkaliemic periodic paralysis type 2
|
|
D020513|170500||hyperkpp
|
|
D020513|170500||hyperpp
|
|
D020513|170500||hypp
|
|
D020513|170500||myotonic periodic paralysis
|
|
D020513|170500||paralysis periodic hyperkalemic familial
|
|
D020513|170500||primary hyperkalemic periodic paralysis
|
|
C563594||melanosis universal
|
|
C563593||melorheostosis with osteopoikilosis
|
|
C537689|610688||joubert syndrome 6
|
|
C537689|610688||jbts6
|
|
C563599||maxillofacial dysostosis
|
|
C563598||median ulnar nerve communications
|
|
C563598||martin gruber median ulnar anastomosis
|
|
606069|C537249||hemochromatosis type 4
|
|
606069|C537249||hemochromatosis autosomal dominant
|
|
606069|C537249||hemochromatosis due to defect in ferroportin
|
|
606069|C537249||hfe4
|
|
613340||epilepsy hot water 2
|
|
613340||hwe2
|
|
D005126||eye burns
|
|
D005126||burn eye
|
|
D005126||burns eye
|
|
D005126||eye burn
|
|
D005129||eye foreign bodies
|
|
D005129||eye foreign body
|
|
D005129||foreign bodies eye
|
|
D005129||foreign body eye
|
|
D005128||eye diseases
|
|
D005128||disease eye
|
|
D005128||diseases eye
|
|
D005128||eye disease
|
|
D006456||hemoglobinuria
|
|
D007787||lactose intolerance
|
|
D007787||alactasia
|
|
D007787||dairy product intolerance
|
|
D007787||hypolactasia
|
|
D007787||intolerance lactose
|
|
D007787||lactose malabsorption
|
|
D007787||malabsorption lactose
|
|
D007787||milk sugar intolerance
|
|
D006453||hemoglobinopathies
|
|
D006453||hemoglobinopathy
|
|
D017490|242300||ichthyosis lamellar
|
|
D017490|242300||arci1
|
|
D017490|242300||baby syndrome collodion
|
|
D017490|242300||baby syndrome harlequin
|
|
D017490|242300||baby syndromes collodion
|
|
D017490|242300||baby syndromes harlequin
|
|
D017490|242300||collodion baby syndrome
|
|
D017490|242300||collodion baby syndromes
|
|
D017490|242300||collodion fetus
|
|
D017490|242300||congenita ichthyosis
|
|
D017490|242300||congenita i ichthyosis
|
|
D017490|242300||congenita ii ichthyosis
|
|
D017490|242300||congenita iis ichthyosis
|
|
D017490|242300||congenita is ichthyosis
|
|
D017490|242300||congenital ichthyosiform erythroderma nonbullous
|
|
D017490|242300||congenital nonbullous ichthyosiform erythroderma
|
|
D017490|242300||congenitas ichthyosis
|
|
D017490|242300||desquamation of newborn
|
|
D017490|242300||erythroderma ichthyosiforme nonbullous
|
|
D017490|242300||erythroderma ichthyosiformes nonbullous
|
|
D017490|242300||fetus collodion
|
|
D017490|242300||fetus harlequin
|
|
D017490|242300||harlequin baby syndrome
|
|
D017490|242300||harlequin baby syndromes
|
|
D017490|242300||harlequin fetus
|
|
D017490|242300||harlequin ichthyoses
|
|
D017490|242300||ichthyose lamellar
|
|
D017490|242300||ichthyoses harlequin
|
|
D017490|242300||ichthyoses lamellar
|
|
D017490|242300||ichthyosiforme nonbullous erythroderma
|
|
D017490|242300||ichthyosiform erythroderma nonbullous congenital
|
|
D017490|242300||ichthyosiformes nonbullous erythroderma
|
|
D017490|242300||ichthyosis congenita
|
|
D017490|242300||ichthyosis congenita i
|
|
D017490|242300||ichthyosis congenita ii
|
|
D017490|242300||ichthyosis congenita iis
|
|
D017490|242300||ichthyosis congenita is
|
|
D017490|242300||ichthyosis congenital autosomal recessive 1
|
|
D017490|242300||ichthyosis congenital autosomal recessive 1 with bathing suit distribution
|
|
D017490|242300||ichthyosis congenitas
|
|
D017490|242300||ichthyosis harlequin
|
|
D017490|242300||ichthyosis lamellar 1
|
|
D017490|242300||ichthyosis lamellar 1 formerly
|
|
D017490|242300||icr2
|
|
D017490|242300||i ichthyosis congenita
|
|
D017490|242300||is ichthyosis congenita
|
|
D017490|242300||lamellar exfoliation of newborn
|
|
D017490|242300||lamellar ichthyose
|
|
D017490|242300||lamellar ichthyoses
|
|
D017490|242300||lamellar ichthyosis
|
|
D017490|242300||lamellar ichthyosis type 1
|
|
D017490|242300||li1 formerly
|
|
D017490|242300||newborn desquamation
|
|
D017490|242300||newborn desquamations
|
|
D017490|242300||newborn lamellar exfoliation
|
|
D017490|242300||newborn lamellar exfoliations
|
|
D017490|242300||nonbullous congenital ichthyosiform erythroderma
|
|
D017490|242300||nonbullous congenital lamellar ichthyosis
|
|
D017490|242300||nonbullous erythroderma ichthyosiforme
|
|
D017490|242300||nonbullous erythroderma ichthyosiformes
|
|
D017490|242300||shcb
|
|
D017490|242300||syndrome collodion baby
|
|
D017490|242300||syndrome harlequin baby
|
|
D017490|242300||syndromes collodion baby
|
|
D017490|242300||syndromes harlequin baby
|
|
D005124||eye abnormalities
|
|
D005124||abnormalities eye
|
|
D005124||abnormality eye
|
|
D005124||eye abnormality
|
|
D005130||eye hemorrhage
|
|
D005130||eye hemorrhages
|
|
D005130||hemophthalmos
|
|
D005130||hemorrhage eye
|
|
D006463||hemolytic uremic syndrome
|
|
D006463||gasser apos s syndrome
|
|
D006463||gassers syndrome
|
|
D006463||gasser syndrome
|
|
D006463||syndrome gasser
|
|
D006463||syndrome hemolytic uremic
|
|
D007794||lameness animal
|
|
D007794||animal gait disorder
|
|
D007794||animal gait disorders
|
|
D007794||animal lameness
|
|
D007794||animal lamenesses
|
|
D007794||disorder animal gait
|
|
D007794||disorders animal gait
|
|
D007794||gait disorder animal
|
|
D007794||gait disorders animal
|
|
D007794||lamenesses animal
|
|
613339||epilepsy hot water 1
|
|
613339||bathing epilepsy
|
|
613339||hwe1
|
|
613339||water immersion epilepsy
|
|
D005132||eye manifestations
|
|
D005132||eye manifestation
|
|
D005132||manifestation eye
|
|
D005132||manifestations eye
|
|
D006461||hemolysis
|
|
D005131||eye injuries
|
|
D005131||eye injury
|
|
D005131||injuries eye
|
|
D005131||injury eye
|
|
D017109||akathisia drug induced
|
|
D017109||acathisia drug induced
|
|
D017109||akathisia tardive
|
|
D017109||drug induced acathisia
|
|
D017109||drug induced akathisia
|
|
D017109||pseudoakathisia
|
|
D017109||tardive akathisia
|
|
C567085|611788||aortic aneurysm familial thoracic 6
|
|
C567085|611788||aat6
|
|
C567085|611788||familial thoracic aortic aneurysm with livedo reticularis and iris flocculi
|
|
D018437||brown sequard syndrome
|
|
D018437||brown sequard disease
|
|
D018437||brown sequard paralysis
|
|
D018437||brown sequard apos s disease
|
|
D018437||brown sequards disease
|
|
D018437||brown sequard apos s paralysis
|
|
D018437||brown sequards paralysis
|
|
D018437||brown sequard apos s syndrome
|
|
D018437||brown sequards syndrome
|
|
D018437||hemicord syndrome
|
|
D018437||hemicord syndromes
|
|
D018437||hemiparaplegic syndrome
|
|
D018437||hemiparaplegic syndromes
|
|
D018437||hemispinal cord syndrome
|
|
D018437||hemispinal cord syndromes
|
|
D018437||paralysis brown sequard apos s
|
|
D018437||spastic spinal monoplegia syndrome
|
|
D018437||syndrome brown sequard
|
|
D018437||syndrome brown sequard apos s
|
|
D018437||syndrome hemicord
|
|
D018437||syndrome hemiparaplegic
|
|
D018437||syndrome hemispinal cord
|
|
D018437||syndromes hemicord
|
|
D018437||syndromes hemiparaplegic
|
|
D018437||syndromes hemispinal cord
|
|
D019767||maxillofacial abnormalities
|
|
D019767||abnormalities maxillofacial
|
|
D019767||abnormality maxillofacial
|
|
D019767||maxillofacial abnormality
|
|
D018438||blue toe syndrome
|
|
D018438||syndrome blue toe
|
|
C563563||muscle cramps familial
|
|
C564894||peripheral neuropathy ataxia focal necrotizing encephalopathy and spongy degeneration of brain
|
|
C537275||cirrhosis familial with deposition of abnormal glycogen
|
|
C565298|605749||cataract autosomal recessive early onset pulverulent
|
|
C565298|605749||caar
|
|
C565298|605749||cataract 26 multiple types
|
|
C565298|605749||ctrct26
|
|
C564893||presentey anomaly
|
|
C564893||eosinophil peroxidase deficiency partial
|
|
C564893||peroxidase and phospholipid deficiency in eosinophils
|
|
C563566||multiple exostoses with spastic tetraparesis
|
|
C563565||cerebellar granule cell hypertrophy and megalencephaly
|
|
C567906|309530||mental retardation x linked 1
|
|
C567906|309530||mrx1
|
|
C567906|309530||mrx18 included
|
|
C567906|309530||mrx mental retardation x linked 18 included
|
|
D007759||labyrinth diseases
|
|
D007759||ear disease inner
|
|
D007759||ear diseases inner
|
|
D007759||inner ear disease
|
|
D007759||inner ear diseases
|
|
D007759||labyrinth disease
|
|
D006429||hemiplegia
|
|
D006429||crossed hemiplegia
|
|
D006429||crossed hemiplegias
|
|
D006429||flaccid hemiplegia
|
|
D006429||flaccid hemiplegias
|
|
D006429||hemiplegia crossed
|
|
D006429||hemiplegia flaccid
|
|
D006429||hemiplegia infantile
|
|
D006429||hemiplegia post ictal
|
|
D006429||hemiplegias
|
|
D006429||hemiplegias crossed
|
|
D006429||hemiplegias flaccid
|
|
D006429||hemiplegias infantile
|
|
D006429||hemiplegia spastic
|
|
D006429||hemiplegias post ictal
|
|
D006429||hemiplegias spastic
|
|
D006429||hemiplegias transient
|
|
D006429||hemiplegia transient
|
|
D006429||infantile hemiplegia
|
|
D006429||infantile hemiplegias
|
|
D006429||monoplegia
|
|
D006429||monoplegias
|
|
D006429||post ictal hemiplegia
|
|
D006429||post ictal hemiplegias
|
|
D006429||spastic hemiplegia
|
|
D006429||spastic hemiplegias
|
|
D006429||transient hemiplegia
|
|
D006429||transient hemiplegias
|
|
C563564||cerebelloparenchymal disorder vi
|
|
C564895||pericardial effusion chronic
|
|
C564895||cholesterol pericarditis
|
|
D007757||laboratory infection
|
|
D007757||infection laboratory
|
|
D007757||infections laboratory
|
|
D007757||laboratory infections
|
|
C538150|212780||syndactyly cenani lenz type
|
|
C538150|212780||cenani lenz syndactyly
|
|
C538150|212780||cenani lenz syndactyly syndrome
|
|
C538150|212780||cenani lenz type syndactyly
|
|
C538150|212780||cenani syndactylism
|
|
C538150|212780||clss
|
|
C538150|212780||syndactyly type 7
|
|
C538150|212780||syndactyly type vii
|
|
C563569||coronary artery disease development of in hiv
|
|
D006425||hemic and lymphatic diseases
|
|
C564899||pelger huet like anomaly and episodic fever with abdominal pain
|
|
C537271||fowler christmas chapple syndrome
|
|
C537271||voiding dysfunction and polycystic ovaries
|
|
D006423||hemianopsia
|
|
D006423||altidudinal hemianopia
|
|
D006423||altidudinal hemianopias
|
|
D006423||altitudinal hemianopsia
|
|
D006423||altitudinal hemianopsias
|
|
D006423||binasal hemianopia
|
|
D006423||binasal hemianopias
|
|
D006423||binasal hemianopsia
|
|
D006423||binasal hemianopsias
|
|
D006423||bitemporal hemianopia
|
|
D006423||bitemporal hemianopias
|
|
D006423||bitemporal hemianopsia
|
|
D006423||bitemporal hemianopsias
|
|
D006423||hemianopia
|
|
D006423||hemianopia altidudinal
|
|
D006423||hemianopia binasal
|
|
D006423||hemianopia bitemporal
|
|
D006423||hemianopia homonymous
|
|
D006423||hemianopias
|
|
D006423||hemianopias altidudinal
|
|
D006423||hemianopias binasal
|
|
D006423||hemianopias bitemporal
|
|
D006423||hemianopias homonymous
|
|
D006423||hemianopsia altitudinal
|
|
D006423||hemianopsia binasal
|
|
D006423||hemianopsia bitemporal
|
|
D006423||hemianopsia homonymous
|
|
D006423||hemianopsias
|
|
D006423||hemianopsias altitudinal
|
|
D006423||hemianopsias binasal
|
|
D006423||hemianopsias bitemporal
|
|
D006423||hemianopsias homonymous
|
|
D006423||homonymous hemianopia
|
|
D006423||homonymous hemianopias
|
|
D006423||homonymous hemianopsia
|
|
D006423||homonymous hemianopsias
|
|
D006423||quadrantanopia
|
|
D006423||quadrantanopias
|
|
D006423||quadrantanopsia
|
|
D006423||quadrantanopsias
|
|
C537272||franceschini vardeu guala syndrome
|
|
D007752||obstetric labor premature
|
|
D007752||labor premature
|
|
D007752||labor premature obstetric
|
|
D007752||labor preterm
|
|
D007752||premature labor
|
|
D007752||premature obstetric labor
|
|
D007752||preterm labor
|
|
C537270||fountain syndrome
|
|
C537270||mental retardation deafnes skeletal abnormalities coarse face with full lips
|
|
C537270||mental retardation sensorineural deafness skeletal abnormalities and coarse face with full lips
|
|
606240||thyroid carcinoma nonmedullary susceptibility to 1
|
|
606240||nmtc1
|
|
251450|C535943||desbuquois syndrome
|
|
251450|C535943||dbqd1
|
|
251450|C535943||desbuquois dysplasia
|
|
251450|C535943||desbuquois dysplasia 1
|
|
251450|C535943||micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
|
|
251450|C535943||micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification desbuquois dysplasia kim variant included
|
|
D020739||brain diseases metabolic inborn
|
|
D020739||brain diseases metabolic familial
|
|
D020739||brain diseases metabolic inherited
|
|
D020739||brain syndrome metabolic inborn
|
|
D020739||central nervous system inborn metabolic diseases
|
|
D020739||central nervous system inborn metabolic disorders
|
|
D020739||cns metabolic disorders inborn
|
|
D020739||encephalopathies metabolic inborn
|
|
D020739||familial metabolic brain diseases
|
|
D020739||familial metabolic disorders brain
|
|
D020739||inborn errors of metabolism brain
|
|
D020739||inborn metabolic brain diseases
|
|
D020739||inborn metabolic brain disorders
|
|
D020739||inborn metabolic disorders brain
|
|
D020739||inherited metabolic brain diseases
|
|
D020739||inherited metabolic disorders brain
|
|
D020739||metabolic brain diseases familial
|
|
D020739||metabolic brain diseases inborn
|
|
D020739||metabolic brain diseases inherited
|
|
D020739||metabolic brain syndrome inborn
|
|
D020739||metabolic diseases inborn brain
|
|
D020739||metabolic diseases inborn central nervous system
|
|
D020739||metabolic disorders brain inherited
|
|
D020739||metabolic disorders cns inborn
|
|
D020739||metabolic disorders familial brain
|
|
D018409||foot injuries
|
|
D018409||foot injury
|
|
D018409||injuries foot
|
|
D018409||injury foot
|
|
C566343|603689||hereditary myopathy with early respiratory failure
|
|
C566343|603689||edstrom myopathy
|
|
C566343|603689||hmerf
|
|
C566343|603689||mprm
|
|
C566343|603689||myopathy proximal with early respiratory muscle involvement
|
|
D018404||isochromosomes
|
|
D018404||isochromosome
|
|
C563654|610842||pseudoxanthoma elasticum like disorder with multiple coagulation factor deficiency
|
|
C563654|610842||pxe like disorder with multiple coagulation factor deficiency
|
|
C563570||monophalangy of great toe
|
|
105200|C538249||amyloidosis familial visceral
|
|
105200|C538249||amyloidosis 8
|
|
105200|C538249||amyloidosis familial renal
|
|
105200|C538249||amyloidosis systemic nonneuropathic
|
|
105200|C538249||amyloidosis viii
|
|
105200|C538249||german type amyloidosis
|
|
105200|C538249||ostertag type amyloidosis
|
|
C567934|188570||thyroid hormone resistance generalized autosomal dominant
|
|
C567934|188570||hyperthyroxinemia familial euthyroid secondary to pituitary and peripheral resistance to thyroid hormones
|
|
C537286||gonadal dysgenesis xx type deafness
|
|
C537286||17 beta hydroxysteroid dehydrogenase 4 deficiency of
|
|
C537286||ovarian dysgenesis with sensorineural deafness
|
|
C537286||peroxisomal bifunctional enzyme complex deficiency
|
|
C537286||perrault syndrome
|
|
C563573||mitral valve prolapse myxomatous 1
|
|
C563573||myxomatous mitral valve prolapse 1
|
|
C537287||goodman camptodactyly
|
|
C537287||acrocephalopolysyndactyly type 4
|
|
C537287||acrocephalopolysyndactyly type iv
|
|
C537287||goodman syndrome
|
|
D018420||ape diseases
|
|
D018420||ape disease
|
|
D018420||disease ape
|
|
D018420||disease pongidae
|
|
D018420||diseases ape
|
|
D018420||diseases pongidae
|
|
D018420||pongidae disease
|
|
D018420||pongidae diseases
|
|
C563572||mitral regurgitation conductive deafness and fusion of cervical vertebrae and of carpal and tarsal bones
|
|
C537284||gombo syndrome
|
|
C537284||growth retardation ocular abnormalities microcephaly brachydactyly and oligophrenia
|
|
239000||paget disease juvenile
|
|
C563578||myopathy cataract hypogonadism syndrome
|
|
C563578||ocular myopathy with hypogonadism
|
|
C563576||progressive external ophthalmoplegia with hypogonadism
|
|
C537288||gordon syndrome
|
|
C537288||arthrogryposis distal type 3
|
|
C537288||arthrogryposis multiplex congenita distal type 2a
|
|
C537288||arthrogryposis multiplex congenita distal type iia
|
|
C537288||camptodactyly cleft palate and clubfoot
|
|
C537288||distal arthrogryposis type 3
|
|
C537289||gorlin bushkell jensen syndrome
|
|
C567193|612717||myopia 15
|
|
C567193|612717||myopia 15 autosomal dominant
|
|
C567193|612717||myp15
|
|
D007766||lacrimal apparatus diseases
|
|
D007766||apparatus disease lacrimal
|
|
D007766||apparatus diseases lacrimal
|
|
D007766||disease lacrimal apparatus
|
|
D007766||diseases lacrimal apparatus
|
|
D007766||epiphora
|
|
D007766||lacrimal apparatus disease
|
|
D007767||lacrimal duct obstruction
|
|
D007767||duct obstruction lacrimal
|
|
D007767||duct obstructions lacrimal
|
|
D007767||lacrimal duct obstructions
|
|
D007767||obstruction lacrimal duct
|
|
D007767||obstructions lacrimal duct
|
|
D020721||nervous system autoimmune disease experimental
|
|
D020721||autoimmune disease models nervous system
|
|
D020721||autoimmune experimental myositis
|
|
D020721||autoimmune myositis experimental
|
|
D020721||disease models autoimmune nervous system
|
|
D020721||experimental autoimmune myositis
|
|
D020721||experimental myositis autoimmune
|
|
D020721||myositis autoimmune experimental
|
|
D020721||myositis experimental autoimmune
|
|
D020721||nervous system autoimmune disease models
|
|
C562656|233910||hyperphenylalaninemia bh4 deficient b
|
|
C562656|233910||gtp cyclohydrolase i deficiency
|
|
C562656|233910||gtp cyclohydrolase i deficiency dystonia dopa responsive with or without hyperphenylalaninemia autosomal recessive included
|
|
C562656|233910||hpabh4b
|
|
C562656|233910||hyperphenylalaninemia tetrahydrobiopterin deficient due to gtp cyclohydrolase i deficiency
|
|
D020720||myasthenia gravis autoimmune experimental
|
|
D020720||autoimmune experimental myasthenia gravis
|
|
D020720||experimental autoimmune myasthenia gravis passive transfer
|
|
D020720||experimental myasthenia
|
|
D020720||experimental myasthenia gravis
|
|
D020720||experimental myasthenias
|
|
D020720||myasthenia experimental
|
|
D020720||myasthenia gravis experimental
|
|
D020720||myasthenia gravis experimental autoimmune
|
|
D020720||myasthenias experimental
|
|
D020720||passive transfer experimental autoimmune myasthenia gravis
|
|
C537282||goldstein hutt syndrome
|
|
C537282||long eyelashes cataract and hereditary spherocytosis
|
|
C537282||trichomegaly cataract and hereditary spherocytosis
|
|
C537283||gollop coates syndrome
|
|
C537283||bifurcation of distal humerus with oligoectro syndactyly
|
|
D006431||hemobilia
|
|
D006431||biliary tract hemorrhage
|
|
D006431||biliary tract hemorrhages
|
|
D006431||hemobilias
|
|
D006431||hemorrhage biliary tract
|
|
D007762||labyrinthitis
|
|
D007762||labyrinthitides
|
|
D007762||otitis interna
|
|
C537280||goldblatt viljoen syndrome
|
|
C537280||autosomal dominant radial ray hypoplasia syndrome
|
|
C537280||goldblatt viljoen radial ray hypoplasia
|
|
C537280||radial ray hypoplasia with choanal hypoplasia
|
|
D018419||primate diseases
|
|
D018419||disease primate
|
|
D018419||diseases primate
|
|
D018419||primate disease
|
|
C563581||microphthalmia isolated with corectopia
|
|
C563581||mcopcr
|
|
C563581||microphthalmia and corectopia
|
|
C563581||microphthalmia with myopia and corectopia
|
|
108900||atrial septal defect 7 with or without atrioventricular conduction defects
|
|
108900||asd7
|
|
108900||asd with or without atrioventricular conduction defects
|
|
D018410||pneumonia bacterial
|
|
D018410||bacterial pneumonia
|
|
D018410||bacterial pneumonias
|
|
D018410||pneumonias bacterial
|
|
C563580||tauopathy and respiratory failure
|
|
C537297||autosomal dominant lateral temporal lobe epilepsy
|
|
C537297||autosomal dominant partial epilepsy with auditory features
|
|
C563540||atrial septal defect 3
|
|
C564871||progesterone resistance
|
|
C564871||pseudocorpus luteum insufficiency
|
|
C537298||autosomal recessive nonsyndromic congenital nuclear cataract
|
|
C537298||congenital nuclear cataract autosomal recessive
|
|
C564870||prolactin deficiency with obesity and enlarged testes
|
|
C537295||granulomatous angiitis of the central nervous system
|
|
C537295||granulomatous angiitis of cns
|
|
C537295||granulomatous angiitis of the nervous system
|
|
C537296||granulosa cell tumor of the ovary
|
|
C537296||adult granulosa cell tumor of the ovary
|
|
C537296||gct of the ovary
|
|
C537296||granulosa theca cell tumor
|
|
C537296||granulosa theca cell tumor of the ovary
|
|
D006408||hematoma subdural
|
|
D006408||hematomas subdural
|
|
D006408||hematomas traumatic subdural
|
|
D006408||hematoma traumatic subdural
|
|
D006408||hemorrhages subdural
|
|
D006408||hemorrhage subdural
|
|
D006408||subdural hematoma
|
|
D006408||subdural hematomas
|
|
D006408||subdural hematomas traumatic
|
|
D006408||subdural hematoma traumatic
|
|
D006408||subdural hemorrhage
|
|
D006408||subdural hemorrhages
|
|
D006408||traumatic subdural hematoma
|
|
D006408||traumatic subdural hematomas
|
|
C563545||continuous muscle fiber activity hereditary
|
|
C564876||polyhydramnios chronic idiopathic
|
|
C564876||lactogen receptor defect of chorion
|
|
D006409||hematometra
|
|
D006409||hematometras
|
|
C564875||bonneau syndrome
|
|
C564875||polysyndactyly with cardiac malformation
|
|
C537140|601101||osler rendu weber syndrome 3
|
|
C537140|601101||hht3
|
|
C537140|601101||telangiectasia hereditary hemorrhagic type 3
|
|
D006406||hematoma
|
|
D006406||hematomas
|
|
C563543||myopathy distal with onset in infancy
|
|
C564874||popliteal pterygium syndrome lethal type
|
|
C564874||aslan multiple pterygium syndrome
|
|
C564874||bartsocas papas syndrome
|
|
C564874||multiple pterygium syndrome aslan type
|
|
C564874||pterygium popliteal lethal type
|
|
D006407||hematoma epidural cranial
|
|
D006407||cranial epidural hematoma
|
|
D006407||cranial epidural hematomas
|
|
D006407||cranial epidural hemorrhage
|
|
D006407||cranial epidural hemorrhages
|
|
D006407||cranial extradural hematoma
|
|
D006407||cranial extradural hematomas
|
|
D006407||cranial extradural hemorrhage
|
|
D006407||cranial extradural hemorrhages
|
|
D006407||epidural hematoma cranial
|
|
D006407||epidural hematoma intracranial
|
|
D006407||epidural hematomas cranial
|
|
D006407||epidural hematomas intracranial
|
|
D006407||epidural hemorrhage cranial
|
|
D006407||epidural hemorrhages cranial
|
|
D006407||extradural hematoma cranial
|
|
D006407||extradural hematomas cranial
|
|
D006407||extradural hemorrhage cranial
|
|
D006407||extradural hemorrhages cranial
|
|
D006407||hematoma cranial epidural
|
|
D006407||hematoma cranial extradural
|
|
D006407||hematoma epidural intracranial
|
|
D006407||hematoma intracranial epidural
|
|
D006407||hematomas cranial epidural
|
|
D006407||hematomas cranial extradural
|
|
D006407||hematomas intracranial epidural
|
|
D006407||hemorrhage cranial epidural
|
|
D006407||hemorrhage cranial extradural
|
|
D006407||hemorrhages cranial epidural
|
|
D006407||hemorrhages cranial extradural
|
|
D006407||intracranial epidural hematoma
|
|
D006407||intracranial epidural hematomas
|
|
C563542||myopathy with storage of glycoproteins and glycosaminoglycans
|
|
D007738||kyphosis
|
|
D007738||kyphoses
|
|
C564873||prenatal bowing
|
|
C563549||myoclonus cerebellar ataxia and deafness
|
|
C564879||polyneuropathy mixed of early onset
|
|
C537290||gorlin chaudhry moss syndrome
|
|
C537290||craniofacial dysostosis patent ductus arteriosus hypertrichosis hypoplasia of labia majora dental and eye anomalies
|
|
C537290||gcm syndrome
|
|
D006402||hematologic diseases
|
|
D006402||blood disease
|
|
D006402||blood diseases
|
|
D006402||disease blood
|
|
D006402||disease hematologic
|
|
D006402||disease hematological
|
|
D006402||diseases blood
|
|
D006402||diseases hematologic
|
|
D006402||diseases hematological
|
|
D006402||hematological disease
|
|
D006402||hematological diseases
|
|
D006402||hematologic disease
|
|
D007733||kyasanur forest disease
|
|
D007733||disease kyasanur forest
|
|
D007733||forest disease kyasanur
|
|
C564878||polyglucosan body disease adult form
|
|
C564878||adult polyglucosan body disease
|
|
C563546||myoglobinuria autosomal dominant
|
|
C564877||polysaccharide storage of unusual
|
|
C537293||grant syndrome
|
|
D007732||kwashiorkor
|
|
D007732||kwashiorkors
|
|
C537294||granulomas congenital cerebral
|
|
C537294||congenital cerebral granulomas
|
|
C537291||gracile bone dysplasia
|
|
C537291||habrodysplasia
|
|
C537291||osteocraniosplenic syndrome
|
|
C537291||osteocraniostenosis
|
|
C537291||skeletal dysplasia lethal with gracile bones
|
|
C537292||graham boyle troxell syndrome
|
|
C537292||cystic hamartomata of lung and kidney
|
|
D005171|227600||factor x deficiency
|
|
D005171|227600||deficiencies factor x
|
|
D005171|227600||deficiency factor x
|
|
D005171|227600||deficiency stuart prower
|
|
D005171|227600||deficiency stuart prower factor
|
|
D005171|227600||f10 deficiency
|
|
D005171|227600||factor x deficiencies
|
|
D005171|227600||stuart prower deficiency
|
|
D005171|227600||stuart prower factor deficiency
|
|
C564767|274230||thymoma familial
|
|
C564767|274230||thymic neoplasia
|
|
D063926||drug hypersensitivity syndrome
|
|
D063926||dress syndrome
|
|
D063926||dress syndromes
|
|
D063926||drug hypersensitivity syndromes
|
|
D063926||drug reaction with eosinophilia and systemic symptoms
|
|
D063926||drug reaction with eosinophilia and systemic symptoms syndrome
|
|
D063926||hypersensitivity syndrome drug
|
|
D063926||hypersensitivity syndromes drug
|
|
D063926||syndrome drug hypersensitivity
|
|
D063926||syndromes drug hypersensitivity
|
|
C538208|176500||dementia familial british
|
|
C538208|176500||cerebral amyloid angiopathy british type
|
|
C538208|176500||cerebral amyloid angiopathy itm2b related 1
|
|
C538208|176500||fbd
|
|
C538208|176500||presenile dementia with spastic ataxia
|
|
C537437|608643||aromatic amino acid decarboxylase deficiency
|
|
C537437|608643||aadc deficiency
|
|
C537437|608643||aromatic l amino acid decarboxylase deficiency
|
|
C537437|608643||ddc deficiency
|
|
C537437|608643||dopa decarboxylase deficiency
|
|
607488|C538002||dystonia 15 myoclonic
|
|
607488|C538002||dyt15
|
|
C563552||myasthenia limb girdle autoimmune
|
|
C563552||myasthenia gravis limb girdle
|
|
C564883||pleoconial myopathy with salt craving
|
|
C536109|237310||n acetyl glutamate synthetase deficiency
|
|
C536109|237310||hyperammonemia due to n acetylglutamate synthetase deficiency
|
|
C536109|237310||n acetylglutamate synthase deficiency
|
|
C536109|237310||n acetylglutamate synthetase deficiency
|
|
C536109|237310||nags deficiency
|
|
C564882||polycystic kidney cataract and congenital blindness
|
|
C563550||myoclonic epilepsy hartung type
|
|
C564881||polycystic kidney disease potter type i with microbrachycephaly hypertelorism and brachymelia
|
|
C564880||polydactyly postaxial with dental and vertebral anomalies
|
|
D006417||hematuria
|
|
D006417||hematurias
|
|
C563554||muscular dystrophy pseudohypertrophic with internalized capillaries
|
|
C564885||plasma clot retraction factor deficiency of
|
|
C563553||muscular hypoplasia congenital universal of krabbe
|
|
C564884||platelet prostacyclin receptor defect
|
|
C564884||vienna hietzing defect
|
|
C563559||muscular atrophy malignant neurogenic
|
|
C563558||muscular dystrophy barnes type
|
|
D007744||obstetric labor complications
|
|
D007744||complication labor
|
|
D007744||complication obstetric labor
|
|
D007744||complications labor
|
|
D007744||complications obstetric labor
|
|
D007744||labor complication
|
|
D007744||labor complication obstetric
|
|
D007744||labor complications
|
|
D007744||labor complications obstetric
|
|
D007744||obstetric labor complication
|
|
101200|D000168||acrocephalosyndactylia
|
|
101200|D000168||acrocephalosyndactylias
|
|
101200|D000168||acrocephalosyndactylies type 1
|
|
101200|D000168||acrocephalosyndactylies type 3
|
|
101200|D000168||acrocephalosyndactylies type i
|
|
101200|D000168||acrocephalosyndactylies type ii
|
|
101200|D000168||acrocephalosyndactylies type iii
|
|
101200|D000168||acrocephalosyndactylies type v
|
|
101200|D000168||acrocephalosyndactyly apert
|
|
101200|D000168||acrocephalosyndactyly iii
|
|
101200|D000168||acrocephalosyndactyly iiis
|
|
101200|D000168||acrocephalosyndactyly type 1
|
|
101200|D000168||acrocephalosyndactyly type 3
|
|
101200|D000168||acrocephalosyndactyly type i
|
|
101200|D000168||acrocephalosyndactyly type ii
|
|
101200|D000168||acrocephalosyndactyly type iii
|
|
101200|D000168||acrocephalosyndactyly type ii included
|
|
101200|D000168||acrocephaly skull asymmetry and mild syndactyly
|
|
101200|D000168||acs1
|
|
101200|D000168||acs i apert crouzon disease included
|
|
101200|D000168||acs ii included
|
|
101200|D000168||apert crouzon disease
|
|
101200|D000168||apert syndrome
|
|
101200|D000168||blepharophimosis epicanthus inversus and ptosis 3 formerly included bpes3 formerly included
|
|
101200|D000168||craniofacial skeletal dermatologic dysplasia
|
|
101200|D000168||disease apert crouzon
|
|
101200|D000168||dysostosis craniofacialis with hypertelorism
|
|
101200|D000168||kurczynski casperson syndrome
|
|
101200|D000168||noack syndrome
|
|
101200|D000168||noack syndromes
|
|
101200|D000168||scs
|
|
101200|D000168||syndactylic oxycephalies
|
|
101200|D000168||syndactylic oxycephaly
|
|
101200|D000168||syndrome apert
|
|
101200|D000168||syndrome chotzen
|
|
101200|D000168||syndrome kurczynski casperson
|
|
101200|D000168||syndrome noack
|
|
101200|D000168||syndrome pfeiffer
|
|
101200|D000168||syndrome saethre chotzen
|
|
101200|D000168||syndromes noack
|
|
101200|D000168||type i acrocephalosyndactylies
|
|
101200|D000168||type i acrocephalosyndactyly
|
|
101200|D000168||type ii acrocephalosyndactylies
|
|
101200|D000168||type ii acrocephalosyndactyly
|
|
101200|D000168||type iii acrocephalosyndactyly
|
|
101200|D000168||type v acrocephalosyndactylies
|
|
101200|D000168||type v acrocephalosyndactyly
|
|
101200|D000168||vogt cephalodactyly included
|
|
D012148|102300||restless legs syndrome
|
|
D012148|102300|C538443||acromelalgia hereditary
|
|
D012148|102300||disease willis ekbom
|
|
D012148|102300||ekbom syndrome
|
|
D012148|102300||periodic limb movements in sleep
|
|
D012148|102300||restless legs
|
|
D012148|102300||restless legs syndrome susceptibility to 1
|
|
D012148|102300||restless legs syndrome susceptibility to 2
|
|
D012148|102300||restless legs syndrome susceptibility to 3
|
|
D012148|102300||restless legs syndrome susceptibility to 4
|
|
D012148|102300||restless legs syndrome susceptibility to 5
|
|
D012148|102300||restless legs syndrome susceptibility to 6
|
|
D012148|102300||restless legs syndrome susceptibility to 7
|
|
D012148|102300||restless leg syndrome
|
|
D012148|102300||rls1
|
|
D012148|102300||rls2
|
|
D012148|102300||rls3
|
|
D012148|102300||rls4
|
|
D012148|102300||rls5
|
|
D012148|102300||rls6
|
|
D012148|102300||rls7
|
|
D012148|102300||syndrome restless leg
|
|
D012148|102300||syndrome willis ekbom
|
|
D012148|102300||syndrome wittmaack ekbom
|
|
D012148|102300||willis ekbom disease
|
|
D012148|102300||willis ekbom syndrome
|
|
D012148|102300||wittmaack ekbom syndrome
|
|
C565251|606187||alzheimer disease 7
|
|
C565251|606187||ad7
|
|
C565251|606187||alzheimer disease familial 7
|
|
C535746|608104||congenital disorder of glycosylation type 1h
|
|
C535746|608104||cdg1h
|
|
C535746|608104||cdgih
|
|
C535746|608104||cdg ih
|
|
C535746|608104||congenital disorder of glycosylation type ih
|
|
300615|C563156||brunner syndrome
|
|
607596|C548069||pontocerebellar hypoplasia type 1
|
|
607596|C548069||pch1
|
|
607596|C548069||pch1a
|
|
607596|C548069||pontocerebellar hypoplasia type 1a
|
|
607596|C548069||pontocerebellar hypoplasia with anterior horn cell disease
|
|
607596|C548069||pontocerebellar hypoplasia with infantile spinal muscular atrophy
|
|
102200|D049912||growth hormone secreting pituitary adenoma
|
|
102200|D049912||acromegaly due to pituitary adenoma
|
|
102200|D049912||acromegaly due to pituitary adenoma pituitary adenoma predisposition included
|
|
102200|D049912||adenoma somatotroph
|
|
102200|D049912||adenomas somatotroph
|
|
102200|D049912||fipa included
|
|
102200|D049912||fis
|
|
102200|D049912||gh secreting pituitary adenoma
|
|
102200|D049912||gh secreting pituitary adenomas
|
|
102200|D049912||ifs
|
|
102200|D049912||isolated familial somatotropinoma
|
|
102200|D049912||pap included
|
|
102200|D049912||pituitary adenoma familial isolated included
|
|
102200|D049912||pituitary adenoma gh secreting
|
|
102200|D049912||pituitary adenoma growth hormone secreting
|
|
102200|D049912||pituitary adenomas gh secreting
|
|
102200|D049912||pituitary growth hormone secreting adenoma
|
|
102200|D049912||somatostatin analog resistance to included
|
|
102200|D049912||somatotroph adenoma
|
|
102200|D049912||somatotroph adenomas
|
|
102200|D049912||somatotrophinoma familial
|
|
102200|D049912||somatotropinoma familial isolated
|
|
301590|C564457||microphthalmia syndromic 4
|
|
301590|C564457||anop1 formerly
|
|
301590|C564457||mcops4
|
|
301590|C564457||microphthalmia with ankyloblepharon and mental retardation
|
|
180100|C538365||retinitis pigmentosa 1
|
|
180100|C538365||rp1
|
|
C537231||samson viljoen syndrome
|
|
C537232||sanderson fraser syndrome
|
|
C537232||proptosis robin association clenched hands and multiple abnormalities
|
|
300158||arthrogryposis congenital lower limb x linked
|
|
300158||acllx
|
|
300158||amcx5 formerly
|
|
300158||arthrogryposis x linked type v formerly
|
|
C537230||samson gardner syndrome
|
|
C537230||craniosynostosis microcephaly hydrancephaly humero radial synostosis and thumb aplasia
|
|
C564854||reese retinal dysplasia
|
|
C538567||hyperinsulinism autosomal recessive
|
|
C537235||santos mateus leal syndrome
|
|
C537235||hirschsprung disease deafness and polydactyly
|
|
C563522||neurofibromatosis pheochromocytoma duodenal carcinoid syndrome
|
|
C563522||duodenal carcinoid syndrome
|
|
C564853||renal and mullerian duct hypoplasia
|
|
D007718||knee injuries
|
|
D007718||injuries knee
|
|
D007718||injury knee
|
|
D007718||knee injury
|
|
C537233||sandhaus ben ami syndrome
|
|
C537233||patella hypoplasia skeletal malformations
|
|
C537234||sandifer syndrome
|
|
C537234||sandifer apos s syndrome
|
|
C563527||retinal degeneration autosomal recessive clumped pigment type
|
|
D007713||klinefelter syndrome
|
|
D007713||48 xxyy syndrome
|
|
D007713||49 xxxxy syndrome
|
|
D007713||klinefelter apos s syndrome
|
|
D007713||klinefelters syndrome
|
|
D007713||klinefelter syndromes
|
|
D007713||klinefelter syndromes variants
|
|
D007713||klinefelter syndrome variants
|
|
D007713||syndrome 48 xxyy
|
|
D007713||syndrome klinefelter
|
|
D007713||syndrome klinefelter apos s
|
|
D007713||syndromes 49 xxxxy
|
|
D007713||syndromes klinefelter
|
|
D007713||syndromes variants klinefelter
|
|
D007713||syndromes xxy
|
|
D007713||syndromes xxyy
|
|
D007713||syndrome variants klinefelter
|
|
D007713||syndrome xxy
|
|
D007713||syndrome xxyy
|
|
D007713||trisomies xxy
|
|
D007713||trisomy xxy
|
|
D007713||xxxy male
|
|
D007713||xxxy males
|
|
D007713||xxy syndrome
|
|
D007713||xxy syndromes
|
|
D007713||xxy trisomies
|
|
D007713||xxy trisomy
|
|
D007713||xxyy syndrome
|
|
D007713||xxyy syndromes
|
|
C563526||retinitis pigmentosa 27
|
|
C564857||radiculoneuropathy fatal neonatal
|
|
D007714||klippel feil syndrome
|
|
D007714||cervical fusion syndrome
|
|
D007714||dystrophia brevicollis congenita
|
|
D007714||dystrophia brevicollis congenitas
|
|
D007714||klippel feil sequence
|
|
D007714||syndrome klippel feil
|
|
D007714||vertebral cervical fusion syndrome
|
|
C564856||radioulnar synostosis unilateral with developmental retardation and hypotonia
|
|
C563524||nf1 microdeletion syndrome
|
|
C535460|246700||chylomicron retention disease
|
|
C535460|246700||andd
|
|
C535460|246700||anderson disease
|
|
C535460|246700||anderson syndrome
|
|
C535460|246700||cmrd
|
|
C535460|246700||hypobetalipoproteinemia with accumulation of apolipoprotein b like protein in intestinal cells
|
|
C535460|246700||lipid transport defect of intestine
|
|
D007710||klebsiella infections
|
|
D007710||infection klebsiella
|
|
D007710||infections klebsiella
|
|
D007710||klebsiella infection
|
|
C563529||myopathy actin congenital with excess of thin myofilaments
|
|
607364|C537653||bartter syndrome type 3
|
|
607364|C537653||bartter syndrome classic
|
|
607364|C537653||bartter syndrome classic bartter syndrome type 3 with hypocalciuria included
|
|
241410|C537157||hypoparathyroidism retardation dysmorphism syndrome
|
|
241410|C537157||hrd
|
|
241410|C537157||hypoparathyroidism congenital associated with dysmorphism growth retardation and developmental delay
|
|
241410|C537157||hypoparathyroidism with short stature mental retardation and seizures
|
|
241410|C537157||sanjad sakati syndrome
|
|
C537228||salcedo syndrome
|
|
C537228||glomerular basement membrane disease nail patella syndrome type
|
|
C537228||nail patella like renal disease
|
|
C537229||sammartino de crecchio syndrome
|
|
C536602|604537||amaurosis congenita of leber type 5
|
|
C536602|604537||lca5
|
|
C536602|604537||leber congenital amaurosis 5
|
|
C536602|604537||leber congenital amaurosis type 5
|
|
C538558||bilateral kienbock apos s disease
|
|
C537226||saito kuba tsuruta syndrome
|
|
C537226||fibuloulnar aplasia or hypoplasia with renal abnormalities
|
|
C537226||fibulo ulnar hypoplasia renal anomalies
|
|
C567649|613309||diamond blackfan anemia 10
|
|
C567649|613309||dba10
|
|
C538557||renal cell carcinoma 1
|
|
C537227||sakati syndrome
|
|
C537227||acps iii
|
|
C537227||acps with leg hypoplasia
|
|
C537227||acrocephalopolysyndactyly type 3
|
|
C537227||acrocephalopolysyndactyly type iii
|
|
C537227||sakati nyhan syndrome
|
|
608864||orofacial cleft 6 susceptibility to
|
|
608864||cleft lip with or without cleft palate nonsyndromic 6
|
|
608864||ofc6
|
|
C580095||familial osteochondritis dissecans
|
|
C564833|268150||rh null regulator type
|
|
C564833|268150||rh deficiency syndrome included
|
|
C564833|268150||rhn
|
|
C564833|268150||rh null disease
|
|
C564833|268150||rh null disease included
|
|
C563530||necrotizing encephalomyelopathy subacute of leigh adult
|
|
C563530||leigh syndrome adult
|
|
C564861||pygmy
|
|
C564861||pygmy african
|
|
C537242||prosopagnosia hereditary
|
|
C537242||face blindness
|
|
C537242||prosopagnosia congenital
|
|
C537243||prostate cancer familial
|
|
C537243||hereditary prostate cancer
|
|
C538572||familial progressive supranuclear palsy
|
|
C537246||hemiplegic migraine familial type 2
|
|
C537246||familial hemiplegic migraine type 2
|
|
C563533||nasal alar collapse bilateral
|
|
C564864||pseudouridinuria and mental defect
|
|
D007729||kuru
|
|
D007729||encephalopathy kuru
|
|
D007729||kuru encephalopathy
|
|
C537247||hemochromatosis type 2
|
|
C537247||hemochromatosis juvenile
|
|
C537247||juvenile hemochromatosis
|
|
C564863||pulmonary bullae causing pneumothorax
|
|
C537244||prostatic malacoplakia associated with prostatic abscess
|
|
C537244||prostatic malacoplakia with prostatic and seminal vesicle abscess
|
|
C564862||pulmonary hypertension primary autosomal recessive
|
|
C537245||prostatic stromal proliferation of uncertain malignant potential
|
|
C564869||pseudohermaphroditism female with skeletal anomalies
|
|
D007724||vulvar lichen sclerosus
|
|
D007724||kraurosis vulvae
|
|
D007724||lichen sclerosus of vulva
|
|
D007724||lichen sclerosus vulvar
|
|
D007724||sclerosus vulvar lichen
|
|
D007724||vulvae kraurosis
|
|
D007724||vulva lichen sclerosus
|
|
C564868||polycystic ovarian disease due to 17 ketosteroid reductase deficiency
|
|
D007725||krukenberg tumor
|
|
D007725||carcinoma krukenberg
|
|
D007725||krukenberg carcinoma
|
|
D007725||krukenberg apos s tumor
|
|
D007725||krukenbergs tumor
|
|
D007725||tumor krukenberg
|
|
D007725||tumor krukenberg apos s
|
|
C563535||myotonic myopathy with cylindrical spirals
|
|
C564866||acrootoocular syndrome
|
|
C564866||pseudopapilledema ocular hypotelorism blepharophimosis and hand anomalies
|
|
C563991|600138||retinitis pigmentosa 11
|
|
C563991|600138||rp11
|
|
C565237|606325||heterotaxy visceral 3 autosomal
|
|
C565237|606325||htx3
|
|
608850||macular dystrophy retinal 3
|
|
608850||mcdr3
|
|
608852||pulmonary function
|
|
608852||lung function accelerated rate of decline in smoking related
|
|
608852||plf
|
|
C564520|300029||retinitis pigmentosa 3
|
|
C564520|300029||choroidoretinal degeneration with retinal reflex in heterozygous women
|
|
C564520|300029||cone rod degeneration x linked
|
|
C564520|300029||retinitis pigmentosa 15
|
|
C564520|300029||rp15
|
|
C564520|300029||rp3
|
|
C537239||mengel konigsmark syndrome
|
|
C537239||conductive hearing loss and malformed low set ears
|
|
C537239||ear deformity and conductive hearing loss
|
|
C537239||familial congenital moderate neural hearing loss
|
|
D019701||hepatitis d chronic
|
|
D019701||chronic delta hepatitides
|
|
D019701||chronic delta hepatitis
|
|
D019701||chronic hepatitis d
|
|
D019701||delta hepatitides chronic
|
|
D019701||delta hepatitis chronic
|
|
D019701||hepatitides chronic delta
|
|
D019701||hepatitis chronic delta
|
|
C537238||melhem fahl syndrome
|
|
C537238||fifteen dorsal vertebrae and rib pairs
|
|
C538585||oral facial digital syndrome type 2
|
|
C538585||orofaciodigital syndrome 2
|
|
C537254||hemorrhagic shock and encephalopathy syndrome
|
|
C563853|608808||transposition of the great arteries dextro looped 1
|
|
C563853|608808||d tga
|
|
C563853|608808||dtga1
|
|
300136||diabetes mellitus insulin dependent x linked susceptibility to
|
|
300136||iddmx
|
|
300136||insulin dependent diabetes mellitus x linked susceptibility to
|
|
C563501||ophthalmomandibulomelic dysplasia
|
|
C563500||ophthalmoplegia familial static
|
|
C563500||external ophthalmoplegia congenital hereditary nonprogressive
|
|
C537258||fibrolamellar hepatocellular carcinoma
|
|
C537258||fibrolamellar variant of hepatocellular carcinoma
|
|
C537258||hepatocellular carcinoma fibrolamellar variant
|
|
C538586||hyperostosis frontalis interna obesity shortness and cognitive impairment
|
|
C537256||vascular purpura
|
|
C563505||olivopontocerebellar atrophy v
|
|
C563505||opca with dementia and extrapyramidal signs
|
|
C563503||onycholysis partial with scleronychia
|
|
162400||neuropathy hereditary sensory and autonomic type ia
|
|
162400||hsan1a
|
|
162400||hsan ia
|
|
162400||hsn1a
|
|
162400||hsn ia
|
|
162400||neuropathy hereditary sensory radicular autosomal dominant type 1a
|
|
162400||neuropathy hereditary sensory type ia
|
|
C563509||schilbach rott syndrome ocular hypotelorism submucosal cleft palate and hypospadias
|
|
C563509||blepharofacioskeletal syndrome
|
|
C563509||cleft palate hypotelorism and hypospadias
|
|
C563509||ocular hypotelorism submucosal cleft palate and hypospadias
|
|
C563508||oculopharyngodistal myopathy
|
|
C564839||retinohepatoendocrinologic syndrome
|
|
C564838||retinopathy pericentral pigmentary autosomal recessive
|
|
C564838||retinitis pigmentosa pericentral
|
|
C537152|154020||hypomagnesemia 2 renal
|
|
C537152|154020||homg2
|
|
C537152|154020||magnesium loss isolated renal
|
|
C537152|154020||magnesium wasting renal
|
|
C563506||onychogryposis pedal with keratosis plantaris and coarse hair
|
|
608840||muscular dystrophy dystroglycanopathy congenital with mental retardation type b 6
|
|
608840||mdc1d
|
|
608840||mddgb6
|
|
608840||muscular dystrophy congenital large related
|
|
277300||scdo1
|
|
277300||vertebral anomalies
|
|
C536856|607152||spastic paraplegia 19 autosomal dominant
|
|
C536856|607152||spg19
|
|
607514||body mass index quantitative trait locus 10
|
|
607514||bmiq10
|
|
C580075||familial acute myeloid leukemia with mutated cebpa
|
|
C580075||cebpa dependent familial acute myeloid leukemia
|
|
C580075||familial acute myeloid leukaemia
|
|
300143||mrx34
|
|
D012288||rickettsiaceae infections
|
|
D012288||infection rickettsiaceae
|
|
D012288||infections rickettsiaceae
|
|
D012288||rickettsiaceae infection
|
|
D012288||rickettsialpox
|
|
C538596||peritoneal retractile mesenteritis
|
|
C538595||mermaid syndrome
|
|
C538595||fused legs and feet
|
|
C538595||mermaid malformation
|
|
C538595||sirenomelia sequence
|
|
C538595||sirenomelus
|
|
300147||prostate cancer hereditary x linked 1
|
|
300147||hpcx1
|
|
300147||pcsx
|
|
300147||prostate cancer susceptibility x linked
|
|
C537263||lamellar ichthyosis autosomal dominant form
|
|
C537263||autosomal dominant lamellar ichthyosis
|
|
C537263||ichthyosiform erythroderma nonbullous dominant form
|
|
C537263||ichthyosis lamellar autosomal dominant
|
|
C537263||lamellar ichthyosis autosomal dominant
|
|
C537263||lamellar ichthyosis dominant
|
|
C563512||noduli cutanei multiple with urinary tract abnormalities
|
|
C537268||formaldehyde poisoning
|
|
C537268||formaldehyde exposure
|
|
C537268||formaldehyde toxicity
|
|
C537268||formalin intoxication
|
|
C537268||formalin toxicity
|
|
C564842||retinitis pigmentosa inversa with deafness
|
|
611376|C548078||mungan syndrome
|
|
611376|C548078||mgs
|
|
611376|C548078||pseudoobstruction chronic idiopathic intestinal with barrett esophagus and cardiac abnormalities
|
|
611376|C548078||visceral neuromyopathy familial with pseudoobstruction megaduodenum barrett esophagus and cardiac abnormalities
|
|
C567166|610532||leukodystrophy hypomyelinating 5
|
|
C567166|610532||hld5
|
|
C567166|610532||hypomyelination and congenital cataract
|
|
C567166|610532||hypomyelination and congenital cataract hcc
|
|
C537269||forney robinson pascoe syndrome
|
|
C537269||congenital heart disease deafness and skeletal malformations
|
|
C564841||retinitis pigmentosa deafness mental retardation and hypogonadism
|
|
C537266||landy donnai syndrome
|
|
C537266||hydrops ectrodactyly syndactyly duplication of the great toes
|
|
C564840||retinitis pigmentosa late adult onset
|
|
C564840||retinitis pigmentosa senile
|
|
256731|C575534||ceroid lipofuscinosis neuronal 5
|
|
256731|C575534||ceroid lipofuscinosis neuronal 5 variable age at onset
|
|
256731|C575534||ceroid lipofuscinosis neuronal 5 variable age at onset neuronal ceroid lipofuscinosis late infantile finnish variant included
|
|
256731|C575534||cln5
|
|
256731|C575534||finnish vlincl
|
|
256731|C575534||finnish vlincl included
|
|
256731|C575534||neuronal ceroid lipofuscinosis 5
|
|
256731|C575534||neuronal ceroid lipofuscinosis finnish variant late infantile
|
|
256731|C575534||vlincl
|
|
C563516||neuropathy with paraprotein in serum cerebrospinal fluid and urine
|
|
C564847||retinal degeneration and epilepsy
|
|
C563514||hypertension resistant to conventional therapy
|
|
D050336|253250||mulibrey nanism
|
|
D050336|253250||mulibrey nanism syndrome
|
|
D050336|253250||muscle liver brain eye nanism
|
|
D050336|253250||nanism mulibrey
|
|
D050336|253250||nanism muscle liver brain eye
|
|
D050336|253250||nanism syndrome mulibrey
|
|
D050336|253250||perheentupa syndrome
|
|
D050336|253250|C538604||pericardial constriction and growth failure
|
|
D050336|253250||syndrome mulibrey nanism
|
|
D050336|253250||syndrome perheentupa
|
|
C564844||retinal dystrophy reticular pigmentary of posterior pole
|
|
C537260||hereditary koilonychia
|
|
C537260||congenital koilonychia
|
|
C537260||familial koilonychia
|
|
C537260||koilonychia hereditary
|
|
C563519||ganglioneuromatosis of the alimentary tract
|
|
C564849||renal genital and middle ear anomalies
|
|
C538590||necrotizing encephalopathy infantile subacute of leigh
|
|
C538590||leigh apos s necrotizing encephalopathy
|
|
C563517||neuropathy hereditary sensorimotor with upper motor neuron visual pathway and autonomic disturbance
|
|
C564848||respiratory underresponsiveness to hypoxia and hypercapnia
|
|
D000130|100800||achondroplasia
|
|
D000130|100800||ach
|
|
D000130|100800||achondroplasias
|
|
D000130|100800||achondroplasia severe with developmental delay and acanthosis nigricans
|
|
D000130|100800||dysplasia saddan
|
|
D000130|100800||dysplasias saddan
|
|
D000130|100800||saddan
|
|
D000130|100800||saddan dysplasia
|
|
D000130|100800||saddan dysplasias
|
|
D000130|100800||saddans
|
|
D000130|100800||severe achondroplasia with developmental delay and acanthosis nigricans
|
|
D000130|100800||skeleton skin brain syndrome
|
|
D000130|100800||skeleton skin brain syndromes
|
|
D000130|100800||syndrome skeleton skin brain
|
|
D000130|100800||syndromes skeleton skin brain
|
|
D062625||cystadenofibroma
|
|
D062625||adenofibroma clear cell
|
|
D062625||adenofibromas clear cell
|
|
D062625||benign clear cell adenofibroma
|
|
D062625||benign cystadenofibroma
|
|
D062625||benign cystadenofibromas
|
|
D062625||borderline clear cell adenofibroma
|
|
D062625||borderline cystadenofibroma
|
|
D062625||borderline cystadenofibromas
|
|
D062625||clear cell adenofibroma
|
|
D062625||clear cell adenofibromas
|
|
D062625||cystadenofibroma benign
|
|
D062625||cystadenofibroma borderline
|
|
D062625||cystadenofibromas
|
|
D062625||cystadenofibromas benign
|
|
D062625||cystadenofibromas borderline
|
|
C580087||familial hyperaldosteronism
|
|
D012295||rift valley fever
|
|
D012295||fever rift valley
|
|
D012298||rigor mortis
|
|
D012298||mortis rigor
|
|
C580083||familial exudative vitreoretinopathy
|
|
C538640||limb girdle muscular dystrophy autosomal recessive
|
|
C563600||masticatory muscles hypertrophy of
|
|
C563600||masseter muscle hypertrophy
|
|
C564931||oliver syndrome
|
|
C564931||postaxial polydactyly and mental retardation
|
|
D012391||root resorption
|
|
D012391||resorption root
|
|
D012391||resorptions root
|
|
D012391||root resorptions
|
|
C564930||olivopontocerebellar atrophy ii autosomal recessive
|
|
C564930||opca ii fickler winkler type
|
|
C567757|613094||microphthalmia isolated 4
|
|
C567757|613094||mcop4
|
|
C538641||congenital facial linear porokeratosis
|
|
C565234|606348||inflammatory bowel disease 5
|
|
C565234|606348||ibd5
|
|
C563604||cataract cortical pulverulent late onset
|
|
C563603||cataract polymorphic and lamellar
|
|
C564934||oculotrichodysplasia
|
|
C563602||mannose binding protein deficiency
|
|
C563602||mannose binding lectin deficiency
|
|
C563602||mannose binding lectin protein deficiency
|
|
C563602||mbl2 deficiency
|
|
C563602||mbl deficiency
|
|
C563602||mbp deficiency
|
|
C563601||mannose 6 phosphate receptor recognition defect lebanese type
|
|
C563601||phosphodiester glycoside deficiency
|
|
C563607||macular dystrophy fenestrated sheen type
|
|
C564938||nystagmus congenital motor autosomal recessive
|
|
C564937||ocular myopathy with curare sensitivity
|
|
D061205||vascular calcification
|
|
D061205||calcifications vascular
|
|
D061205||calcification vascular
|
|
D061205||calcinoses vascular
|
|
D061205||calcinosis vascular
|
|
D061205||vascular calcifications
|
|
D061205||vascular calcinoses
|
|
D061205||vascular calcinosis
|
|
D061206||neoplasm micrometastasis
|
|
D061206||micrometastase neoplasm
|
|
D061206||micrometastases
|
|
D061206||micrometastases neoplasm
|
|
D061206||micrometastasis
|
|
D061206||micrometastasis neoplasm
|
|
D061206||neoplasm micrometastase
|
|
D061206||neoplasm micrometastases
|
|
C537848|257320||norman roberts lissencephaly syndrome
|
|
C537848|257320||lis2
|
|
C537848|257320||lissencephaly 2
|
|
C537848|257320||lissencephaly syndrome norman roberts type
|
|
C537848|257320||norman roberts syndrome
|
|
D011668|265450||pulmonary veno occlusive disease
|
|
D011668|265450||diseases pulmonary veno occlusive
|
|
D011668|265450||pulmonary venoocclusive disease
|
|
D011668|265450||pulmonary venoocclusive disease 1 autosomal dominant
|
|
D011668|265450||pulmonary venoocclusive diseases
|
|
D011668|265450||pulmonary veno occlusive diseases
|
|
D011668|265450||pvod
|
|
D011668|265450||pvod1
|
|
D011668|265450||venoocclusive disease pulmonary
|
|
D011668|265450||veno occlusive disease pulmonary
|
|
D011668|265450||venoocclusive diseases pulmonary
|
|
D011668|265450||veno occlusive diseases pulmonary
|
|
D011052||poliomyelitis bulbar
|
|
D011052||bulbar polio
|
|
D011052||bulbar poliomyelitis
|
|
D011052||medullary involvement poliomyelitis
|
|
D011052||polio bulbar
|
|
D011052||poliomyelitis medullary involvement
|
|
C538637||autosomal dominant diffuse lewy body disease
|
|
C537305||groll hirschowitz syndrome
|
|
C537305||deafness nerve type with mesenteric diverticula of small bowel and progressive sensory neuropathy
|
|
D011051||poliomyelitis
|
|
D011051||acute poliomyelitis
|
|
D011051||acute poliomyelitis epidemic
|
|
D011051||encephalitis polio
|
|
D011051||epidemic acute poliomyelitis
|
|
D011051||infantile paralysis
|
|
D011051||nonpoliovirus poliomyelitis
|
|
D011051||paralysis infantile
|
|
D011051||polio
|
|
D011051||polio encephalitis
|
|
D011051||poliomyelitides preparalytic
|
|
D011051||poliomyelitis acute
|
|
D011051||poliomyelitis epidemic acute
|
|
D011051||poliomyelitis nonpoliovirus
|
|
D011051||poliomyelitis preparalytic
|
|
D011051||polios
|
|
D011051||preparalytic poliomyelitis
|
|
C537835|136550||macular dystrophy retinal 1 north carolina type
|
|
C537835|136550||caped
|
|
C537835|136550||central areolar pigment epithelial dystrophy
|
|
C537835|136550||foveal dystrophy progressive
|
|
C537835|136550||mcdr1
|
|
C537835|136550||ncmd
|
|
C537835|136550||north carolina macular dystrophy
|
|
C537835|136550||retinal pigment epithelial dystrophy central
|
|
C538636||familial letterer siwe disease
|
|
C538636||histiocytosis x acute disseminated
|
|
C537306||grover apos s disease
|
|
C537306||grover disease
|
|
C537306||transient acantholytic dermatosis
|
|
C580174||huntington disease like syndrome
|
|
C580174||huntington disease like syndromes
|
|
C580174||huntington apos s disease like syndromes
|
|
C580174||huntington apos s disease phenocopies
|
|
C580174||huntington apos s disease phenocopy syndromes
|
|
300244||terminal osseous dysplasia
|
|
300244||odpd
|
|
300244||odpf
|
|
300244||odpf syndrome
|
|
300244||tod
|
|
300244||todpd
|
|
C537320||microcephalic osteodysplastic primordial dwarfism type 3
|
|
C537320||microcephalic osteodysplastic primordial dwarfism caroline crachami type
|
|
C537320||microcephalic osteodysplastic primordial dwarfism sicilian fairy type
|
|
C537320||microcephalic osteodysplastic primordial dwarfism type iii
|
|
C537320||mopd iii
|
|
C537320||osteodysplastic primordial dwarfism type 3
|
|
C537320||osteodysplastic primordial dwarfism type iii
|
|
D007805||language development disorders
|
|
D007805||auditory processing disorder central
|
|
D007805||central auditory processing disorder
|
|
D007805||delay speech
|
|
D007805||delays speech
|
|
D007805||developmental disorder speech or language
|
|
D007805||developmental language disorder
|
|
D007805||developmental language disorders
|
|
D007805||development disorder language
|
|
D007805||language delay
|
|
D007805||language delays
|
|
D007805||language development disorder
|
|
D007805||language disorder developmental
|
|
D007805||language disorders developmental
|
|
D007805||semantic pragmatic disorder
|
|
D007805||semantic pragmatic disorders
|
|
D007805||speech delay
|
|
D007805||speech delays
|
|
D007805||speech or language developmental disorder
|
|
C564942||neutrophil actin dysfunction
|
|
C537323||microcephaly autosomal dominant
|
|
C537323||microcephaly with autosomal dominant inheritance
|
|
C563610||sebaceous tumors somatic
|
|
D007806||language disorders
|
|
D007806||acquired language disorder
|
|
D007806||acquired language disorders
|
|
D007806||language disorder
|
|
D007806||language disorder acquired
|
|
D007806||language disorders acquired
|
|
C564941||niemann pick disease nova scotian type
|
|
C537321||microcephalic primordial dwarfism toriello type
|
|
C537321||microcephalic primordial dwarfism and cataracts
|
|
C537322||microcephaly albinism digital anomalies syndrome
|
|
C537322||albinism microcephaly digital anomalies syndrome
|
|
C564946||neuropathy hereditary sensory atypical
|
|
C564945||neuropathy painful
|
|
C563613||lumbar stenosis familial
|
|
C564944||neurovisceral storage disease with curvilinear bodies
|
|
C563612||lymphedema and cerebral arteriovenous anomaly
|
|
C564943||neutropenia lethal congenital with eosinophilia
|
|
C563618||lp a deficiency congenital
|
|
C563618||lipoprotein a deficiency congenital
|
|
C537698|601553||juvenile macular degeneration and hypotrichosis
|
|
C537698|601553||hjmd
|
|
C537698|601553||hypotrichosis congenital with juvenile macular dystrophy
|
|
C537698|601553||hypotrichosis with cone rod dystrophy
|
|
C537698|601553||juvenile macular dystrophy and congenital hypotrichosis
|
|
C563617||lipoprotein types lp system lp a hyperlipoproteinemia
|
|
C565210|610250||spastic paraplegia 31 autosomal dominant
|
|
C565210|610250||spg31
|
|
C564947||neuropathy hereditary motor and sensory with excessive myelin folding complex autosomal recessive
|
|
C564947||charcot marie tooth disease with excessive myelin folding autosomal recessive
|
|
C563873|608696||glaucoma 1 open angle k
|
|
C563873|608696||glaucoma primary open angle juvenile onset 3
|
|
C563873|608696||glc1k
|
|
C563873|608696||joag3
|
|
220600|C565647||split hand foot malformation with sensorineural hearing loss
|
|
220600|C565647||deafness congenital and split hands and feet
|
|
220600|C565647||deafness congenital with split hands and feet
|
|
220600|C565647||shfm1d
|
|
220600|C565647||split hand foot malformation 1 with sensorineural hearing loss autosomal recessive
|
|
C032598||heavy chain disease proteins human
|
|
C538648||lysosomal alpha n acetylgalactosaminidase deficiency
|
|
C535717|604484||neuropathy hereditary motor and sensory okinawa type
|
|
C535717|604484||hereditary motor and sensory neuropathy proximal type
|
|
C535717|604484||hmsno
|
|
C535717|604484||hmsnp
|
|
C538646||high serum cholesterol familial
|
|
C538646||hyperlipidema familial
|
|
C538646||hyperlipoproteinemia type 2 a
|
|
D012393||rosacea
|
|
D012393||acne rosacea
|
|
D012393||erythematotelangiectatic rosacea
|
|
D012393||granulomatous rosacea
|
|
D012393||ocular rosacea
|
|
D012393||papulopustular rosacea
|
|
D012393||phymatous rosacea
|
|
D012393||rosacea erythematotelangiectatic
|
|
D012393||rosacea granulomatous
|
|
D012393||rosacea ocular
|
|
D012393||rosacea papulopustular
|
|
D012393||rosacea phymatous
|
|
C537318||splenogonadal fusion limb defects micrognatia
|
|
C537318||splenogonadal fusion limb defects syndrome
|
|
C537318||splenogonadal fusion limb defect syndrome
|
|
C537318||splenogonadal fusion with limb defects and micrognathia
|
|
C580182||hyperparathyroidism jaw tumor syndrome
|
|
C580182||familial cystic parathyroid adenomatosis
|
|
C580182||familial primary hyperparathyroidism with multiple ossifying jaw fibromas
|
|
C580182||hereditary hyperparathyroidism jaw tumor syndrome
|
|
C580182||hpt jt
|
|
C537319||split hand split foot nystagmus
|
|
C537319||karsch neugebauer syndrome
|
|
C537319||nystagmus split hand syndrome
|
|
C537319||split hand nystagmus syndrome
|
|
C537319||split hand with congenital nystagmus fundal changes and cataracts
|
|
C538662||recurrent trigger thumb
|
|
C538662||bilateral trigger thumb
|
|
C538662||congenital trigger thumb
|
|
C536130|606129||anemia diamond blackfan 2
|
|
C536130|606129||dba2
|
|
C536130|606129||diamond blackfan anemia 2
|
|
D056734|158000||monilethrix
|
|
D056734|158000||hair nodose
|
|
D056734|158000||hairs nodose
|
|
D056734|158000||monilethrices
|
|
D056734|158000||nodose hair
|
|
D056734|158000||nodose hairs
|
|
C536000||acanthosis nigricans muscle cramps acral enlargement
|
|
C536000||acanthosis nigricans with muscle cramps and acral enlargement
|
|
C536003||accessory pancreas
|
|
C537334||sideroblastic anemia autosomal
|
|
C537334||sideroblastic anemia autosomal recessive inheritance
|
|
C538665||watermelon stomach disease
|
|
C567462|300758||hypospadias 2 x linked
|
|
C567462|300758||hysp2
|
|
C537335||siegler brewer carey syndrome
|
|
C538664||pica syndrome
|
|
C538664||vertebral artery syndrome
|
|
C536001||accessory deep peroneal nerve
|
|
C536001||peroneal nerve accessory deep
|
|
C536002||accessory navicular bone
|
|
C536002||navicular bone accessory
|
|
D061220||oculomotor nerve injuries
|
|
D061220||avulsion oculomotor nerve
|
|
D061220||avulsions oculomotor nerve
|
|
D061220||contusion oculomotor nerve
|
|
D061220||contusions oculomotor nerve
|
|
D061220||cranial nerve iii injury
|
|
D061220||injuries oculomotor nerve
|
|
D061220||injury cranial nerve iii
|
|
D061220||injury oculomotor nerve
|
|
D061220||injury third cranial nerve
|
|
D061220||nerve avulsion oculomotor
|
|
D061220||nerve avulsions oculomotor
|
|
D061220||nerve contusion oculomotor
|
|
D061220||nerve contusions oculomotor
|
|
D061220||nerve injuries oculomotor
|
|
D061220||nerve injury oculomotor
|
|
D061220||nerve transection oculomotor
|
|
D061220||nerve transections oculomotor
|
|
D061220||nerve trauma oculomotor
|
|
D061220||nerve traumas oculomotor
|
|
D061220||neuropathies traumatic oculomotor
|
|
D061220||neuropathy traumatic oculomotor
|
|
D061220||oculomotor nerve avulsion
|
|
D061220||oculomotor nerve avulsions
|
|
D061220||oculomotor nerve contusion
|
|
D061220||oculomotor nerve contusions
|
|
D061220||oculomotor nerve injury
|
|
D061220||oculomotor nerve transection
|
|
D061220||oculomotor nerve transections
|
|
D061220||oculomotor nerve trauma
|
|
D061220||oculomotor nerve traumas
|
|
D061220||oculomotor neuropathies traumatic
|
|
D061220||oculomotor neuropathy traumatic
|
|
D061220||palsies traumatic third nerve
|
|
D061220||palsy traumatic third nerve
|
|
D061220||third cranial nerve injuries
|
|
D061220||third cranial nerve injury
|
|
D061220||third nerve palsies traumatic
|
|
D061220||third nerve palsy traumatic
|
|
D061220||third nerve trauma
|
|
D061220||third nerve traumas
|
|
D061220||transection oculomotor nerve
|
|
D061220||transections oculomotor nerve
|
|
D061220||trauma oculomotor nerve
|
|
D061220||traumas oculomotor nerve
|
|
D061220||traumas third nerve
|
|
D061220||trauma third nerve
|
|
D061220||traumatic oculomotor neuropathies
|
|
D061220||traumatic oculomotor neuropathy
|
|
D061220||traumatic third nerve palsies
|
|
D061220||traumatic third nerve palsy
|
|
C564912||otoonychoperoneal syndrome
|
|
D000382||agricultural workers apos diseases
|
|
D000382||agricultural worker disease
|
|
D000382||agricultural worker diseases
|
|
D000382||agricultural worker apos s disease
|
|
D000382||agricultural workers disease
|
|
D000382||agricultural workers apos disease
|
|
D000382||agricultural worker apos s diseases
|
|
D000382||agricultural workers diseases
|
|
D000382||disease agricultural worker
|
|
D000382||disease agricultural worker apos s
|
|
D000382||disease agricultural workers apos
|
|
D000382||diseases agricultural worker
|
|
D000382||diseases agricultural worker apos s
|
|
D000382||diseases agricultural workers apos
|
|
D000382||worker disease agricultural
|
|
D000382||worker diseases agricultural
|
|
D000382||worker apos s disease agricultural
|
|
D000382||workers apos disease agricultural
|
|
D000382||worker apos s diseases agricultural
|
|
D000382||workers apos diseases agricultural
|
|
D061221||trigeminal nerve injuries
|
|
D061221||avulsions trigeminal nerve
|
|
D061221||avulsion trigeminal nerve
|
|
D061221||contusions trigeminal nerve
|
|
D061221||contusion trigeminal nerve
|
|
D061221||cranial nerve v injury
|
|
D061221||fifth cranial nerve injuries
|
|
D061221||fifth cranial nerve injury
|
|
D061221||fifth nerve palsies traumatic
|
|
D061221||fifth nerve palsy traumatic
|
|
D061221||fifth nerve trauma
|
|
D061221||fifth nerve traumas
|
|
D061221||injuries trigeminal nerve
|
|
D061221||injury cranial nerve v
|
|
D061221||injury fifth cranial nerve
|
|
D061221||injury trigeminal nerve
|
|
D061221||nerve avulsions trigeminal
|
|
D061221||nerve avulsion trigeminal
|
|
D061221||nerve contusions trigeminal
|
|
D061221||nerve contusion trigeminal
|
|
D061221||nerve injuries trigeminal
|
|
D061221||nerve injury trigeminal
|
|
D061221||nerve transections trigeminal
|
|
D061221||nerve transection trigeminal
|
|
D061221||nerve traumas trigeminal
|
|
D061221||nerve trauma trigeminal
|
|
D061221||neuropathies traumatic trigeminal
|
|
D061221||neuropathy traumatic trigeminal
|
|
D061221||palsies traumatic fifth nerve
|
|
D061221||palsy traumatic fifth nerve
|
|
D061221||transections trigeminal nerve
|
|
D061221||transection trigeminal nerve
|
|
D061221||trauma fifth nerve
|
|
D061221||traumas fifth nerve
|
|
D061221||traumas trigeminal nerve
|
|
D061221||traumatic fifth nerve palsies
|
|
D061221||traumatic fifth nerve palsy
|
|
D061221||traumatic trigeminal neuropathies
|
|
D061221||traumatic trigeminal neuropathy
|
|
D061221||trauma trigeminal nerve
|
|
D061221||trigeminal nerve avulsion
|
|
D061221||trigeminal nerve avulsions
|
|
D061221||trigeminal nerve contusion
|
|
D061221||trigeminal nerve contusions
|
|
D061221||trigeminal nerve injury
|
|
D061221||trigeminal nerve transection
|
|
D061221||trigeminal nerve transections
|
|
D061221||trigeminal nerve trauma
|
|
D061221||trigeminal nerve traumas
|
|
D061221||trigeminal neuropathies traumatic
|
|
D061221||trigeminal neuropathy traumatic
|
|
D000381||agraphia
|
|
D000381||acquired agraphia
|
|
D000381||acquired agraphias
|
|
D000381||acquired dysgraphia
|
|
D000381||acquired dysgraphias
|
|
D000381||agraphia acquired
|
|
D000381||agraphia constructional
|
|
D000381||agraphia developmental
|
|
D000381||agraphia pure
|
|
D000381||agraphias
|
|
D000381||agraphias acquired
|
|
D000381||agraphias constructional
|
|
D000381||agraphias developmental
|
|
D000381||agraphias pure
|
|
D000381||constructional agraphia
|
|
D000381||constructional agraphias
|
|
D000381||developmental agraphia
|
|
D000381||developmental agraphias
|
|
D000381||developmental dysgraphia
|
|
D000381||developmental dysgraphias
|
|
D000381||dysgraphia
|
|
D000381||dysgraphia acquired
|
|
D000381||dysgraphia developmental
|
|
D000381||dysgraphias
|
|
D000381||dysgraphias acquired
|
|
D000381||dysgraphias developmental
|
|
D000381||pure agraphia
|
|
D000381||pure agraphias
|
|
D061222||lingual nerve injuries
|
|
D061222||contusion lingual nerve
|
|
D061222||contusions lingual nerve
|
|
D061222||injuries lingual nerve
|
|
D061222||injury lingual nerve
|
|
D061222||lingual nerve contusion
|
|
D061222||lingual nerve contusions
|
|
D061222||lingual nerve injury
|
|
D061222||lingual nerve transection
|
|
D061222||lingual nerve transections
|
|
D061222||lingual neuropathy traumatic
|
|
D061222||nerve contusion lingual
|
|
D061222||nerve contusions lingual
|
|
D061222||nerve injuries lingual
|
|
D061222||nerve injury lingual
|
|
D061222||nerve transection lingual
|
|
D061222||nerve transections lingual
|
|
D061222||transection lingual nerve
|
|
D061222||transections lingual nerve
|
|
C564910||pallidal degeneration progressive with retinitis pigmentosa
|
|
D061223||vagus nerve injuries
|
|
D061223||avulsions vagus nerve
|
|
D061223||avulsion vagus nerve
|
|
D061223||contusions vagus nerve
|
|
D061223||contusion vagus nerve
|
|
D061223||cranial nerve x injury
|
|
D061223||injuries vagus nerve
|
|
D061223||injury cranial nerve x
|
|
D061223||injury tenth cranial nerve
|
|
D061223||injury vagus nerve
|
|
D061223||nerve avulsions vagus
|
|
D061223||nerve avulsion vagus
|
|
D061223||nerve contusions vagus
|
|
D061223||nerve contusion vagus
|
|
D061223||nerve injuries vagus
|
|
D061223||nerve injury vagus
|
|
D061223||nerve transections vagus
|
|
D061223||nerve transection vagus
|
|
D061223||nerve traumas vagus
|
|
D061223||nerve trauma vagus
|
|
D061223||neuropathies traumatic vagus
|
|
D061223||neuropathy traumatic vagus
|
|
D061223||palsies traumatic tenth nerve
|
|
D061223||palsy traumatic tenth nerve
|
|
D061223||tenth cranial nerve injuries
|
|
D061223||tenth cranial nerve injury
|
|
D061223||tenth nerve palsies traumatic
|
|
D061223||tenth nerve palsy traumatic
|
|
D061223||tenth nerve trauma
|
|
D061223||tenth nerve traumas
|
|
D061223||transections vagus nerve
|
|
D061223||transection vagus nerve
|
|
D061223||traumas tenth nerve
|
|
D061223||traumas vagus nerve
|
|
D061223||trauma tenth nerve
|
|
D061223||traumatic tenth nerve palsies
|
|
D061223||traumatic tenth nerve palsy
|
|
D061223||traumatic vagus neuropathies
|
|
D061223||traumatic vagus neuropathy
|
|
D061223||trauma vagus nerve
|
|
D061223||vagus nerve avulsion
|
|
D061223||vagus nerve avulsions
|
|
D061223||vagus nerve contusion
|
|
D061223||vagus nerve contusions
|
|
D061223||vagus nerve injury
|
|
D061223||vagus nerve transection
|
|
D061223||vagus nerve transections
|
|
D061223||vagus nerve trauma
|
|
D061223||vagus nerve traumas
|
|
D061223||vagus neuropathies traumatic
|
|
D061223||vagus neuropathy traumatic
|
|
C564917||osteoma of middle ear
|
|
D000387||ainhum
|
|
D000387||dactylolyses spontaneous
|
|
D000387||dactylolysis spontanea
|
|
D000387||dactylolysis spontaneous
|
|
D000387||spontaneous dactylolyses
|
|
D000387||spontaneous dactylolysis
|
|
C567672|608980||bifid nose with or without anorectal and renal anomalies
|
|
C567672|608980||bnar
|
|
D061224||laryngeal nerve injuries
|
|
D061224||avulsion laryngeal nerve
|
|
D061224||avulsions laryngeal nerve
|
|
D061224||contusion laryngeal nerve
|
|
D061224||contusions laryngeal nerve
|
|
D061224||injuries laryngeal nerve
|
|
D061224||injury laryngeal nerve
|
|
D061224||laryngeal nerve avulsion
|
|
D061224||laryngeal nerve avulsions
|
|
D061224||laryngeal nerve contusion
|
|
D061224||laryngeal nerve contusions
|
|
D061224||laryngeal nerve injury
|
|
D061224||laryngeal nerve transection
|
|
D061224||laryngeal nerve transections
|
|
D061224||laryngeal nerve trauma
|
|
D061224||laryngeal nerve traumas
|
|
D061224||laryngeal neuropathies traumatic
|
|
D061224||laryngeal neuropathy traumatic
|
|
D061224||nerve avulsion laryngeal
|
|
D061224||nerve avulsions laryngeal
|
|
D061224||nerve contusion laryngeal
|
|
D061224||nerve contusions laryngeal
|
|
D061224||nerve injuries laryngeal
|
|
D061224||nerve injury laryngeal
|
|
D061224||nerve transection laryngeal
|
|
D061224||nerve transections laryngeal
|
|
D061224||nerve trauma laryngeal
|
|
D061224||nerve traumas laryngeal
|
|
D061224||neuropathies traumatic laryngeal
|
|
D061224||neuropathy traumatic laryngeal
|
|
D061224||transection laryngeal nerve
|
|
D061224||transections laryngeal nerve
|
|
D061224||trauma laryngeal nerve
|
|
D061224||traumas laryngeal nerve
|
|
D061224||traumatic laryngeal neuropathies
|
|
D061224||traumatic laryngeal neuropathy
|
|
C564916||osteomalacia sclerosing with cerebral calcification
|
|
D000386||aids related complex
|
|
D000386||arc
|
|
D000386||complex aids related
|
|
D000386||lymphadenopathy syndrome
|
|
D000386||lymphadenopathy syndromes
|
|
D000386||syndrome lymphadenopathy
|
|
D000386||syndromes lymphadenopathy
|
|
D061226||recurrent laryngeal nerve injuries
|
|
D061226||recurrent laryngeal nerve contusion
|
|
D061226||recurrent laryngeal nerve injury
|
|
D061226||recurrent laryngeal nerve transection
|
|
D061226||recurrent laryngeal nerve trauma
|
|
D061226||recurrent laryngeal neuropathy traumatic
|
|
D061227||accessory nerve injuries
|
|
D061227||accessory nerve avulsion
|
|
D061227||accessory nerve avulsions
|
|
D061227||accessory nerve contusion
|
|
D061227||accessory nerve contusions
|
|
D061227||accessory nerve injury
|
|
D061227||accessory nerve transection
|
|
D061227||accessory nerve transections
|
|
D061227||accessory nerve trauma
|
|
D061227||accessory nerve traumas
|
|
D061227||accessory neuropathies traumatic
|
|
D061227||accessory neuropathy traumatic
|
|
D061227||avulsion accessory nerve
|
|
D061227||avulsions accessory nerve
|
|
D061227||contusion accessory nerve
|
|
D061227||contusions accessory nerve
|
|
D061227||cranial nerve xi injury
|
|
D061227||eleventh cranial nerve injuries
|
|
D061227||eleventh cranial nerve injury
|
|
D061227||eleventh nerve palsies traumatic
|
|
D061227||eleventh nerve palsy traumatic
|
|
D061227||eleventh nerve trauma
|
|
D061227||eleventh nerve traumas
|
|
D061227||injuries accessory nerve
|
|
D061227||injury accessory nerve
|
|
D061227||injury cranial nerve xi
|
|
D061227||injury eleventh cranial nerve
|
|
D061227||nerve avulsion accessory
|
|
D061227||nerve avulsions accessory
|
|
D061227||nerve contusion accessory
|
|
D061227||nerve contusions accessory
|
|
D061227||nerve injuries accessory
|
|
D061227||nerve injury accessory
|
|
D061227||nerve transection accessory
|
|
D061227||nerve transections accessory
|
|
D061227||nerve trauma accessory
|
|
D061227||nerve traumas accessory
|
|
D061227||neuropathies traumatic accessory
|
|
D061227||neuropathy traumatic accessory
|
|
D061227||palsies traumatic eleventh nerve
|
|
D061227||palsy traumatic eleventh nerve
|
|
D061227||spinal accessory nerve avulsion
|
|
D061227||spinal accessory nerve contusion
|
|
D061227||spinal accessory nerve injury
|
|
D061227||spinal accessory nerve transection
|
|
D061227||spinal accessory nerve trauma
|
|
D061227||spinal accessory neuropathy traumatic
|
|
D061227||transection accessory nerve
|
|
D061227||transections accessory nerve
|
|
D061227||trauma accessory nerve
|
|
D061227||trauma eleventh nerve
|
|
D061227||traumas accessory nerve
|
|
D061227||traumas eleventh nerve
|
|
D061227||traumatic accessory neuropathies
|
|
D061227||traumatic accessory neuropathy
|
|
D061227||traumatic eleventh nerve palsies
|
|
D061227||traumatic eleventh nerve palsy
|
|
C567190||keratosis familial actinic
|
|
D061228||hypoglossal nerve injuries
|
|
D061228||avulsion hypoglossal nerve
|
|
D061228||avulsions hypoglossal nerve
|
|
D061228||contusion hypoglossal nerve
|
|
D061228||contusions hypoglossal nerve
|
|
D061228||cranial nerve xii injury
|
|
D061228||hypoglossal nerve avulsion
|
|
D061228||hypoglossal nerve avulsions
|
|
D061228||hypoglossal nerve contusion
|
|
D061228||hypoglossal nerve contusions
|
|
D061228||hypoglossal nerve injury
|
|
D061228||hypoglossal nerve transection
|
|
D061228||hypoglossal nerve transections
|
|
D061228||hypoglossal nerve trauma
|
|
D061228||hypoglossal nerve traumas
|
|
D061228||hypoglossal neuropathies traumatic
|
|
D061228||hypoglossal neuropathy traumatic
|
|
D061228||injuries hypoglossal nerve
|
|
D061228||injury cranial nerve xii
|
|
D061228||injury hypoglossal nerve
|
|
D061228||injury twelfth cranial nerve
|
|
D061228||nerve avulsion hypoglossal
|
|
D061228||nerve avulsions hypoglossal
|
|
D061228||nerve contusion hypoglossal
|
|
D061228||nerve contusions hypoglossal
|
|
D061228||nerve injuries hypoglossal
|
|
D061228||nerve injury hypoglossal
|
|
D061228||nerve transection hypoglossal
|
|
D061228||nerve transections hypoglossal
|
|
D061228||nerve trauma hypoglossal
|
|
D061228||nerve traumas hypoglossal
|
|
D061228||neuropathies traumatic hypoglossal
|
|
D061228||neuropathy traumatic hypoglossal
|
|
D061228||palsies traumatic twelfth nerve
|
|
D061228||palsy traumatic twelfth nerve
|
|
D061228||transection hypoglossal nerve
|
|
D061228||transections hypoglossal nerve
|
|
D061228||trauma hypoglossal nerve
|
|
D061228||traumas hypoglossal nerve
|
|
D061228||traumas twelfth nerve
|
|
D061228||traumatic hypoglossal neuropathies
|
|
D061228||traumatic hypoglossal neuropathy
|
|
D061228||traumatic twelfth nerve palsies
|
|
D061228||traumatic twelfth nerve palsy
|
|
D061228||trauma twelfth nerve
|
|
D061228||twelfth cranial nerve injuries
|
|
D061228||twelfth cranial nerve injury
|
|
D061228||twelfth nerve palsies traumatic
|
|
D061228||twelfth nerve palsy traumatic
|
|
D061228||twelfth nerve trauma
|
|
D061228||twelfth nerve traumas
|
|
C567816|613008||biliary cirrhosis primary 3
|
|
C567816|613008||pbc3
|
|
D011030||pneumothorax
|
|
D011030||pneumothorax pressure
|
|
D011030||pneumothorax spontaneous
|
|
D011030||pneumothoraxs pressure
|
|
D011030||pneumothoraxs primary spontaneous
|
|
D011030||pneumothoraxs spontaneous
|
|
D011030||pneumothoraxs tension
|
|
D011030||pneumothorax tension
|
|
D011030||pressure pneumothorax
|
|
D011030||pressure pneumothoraxs
|
|
D011030||primary spontaneous pneumothorax
|
|
D011030||primary spontaneous pneumothoraxs
|
|
D011030||spontaneous pneumothorax
|
|
D011030||spontaneous pneumothorax primary
|
|
D011030||spontaneous pneumothoraxs
|
|
D011030||spontaneous pneumothoraxs primary
|
|
D011030||tension pneumothorax
|
|
D011030||tension pneumothoraxs
|
|
C567198||microcephaly primary autosomal recessive 7
|
|
C537327||short syndrome
|
|
C537327||lipodystrophy partial with rieger anomaly and short stature
|
|
C538657||van der hoeve halbertsma waardenburg gualdi syndrome
|
|
C538657||mende syndrome
|
|
C538657||ptosis epicanthus syndrome
|
|
C537325||microcephaly cervical spine fusion anomalies
|
|
C537325||microcephaly mild mental retardation short stature and skeletal anomalies
|
|
C537325||microcephaly with cervical spine fusion anomalies
|
|
C567199||kallmann syndrome 6
|
|
C537326||microcephaly deafness syndrome
|
|
C537326||kawashima tsuji syndrome
|
|
C537326||syndrome of microcephaly deafness malformed ears mental retardation and peculiar facies
|
|
C580150||hereditary diffuse leukoencephalopathy with spheroids
|
|
C580150||adult onset leukodystrophy with neuroaxonal spheroids
|
|
C580150||autosomal dominant leukoencephalopathy with neuroaxonal spheroids
|
|
C580150||hereditary diffuse leukoencephalopathy with axonal spheroids
|
|
C580150||neuroaxonal leukodystrophy
|
|
C567513|611820||long qt syndrome 11
|
|
C567513|611820||lqt11
|
|
C537329||shprintzen omphalocele syndrome
|
|
C537329||laryngeal and pharyngeal hypoplasia with omphalocele
|
|
C537329||pharynx and larynx hypoplasia with omphalocele
|
|
C537329||shprintzen goldberg omphalocele syndrome
|
|
607501|D020326||migraine without aura
|
|
607501|D020326||common migraine
|
|
607501|D020326||common migraines
|
|
607501|D020326||mgoa
|
|
607501|D020326||mgr4
|
|
607501|D020326||migraine common
|
|
607501|D020326||migraines common
|
|
607501|D020326||migraine without aura susceptibility to 4
|
|
C536010||achalasia microcephaly
|
|
C536010||achalasia microcephaly syndrome
|
|
C537341||singh chhaparwal dhanda syndrome
|
|
C538670||x linked infantile spasm syndrome
|
|
C538670||early infantile epileptic encephalopathy
|
|
C538670||x linked infantile spasms
|
|
C538670||x linked west syndrome
|
|
C538676||melanodermic leukodystrophy
|
|
C537346||mesangial sclerosis diffuse
|
|
C537346||diffuse isolated mesangial sclerosis
|
|
C537346||diffuse mesangial sclerosis
|
|
C537346||familial mesangial sclerosis
|
|
C537346||isolated diffuse mesangial sclerosis
|
|
C537346||mesangial sclerosis familial
|
|
C537346||mesangial sclerosis isolated diffuse
|
|
C537346||nephrotic syndrome early onset with diffuse mesangial sclerosis
|
|
C536012||achard syndrome
|
|
C536012||arachnodactyly receding lower jaw and joint laxity limited to the hands and feet
|
|
C536012||dysostoses and increased ligament laxity
|
|
C536013||achard thiers syndrome
|
|
C536013||adenoma associated virilism of older women
|
|
C536013||bearded female with diabetes
|
|
C536013||diabetes in bearded women
|
|
C536013||diabetic bearded woman syndrome
|
|
C537344||sinonasal undifferentiated carcinoma
|
|
C564923||osteodysplasia familial anderson type
|
|
C567384|612244||inflammatory bowel disease 13
|
|
C567384|612244||ibd13
|
|
C564992|136900||fundus dystrophy pseudoinflammatory of sorsby
|
|
C564992|136900||macular dystrophy hemorrhagic
|
|
C564992|136900||sfd
|
|
C564922||osteodysplasty precocious of danks mayne and kozlowski
|
|
C564927||ophthalmoplegia totalis with ptosis and miosis
|
|
D024343||open bite
|
|
D024343||apertognathia
|
|
D024343||bite open
|
|
D024343||nonocclusion
|
|
D024343||openbite
|
|
C564925||ophthalmoplegic neuromuscular disorder with abnormal mitochondria
|
|
C565315|605598||diabetes mellitus insulin dependent 18
|
|
C565315|605598||iddm18
|
|
C565315|605598||insulin dependent diabetes mellitus 18
|
|
D061218||depressive disorder treatment resistant
|
|
D061218||depression refractory
|
|
D061218||depressions refractory
|
|
D061218||depressions therapy resistant
|
|
D061218||depressions treatment resistant
|
|
D061218||depression therapy resistant
|
|
D061218||depression treatment resistant
|
|
D061218||depressive disorders treatment resistant
|
|
D061218||disorders treatment resistant depressive
|
|
D061218||disorder treatment resistant depressive
|
|
D061218||refractory depression
|
|
D061218||refractory depressions
|
|
D061218||resistant depressions treatment
|
|
D061218||resistant depression treatment
|
|
D061218||therapy resistant depression
|
|
D061218||therapy resistant depressions
|
|
D061218||treatment resistant depression
|
|
D061218||treatment resistant depressions
|
|
D061218||treatment resistant depressive disorder
|
|
D061218||treatment resistant depressive disorders
|
|
D061219||olfactory nerve injuries
|
|
D061219||avulsion olfactory nerve
|
|
D061219||avulsions olfactory nerve
|
|
D061219||contusion olfactory nerve
|
|
D061219||contusions olfactory nerve
|
|
D061219||cranial nerve i injury
|
|
D061219||first cranial nerve injuries
|
|
D061219||first cranial nerve injury
|
|
D061219||first nerve palsies traumatic
|
|
D061219||first nerve palsy traumatic
|
|
D061219||first nerve trauma
|
|
D061219||first nerve traumas
|
|
D061219||injuries olfactory nerve
|
|
D061219||injury cranial nerve i
|
|
D061219||injury first cranial nerve
|
|
D061219||injury olfactory nerve
|
|
D061219||nerve avulsion olfactory
|
|
D061219||nerve avulsions olfactory
|
|
D061219||nerve contusion olfactory
|
|
D061219||nerve contusions olfactory
|
|
D061219||nerve injuries olfactory
|
|
D061219||nerve injury olfactory
|
|
D061219||nerve transection olfactory
|
|
D061219||nerve transections olfactory
|
|
D061219||nerve trauma olfactory
|
|
D061219||nerve traumas olfactory
|
|
D061219||neuropathies traumatic olfactory
|
|
D061219||neuropathy traumatic olfactory
|
|
D061219||olfactory nerve avulsion
|
|
D061219||olfactory nerve avulsions
|
|
D061219||olfactory nerve contusion
|
|
D061219||olfactory nerve contusions
|
|
D061219||olfactory nerve injury
|
|
D061219||olfactory nerve transection
|
|
D061219||olfactory nerve transections
|
|
D061219||olfactory nerve trauma
|
|
D061219||olfactory nerve traumas
|
|
D061219||olfactory neuropathies traumatic
|
|
D061219||olfactory neuropathy traumatic
|
|
D061219||palsies traumatic first nerve
|
|
D061219||palsy traumatic first nerve
|
|
D061219||transection olfactory nerve
|
|
D061219||transections olfactory nerve
|
|
D061219||trauma first nerve
|
|
D061219||trauma olfactory nerve
|
|
D061219||traumas first nerve
|
|
D061219||traumas olfactory nerve
|
|
D061219||traumatic first nerve palsies
|
|
D061219||traumatic first nerve palsy
|
|
D061219||traumatic olfactory neuropathies
|
|
D061219||traumatic olfactory neuropathy
|
|
C536974|107480||townes brocks syndrome
|
|
C536974|107480||anal ear renal radial malformation syndrome
|
|
C536974|107480||anus imperforate with hand foot and ear anomalies
|
|
C536974|107480||deafness imperforate anus hypoplastic thumbs syndrome
|
|
C536974|107480||deafness sensorineural with imperforate anus and hypoplastic thumbs
|
|
C536974|107480||deafness sensorineural with imperforate anus and thumb anomalies
|
|
C536974|107480||deafness sensorineural with imperforate anus and thumb anomalies townes brocks branchiootorenal like syndrome included
|
|
C536974|107480||imperforate anus hand and foot anomalies syndrome
|
|
C536974|107480||rear syndrome
|
|
C536974|107480||renal ear anal radial syndrome
|
|
C536974|107480||renal ear anal radial syndrome rear
|
|
C536974|107480||sensorineural deafness imperforate anus hypoplastic thumbs syndrome
|
|
C536974|107480||tbs
|
|
C536974|107480||townes syndrome
|
|
D011041||poisoning
|
|
D011041||poisonings
|
|
D012373||rocky mountain spotted fever
|
|
D012373||sao paulo typhus
|
|
D012373||typhus sao paulo
|
|
C537338||sillence syndrome
|
|
C537338||brachydactyly distal symphalangism syndrome
|
|
D011040||dermatitis toxicodendron
|
|
D011040||dermatitides poison ivy
|
|
D011040||dermatitides rhus
|
|
D011040||dermatitides toxicodendron
|
|
D011040||dermatitis poison ivy
|
|
D011040||dermatitis rhus
|
|
D011040||poison ivy dermatitides
|
|
D011040||poison ivy dermatitis
|
|
D011040||rhus dermatitides
|
|
D011040||rhus dermatitis
|
|
D011040||toxicodendron dermatitides
|
|
D011040||toxicodendron dermatitis
|
|
C538013|208920||early onset ataxia with oculomotor apraxia and hypoalbuminemia
|
|
C538013|208920||aoa
|
|
C538013|208920||aoa1
|
|
C538013|208920||ataxia adult onset with oculomotor apraxia
|
|
C538013|208920||ataxia early onset with oculomotor apraxia and hypoalbuminemia
|
|
C538013|208920||ataxia oculomotor apraxia 1
|
|
C538013|208920||ataxia oculomotor apraxia syndrome
|
|
C538013|208920||ataxia telangiectasia like syndrome
|
|
C538013|208920||cerebellar ataxia early onset with hypoalbuminemia
|
|
C538013|208920||cerebellar ataxia early onset with hypoalbuminemia eoca ha ataxia adult onset with oculomotor apraxia included
|
|
C538013|208920||eaoh
|
|
C538013|208920||early onset ataxia with ocular motor apraxia and hypoalbuminemia
|
|
C538013|208920||early onset cerebellar ataxia with hypoalbuminemia
|
|
C538669||korsakoff apos s amnesic syndrome
|
|
C537339||simosa cranio facial syndrome
|
|
C537339||simosa craniofacial syndrome
|
|
C536005||cytosolic acetoacetyl coa thiolase deficiency
|
|
C536005||acat2 deficiency
|
|
C536005||acetocoenzyme a acetyltransferase 2 deficiency
|
|
C536005||acetyl coa acetyltransferase 2 deficiency
|
|
C537336||silengo lerone pelizza syndrome
|
|
C538667||midline granulomatosis
|
|
C536006||acetylcarnitine deficiency
|
|
C537337||silicosiderosis
|
|
C537337||hematite pneumoconiosis
|
|
C537337||iron miners lung
|
|
D011045||poland syndrome
|
|
D011045||anomaly poland
|
|
D011045||poland anomaly
|
|
D011045||poland sequence
|
|
D011045||poland syndactyly
|
|
D011045||syndactyly poland
|
|
D011045||syndrome poland
|
|
C580162||hereditary sensory and autonomic neuropathy type ie
|
|
C580162||dnmt1 related dementia deafness and sensory neuropathy
|
|
C580162||hereditary sensory and autonomic neuropathy type 1 with dementia and hearing loss
|
|
C580162||hereditary sensory neuropathy type ie
|
|
C580162||hsnie
|
|
C580162||hsn ie
|
|
C563714|609464||sarcoidosis early onset
|
|
D012376||rodent diseases
|
|
D012376||disease rodent
|
|
D012376||diseases rodent
|
|
D012376||rodent disease
|
|
105150|D028243||cerebral amyloid angiopathy familial
|
|
105150|D028243||amyloidosis cerebroarterial icelandic type
|
|
105150|D028243||amyloidosis icelandic type
|
|
105150|D028243||amyloidosis vi
|
|
105150|D028243||amyloidosis vis
|
|
105150|D028243||autosomal dominant cerebrovascular amyloidosis
|
|
105150|D028243||cerebral amyloid angiopathy cst3 related
|
|
105150|D028243||cerebral amyloid angiopathy genetic
|
|
105150|D028243||cerebral amyloid angiopathy hereditary
|
|
105150|D028243||cerebral hemorrhage hereditary with amyloidosis
|
|
105150|D028243||dutch type hereditary cerebral amyloid angiopathy
|
|
105150|D028243||familial cerebral amyloid angiopathy
|
|
105150|D028243||hchwa
|
|
105150|D028243||hereditary cerebral amyloid angiopathy
|
|
105150|D028243||hereditary cerebral amyloid angiopathy dutch type
|
|
105150|D028243||hereditary cerebral amyloid angiopathy icelandic type
|
|
105150|D028243||hereditary cerebral hemorrhage with amyloidosis
|
|
105150|D028243||icelandic type amyloidosis
|
|
105150|D028243||icelandic type hereditary cerebral amyloid angiopathy
|
|
C564685|606658||spinocerebellar ataxia 15
|
|
C564685|606658||sca16 formerly
|
|
C564685|606658||spinocerebellar ataxia 15 sca15 spinocerebellar ataxia 16 formerly
|
|
C567168||leydig cell adenoma somatic with male limited precocious puberty
|
|
D061247||trochlear nerve injuries
|
|
D061247||avulsions trochlear nerve
|
|
D061247||avulsion trochlear nerve
|
|
D061247||contusions trochlear nerve
|
|
D061247||contusion trochlear nerve
|
|
D061247||cranial nerve iv injury
|
|
D061247||fourth cranial nerve injuries
|
|
D061247||fourth cranial nerve injury
|
|
D061247||fourth nerve palsies traumatic
|
|
D061247||fourth nerve palsy traumatic
|
|
D061247||fourth nerve trauma
|
|
D061247||fourth nerve traumas
|
|
D061247||injuries trochlear nerve
|
|
D061247||injury cranial nerve iv
|
|
D061247||injury fourth cranial nerve
|
|
D061247||injury trochlear nerve
|
|
D061247||nerve avulsions trochlear
|
|
D061247||nerve avulsion trochlear
|
|
D061247||nerve contusions trochlear
|
|
D061247||nerve contusion trochlear
|
|
D061247||nerve injuries trochlear
|
|
D061247||nerve injury trochlear
|
|
D061247||nerve transections trochlear
|
|
D061247||nerve transection trochlear
|
|
D061247||nerve traumas trochlear
|
|
D061247||nerve trauma trochlear
|
|
D061247||neuropathies traumatic trochlear
|
|
D061247||neuropathy traumatic trochlear
|
|
D061247||palsies traumatic fourth nerve
|
|
D061247||palsy traumatic fourth nerve
|
|
D061247||transections trochlear nerve
|
|
D061247||transection trochlear nerve
|
|
D061247||trauma fourth nerve
|
|
D061247||traumas fourth nerve
|
|
D061247||traumas trochlear nerve
|
|
D061247||traumatic fourth nerve palsies
|
|
D061247||traumatic fourth nerve palsy
|
|
D061247||traumatic trochlear neuropathies
|
|
D061247||traumatic trochlear neuropathy
|
|
D061247||trauma trochlear nerve
|
|
D061247||trochlear nerve avulsion
|
|
D061247||trochlear nerve avulsions
|
|
D061247||trochlear nerve contusion
|
|
D061247||trochlear nerve contusions
|
|
D061247||trochlear nerve injury
|
|
D061247||trochlear nerve transection
|
|
D061247||trochlear nerve transections
|
|
D061247||trochlear nerve trauma
|
|
D061247||trochlear nerve traumas
|
|
D061247||trochlear neuropathies traumatic
|
|
D061247||trochlear neuropathy traumatic
|
|
D011016||pneumonia atypical interstitial of cattle
|
|
D011016||adenomatoses bovine pulmonary
|
|
D011016||adenomatosis bovine pulmonary
|
|
D011016||adenomatosis pulmonary bovine
|
|
D011016||atypical interstitial pneumonia of cattle
|
|
D011016||bovine pulmonary adenomatoses
|
|
D011016||bovine pulmonary adenomatosis
|
|
D011016||emphysema acute bovine pulmonary
|
|
D011016||fever fog
|
|
D011016||fog fever
|
|
D011016||pulmonary adenomatoses bovine
|
|
D011016||pulmonary adenomatosis bovine
|
|
C538371|268130||revesz debuse syndrome
|
|
C538371|268130||dkca5
|
|
C538371|268130||dyskeratosis congenita autosomal dominant 5
|
|
C538371|268130||exudative retinopathy with bone marrow failure
|
|
C538371|268130||revesz syndrome
|
|
D011015||pneumonia aspiration
|
|
D011015||acid aspiration syndrome
|
|
D011015||acid aspiration syndromes
|
|
D011015||aspiration pneumonia
|
|
D011015||aspiration pneumonias
|
|
D011015||gastric acid aspiration syndrome
|
|
D011015||mendelson apos s syndrome
|
|
D011015||mendelsons syndrome
|
|
D011015||mendelson syndrome
|
|
D011015||pneumonias aspiration
|
|
D011015||syndrome acid aspiration
|
|
D011015||syndrome mendelson
|
|
D011015||syndrome mendelson apos s
|
|
D011015||syndromes acid aspiration
|
|
125851|C564219||maturity onset diabetes of the young type 2
|
|
125851|C564219||mody2
|
|
125851|C564219||mody glucokinase related
|
|
125851|C564219||mody glucokinase related diabetes gestational included
|
|
125851|C564219||mody type 2
|
|
D011018||pneumonia pneumococcal
|
|
D011018||pneumococcal pneumonia
|
|
D011018||pneumococcal pneumonias
|
|
D011018||pneumonias pneumococcal
|
|
D011017||pneumonia lipid
|
|
D011017||lipid pneumonia
|
|
D011017||lipid pneumonias
|
|
D011017||pneumonias lipid
|
|
D011019||pneumonia mycoplasma
|
|
D011019||atypical pneumonia primary
|
|
D011019||atypical pneumonias primary
|
|
D011019||mycoplasma pneumonia
|
|
D011019||mycoplasma pneumonias
|
|
D011019||pneumonia primary atypical
|
|
D011019||pneumonias mycoplasma
|
|
D011019||pneumonias primary atypical
|
|
D011019||primary atypical pneumonia
|
|
D011019||primary atypical pneumonias
|
|
C567084|608634||neuronopathy distal hereditary motor type iib
|
|
C567084|608634||dhmn2b
|
|
C567084|608634||hmn2b
|
|
C567084|608634||hmn iib
|
|
C567084|608634||neuropathy distal hereditary motor type iib
|
|
C565717|610153||deafness autosomal recessive 49
|
|
C565717|610153||dfnb49
|
|
C567176||faciocardiomelic syndrome
|
|
607499|D052018||bulimia nervosa
|
|
607499|D052018||anon2 included
|
|
607499|D052018||anorexia nervosa susceptibility to 2 included
|
|
607499|D052018||bn
|
|
607499|D052018||bulimia nervosa susceptibility to 1
|
|
607499|D052018||bulimia nervosa susceptibility to 2
|
|
607499|D052018||buln1
|
|
607499|D052018||buln2
|
|
607499|D052018||nervosa bulimia
|
|
C580130||glycogen storage disease type ix
|
|
C580130||gsdix
|
|
C580130||gsd ix
|
|
C580130||phk deficiency
|
|
C580130||phosphorylase b kinase deficiency
|
|
C580130||phosphorylase kinase deficiency
|
|
C567172||osteopenic nonfracture syndrome
|
|
300200||adrenal insufficiency progressive and hypogonadotropic hypogonadism included
|
|
300200||ahc
|
|
300200||ahch
|
|
300200||ahc with hhg
|
|
300200||ahc with isolated gonadotropin deficiency adrenal hypoplasia congenital with precocious puberty included
|
|
300200||ahx
|
|
300200||mineralocorticoid deficiency isolated included
|
|
C567171||osteolysis hereditary of carpal bones with or without nephropathy
|
|
C567171||multicentric osteolysis autosomal dominant
|
|
D011014||pneumonia
|
|
D011014||experimental lung inflammation
|
|
D011014||experimental lung inflammations
|
|
D011014||inflammation experimental lung
|
|
D011014||inflammation lung
|
|
D011014||inflammation pulmonary
|
|
D011014||inflammations lung
|
|
D011014||inflammations pulmonary
|
|
D011014||lobar pneumonia
|
|
D011014||lung inflammation
|
|
D011014||lung inflammation experimental
|
|
D011014||lung inflammations
|
|
D011014||lung inflammations experimental
|
|
D011014||pneumonia lobar
|
|
D011014||pneumonias
|
|
D011014||pneumonitides
|
|
D011014||pneumonitis
|
|
D011014||pulmonary inflammation
|
|
D011014||pulmonary inflammations
|
|
C567174||myokymia 1
|
|
C567173||nf1 microduplication syndrome
|
|
D000379||agoraphobia
|
|
D000379||agoraphobias
|
|
169150|C536309||patterned dystrophy of retinal pigment epithelium
|
|
169150|C536309||butterfly dystrophy of retinal pigment epithelium
|
|
169150|C536309||butterfly shaped pigment dystrophy of the fovea
|
|
169150|C536309||macular dystrophy butterfly shaped pigmentary
|
|
169150|C536309||macular dystrophy butterfly shaped pigmentary 2
|
|
D000370||ageusia
|
|
D000370||ageusia hysterical
|
|
D000370||ageusias hysterical
|
|
D000370||hypogeusia
|
|
D000370||hypogeusias
|
|
D000370||hysterical ageusia
|
|
D000370||hysterical ageusias
|
|
D000370||taste blindness
|
|
D000377||agnosia
|
|
D000377||agnosia auditory
|
|
D000377||agnosia body image
|
|
D000377||agnosia congenital auditory
|
|
D000377||agnosia developmental
|
|
D000377||agnosia finger
|
|
D000377||agnosia for pain
|
|
D000377||agnosia for smell
|
|
D000377||agnosia for taste
|
|
D000377||agnosia for tastes
|
|
D000377||agnosia for temperature
|
|
D000377||agnosia gustatory
|
|
D000377||agnosia ideational
|
|
D000377||agnosia olfactory
|
|
D000377||agnosia position
|
|
D000377||agnosias
|
|
D000377||agnosias auditory
|
|
D000377||agnosias body image
|
|
D000377||agnosias congenital auditory
|
|
D000377||agnosias developmental
|
|
D000377||agnosia sensory
|
|
D000377||agnosias finger
|
|
D000377||agnosias ideational
|
|
D000377||agnosias olfactory
|
|
D000377||agnosia somatosensory
|
|
D000377||agnosias position
|
|
D000377||agnosias sensory
|
|
D000377||agnosias somatosensory
|
|
D000377||agnosias tactile
|
|
D000377||agnosias time
|
|
D000377||agnosias topographical
|
|
D000377||agnosias visual
|
|
D000377||agnosias visuospatial
|
|
D000377||agnosia tactile
|
|
D000377||agnosia time
|
|
D000377||agnosia topographical
|
|
D000377||agnosia visual
|
|
D000377||agnosia visuospatial
|
|
D000377||anosognosia
|
|
D000377||anosognosias
|
|
D000377||auditory agnosia
|
|
D000377||auditory agnosia congenital
|
|
D000377||auditory agnosias
|
|
D000377||auditory agnosias congenital
|
|
D000377||body image agnosia
|
|
D000377||body image agnosias
|
|
D000377||congenital auditory agnosia
|
|
D000377||congenital auditory agnosias
|
|
D000377||developmental agnosia
|
|
D000377||developmental agnosias
|
|
D000377||finger agnosia
|
|
D000377||finger agnosias
|
|
D000377||gustatory agnosia
|
|
D000377||ideational agnosia
|
|
D000377||ideational agnosias
|
|
D000377||olfactory agnosia
|
|
D000377||olfactory agnosias
|
|
D000377||position agnosia
|
|
D000377||position agnosias
|
|
D000377||sensory agnosia
|
|
D000377||sensory agnosias
|
|
D000377||somatosensory agnosia
|
|
D000377||somatosensory agnosias
|
|
D000377||syndromes visual disorientation
|
|
D000377||syndrome visual disorientation
|
|
D000377||tactile agnosia
|
|
D000377||tactile agnosias
|
|
D000377||time agnosia
|
|
D000377||time agnosias
|
|
D000377||topographical agnosia
|
|
D000377||topographical agnosias
|
|
D000377||visual agnosia
|
|
D000377||visual agnosia for objects
|
|
D000377||visual agnosias
|
|
D000377||visual disorientation syndrome
|
|
D000377||visual disorientation syndromes
|
|
D000377||visuospatial agnosia
|
|
D000377||visuospatial agnosias
|
|
C564906||pancreatitis sclerosing cholangitis and sicca complex
|
|
C564905||parana hard skin syndrome
|
|
D011027||pneumoperitoneum
|
|
D011026||pneumopericardium
|
|
D011026||pneumopericardiums
|
|
C562873|245480||specific granule deficiency
|
|
C562873|245480||lactoferrin deficient neutrophils
|
|
C562873|245480||neutrophil lactoferrin deficiency
|
|
C562873|245480||sgd
|
|
C567181||loeys dietz syndrome type 1b
|
|
D000380||agranulocytosis
|
|
D000380||agranulocytoses
|
|
D000380||granulocytopenia
|
|
D000380||granulocytopenias
|
|
607485||frontotemporal lobar degeneration with tdp43 inclusions grn related
|
|
607485||dementia hereditary dysphasic disinhibition hddd aphasia primary progressive included
|
|
607485||frontotemporal dementia with tdp43 inclusions grn related
|
|
607485||ftdu
|
|
607485||ftld tdp grn related
|
|
607485||ftldu
|
|
607485||ppa included
|
|
C538604||pericardial constriction with growth failure
|
|
C567187||best vitelliform macular dystrophy multifocal
|
|
D011021||pneumonia progressive interstitial of sheep
|
|
D011021||maedi
|
|
D011021||progressive interstitial pneumonia of sheep
|
|
C538602||mucolipidosis 2
|
|
C567189||li fraumeni like syndrome
|
|
D011020||pneumonia pneumocystis
|
|
D011020||pneumocystis carinii pneumonia
|
|
D011020||pneumocystis pneumonia
|
|
D011020||pneumocystis pneumonias
|
|
D011020||pneumocystoses
|
|
D011020||pneumocystosis
|
|
D011020||pneumonia interstitial plasma cell
|
|
D011020||pneumonia pneumocystis carinii
|
|
D011020||pneumonias pneumocystis
|
|
D011020||pneumonias pneumocystis carinii
|
|
C536195|130010||ehlers danlos syndrome type 2
|
|
C536195|130010||eds2
|
|
C536195|130010||eds ii
|
|
C536195|130010||ehlers danlos syndrome mild classic type
|
|
C536195|130010||ehlers danlos syndrome mitis type
|
|
C536195|130010||ehlers danlos syndrome type ii
|
|
C567188||lymphedema distichiasis syndrome with renal disease and diabetes mellitus
|
|
D011023||pneumonia staphylococcal
|
|
D011023||pneumonias staphylococcal
|
|
D011023||pneumonias staphylococcus aureus
|
|
D011023||pneumonia staphylococcus aureus
|
|
D011023||staphylococcal pneumonia
|
|
D011023||staphylococcal pneumonias
|
|
D011023||staphylococcus aureus pneumonia
|
|
D011023||staphylococcus aureus pneumonias
|
|
D011022||pneumonia rickettsial
|
|
D011022||pneumonias rickettsial
|
|
D011022||rickettsial pneumonia
|
|
D011022||rickettsial pneumonias
|
|
C567182||chromosome 10q26 deletion syndrome
|
|
C567182||terminal chromosome 10q26 deletion syndrome
|
|
D013684||telangiectasis
|
|
D013684||spider vein
|
|
D013684||spider veins
|
|
D013684||telangiectases
|
|
D013684||telangiectasia
|
|
D013684||telangiectasias
|
|
D013684||vein spider
|
|
D013684||veins spider
|
|
C567185||dandy walker malformation with occipital cephalocele autosomal dominant
|
|
C567185||addwoc
|
|
D011024||pneumonia viral
|
|
D011024||pneumonias viral
|
|
D011024||viral pneumonia
|
|
D011024||viral pneumonias
|
|
C567184||chromosome 3q29 deletion syndrome
|
|
C567184||microdeletion 3q29 syndrome
|
|
D000347||afibrinogenemia
|
|
D000347||afibrinogenemias
|
|
D000347||congenital afibrinogenemia
|
|
D000347||deficiencies fibrinogen
|
|
D000347||deficiency fibrinogen
|
|
D000347||familial afibrinogenemia
|
|
D000347||fibrinogen deficiencies
|
|
D000347||fibrinogen deficiency
|
|
152700|D008180||lupus erythematosus systemic
|
|
152700|D008180||disease libman sacks
|
|
152700|D008180||excess lmw dna included
|
|
152700|D008180||excess lymphocyte low molecular weight dna included
|
|
152700|D008180||libman sacks disease
|
|
152700|D008180||lupus erythematosus disseminatus
|
|
152700|D008180||sle
|
|
152700|D008180||sleb1
|
|
152700|D008180||sleb10
|
|
152700|D008180||sleb11
|
|
152700|D008180||sleb12
|
|
152700|D008180||sleb13
|
|
152700|D008180||sleb14
|
|
152700|D008180||sleb15
|
|
152700|D008180||sleb2
|
|
152700|D008180||sleb3
|
|
152700|D008180||sleb4
|
|
152700|D008180||sleb5
|
|
152700|D008180||sleb6
|
|
152700|D008180||sleb7
|
|
152700|D008180||sleb8
|
|
152700|D008180||sleb9
|
|
152700|D008180||systemic lupus erythematosus
|
|
152700|D008180||systemic lupus erythematosus resistance to 1 included
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 1
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 10
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 11
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 12
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 13
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 14
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 15
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 2
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 3
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 4
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 5
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 6
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 7
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 8
|
|
152700|D008180||systemic lupus erythematosus susceptibility to 9
|
|
C537502|601559||stuve wiedemann syndrome
|
|
C537502|601559||schwartz jampel syndrome neonatal
|
|
C537502|601559||schwartz jampel syndrome type 2
|
|
C537502|601559||schwartz jampel type 2 syndrome
|
|
C537502|601559||sjs2
|
|
C537502|601559||stuve wiedemann schwartz jampel type 2 syndrome
|
|
C537502|601559||stws
|
|
C537502|601559||sws
|
|
604129|C563192||epidermolysis bullosa pruriginosa
|
|
604129|C563192||deb pruriginosa
|
|
604129|C563192||dystrophic epidermolysis bullosa pruriginosa
|
|
C567685|613244||colorectal cancer hereditary nonpolyposis type 8
|
|
C567685|613244||hnpcc8
|
|
C538620||acute brachial neuritis
|
|
C538620||acute brachial neuritis syndrome
|
|
C538620||acute brachial radiculitis syndrome
|
|
C538620||acute shoulder neuritis
|
|
D000343||afferent loop syndrome
|
|
D000343||afferent loop syndromes
|
|
D000343||loop syndrome afferent
|
|
D000343||loop syndromes afferent
|
|
D000343||syndrome afferent loop
|
|
D000343||syndromes afferent loop
|
|
D000341||affective disorders psychotic
|
|
D000341||affective disorder psychotic
|
|
D000341||affective psychoses
|
|
D000341||depression reactive psychotic
|
|
D000341||disorder psychotic affective
|
|
D000341||disorders psychotic affective
|
|
D000341||mood disorder psychotic
|
|
D000341||mood disorders psychotic
|
|
D000341||psychoses affective
|
|
D000341||psychotic affective disorder
|
|
D000341||psychotic affective disorders
|
|
D000341||psychotic mood disorder
|
|
D000341||psychotic mood disorders
|
|
607473||vitamin k dependent clotting factors combined deficiency of 2
|
|
218700|C566852||hypothyroidism congenital nongoitrous 2
|
|
218700|C566852||athyreotic hypothyroidism
|
|
218700|C566852||chng2
|
|
218700|C566852||hypothyroidism athyreotic
|
|
218700|C566852||hypothyroidism congenital due to thyroid dysgenesis
|
|
D012327||rna virus infections
|
|
D012327||infection rna virus
|
|
D012327||infections rna virus
|
|
D012327||rna virus infection
|
|
D012327||virus infection rna
|
|
D012327||virus infections rna
|
|
D014987||xerostomia
|
|
D014987||asialia
|
|
D014987||asialias
|
|
D014987||dryness mouth
|
|
D014987||hyposalivation
|
|
D014987||hyposalivations
|
|
D014987||mouth dryness
|
|
D014987||xerostomias
|
|
C567154|D003093|191390||inflammatory bowel disease 11
|
|
C538614||papillary renal cell carcinoma sporadic
|
|
C538614||papillary renal carcinoma malignant
|
|
C538614||papillary renal cell carcinoma bilateral
|
|
C538614||papillary renal cell carcinoma familial
|
|
C538614||papillary renal cell carcinoma multiple
|
|
C567156||loeys dietz syndrome type 2a
|
|
C567155||skin hair eye pigmentation variation in 7
|
|
C567155||shep7
|
|
C567155||skin hair eye pigmentation 7 blond brown hair
|
|
C567155||skin hair eye pigmentation 7 dark light skin
|
|
D014985||xerophthalmia
|
|
D014985||xerophthalmias
|
|
C538618||donath landsteiner hemolytic anemia
|
|
C538618||donath landsteiner syndrome
|
|
C538618||dressler syndrome
|
|
C538618||harley syndrome
|
|
C538618||immune hemolytic anemia paroxysmal cold
|
|
D013651||taste disorders
|
|
D013651||metallic taste
|
|
D013651||metallic tastes
|
|
D013651||primary taste disorder
|
|
D013651||primary taste disorders
|
|
D013651||secondary taste disorder
|
|
D013651||secondary taste disorders
|
|
D013651||taste disorder
|
|
D013651||taste disorder anterior tongue
|
|
D013651||taste disorder posterior tongue
|
|
D013651||taste disorder primary
|
|
D013651||taste disorder primary bitter
|
|
D013651||taste disorder primary salt
|
|
D013651||taste disorder primary sweet
|
|
D013651||taste disorder secondary
|
|
D013651||taste disorder secondary bitter
|
|
D013651||taste disorder secondary salt
|
|
D013651||taste disorder secondary sweet
|
|
D013651||taste disorders primary
|
|
D013651||taste disorders secondary
|
|
D013651||taste metallic
|
|
D013651||tastes metallic
|
|
C567688|613235||factor xiii b subunit deficiency of
|
|
D000357||african swine fever
|
|
D000357||swine fever african
|
|
D000357||wart hog disease
|
|
D000357||wart hog diseases
|
|
C562782|307700||hypoparathyroidism x linked
|
|
C562782|307700||hypx
|
|
604145|C565824||cardiomyopathy dilated 1g
|
|
604145|C565824||cmd1g
|
|
C538631||olivopontocerebellar atrophy 3
|
|
C538631||autosomal dominant cerebellar ataxia type 2
|
|
C567088|611773||angiopathy hereditary with nephropathy aneurysms and muscle cramps
|
|
C567088|611773||autosomal dominant familial hematuria retinal arteriolar tortuosity contractures
|
|
C567088|611773||hanac
|
|
C567088|611773||hanac syndrome
|
|
C567088|611773||hereditary angiopathy with nephropathy aneurysm and muscle cramps syndrome
|
|
C567088|611773||hereditary angiopathy with nephropathy aneurysms and muscle cramps syndrome
|
|
C565186|610753||alopecia areata 2
|
|
C565186|610753||aa2
|
|
D000355||african horse sickness
|
|
D000355||african horsesickness
|
|
D000355||african horsesicknesses
|
|
D000355||african horse sicknesses
|
|
D000355||equine plague
|
|
D000355||equine plagues
|
|
D000355||horsesickness african
|
|
D000355||horse sickness african
|
|
D000355||horsesicknesses african
|
|
D000355||horse sicknesses african
|
|
D000355||plague equine
|
|
D000355||plagues equine
|
|
D000355||sickness african horse
|
|
D000355||sicknesses african horse
|
|
D011004||plummer vinson syndrome
|
|
D011004||kelly apos s syndrome
|
|
D011004||kellys syndrome
|
|
D011004||patterson brown kelly syndrome
|
|
D011004||patterson kelly syndrome
|
|
D011004||patterson apos s syndrome
|
|
D011004||pattersons syndrome
|
|
D011004||patterson syndrome
|
|
D011004||syndrome kelly apos s
|
|
D011004||syndrome patterson brown kelly
|
|
D011004||syndrome patterson kelly
|
|
D011004||syndrome patterson apos s
|
|
D011004||syndrome plummer vinson
|
|
D011007||pneumocephalus
|
|
D011007||airocele cranial
|
|
D011007||airoceles cranial
|
|
D011007||cranial airocele
|
|
D011007||cranial airoceles
|
|
D011007||cranial pneumocyst
|
|
D011007||cranial pneumocysts
|
|
D011007||epidural pneumocephalus
|
|
D011007||gas intracranial
|
|
D011007||intracranial gas
|
|
D011007||pneumocephalus epidural
|
|
D011007||pneumocephalus pressure
|
|
D011007||pneumocephalus tension
|
|
D011007||pneumocephalus traumatic
|
|
D011007||pneumocyst cranial
|
|
D011007||pneumocysts cranial
|
|
D011007||pressure pneumocephalus
|
|
D011007||tension pneumocephalus
|
|
D011007||traumatic pneumocephalus
|
|
D011006||pneumatosis cystoides intestinalis
|
|
D011006||cystoides intestinalis pneumatosis
|
|
D011006||intestinalis pneumatosis cystoides
|
|
D014997||xyy karyotype
|
|
D014997||karyotypes xyy
|
|
D014997||karyotype xyy
|
|
D014997||xyy karyotypes
|
|
D011009||pneumoconiosis
|
|
D011009||bagassosis
|
|
D011009||pneumoconioses
|
|
222100|D003922||diabetes mellitus type 1
|
|
222100|D003922||autoimmune diabetes
|
|
222100|D003922||brittle diabetes mellitus
|
|
222100|D003922||diabetes autoimmune
|
|
222100|D003922||diabetes juvenile onset
|
|
222100|D003922||diabetes mellitus brittle
|
|
222100|D003922||diabetes mellitus insulin dependent
|
|
222100|D003922||diabetes mellitus insulin dependent 1
|
|
222100|D003922||diabetes mellitus juvenile onset
|
|
222100|D003922||diabetes mellitus ketosis prone
|
|
222100|D003922||diabetes mellitus sudden onset
|
|
222100|D003922||diabetes mellitus type i
|
|
222100|D003922||iddm
|
|
222100|D003922||iddm1 included
|
|
222100|D003922||insulin dependent diabetes mellitus
|
|
222100|D003922||insulin dependent diabetes mellitus 1
|
|
222100|D003922||insulin dependent diabetes mellitus 1 included
|
|
222100|D003922||juvenile onset diabetes
|
|
222100|D003922||juvenile onset diabetes jod diabetes mellitus insulin dependent 1 included
|
|
222100|D003922||juvenile onset diabetes mellitus
|
|
222100|D003922||ketosis prone diabetes mellitus
|
|
222100|D003922||kpd
|
|
222100|D003922||mellitus sudden onset diabetes
|
|
222100|D003922||sudden onset diabetes mellitus
|
|
222100|D003922||type 1 diabetes mellitus
|
|
D011008||pneumococcal infections
|
|
D011008||infection pneumococcal
|
|
D011008||infections pneumococcal
|
|
D011008||infections streptococcus pneumoniae
|
|
D011008||infection streptococcus pneumoniae
|
|
D011008||pneumococcal infection
|
|
D011008||pneumoniae infections streptococcus
|
|
D011008||pneumoniae infection streptococcus
|
|
D011008||streptococcus pneumoniae infection
|
|
D011008||streptococcus pneumoniae infections
|
|
C538626||olivopontocerebellar atrophy 1
|
|
C538626||menzel type olivopontocerebellar atrophy
|
|
C538626||olivopontocerebellar atrophy 4
|
|
C538626||schut haymaker type olivopontocerebellar atrophy
|
|
C538626||spinocerebellar atrophy 1
|
|
C567165||palmoplantar hyperkeratosis and true hermaphroditism
|
|
C567164||protein c deficiency acquired
|
|
C536990|235730||mowat wilson syndrome
|
|
C536990|235730||hirschsprung disease mental retardation syndrome
|
|
C536990|235730||microcephaly mental retardation and distinct facial features with or without hirschsprung disease
|
|
C536990|235730||mows
|
|
C562600|223000||lactase deficiency congenital
|
|
C562600|223000||alactasia congenital
|
|
C562600|223000||disaccharide intolerance ii
|
|
D011001||pleuropneumonia
|
|
D011001||pleuropneumonias
|
|
D011000||pleurodynia epidemic
|
|
D011000||bornholm disease
|
|
D011000||epidemic myalgia
|
|
D011000||epidemic myalgias
|
|
D011000||epidemic pleurodynia
|
|
D011000||epidemic pleurodynias
|
|
D011000||myalgia epidemic
|
|
D011000||myalgias epidemic
|
|
D011000||pleurodynias epidemic
|
|
C567160||anemia sideroblastic autosomal dominant
|
|
145680|C567719||dystransthyretinemic euthyroidal hyperthyroxinemia
|
|
145680|C567719||hyperthyroxinemia dysprealbuminemic
|
|
145680|C567719||hyperthyroxinemia dystransthyretinemic
|
|
C567163||thrombophilia hereditary due to protein c deficiency autosomal dominant
|
|
C567163||proc deficiency autosomal dominant
|
|
D011002||pleuropneumonia contagious
|
|
D011002||contagious pleuropneumonia
|
|
D011002||contagious pleuropneumonias
|
|
D011002||pleuropneumonias contagious
|
|
C567162||neuromuscular disease congenital with uniform type 1 fiber
|
|
C567162||cnmdu1
|
|
D001657||biliary dyskinesia
|
|
D001657||biliary dyskinesias
|
|
D001657||dyskinesia biliary
|
|
D001657||dyskinesia gallbladder
|
|
D001657||dyskinesias biliary
|
|
D001657||dyskinesias gallbladder
|
|
D001657||gallbladder dyskinesia
|
|
D001657||gallbladder dyskinesias
|
|
D001656||biliary atresia
|
|
D001656||atresia biliary
|
|
D001656||atresia extrahepatic biliary
|
|
D001656||atresias extrahepatic biliary
|
|
D001656||biliary atresia extrahepatic
|
|
D001656||biliary atresias extrahepatic
|
|
D001656||extrahepatic biliary atresia
|
|
D001656||extrahepatic biliary atresias
|
|
D001656||familial extrahepatic biliary atresia
|
|
D001656||idiopathic extrahepatic biliary atresia
|
|
C567128||spondyloepiphyseal dysplasia brachydactyly and distinctive speech
|
|
C567128||fantasy island syndrome
|
|
C567128||sed bds
|
|
C567128||tattoo dysplasia
|
|
D001655||bile reflux
|
|
D001655||reflux bile
|
|
C536979|131705||transient bullous dermolysis of the newborn
|
|
C536979|131705||dystrophic epidermolysis bullosa dominant neonatal
|
|
C536979|131705||dystrophic epidermolysis bullosa neonatal
|
|
C536979|131705||epidermolysis bullosa dystrophica dominant neonatal form
|
|
C536979|131705||epidermolysis bullosa dystrophica neonatal form
|
|
C536979|131705||tbdn
|
|
C567124||ectopia lentis isolated autosomal recessive
|
|
D001658||biliary fistula
|
|
D001658||biliary fistulas
|
|
D001658||fistula biliary
|
|
D001658||fistulas biliary
|
|
D061285||vestibulocochlear nerve injuries
|
|
D061285||avulsions vestibulocochlear nerve
|
|
D061285||avulsion vestibulocochlear nerve
|
|
D061285||contusions vestibulocochlear nerve
|
|
D061285||contusion vestibulocochlear nerve
|
|
D061285||cranial nerve viii injury
|
|
D061285||eighth cranial nerve injuries
|
|
D061285||eighth cranial nerve injury
|
|
D061285||eighth nerve palsies traumatic
|
|
D061285||eighth nerve palsy traumatic
|
|
D061285||eighth nerve trauma
|
|
D061285||eighth nerve traumas
|
|
D061285||injuries vestibulocochlear nerve
|
|
D061285||injury cranial nerve viii
|
|
D061285||injury eighth cranial nerve
|
|
D061285||injury vestibulocochlear nerve
|
|
D061285||nerve avulsions vestibulocochlear
|
|
D061285||nerve avulsion vestibulocochlear
|
|
D061285||nerve contusions vestibulocochlear
|
|
D061285||nerve contusion vestibulocochlear
|
|
D061285||nerve injuries vestibulocochlear
|
|
D061285||nerve injury vestibulocochlear
|
|
D061285||nerve transections vestibulocochlear
|
|
D061285||nerve transection vestibulocochlear
|
|
D061285||nerve traumas vestibulocochlear
|
|
D061285||nerve trauma vestibulocochlear
|
|
D061285||neuropathies traumatic vestibulocochlear
|
|
D061285||neuropathy traumatic vestibulocochlear
|
|
D061285||palsies traumatic eighth nerve
|
|
D061285||palsy traumatic eighth nerve
|
|
D061285||transections vestibulocochlear nerve
|
|
D061285||transection vestibulocochlear nerve
|
|
D061285||trauma eighth nerve
|
|
D061285||traumas eighth nerve
|
|
D061285||traumas vestibulocochlear nerve
|
|
D061285||traumatic eighth nerve palsies
|
|
D061285||traumatic eighth nerve palsy
|
|
D061285||traumatic vestibulocochlear neuropathies
|
|
D061285||traumatic vestibulocochlear neuropathy
|
|
D061285||trauma vestibulocochlear nerve
|
|
D061285||vestibulocochlear nerve avulsion
|
|
D061285||vestibulocochlear nerve avulsions
|
|
D061285||vestibulocochlear nerve contusion
|
|
D061285||vestibulocochlear nerve contusions
|
|
D061285||vestibulocochlear nerve injury
|
|
D061285||vestibulocochlear nerve transection
|
|
D061285||vestibulocochlear nerve transections
|
|
D061285||vestibulocochlear nerve trauma
|
|
D061285||vestibulocochlear nerve traumas
|
|
D061285||vestibulocochlear neuropathies traumatic
|
|
D061285||vestibulocochlear neuropathy traumatic
|
|
C564713|300115||mental retardation x linked 50
|
|
C564713|300115||mrx50
|
|
D061287||glossopharyngeal nerve injuries
|
|
D061287||avulsion glossopharyngeal nerve
|
|
D061287||avulsions glossopharyngeal nerve
|
|
D061287||contusion glossopharyngeal nerve
|
|
D061287||contusions glossopharyngeal nerve
|
|
D061287||cranial nerve ix injury
|
|
D061287||glossopharyngeal nerve avulsion
|
|
D061287||glossopharyngeal nerve avulsions
|
|
D061287||glossopharyngeal nerve contusion
|
|
D061287||glossopharyngeal nerve contusions
|
|
D061287||glossopharyngeal nerve injury
|
|
D061287||glossopharyngeal nerve transection
|
|
D061287||glossopharyngeal nerve transections
|
|
D061287||glossopharyngeal nerve trauma
|
|
D061287||glossopharyngeal nerve traumas
|
|
D061287||glossopharyngeal neuropathies traumatic
|
|
D061287||glossopharyngeal neuropathy traumatic
|
|
D061287||injuries glossopharyngeal nerve
|
|
D061287||injury cranial nerve ix
|
|
D061287||injury glossopharyngeal nerve
|
|
D061287||injury ninth cranial nerve
|
|
D061287||nerve avulsion glossopharyngeal
|
|
D061287||nerve avulsions glossopharyngeal
|
|
D061287||nerve contusion glossopharyngeal
|
|
D061287||nerve contusions glossopharyngeal
|
|
D061287||nerve injuries glossopharyngeal
|
|
D061287||nerve injury glossopharyngeal
|
|
D061287||nerve transection glossopharyngeal
|
|
D061287||nerve transections glossopharyngeal
|
|
D061287||nerve trauma glossopharyngeal
|
|
D061287||nerve traumas glossopharyngeal
|
|
D061287||neuropathies traumatic glossopharyngeal
|
|
D061287||neuropathy traumatic glossopharyngeal
|
|
D061287||ninth cranial nerve injuries
|
|
D061287||ninth cranial nerve injury
|
|
D061287||ninth nerve palsies traumatic
|
|
D061287||ninth nerve palsy traumatic
|
|
D061287||ninth nerve trauma
|
|
D061287||ninth nerve traumas
|
|
D061287||palsies traumatic ninth nerve
|
|
D061287||palsy traumatic ninth nerve
|
|
D061287||transection glossopharyngeal nerve
|
|
D061287||transections glossopharyngeal nerve
|
|
D061287||trauma glossopharyngeal nerve
|
|
D061287||trauma ninth nerve
|
|
D061287||traumas glossopharyngeal nerve
|
|
D061287||traumas ninth nerve
|
|
D061287||traumatic glossopharyngeal neuropathies
|
|
D061287||traumatic glossopharyngeal neuropathy
|
|
D061287||traumatic ninth nerve palsies
|
|
D061287||traumatic ninth nerve palsy
|
|
C564546|300273||goiter multinodular 2
|
|
C564546|300273||mng2
|
|
304700|C535808||mohr tranebjaerg syndrome
|
|
304700|C535808||ddp
|
|
304700|C535808||deafness dfn 1 dystonia mental deficiency and blindness
|
|
304700|C535808||deafness dystonia optic atrophy syndrome
|
|
304700|C535808||deafness dystonia optic neuronopathy syndrome
|
|
304700|C535808||deafness dystonia syndrome
|
|
304700|C535808||deafness syndrome progressive with blindness dystonia fractures and mental deficiency
|
|
304700|C535808||dystonia deafness syndrome
|
|
304700|C535808||mohr tranebj 230 rg syndrome
|
|
304700|C535808||mts
|
|
D001651||cholestasis extrahepatic
|
|
D001651||bile duct obstruction extrahepatic
|
|
D001651||biliary stasis extrahepatic
|
|
D001651||extrahepatic biliary stasis
|
|
D001651||extrahepatic cholestasis
|
|
D001650||bile duct neoplasms
|
|
D001650||bile duct cancer
|
|
D001650||bile duct cancers
|
|
D001650||bile duct neoplasm
|
|
D001650||cancer bile duct
|
|
D001650||cancer of bile duct
|
|
D001650||cancer of the bile duct
|
|
D001650||cancers bile duct
|
|
D001650||neoplasm bile duct
|
|
D001650||neoplasms bile duct
|
|
C567075|611536||major affective disorder 6
|
|
C567075|611536||mafd6
|
|
D012303||ring chromosomes
|
|
D012303||chromosome ring
|
|
D012303||chromosomes ring
|
|
D012303||ring chromosome
|
|
C567132||dibasic amino aciduria i
|
|
C567131||dystonia with cerebellar atrophy
|
|
D012301||rinderpest
|
|
D012301||cattle plague
|
|
D012301||plague cattle
|
|
C567139||skin hair eye pigmentation variation in 6
|
|
C567139||shep6
|
|
C567139||skin hair eye pigmentation 6 blond brown hair
|
|
C567139||skin hair eye pigmentation 6 blue green eyes
|
|
D000334||aerophagy
|
|
D000334||air swallowing
|
|
D000334||swallowing air
|
|
D061270||nasal septal perforation
|
|
D061270||nasal septal perforations
|
|
D061270||nasal septum perforation
|
|
D061270||nasal septum perforations
|
|
D061270||perforation nasal septal
|
|
D061270||perforation nasal septum
|
|
D061270||perforations nasal septal
|
|
D061270||perforations nasal septum
|
|
D061270||septal perforation nasal
|
|
D061270||septal perforations nasal
|
|
D061270||septum perforation nasal
|
|
D061270||septum perforations nasal
|
|
C567138||camptodactyly syndrome guadalajara type ii
|
|
C567137||ciliary dyskinesia with transposition of ciliary microtubules
|
|
D001660||biliary tract diseases
|
|
D001660||biliary tract disease
|
|
D001660||disease biliary tract
|
|
D001660||diseases biliary tract
|
|
D001660||tract disease biliary
|
|
D001660||tract diseases biliary
|
|
C538417|271150||spinal muscular atrophy 4
|
|
C538417|271150||sma4
|
|
C536426|303400||cleft palate x linked
|
|
C536426|303400||cleft palate with or without ankyloglossia x linked
|
|
C536426|303400||cpx
|
|
C536426|303400||x linked cleft palate
|
|
C580109||fragile x associated tremor ataxia syndrome
|
|
D001661||biliary tract neoplasms
|
|
D001661||biliary tract cancer
|
|
D001661||biliary tract cancers
|
|
D001661||biliary tract neoplasm
|
|
D001661||cancer biliary tract
|
|
D001661||cancer of biliary tract
|
|
D001661||cancer of the biliary tract
|
|
D001661||cancers biliary tract
|
|
D001661||neoplasm biliary tract
|
|
D001661||neoplasms biliary tract
|
|
C580102||dysmyelinating leukodystrophy and spastic paraparesis
|
|
C580102||spastic paraplegia 35
|
|
610551|D020803||encephalitis herpes simplex
|
|
610551|D020803||acute necrotizing encephalitis herpetic
|
|
610551|D020803||encephalitides herpes simplex
|
|
610551|D020803||encephalitides herpetic
|
|
610551|D020803||encephalitis herpes
|
|
610551|D020803||encephalitis herpetic
|
|
610551|D020803||encephalopathy acute infection induced susceptibility to 1
|
|
610551|D020803||encephalopathy acute infection induced susceptibility to 2
|
|
610551|D020803||herpes encephalitis
|
|
610551|D020803||herpes simplex encephalitides
|
|
610551|D020803||herpes simplex encephalitis
|
|
610551|D020803||herpes simplex encephalitis susceptibility to 1
|
|
610551|D020803||herpes simplex encephalitis susceptibility to 2
|
|
610551|D020803||herpes simplex meningoencephalitides
|
|
610551|D020803||herpes simplex meningoencephalitis
|
|
610551|D020803||herpetic acute necrotizing encephalitis
|
|
610551|D020803||herpetic encephalitides
|
|
610551|D020803||herpetic encephalitis
|
|
610551|D020803||herpetic meningoencephalitides
|
|
610551|D020803||herpetic meningoencephalitis
|
|
610551|D020803||iiae1
|
|
610551|D020803||iiae2
|
|
610551|D020803||meningoencephalitides herpes simplex
|
|
610551|D020803||meningoencephalitides herpetic
|
|
610551|D020803||meningoencephalitis herpes simplex
|
|
610551|D020803||meningoencephalitis herpes simplex virus
|
|
610551|D020803||meningoencephalitis herpetic
|
|
D014973||xanthomatosis
|
|
D014973||xanthoma
|
|
D014973||xanthomas
|
|
D014973||xanthomatoses
|
|
D014972||xanthogranuloma juvenile
|
|
D014972||juvenile xanthogranuloma
|
|
D014972||juvenile xanthogranulomas
|
|
D014972||juvenile xanthoma
|
|
D014972||juvenile xanthomas
|
|
D014972||nevoxanthoendothelioma
|
|
D014972||nevoxanthoendotheliomas
|
|
D014972||xanthogranulomas juvenile
|
|
D014972||xanthoma juvenile
|
|
D014972||xanthomas juvenile
|
|
C567141||bardet biedl syndrome 14
|
|
D013641||tarsal tunnel syndrome
|
|
D013641||entrapment neuropathy tarsal tunnel
|
|
D013641||posterior tibial nerve neuralgia
|
|
D013641||syndromes tarsal tunnel
|
|
D013641||syndrome tarsal tunnel
|
|
D013641||tarsal tunnel entrapment neuropathy
|
|
D013641||tarsal tunnel syndromes
|
|
D013641||tarsal tunnel tibial neuropathy
|
|
D013641||tibial neuropathy tarsal tunnel
|
|
D013641||tunnel syndromes tarsal
|
|
D013641||tunnel syndrome tarsal
|
|
C567140||bardet biedl syndrome 13
|
|
C567107||hypophosphatasia perinatal lethal
|
|
D000303||adrenal cortex diseases
|
|
D000303||adrenal cortex disease
|
|
D000303||cortex disease adrenal
|
|
D000303||cortex diseases adrenal
|
|
D000303||disease adrenal cortex
|
|
D000303||diseases adrenal cortex
|
|
C567109||hypergonadotropic hypogonadism and partial alopecia
|
|
C567108||hypogonadism and testicular atrophy
|
|
D000308||adrenocortical hyperfunction
|
|
D000308||adrenal gland hyperfunction
|
|
D000308||hyperadrenalism
|
|
D000308||hyperadrenocorticism
|
|
D000308||hypercorticism
|
|
D000308||hyperfunction adrenal gland
|
|
D000308||hyperfunction adrenocortical
|
|
D000307||adrenal gland diseases
|
|
D000307||adrenal gland disease
|
|
D000307||disease adrenal gland
|
|
D000307||diseases adrenal gland
|
|
D000307||gland disease adrenal
|
|
D000307||gland diseases adrenal
|
|
D000306||adrenal cortex neoplasms
|
|
D000306||adrenal cortex cancer
|
|
D000306||adrenal cortex cancers
|
|
D000306||adrenal cortex neoplasm
|
|
D000306||adrenocortical cancer
|
|
D000306||adrenocortical cancers
|
|
D000306||cancer adrenal cortex
|
|
D000306||cancer adrenocortical
|
|
D000306||cancer of adrenal cortex
|
|
D000306||cancer of the adrenal cortex
|
|
D000306||cancers adrenal cortex
|
|
D000306||cancers adrenocortical
|
|
D000306||neoplasm adrenal cortex
|
|
D000306||neoplasms adrenal cortex
|
|
D001630||bezoars
|
|
D001630||ball hair
|
|
D001630||balls hair
|
|
D001630||bezoar
|
|
D001630||hair ball
|
|
D001630||hair balls
|
|
D001630||trichobezoar
|
|
D001630||trichobezoars
|
|
D013613||tachycardia ectopic junctional
|
|
D013613||ectopic junctional tachycardia
|
|
D013613||ectopic junctional tachycardias
|
|
D013613||ectopic tachycardia junctional
|
|
D013613||ectopic tachycardias junctional
|
|
D013613||junctional ectopic tachycardia
|
|
D013613||junctional ectopic tachycardias
|
|
D013613||junctional tachycardia ectopic
|
|
D013613||junctional tachycardias ectopic
|
|
D013613||tachycardia junctional ectopic
|
|
D013613||tachycardias ectopic junctional
|
|
D013613||tachycardias junctional ectopic
|
|
D013614||tachycardia paroxysmal
|
|
D013614||paroxysmal reciprocal tachycardia
|
|
D013614||paroxysmal reciprocal tachycardias
|
|
D013614||paroxysmal tachycardia
|
|
D013614||paroxysmal tachycardias
|
|
D013614||reciprocal tachycardia paroxysmal
|
|
D013614||reciprocal tachycardias paroxysmal
|
|
D013614||tachycardia paroxysmal reciprocal
|
|
D013614||tachycardias paroxysmal
|
|
D013614||tachycardias paroxysmal reciprocal
|
|
D013611||tachycardia atrioventricular nodal reentry
|
|
D013611||atrioventricular nodal reentrant tachycardia
|
|
D013611||atrioventricular nodal reentry tachycardia
|
|
D013611||av nodal reentrant tachycardia
|
|
D013611||tachycardia av nodal reentrant
|
|
D013612||tachycardia ectopic atrial
|
|
D013612||atrial ectopic tachycardia
|
|
D013612||atrial ectopic tachycardias
|
|
D013612||atrial tachycardia ectopic
|
|
D013612||atrial tachycardias ectopic
|
|
D013612||ectopic atrial tachycardia
|
|
D013612||ectopic atrial tachycardias
|
|
D013612||ectopic tachycardia atrial
|
|
D013612||ectopic tachycardias atrial
|
|
D013612||tachycardia atrial ectopic
|
|
D013612||tachycardias atrial ectopic
|
|
D013612||tachycardias ectopic atrial
|
|
D014949||wounds nonpenetrating
|
|
D014949||blunt injuries
|
|
D014949||blunt injury
|
|
D014949||injuries blunt
|
|
D014949||injuries nonpenetrating
|
|
D014949||injury blunt
|
|
D014949||injury nonpenetrating
|
|
D014949||nonpenetrating injuries
|
|
D014949||nonpenetrating injury
|
|
D014949||nonpenetrating wound
|
|
D014949||nonpenetrating wounds
|
|
D014949||wound nonpenetrating
|
|
D013617||tachycardia supraventricular
|
|
D013617||supraventricular tachycardia
|
|
D013617||supraventricular tachycardias
|
|
D013617||tachycardias supraventricular
|
|
D007877|608556||legionnaires apos disease
|
|
D007877|608556||disease legionnaire
|
|
D007877|608556||disease legionnaires apos
|
|
D007877|608556||infection legionella pneumophila
|
|
D007877|608556||infections legionella pneumophila
|
|
D007877|608556||legionella pneumophila infection
|
|
D007877|608556||legionella pneumophila infections
|
|
D007877|608556||legionnaire disease
|
|
D007877|608556||legionnaire disease susceptibility to
|
|
D007877|608556||legionnaire apos s disease
|
|
D007877|608556||legionnaires disease
|
|
D007877|608556||pneumophila infection legionella
|
|
D007877|608556||pneumophila infections legionella
|
|
C536330|174050||polycystic liver disease
|
|
C536330|174050||isolated autosomal dominant polycystic liver disease
|
|
C536330|174050||isolated polycystic liver disease
|
|
C536330|174050||pcld
|
|
D014948||wounds gunshot
|
|
D014948||gunshot wound
|
|
D014948||gunshot wounds
|
|
D014948||wound gunshot
|
|
D014947||wounds and injuries
|
|
D014947||injuries
|
|
D014947||injuries and wounds
|
|
D014947||injuries wounds
|
|
D014947||injury
|
|
D014947||injury and wounds
|
|
D014947||trauma
|
|
D014947||traumas
|
|
D014947||wound
|
|
D014947||wounds
|
|
D014947||wounds and injury
|
|
D014947||wounds injury
|
|
D013615||tachycardia sinoatrial nodal reentry
|
|
D013615||sinoatrial nodal reentry tachycardia
|
|
D013615||sinus node reentrant tachycardia
|
|
D013615||tachycardia sa nodal reentrant
|
|
D014946||wound infection
|
|
D014946||infections wound
|
|
D014946||infection wound
|
|
D014946||wound infections
|
|
D013616||tachycardia sinus
|
|
D013616||sinus tachycardia
|
|
D013616||sinus tachycardias
|
|
D013616||tachycardias sinus
|
|
C565836|603896||vanishing white matter leukodystrophy with ovarian failure
|
|
C565836|603896||cach
|
|
C565836|603896||cree leukoencephalopathy cle vanishing white matter leukodystrophy with ovarian failure included
|
|
C565836|603896||ovarioleukodystrophy
|
|
C565836|603896||ovarioleukodystrophy included
|
|
C565836|603896||vwm
|
|
D000309||adrenal insufficiency
|
|
D000309||adrenal gland hypofunction
|
|
D000309||adrenal insufficiencies
|
|
D000309||hypoadrenalism
|
|
D000309||hypofunction adrenal gland
|
|
208230|C535387||arthropathy progressive pseudorheumatoid of childhood
|
|
208230|C535387||ppac
|
|
208230|C535387||ppd
|
|
208230|C535387||progressive pseudorheumatoid arthropathy of childhood
|
|
208230|C535387||progressive pseudorheumatoid dysplasia
|
|
208230|C535387||sedt pa
|
|
208230|C535387||spondyloepiphyseal dysplasia tarda with progressive arthropathy
|
|
C566672|182980||spinal muscular atrophy proximal adult autosomal dominant
|
|
C566672|182980||smafk
|
|
D013610||tachycardia
|
|
D013610||tachyarrhythmia
|
|
D013610||tachyarrhythmias
|
|
D013610||tachycardias
|
|
D000012|200100||abetalipoproteinemia
|
|
D000012|200100||abl
|
|
D000012|200100||acanthocytoses
|
|
D000012|200100||acanthocytosis
|
|
D000012|200100||bassen kornzweig disease
|
|
D000012|200100||bassen kornzweig syndrome
|
|
D000012|200100||betalipoprotein deficiency disease
|
|
D000012|200100||betalipoprotein deficiency diseases
|
|
D000012|200100||deficiency disease betalipoprotein
|
|
D000012|200100||deficiency diseases betalipoprotein
|
|
D000012|200100||disease betalipoprotein deficiency
|
|
D000012|200100||diseases betalipoprotein deficiency
|
|
D000012|200100||microsomal triglyceride transfer protein deficiency
|
|
D000012|200100||microsomal triglyceride transfer protein deficiency disease
|
|
D000012|200100||mtp deficiency
|
|
D000314||adrenal rest tumor
|
|
D000314||adrenal cortical rest tumor
|
|
D000314||adrenal rest tumors
|
|
D000314||rest tumor adrenal
|
|
D000314||rest tumors adrenal
|
|
D000314||tumor adrenal rest
|
|
D000314||tumors adrenal rest
|
|
D000312||adrenal hyperplasia congenital
|
|
D000312||adrenal hyperplasias congenital
|
|
D000312||congenital adrenal hyperplasia
|
|
D000312||congenital adrenal hyperplasias
|
|
D000312||hyperplasia congenital adrenal
|
|
D000312||hyperplasias congenital adrenal
|
|
C567119||skin hair eye pigmentation variation in 5
|
|
C567119||shep5
|
|
C567119||skin hair eye pigmentation 5 black nonblack hair
|
|
C567119||skin hair eye pigmentation 5 dark fair skin
|
|
C567119||skin hair eye pigmentation 5 dark light eyes
|
|
D001649||bile duct diseases
|
|
D001649||bile duct disease
|
|
D001649||disease bile duct
|
|
D001649||diseases bile duct
|
|
D001649||duct disease bile
|
|
D001649||duct diseases bile
|
|
C567116||kininogen deficiency high molecular weight and low molecular weight
|
|
C564106|309545||mental retardation x linked syndromic 12
|
|
C564106|309545||mrxs12
|
|
D002971||cleft lip
|
|
D002971||cleft lips
|
|
D002971||harelip
|
|
D002971||harelips
|
|
D002971||lip cleft
|
|
D002971||lips cleft
|
|
C564682|606668||inflammatory bowel disease 8
|
|
C564682|606668||ibd8
|
|
D002972||cleft palates
|
|
D002972||palate cleft
|
|
D002972||palates cleft
|
|
C564794|271665||spondylometaepiphyseal dysplasia short limb hand type
|
|
C564794|271665||smed short limb abnormal calcification type
|
|
C564794|271665||smed short limb hand type
|
|
C564794|271665||smed sl
|
|
C564794|271665||smed sl ac
|
|
C564794|271665||smed type ii
|
|
C564794|271665||spondylometaepiphyseal dysplasia short limb abnormal calcification type
|
|
D000310||adrenal gland neoplasms
|
|
D000310||adrenal cancer
|
|
D000310||adrenal cancers
|
|
D000310||adrenal gland cancer
|
|
D000310||adrenal gland cancers
|
|
D000310||adrenal gland neoplasm
|
|
D000310||adrenal neoplasm
|
|
D000310||adrenal neoplasms
|
|
D000310||cancer adrenal
|
|
D000310||cancer adrenal gland
|
|
D000310||cancer of the adrenal gland
|
|
D000310||cancers adrenal
|
|
D000310||cancers adrenal gland
|
|
D000310||neoplasm adrenal
|
|
D000310||neoplasm adrenal gland
|
|
D000310||neoplasms adrenal
|
|
D000310||neoplasms adrenal gland
|
|
D038901||mental retardation x linked
|
|
D038901||retardation x linked mental
|
|
D038901||x linked mental retardation
|
|
D038901||x linked mental retardation disorders
|
|
D038901||x linked mental retardations
|
|
D038901||x linked mental retardation syndromes
|
|
D013625||takayasu arteritis
|
|
D013625||aortitis syndrome
|
|
D013625||arteritides young female
|
|
D013625||arteritis takayasu
|
|
D013625||arteritis takayasus
|
|
D013625||arteritis takayasu apos s
|
|
D013625||arteritis young female
|
|
D013625||disease takayasu
|
|
D013625||female arteritides young
|
|
D013625||female arteritis young
|
|
D013625||pulseless disease
|
|
D013625||syndrome aortitis
|
|
D013625||takayasu disease
|
|
D013625||takayasu apos s arteritis
|
|
D013625||takayasus arteritis
|
|
D013625||takayasu syndrome
|
|
D013625||young female arteritides
|
|
D013625||young female arteritis
|
|
D014954||wrist injuries
|
|
D014954||injuries wrist
|
|
D014954||injury wrist
|
|
D014954||wrist injury
|
|
D013622||taeniasis
|
|
D013622||infections taenia
|
|
D013622||infection taenia
|
|
D013622||taenia infection
|
|
D013622||taenia infections
|
|
D013622||taeniases
|
|
C537425|229100||glutamate formiminotransferase deficiency
|
|
C537425|229100||arakawa syndrome 1
|
|
C537425|229100||figlu uria
|
|
C537425|229100||formiminoglutamic aciduria
|
|
C537425|229100||formiminoglutamicaciduria figlu uria
|
|
C537425|229100||formiminotransferase deficiency
|
|
C537425|229100||formiminotransferase deficiency syndrome
|
|
C567121||epidermolysis bullosa dystrophica autosomal recessive localisata variant
|
|
C567122||epidermolysis bullosa dystrophica inversa autosomal recessive
|
|
C566899|611638||microphthalmia isolated with coloboma 5
|
|
C566899|611638||mcopcb5
|
|
D014951||wounds stab
|
|
D014951||stab wound
|
|
D014951||stab wounds
|
|
D014951||wound stab
|
|
D014950||wounds penetrating
|
|
D014950||penetrating wound
|
|
D014950||penetrating wounds
|
|
D014950||wound penetrating
|
|
248370|C535705||mandibuloacral dysplasia with type a lipodystrophy
|
|
248370|C535705||craniomandibular dermatodysostosis
|
|
248370|C535705||craniomandibular dermatodysostosis mandibuloacral dysplasia with type a lipodystrophy atypical included
|
|
248370|C535705||lipodystrophy type a associated with mandibuloacral dysplasia
|
|
248370|C535705||mada
|
|
248370|C535705||mandibuloacral dysplasia with type a lipodystrophy atypical
|
|
C563687|609918||gallbladder disease 2
|
|
C563687|609918||gbd2
|
|
C537854|164100||nystagmus 2 congenital autosomal dominant
|
|
C537854|164100||nys2
|
|
C537854|164100||nystagmus congenital motor 2
|
|
C537871|245590||laron syndrome type 2
|
|
C537871|245590||growth hormone insensitivity due to postreceptor defect
|
|
C537871|245590||growth hormone insensitivity with immunodeficiency
|
|
C537871|245590||laron syndrome due to postreceptor defect
|
|
C537871|245590||laron type dwarfism 2
|
|
601308||myeloid tumor suppressor
|
|
601308||mlrl
|
|
601308||myeloid leukemia related locus
|
|
C563919|608520||major depressive disorder 1
|
|
C563919|608520||mdd1
|
|
C563919|608520||unipolar depression 1
|
|
C535866|300258||roifman syndrome
|
|
C535866|300258||spondyloepiphseal dysplasia retinal dystrophy and antibody deficiency
|
|
C535866|300258||spondyloepiphyseal dysplasia retinal dystrophy and antibody deficiency
|
|
D002051|113970||burkitt lymphoma
|
|
D002051|113970||african lymphoma
|
|
D002051|113970||bl
|
|
D002051|113970||burkitt cell leukemia
|
|
D002051|113970||burkitt leukemia
|
|
D002051|113970||burkitt apos s leukemia
|
|
D002051|113970||burkitts leukemia
|
|
D002051|113970||burkitt apos s lymphoma
|
|
D002051|113970||burkitts lymphoma
|
|
D002051|113970||burkitt apos s tumor
|
|
D002051|113970||burkitts tumor
|
|
D002051|113970||burkitt tumor
|
|
D002051|113970||cell leukemia burkitt
|
|
D002051|113970||l3 lymphocytic leukemia
|
|
D002051|113970||l3 lymphocytic leukemias
|
|
D002051|113970||leukemia burkitt
|
|
D002051|113970||leukemia burkitt cell
|
|
D002051|113970||leukemia burkitt apos s
|
|
D002051|113970||leukemia l3 lymphocytic
|
|
D002051|113970||leukemia lymphoblastic burkitt type
|
|
D002051|113970||leukemia lymphocytic l3
|
|
D002051|113970||leukemias l3 lymphocytic
|
|
D002051|113970||lymphocytic leukemia l3
|
|
D002051|113970||lymphocytic leukemias l3
|
|
D002051|113970||lymphoma african
|
|
D002051|113970||lymphoma burkitt
|
|
D002051|113970||lymphoma burkitt apos s
|
|
D002051|113970||tumor burkitt
|
|
D002051|113970||tumor burkitt apos s
|
|
C562460|612759||synesthesia
|
|
C562460|612759||synsth
|
|
D014924||wissler apos s syndrome
|
|
D014924||subsepsis allergica
|
|
D014924||subsepsis hyperergica
|
|
D014924||syndrome wissler fanconi
|
|
D014924||syndrome wissler apos s
|
|
D014924||wissler fanconi syndrome
|
|
D014924||wisslers syndrome
|
|
D014924||wissler syndrome
|
|
143200|C536075||hyaloideoretinal degeneration of wagner
|
|
143200|C536075||erosive vitreoretinopathy
|
|
143200|C536075||ervr
|
|
143200|C536075||vcan related vitreoretinopathy
|
|
143200|C536075||wagner disease
|
|
143200|C536075||wagner syndrome
|
|
143200|C536075||wagner syndrome 1
|
|
143200|C536075||wagner syndrome type 1
|
|
143200|C536075||wagner vitreoretinal degeneration
|
|
143200|C536075||wagner vitreoretinopathy
|
|
143200|C536075||wgn1
|
|
143200|C536075||wgvrp
|
|
D058502|313850||pentalogy of cantrell
|
|
D058502|313850||cantrell haller ravitch syndrome
|
|
D058502|313850||cantrell pentalogy
|
|
D058502|313850||cantrell apos s pentalogy
|
|
D058502|313850||cantrells pentalogy
|
|
D058502|313850||pentalogy cantrell
|
|
D058502|313850||pentalogy cantrell apos s
|
|
D058502|313850||pentalogy of cantrell included
|
|
D058502|313850||tas midline defects x linked included
|
|
D058502|313850||thas
|
|
D058502|313850||thoracoabdominal syndrome
|
|
D058502|313850||thoracoabdominal syndromes
|
|
202110|C538237||adrenal hyperplasia congenital type 5
|
|
202110|C538237||17 alpha hydroxylase 17 20 lyase deficiency combined complete included
|
|
202110|C538237||17 alpha hydroxylase 17 20 lyase deficiency combined partial included
|
|
202110|C538237||17 alpha hydroxylase deficiency
|
|
202110|C538237||17 alpha hydroxylase deficiency 17 20 lyase deficiency isolated included
|
|
202110|C538237||adrenal hyperplasia congenital due to 17 alpha hydroxylase deficiency
|
|
202110|C538237||adrenal hyperplasia v
|
|
D013606||tabes dorsalis
|
|
D013606||ataxia locomotor
|
|
D013606||ataxias locomotor
|
|
D013606||locomotor ataxia
|
|
D013606||locomotor ataxias
|
|
D013606||meningomyelitides syphilitic
|
|
D013606||meningomyelitis syphilitic
|
|
D013606||meningovascular syphilis spinal
|
|
D013606||myelosyphilis
|
|
D013606||neurosyphilis tabetic
|
|
D013606||spinal cord syphilis
|
|
D013606||spinalis tabes
|
|
D013606||spinal meningovascular syphilis
|
|
D013606||syphilis spinal cord
|
|
D013606||syphilis spinal meningovascular
|
|
D013606||syphilitic meningomyelitides
|
|
D013606||syphilitic meningomyelitis
|
|
D013606||tabes spinalis
|
|
D013606||tabetic neurosyphilis
|
|
611147|C567001||paroxysmal nonkinesigenic dyskinesia 2
|
|
611147|C567001||dystonia 20
|
|
611147|C567001||dyt20
|
|
611147|C567001||pnkd2
|
|
D005922|161950||glomerulonephritis iga
|
|
D005922|161950||berger disease
|
|
D005922|161950||berger apos s disease
|
|
D005922|161950||bergers disease
|
|
D005922|161950||glomerulonephritides iga
|
|
D005922|161950||iga glomerulonephritis
|
|
D005922|161950||igan
|
|
D005922|161950||igan1
|
|
D005922|161950||igan2
|
|
D005922|161950||iga nephropathy
|
|
D005922|161950||iga nephropathy 1
|
|
D005922|161950||iga nephropathy susceptibility to 1
|
|
D005922|161950||iga nephropathy susceptibility to 2
|
|
D005922|161950||iga type nephritis
|
|
D005922|161950||immunoglobulin a nephropathy
|
|
D005922|161950||nephritis iga type
|
|
D005922|161950||nephropathy 1 iga
|
|
D005922|161950||nephropathy iga
|
|
D005922|161950||nephropathy immunoglobulin a
|
|
D002925||ciliary motility disorders
|
|
D002925||ciliary dyskinesia
|
|
D002925||ciliary dyskinesias
|
|
D002925||ciliary motility disorder
|
|
D002925||cilia syndrome immotile
|
|
D002925||cilia syndromes immotile
|
|
D002925||disorder ciliary motility
|
|
D002925||disorders ciliary motility
|
|
D002925||dyskinesia ciliary
|
|
D002925||dyskinesias ciliary
|
|
D002925||immotile cilia syndromes
|
|
D002925||syndrome immotile cilia
|
|
D002925||syndromes immotile cilia
|
|
D017188||adenophorea infections
|
|
D017188||adenophorea infection
|
|
D017188||aphasmidia infection
|
|
D017188||aphasmidia infections
|
|
D017188||infection adenophorea
|
|
D017188||infection aphasmidia
|
|
D017188||infections adenophorea
|
|
D017188||infections aphasmidia
|
|
D002921||cicatrix
|
|
D002921||cicatrization
|
|
D002921||scar
|
|
D002921||scarring
|
|
D002921||scars
|
|
300518|C564496||mental retardation x linked 82
|
|
300518|C564496||mrx82
|
|
D017180||tachycardia ventricular
|
|
D017180||tachycardias ventricular
|
|
D017180||ventricular tachycardia
|
|
D017180||ventricular tachycardias
|
|
D042101||acalculous cholecystitis
|
|
D042101||acalculous gallbladder inflammation
|
|
D042101||cholecystitis acalculous
|
|
D042101||gallbladder inflammation acalculous
|
|
606054|D056693||propionic acidemia
|
|
606054|D056693||acidemia propionic
|
|
606054|D056693||acidemia propionics
|
|
606054|D056693||acidemias propionic
|
|
606054|D056693||aciduria propionic
|
|
606054|D056693||acidurias propionic
|
|
606054|D056693||carboxylase deficiencies propionyl coa
|
|
606054|D056693||carboxylase deficiency propionyl coa
|
|
606054|D056693||deficiencies pcc
|
|
606054|D056693||deficiencies propionyl coa carboxylase
|
|
606054|D056693||deficiency pcc
|
|
606054|D056693||deficiency propionyl coa carboxylase
|
|
606054|D056693||glycinemia ketotic
|
|
606054|D056693||glycinemias ketotic
|
|
606054|D056693||hyperglycinemia ketotic
|
|
606054|D056693||hyperglycinemias ketotic
|
|
606054|D056693||hyperglycinemia with ketoacidosis and leukopenia
|
|
606054|D056693||ketotic glycinemia
|
|
606054|D056693||ketotic glycinemias
|
|
606054|D056693||ketotic hyperglycinemia
|
|
606054|D056693||ketotic hyperglycinemias
|
|
606054|D056693||pcc deficiencies
|
|
606054|D056693||pcc deficiency
|
|
606054|D056693||propionicacidemia
|
|
606054|D056693||propionicacidemias
|
|
606054|D056693||propionic acidemias
|
|
606054|D056693||propionicaciduria
|
|
606054|D056693||propionic aciduria
|
|
606054|D056693||propionicacidurias
|
|
606054|D056693||propionic acidurias
|
|
606054|D056693||propionics acidemia
|
|
606054|D056693||propionyl coa carboxylase deficiencies
|
|
606054|D056693||propionyl coa carboxylase deficiency
|
|
C567433|612020||spastic paraplegia 39 autosomal recessive
|
|
C567433|612020||ntemnd
|
|
C567433|612020||nte related motor neuron disorder
|
|
C567433|612020||spg39
|
|
C564523|300378||radial ray deficiency x linked
|
|
C564523|300378||rrdx
|
|
D001602||beriberi
|
|
D017196||rhabditida infections
|
|
D017196||infection rhabditida
|
|
D017196||infections rhabditida
|
|
D017196||rhabditida infection
|
|
603933||microvascular complications of diabetes susceptibility to 1
|
|
603933||end stage renal disease diabetic susceptibility to included
|
|
603933||microvascular complications of diabetes protection against included
|
|
603933||mvcd1
|
|
603933||nephropathy diabetic susceptibility to included
|
|
603933||neuropathy diabetic susceptibility to included
|
|
603933||nonproliferative retinopathy diabetic susceptibility to included
|
|
603933||nonproliferative retinopathy diabetic susceptibility to microvascular complications of diabetes susceptibility to included
|
|
603933||proliferative retinopathy diabetic susceptibility to included
|
|
C535742|601110||congenital disorder of glycosylation type 1d
|
|
C535742|601110||carbohydrate deficient glycoprotein syndrome type 4
|
|
C535742|601110||carbohydrate deficient glycoprotein syndrome type iv formerly
|
|
C535742|601110||cdg1d
|
|
C535742|601110||cdgid
|
|
C535742|601110||cdg id
|
|
C535742|601110||cdgs4 formerly
|
|
C535742|601110||cdgs type iv formerly
|
|
C535742|601110||congenital disorder of glycosylation type id
|
|
D017192||skin diseases bacterial
|
|
D017192||bacterial skin disease
|
|
D017192||bacterial skin diseases
|
|
D017192||disease bacterial skin
|
|
D017192||diseases bacterial skin
|
|
D017192||skin disease bacterial
|
|
D017193||skin diseases viral
|
|
D017193||diseases viral skin
|
|
D017193||disease viral skin
|
|
D017193||skin disease viral
|
|
D017193||viral skin disease
|
|
D017193||viral skin diseases
|
|
D017194||oxyurida infections
|
|
D017194||infection oxyurida
|
|
D017194||infections oxyurida
|
|
D017194||oxyurida infection
|
|
D015799|258870||gyrate atrophy
|
|
D015799|258870||atrophy gyrate
|
|
D015799|258870||deficiency oat
|
|
D015799|258870||deficiency okt
|
|
D015799|258870||deficiency ornithine aminotransferase
|
|
D015799|258870||deficiency ornithine delta aminotransferase
|
|
D015799|258870||gacr
|
|
D015799|258870||gyrate atrophy of choroid and retina
|
|
D015799|258870||gyrate atrophy of the choroid and retina
|
|
D015799|258870||hoga
|
|
D015799|258870||hyperornithinemia with gyrate atrophy of choroid and retina
|
|
D015799|258870||oat deficiency
|
|
D015799|258870||okt deficiency
|
|
D015799|258870||ornithine aminotransferase deficiency
|
|
D015799|258870||ornithine delta aminotransferase deficiency
|
|
D015799|258870||ornithine ketoacid aminotransferase deficiency
|
|
D015799|258870||ornithine keto acid aminotransferase deficiency
|
|
D015799|258870||ornithinemia with gyrate atrophy
|
|
605388|C562856||cerebral palsy ataxic autosomal recessive
|
|
605388|C562856||acp
|
|
605388|C562856||ataxic cerebral palsy
|
|
D017190||secernentea infections
|
|
D017190||infection phasmidia
|
|
D017190||infection secernentea
|
|
D017190||infections phasmidia
|
|
D017190||infections secernentea
|
|
D017190||phasmidia infection
|
|
D017190||phasmidia infections
|
|
D017190||secernentea infection
|
|
D017191||ascaridida infections
|
|
D017191||ascaridida infection
|
|
D017191||infection ascaridida
|
|
D017191||infections ascaridida
|
|
D014917||whooping cough
|
|
D014917||bordetella pertussis infection respiratory
|
|
D014917||cough whooping
|
|
D014917||pertusses
|
|
D014917||pertussis
|
|
239100|D010009||osteochondrodysplasias
|
|
239100|D010009||buchem diseases van
|
|
239100|D010009||buchem disease van
|
|
239100|D010009||chondrodystrophic myotonias
|
|
239100|D010009||chondrodystrophies myotonic
|
|
239100|D010009||chondrodystrophy myotonic
|
|
239100|D010009||diseases van buchem
|
|
239100|D010009||disease van buchem
|
|
239100|D010009||dyschondroplasias
|
|
239100|D010009||dysplasia multiple epiphyseal
|
|
239100|D010009||dysplasias multiple epiphyseal
|
|
239100|D010009||dysplasia spondyloepiphyseal
|
|
239100|D010009||dysplasias spondyloepiphyseal
|
|
239100|D010009||endosteal hyperostosis autosomal recessive
|
|
239100|D010009||epiphyseal dysplasia multiple
|
|
239100|D010009||epiphyseal dysplasias multiple
|
|
239100|D010009||hyperostosis corticalis generalisata
|
|
239100|D010009||hyperphosphatasemia tarda
|
|
239100|D010009||hyperphosphatasemia tardas
|
|
239100|D010009||late onset spondyloepiphyseal dysplasia
|
|
239100|D010009||melnick needles osteodysplasty
|
|
239100|D010009||melnick needles syndrome
|
|
239100|D010009||mns
|
|
239100|D010009||multiple epiphyseal dysplasia
|
|
239100|D010009||multiple epiphyseal dysplasias
|
|
239100|D010009||myotonia chondrodystrophic
|
|
239100|D010009||myotonias chondrodystrophic
|
|
239100|D010009||myotonic chondrodystrophies
|
|
239100|D010009||myotonic chondrodystrophy
|
|
239100|D010009||osteochondrodysplasia
|
|
239100|D010009||osteodysplasty melnick needles
|
|
239100|D010009||osteodysplasty of melnick and needles
|
|
239100|D010009||schwartz jampel syndrome
|
|
239100|D010009||sed tarda
|
|
239100|D010009||sja syndromes
|
|
239100|D010009||sjs1
|
|
239100|D010009||sost related sclerosing bone dysplasia
|
|
239100|D010009||sost sclerosing bone dysplasia
|
|
239100|D010009||spondylo epimetaphyseal dysplasia with myotonia
|
|
239100|D010009||spondyloepiphyseal dysplasia
|
|
239100|D010009||spondyloepiphyseal dysplasias
|
|
239100|D010009||syndrome melnick needles
|
|
239100|D010009||syndrome schwartz jampel
|
|
239100|D010009||syndrome schwartz jampel aberfeld
|
|
239100|D010009||syndrome sja
|
|
239100|D010009||syndromes sja
|
|
239100|D010009||van buchem disease
|
|
239100|D010009||van buchem diseases
|
|
239100|D010009||vbch
|
|
239100|D010009||x linked sed
|
|
239100|D010009||x linked sedt
|
|
239100|D010009||x linked spondyloepiphyseal dysplasia tarda
|
|
D014912||white muscle disease
|
|
D014912||diseases white muscle
|
|
D014912||disease white muscle
|
|
D014912||muscle diseases white
|
|
D014912||muscle disease white
|
|
D014912||white muscle diseases
|
|
D014911||whiplash injuries
|
|
D014911||injuries whiplash
|
|
D014911||injury whiplash
|
|
D014911||whiplash injury
|
|
C563433|600883||diabetes mellitus insulin dependent 8
|
|
C563433|600883||iddm8
|
|
C563433|600883||insulin dependent diabetes mellitus 8
|
|
D001607||berylliosis
|
|
D001607||beryllioses
|
|
D001607||beryllium disease
|
|
612541|C567260||neutropenia severe congenital autosomal recessive 4
|
|
612541|C567260||dursun syndrome included
|
|
612541|C567260||neutropenia severe congenital 4 autosomal recessive
|
|
612541|C567260||pulmonary arterial hypertension leukopenia and atrial septal defect included
|
|
612541|C567260||scn4
|
|
D017189||enoplida infections
|
|
D017189||dioctophyma renale infection
|
|
D017189||dioctophyma renale infections
|
|
D017189||enoplida infection
|
|
D017189||infection dioctophyma renale
|
|
D017189||infection enoplida
|
|
D017189||infections dioctophyma renale
|
|
D017189||infections enoplida
|
|
606391|C562772||mason type diabetes
|
|
606391|C562772||maturity onset diabetes of the young
|
|
D017285||polymyositis
|
|
D017285||idiopathic polymyositides
|
|
D017285||idiopathic polymyositis
|
|
D017285||multiple myositis
|
|
D017285||myositides multiple
|
|
D017285||myositis multiple
|
|
D017285||ossificans polymyositis
|
|
D017285||polymyositides
|
|
D017285||polymyositides idiopathic
|
|
D017285||polymyositis idiopathic
|
|
D017285||polymyositis ossificans
|
|
613290||hearing loss cisplatin induced susceptibility to
|
|
613290||cihl
|
|
194072|D017624||wagr syndrome
|
|
194072|D017624||11p partial monosomy syndrome
|
|
194072|D017624||chromosome 11p13 deletion syndrome
|
|
194072|D017624||complex wagr
|
|
194072|D017624||contiguous gene syndrome wagr
|
|
194072|D017624||syndrome wagr
|
|
194072|D017624||wagr
|
|
194072|D017624||wagr complex
|
|
194072|D017624||wagr complices
|
|
194072|D017624||wagr contiguous gene syndrome
|
|
194072|D017624||wagr syndromes
|
|
194072|D017624||wilms tumor aniridia genital anomalies retardation syndrome
|
|
194072|D017624||wilms tumor aniridia genitourinary anomalies and mental retardation syndrome
|
|
194072|D017624||wilms tumor aniridia genitourinary anomalies mental retardation syndrome
|
|
194072|D017624||wilms tumor aniridia genitourinary anomalies mr syndrome
|
|
194072|D017624||wilms tumor aniridia gonadoblastoma mental retardation syndrome
|
|
D017282||tick borne diseases
|
|
D017282||diseases tick borne
|
|
D017282||disease tick borne
|
|
D017282||infections tick borne
|
|
D017282||infection tick borne
|
|
D017282||tick borne disease
|
|
D017282||tick borne infection
|
|
D017282||tick borne infections
|
|
C564969|255320||minicore myopathy with external ophthalmoplegia
|
|
C564969|255320||minicore disease
|
|
C564969|255320||minicore myopathy
|
|
C564969|255320||multicore disease
|
|
C564969|255320||multicore myopathy
|
|
C564969|255320||multicore myopathy with external ophthalmoplegia
|
|
C564969|255320||multiminicore disease
|
|
C564969|255320||multi minicore disease
|
|
C564969|255320||multiminicore disease with external ophthalmoplegia
|
|
C564969|255320||multiminicore myopathy
|
|
C564969|255320||multiminicore myopathy multicore myopathy with external ophthalmoplegia
|
|
C537203|609306||spinocerebellar ataxia 26
|
|
C537203|609306||sca26
|
|
C537203|609306||spinocerebellar ataxia type 26
|
|
D054222||cobblestone lissencephaly
|
|
D054222||cobblestone complex
|
|
D054222||cobblestone dysplasia
|
|
D054222||cobblestone dysplasias
|
|
D054222||cobblestone lissencephalies
|
|
D054222||dysplasia cobblestone
|
|
D054222||dysplasias cobblestone
|
|
D054222||lissencephalies cobblestone
|
|
D054222||lissencephaly cobblestone
|
|
D054222||lissencephaly type 2
|
|
D054220||malformations of cortical development
|
|
D054220||cerebral cortical dysplasia
|
|
D054220||cerebral cortical dysplasias
|
|
D054220||cortical development malformation
|
|
D054220||cortical development malformations
|
|
D054220||cortical dysplasia
|
|
D054220||cortical dysplasia cerebral
|
|
D054220||cortical dysplasias
|
|
D054220||cortical dysplasias cerebral
|
|
D054220||development malformation cortical
|
|
D054220||development malformations cortical
|
|
D054220||dysplasia cerebral cortical
|
|
D054220||dysplasia cortical
|
|
D054220||dysplasias cerebral cortical
|
|
D054220||dysplasias cortical
|
|
D054220||hemimegalencephalies
|
|
D054220||hemimegalencephaly
|
|
D054220||malformations of cerebral cortex development
|
|
D054220||polymicrogyria
|
|
D054220||polymicrogyrias
|
|
D054220||schizencephalies
|
|
D056886||contrecoup injury
|
|
D056886||contre coup injuries
|
|
D056886||contrecoup injuries
|
|
D056886||contre coup injury
|
|
D056886||injuries contrecoup
|
|
D056886||injuries contre coup
|
|
D056886||injury contrecoup
|
|
D056886||injury contre coup
|
|
122700|C563039||coumarin resistance
|
|
122700|C563039||coumarin poor metabolism of
|
|
122700|C563039||warfarin resistance
|
|
122700|C563039||warfarin resistance coumarin sensitivity included
|
|
122700|C563039||warfarin sensitivity included
|
|
C536058|259730||osteopetrosis with renal tubular acidosis
|
|
C536058|259730||carbonic anhydrase 2 deficiency
|
|
C536058|259730||carbonic anhydrase ii deficiency
|
|
C536058|259730||guibaud vainsel syndrome
|
|
C536058|259730||marble brain disease
|
|
C536058|259730||optb3
|
|
C536058|259730||osteopetrosis autosomal recessive 3
|
|
613285||deafness autosomal recessive 25
|
|
613285||dfnb25
|
|
D011371|176670||progeria
|
|
D011371|176670||hgps
|
|
D011371|176670||hutchinson gilford progeria syndrome
|
|
D011371|176670||hutchinson gilford progeria syndromes
|
|
D011371|176670||hutchinson gilford syndrome
|
|
D011371|176670||progeria progeria syndrome childhood onset included
|
|
D011371|176670||progeria syndrome hutchinson gilford
|
|
D011371|176670||progeria syndromes hutchinson gilford
|
|
137100|C536290||immunoglobulin a deficiency 1
|
|
137100|C536290||gamma a globulin selective deficiency of
|
|
137100|C536290||igad1
|
|
137100|C536290||iga selective deficiency of
|
|
137100|C536290||immunoglobulin a selective deficiency of
|
|
C536335|174810||polyostotic osteolytic dysplasia hereditary expansile
|
|
C536335|174810||eof
|
|
C536335|174810||expansile osteolysis familial
|
|
C536335|174810||familial expansile osteolysis
|
|
C536335|174810||feo
|
|
C536335|174810||hepod
|
|
C536335|174810||mccabe disease
|
|
C536335|174810||osteolysis familial expansile
|
|
C565720|611755||leber congenital amaurosis 10
|
|
C565720|611755||lca10
|
|
D007965|245200||leukodystrophy globoid cell
|
|
D007965|245200||beta galactosidase deficiencies galactosylceramide
|
|
D007965|245200||beta galactosidase deficiency galactosylceramide
|
|
D007965|245200||cell leukodystrophies globoid
|
|
D007965|245200||cell leukodystrophy globoid
|
|
D007965|245200||cell leukoencephalopathies globoid
|
|
D007965|245200||cell leukoencephalopathy globoid
|
|
D007965|245200||classic globoid cell leukodystrophy
|
|
D007965|245200||deficiencies galactocerebrosidase
|
|
D007965|245200||deficiencies galactosylceramide beta galactosidase
|
|
D007965|245200||deficiencies galc
|
|
D007965|245200||deficiency disease galactosylceramidase
|
|
D007965|245200||deficiency disease galactosylceramide beta galactosidase
|
|
D007965|245200||deficiency diseases galactosylceramidase
|
|
D007965|245200||deficiency diseases galactosylceramide beta galactosidase
|
|
D007965|245200||deficiency galactocerebrosidase
|
|
D007965|245200||deficiency galactosylceramide beta galactosidase
|
|
D007965|245200||deficiency galc
|
|
D007965|245200||diffuse globoid body sclerosis
|
|
D007965|245200||disease galactosylceramidase deficiency
|
|
D007965|245200||disease galactosylceramide beta galactosidase deficiency
|
|
D007965|245200||diseases galactosylceramidase deficiency
|
|
D007965|245200||diseases galactosylceramide beta galactosidase deficiency
|
|
D007965|245200||early onset globoid cell leukodystrophy
|
|
D007965|245200||galactocerebrosidase deficiencies
|
|
D007965|245200||galactocerebrosidase deficiency
|
|
D007965|245200||galactosylceramidase deficiency disease
|
|
D007965|245200||galactosylceramidase deficiency diseases
|
|
D007965|245200||galactosylceramide beta galactosidase deficiencies
|
|
D007965|245200||galactosylceramide beta galactosidase deficiency
|
|
D007965|245200||galactosylceramide beta galactosidase deficiency disease
|
|
D007965|245200||galactosylceramide beta galactosidase deficiency diseases
|
|
D007965|245200||galactosylceramide lipidosis
|
|
D007965|245200||galactosylcerebrosidase deficiency
|
|
D007965|245200||galactosylsphingosine lipidosis
|
|
D007965|245200||galc deficiencies
|
|
D007965|245200||galc deficiency
|
|
D007965|245200||gcl
|
|
D007965|245200||gld
|
|
D007965|245200||globoid body sclerosis diffuse
|
|
D007965|245200||globoid cell leukodystrophies
|
|
D007965|245200||globoid cell leukodystrophy
|
|
D007965|245200||globoid cell leukoencephalopathies
|
|
D007965|245200||globoid cell leukoencephalopathy
|
|
D007965|245200||globoid leukodystrophies
|
|
D007965|245200||globoid leukodystrophy
|
|
D007965|245200||infantile globoid cell leukodystrophy
|
|
D007965|245200||krabbe disease
|
|
D007965|245200||krabbe leukodystrophy
|
|
D007965|245200||krabbe apos s disease
|
|
D007965|245200||krabbes disease
|
|
D007965|245200||krabbe apos s leukodystrophy
|
|
D007965|245200||krabbes leukodystrophy
|
|
D007965|245200||late onset globoid cell leukodystrophy
|
|
D007965|245200||leukodystrophies globoid
|
|
D007965|245200||leukodystrophies globoid cell
|
|
D007965|245200||leukodystrophy globoid
|
|
D007965|245200||leukodystrophy globoid cell classic
|
|
D007965|245200||leukodystrophy globoid cell early onset
|
|
D007965|245200||leukodystrophy globoid cell infantile
|
|
D007965|245200||leukodystrophy globoid cell late onset
|
|
D007965|245200||leukodystrophy krabbe
|
|
D007965|245200||leukodystrophy krabbe apos s
|
|
D007965|245200||leukoencephalopathies globoid cell
|
|
D007965|245200||leukoencephalopathy globoid cell
|
|
D007965|245200||psychosine lipidosis
|
|
C562590|610651||xeroderma pigmentosum complementation group b
|
|
C562590|610651||xeroderma pigmentosum group b
|
|
C562590|610651||xpb
|
|
C562590|610651||xpb cs included
|
|
C562590|610651||xp group b xpbc xeroderma pigmentosum b cockayne syndrome included
|
|
C571911||gastrointestinal anthrax
|
|
D030243||hemorrhagic syndrome bovine
|
|
D030243||bovine hemorrhagic syndrome
|
|
C571912||inhalation anthrax
|
|
612540|C567261||myopathy congenital compton north
|
|
D054243||vesicular stomatitis
|
|
D054243||stomatitides vesicular
|
|
D054243||stomatitis vesicular
|
|
D054243||vesicular stomatitides
|
|
C564708|606438||huntington disease like 2
|
|
C564708|606438||hdl2
|
|
253220|D016538||mucopolysaccharidosis vii
|
|
253220|D016538||beta glucuronidase deficiencies
|
|
253220|D016538||beta glucuronidase deficiency
|
|
253220|D016538||deficiencies beta glucuronidase
|
|
253220|D016538||deficiencies gusb
|
|
253220|D016538||deficiency beta glucuronidase
|
|
253220|D016538||deficiency gusb
|
|
253220|D016538||disease sly
|
|
253220|D016538||gusb deficiencies
|
|
253220|D016538||gusb deficiency
|
|
253220|D016538||mps7
|
|
253220|D016538||mps vii
|
|
253220|D016538||mucopolysaccharidosis 7
|
|
253220|D016538||mucopolysaccharidosis type vii
|
|
253220|D016538||mucopolysaccharidosis type viis
|
|
253220|D016538||mucopolysaccharidosis viis
|
|
253220|D016538||sly disease
|
|
253220|D016538||sly syndrome
|
|
253220|D016538||syndrome sly
|
|
253220|D016538||type vii mucopolysaccharidosis
|
|
253220|D016538||type viis mucopolysaccharidosis
|
|
253220|D016538||viis mucopolysaccharidosis
|
|
271245||mitochondrial dna depletion syndrome 7 hepatocerebral type
|
|
271245||iosca
|
|
271245||mtdps7
|
|
271245||sca8 formerly
|
|
271245||spinocerebellar ataxia 8 formerly
|
|
271245||spinocerebellar ataxia infantile onset
|
|
D018589||gastroparesis
|
|
D018589||gastric stases
|
|
D018589||gastric stasis
|
|
D018589||gastropareses
|
|
D018589||stases gastric
|
|
D018589||stasis gastric
|
|
180300|D001172||arthritis rheumatoid
|
|
180300|D001172||ra
|
|
180300|D001172||rheumatoid arthritis
|
|
180300|D001172||rheumatoid arthritis susceptibility to
|
|
C566909|611597||cataract autosomal dominant multiple types 1
|
|
C566909|611597||cataract 12 multiple types
|
|
C566909|611597||ctrct12
|
|
D000795|301500||fabry disease
|
|
D000795|301500||alpha galactosidase a deficiency
|
|
D000795|301500||alpha galactosidase a deficiency disease
|
|
D000795|301500||anderson fabry disease
|
|
D000795|301500||angiokeratoma corporis diffusum
|
|
D000795|301500||angiokeratoma diffuse
|
|
D000795|301500||ceramide trihexosidase deficiency
|
|
D000795|301500||ceramide trihexosidase deficiency fabry disease cardiac variant included
|
|
D000795|301500||deficiency alpha galactosidase a
|
|
D000795|301500||deficiency ceramide trihexosidase
|
|
D000795|301500||deficiency gla
|
|
D000795|301500||diffuse angiokeratoma
|
|
D000795|301500||fabry apos s disease
|
|
D000795|301500||gla deficiency
|
|
D000795|301500||hereditary dystopic lipidosis
|
|
D000795|301500||lipidosis hereditary dystopic
|
|
D017271||craniomandibular disorders
|
|
D017271||craniomandibular disease
|
|
D017271||craniomandibular diseases
|
|
D017271||craniomandibular disorder
|
|
D017271||disease craniomandibular
|
|
D017271||diseases craniomandibular
|
|
D017271||disorder craniomandibular
|
|
D017271||disorders craniomandibular
|
|
C537423|257550||apraxia oculomotor cogan type
|
|
C537423|257550||cogan apos s syndrome type 2
|
|
C537423|257550||congenital oculomotor apraxia
|
|
C537423|257550||ocular motor apraxia
|
|
C537423|257550||oculomotor apraxia cogan type
|
|
C537423|257550||saccade initiation failure congenital
|
|
C567213|612645||deafness autosomal recessive 1b
|
|
C567213|612645||dfnb1b
|
|
D000741|609135||anemia aplastic
|
|
D000741|609135||anemia hypoplastic
|
|
D000741|609135||anemias aplastic
|
|
D000741|609135||anemias hypoplastic
|
|
D000741|609135||aplastic anemia
|
|
D000741|609135||aplastic anemias
|
|
D000741|609135||aplastic anemia susceptibility to included
|
|
D000741|609135||hypoplastic anemia
|
|
D000741|609135||hypoplastic anemias
|
|
C565231|606394||mody type 6
|
|
C565231|606394||maturity onset diabetes of the young type 6
|
|
C565231|606394||mody6
|
|
D055589||pancreatitis graft
|
|
D055589||graft pancreatitis
|
|
C563485||osteomas of mandible
|
|
C563484||osteopoikilosis isolated
|
|
C563483||osteosclerosis with ichthyosis and fractures
|
|
C563483||cortical thickening of long bones with bowing and ichthyosis
|
|
D017243||merrf syndrome
|
|
D017243||fukuhara disease
|
|
D017243||fukuhara syndrome
|
|
D017243||merrf
|
|
D017243||myoclonic epilepsy and ragged red fibers
|
|
D017243||myoclonic epilepsy associated with ragged red fibers
|
|
D017243||myoclonic epilepsy with ragged red fibers
|
|
D017243||myoclonus with epilepsy with ragged red fibers
|
|
D017243||myoencephalopathy ragged red fiber disease
|
|
D017243||syndrome fukuhara
|
|
D017243||syndrome merrf
|
|
146200|C537156||hypoparathyroidism familial isolated
|
|
146200|C537156||fih
|
|
146200|C537156||hypoparathyroidism autosomal dominant hypoparathyroidism autosomal recessive included
|
|
C563488||ossified ear cartilages
|
|
C563487||osteogenesis imperfecta with opalescent teeth blue sclerae and wormian bones but without fractures
|
|
C537190||ruvalcaba churesigaew myhre syndrome
|
|
D005258||felty syndrome
|
|
D005258||familial felty apos s syndrome
|
|
D005258||familial feltys syndrome
|
|
D005258||familial felty syndrome
|
|
D005258||felty apos s syndrome
|
|
D005258||feltys syndrome
|
|
D005258||felty apos s syndrome familial
|
|
D005258||felty syndrome familial
|
|
D005258||rheumatoid arthritis splenomegaly and neutropenia
|
|
D005258||syndrome familial felty
|
|
D005258||syndrome familial felty apos s
|
|
D005258||syndrome felty
|
|
D005258||syndrome felty apos s
|
|
D004437|224700||ebstein anomaly
|
|
D004437|224700||anomaly ebstein
|
|
D004437|224700||anomaly ebstein apos s
|
|
D004437|224700||ebstein malformation
|
|
D004437|224700||ebstein apos s anomaly
|
|
D004437|224700||ebsteins anomaly
|
|
D004437|224700||ebstein apos s anomaly familial
|
|
D004437|224700||ebstein apos s malformation
|
|
D004437|224700||ebsteins malformation
|
|
D004437|224700||familial ebstein anomaly
|
|
D004437|224700||familial ebstein apos s anomaly
|
|
D004437|224700||familial ebsteins anomaly
|
|
D004437|224700||malformation ebstein apos s
|
|
D020896||hypovolemia
|
|
D020896||hypovolemias
|
|
D020896||hypovolemic
|
|
D020896||hypovolemics
|
|
D005254||feline panleukopenia
|
|
D005254||agranulocytoses feline
|
|
D005254||agranulocytosis feline
|
|
D005254||ataxia feline
|
|
D005254||ataxias feline
|
|
D005254||cat plague
|
|
D005254||cat plagues
|
|
D005254||distemper feline
|
|
D005254||distempers feline
|
|
D005254||enteritides feline infectious
|
|
D005254||enteritis feline infectious
|
|
D005254||feline agranulocytoses
|
|
D005254||feline agranulocytosis
|
|
D005254||feline ataxia
|
|
D005254||feline ataxias
|
|
D005254||feline distemper
|
|
D005254||feline distempers
|
|
D005254||feline infectious enteritides
|
|
D005254||feline infectious enteritis
|
|
D005254||feline panleukopenias
|
|
D005254||fever show
|
|
D005254||fevers show
|
|
D005254||infectious enteritides feline
|
|
D005254||infectious enteritis feline
|
|
D005254||panleukopenia feline
|
|
D005254||panleukopenias feline
|
|
D005254||plague cat
|
|
D005254||plagues cat
|
|
D005254||show fever
|
|
D005254||show fevers
|
|
C537192||ruzicka goerz anton syndrome
|
|
C537192||ichthyosis deafness mental retardation skeletal anomalies
|
|
C537193||saal bulas syndrome
|
|
C537193||ectrodactyly diaphragmatic hernia congenital heart defect and agenesis of the corpus callosum
|
|
D005262||feminization
|
|
D005262||feminizations
|
|
D005261||female urogenital diseases and pregnancy complications
|
|
D005264||femoral fractures
|
|
D005264||femoral fracture
|
|
D005264||fracture femoral
|
|
D005264||fractures femoral
|
|
D017237||mitochondrial encephalomyopathies
|
|
D017237||encephalomyopathies mitochondrial
|
|
D017237||encephalomyopathy mitochondrial
|
|
D017237||mitochondrial encephalomyopathy
|
|
C563493||optic nerve aplasia bilateral
|
|
D004062|188400||digeorge syndrome
|
|
D004062|188400||22q11 2 deletion syndrome
|
|
D004062|188400||22q11 2ds
|
|
D004062|188400||autosomal dominant opitz g bbb syndrome
|
|
D004062|188400||catch22
|
|
D004062|188400||catch22 included
|
|
D004062|188400||chromosome 22q11 2 deletion syndrome
|
|
D004062|188400||conotruncal anomaly face syndrome
|
|
D004062|188400||conotruncal anomaly face syndrome ctaf
|
|
D004062|188400||deletion 22q11 2 syndrome
|
|
D004062|188400||deletion syndrome 22q11 2
|
|
D004062|188400||dgcr included
|
|
D004062|188400||dgs
|
|
D004062|188400||digeorge anomaly
|
|
D004062|188400||digeorge sequence
|
|
D004062|188400||familial third and fourth pharyngeal pouch syndrome
|
|
D004062|188400||hypoplasia of thymus and parathyroids
|
|
D004062|188400||pharyngeal pouch syndrome
|
|
D004062|188400||sedlackova syndrome
|
|
D004062|188400||shprintzen syndrome
|
|
D004062|188400||shprintzen vcf syndrome
|
|
D004062|188400||syndrome digeorge
|
|
D004062|188400||syndrome sedlackova
|
|
D004062|188400||syndrome shprintzen
|
|
D004062|188400||syndrome vcf
|
|
D004062|188400||syndrome velocardiofacial
|
|
D004062|188400||syndrome velo cardio facial
|
|
D004062|188400||takao vcf syndrome included
|
|
D004062|188400||third and fourth pharyngeal pouch syndrome
|
|
D004062|188400||third and fourth pharyngeal pouch syndrome digeorge syndrome chromosome region included
|
|
D004062|188400||thymic aplasia syndrome
|
|
D004062|188400||vcfs
|
|
D004062|188400||vcf syndrome
|
|
D004062|188400||velocardiofacial syndrome
|
|
D004062|188400||velo cardio facial syndrome
|
|
D018567||breast neoplasms male
|
|
D018567||breast cancer male
|
|
D018567||breast carcinoma male
|
|
D018567||breast neoplasm male
|
|
D018567||breast tumor male
|
|
D018567||breast tumors male
|
|
D018567||cancer male breast
|
|
D018567||carcinoma male breast
|
|
D018567||male breast cancer
|
|
D018567||male breast carcinoma
|
|
D018567||male breast neoplasm
|
|
D018567||male breast neoplasms
|
|
D018567||male breast tumor
|
|
D018567||male breast tumors
|
|
D018567||neoplasm male breast
|
|
D018567||neoplasms breast male
|
|
D018567||neoplasms male breast
|
|
D018567||tumor male breast
|
|
D018567||tumors breast male
|
|
D018567||tumors male breast
|
|
C563491||orofaciodigital syndrome x
|
|
C563491||oral facial digital syndrome type x
|
|
C563491||oral facial digital syndrome with fibular aplasia
|
|
C563491||orofaciodigital syndrome with fibular aplasia
|
|
C566552|602404||parkinson disease 3 autosomal dominant lewy body
|
|
C566552|602404||park3
|
|
C566552|602404||parkinson disease 3 autosomal dominant
|
|
C563490||orbital margin hypoplasia of
|
|
C563497||optic atrophy hearing loss and peripheral neuropathy autosomal dominant
|
|
C563496||optic atrophy with demyelinating disease of cns
|
|
D017253||neurofibromatoses
|
|
D017253||multiple neurofibroma
|
|
D017253||multiple neurofibromas
|
|
D017253||neurofibroma multiple
|
|
D017253||neurofibromas multiple
|
|
D017253||neurofibromatosis
|
|
D017253||neurofibromatosis 3
|
|
D017253||neurofibromatosis 3s
|
|
D017253||neurofibromatosis syndrome
|
|
D017253||neurofibromatosis syndromes
|
|
D017253||neurofibromatosis type 3
|
|
D017253||neurofibromatosis type 3s
|
|
D017253||syndrome neurofibromatosis
|
|
D017253||syndromes neurofibromatosis
|
|
D017253||type 3 neurofibromatosis
|
|
C563494||optic atrophy with negative electroretinograms
|
|
D017254||leukemic infiltration
|
|
D017254||infiltration leukemic
|
|
D017254||infiltrations leukemic
|
|
D017254||leukemic infiltrations
|
|
C563499||ophthalmoplegia familial total with iris transillumination
|
|
C563498||ophthalmoplegia progressive with scrotal tongue and mental deficiency
|
|
D017250||caliciviridae infections
|
|
D017250||caliciviridae infection
|
|
D017250||calicivirus infection
|
|
D017250||calicivirus infections
|
|
D017250||infection caliciviridae
|
|
D017250||infection calicivirus
|
|
D017250||infections caliciviridae
|
|
D017250||infections calicivirus
|
|
C563399|601068||epilepsy myoclonic benign adult familial type 1
|
|
C563399|601068||bafme1
|
|
C563399|601068||benign adult familial myoclonic epilepsy 1
|
|
C563399|601068||cortical myoclonic tremor with epilepsy familial
|
|
C563399|601068||cortical myoclonic tremor with epilepsy familial 1
|
|
C563399|601068||cortical tremor familial
|
|
C563399|601068||epilepsy familial adult myoclonic 1
|
|
C563399|601068||fame1
|
|
C563399|601068||fcmte1
|
|
D020886||somatosensory disorders
|
|
D020886||diminished pain sensation
|
|
D020886||diminished pinprick sensation
|
|
D020886||diminisheds pain sensation
|
|
D020886||diminisheds pinprick sensation
|
|
D020886||impairment light touch sensation
|
|
D020886||light touch sensation impairment
|
|
D020886||pain sensation diminished
|
|
D020886||pain sensation diminisheds
|
|
D020886||pinprick sensation diminished
|
|
D020886||pinprick sensation diminisheds
|
|
D020886||position sense disorder
|
|
D020886||position sense disorders
|
|
D020886||proprioceptive disorder
|
|
D020886||proprioceptive disorders
|
|
D020886||sensation diminished pain
|
|
D020886||sensation diminished pinprick
|
|
D020886||sensation diminisheds pain
|
|
D020886||sensation diminisheds pinprick
|
|
D020886||sensation disorder somatic
|
|
D020886||sensation disorders somatic
|
|
D020886||sensation disorders thermal
|
|
D020886||sensation disorder thermal
|
|
D020886||sense disorder position
|
|
D020886||sense disorders position
|
|
D020886||somatic sensation disorder
|
|
D020886||somatic sensation disorders
|
|
D020886||somatosensory disorder
|
|
D020886||thermal sensation disorder
|
|
D020886||thermal sensation disorders
|
|
D005266||femoral neoplasms
|
|
D005266||femoral neoplasm
|
|
D005266||neoplasm femoral
|
|
D005266||neoplasms femoral
|
|
D005265||femoral neck fractures
|
|
D005265||femoral neck fracture
|
|
D005265||femur neck fracture
|
|
D005265||femur neck fractures
|
|
181430||spmd
|
|
181430||spmm
|
|
613239||thyrotoxic periodic paralysis susceptibility to 2
|
|
613239||ttpp2
|
|
C563492|165550||optic nerve hypoplasia bilateral
|
|
C563492|165550||optic nerve aplasia bilateral included
|
|
C566982|611263||asphyxiating thoracic dystrophy 2
|
|
C566982|611263||atd2
|
|
C566982|611263||short rib thoracic dysplasia 2 with or without polydactyly
|
|
C566982|611263||srtd2
|
|
D017246||ophthalmoplegia chronic progressive external
|
|
D017246||chronic progressive external ophthalmoplegia
|
|
D017246||cpeo
|
|
D017246||disease graefe
|
|
D017246||dystrophy ocular muscular
|
|
D017246||external ophthalmoplegia progressive
|
|
D017246||graefe disease
|
|
D017246||graefe apos s disease
|
|
D017246||mitochondrial ocular myopathy
|
|
D017246||muscular dystrophies ocular
|
|
D017246||muscular dystrophy ocular
|
|
D017246||myopathy mitochondrial ocular
|
|
D017246||ocular muscular dystrophies
|
|
D017246||ocular muscular dystrophy
|
|
D017246||ocular myopathy mitochondrial
|
|
D017246||ocular myopathy of von graefe fuchs
|
|
D017246||ophthalmoplegia progressive external
|
|
D017246||progressive external ophthalmoplegia
|
|
C563464||orofacial cleft 7
|
|
C566585|602085||polydactyly postaxial type a2
|
|
C566585|602085||papa2
|
|
C566585|602085||postaxial polydactyly type a2
|
|
C564793||subaortic stenosis membranous
|
|
C564792||sucrosuria hiatus hernia and mental retardation
|
|
C563468||cleft lip congenital healed
|
|
C563468||congenital healed cleft lip
|
|
C564799||spondylocostal dysostosis with anal atresia and urogenital anomalies
|
|
C564799||casamassima morton nance syndrome
|
|
C563467||hypertryptophanemia familial
|
|
181405||spsma
|
|
C563466||uv sensitive syndrome
|
|
C564797||spondyloepiphyseal dysplasia tarda autosomal recessive
|
|
C564796||spondyloepiphyseal dysplasia tarda with mental retardation
|
|
D014923|301000||wiskott aldrich syndrome
|
|
D014923|301000||aldrich syndrome
|
|
D014923|301000||eczema thrombocytopenia immunodeficiency syndrome
|
|
D014923|301000||eczema thrombocytopenia immunodeficiency syndromes
|
|
D014923|301000||imd2
|
|
D014923|301000||immunodeficiency 2
|
|
D014923|301000||syndrome aldrich
|
|
D014923|301000||syndrome eczema thrombocytopenia immunodeficiency
|
|
D014923|301000||syndromes eczema thrombocytopenia immunodeficiency
|
|
D014923|301000||syndrome wiskott aldrich
|
|
D014923|301000||was
|
|
D014923|301000||was1
|
|
D014923|301000||wiskott aldrich syndrome 1
|
|
D014923|301000||wiskott syndrome
|
|
C565225|609812||maturity onset diabetes of the young type 8 with exocrine dysfunction
|
|
C565225|609812||diabetes and pancreatic exocrine dysfunction
|
|
C565225|609812||diabetes pancreatic exocrine dysfunction syndrome
|
|
C565225|609812||dped
|
|
C565225|609812||mody8
|
|
D005236||favism
|
|
D005236||favisms
|
|
215140||grbgd
|
|
213200|C565865||spinocerebellar ataxia autosomal recessive 2
|
|
213200|C565865||cerebellar granular cell hypoplasia and mental retardation congenital
|
|
213200|C565865||cerebellar hypoplasia nonprogressive norman type
|
|
213200|C565865||cerebelloparenchymal disorder iii
|
|
213200|C565865||cpd3
|
|
213200|C565865||cpd iii
|
|
213200|C565865||scar2
|
|
D007896||leishmaniasis
|
|
D007896||leishmaniases
|
|
D006566||herpesviridae infections
|
|
D006566||herpesviridae infection
|
|
D006566||herpesvirus infection
|
|
D006566||herpesvirus infections
|
|
D006566||infection herpesviridae
|
|
D006566||infection herpesvirus
|
|
D006566||infections herpesviridae
|
|
D006566||infections herpesvirus
|
|
D007897||leishmaniasis mucocutaneous
|
|
D007897||leishmaniases mucocutaneous
|
|
D007897||mucocutaneous leishmaniases
|
|
D007897||mucocutaneous leishmaniasis
|
|
D006563||herpes zoster ophthalmicus
|
|
D006563||herpes zoster ocular
|
|
D006563||ocular herpes zoster
|
|
D005235||fatty liver alcoholic
|
|
D005235||alcoholic fatty liver
|
|
D005235||alcoholic steatohepatitis
|
|
D005234||fatty liver
|
|
D005234||liver fatty
|
|
D005234||liver steatoses
|
|
D005234||liver steatosis
|
|
D005234||steatohepatitides
|
|
D005234||steatohepatitis
|
|
D005234||steatoses liver
|
|
D005234||steatosis liver
|
|
D005234||visceral steatosis
|
|
613238||spondyloarthropathy susceptibility to 3
|
|
613238||spda3
|
|
C536703|314580||wieacker syndrome
|
|
C536703|314580||apraxia oculomotor with congenital contractures and muscle atrophy
|
|
C536703|314580||contractures of feet muscle atrophy and oculomotor apraxia
|
|
C536703|314580||wieacker wolff syndrome
|
|
C536703|314580||wrwf
|
|
D005242||fecal incontinence
|
|
D005242||fecal incontinences
|
|
D005242||incontinence fecal
|
|
D005242||incontinences fecal
|
|
C567639|613330||spondylo megaepiphyseal metaphyseal dysplasia
|
|
C567639|613330||smmd
|
|
D017219||gastric outlet obstruction
|
|
D017219||gastric outlet obstructions
|
|
D017219||obstruction gastric outlet
|
|
D017219||obstructions gastric outlet
|
|
D017219||outlet obstruction gastric
|
|
D017219||outlet obstructions gastric
|
|
600081|C564005||vitamin d hydroxylation deficient rickets type 1b
|
|
600081|C564005||25 hydroxyvitamin d3 deficiency selective
|
|
600081|C564005||pseudovitamin d3 deficiency rickets due to 25 hydroxylase deficiency
|
|
600081|C564005||vddr1b
|
|
600081|C564005||vitamin d dependent rickets type 1b
|
|
D020879||neuromuscular manifestations
|
|
D020879||disease manifestation muscle
|
|
D020879||disease manifestations muscle
|
|
D020879||manifestation muscle disease
|
|
D020879||manifestation neuromuscular
|
|
D020879||manifestations muscle disease
|
|
D020879||manifestations neuromuscular
|
|
D020879||muscle disease manifestation
|
|
D020879||muscle disease manifestations
|
|
D020879||neuromuscular manifestation
|
|
D020879||neuromuscular signs and symptoms
|
|
D020879||signs and symptoms neuromuscular
|
|
214500|D002609||chediak higashi syndrome
|
|
214500|D002609||chs
|
|
214500|D002609||oculocutaneous albinism with leukocyte defect
|
|
214500|D002609||syndrome chediak higashi
|
|
D018549||cryptogenic organizing pneumonia
|
|
D018549||boop
|
|
D018549||bronchiolitis obliterans organizing pneumonia
|
|
D018549||cryptogenic organizing pneumonias
|
|
D018549||organizing pneumonia cryptogenic
|
|
D018549||organizing pneumonias cryptogenic
|
|
D018549||pneumonia cryptogenic organizing
|
|
D018549||pneumonias cryptogenic organizing
|
|
187800|C566061||glanzmann thrombasthenia autosomal dominant
|
|
187800|C566061||bdplt16
|
|
187800|C566061||bleeding disorder platelet type 16
|
|
187800|C566061||thrombasthenia of glanzmann and naegeli autosomal dominant
|
|
D058088|608099||sarcoglycanopathies
|
|
D058088|608099||adhalinopathies
|
|
D058088|608099||adhalinopathies primary
|
|
D058088|608099||adhalinopathy primary
|
|
D058088|608099||alpha sarcoglycanopathies
|
|
D058088|608099||alpha sarcoglycanopathy
|
|
D058088|608099||dmda2
|
|
D058088|608099||duchenne like autosomal recessive muscular dystrophy type 2
|
|
D058088|608099||lgmd2d
|
|
D058088|608099||limb girdle muscular dystrophy type 2d
|
|
D058088|608099||muscular dystrophy limb girdle type 2d
|
|
D058088|608099||muscular dystrophy limb girdle with alpha sarcoglycan deficiency
|
|
D058088|608099||primary adhalinopathies
|
|
D058088|608099||primary adhalinopathy
|
|
D058088|608099||sarcoglycanopathy
|
|
D019873||schnitzler syndrome
|
|
C563470||setting sun phenomenon familial benign
|
|
D056846|277600||weill marchesani syndrome
|
|
D056846|277600||congenital mesodermal dysmorphodystrophies
|
|
D056846|277600||congenital mesodermal dysmorphodystrophy
|
|
D056846|277600||dysmorphodystrophies congenital mesodermal
|
|
D056846|277600||dysmorphodystrophy congenital mesodermal
|
|
D056846|277600||gemss
|
|
D056846|277600||glaucoma lens ectopia microspherophakia stiffness shortness syndrome
|
|
D056846|277600||marchesani syndrome
|
|
D056846|277600||marchesani weill syndrome
|
|
D056846|277600||marchesani weill syndromes
|
|
D056846|277600||mesodermal dysmorphodystrophies congenital
|
|
D056846|277600||mesodermal dysmorphodystrophy congenital
|
|
D056846|277600||spherophakia brachymorphia syndrome
|
|
D056846|277600||spherophakia brachymorphia syndromes
|
|
D056846|277600||syndrome spherophakia brachymorphia
|
|
D056846|277600||syndromes spherophakia brachymorphia
|
|
D056846|277600||weill marchesani syndrome 1
|
|
D056846|277600||weill marchesani syndrome 2
|
|
D056846|277600||weill marchesani syndrome autosomal dominant
|
|
D056846|277600||weill marchesani syndrome autosomal recessive
|
|
D056846|277600||wms1
|
|
D056846|277600||wms2
|
|
D017213||root caries
|
|
D017213||caries cervical
|
|
D017213||caries root
|
|
D017213||cary cervical
|
|
D017213||cervical caries
|
|
D017213||cervical cary
|
|
C563472||spondyloepiphyseal dysplasia with atlantoaxial instability
|
|
C563479||ovalocytosis hereditary hemolytic with defective erythropoiesis
|
|
C563477||nephrolithiasis calcium oxalate
|
|
C563477||urolithiasis calcium oxalate
|
|
113300||brachydactyly type e1
|
|
113300||bde
|
|
113300||bde1
|
|
215150||osmed
|
|
D012021|145290||reflex abnormal
|
|
D012021|145290||abnormal deep tendon reflex
|
|
D012021|145290||abnormal reflex
|
|
D012021|145290||abnormal reflexes
|
|
D012021|145290||absent reflex
|
|
D012021|145290||bulbocavernosus reflex decreased
|
|
D012021|145290||bulbocavernousus reflex absent
|
|
D012021|145290||decreased bulbocavernosus reflex
|
|
D012021|145290||decreased reflex
|
|
D012021|145290||hoffman apos s reflex
|
|
D012021|145290||hrx
|
|
D012021|145290||hyperreflexia
|
|
D012021|145290||hyporeflexia
|
|
D012021|145290||palmo mental reflex
|
|
D012021|145290||pendular reflex
|
|
D012021|145290||reflex absent
|
|
D012021|145290||reflex absent bulbocavernousus
|
|
D012021|145290||reflex acoustic abnormal
|
|
D012021|145290||reflex anal absent
|
|
D012021|145290||reflex anal decreased
|
|
D012021|145290||reflex ankle abnormal
|
|
D012021|145290||reflex ankle absent
|
|
D012021|145290||reflex ankle decreased
|
|
D012021|145290||reflex biceps abnormal
|
|
D012021|145290||reflex biceps absent
|
|
D012021|145290||reflex biceps decreased
|
|
D012021|145290||reflex corneal absent
|
|
D012021|145290||reflex corneal decreased
|
|
D012021|145290||reflex decreased
|
|
D012021|145290||reflex decreased bulbocavernosus
|
|
D012021|145290||reflex deep tendon abnormal
|
|
D012021|145290||reflex deep tendon absent
|
|
D012021|145290||reflexes abnormal
|
|
D012021|145290||reflex gag absent
|
|
D012021|145290||reflex gag decreased
|
|
D012021|145290||reflex hoffman apos s
|
|
D012021|145290||reflex knee abnormal
|
|
D012021|145290||reflex knee decreased
|
|
D012021|145290||reflex moro asymmetric
|
|
D012021|145290||reflex palmo mental
|
|
D012021|145290||reflex pendular
|
|
D012021|145290||reflex triceps abnormal
|
|
D012021|145290||reflex triceps absent
|
|
D012021|145290||reflex triceps decreased
|
|
D020863||central nervous system cysts
|
|
D020863||cleft cysts rathke apos s
|
|
D020863||cysts central nervous system
|
|
D020863||cysts rathke cleft
|
|
D020863||cysts suprasellar
|
|
D020863||cyst suprasellar
|
|
D020863||rathke cleft cysts
|
|
D020863||rathke apos s cleft cysts
|
|
D020863||rathkes cleft cysts
|
|
D020863||suprasellar cyst
|
|
D020863||suprasellar cysts
|
|
D005244||fecal impaction
|
|
D005244||fecalith
|
|
D005244||feces impacted
|
|
D005244||impaction fecal
|
|
D020734|600116||parkinsonian disorders
|
|
D020734|600116||autosomal dominant juvenile parkinson disease
|
|
D020734|600116||autosomal dominant juvenile parkinsonism
|
|
D020734|600116||autosomal dominant parkinsonism
|
|
D020734|600116||autosomal recessive juvenile parkinson disease
|
|
D020734|600116||autosomal recessive parkinsonism
|
|
D020734|600116||autosomal recesssive juvenile parkinsonism
|
|
D020734|600116||chromosome 6 linked autosomal recessive parkinsonism
|
|
D020734|600116||diseases experimental parkinson
|
|
D020734|600116||dominant parkinsonism autosomal
|
|
D020734|600116||epdf
|
|
D020734|600116||experimental parkinson disease
|
|
D020734|600116||experimental parkinson diseases
|
|
D020734|600116||experimental parkinsonism
|
|
D020734|600116||experimental parkinsonism mptp induced
|
|
D020734|600116||experimental parkinsonisms
|
|
D020734|600116||familial juvenile parkinsonism
|
|
D020734|600116||familial parkinson disease autosomal recessive
|
|
D020734|600116||juvenile parkinson disease
|
|
D020734|600116||juvenile parkinson disease autosomal dominant
|
|
D020734|600116||juvenile parkinson disease autosomal recessive
|
|
D020734|600116||juvenile parkinsonism
|
|
D020734|600116||juvenile parkinsonism autosomal dominant
|
|
D020734|600116||juvenile parkinsonism autosomal recessive
|
|
D020734|600116||juvenile parkinsonism familial
|
|
D020734|600116||juvenile parkinsonisms
|
|
D020734|600116||mptp induced experimental parkinsonism
|
|
D020734|600116||park2
|
|
D020734|600116||parkinson disease 2
|
|
D020734|600116||parkinson disease 2 autosomal recessive juvenile
|
|
D020734|600116||parkinson disease autosomal dominant juvenile
|
|
D020734|600116||parkinson disease autosomal recessive early onset
|
|
D020734|600116||parkinson disease experimental
|
|
D020734|600116||parkinson disease familial autosomal recessive
|
|
D020734|600116||parkinson disease juvenile
|
|
D020734|600116||parkinson disease juvenile autosomal dominant
|
|
D020734|600116||parkinson disease juvenile autosomal recessive
|
|
D020734|600116||parkinson diseases experimental
|
|
D020734|600116||parkinsonian diseases
|
|
D020734|600116||parkinsonian syndrome
|
|
D020734|600116||parkinsonian syndromes
|
|
D020734|600116||parkinsonism
|
|
D020734|600116||parkinsonism autosomal dominant
|
|
D020734|600116||parkinsonism autosomal recessive
|
|
D020734|600116||parkinsonism early onset with diurnal fluctuation
|
|
D020734|600116||parkinsonism experimental
|
|
D020734|600116||parkinsonism familial juvenile
|
|
D020734|600116||parkinsonism juvenile
|
|
D020734|600116||parkinsonism juvenile autosomal dominant
|
|
D020734|600116||parkinsonism juvenile autosomal recessive
|
|
D020734|600116||parkinsonism mptp induced experimental
|
|
D020734|600116||parkinsonisms experimental
|
|
D020734|600116||parkinsonisms juvenile
|
|
D020734|600116||pdj
|
|
D020734|600116||ramsay hunt paralysis syndrome
|
|
D020734|600116||recessive parkinsonism autosomal
|
|
D017227||toxascariasis
|
|
D017227||toxascariases
|
|
D017229||enterobiasis
|
|
D017229||enterobiases
|
|
D017229||enterobius vermicularis infection
|
|
D017229||enterobius vermicularis infections
|
|
D017229||infection enterobius vermicularis
|
|
D017229||infection oxyuris vermicularis
|
|
D017229||infections enterobius vermicularis
|
|
D017229||infections oxyuris vermicularis
|
|
D017229||oxyuris vermicularis infection
|
|
D017229||oxyuris vermicularis infections
|
|
C563482||otodental dysplasia
|
|
C563482||chromosome 11q13 deletion syndrome
|
|
C563482||oculootodental syndrome
|
|
C563482||otodental syndrome
|
|
C563482||otodental syndrome with coloboma
|
|
607847|C564320||neutropenia nonimmune chronic idiopathic adult
|
|
607847|C564320||neutropenia nonimmune chronic idiopathic of adults
|
|
607847|C564320||ni cina
|
|
607847|C564320||nonimmune chronic idiopathic neutropenia of adults
|
|
C563480||ovalocytosis hereditary hemolytic
|
|
C564773||thoracomelic dysplasia
|
|
C564773||thoraco limb dysplasia
|
|
C537154||hypomandibular faciocranial dysostosis
|
|
C537155||hypomelia mullerian duct anomalies
|
|
C537155||hypomelia with mullerian duct anomalies
|
|
C537155||limb uterus syndrome
|
|
C537155||severe upper limb hypoplasia and mullerian duct anomalies
|
|
C564771||tetraphocomelia thrombocytopenia syndrome
|
|
C564770||thumb agenesis short stature and immunodeficiency
|
|
C564777||male germ cell tumor
|
|
C538489||familial hyperchylomicronemia syndrome
|
|
C538489||hyperlipoproteinemia type 1
|
|
D005218||fat necrosis
|
|
D005218||fat necroses
|
|
D005218||necrosis fat
|
|
D005218||steatonecroses
|
|
D005218||steatonecrosis
|
|
C537159||hypotonia congenital nystagmus ataxia and abnormal auditory brainstem response
|
|
C537159||hypotonia congenital nystagmus ataxia and abnormal auditory brainstem responses
|
|
106260|C535847||hay wells syndrome
|
|
106260|C535847||aec syndrome
|
|
106260|C535847||ankyloblepharon ectodermal defects cleft lip and palate syndrome
|
|
106260|C535847||ankyloblepharon ectodermal defects cleft lip cleft palate
|
|
106260|C535847||ankyloblepharon ectodermal defects cleft lip palate
|
|
106260|C535847||hay wells syndrome dominant form
|
|
D006549||hernia diaphragmatic traumatic
|
|
D006549||diaphragmatic hernias traumatic
|
|
D006549||diaphragmatic hernia traumatic
|
|
D006549||hernias traumatic diaphragmatic
|
|
D006549||hernia traumatic diaphragmatic
|
|
D006549||traumatic diaphragmatic hernia
|
|
D006549||traumatic diaphragmatic hernias
|
|
C564774||thoracic dysplasia hydrocephalus syndrome
|
|
D006547||hernia
|
|
D006547||enterocele
|
|
D006547||hernias
|
|
C536872|600146||spastic paraplegia type 5b recessive
|
|
C536872|600146||spastic paraplegia 5b autosomal recessive
|
|
C536872|600146||spg5b
|
|
D006548||hernia diaphragmatic
|
|
D006548||diaphragmatic hernia
|
|
D006548||diaphragmatic hernias
|
|
D006548||hernias diaphragmatic
|
|
D007876||legionellosis
|
|
D007876||legionelloses
|
|
C563425|606176||diabetes mellitus permanent neonatal
|
|
C563425|606176||dend included
|
|
C563425|606176||developmental delay epilepsy and neonatal diabetes included
|
|
C563425|606176||diabetes mellitus permanent of infancy
|
|
C563425|606176||diabetes mellitus permanent of infancy pdmi diabetes mellitus permanent neonatal with neurologic features included
|
|
C563425|606176||permanent neonatal diabetes mellitus
|
|
C563425|606176||pndm
|
|
C563447||dwarfism familial with muscle spasms
|
|
D020852||lyme neuroborreliosis
|
|
D020852||borrelia burgdorferi neuroborreliosis
|
|
D020852||central nervous system lyme disease
|
|
D020852||encephalopathies lyme disease
|
|
D020852||encephalopathy lyme disease
|
|
D020852||lyme borreliosis nervous system
|
|
D020852||lyme disease central nervous system
|
|
D020852||lyme disease encephalopathies
|
|
D020852||lyme disease encephalopathy
|
|
D020852||lyme disease mononeuritis multiplex
|
|
D020852||lyme disease nervous system
|
|
D020852||lyme meningoencephalitis
|
|
D020852||lyme meningoradiculitis
|
|
D020852||lyme polyradiculitides
|
|
D020852||lyme polyradiculitis
|
|
D020852||lyme polyradiculopathies
|
|
D020852||lyme polyradiculopathy
|
|
D020852||meningoencephalitis lyme
|
|
D020852||meningoradiculitis lyme
|
|
D020852||mononeuritis multiplex lyme disease
|
|
D020852||nervous system lyme borreliosis
|
|
D020852||nervous system lyme disease
|
|
D020852||neuroborrelioses borrelia burgdorferi
|
|
D020852||neuroborreliosis borrelia burgdorferi
|
|
D020852||neuroborreliosis lyme
|
|
D020852||peripheral nervous system lyme disease
|
|
D020852||polyradiculitides lyme
|
|
D020852||polyradiculitis lyme
|
|
D020852||polyradiculopathies lyme
|
|
D020852||polyradiculopathy lyme
|
|
C538482||monosomy 5p
|
|
D005211||fascioliasis
|
|
D005211||fascioliases
|
|
C538481||acquired cjd
|
|
C538481||sporadic cjd
|
|
D005213||fascioloidiasis
|
|
D005213||fascioloidiases
|
|
D006550||hernia femoral
|
|
D006550||femoral hernia
|
|
D006550||femoral hernias
|
|
D006550||hernias femoral
|
|
D006551||hernia hiatal
|
|
D006551||esophageal hernia
|
|
D006551||esophageal hernias
|
|
D006551||esophageal hernia sliding
|
|
D006551||esophageal hernias sliding
|
|
D006551||hernia esophageal
|
|
D006551||hernia hiatus
|
|
D006551||hernia paraesophageal
|
|
D006551||hernia paraesophageal hiatal
|
|
D006551||hernias esophageal
|
|
D006551||hernias hiatal
|
|
D006551||hernias hiatus
|
|
D006551||hernia sliding esophageal
|
|
D006551||hernia sliding hiatal
|
|
D006551||hernias paraesophageal
|
|
D006551||hernias paraesophageal hiatal
|
|
D006551||hernias sliding esophageal
|
|
D006551||hernias sliding hiatal
|
|
D006551||hiatal hernia
|
|
D006551||hiatal hernia paraesophageal
|
|
D006551||hiatal hernias
|
|
D006551||hiatal hernia sliding
|
|
D006551||hiatal hernias paraesophageal
|
|
D006551||hiatal hernias sliding
|
|
D006551||hiatus hernia
|
|
D006551||hiatus hernias
|
|
D006551||paraesophageal hernia
|
|
D006551||paraesophageal hernias
|
|
D006551||paraesophageal hiatal hernia
|
|
D006551||paraesophageal hiatal hernias
|
|
D006551||sliding esophageal hernia
|
|
D006551||sliding esophageal hernias
|
|
D006551||sliding hiatal hernia
|
|
D006551||sliding hiatal hernias
|
|
D020859||hallux rigidus
|
|
D020859||rigidus hallux
|
|
D020857||hallux limitus
|
|
D020857||limitus hallux
|
|
C535328|212200||homocarnosinosis
|
|
C535328|212200||carnosinase deficiency
|
|
C535328|212200||carnosinemia
|
|
C535328|212200||homocarnosinase deficiency
|
|
D004832|600131||epilepsy absence
|
|
D004832|600131||absence epilepsies childhood
|
|
D004832|600131||absence epilepsies juvenile
|
|
D004832|600131||absence epilepsy
|
|
D004832|600131||absence epilepsy childhood
|
|
D004832|600131||absence epilepsy juvenile
|
|
D004832|600131||absence seizure
|
|
D004832|600131||absence seizure atonic
|
|
D004832|600131||absence seizure disorder
|
|
D004832|600131||absence seizure disorders
|
|
D004832|600131||absence seizures
|
|
D004832|600131||absence seizures atonic
|
|
D004832|600131||akinetic petit mal
|
|
D004832|600131||atonic absence seizure
|
|
D004832|600131||atonic absence seizures
|
|
D004832|600131||childhood absence epilepsies
|
|
D004832|600131||childhood absence epilepsy
|
|
D004832|600131||convulsion petit mal
|
|
D004832|600131||eca1
|
|
D004832|600131||eca2
|
|
D004832|600131||eca5
|
|
D004832|600131||eca6
|
|
D004832|600131||eig6 included
|
|
D004832|600131||eja1
|
|
D004832|600131||epilepsies childhood absence
|
|
D004832|600131||epilepsies juvenile absence
|
|
D004832|600131||epilepsy absence atypical
|
|
D004832|600131||epilepsy childhood absence
|
|
D004832|600131||epilepsy childhood absence susceptibility to 1
|
|
D004832|600131||epilepsy childhood absence susceptibility to 2
|
|
D004832|600131||epilepsy childhood absence susceptibility to 5
|
|
D004832|600131||epilepsy childhood absence susceptibility to 6
|
|
D004832|600131||epilepsy idiopathic generalized susceptibility to 6 included
|
|
D004832|600131||epilepsy juvenile absence
|
|
D004832|600131||epilepsy juvenile absences
|
|
D004832|600131||epilepsy juvenile absence susceptibility to 1
|
|
D004832|600131||epilepsy minor
|
|
D004832|600131||epilepsy petit mal
|
|
D004832|600131||jae1
|
|
D004832|600131||juvenile absence epilepsies
|
|
D004832|600131||juvenile absence epilepsy
|
|
D004832|600131||juvenile absences epilepsy
|
|
D004832|600131||minor epilepsies
|
|
D004832|600131||minor epilepsy
|
|
D004832|600131||petit mal akinetic
|
|
D004832|600131||petit mal convulsion
|
|
D004832|600131||petit mal epilepsies
|
|
D004832|600131||petit mal epilepsy
|
|
D004832|600131||pykno epilepsies
|
|
D004832|600131||pykno epilepsy
|
|
D004832|600131||pyknolepsies
|
|
D004832|600131||pyknolepsy
|
|
D004832|600131||seizure absence
|
|
D004832|600131||seizure atonic absence
|
|
D004832|600131||seizure disorder absence
|
|
D004832|600131||seizure disorders absence
|
|
D004832|600131||seizures atonic absence
|
|
C563453||proximal myopathy with focal depletion of mitochondria
|
|
C564784||gm2 gangliosidosis adult chronic type
|
|
100070||aaa
|
|
100070||aaa1
|
|
C538497||irresistible sleepiness cataplexy and onset of sleep in desynchronized phase
|
|
C564783||hexosaminidase a deficiency adult type
|
|
C538496||dilated cardiomyopathy neutropenia skeletal myopathy and abnormal mitochondria
|
|
C564782||tay sachs disease juvenile
|
|
C537163||pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections
|
|
C538494||aplastic anemia idiopathic
|
|
C537164||panostotic fibrous dysplasia
|
|
C564788||tapetoretinal degeneration with ataxia
|
|
C537169||papular urticaria
|
|
C537169||bullous papular urticaria type
|
|
C563456||colorectal cancer hereditary nonpolyposis type 5
|
|
C563456||hnpcc5
|
|
300624|D005600||fragile x mental retardation syndrome fragile x syndrome
|
|
300624|D005600||mental retardation x linked associated with marxq28
|
|
300624|D005600||x linked mental retardation and macroorchidism
|
|
300624|D005600||marker x syndrome
|
|
300624|D005600||martin bell syndrome primary ovarian insufficiency fragile x associated included
|
|
300624|D005600||fragile x premature ovarian failure included
|
|
C564787||tatsumi factor deficiency
|
|
C563455||dermoid cysts familial frontonasal
|
|
C564786||tay sachs disease pseudo ab variant
|
|
C538499||erythema migrans
|
|
C537167||papillomatosis florid of nipple
|
|
C537167||florid papillomatosis of the nipple
|
|
C564785||tay sachs disease variant b1
|
|
D006558||herpes genitalis
|
|
D006558||genital herpes
|
|
D006558||genital herpes simplex
|
|
D006558||herpes genital
|
|
D006558||herpes simplex genital
|
|
D006558||herpes simplex virus genital infection
|
|
D007889||leiomyoma
|
|
D007889||fibroid
|
|
D007889||fibroids
|
|
D007889||fibroids uterine
|
|
D007889||fibroid tumor
|
|
D007889||fibroid tumors
|
|
D007889||fibroid uterine
|
|
D007889||fibroid uterus
|
|
D007889||fibromas uterine
|
|
D007889||fibroma uterine
|
|
D007889||fibromyoma
|
|
D007889||fibromyomas
|
|
D007889||leiomyomas
|
|
D007889||leiomyoma uterine
|
|
D007889||tumor fibroid
|
|
D007889||tumors fibroid
|
|
D007889||uterine fibroid
|
|
D007889||uterine fibroids
|
|
D007889||uterine fibroma
|
|
D007889||uterine fibromas
|
|
D007889||uterus fibroid
|
|
C535483|193700||freeman sheldon syndrome
|
|
C535483|193700||arthrogryposis distal type 2a
|
|
C535483|193700||craniocarpotarsal dysplasia
|
|
C535483|193700||craniocarpotarsal dystrophy
|
|
C535483|193700||da2a
|
|
C535483|193700||distal arthrogryposis type 2a
|
|
C535483|193700||fss
|
|
C535483|193700||whistling face syndrome
|
|
C535483|193700||whistling face windmill vane hand syndrome
|
|
D006559||pemphigoid gestationis
|
|
D006559||gestational pemphigoid
|
|
D006559||gestational pemphigoids
|
|
D006559||gestationi pemphigoid
|
|
D006559||gestationis pemphigoid
|
|
D006559||herpes gestationis
|
|
D006559||pemphigoid gestational
|
|
D006559||pemphigoid gestationi
|
|
D006559||pemphigoids gestational
|
|
254780|D020192||lafora disease
|
|
254780|D020192||disease lafora
|
|
254780|D020192||disease lafora body
|
|
254780|D020192||disorder lafora body
|
|
254780|D020192||epilepsy progressive myoclonic 2
|
|
254780|D020192||epilepsy progressive myoclonic 2a
|
|
254780|D020192||epilepsy progressive myoclonic lafora
|
|
254780|D020192||epm2a
|
|
254780|D020192||epm2b included
|
|
254780|D020192||epm2 epilepsy progressive myoclonic 2b included
|
|
254780|D020192||lafora body disease
|
|
254780|D020192||lafora body disease late onset
|
|
254780|D020192||lafora body disorder
|
|
254780|D020192||lafora myoclonic epilepsy
|
|
254780|D020192||lafora progressive myoclonic epilepsy
|
|
254780|D020192||lafora progressive myoclonus epilepsy
|
|
254780|D020192||lafora type progressive myoclonic epilepsy
|
|
254780|D020192||late onset lafora body disease
|
|
254780|D020192||lbd
|
|
254780|D020192||melf
|
|
254780|D020192||myoclonic epilepsy of lafora
|
|
254780|D020192||progressive myoclonic epilepsy lafora
|
|
254780|D020192||progressive myoclonic epilepsy lafora type
|
|
254780|D020192||progressive myoclonic epilepsy type 2
|
|
254780|D020192||progressive myoclonus epilepsy lafora type
|
|
D006556||heroin dependence
|
|
D006556||abuse heroin
|
|
D006556||addiction heroin
|
|
D006556||dependence heroin
|
|
D006556||heroin abuse
|
|
D006556||heroin addiction
|
|
D006557||herpangina
|
|
D006557||herpanginas
|
|
C563458||varicella severe recurrent
|
|
D012559|181500||schizophrenia
|
|
D012559|181500||dementia praecox
|
|
D012559|181500||disorder schizophrenic
|
|
D012559|181500||disorders schizophrenic
|
|
D012559|181500||schizoaffective disorder included
|
|
D012559|181500||schizophrenia 1
|
|
D012559|181500||schizophrenia 11
|
|
D012559|181500||schizophrenia 12
|
|
D012559|181500||schizophrenia 13
|
|
D012559|181500||schizophrenia 14
|
|
D012559|181500||schizophrenia 2
|
|
D012559|181500||schizophrenia 3
|
|
D012559|181500||schizophrenia 4
|
|
D012559|181500||schizophrenia 5
|
|
D012559|181500||schizophrenia 6
|
|
D012559|181500||schizophrenia 7
|
|
D012559|181500||schizophrenia 8
|
|
D012559|181500||schizophrenia 9
|
|
D012559|181500||schizophrenias
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 10q related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 11q related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 13q related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 15q13 q14 related schizophrenia neurophysiologic defect in included
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 18 related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 1p related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 1q42 related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 22q11 related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 2q32 related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 5 related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 6q related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 6 related
|
|
D012559|181500||schizophrenia susceptibility locus chromosome 8p related
|
|
D012559|181500||schizophrenic disorder
|
|
D012559|181500||schizophrenic disorders
|
|
D012559|181500||sczd
|
|
D012559|181500||sczd1
|
|
D012559|181500||sczd11
|
|
D012559|181500||sczd12
|
|
D012559|181500||sczd13
|
|
D012559|181500||sczd14
|
|
D012559|181500||sczd2
|
|
D012559|181500||sczd3
|
|
D012559|181500||sczd4
|
|
D012559|181500||sczd5
|
|
D012559|181500||sczd6
|
|
D012559|181500||sczd7
|
|
D012559|181500||sczd8
|
|
D012559|181500||sczd9
|
|
D006554||hernia umbilical
|
|
D006554||exomphalos
|
|
D006554||hernias umbilical
|
|
D006554||omphalocele
|
|
D006554||omphaloceles
|
|
D006554||umbilical hernia
|
|
D006554||umbilical hernias
|
|
C538493||familial burkitt apos s lymphoma
|
|
D005222||mental fatigue
|
|
D005222||fatigue mental
|
|
D006555||hernia ventral
|
|
D006555||hernias ventral
|
|
D006555||ventral hernia
|
|
D006555||ventral hernias
|
|
D005221||fatigue
|
|
D005221||lassitude
|
|
C537162||pancreatoblastoma
|
|
D006552||hernia inguinal
|
|
D006552||direct inguinal hernia
|
|
D006552||direct inguinal hernias
|
|
D006552||hernia direct inguinal
|
|
D006552||hernia indirect inguinal
|
|
D006552||hernias direct inguinal
|
|
D006552||hernias indirect inguinal
|
|
D006552||hernias inguinal
|
|
D006552||indirect inguinal hernia
|
|
D006552||indirect inguinal hernias
|
|
D006552||inguinal hernia
|
|
D006552||inguinal hernia direct
|
|
D006552||inguinal hernia indirect
|
|
D006552||inguinal hernias
|
|
D006552||inguinal hernias direct
|
|
D006552||inguinal hernias indirect
|
|
D006553||hernia obturator
|
|
D006553||hernias obturator
|
|
D006553||obturator hernia
|
|
D006553||obturator hernias
|
|
D006561||herpes simplex
|
|
D006562||herpes zoster
|
|
D006562||shingles
|
|
D006562||zona
|
|
D006562||zoster
|
|
D007890||leiomyosarcoma
|
|
D007890||epithelioid leiomyosarcoma
|
|
D007890||epithelioid leiomyosarcomas
|
|
D007890||leiomyosarcoma epithelioid
|
|
D007890||leiomyosarcoma myxoid
|
|
D007890||leiomyosarcomas
|
|
D007890||leiomyosarcomas epithelioid
|
|
D007890||leiomyosarcomas myxoid
|
|
D007890||myxoid leiomyosarcoma
|
|
D007890||myxoid leiomyosarcomas
|
|
208550|C565935||asthma nasal polyps and aspirin intolerance
|
|
208550|C565935||asa triad
|
|
208550|C565935||asa triad asthma aspirin induced susceptibility to included
|
|
208550|C565935||asthma and nasal polyps included
|
|
D006560||herpes labialis
|
|
D006560||blister fever
|
|
D006560||blisters fever
|
|
D006560||cold sore
|
|
D006560||cold sores
|
|
D006560||fever blister
|
|
D006560||fever blisters
|
|
D006560||herpes simplex labial
|
|
D006560||labial herpes simplex
|
|
D006560||sore cold
|
|
D006560||sores cold
|
|
203450|D038261||alexander disease
|
|
203450|D038261||alexander apos s disease
|
|
203450|D038261||alexanders disease
|
|
203450|D038261||demyelinogenic leukodystrophy
|
|
203450|D038261||dysmyelinogenic leukodystrophy
|
|
203450|D038261||fibrinoid degeneration of astrocytes
|
|
203450|D038261||leukodystrophy with rosenthal fibers
|
|
D019867||anti glomerular basement membrane disease
|
|
D019867||anti gbm disease
|
|
D019867||goodpasture apos s syndrome
|
|
D019867||goodpastures syndrome
|
|
D019867||goodpasture syndrome
|
|
D019867||lung purpura with nephritis
|
|
D019867||syndrome goodpasture
|
|
D019867||syndrome goodpasture apos s
|
|
D017205||spirurida infections
|
|
D017205||habronemiases
|
|
D017205||habronemiasis
|
|
D017205||infection spirurida
|
|
D017205||infections spirurida
|
|
D017205||spirurida infection
|
|
607447||body mass index quantitative trait locus 4
|
|
607447||bmiq4
|
|
C536596|606889||alzheimer disease type 4
|
|
C536596|606889||ad4
|
|
C536596|606889||alzheimer disease 4
|
|
C536596|606889||alzheimer disease familial 4
|
|
C536596|606889||alzheimer disease familial type 4
|
|
D017206||strongylida infections
|
|
D017206||dentatus infections stephanurus
|
|
D017206||dentatus infection stephanurus
|
|
D017206||infections stephanurus dentatus
|
|
D017206||infections strongylida
|
|
D017206||infection stephanurus dentatus
|
|
D017206||infection strongylida
|
|
D017206||stephanurus dentatus infection
|
|
D017206||stephanurus dentatus infections
|
|
D017206||strongylida infection
|
|
D017206||syngamiases
|
|
D017206||syngamiasis
|
|
D013341|608355||sturge weber syndrome
|
|
D013341|608355||angiomatosis meningo oculo facial
|
|
D013341|608355||angiomatosis oculoorbital thalamic syndrome
|
|
D013341|608355||encephalofacial hemangiomatosis syndrome
|
|
D013341|608355||hemangiomatosis syndrome encephalofacial
|
|
D013341|608355||meningofacial angiomatosis cerebral calcification syndrome
|
|
D013341|608355||meningo oculo facial angiomatosis
|
|
D013341|608355||neuroretinoangiomatosis
|
|
D013341|608355||parkes weber syndrome
|
|
D013341|608355||phakomatosis sturge weber
|
|
D013341|608355||pkws
|
|
D013341|608355||sturge disease
|
|
D013341|608355||sturge kalischer weber syndrome
|
|
D013341|608355||sturge apos s syndrome
|
|
D013341|608355||sturge syndrome
|
|
D013341|608355||sturge weber dimitri syndrome
|
|
D013341|608355||sturge weber krabbe syndrome
|
|
D013341|608355||sturge weber phakomatosis
|
|
D013341|608355||syndrome encephalofacial hemangiomatosis
|
|
D013341|608355||syndrome parkes weber
|
|
D013341|608355||syndrome sturge
|
|
D013341|608355||syndrome sturge kalischer weber
|
|
D013341|608355||syndrome sturge apos s
|
|
D013341|608355||syndrome sturge weber
|
|
D013341|608355||syndrome sturge weber dimitri
|
|
D013341|608355||syndrome sturge weber krabbe
|
|
C535598|300352||creatine deficiency x linked
|
|
C535598|300352||ccds1
|
|
C535598|300352||cerebral creatine deficiency syndrome 1
|
|
C535598|300352||creatine deficiency syndrome x linked
|
|
C535598|300352||creatine transporter defect
|
|
C535598|300352||creatine transporter deficiency
|
|
C535598|300352||mental retardation x linked with creatine transport deficiency
|
|
C535598|300352||mental retardation x linked with seizures short stature and midface hypoplasia
|
|
C535598|300352||slc6a8 deficiency
|
|
C535598|300352||slc6a8 related creatine transporter deficiency
|
|
C535598|300352||x linked creatine deficiency
|
|
C535598|300352||x linked creatine deficiency syndrome
|
|
C535598|300352||x linked creatine transporter deficiency
|
|
D017202||myocardial ischemia
|
|
D017202||disease ischemic heart
|
|
D017202||diseases ischemic heart
|
|
D017202||heart disease ischemic
|
|
D017202||heart diseases ischemic
|
|
D017202||ischemia myocardial
|
|
D017202||ischemias myocardial
|
|
D017202||ischemic heart disease
|
|
D017202||ischemic heart diseases
|
|
D017202||myocardial ischemias
|
|
C563420||epiphyseal dysplasia multiple with myopathy
|
|
C564751|C536521|276950||vacterl association with hydrocephalus
|
|
C564751||vacterl h
|
|
D050723||fractures bone
|
|
D050723||bone broken
|
|
D050723||bone fracture
|
|
D050723||bone fractures
|
|
D050723||bones broken
|
|
D050723||broken bone
|
|
D050723||broken bones
|
|
D050723||fracture bone
|
|
C537176||parkinson disease 3
|
|
C564750||vascular hyalinosis
|
|
C565840|603830||long qt syndrome 3
|
|
C565840|603830|C563614|613688||long qt syndrome 2 3 digenic included lqt2 3 digenic included
|
|
C565840|603830||long qt syndrome 3 acquired susceptibility to included
|
|
C565840|603830||lqt3
|
|
C537174||parc syndrome
|
|
C537174||poikiloderma alopecia retrognathism and cleft palate
|
|
D050724||fractures cartilage
|
|
D050724||cartilage fracture
|
|
D050724||cartilage fractures
|
|
D050724||fracture cartilage
|
|
D006529||hepatomegaly
|
|
D006529||enlarged liver
|
|
D006529||liver enlarged
|
|
C563424||diabetes mellitus permanent neonatal with neurologic features
|
|
C564755||usher syndrome type ib
|
|
D007859||learning disorders
|
|
D007859||academic disorder developmental
|
|
D007859||academic disorders developmental
|
|
D007859||adult learning disorder
|
|
D007859||adult learning disorders
|
|
D007859||developmental academic disorder
|
|
D007859||developmental academic disorders
|
|
D007859||developmental disorders of scholastic skills
|
|
D007859||disabilities learning
|
|
D007859||disability learning
|
|
D007859||disturbance learning
|
|
D007859||disturbances learning
|
|
D007859||learning disabilities
|
|
D007859||learning disability
|
|
D007859||learning disorder
|
|
D007859||learning disorder adult
|
|
D007859||learning disorders adult
|
|
D007859||learning disturbance
|
|
D007859||learning disturbances
|
|
D007859||scholastic skills development disorders
|
|
C564752||vater association with hydrocephalus
|
|
C564752||vater association with macrocephaly and ventriculomegaly
|
|
D006525||hepatitis viral human
|
|
C563428||long qt syndrome 4
|
|
C564759||trigonobrachycephaly bulbous bifid nose micrognathia and abnormalities of the hands and feet
|
|
D020833||diffuse axonal injury
|
|
D020833||axonal injuries diffuse
|
|
D020833||axonal injury diffuse
|
|
D020833||dai diffuse axonal injury
|
|
D020833||dais diffuse axonal injury
|
|
D020833||diffuse axonal injuries
|
|
D020833||injuries diffuse axonal
|
|
D020833||injury diffuse axonal
|
|
C535314|273750||miller mckusick malvaux syndrome 3m syndrome
|
|
C535314|273750||3m1
|
|
C535314|273750||3 m syndrome
|
|
C535314|273750||3m syndrome
|
|
C535314|273750||dolichospondylic dysplasia
|
|
C535314|273750||gloomy face syndrome
|
|
C535314|273750||gloomy face syndrome yakut short stature syndrome included
|
|
C535314|273750||le merrer syndrome
|
|
C535314|273750||three m slender boned nanism
|
|
C535314|273750||three m syndrome
|
|
C535314|273750||three m syndrome 1
|
|
C535314|273750||yakut short stature syndrome
|
|
C563426||cataract pulverulent
|
|
C564757||ulnar hypoplasia with mental retardation
|
|
D006524||hepatitis viral animal
|
|
D007855||lead poisoning
|
|
D007855||lead poisonings
|
|
D007855||poisoning lead
|
|
D007855||poisonings lead
|
|
C564756||ulnar agenesis and endocardial fibroelastosis
|
|
D006521||hepatitis chronic
|
|
D006521||chronic active hepatitis
|
|
D006521||chronic hepatitis
|
|
D006521||chronic hepatitis cryptogenic
|
|
D006521||chronic persistent hepatitides
|
|
D006521||chronic persistent hepatitis
|
|
D006521||cryptogenic chronic hepatitis
|
|
D006521||hepatitis chronic active
|
|
D006521||hepatitis chronic cryptogenic
|
|
D006521||hepatitis chronic persistent
|
|
D006521||hepatitis cryptogenic chronic
|
|
D000474|203500||alkaptonuria
|
|
D000474|203500||aku
|
|
D000474|203500||alcaptonuria
|
|
D000474|203500||alcaptonurias
|
|
D000474|203500||homogentisic acid oxidase deficiency
|
|
D000474|203500||homogentisic acidura
|
|
D006522||hepatitis infectious canine
|
|
D006522||canine hepatitides infectious
|
|
D006522||canine hepatitis infectious
|
|
D006522||canine infectious hepatitides
|
|
D006522||canine infectious hepatitis
|
|
D006522||hepatitides canine infectious
|
|
D006522||hepatitides infectious canine
|
|
D006522||hepatitis canine infectious
|
|
D006522||infectious canine hepatitides
|
|
D006522||infectious canine hepatitis
|
|
D006522||infectious hepatitides canine
|
|
D006522||infectious hepatitis canine
|
|
C537173||parathyroid cancer adult
|
|
C537173||parathyroid carcinoma adult
|
|
C537173||parathyroid neoplasm adult
|
|
C537170||paraomphalocele
|
|
C537170||paraomphalocele epigastric
|
|
C537170||paraomphalocele hypogastric
|
|
D006520||hepatitis animal
|
|
D006520||animal hepatitides
|
|
D006520||animal hepatitis
|
|
D006520||hepatitides animal
|
|
C563429||agonadism xy with mental retardation short stature retarded bone age and multiple extragenital malformations
|
|
C537171||paraquat lung
|
|
C537171||paraquat induced lung disease
|
|
C536521|276950||vacterl hydrocephaly
|
|
C536521|276950||vacterl association with hydrocephaly
|
|
C536521|276950||vacterl h vater association with hydrocephalus included
|
|
C536521|276950||vater association with macrocephaly and ventriculomegaly included
|
|
C564503|300498||mental retardation x linked 45
|
|
C564503|300498||mrx45
|
|
D019838||neck injuries
|
|
D019838||injuries neck
|
|
D019838||injury neck
|
|
D019838||neck injury
|
|
C563396|601071||deafness autosomal recessive 9
|
|
C563396|601071||auditory neuropathy autosomal recessive 1
|
|
C563396|601071||auditory neuropathy nonsyndromic recessive included
|
|
C563396|601071||aunb1 included
|
|
C563396|601071||dfnb9
|
|
C563396|601071||neurosensory nonsyndromic recessive deafness 9
|
|
C563396|601071||neurosensory nonsyndromic recessive deafness 9 nsrd9 auditory neuropathy autosomal recessive 1 included
|
|
C563396|601071||nsran included
|
|
608765||scoliosis idiopathic susceptibility to 3
|
|
608765||is3
|
|
C563431||wiskott aldrich syndrome autosomal dominant form
|
|
C564762||tricarboxylic acid cycle defect of
|
|
C537187||pili annulati
|
|
C537187||ringed hair
|
|
C563430||enamel hypoplasia cataracts and aqueductal stenosis
|
|
C537188||pili multigemini
|
|
C537188||compound hairs
|
|
C564760||trichoodontoonychial dysplasia
|
|
100050||aarskog syndrome autosomal dominant
|
|
278150|D007039||hypotrichosis
|
|
278150|D007039||ah
|
|
278150|D007039||arwh1 included
|
|
278150|D007039||arwh2 included
|
|
278150|D007039||htl
|
|
278150|D007039||hypotrichoses
|
|
278150|D007039||hypotrichosis 10
|
|
278150|D007039||hypotrichosis 6
|
|
278150|D007039||hypotrichosis 7
|
|
278150|D007039||hypotrichosis 8
|
|
278150|D007039||hypotrichosis 9
|
|
278150|D007039||hypotrichosis localized autosomal recessive 3 lah3 woolly hair autosomal recessive 1 with or without hypotrichosis included
|
|
278150|D007039||hypotrichosis total mari type woolly hair autosomal recessive 2 with or without hypotrichosis included
|
|
278150|D007039||hypt10
|
|
278150|D007039||hypt6
|
|
278150|D007039||hypt7
|
|
278150|D007039||hypt8
|
|
278150|D007039||hypt9
|
|
278150|D007039||lah
|
|
278150|D007039||lah1
|
|
278150|D007039||lah2
|
|
278150|D007039||wh ht included
|
|
C537186||pigmented purpuric eruption
|
|
C537186||familial pigmented purpuric eruption
|
|
C537186||familial schamberg apos s disease
|
|
C537186||schamberg purpura
|
|
D050738||mesomycetozoea infections
|
|
D050738||infection mesomycetozoea
|
|
D050738||infections mesomycetozoea
|
|
D050738||mesomycetozoea infection
|
|
D005208||fasciitis
|
|
D005208||fasciitides
|
|
D005208||fascitides
|
|
D005208||fascitis
|
|
C564765||thyrotropin biologically inactive
|
|
D005207||fasciculation
|
|
D005207||benign fasciculation
|
|
D005207||benign fasciculations
|
|
D005207||fasciculation benign
|
|
D005207||fasciculation muscular
|
|
D005207||fasciculation neural
|
|
D005207||fasciculations
|
|
D005207||fasciculations benign
|
|
D005207||fasciculation skeletal muscle
|
|
D005207||fasciculations muscular
|
|
D005207||fasciculations neural
|
|
D005207||fasciculations skeletal muscle
|
|
D005207||fasciculations tongue
|
|
D005207||fasciculation tongue
|
|
D005207||muscle fasciculation skeletal
|
|
D005207||muscle fasciculations skeletal
|
|
D005207||muscular fasciculation
|
|
D005207||muscular fasciculations
|
|
D005207||neural fasciculation
|
|
D005207||neural fasciculations
|
|
D005207||skeletal muscle fasciculation
|
|
D005207||skeletal muscle fasciculations
|
|
D005207||tongue fasciculation
|
|
D005207||tongue fasciculations
|
|
D007869||leg injuries
|
|
D007869||injuries leg
|
|
D007869||injury leg
|
|
D007869||leg injury
|
|
C564764||tibia absence of with congenital deafness
|
|
C537189||rufous oca
|
|
D007868||leg dermatoses
|
|
D007868||dermatoses leg
|
|
D007868||dermatosis leg
|
|
D007868||leg dermatosis
|
|
C564769||thumb hypoplastic with choroid coloboma poorly developed antihelix and deafness
|
|
D005203||farmer apos s lung
|
|
D005203||farmer lung
|
|
D005203||farmers lung
|
|
D005203||farmer apos s lungs
|
|
D005203||mushroom worker lung
|
|
D005203||mushroom worker apos s lung
|
|
D005203||mushroom workers lung
|
|
D005203||mushroom worker apos s lungs
|
|
C537180||familial paroxysmal dystonia
|
|
C567127|611718||hypomagnesemia 4 renal
|
|
C567127|611718||homg4
|
|
C567127|611718||hypomagnesemia renal normocalciuric
|
|
C564768||thymic aplasia with fetal death
|
|
D020821||dystonic disorders
|
|
D020821||adult onset dystonia
|
|
D020821||adult onset dystonias
|
|
D020821||adult onset idiopathic focal dystonias
|
|
D020821||adult onset idiopathic torsion dystonias
|
|
D020821||autosomal dominant familial dystonia
|
|
D020821||autosomal recessive familial dystonia
|
|
D020821||childhood onset dystonia
|
|
D020821||childhood onset dystonias
|
|
D020821||dystonia adult onset
|
|
D020821||dystonia childhood onset
|
|
D020821||dystonia disorder
|
|
D020821||dystonia disorders
|
|
D020821||dystonia familial
|
|
D020821||dystonia focal
|
|
D020821||dystonia hereditary
|
|
D020821||dystonia idiopathic familial
|
|
D020821||dystonia primary
|
|
D020821||dystonia psychogenic
|
|
D020821||dystonias adult onset
|
|
D020821||dystonias childhood onset
|
|
D020821||dystonia secondary
|
|
D020821||dystonias familial
|
|
D020821||dystonias focal
|
|
D020821||dystonias hereditary
|
|
D020821||dystonias idiopathic familial
|
|
D020821||dystonia sporadic
|
|
D020821||dystonias primary
|
|
D020821||dystonias psychogenic
|
|
D020821||dystonias secondary
|
|
D020821||dystonias sporadic
|
|
D020821||dystonic disorder
|
|
D020821||familial dystonia
|
|
D020821||familial dystonia autosomal dominant
|
|
D020821||familial dystonia autosomal recessive
|
|
D020821||familial dystonia idiopathic
|
|
D020821||familial dystonias
|
|
D020821||familial dystonias idiopathic
|
|
D020821||focal dystonia
|
|
D020821||focal dystonias
|
|
D020821||hereditary dystonia
|
|
D020821||hereditary dystonias
|
|
D020821||idiopathic familial dystonia
|
|
D020821||idiopathic familial dystonias
|
|
D020821||primary dystonia
|
|
D020821||primary dystonias
|
|
D020821||pseudodystonia
|
|
D020821||pseudodystonias
|
|
D020821||psychogenic dystonia
|
|
D020821||psychogenic dystonias
|
|
D020821||secondary dystonia
|
|
D020821||secondary dystonias
|
|
D020821||sporadic dystonia
|
|
D020821||sporadic dystonias
|
|
D020821||writer cramp
|
|
D020821||writer apos s cramp
|
|
D020821||writers cramp
|
|
D020820||dyskinesias
|
|
D020820||abnormal movement
|
|
D020820||abnormal movements
|
|
D020820||asterixis
|
|
D020820||ballismus
|
|
D020820||dyskinesia
|
|
D020820||hemiballism
|
|
D020820||hemiballismus
|
|
D020820||involuntary movement
|
|
D020820||involuntary movements
|
|
D020820||movement abnormal
|
|
D020820||movement involuntary
|
|
D020820||movements abnormal
|
|
D020820||movements involuntary
|
|
300551|C564489||mental retardation x linked 78
|
|
300551|C564489||mrx78
|
|
C537183||robinow sorauf syndrome
|
|
C537183||acrocephalosyndactyly robinow sorauf type
|
|
C537183||craniosynostosis bifid hallux syndrome
|
|
D003550|219700||cystic fibrosis
|
|
D003550|219700||cf
|
|
D003550|219700||cystic fibrosis of pancreas
|
|
D003550|219700||cystic fibrosis pancreatic
|
|
D003550|219700||cystic fibrosis pulmonary
|
|
D003550|219700||fibrocystic disease of pancreas
|
|
D003550|219700||fibrosis cystic
|
|
D003550|219700||mucoviscidosis
|
|
D003550|219700||pancreas fibrocystic disease
|
|
D003550|219700||pancreas fibrocystic diseases
|
|
D003550|219700||pancreatic cystic fibrosis
|
|
D003550|219700||pulmonary cystic fibrosis
|
|
D006530||hepatorenal syndrome
|
|
D006530||syndrome hepatorenal
|
|
D007870||leg length inequality
|
|
D007870||inequalities leg length
|
|
D007870||inequality leg length
|
|
D007870||leg length inequalities
|
|
D007870||length inequalities leg
|
|
D007870||length inequality leg
|
|
D007871||leg ulcer
|
|
D007871||leg ulcers
|
|
D007871||ulcer leg
|
|
D007871||ulcers leg
|
|
D020828||pseudobulbar palsy
|
|
D020828||bulbar palsies spastic
|
|
D020828||bulbar palsy spastic
|
|
D020828||dysarthria pseudobulbar
|
|
D020828||dysarthrias pseudobulbar
|
|
D020828||mutism pseudobulbar
|
|
D020828||mutisms pseudobulbar
|
|
D020828||palsies pseudobulbar
|
|
D020828||palsies spastic bulbar
|
|
D020828||palsy pseudobulbar
|
|
D020828||palsy spastic bulbar
|
|
D020828||paralyses pseudobulbar
|
|
D020828||paralysis pseudobulbar
|
|
D020828||pareses pseudobulbar
|
|
D020828||paresis pseudobulbar
|
|
D020828||pseudobulbar dysarthria
|
|
D020828||pseudobulbar dysarthrias
|
|
D020828||pseudobulbar mutism
|
|
D020828||pseudobulbar mutisms
|
|
D020828||pseudobulbar palsies
|
|
D020828||pseudobulbar paralyses
|
|
D020828||pseudobulbar paralysis
|
|
D020828||pseudobulbar pareses
|
|
D020828||pseudobulbar paresis
|
|
D020828||pseudobulbar syndrome
|
|
D020828||pseudobulbar syndromes
|
|
D020828||spastic bulbar palsies
|
|
D020828||spastic bulbar palsy
|
|
D020828||syndrome pseudobulbar
|
|
D020828||syndromes pseudobulbar
|
|
D062706||prodromal symptoms
|
|
D062706||characteristic prodromal
|
|
D062706||characteristics prodromal
|
|
D062706||period prodromal
|
|
D062706||periods prodromal
|
|
D062706||prodromal characteristic
|
|
D062706||prodromal characteristics
|
|
D062706||prodromal period
|
|
D062706||prodromal periods
|
|
D062706||prodromal sign
|
|
D062706||prodromal signs
|
|
D062706||prodromal stage
|
|
D062706||prodromal stages
|
|
D062706||prodromal state
|
|
D062706||prodromal states
|
|
D062706||prodromal symptom
|
|
D062706||prodromal syndrome
|
|
D062706||prodromal syndromes
|
|
D062706||sign prodromal
|
|
D062706||signs prodromal
|
|
D062706||stage prodromal
|
|
D062706||stages prodromal
|
|
D062706||state prodromal
|
|
D062706||states prodromal
|
|
D062706||symptom prodromal
|
|
D062706||symptoms prodromal
|
|
D062706||syndrome prodromal
|
|
D062706||syndromes prodromal
|
|
607426||coenzyme q10 deficiency primary 1
|
|
607426||coenzyme q deficiency 1
|
|
607426||coq10d1
|
|
607426||coq10 deficiency primary 1
|
|
607426||coq deficiency 1
|
|
607426||ubiquinone deficiency 1
|
|
D019846||miller fisher syndrome
|
|
D019846||fisher syndrome
|
|
D019846||guillain barre syndrome miller fisher variant
|
|
D019846||miller fisher variant of guillain barre syndrome
|
|
D019846||ophthalmoplegia ataxia and areflexia syndrome
|
|
D019846||syndrome fisher
|
|
D019846||syndrome miller fisher
|
|
D018512||parasitemia
|
|
D018512||parasitemias
|
|
C567364|612285||joubert syndrome 9
|
|
C567364|612285||jbts9
|
|
C567364|612285||joubert syndrome 9 15 digenic included
|
|
C538442||aase smith syndrome 2
|
|
C538442||anemia and triphalangeal thumbs
|
|
C538442||congenital anemia and triphalangeal thumbs
|
|
C538442||hypoplastic anemia triphalangeal thumbs aase smith type
|
|
C537110||chromosome 21 monosomy 21q22
|
|
C537110||deletion 21q22
|
|
C537110||monosomy 21q22
|
|
C567767|613078||nijmegen breakage syndrome like disorder
|
|
C567767|613078||microcephaly and spontaneous chromosome instability without immunodeficiency
|
|
C567767|613078||nbsld
|
|
C567767|613078||nbs like disorder
|
|
C567767|613078||rad50 deficiency
|
|
C563402||ichthyosis mental retardation syndrome with large keratohyalin granules in the skin
|
|
C564733||trichothiodystrophy with sun sensitivity
|
|
C538446||speech disturbance use of faulty phrasing and unrelated words
|
|
C538445||clear cell metastatic renal cell carcinoma
|
|
C538445||clear cell rcc
|
|
C538445||cystic multilocular variant
|
|
C537115||lenz majewski hyperostotic dwarfism
|
|
C537115||delayed closure of fontanel proximal symphalangism prominent cutaneous veins mental retardation and progressive skeletal sclerosis
|
|
C537115||multiple congenital anomalies mental retardation and progressive skeletal sclerosis
|
|
D006505||hepatitis
|
|
D006505||hepatitides
|
|
C564731||xeroderma pigmentosum ix
|
|
C564731||xeroderma pigmentosum complementation group i
|
|
C564731||xp9
|
|
C564731||xp group i
|
|
C538444||ctnl1
|
|
D006506||hepatitis a
|
|
D006506||hepatitides infectious
|
|
D006506||hepatitis infectious
|
|
D006506||infectious hepatitides
|
|
D006506||infectious hepatitis
|
|
C564730||xylosidase deficiency
|
|
C538443||restless legs syndrome 1
|
|
C563405||migraine sporadic hemiplegic
|
|
D006504||hepatic veno occlusive disease
|
|
D006504||disease hepatic veno occlusive
|
|
D006504||hepatic veno occlusive diseases
|
|
D006504||sinusoidal obstruction syndrome
|
|
D006504||syndrome sinusoidal obstruction
|
|
D006504||veno occlusive disease hepatic
|
|
C564736||wolman disease with hypolipoproteinemia and acanthocytosis
|
|
D007835||lassa fever
|
|
D007835||fever lassa
|
|
D007835||fevers lassa
|
|
D007835||lassa fevers
|
|
C536382|133780||exudative vitreoretinopathy 1
|
|
C536382|133780||criswick schepens syndrome
|
|
C536382|133780||criswick schepens syndrome retinopathy of prematurity included
|
|
C536382|133780||evr1
|
|
C536382|133780||exudative vitreoretinopathy familial autosomal dominant
|
|
C536382|133780||fevr autosomal dominant
|
|
C536382|133780||rop included
|
|
D006501||hepatic encephalopathy
|
|
D006501||coma hepatic
|
|
D006501||comas hepatic
|
|
D006501||encephalopathies hepatic
|
|
D006501||encephalopathies hepatocerebral
|
|
D006501||encephalopathies portal systemic
|
|
D006501||encephalopathies portosystemic
|
|
D006501||encephalopathy hepatic
|
|
D006501||encephalopathy hepatocerebral
|
|
D006501||encephalopathy portal systemic
|
|
D006501||encephalopathy portosystemic
|
|
D006501||fulminant hepatic failure with cerebral edema
|
|
D006501||hepatic coma
|
|
D006501||hepatic comas
|
|
D006501||hepatic encephalopathies
|
|
D006501||hepatic stupor
|
|
D006501||hepatic stupors
|
|
D006501||hepatocerebral encephalopathies
|
|
D006501||hepatocerebral encephalopathy
|
|
D006501||portal systemic encephalopathies
|
|
D006501||portal systemic encephalopathy
|
|
D006501||portosystemic encephalopathies
|
|
D006501||portosystemic encephalopathy
|
|
D006501||stupor hepatic
|
|
D006501||stupors hepatic
|
|
C564735||woolly hair autosomal recessive
|
|
C563403||tibia absence or hypoplasia of with polydactyly retrocerebellar arachnoid cyst and other anomalies
|
|
C564734||trichothiodystrophy type 1
|
|
C564739||vitiligo progressive with mental retardation and urethral duplication
|
|
C563407||portal vein cavernous transformation of
|
|
C564738|277470||pontocerebellar hypoplasia type 2a
|
|
C564738|277470||pontocerebellar hypoplasia with progressive cerebral atrophy
|
|
C564738|277470||volendam neurodegenerative disease
|
|
D020819||perimeningeal infections
|
|
D020819||infection parameningeal
|
|
D020819||infection perimeningeal
|
|
D020819||infections parameningeal
|
|
D020819||infections perimeningeal
|
|
D020819||parameningeal infection
|
|
D020819||parameningeal infections
|
|
D020819||perimeningeal infection
|
|
D020818||neuroschistosomiasis
|
|
D020818||central nervous system schistosomiasis
|
|
D020818||myelitis schistosomal
|
|
D020818||myelopathies schistosomal
|
|
D020818||myelopathy schistosomal
|
|
D020818||myeloradiculopathies schistosomal
|
|
D020818||myeloradiculopathy schistosomal
|
|
D020818||neuroschistosomiases
|
|
D020818||schistosomal myelitis
|
|
D020818||schistosomal myelopathies
|
|
D020818||schistosomal myelopathy
|
|
D020818||schistosomal myeloradiculopathies
|
|
D020818||schistosomal myeloradiculopathy
|
|
D020818||schistosomiasis central nervous system
|
|
D020814||meningitis escherichia coli
|
|
D020814||escherichia coli meningitides
|
|
D020814||escherichia coli meningitis
|
|
D020814||meningitides escherichia coli
|
|
C537108||chromosome 21 monosomy
|
|
C537108||monosomy 21
|
|
C538437||immuno hemolytic anemia
|
|
C538437||familial auto immune hemolytic anemia
|
|
C538436||auditory perceptual impairment
|
|
C563363|601238||cerebellar ataxia cayman type
|
|
C563363|601238||atcay
|
|
C537709|608233||hermansky pudlak syndrome 2
|
|
C537709|608233||hps2
|
|
C537709|608233||platelet defects and oculocutaneous albinism
|
|
C565193|610713||brachydactyly syndactyly syndrome
|
|
C565193|610713||bdsd
|
|
C537109||chromosome 21 ring
|
|
C537109||ring 21 chromosome
|
|
C537121||short stature syndrome brussels type
|
|
C537121||mievis verellen dumoulin syndrome
|
|
248500|D008363||alpha mannosidosis
|
|
248500|D008363||alpha d mannosidase deficiencies lysosomal
|
|
248500|D008363||alpha d mannosidase deficiency lysosomal
|
|
248500|D008363||alpha d mannosidosis
|
|
248500|D008363||alpha mannosidase b deficiency
|
|
248500|D008363||alpha mannosidase deficiencies
|
|
248500|D008363||alpha mannosidase deficiency
|
|
248500|D008363||alpha mannosidoses
|
|
248500|D008363||alpha mannosidosis type i
|
|
248500|D008363||deficiencies alpha mannosidase
|
|
248500|D008363||deficiencies lysosomal alpha d mannosidase
|
|
248500|D008363||deficiency alpha mannosidase
|
|
248500|D008363||deficiency lysosomal alpha d mannosidase
|
|
248500|D008363||lysosomal alpha b mannosidosis
|
|
248500|D008363||lysosomal alpha d mannosidase deficiencies
|
|
248500|D008363||lysosomal alpha d mannosidase deficiency
|
|
248500|D008363||mannosidosis alpha b lysosomal
|
|
248500|D008363||mansa
|
|
C537122||opsismodysplasia
|
|
C563413||hydrocephalus skeletal anomalies and mental disturbance
|
|
D007849||laurence moon syndrome
|
|
D007849||laurence moon biedl syndrome
|
|
D007849||syndrome laurence moon
|
|
D007849||syndrome laurence moon biedl
|
|
C538457||segmental glomerulosclerosis
|
|
C538457||focal sclerosis with hyalinosis
|
|
211600|C535933||cholestasis progressive familial intrahepatic 1
|
|
211600|C535933||bric1
|
|
211600|C535933||byler disease
|
|
211600|C535933||byler apos s disease
|
|
211600|C535933||cholestasis benign recurrent intrahepatic 1
|
|
211600|C535933||cholestasis fatal intrahepatic
|
|
211600|C535933||fic1 deficiency
|
|
211600|C535933||pfic1
|
|
211600|C535933||progressive familial intrahepatic cholestasis
|
|
211600|C535933||progressive familial intrahepatic cholestasis type 1 pfic 1
|
|
211600|C535933||progressive familial intrahepatic cholestasis type 1 pfic1
|
|
211600|C535933||summerskill syndrome
|
|
D007562|123400||creutzfeldt jakob syndrome
|
|
D007562|123400||cjd
|
|
D007562|123400||cjd creutzfeldt jakob disease
|
|
D007562|123400||creutzfeldt jacob disease
|
|
D007562|123400||creutzfeldt jakob disease
|
|
D007562|123400||creutzfeldt jakob disease familial
|
|
D007562|123400||creutzfeldt jakob disease familial creutzfeldt jakob disease sporadic included
|
|
D007562|123400||creutzfeldt jakob disease heidenhain variant included
|
|
D007562|123400||creutzfeldt jakob disease new variant
|
|
D007562|123400||creutzfeldt jakob diseases familial
|
|
D007562|123400||creutzfeldt jakob disease variant
|
|
D007562|123400||creutzfeldt jakob disease variant included
|
|
D007562|123400||disease creutzfeldt jacob
|
|
D007562|123400||disease creutzfeldt jakob
|
|
D007562|123400||disease familial creutzfeldt jakob
|
|
D007562|123400||disease jakob creutzfeldt
|
|
D007562|123400||encephalopathies subacute spongiform
|
|
D007562|123400||encephalopathy subacute spongiform
|
|
D007562|123400||familial creutzfeldt jakob disease
|
|
D007562|123400||familial creutzfeldt jakob diseases
|
|
D007562|123400||jacob disease creutzfeldt
|
|
D007562|123400||jakob creutzfeldt disease
|
|
D007562|123400||jakob creutzfeldt syndrome
|
|
D007562|123400||new variant creutzfeldt jakob disease
|
|
D007562|123400||scjd included
|
|
D007562|123400||spongiform encephalopathies subacute
|
|
D007562|123400||spongiform encephalopathy subacute
|
|
D007562|123400||subacute spongiform encephalopathies
|
|
D007562|123400||subacute spongiform encephalopathy
|
|
D007562|123400||syndrome creutzfeldt jakob
|
|
D007562|123400||syndrome jakob creutzfeldt
|
|
D007562|123400||variant creutzfeldt jakob disease
|
|
D007562|123400||vcjd included
|
|
D007562|123400||v cjd variant creutzfeldt jakob disease
|
|
D006519||hepatitis alcoholic
|
|
D006519||alcoholic hepatitis
|
|
D006519||alcoholic hepatitis chronic
|
|
D006519||chronic alcoholic hepatitides
|
|
D006519||chronic alcoholic hepatitis
|
|
D006519||hepatitis alcoholic chronic
|
|
C564742||chondrodysplasia punctata with coagulation factor deficiency
|
|
C563414||cardiac malformation cleft lip palate microcephaly and digital anomalies
|
|
C537774|601202||anterior polar cataract 2
|
|
C537774|601202||cataract 24
|
|
C537774|601202||cataract 24 anterior polar
|
|
C537774|601202||cataract anterior polar 2
|
|
C537774|601202||ctaa2
|
|
C537774|601202||ctrct24
|
|
C563661|610805||renal hypodysplasia nonsyndromic 1
|
|
C563661|610805||congenital anomalies of kidney and urinary tract susceptibility to
|
|
C563661|610805||rhdns1
|
|
D007842||lathyrism
|
|
D007842||neurolathyrism
|
|
D020809||central nervous system helminthiasis
|
|
D020809||cerebral helminthiasis
|
|
D020809||helminthiasis central nervous system
|
|
D020809||helminthiasis cerebral
|
|
D020808||central nervous system protozoal infections
|
|
D020808||amebic meningoencephalitides
|
|
D020808||amebic meningoencephalitis
|
|
D020808||cerebral protozoal infection
|
|
D020808||cerebral protozoal infections
|
|
D020808||infection central nervous system protozoal
|
|
D020808||infection cerebral protozoal
|
|
D020808||infections cerebral protozoal
|
|
D020808||infections protozoal central nervous system
|
|
D020808||meningoencephalitides amebic
|
|
D020808||meningoencephalitides protozoal
|
|
D020808||meningoencephalitis amebic
|
|
D020808||meningoencephalitis protozoal
|
|
D020808||protozoal infection cerebral
|
|
D020808||protozoal infections central nervous system
|
|
D020808||protozoal infections cerebral
|
|
D020808||protozoal meningoencephalitides
|
|
D020808||protozoal meningoencephalitis
|
|
D020807||central nervous system parasitic infections
|
|
D020807||infections central nervous system parasitic
|
|
D020807||infections parasitic central nervous system
|
|
D020807||parasitic infections central nervous system
|
|
D020806||central nervous system bacterial infections
|
|
D020806||bacterial infections central nervous system
|
|
D020806||infections bacterial central nervous system
|
|
D020805||central nervous system viral diseases
|
|
D020805||central nervous system viral infections
|
|
D020805||cns infections viral
|
|
D020805||cns infection viral
|
|
D020805||infections cns viral
|
|
D020805||infections viral cns
|
|
D020805||infection viral cns
|
|
D020805||viral cns infection
|
|
D020805||viral cns infections
|
|
D020805||viral diseases central nervous system
|
|
D020805||viral infections central nervous system
|
|
D020804||encephalitis varicella zoster
|
|
D020804||encephalitis herpes zoster
|
|
D020804||encephalitis human herpesvirus 3
|
|
D020804||encephalitis varicella
|
|
D020804||encephalitis vz virus
|
|
D020804||herpes zoster encephalitis
|
|
D020804||herpes zoster meningoencephalitis
|
|
D020804||meningoencephalitis herpes zoster
|
|
D020804||varicella encephalitides
|
|
D020804||varicella encephalitis
|
|
D020804||varicella zoster encephalitis
|
|
D020804||virus encephalitis vz
|
|
D020804||zoster encephalitis herpes
|
|
D020804||zoster encephalitis varicella
|
|
D020802||epidural abscess
|
|
D020802||abscess cranial epidural
|
|
D020802||abscess cranial extradural
|
|
D020802||abscess epidural
|
|
D020802||abscesses intracranial extradural
|
|
D020802||abscess extradural
|
|
D020802||abscess intracranial epidural
|
|
D020802||abscess intracranial extradural
|
|
D020802||abscess spinal epidural
|
|
D020802||abscess spinal extradural
|
|
D020802||cranial epidural abscess
|
|
D020802||cranial extradural abscess
|
|
D020802||epidural abscess cranial
|
|
D020802||epidural abscess intracranial
|
|
D020802||epidural abscess spinal
|
|
D020802||extradural abscess
|
|
D020802||extradural abscesses intracranial
|
|
D020802||extradural abscess intracranial
|
|
D020802||extradural abscess spinal
|
|
D020802||intracranial epidural abscess
|
|
D020802||intracranial extradural abscess
|
|
D020802||intracranial extradural abscesses
|
|
D020802||spinal epidural abscess
|
|
D020802||spinal extradural abscess
|
|
C537118||leri pleonosteosis
|
|
C537118||leri apos s pleonosteosis
|
|
C537118||leri type pleonosteosis
|
|
300259||mycobacterium tuberculosis susceptibility to x linked
|
|
300259||mtbsx
|
|
C537133||orofaciodigital syndrome 4
|
|
C537133||baraitser burn syndrome
|
|
C537133||ofd syndrome baraitser burn type
|
|
C537133||ofd syndrome with tibial defects
|
|
C537133||oral facial digital syndrome type iv
|
|
C537133||orofaciodigital syndrome iv
|
|
C537133||orofaciodigital syndrome with tibial dysplasia
|
|
D007818||laryngeal diseases
|
|
D007818||disease laryngeal
|
|
D007818||disease larynx
|
|
D007818||diseases laryngeal
|
|
D007818||diseases larynx
|
|
D007818||laryngeal disease
|
|
D007818||laryngeal perichondritides
|
|
D007818||laryngeal perichondritis
|
|
D007818||larynx disease
|
|
D007818||larynx diseases
|
|
D007818||perichondritides laryngeal
|
|
D007818||perichondritis laryngeal
|
|
608264|C564266||deafness autosomal recessive 40
|
|
608264|C564266||dfnb40
|
|
C537130||optic nerve hypoplasia familial bilateral
|
|
C537130||familial bilateral optic nerve hypoplasia
|
|
D007819||laryngeal edema
|
|
D007819||edema laryngeal
|
|
D007819||edemas laryngeal
|
|
D007819||laryngeal edemas
|
|
C537131||orbital lymphoma
|
|
C537131||lymphoma of the orbit
|
|
C537131||primary orbital lymphoma
|
|
D011081||polychondritis relapsing
|
|
D011081||atrophic polychondritides chronic
|
|
D011081||atrophic polychondritis chronic
|
|
D011081||chronic atrophic polychondritides
|
|
D011081||chronic atrophic polychondritis
|
|
D011081||polychondritides chronic atrophic
|
|
D011081||polychondritides relapsing
|
|
D011081||polychondritis chronic atrophic
|
|
D011081||relapsing polychondritides
|
|
D011081||relapsing polychondritis
|
|
D007816||larva migrans visceral
|
|
D007816||larva migran visceral
|
|
D007816||migrans visceral larva
|
|
D007816||migran visceral larva
|
|
D007816||visceral larva migran
|
|
D007816||visceral larva migrans
|
|
D007816||visceral larva migrans syndrome
|
|
C537137||orstavik lindemann solberg syndrome
|
|
C537137||congenital heart defects hamartomas of tongue and polysyndactyly
|
|
D007815||larva migrans
|
|
D007815||creeping eruption
|
|
D007815||creeping eruptions
|
|
D007815||cutaneous larva migrans
|
|
D007815||dew itch
|
|
D007815||dew itchs
|
|
D007815||eruption creeping
|
|
D007815||eruptions creeping
|
|
D007815||ground itch
|
|
D007815||ground itchs
|
|
D007815||itch dew
|
|
D007815||itch ground
|
|
D007815||itchs dew
|
|
D007815||itchs ground
|
|
D007815||larva migrans cutaneous
|
|
D007815||larva migrans ocular
|
|
D007815||ocular larva migrans
|
|
C538465||hla class 1 deficiency
|
|
C564714||spondyloepimetaphyseal dysplasia x linked
|
|
C564714||semd x linked
|
|
C564712||mental retardation x linked with isolated growth hormone deficiency
|
|
C563614|613688||long qt syndrome 2
|
|
C563614|613688||long qt syndrome 1 2 digenic included lqt1 2 digenic included
|
|
C563614|613688||long qt syndrome 2 acquired susceptibility to included
|
|
C563614|613688||lqt2
|
|
C564716||x inactivation familial skewed 1
|
|
C537710|153400||lymphedema distichiasis syndrome
|
|
C537710|153400||hereditary lymphedema distichiasis syndrome
|
|
C537710|153400||lymphedema with distichiasis
|
|
C537710|153400||lymphedema with distichiasis lymphedema distichiasis syndrome with renal disease and diabetes mellitus included
|
|
D007926|300322||lesch nyhan syndrome
|
|
D007926|300322||choreoathetosis self mutilation hyperuricemia syndrome
|
|
D007926|300322||choreoathetosis self mutilation syndrome
|
|
D007926|300322||choreoathetosis self mutilation syndromes
|
|
D007926|300322||complete hgprt deficiency disease
|
|
D007926|300322||complete hprt deficiencies
|
|
D007926|300322||complete hprt deficiency
|
|
D007926|300322||complete hypoxanthine guanine phosphoribosyltransferase deficiency
|
|
D007926|300322||deficiencies complete hprt
|
|
D007926|300322||deficiencies hgprt
|
|
D007926|300322||deficiencies hypoxanthine phosphoribosyltransferase
|
|
D007926|300322||deficiencies total hprt
|
|
D007926|300322||deficiency complete hprt
|
|
D007926|300322||deficiency disease complete hgprt
|
|
D007926|300322||deficiency disease hypoxanthine phosphoribosyl transferase
|
|
D007926|300322||deficiency diseases hypoxanthine phosphoribosyl transferase
|
|
D007926|300322||deficiency hgprt
|
|
D007926|300322||deficiency hypoxanthine phosphoribosyltransferase
|
|
D007926|300322||deficiency of guanine phosphoribosyltransferase
|
|
D007926|300322||deficiency of hypoxanthine phosphoribosyltransferase
|
|
D007926|300322||deficiency total hprt
|
|
D007926|300322||guanine phosphoribosyltransferase deficiencies
|
|
D007926|300322||guanine phosphoribosyltransferase deficiency
|
|
D007926|300322||hgprt deficiencies
|
|
D007926|300322||hgprt deficiency
|
|
D007926|300322||hgprt deficiency disease complete
|
|
D007926|300322||hprt1 deficiency
|
|
D007926|300322||hprt deficiencies complete
|
|
D007926|300322||hprt deficiencies total
|
|
D007926|300322||hprt deficiency
|
|
D007926|300322||hprt deficiency complete
|
|
D007926|300322||hprt deficiency complete hprt deficiency neurologic variant included
|
|
D007926|300322||hprt deficiency total
|
|
D007926|300322||hyperuricemias x linked
|
|
D007926|300322||hyperuricemias x linked primary
|
|
D007926|300322||hyperuricemia syndrome juvenile
|
|
D007926|300322||hyperuricemia syndrome primary
|
|
D007926|300322||hyperuricemia syndromes juvenile
|
|
D007926|300322||hyperuricemia syndromes primary
|
|
D007926|300322||hyperuricemia x linked
|
|
D007926|300322||hyperuricemia x linked primary
|
|
D007926|300322||hypoxanthine guanine phosphoribosyltransferase 1 deficiency
|
|
D007926|300322||hypoxanthine guanine phosphoribosyltransferase deficiency
|
|
D007926|300322||hypoxanthine phosphoribosyltransferase deficiencies
|
|
D007926|300322||hypoxanthine phosphoribosyltransferase deficiency
|
|
D007926|300322||hypoxanthine phosphoribosyl transferase deficiency disease
|
|
D007926|300322||hypoxanthine phosphoribosyl transferase deficiency diseases
|
|
D007926|300322||juvenile gout choreoathetosis mental retardation syndrome
|
|
D007926|300322||juvenile hyperuricemia syndrome
|
|
D007926|300322||juvenile hyperuricemia syndromes
|
|
D007926|300322||lesch nyhan disease
|
|
D007926|300322||lesch nyhan syndrome neurologic variant included
|
|
D007926|300322||lns
|
|
D007926|300322||phosphoribosyltransferase deficiencies guanine
|
|
D007926|300322||phosphoribosyltransferase deficiencies hypoxanthine
|
|
D007926|300322||phosphoribosyltransferase deficiency guanine
|
|
D007926|300322||phosphoribosyltransferase deficiency hypoxanthine
|
|
D007926|300322||primary hyperuricemias x linked
|
|
D007926|300322||primary hyperuricemia syndrome
|
|
D007926|300322||primary hyperuricemia syndromes
|
|
D007926|300322||primary hyperuricemia x linked
|
|
D007926|300322||self mutilation syndrome choreoathetosis
|
|
D007926|300322||self mutilation syndromes choreoathetosis
|
|
D007926|300322||syndrome choreoathetosis self mutilation
|
|
D007926|300322||syndrome juvenile hyperuricemia
|
|
D007926|300322||syndrome primary hyperuricemia
|
|
D007926|300322||syndromes choreoathetosis self mutilation
|
|
D007926|300322||syndromes juvenile hyperuricemia
|
|
D007926|300322||syndromes primary hyperuricemia
|
|
D007926|300322||total hprt deficiencies
|
|
D007926|300322||total hprt deficiency
|
|
D007926|300322||total hypoxanthine guanine phosphoribosyl transferase deficiency
|
|
D007926|300322||x linked hyperuricemia
|
|
D007926|300322||x linked hyperuricemias
|
|
D007926|300322||x linked primary hyperuricemia
|
|
D007926|300322||x linked primary hyperuricemias
|
|
C538459||ovarian gynandroblastoma
|
|
C538458||rapidly progressive glomerulonephritis with pulmonary hemorrhage
|
|
C538458||anti glomerular basement membrane antibody disease
|
|
C538458||glomerulonephritis pulmonary hemorrhage
|
|
C538458||pulmonary renal syndrome
|
|
C563353|601317||deafness autosomal dominant 11
|
|
C563353|601317||dfna11
|
|
C538475||double cortex
|
|
607864|C564315||caudal duplication anomaly
|
|
C537144||osteoarthropathy of fingers familial
|
|
C537144||thiemann epiphyseal disease
|
|
C537144||thiemann apos s disease
|
|
D007829||laryngostenosis
|
|
D007829||acquired laryngeal stenoses
|
|
D007829||acquired laryngeal stenosis
|
|
D007829||acquired subglottic stenoses
|
|
D007829||acquired subglottic stenosis
|
|
D007829||congenital subglottic stenoses
|
|
D007829||congenital subglottic stenosis
|
|
D007829||laryngeal stenoses
|
|
D007829||laryngeal stenoses acquired
|
|
D007829||laryngeal stenosis
|
|
D007829||laryngeal stenosis acquired
|
|
D007829||laryngostenoses
|
|
D007829||stenoses acquired laryngeal
|
|
D007829||stenoses acquired subglottic
|
|
D007829||stenoses congenital subglottic
|
|
D007829||stenoses laryngeal
|
|
D007829||stenosis acquired laryngeal
|
|
D007829||stenosis acquired subglottic
|
|
D007829||stenosis congenital subglottic
|
|
D007829||stenosis laryngeal
|
|
D007829||subglottic stenoses acquired
|
|
D007829||subglottic stenoses congenital
|
|
D007829||subglottic stenosis acquired
|
|
D007829||subglottic stenosis congenital
|
|
C537142||ossicular malformations familial
|
|
C537142||familial middle ear ossicular anomalies
|
|
C537142||familial ossicular malformations
|
|
C564722||subcortical band heterotopia x linked
|
|
D007827||laryngitis
|
|
D007827||laryngitides
|
|
C564721||cardiomyopathy dilated 3a
|
|
C564721||cardiomyopathy dilated x linked fatal infantile
|
|
C537148||hypodontia x linked
|
|
C537148||x linked hypodontia
|
|
D007826||laryngismus
|
|
D007826||laryngeal spasm
|
|
D007826||laryngeal spasms
|
|
D007826||laryngospasm
|
|
D007826||laryngospasms
|
|
D007826||spasm laryngeal
|
|
D007826||spasms laryngeal
|
|
C564725||heterotopia periventricular nodular with frontometaphyseal dysplasia
|
|
D004387|126900||dupuytren contracture
|
|
D004387|126900||contracture dupuytren
|
|
D004387|126900||contracture dupuytren apos s
|
|
D004387|126900||dupc1 included
|
|
D004387|126900||dupuytren contracture 1 included
|
|
D004387|126900||dupuytren disease
|
|
D004387|126900||dupuytren apos s contracture
|
|
D004387|126900||dupuytrens contracture
|
|
D004387|126900||dupuytren apos s disease
|
|
D004387|126900||dupuytrens disease
|
|
D004387|126900||plantar fibromas included
|
|
D004387|126900||plantar fibromatosis familial included
|
|
C536863|609727||spastic paraplegia 29 autosomal dominant
|
|
C536863|609727||spg29
|
|
D007822||laryngeal neoplasms
|
|
D007822||cancer laryngeal
|
|
D007822||cancer larynx
|
|
D007822||cancer of larynx
|
|
D007822||cancer of the larynx
|
|
D007822||cancers laryngeal
|
|
D007822||cancers larynx
|
|
D007822||laryngeal cancer
|
|
D007822||laryngeal cancers
|
|
D007822||laryngeal neoplasm
|
|
D007822||larynx cancer
|
|
D007822||larynx cancers
|
|
D007822||larynx neoplasm
|
|
D007822||larynx neoplasms
|
|
D007822||neoplasm laryngeal
|
|
D007822||neoplasm larynx
|
|
D007822||neoplasms laryngeal
|
|
D007822||neoplasms larynx
|
|
C564729||ichthyosis x linked without steroid sulfatase deficiency
|
|
605258|D053306||hyper igm immunodeficiency syndrome
|
|
605258|D053306||higm2
|
|
605258|D053306||higm2 syndrome
|
|
605258|D053306||higm2 syndromes
|
|
605258|D053306||higm3
|
|
605258|D053306||higm3 syndrome
|
|
605258|D053306||higm3 syndromes
|
|
605258|D053306||higm5
|
|
605258|D053306||higm5 syndrome
|
|
605258|D053306||higm5 syndromes
|
|
605258|D053306||hyper igm immunodeficiency syndromes
|
|
605258|D053306||hyper igm immunodeficiency syndrome type 2
|
|
605258|D053306||hyper igm immunodeficiency syndrome type 3
|
|
605258|D053306||hyper igm immunodeficiency syndrome type 5
|
|
605258|D053306||hyper igm syndrome 2
|
|
605258|D053306||hyper igm syndrome 3
|
|
605258|D053306||hyper igm syndrome 5
|
|
605258|D053306||hyper igm syndrome 5s
|
|
605258|D053306||hyper igm syndromes
|
|
605258|D053306||immunodeficiency syndrome hyper igm
|
|
605258|D053306||immunodeficiency syndromes hyper igm
|
|
605258|D053306||immunodeficiency with hyper igm syndrome
|
|
605258|D053306||immunodeficiency with hyper igm type 2
|
|
605258|D053306||immunodeficiency with hyper igm type 3
|
|
605258|D053306||immunodeficiency with hyper igm type 5
|
|
605258|D053306||syndrome hyper igm immunodeficiency
|
|
605258|D053306||syndromes hyper igm immunodeficiency
|
|
C563890|608641||deafness autosomal dominant 28
|
|
C563890|608641||dfna28
|
|
C536425|119100||split hand foot malformation with long bone deficiency
|
|
C536425|119100||aplasia of tibia with ectrodactyly
|
|
C536425|119100||cleft hand absent tibia
|
|
C536425|119100||cleft hand and absent tibia
|
|
C536425|119100||ectrodactyly with aplasia of long bones
|
|
C536425|119100||shfld
|
|
C536425|119100||shfld1
|
|
C536425|119100||split hand foot malformation with long bone deficiency 1
|
|
C536425|119100||tibial aplasia with split hand split foot deformity
|
|
C564516|300423||mental retardation x linked with epilepsy
|
|
C564516|300423||mental retardation x linked syndromic hedera type
|
|
C564516|300423||mrxe
|
|
C564516|300423||mrxsh
|
|
608716||microcephaly 5 primary autosomal recessive
|
|
608716||mcph5
|
|
C537138||oslam syndrome
|
|
D011086||polycythemia
|
|
D011086||erythrocytoses
|
|
D011086||erythrocytosis
|
|
D011086||polycythemias
|
|
133700||ext
|
|
133700||ext1
|
|
300534|C564494||mental retardation x linked syndromic jarid1c related
|
|
300534|C564494||mental retardation x linked syndromic claes jensen type
|
|
300534|C564494||mrxscj
|
|
300534|C564494||mrxsj
|
|
133701||ext2
|
|
D011180||postmortem changes
|
|
D011180||adipocere
|
|
D011180||algor mortis
|
|
D011180||change postmortem
|
|
D011180||changes postmortem
|
|
D011180||cruor
|
|
D011180||livor mortis
|
|
D011180||postmortem change
|
|
C564810||spastic paraplegia with myoclonic epilepsy
|
|
C538523||free sialic acid storage disease
|
|
C538523||n acetylneuraminic acid nana storage disease nsd
|
|
C538521||bilateral temporal lobe disorder
|
|
C538521||memory loss extreme sexual behavior placidity and visual distractibility
|
|
C538521||post encephalitic kluver bucy syndrome
|
|
C538521||post traumatic kluver bucy syndrome
|
|
D007911||lentigo
|
|
D007911||lentigines
|
|
D007911||lentiginoses
|
|
D007911||lentiginosis
|
|
D007911||lentigos
|
|
C564817||insulin like growth factor i resistance to due to increased binding protein
|
|
D061325||hereditary breast and ovarian cancer syndrome
|
|
D061325||hboc syndrome
|
|
D061325||hboc syndromes
|
|
D061325||syndrome hboc
|
|
D061325||syndromes hboc
|
|
C564815||spastic ataxia
|
|
C535698|601887||malignant hyperthermia susceptibility type 5
|
|
C535698|601887||malignant hyperpyrexia susceptibility type 5
|
|
C535698|601887||malignant hyperthermia susceptibility to 5
|
|
C535698|601887||mhs5
|
|
C567091||skin hair eye pigmentation variation in 9
|
|
C567091||shep9
|
|
C567091||skin hair eye pigmentation 9 brown nonbrown eyes
|
|
C567091||skin hair eye pigmentation 9 dark light hair
|
|
C567091||skin hair eye pigmentation 9 freckling and burning
|
|
C567091||skin hair eye pigmentation 9 red nonred hair
|
|
C536736|189500||witkop syndrome
|
|
C536736|189500||dysplasia of nails with hypodontia
|
|
C536736|189500||ectd3
|
|
C536736|189500||ectodermal dysplasia 3 tooth nail type
|
|
C536736|189500||ectodermal dysplasia 3 witkop type
|
|
C536736|189500||nail dysplasia with hypodontia
|
|
C536736|189500||tns
|
|
C536736|189500||tooth and nail syndrome
|
|
C567203|612674||polyneuropathy hearing loss ataxia retinitis pigmentosa and cataract
|
|
C567203|612674||pharc
|
|
C567093||short stature facial dysmorphism severe brachydactyly and syndactyly
|
|
C567093||dauwerse peters syndrome
|
|
C564819||skeletal dysplasia with telangiectases and mesodermal dysgenesis of the iris
|
|
D010001|167250||osteitis deformans
|
|
D010001|167250||osseous paget apos s disease
|
|
D010001|167250||paget disease bone
|
|
D010001|167250||paget disease of bone
|
|
D010001|167250||paget disease of bone 1
|
|
D010001|167250||pagets disease bone
|
|
D010001|167250||paget apos s disease of bone
|
|
D010001|167250||pdb
|
|
D010001|167250||pdb1
|
|
C580055||early onset glaucoma
|
|
C580055||hereditary glaucoma
|
|
C567099||mucolipidosis iii alpha beta atypical
|
|
C567095||epilepsy progressive myoclonic 3
|
|
300614|C564472||deafness x linked 5
|
|
300614|C564472||auditory neuropathy x linked 1 with peripheral sensory neuropathy
|
|
300614|C564472||aunx1
|
|
300614|C564472||dfnx5
|
|
D011178||postgastrectomy syndromes
|
|
D011178||postgastrectomy syndrome
|
|
D011178||syndrome postgastrectomy
|
|
D011178||syndromes postgastrectomy
|
|
C567096||skin hair eye pigmentation variation in 8
|
|
C567096||shep8
|
|
C567096||skin hair eye pigmentation 8 freckling
|
|
300367||thrombocytopenia x linked with or without dyserythropoietic anemia
|
|
300367||xltda
|
|
C538400|601680||distal arthrogryposis type 2b
|
|
C538400|601680||arthrogryposis distal type 2b
|
|
C538400|601680||arthrogryposis multiplex congenita distal type 2b
|
|
C538400|601680||arthrogryposis multiplex congenita distal type ii with craniofacial abnormalities
|
|
C538400|601680||arthrogryposis multiplex congenita type 2b
|
|
C538400|601680||da2b
|
|
C538400|601680||freeman sheldon syndrome variant
|
|
C538400|601680||fssv
|
|
C538400|601680||sheldon hall syndrome
|
|
D011191||potassium deficiency
|
|
D011191||deficiencies potassium
|
|
D011191||deficiency potassium
|
|
D011191||potassium deficiencies
|
|
C564821||short stature obesity syndrome
|
|
C538534||hypogonadotropic hypogonadism and anosmia autosomal dominant
|
|
C538533||juvenile giant cell arteritis
|
|
C538533||juvenile cranial arteritis
|
|
C538533||juvenile polymyalgia rheumatica
|
|
D007925||leriche syndrome
|
|
D007925||leriche apos s syndrome
|
|
D007925||leriches syndrome
|
|
D007925||syndrome leriche
|
|
D007925||syndrome leriche apos s
|
|
D007922||leptospirosis
|
|
D007922||leptospiroses
|
|
C564825||sandhoff disease adult type
|
|
C564824||second metatarsal metacarpal syndrome
|
|
C564823||epilepsy benign neonatal autosomal recessive
|
|
C564823||convulsions benign familial neonatal autosomal recessive
|
|
C564823||seizures benign familial neonatal autosomal recessive
|
|
C564829||rod cone dystrophy sensorineural deafness and fanconi type renal dysfunction
|
|
C564827||sandhoff disease infantile type
|
|
C564826||sandhoff disease juvenile type
|
|
C567292|612469||wilms tumor aniridia genitourinary anomalies mental retardation and obesity syndrome
|
|
C567292|612469||chromosome 11p13 p12 deletion syndrome
|
|
C567292|612469||wagro
|
|
C567292|612469||wagro syndrome
|
|
C567292|612469||wagr syndrome with obesity
|
|
121700||corneal endothelial dystrophy 1 autosomal dominant
|
|
121700||ched
|
|
121700||ched1
|
|
C566464|609637||holoprosencephaly 5
|
|
C566464|609637||hpe5
|
|
612318|C563016||pseudofolliculitis barbae
|
|
612318|C563016||ingrown hairs
|
|
612318|C563016||pfb
|
|
612318|C563016||pili incarnati
|
|
D011183||postoperative complications
|
|
D011183||complication postoperative
|
|
D011183||complications postoperative
|
|
D011183||postoperative complication
|
|
C537806|203400||18 hydroxylase deficiency
|
|
C537806|203400||18 alpha hydroxylase deficiency
|
|
C537806|203400||18 oxidase deficiency
|
|
C537806|203400||aldosterone deficiency 1
|
|
C537806|203400||aldosterone deficiency due to defect in 18 hydroxylase
|
|
C537806|203400||aldosterone deficiency due to defect in steroid 18 hydroxylase
|
|
C537806|203400||aldosterone deficiency due to deficiency of steroid 18 oxidase
|
|
C537806|203400||aldosterone deficiency i
|
|
C537806|203400||aldosterone deficiency ii
|
|
C537806|203400||aldosterone deficiency type i
|
|
C537806|203400||aldosterone deficiency type ii
|
|
C537806|203400||cmo i deficiency
|
|
C537806|203400||cmo ii deficiency
|
|
C537806|203400||corticosterone methyloxidase type 1 deficiency
|
|
C537806|203400||corticosterone methyloxidase type i deficiency
|
|
C537806|203400||corticosterone methyloxidase type ii deficiency
|
|
C537806|203400||fhha1a
|
|
C537806|203400||fhha1b
|
|
C537806|203400||hyperreninemic hypoaldosteronism familial 1
|
|
C537806|203400||hyperreninemic hypoaldosteronism familial type i
|
|
C537806|203400||steroid 18 hydroxylase deficiency
|
|
C537806|203400||steroid 18 oxidase deficiency
|
|
D011186||postphlebitic syndrome
|
|
D011186||disease postphlebitic
|
|
D011186||diseases postphlebitic
|
|
D011186||postphlebitic disease
|
|
D011186||postphlebitic diseases
|
|
D011186||postphlebitic syndromes
|
|
D011186||postphlebitic ulcer
|
|
D011186||postphlebitic ulcers
|
|
D011186||syndrome postphlebitic
|
|
D011186||syndromes postphlebitic
|
|
D011186||ulcer postphlebitic
|
|
D011186||ulcers postphlebitic
|
|
C538525||mitochondrial encephalopathy
|
|
D011185||postpericardiotomy syndrome
|
|
D011185||postcommissurotomy syndrome
|
|
D011185||postcommissurotomy syndromes
|
|
D011185||postpericardiotomy syndromes
|
|
D011185||syndrome postcommissurotomy
|
|
D011185||syndrome postpericardiotomy
|
|
D011185||syndromes postcommissurotomy
|
|
D011185||syndromes postpericardiotomy
|
|
C580065||episodic ataxia
|
|
C566510|609597||parietal foramina 2
|
|
C566510|609597||pfm2
|
|
C580062||epidermal nevus
|
|
C580062||epidermal naevus
|
|
400042|C537587||sertoli cell only syndrome y linked
|
|
400042|C537587||hypospermatogenesis included
|
|
400042|C537587||incomplete sertoli cell only syndrome included
|
|
400042|C537587||sertoli cell only syndrome type 1
|
|
400042|C537587||sertoli cell only syndrome type i
|
|
400042|C537587||sertoli cell only syndrome type i sertoli cell only syndrome type ii included
|
|
400042|C537587||spermatogenic failure y linked 1
|
|
400042|C537587||spgfy1
|
|
C538540||hirschsprung disease 1
|
|
C538540||hirschsprung disease type 1
|
|
108721||ao3
|
|
109720|D008105||liver cirrhosis biliary
|
|
109720|D008105||biliary cirrhosis
|
|
109720|D008105||biliary cirrhosis primary
|
|
109720|D008105||biliary cirrhosis primary 1
|
|
109720|D008105||biliary cirrhosis primary 4
|
|
109720|D008105||biliary cirrhosis primary 5
|
|
109720|D008105||biliary cirrhosis secondary
|
|
109720|D008105||cholangitis chronic nonsuppurative destructive
|
|
109720|D008105||cirrhosis biliary
|
|
109720|D008105||cirrhosis secondary biliary
|
|
109720|D008105||liver cirrhoses biliary
|
|
109720|D008105||liver cirrhosis obstructive
|
|
109720|D008105||obstructive liver cirrhosis
|
|
109720|D008105||pbc
|
|
109720|D008105||pbc1
|
|
109720|D008105||pbc4
|
|
109720|D008105||pbc5
|
|
109720|D008105||primary biliary cirrhosis
|
|
109720|D008105||secondary biliary cirrhosis
|
|
C537213||kohlschutter tonz syndrome
|
|
C537213||epilepsy and yellow teeth
|
|
C537213||epilepsy dementia amelogenesis imperfecta
|
|
C537213||epilepsy dementia and amelogenesis imperfecta
|
|
C537213||kohlschutter syndrome
|
|
C538544||familial primary biliary cirrhosis
|
|
C537214||konigsmark knox hussels syndrome
|
|
C537214||deafness optic atrophy syndrome
|
|
C537214||dominant congenital deafness and progressive optic nerve atrophy
|
|
C567069||mental retardation x linked with brachydactyly and macroglossia
|
|
C567069|300354||cabezas syndrome
|
|
C567069|300354||cabezas x linked mental retardation syndrome
|
|
C567069|300354||mental retardation x linked syndromic 15
|
|
C567069||mental retardation x linked with short stature small testes muscle wasting and tremor
|
|
C567069|300354||mrxs15
|
|
300337||hypomelanosis of ito
|
|
300337||hmi
|
|
300337||incontinentia pigmenti type i formerly
|
|
300337||ip1 formerly
|
|
300337||ipa
|
|
300337||ito
|
|
300337||ito hypomelanosis
|
|
C538543||preeclamptic toxemia
|
|
C537211||kocher debre semelaigne syndrome
|
|
C537211||kocher debre semelaigne disease
|
|
C566582|602088||nephronophthisis 2
|
|
C566582|602088||nephronophthisis infantile
|
|
C566582|602088||nph2
|
|
C566582|602088||nphp2
|
|
C538542||sexual precocity
|
|
C538542||familial precocious puberty
|
|
C538542||idiopathic sexual precocity
|
|
277470||pch2
|
|
277470||pch2a
|
|
D016471|608115||ovarian hyperstimulation syndrome
|
|
D016471|608115||hyperstimulation syndrome ovarian
|
|
D016471|608115||hyperstimulation syndromes ovarian
|
|
D016471|608115||ohss
|
|
D016471|608115||ovarian hyperstimulation syndrome familial gestational spontaneous
|
|
D016471|608115||ovarian hyperstimulation syndromes
|
|
C580039||deoxyguanosine kinase deficiency
|
|
C580039||dguok related mitochondrial dna depletion syndrome
|
|
C580039||hepatocerebral mitochondrial dna depletion syndrome
|
|
C580039||mitochondrial dna depletion syndrome hepatocerebral form
|
|
C537454|300062||mental retardation x linked 14
|
|
C537454|300062||mental retardation x linked nonspecific type 14
|
|
C537454|300062||mrx14
|
|
D011151||popliteal cyst
|
|
D011151||baker cyst
|
|
D011151||baker cysts
|
|
D011151||baker apos s cyst
|
|
D011151||cyst baker
|
|
D011151||cyst popliteal
|
|
D011151||cysts baker
|
|
D011151||cysts popliteal
|
|
D011151||popliteal cysts
|
|
C567077||acquired protein s deficiency
|
|
C565071|129150||echo virus 11 sensitivity
|
|
C565071|129150||e11s
|
|
C567076||17 20 lyase deficiency isolated
|
|
C567076||17 alpha hydroxylase 17 20 lyase deficiency combined complete
|
|
C567076||17 alpha hydroxylase 17 20 lyase deficiency combined partial
|
|
D012481||salmonella infections animal
|
|
D012481||animal salmonella infection
|
|
D012481||animal salmonella infections
|
|
D012481||infection animal salmonella
|
|
D012481||infections animal salmonella
|
|
D012481||salmonella infection animal
|
|
C567079||deafness unilateral
|
|
D012488||salpingitis
|
|
D012488||salpingitides
|
|
C537208||kniest like dysplasia lethal
|
|
C537208||arthrosis flat face hypotonia short neck and macrocephaly
|
|
C537208||lethal kniest like dysplasia
|
|
D007906||lens subluxation
|
|
D007906||dislocation lens
|
|
D007906||dislocations lens
|
|
D007906||lens dislocation
|
|
D007906||lens dislocation and subluxation
|
|
D007906||lens dislocations
|
|
D007906||lens subluxations
|
|
D007906||subluxation lens
|
|
D007906||subluxations lens
|
|
C538550||subvalvular aortic stenosis eisenberg type
|
|
C537224||sacral plexopathy
|
|
D007905||lens diseases
|
|
D007905||disease lens
|
|
D007905||diseases lens
|
|
D007905||lens disease
|
|
C537225||sacrococcygeal dysgenesis association
|
|
C538554||diminished galc activity
|
|
C537222||sacral hemangiomas multiple congenital abnormalities
|
|
C538553||familial subependymomas
|
|
C537223||sacral meningocele conotruncal heart defects
|
|
C537223||kousseff syndrome
|
|
C564802||spinocerebellar ataxia with dysmorphism
|
|
C564807||spinal muscular atrophy with mental retardation
|
|
D013494|601104||supranuclear palsy progressive
|
|
D013494|601104||ophthalmoplegia progressive supranuclear
|
|
D013494|601104||palsy progressive supranuclear
|
|
D013494|601104||progressive supranuclear ophthalmoplegia
|
|
D013494|601104||progressive supranuclear palsies
|
|
D013494|601104||progressive supranuclear palsy
|
|
D013494|601104||psnp1
|
|
D013494|601104||richardson apos s syndrome
|
|
D013494|601104||richardson syndrome
|
|
D013494|601104||steele richardson olszewski disease
|
|
D013494|601104||steele richardson olszewski syndrome
|
|
D013494|601104||supranuclear ophthalmoplegia progressive
|
|
D013494|601104||supranuclear palsies progressive
|
|
D013494|601104||supranuclear palsy progressive 1
|
|
D013494|601104||syndrome richardson apos s
|
|
D013494|601104||syndrome steele richardson olszewski
|
|
C564806||spinal muscular atrophy with microcephaly and mental subnormality
|
|
C564805||spinal muscular atrophy type i with congenital bone fractures
|
|
C536446|218000||corpus callosum agenesis neuronopathy
|
|
C536446|218000||accpn
|
|
C536446|218000||agenesis of corpus callosum with neuronopathy
|
|
C536446|218000||agenesis of corpus callosum with peripheral neuropathy
|
|
C536446|218000||agenesis of corpus callosum with polyneuropathy
|
|
C536446|218000||agenesis of the corpus callosum with peripheral neuropathy
|
|
C536446|218000||andermann syndrome
|
|
C536446|218000||charlevoix disease
|
|
C536446|218000||corpus callosum agenesis of with neuronopathy
|
|
C536446|218000||hereditary motor and sensory neuropathy with agenesis of the corpus callosum
|
|
C536446|218000||polyneuropathy sensorimotor with or without agenesis of the corpus callosum
|
|
C567080||warfarin sensitivity
|
|
188890||tobacco addiction susceptibility to
|
|
188890||cigarette habituation susceptibility to
|
|
188890||nicotine addiction susceptibility to
|
|
188890||nicotine dependence susceptibility to
|
|
188890||smoking habit susceptibility to
|
|
C564809||spastic paresis glaucoma and mental retardation
|
|
C564808||spastic quadriplegia retinitis pigmentosa and mental retardation
|
|
C567509|611875||brugada syndrome 3
|
|
C567509|611875||brgda3
|
|
C580044||distal hereditary motor neuropathy type ii
|
|
C580044||distal hereditary motor neuronopathy type ii
|
|
C562770|274800||thyroid dyshormonogenesis 4
|
|
C562770|274800||deiodinase deficiency
|
|
C562770|274800||hypothyroidism congenital due to dyshormonogenesis 4
|
|
C562770|274800||iodotyrosine dehalogenase deficiency
|
|
C562770|274800||tdh4
|
|
C562770|274800||thyroid hormonogenesis genetic defect in 4
|
|
D011164||porphyrias
|
|
D011164||disorder porphyrin
|
|
D011164||disorders porphyrin
|
|
D011164||porphyria
|
|
D011164||porphyrin disorder
|
|
D011164||porphyrin disorders
|
|
C564506|300489||spinal muscular atrophy distal x linked 3
|
|
C564506|300489||dsmax
|
|
C564506|300489||smax3
|
|
C564506|300489||spinal muscular atrophy distal x linked recessive
|
|
187601|C536508||thanatophoric dysplasia type 2
|
|
187601|C536508||cloverleaf skull with thanatophoric dwarfism
|
|
187601|C536508||td2
|
|
187601|C536508||thanatophoric dysplasia type ii
|
|
187601|C536508||thanatophoric dysplasia with kleeblattschaedel
|
|
187601|C536508||thanatophoric dysplasia with straight femurs and cloverleaf skull
|
|
C566500|609634||migraine familial hemiplegic 3
|
|
C566500|609634||fhm3
|
|
300354||mental retardation x linked with short stature hypogonadism and abnormal gait
|
|
300354||mrxsc
|
|
300351||graves disease susceptibility to x linked 1
|
|
300351||grdx1 graves disease susceptibility to x linked 2 included
|
|
300351||grdx2 included
|
|
C564702|606483||charcot marie tooth disease dominant intermediate a
|
|
C564702|606483||charcot marie tooth neuropathy dominant intermediate a
|
|
C564702|606483||cmtdia
|
|
C564702|606483||di cmta
|
|
C537219||sackey sakati aur syndrome
|
|
C537219||aur syndrome
|
|
C537219||multiple dysmorphic features and pancytopenia
|
|
C537219||pancytopenia multiple congenital anomalies
|
|
608265|C564265||deafness autosomal recessive 39
|
|
608265|C564265||dfnb39
|
|
C567049||pulmonary alveolar proteinosis acquired
|
|
C567049||pulmonary alveolar lipoproteinosis acquired
|
|
C567049||pulmonary alveolar proteinosis autoimmune
|
|
D059041||plagiocephaly
|
|
D059041||plagiocephalies
|
|
C563513|163800||sick sinus syndrome 2 autosomal dominant
|
|
C563513|163800||atrial fibrillation with bradyarrhythmia
|
|
C563513|163800||sinus bradycardia syndrome familial autosomal dominant
|
|
C563513|163800||sinus node disease familial autosomal dominant
|
|
C563513|163800||sss2
|
|
C563513|163800||sss autosomal dominant
|
|
D013798||thecoma
|
|
D013798||theca cell tumor
|
|
D013798||theca cell tumors
|
|
D013798||thecomas
|
|
D013798||tumors theca cell
|
|
D013798||tumor theca cell
|
|
D012467||salivary gland fistula
|
|
D012467||fistula salivary gland
|
|
D012467||fistulas salivary gland
|
|
D012467||gland fistula salivary
|
|
D012467||gland fistulas salivary
|
|
D012467||salivary gland fistulas
|
|
C580017||congenital plasminogen deficiency
|
|
C580017||hypoplasminogenemia
|
|
D012468||salivary gland neoplasms
|
|
D012468||cancer of salivary gland
|
|
D012468||cancer of the salivary gland
|
|
D012468||cancer salivary gland
|
|
D012468||cancers salivary gland
|
|
D012468||gland neoplasm salivary
|
|
D012468||gland neoplasms salivary
|
|
D012468||neoplasm salivary gland
|
|
D012468||neoplasms salivary gland
|
|
D012468||salivary gland cancer
|
|
D012468||salivary gland cancers
|
|
D012468||salivary gland neoplasm
|
|
C536370|206700||aniridia cerebellar ataxia mental deficiency
|
|
C536370|206700||aniridia cerebellar ataxia and mental deficiency
|
|
C536370|206700||aniridia cerebellar ataxia and mental retardation
|
|
C536370|206700||aniridia partial cerebellar ataxia mental retardation
|
|
C536370|206700||aniridia partial cerebellar ataxia oligophrenia
|
|
C536370|206700||gillespie syndrome
|
|
C580013||congenital hepatic fibrosis
|
|
C580013||congenital fibrose liver
|
|
C580011||congenital myopathy with fiber type disproportion
|
|
C567055||sakoda complex
|
|
C567055||sakoda spectrum
|
|
C567055||sphenoethmoidal encephalomeningocele agenesis of the corpus callosum and cleft lip palate
|
|
C580012||congenital fibrosis of the extraocular muscles
|
|
C580012||cfeom
|
|
C580012||congenital external ophthalmoplegia
|
|
C580012||congenital fibrosis of extraocular muscles
|
|
C580012||congenital fibrosis syndrome
|
|
C580012||general fibrosis syndrome
|
|
C567351|612310||premature ovarian failure 6
|
|
C567351|612310||pof6
|
|
D013796||thanatophoric dysplasia
|
|
D013796||dwarfisms thanatophoric
|
|
D013796||dwarfism thanatophoric
|
|
D013796||dysplasias thanatophoric
|
|
D013796||dysplasia thanatophoric
|
|
D013796||thanatophoric dwarfism
|
|
D013796||thanatophoric dwarfisms
|
|
D013796||thanatophoric dysplasias
|
|
D013796||thanatophoric short stature
|
|
D012465||salivary duct calculi
|
|
D012465||calculi salivary duct
|
|
D012465||calculus salivary duct
|
|
D012465||duct calculi salivary
|
|
D012465||duct calculus salivary
|
|
D012465||duct stone salivary
|
|
D012465||duct stones salivary
|
|
D012465||parotid duct calculi
|
|
D012465||salivary duct calculus
|
|
D012465||salivary duct stone
|
|
D012465||salivary duct stones
|
|
D012465||sialolithiases ductal
|
|
D012465||sialolithiasis ductal
|
|
D012465||stone salivary duct
|
|
D012465||stones salivary duct
|
|
D012465||submandibular duct calculi
|
|
C535576|314400||cardiac valvular dysplasia x linked
|
|
C535576|314400||cvd1
|
|
C535576|314400||myxomatous valvular dystrophy x linked
|
|
C535576|314400||valvular heart disease congenital
|
|
C535576|314400||xmvd
|
|
D012466||salivary gland diseases
|
|
D012466||disease salivary gland
|
|
D012466||diseases salivary gland
|
|
D012466||gland disease salivary
|
|
D012466||gland diseases salivary
|
|
D012466||salivary gland disease
|
|
D012480||salmonella infections
|
|
D012480||infection salmonella
|
|
D012480||infections salmonella
|
|
D012480||salmonella infection
|
|
D012480||salmonelloses
|
|
D012480||salmonellosis
|
|
C562851|601152||hereditary motor and sensory neuropathy vi
|
|
C562851|601152||charcot marie tooth disease type 6
|
|
C562851|601152||cmt6
|
|
C562851|601152||hmsn6
|
|
C562851|601152||hmsn vi
|
|
C562851|601152||hsmn6
|
|
C562851|601152||neuropathy hereditary motor and sensory type vi
|
|
C562851|601152||peripheral neuropathy and optic atrophy
|
|
C537384|607855||muscular dystrophy congenital merosin negative
|
|
C537384|607855||mdc1a
|
|
C537384|607855||merosin deficient congenital muscular dystrophy
|
|
C537384|607855||merosin negative congenital muscular dystrophy
|
|
C537384|607855||muscular dystrophy congenital merosin deficient
|
|
C537384|607855||muscular dystrophy congenital merosin deficient 1a
|
|
C537384|607855||muscular dystrophy congenital merosin deficient muscular dystrophy congenital due to partial lama2 deficiency included
|
|
D062688||buschke lowenstein tumor
|
|
D062688||anogenital type verrucous carcinoma
|
|
D062688||buschke l 246 wenstein tumor
|
|
D062688||condyloma acuminatum giant
|
|
D062688||condyloma acuminatums giant
|
|
D062688||giant condyloma acuminatum
|
|
D062688||giant condyloma acuminatums
|
|
D062688||giant condyloma of buschke and lowenstein
|
|
D062688||giant condyloma of buschke and l 246 wenstein
|
|
D062688||lowenstein tumor buschke
|
|
D062688||l 246 wenstein tumor buschke
|
|
D062688||tumor buschke lowenstein
|
|
D062688||tumor buschke l 246 wenstein
|
|
D062689||lipoblastoma
|
|
D062689||lipoblastomas
|
|
D062689||lipoblastomatoses
|
|
D062689||lipoblastomatosis
|
|
C536492|605472||usher syndrome type 2c
|
|
C536492|605472||ush2c
|
|
C536492|605472||usher syndrome type iib formerly included ush2b formerly included
|
|
C536492|605472||usher syndrome type iic
|
|
C536492|605472||usher syndrome type iic gpr98 pdzd7 digenic included
|
|
C538159|236700||mckusick kaufman syndrome
|
|
C538159|236700||hmcs
|
|
C538159|236700||hydrometrocolpos postaxial polydactyly and congenital heart malformation
|
|
C538159|236700||hydrometrocolpos syndrome
|
|
C538159|236700||kaufman mckusick syndrome
|
|
C538159|236700||mkks
|
|
D012478||salmonella food poisoning
|
|
D012478||food poisoning salmonella
|
|
D012478||food poisonings salmonella
|
|
D012478||poisoning salmonella food
|
|
D012478||poisonings salmonella food
|
|
D012478||salmonella food poisonings
|
|
C535535|601631||iridogoniodysgenesis type1
|
|
C535535|601631||glaucoma iridogoniodysplasia familial included
|
|
C535535|601631||irid1
|
|
C535535|601631||iridogoniodysgenesis anomaly autosomal dominant
|
|
C535535|601631||iridogoniodysgenesis anomaly autosomal dominant igda iris hypoplasia with glaucoma included
|
|
C535535|601631||iridogoniodysgenesis type 1
|
|
606035||fasting insulin level quantitative trait locus 1
|
|
606035||fiqtl1
|
|
C564915|259700||osteopetrosis autosomal recessive 1
|
|
C564915|259700||albers schonberg disease autosomal recessive
|
|
C564915|259700||marble bones autosomal recessive
|
|
C564915|259700||optb1
|
|
C564915|259700||osteopetrosis infantile malignant 1
|
|
C567361|612288||inflammatory bowel disease 20
|
|
C567361|612288||ibd20
|
|
D011141||polyuria
|
|
D011141||polyurias
|
|
300331||thrombocythemia x linked
|
|
300331||thcytx
|
|
300331||thrombocytosis x linked
|
|
C567062||fabry disease cardiac variant
|
|
C567061||xeroderma pigmentosum b cockayne syndrome
|
|
D011146||eczema dyshidrotic
|
|
D011146||dyshidrotic eczema
|
|
D011146||dyshidrotic eczemas
|
|
D011146||dyshydrotic eczema
|
|
D011146||dyshydrotic eczemas
|
|
D011146||eczema dyshydrotic
|
|
D011146||eczemas dyshidrotic
|
|
D011146||eczemas dyshydrotic
|
|
D011146||eczemas vesicular palmoplantar
|
|
D011146||eczema vesicular palmoplantar
|
|
D011146||palmoplantar eczemas vesicular
|
|
D011146||palmoplantar eczema vesicular
|
|
D011146||pompholyx
|
|
D011146||vesicular palmoplantar eczema
|
|
D011146||vesicular palmoplantar eczemas
|
|
C567751|613102||hypotrichosis and recurrent skin vesicles
|
|
117550|D058495||sotos syndrome
|
|
117550|D058495||cerebral gigantism
|
|
117550|D058495||cerebral gigantisms
|
|
117550|D058495||chromosome 5q35 deletion syndrome
|
|
117550|D058495||gigantism cerebral
|
|
117550|D058495||gigantisms cerebral
|
|
117550|D058495||sequence sotos
|
|
117550|D058495||sotos1
|
|
117550|D058495||sotos sequence
|
|
117550|D058495||soto apos s syndrome
|
|
117550|D058495||sotos apos syndrome
|
|
117550|D058495||sotos syndrome 1
|
|
117550|D058495||soto syndrome
|
|
117550|D058495||syndrome sotos
|
|
117550|D058495||syndrome sotos apos
|
|
D001791||blood platelet disorders
|
|
D001791||blood platelet disorder
|
|
D001791||disorder blood platelet
|
|
D001791||disorders blood platelet
|
|
D001791||platelet disorder blood
|
|
D001791||platelet disorders blood
|
|
D001791||thrombocytopathies
|
|
D001791||thrombocytopathy
|
|
D061387||chlamydial pneumonia
|
|
D061387||chlamydial pneumonias
|
|
D061387||chlamydophila pneumonia
|
|
D061387||chlamydophila pneumonias
|
|
D061387||pneumonia chlamydial
|
|
D061387||pneumonia chlamydophila
|
|
D061387||pneumonias chlamydial
|
|
D061387||pneumonias chlamydophila
|
|
D001796||blood protein disorders
|
|
D001796||blood protein disorder
|
|
D001796||disorder blood protein
|
|
D001796||disorders blood protein
|
|
D001796||protein disorder blood
|
|
D001796||protein disorders blood
|
|
D011115||polyneuropathies
|
|
D011115||acquired polyneuropathies
|
|
D011115||acquired polyneuropathy
|
|
D011115||critical illness polyneuropathies
|
|
D011115||critical illness polyneuropathy
|
|
D011115||familial polyneuropathies
|
|
D011115||familial polyneuropathy
|
|
D011115||inherited polyneuropathies
|
|
D011115||inherited polyneuropathy
|
|
D011115||motor polyneuropathies
|
|
D011115||motor polyneuropathy
|
|
D011115||polyneuropathies acquired
|
|
D011115||polyneuropathies critical illness
|
|
D011115||polyneuropathies familial
|
|
D011115||polyneuropathies inherited
|
|
D011115||polyneuropathies motor
|
|
D011115||polyneuropathy
|
|
D011115||polyneuropathy acquired
|
|
D011115||polyneuropathy critical illness
|
|
D011115||polyneuropathy familial
|
|
D011115||polyneuropathy inherited
|
|
D011115||polyneuropathy motor
|
|
C566471|610476||arrhythmogenic right ventricular dysplasia familial 11
|
|
C566471|610476||arrhythmogenic right ventricular cardiomyopathy 11
|
|
C566471|610476||arrhythmogenic right ventricular cardiomyopathy 11 arvc11 arrhythmogenic right ventricular dysplasia familial 11 with mild palmoplantar keratoderma and woolly hair included
|
|
C566471|610476||arvd11
|
|
D060048||slipped capital femoral epiphyses
|
|
D060048||adolescent coxa vara
|
|
D060048||adolescent coxa varas
|
|
D060048||bilateral slipped capital femoral epiphyses
|
|
D060048||bilateral slipped capital femoral epiphysis
|
|
D060048||coxa vara adolescent
|
|
D060048||coxa varas adolescent
|
|
D060048||epiphysiolysis capitis femoris
|
|
D060048||slipped capital femoral epiphysis
|
|
D060048||slipped femoral capital epiphyses
|
|
D060048||unilateral slipped capital femoral epiphyses
|
|
D060048||unilateral slipped capital femoral epiphysis
|
|
D012448||sadism
|
|
D012448||sadisms
|
|
D012448||sadism sexual
|
|
D012448||sadisms sexual
|
|
D012448||sexual sadism
|
|
D012448||sexual sadisms
|
|
180200|D012175||retinoblastoma
|
|
180200|D012175||eye cancer retinoblastoma
|
|
180200|D012175||familial retinoblastoma
|
|
180200|D012175||familial retinoblastomas
|
|
180200|D012175||glioblastoma retinal
|
|
180200|D012175||glioblastomas retinal
|
|
180200|D012175||glioma retinal
|
|
180200|D012175||gliomas retinal
|
|
180200|D012175||hereditary retinoblastoma
|
|
180200|D012175||hereditary retinoblastomas
|
|
180200|D012175||neuroblastoma retinal
|
|
180200|D012175||neuroblastomas retinal
|
|
180200|D012175||rb
|
|
180200|D012175||rb1
|
|
180200|D012175||retinal glioblastoma
|
|
180200|D012175||retinal glioblastomas
|
|
180200|D012175||retinal glioma
|
|
180200|D012175||retinal gliomas
|
|
180200|D012175||retinal neuroblastoma
|
|
180200|D012175||retinal neuroblastomas
|
|
180200|D012175||retinoblastoma familial
|
|
180200|D012175||retinoblastoma hereditary
|
|
180200|D012175||retinoblastomas
|
|
180200|D012175||retinoblastomas familial
|
|
180200|D012175||retinoblastomas hereditary
|
|
180200|D012175||retinoblastoma sporadic
|
|
180200|D012175||retinoblastomas sporadic
|
|
180200|D012175||sporadic retinoblastoma
|
|
180200|D012175||sporadic retinoblastomas
|
|
C563909|608562||polydactyly postaxial type a4
|
|
C563909|608562||papa4
|
|
C563909|608562||postaxial polydactyly type a4
|
|
608681||scdo2
|
|
607354||scoliosis idiopathic susceptibility to 2
|
|
607354||is2
|
|
607354||scoliosis adolescent idiopathic 2
|
|
138000|C536827||glomus vagale tumors
|
|
138000|C536827||glomangiomas multiple
|
|
138000|C536827||glomus tumors multiple
|
|
138000|C536827||glomuvenous malformations
|
|
138000|C536827||gvm
|
|
138000|C536827||venous malformations with glomus cells
|
|
138000|C536827||vmglom
|
|
C567033||glomerulonephritis with isolated c3 deposits and factor i deficiency
|
|
218330|C562966||cranioectodermal dysplasia
|
|
218330|C562966||ced1
|
|
218330|C562966||cranioectodermal dysplasia 1
|
|
218330|C562966||levin syndrome i
|
|
218330|C562966||sensenbrenner syndrome
|
|
D011111||polymyalgia rheumatica
|
|
D011111||forestier certonciny syndrome
|
|
D011111||peri extra articular rheumatism
|
|
D011111||pseudopolyarthritides rhizomelic
|
|
D011111||pseudopolyarthritis rhizomelic
|
|
D011111||rheumatism peri extra articular
|
|
D011111||rhizomelic pseudopolyarthritides
|
|
D011111||rhizomelic pseudopolyarthritis
|
|
D011111||syndrome forestier certonciny
|
|
608688||aicar transformylase imp cyclohydrolase deficiency
|
|
608688||atic deficiency
|
|
611553|C548083||noonan syndrome 5
|
|
611553|C548083||ns5
|
|
607317|C537310||spinocerebellar ataxia autosomal recessive 4
|
|
607317|C537310||sca24 formerly
|
|
607317|C537310||scar4
|
|
607317|C537310||scasi
|
|
607317|C537310||spinocerebellar ataxia 24 formerly
|
|
607317|C537310||spinocerebellar ataxia with saccadic intrusions
|
|
300306||body mass index quantitative trait locus 11
|
|
300306||bmiq11
|
|
C538511||cancer of the oviduct
|
|
C567039||facial dysmorphism selective tooth agenesis and choroid calcification
|
|
D000472||alkalosis respiratory
|
|
D000472||alkaloses respiratory
|
|
D000472||respiratory alkaloses
|
|
D000472||respiratory alkalosis
|
|
D000471||alkalosis
|
|
D000471||alkaloses
|
|
608673||charcot marie tooth disease axonal type 2l
|
|
D013789||thalassemia
|
|
D013789||thalassemias
|
|
C580009||congenital deafness with labyrinthine aplasia microtia and microdontia
|
|
C580009||congenital deafness with inner ear agenesis microtia and microdontia
|
|
C580009||lamm syndrome
|
|
D011128||polyradiculopathy
|
|
D011128||abdominal polyradiculopathies
|
|
D011128||abdominal polyradiculopathy
|
|
D011128||cauda equina syndrome
|
|
D011128||cauda equina syndromes
|
|
D011128||polyradiculitides
|
|
D011128||polyradiculitis
|
|
D011128||polyradiculopathies
|
|
D011128||polyradiculopathies abdominal
|
|
D011128||polyradiculopathy abdominal
|
|
D011128||syndrome cauda equina
|
|
D011128||syndromes cauda equina
|
|
D011127||polyps
|
|
D011127||polyp
|
|
D011129||polyradiculoneuropathy
|
|
D011129||autoimmune demyelinating disease peripheral
|
|
D011129||demyelinating autoimmune disease peripheral
|
|
D011129||demyelinating disease peripheral autoimmune
|
|
D011129||peripheral autoimmune demyelinating disease
|
|
D011129||polyradiculoneuritides
|
|
D011129||polyradiculoneuritis
|
|
D011129||polyradiculoneuropathies
|
|
C580002||combined malonic and methylmalonic aciduria
|
|
C580002||cmamma
|
|
C580003||combined pituitary hormone deficiency
|
|
C538505||cytomegalic inclusion body disease
|
|
D060051||occupational injuries
|
|
D060051||injuries occupational
|
|
D060051||injury occupational
|
|
D060051||occupational injury
|
|
D060050||angina stable
|
|
D060050||angina chronic stable
|
|
D060050||angina pectoris stable
|
|
D060050||angina pectori stable
|
|
D060050||anginas chronic stable
|
|
D060050||anginas stable
|
|
D060050||chronic stable angina
|
|
D060050||chronic stable anginas
|
|
D060050||pectoris stable angina
|
|
D060050||pectori stable angina
|
|
D060050||stable angina
|
|
D060050||stable angina chronic
|
|
D060050||stable angina pectori
|
|
D060050||stable angina pectoris
|
|
D060050||stable anginas
|
|
D060050||stable anginas chronic
|
|
C537221|600145||sacral defect and anterior sacral meningocele
|
|
C537221|600145||agenesis of sacrum
|
|
C537221|600145||caudal dysgenesis syndrome
|
|
C537221|600145||caudal regression syndrome included
|
|
C537221|600145||hypoplasia of sacrum
|
|
C537221|600145||lumbosacral agenesis
|
|
C537221|600145||sacral agenesis
|
|
C537221|600145||sacral agenesis included
|
|
C537221|600145||sacral defect anterior meningocele
|
|
C537221|600145||sacral defect with anterior meningocele
|
|
C537221|600145||sdam caudal dysgenesis syndrome included
|
|
C537221|600145||sirenomelia included
|
|
D013786||thalamic diseases
|
|
D013786||dejerine roussy syndrome
|
|
D013786||diseases thalamic
|
|
D013786||disease thalamic
|
|
D013786||syndrome dejerine roussy
|
|
D013786||syndromes thalamic
|
|
D013786||syndrome thalamic
|
|
D013786||thalamic disease
|
|
D013786||thalamic syndrome
|
|
D013786||thalamic syndromes
|
|
D011123||polyploidy
|
|
D011123||cell polyploid
|
|
D011123||cells polyploid
|
|
D011123||polyploid
|
|
D011123||polyploid cell
|
|
D011123||polyploid cells
|
|
D011123||polyploidies
|
|
D011123||polyploids
|
|
C543092||lubinsky syndrome
|
|
C543092||cataracts and testicular failure
|
|
C543092||hypogonadism cataract syndrome
|
|
C567041||osteogenesis imperfecta type vi
|
|
C567041||oi6
|
|
C567041||oi type vi
|
|
D001778||blood coagulation disorders
|
|
D001778||blood coagulation disorder
|
|
D001778||coagulation disorder blood
|
|
D001778||coagulation disorders blood
|
|
D001778||disorder blood coagulation
|
|
D001778||disorders blood coagulation
|
|
C567004||meckel like cerebrorenodigital syndrome
|
|
D056806||urea cycle disorders inborn
|
|
D056806||disorders urea cycle
|
|
D056806||disorder urea cycle
|
|
D056806||inborn urea cycle disorder
|
|
D056806||urea cycle disorder
|
|
D056806||urea cycle disorders
|
|
C563451|606392||maturity onset diabetes of the young type 4
|
|
C563451|606392||mody4
|
|
C563451|606392||mody type 4
|
|
C567813|613021||bronchiectasis with or without elevated sweat chloride 2
|
|
C567813|613021||besc2
|
|
208250|C537560||jacobs syndrome
|
|
208250|C537560||arthropathy camptodactyly syndrome
|
|
208250|C537560||cacp
|
|
208250|C537560||camptodactyly arthropathy coxa vara pericarditis syndrome
|
|
208250|C537560||camptodactyly arthropathy pericarditis syndrome
|
|
208250|C537560||congenital familial hypertrophic synovitis
|
|
208250|C537560||fibrosing serositis familial
|
|
208250|C537560||hypertrophic synovitis congenital familial
|
|
208250|C537560||pac syndrome
|
|
208250|C537560||pericarditis arthropathy camptodactyly syndrome
|
|
607812|C564332||craniolenticulosutural dysplasia
|
|
607812|C564332||boyadjiev jabs syndrome
|
|
607812|C564332||clsd
|
|
D003093|191390||colitis ulcerative
|
|
D003093|191390||colitis gravis
|
|
D003093|191390||ibd11
|
|
D003093|191390||idiopathic proctocolitis
|
|
D003093|191390||inflammatory bowel disease ulcerative colitis type
|
|
D003093|191390||ulcerative colitis
|
|
613207||asthma related traits susceptibility to 8
|
|
613207||asrt8
|
|
613207||rhinoconjunctivitis susceptibility to included
|
|
C565102|612908||keratosis palmoplantaris striata ii
|
|
C565102|612908||keratoderma palmoplantar striate form ii
|
|
C565102|612908||kpps2
|
|
C565102|612908||ppks2
|
|
C565102|612908||sppk2
|
|
C565102|612908||striate palmoplantar keratoderma ii
|
|
C557675||congenital tracheomalacia
|
|
C557675||tracheomalacia congenital
|
|
C557675||type 1 tracheomalacia
|
|
607086|C562834||aortic aneurysm familial thoracic 1
|
|
607086|C562834||aat1
|
|
607086|C562834||aneurysm thoracic aortic erdheim cystic medial necrosis of aorta included
|
|
607086|C562834||annuloaortic ectasia
|
|
607086|C562834||aortic aneurysm familial thoracic
|
|
607086|C562834||aortic dissection familial
|
|
607086|C562834||faa1
|
|
607086|C562834||familial aortic aneurysm
|
|
607086|C562834||familial aortic dissection
|
|
607086|C562834||familial taad
|
|
607086|C562834||familial thoracic aortic aneurysm
|
|
607086|C562834||familial thoracic aortic aneurysm and dissection
|
|
D012421||rupture
|
|
D012421||ruptures
|
|
C563717|609454||supranuclear palsy progressive 2
|
|
C563717|609454||psnp2
|
|
D012422||rupture spontaneous
|
|
D012422||ruptures spontaneous
|
|
D012422||spontaneous rupture
|
|
D012422||spontaneous ruptures
|
|
C563541|160700||myopia 2
|
|
C563541|160700||myopia 2 autosomal dominant
|
|
C563541|160700||myp2
|
|
150250|C537873||larsen syndrome dominant type
|
|
150250|C537873||larsen syndrome autosomal dominant
|
|
150250|C537873||lrs
|
|
D001787||blood group incompatibility
|
|
D001787||blood group incompatibilities
|
|
D001787||group incompatibilities blood
|
|
D001787||group incompatibility blood
|
|
D001787||incompatibilities blood group
|
|
D001787||incompatibility blood group
|
|
D001787||reactions transfusion
|
|
D001787||reaction transfusion
|
|
D001787||transfusion reaction
|
|
D001787||transfusion reactions
|
|
D000453||aleutian mink disease
|
|
D000453||aleutian disease of mink
|
|
D000453||disease aleutian mink
|
|
D000453||mink disease aleutian
|
|
C565833|603909||autoimmune lymphoproliferative syndrome type iia
|
|
C565833|603909||alps2a
|
|
148500|C536164||keratosis palmoplantaris with esophageal cancer
|
|
148500|C536164||howell evans syndrome
|
|
148500|C536164||keratosis palmaris et plantaris with esophageal cancer
|
|
148500|C536164||toc
|
|
148500|C536164||tylosis with esophageal cancer
|
|
D000425||alcohol amnestic disorder
|
|
D000425||alcohol amnestic disorders
|
|
D000425||alcohol amnestic syndrome
|
|
D000425||alcohol amnestic syndromes
|
|
D000425||alcoholic korsakoff syndrome
|
|
D000425||alcoholic korsakoff syndromes
|
|
D000425||alcohol induced amnestic psychoses
|
|
D000425||alcohol induced amnestic psychosis
|
|
D000425||alcohol induced amnestic syndrome
|
|
D000425||alcohol induced amnestic syndromes
|
|
D000425||alcohol induced dysmnesic psychoses
|
|
D000425||alcohol induced dysmnesic psychosis
|
|
D000425||alcohol induced dysmnesic syndrome
|
|
D000425||alcohol induced dysmnesic syndromes
|
|
D000425||alcohol induced korsakoff syndrome
|
|
D000425||alcohol induced korsakoff syndromes
|
|
D000425||alcohol induced persisting amnestic disorder
|
|
D000425||amnestic disorder alcohol
|
|
D000425||amnestic disorders alcohol
|
|
D000425||amnestic psychoses alcohol induced
|
|
D000425||amnestic psychosis alcohol induced
|
|
D000425||amnestic syndrome alcohol
|
|
D000425||amnestic syndrome alcohol induced
|
|
D000425||amnestic syndromes alcohol
|
|
D000425||amnestic syndromes alcohol induced
|
|
D000425||dysmnesic psychoses alcohol induced
|
|
D000425||dysmnesic psychosis alcohol induced
|
|
D000425||dysmnesic syndrome alcohol induced
|
|
D000425||dysmnesic syndromes alcohol induced
|
|
D000425||korsakoff syndrome alcoholic
|
|
D000425||korsakoff syndrome alcohol induced
|
|
D000425||korsakoff syndromes alcoholic
|
|
D000425||korsakoff syndromes alcohol induced
|
|
D000425||psychoses alcohol induced amnestic
|
|
D000425||psychoses alcohol induced dysmnesic
|
|
D000425||psychosis alcohol induced amnestic
|
|
D000425||psychosis alcohol induced dysmnesic
|
|
D000425||syndrome alcohol amnestic
|
|
D000425||syndrome alcoholic korsakoff
|
|
D000425||syndrome alcohol induced amnestic
|
|
D000425||syndrome alcohol induced dysmnesic
|
|
D000425||syndrome alcohol induced korsakoff
|
|
D000425||syndromes alcohol amnestic
|
|
D000425||syndromes alcoholic korsakoff
|
|
D000425||syndromes alcohol induced amnestic
|
|
D000425||syndromes alcohol induced dysmnesic
|
|
D000425||syndromes alcohol induced korsakoff
|
|
D001753||blast injuries
|
|
D001753||blast injury
|
|
D001753||injuries blast
|
|
D001753||injury blast
|
|
D001759||blastomycosis
|
|
D001759||blastomycoses
|
|
D001759||blastomycosis north american
|
|
D001759||gilchrist disease
|
|
D001759||gilchrist apos s disease
|
|
D001759||gilchrists disease
|
|
D001759||north american blastomycosis
|
|
194380|C566369||dehydrated hereditary stomatocytosis pseudohyperkalemia and perinatal edema
|
|
194380|C566369||dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and or perinatal edema
|
|
194380|C566369||dhs
|
|
194380|C566369||pseudohyperkalemia edinburgh
|
|
194380|C566369||pseudohyperkalemia familial 1 due to red cell leak
|
|
194380|C566369||pshk1
|
|
D056829||hereditary angioedema types i and ii
|
|
D056829||angioedema hereditary type ii
|
|
D056829||angioedema hereditary types i and ii
|
|
D056829||c1 esterase inhibitor deficiency of
|
|
D056829||deficiency of c1 esterase inhibitor
|
|
D056829||hereditary angioedema type 1
|
|
D056829||hereditary angioedema type i
|
|
D056829||hereditary angioedema type ii
|
|
604403|C565810||generalized epilepsy with febrile seizures plus type 2
|
|
604403|C565810||feb3a included
|
|
604403|C565810||gefsp2
|
|
604403|C565810||gefs type 2
|
|
604403|C565810||gefs type 2 gefs 2 febrile seizures familial 3a included
|
|
C563273|145001||hyperparathyroidism 2
|
|
C563273|145001||hrpt2
|
|
C563273|145001||hyperparathyroidism familial primary with multiple ossifying jaw fibromas
|
|
C563273|145001||hyperparathyroidism jaw tumor syndrome hereditary
|
|
C563273|145001||hyperparathyroidism jaw tumor syndrome hereditary hpt jt parathyroid adenomatosis familial cystic included
|
|
C565328|605432||radioulnar synostosis with amegakaryocytic thrombocytopenia
|
|
C565328|605432||ctrus
|
|
C565328|605432||rusat
|
|
C565328|605432||thrombocytopenia congenital with radioulnar synostosis
|
|
D012409||rubella
|
|
D012409||german measles
|
|
D012409||measles german
|
|
D012409||measles three day
|
|
D012409||measle three day
|
|
D012409||rubellas
|
|
D012409||three day measle
|
|
D012409||three day measles
|
|
D001752||blast crisis
|
|
D001752||blast crises
|
|
D001752||blast phase
|
|
D001752||blast phases
|
|
D001752||crises blast
|
|
D001752||crisis blast
|
|
D001752||phase blast
|
|
D001752||phases blast
|
|
D001750||urinary bladder neurogenic
|
|
D001750||atonic neurogenic bladder
|
|
D001750||bladder disorder neurogenic
|
|
D001750||bladder neurogenesis
|
|
D001750||bladder neurogenic
|
|
D001750||neurogenesis bladder
|
|
D001750||neurogenesis urinary bladder
|
|
D001750||neurogenic bladder
|
|
D001750||neurogenic bladder atonic
|
|
D001750||neurogenic bladder disorder
|
|
D001750||neurogenic bladder disorders
|
|
D001750||neurogenic bladder spastic
|
|
D001750||neurogenic bladder uninhibited
|
|
D001750||neurogenic dysfunction of the urinary bladder
|
|
D001750||neurogenic urinary bladder
|
|
D001750||neurogenic urinary bladder atonic
|
|
D001750||neurogenic urinary bladder disorder
|
|
D001750||neurogenic urinary bladder spastic
|
|
D001750||neurogenic urinary bladder uninhibited
|
|
D001750||neuropathic bladder
|
|
D001750||spastic neurogenic bladder
|
|
D001750||uninhibited neurogenic bladder
|
|
D001750||urinary bladder disorder neurogenic
|
|
D001750||urinary bladder neurogenesis
|
|
D001750||urinary bladder neurogenic dysfunction
|
|
D013733||testicular diseases
|
|
D013733||diseases testicular
|
|
D013733||disease testicular
|
|
D013733||testicular disease
|
|
D013736||testicular neoplasms
|
|
D013736||cancer of testis
|
|
D013736||cancer of the testes
|
|
D013736||cancer of the testis
|
|
D013736||cancers testicular
|
|
D013736||cancers testis
|
|
D013736||cancer testicular
|
|
D013736||cancer testis
|
|
D013736||neoplasms testicular
|
|
D013736||neoplasms testis
|
|
D013736||neoplasm testicular
|
|
D013736||neoplasm testis
|
|
D013736||rete testis tumor
|
|
D013736||rete testis tumors
|
|
D013736||testicular cancer
|
|
D013736||testicular cancers
|
|
D013736||testicular neoplasm
|
|
D013736||testicular tumors
|
|
D013736||testis cancer
|
|
D013736||testis cancers
|
|
D013736||testis neoplasm
|
|
D013736||testis neoplasms
|
|
D013736||testis tumor rete
|
|
D013736||testis tumors rete
|
|
D013736||tumor of rete testis
|
|
D060085||coinfection
|
|
D060085||co infection
|
|
D060085||coinfections
|
|
D060085||co infections
|
|
D060085||infection mixed
|
|
D060085||infection polymicrobial
|
|
D060085||infection secondary
|
|
D060085||infections mixed
|
|
D060085||infections polymicrobial
|
|
D060085||infections secondary
|
|
D060085||mixed infection
|
|
D060085||mixed infections
|
|
D060085||polymicrobial infection
|
|
D060085||polymicrobial infections
|
|
D060085||secondary infection
|
|
D060085||secondary infections
|
|
D056824||upper extremity deep vein thrombosis
|
|
D056824||central venous catheter thrombosis
|
|
D056824||effort induced upper extremity deep vein thrombosis
|
|
D056824||effort related upper extremity deep vein thrombosis
|
|
D056824||exercise induced upper extremity deep vein thrombosis
|
|
D056824||idiopathic upper extremity deep vein thrombosis
|
|
D056824||paget schroetter syndrome
|
|
D056824||syndrome paget schroetter
|
|
D056824||upper extremity deep vein thrombosis primary
|
|
D056824||upper extremity deep vein thrombosis secondary
|
|
D012400||rotavirus infections
|
|
D012400||infection rotavirus
|
|
D012400||infections rotavirus
|
|
D012400||rotavirus infection
|
|
D056685|218040||costello syndrome
|
|
D056685|218040||cmems included
|
|
D056685|218040||faciocutaneoskeletal syndrome
|
|
D056685|218040||faciocutaneoskeletal syndromes
|
|
D056685|218040||fcs syndrome
|
|
D056685|218040||fcs syndrome myopathy congenital with excess of muscle spindles included
|
|
D056685|218040||fcs syndromes
|
|
D056685|218040||syndrome costello
|
|
D056685|218040||syndrome faciocutaneoskeletal
|
|
D056685|218040||syndrome fcs
|
|
D056685|218040||syndromes faciocutaneoskeletal
|
|
D056685|218040||syndromes fcs
|
|
D001766||blindness
|
|
D001766||acquired blindness
|
|
D001766||amauroses
|
|
D001766||amaurosis
|
|
D001766||blindness acquired
|
|
D001766||blindness complete
|
|
D001766||blindness hysterical
|
|
D001766||blindness legal
|
|
D001766||blindness monocular
|
|
D001766||blindness transient
|
|
D001766||complete blindness
|
|
D001766||hysterical blindness
|
|
D001766||legal blindness
|
|
D001766||monocular blindness
|
|
D001766||transient blindness
|
|
D000435||alcoholic intoxication
|
|
D000435||drunkenness
|
|
D000435||drunkennesses
|
|
D000435||intoxication alcoholic
|
|
D001765||blind loop syndrome
|
|
D001765||bacterial overgrowth syndrome
|
|
D001765||loop syndromes stagnant
|
|
D001765||loop syndrome stagnant
|
|
D001765||stagnant loop syndrome
|
|
D001765||stagnant loop syndromes
|
|
D001765||syndrome bacterial overgrowth
|
|
D001765||syndrome blind loop
|
|
D001765||syndromes stagnant loop
|
|
D001765||syndrome stagnant loop
|
|
D001764||blepharospasm
|
|
D001764||blepharospasms
|
|
D001768||blister
|
|
D001768||bleb
|
|
D001768||blebs
|
|
D001768||blisters
|
|
D001768||bulla
|
|
D001768||bullae
|
|
D001768||bullous lesion
|
|
D001768||bullous lesions
|
|
D001768||lesion bullous
|
|
D001768||lesions bullous
|
|
D001768||vesication
|
|
D001768||vesications
|
|
194070|D009396||wilms tumor
|
|
194070|D009396||bilateral wilms tumor
|
|
194070|D009396||nephroblastoma
|
|
194070|D009396||nephroblastomas
|
|
194070|D009396||tumor bilateral wilms
|
|
194070|D009396||tumor wilms
|
|
194070|D009396||tumor wilms apos
|
|
194070|D009396||wilm apos s tumor
|
|
194070|D009396||wilms apos tumor
|
|
194070|D009396||wilms tumor 1
|
|
194070|D009396||wilms tumor bilateral
|
|
194070|D009396||wilm tumor
|
|
194070|D009396||wt1
|
|
D001763||blepharoptosis
|
|
D001763||blepharoptoses
|
|
D001763||eyelid ptoses
|
|
D001763||eyelid ptosis
|
|
D001763||ptoses eyelid
|
|
D001763||ptosis eyelid
|
|
D001762||blepharitis
|
|
D001762||blepharitides
|
|
D000430||alcohol withdrawal delirium
|
|
D000430||alcohol withdrawal associated autonomic hyperactivity
|
|
D000430||alcohol withdrawal hallucinosis
|
|
D000430||alcohol withdrawal induced delirium tremens
|
|
D000430||autonomic hyperactivity alcohol withdrawal associated
|
|
D000430||delirium alcohol withdrawal
|
|
D000430||delirium tremens
|
|
D000430||delirium tremens alcohol withdrawal induced
|
|
D000430||hallucinosis alcohol withdrawal
|
|
D013746||tetany
|
|
D013746||neonatal tetanies
|
|
D013746||neonatal tetany
|
|
D013746||spasmophilia
|
|
D013746||spasmophilias
|
|
D013746||tetanies
|
|
D013746||tetanies neonatal
|
|
D013746||tetanilla
|
|
D013746||tetanillas
|
|
D013746||tetany neonatal
|
|
C536546|602134||tremor hereditary essential 2
|
|
C536546|602134||etm2
|
|
203800|D056769||alstrom syndrome
|
|
203800|D056769||alms
|
|
203800|D056769||alss
|
|
203800|D056769||alstrom hallgren syndrome
|
|
203800|D056769||alstrom apos s syndrome
|
|
203800|D056769||alstroms syndrome
|
|
203800|D056769||alstr 246 m syndrome
|
|
203800|D056769||syndrome alstrom
|
|
203800|D056769||syndrome alstr 246 m
|
|
203800|D056769||syndrome alstrom hallgren
|
|
203800|D056769||syndrome alstrom apos s
|
|
C567002||epilepsy childhood absence susceptibility to 4
|
|
D056830||isolated noncompaction of the ventricular myocardium
|
|
D056830||isolated noncompaction of the left ventricular myocardium x linked
|
|
D056830||isolated non compaction of the ventricular myocardium
|
|
D056830||noncompaction of the left ventricular myocardium autosomal dominant
|
|
D012410||rubella syndrome congenital
|
|
D012410||congenital rubella syndrome
|
|
D012410||congenital rubella syndromes
|
|
D012410||rubella syndromes congenital
|
|
D012410||syndrome congenital rubella
|
|
D012410||syndromes congenital rubella
|
|
D013742||tetanus
|
|
C536271|608649||ichthyosis prematurity syndrome
|
|
C536271|608649||aniridia partial with unilateral renal agenesis and psychomotor retardation
|
|
C536271|608649||aniridia renal agenesis psychomotor retardation
|
|
C536271|608649||ichthyosis congenita iv
|
|
C536271|608649||ips
|
|
D055501||macrophage activation syndrome
|
|
D055501||syndrome macrophage activation
|
|
D056833||central serous chorioretinopathy
|
|
D056833||central serous chorioretinopathies
|
|
D056833||central serous retinopathies
|
|
D056833||central serous retinopathy
|
|
D056833||chorioretinopathies central serous
|
|
D056833||chorioretinopathy central serous
|
|
D056833||retinopathies central serous
|
|
D056833||retinopathy central serous
|
|
D056833||serous chorioretinopathies central
|
|
D056833||serous chorioretinopathy central
|
|
D056833||serous retinopathies central
|
|
D056833||serous retinopathy central
|
|
D001734||bites human
|
|
D001734||bite human
|
|
D001734||human bite
|
|
D001734||human bites
|
|
D001733||bites and stings
|
|
D001733||bite
|
|
D001733||bites
|
|
D001733||sting
|
|
D001733||stings
|
|
D001733||stings and bites
|
|
D000402||airway obstruction
|
|
D000402||airway obstructions
|
|
D000402||choking
|
|
D000402||obstruction airway
|
|
D000402||obstructions airway
|
|
143100|D006816||huntington disease
|
|
143100|D006816||akinetic rigid variant of huntington disease
|
|
143100|D006816||chorea chronic progressive hereditary huntington
|
|
143100|D006816||chorea huntington
|
|
143100|D006816||chorea huntington apos s
|
|
143100|D006816||chronic progressive hereditary chorea huntington
|
|
143100|D006816||hd
|
|
143100|D006816||huntington chorea
|
|
143100|D006816||huntington chronic progressive hereditary chorea
|
|
143100|D006816||huntington disease akinetic rigid variant
|
|
143100|D006816||huntington disease juvenile
|
|
143100|D006816||huntington disease juvenile onset
|
|
143100|D006816||huntington disease late onset
|
|
143100|D006816||huntington apos s chorea
|
|
143100|D006816||huntington apos s disease
|
|
143100|D006816||juvenile huntington disease
|
|
143100|D006816||juvenile onset huntington disease
|
|
143100|D006816||late onset huntington disease
|
|
143100|D006816||progressive chorea chronic hereditary huntington
|
|
143100|D006816||progressive chorea hereditary chronic huntington
|
|
D008881|157300||migraine disorders
|
|
D008881|157300||abdominal migraine
|
|
D008881|157300||abdominal migraines
|
|
D008881|157300||acute confusional migraine
|
|
D008881|157300||acute confusional migraines
|
|
D008881|157300||cervical migraine syndrome
|
|
D008881|157300||cervical migraine syndromes
|
|
D008881|157300||disorder migraine
|
|
D008881|157300||disorders migraine
|
|
D008881|157300||fhm4 included
|
|
D008881|157300||headache migraine
|
|
D008881|157300||headache sick
|
|
D008881|157300||headaches migraine
|
|
D008881|157300||headaches sick
|
|
D008881|157300||hemicrania migraine
|
|
D008881|157300||hemicrania migraines
|
|
D008881|157300||ma
|
|
D008881|157300||mgau
|
|
D008881|157300||mgr1
|
|
D008881|157300||mgr12
|
|
D008881|157300||mgr13
|
|
D008881|157300||mgr3
|
|
D008881|157300||mgr5
|
|
D008881|157300||mgr6 migraine familial hemiplegic 4 included
|
|
D008881|157300||mgr8
|
|
D008881|157300||migraine
|
|
D008881|157300||migraine abdominal
|
|
D008881|157300||migraine acute confusional
|
|
D008881|157300||migraine disorder
|
|
D008881|157300||migraine headache
|
|
D008881|157300||migraine headaches
|
|
D008881|157300||migraine hemicrania
|
|
D008881|157300||migraines
|
|
D008881|157300||migraines abdominal
|
|
D008881|157300||migraines acute confusional
|
|
D008881|157300||migraines hemicrania
|
|
D008881|157300||migraine syndrome cervical
|
|
D008881|157300||migraine syndromes cervical
|
|
D008881|157300||migraine variant
|
|
D008881|157300||migraine variants
|
|
D008881|157300||migraine with or without aura susceptibility to 1
|
|
D008881|157300||migraine with or without aura susceptibility to 12
|
|
D008881|157300||migraine with or without aura susceptibility to 13
|
|
D008881|157300||migraine with or without aura susceptibility to 3
|
|
D008881|157300||migraine with or without aura susceptibility to 5
|
|
D008881|157300||migraine with or without aura susceptibility to 6
|
|
D008881|157300||migraine with or without aura susceptibility to 8
|
|
D008881|157300||sick headache
|
|
D008881|157300||sick headaches
|
|
D008881|157300||status migrainosus
|
|
D008881|157300||variant migraine
|
|
D008881|157300||variants migraine
|
|
C563668|610422||alopecia mental retardation syndrome 2
|
|
C563668|610422||apmr2
|
|
C566599|601954||muscular dystrophy limb girdle type 2g
|
|
C566599|601954||lgmd2g
|
|
D000405||akinetic mutism
|
|
D000405||akinetic autism
|
|
D000405||akinetic mutisms
|
|
D000405||autism akinetic
|
|
D000405||coma vigil
|
|
D000405||coma vigilans
|
|
D000405||mutism akinetic
|
|
D000405||vigil coma
|
|
D000405||vigils coma
|
|
C564539|300299||neutropenia severe congenital x linked
|
|
C564539|300299||scnx
|
|
C564539|300299||xln
|
|
122200|C537881||lattice corneal dystrophy type 1
|
|
122200|C537881||biber haab dimmer dystrophy
|
|
122200|C537881||cdl1
|
|
122200|C537881||corneal dystrophy lattice type 1
|
|
122200|C537881||corneal dystrophy lattice type i
|
|
122200|C537881||lattice corneal dystrophy type i
|
|
122200|C537881||lcd
|
|
122200|C537881||lcd1
|
|
244460|C537021||kenny caffey syndrome type 1
|
|
244460|C537021||kcs
|
|
244460|C537021||kcs1
|
|
244460|C537021||kenny caffey syndrome autosomal recessive
|
|
244460|C537021||kenny caffey syndrome autosomal recessive form
|
|
D013716||tennis elbow
|
|
D013716||elbows tennis
|
|
D013716||elbow tennis
|
|
D013716||epicondylitides lateral humeral
|
|
D013716||epicondylitis lateral humeral
|
|
D013716||humeral epicondylitides lateral
|
|
D013716||humeral epicondylitis lateral
|
|
D013716||lateral humeral epicondylitides
|
|
D013716||lateral humeral epicondylitis
|
|
D013716||tennis elbows
|
|
D013717||tenosynovitis
|
|
D013717||tenosynovitides
|
|
D010673|171300||pheochromocytoma
|
|
D010673|171300||extra adrenal pheochromocytoma
|
|
D010673|171300||extra adrenal pheochromocytomas
|
|
D010673|171300||pheochromocytoma extra adrenal
|
|
D010673|171300||pheochromocytoma pheochromocytoma susceptibility to
|
|
D010673|171300||pheochromocytomas
|
|
D010673|171300||pheochromocytomas extra adrenal
|
|
603855||cystic fibrosis modifier of 1
|
|
603855||cfm1
|
|
603855||meconium ileus in cystic fibrosis susceptibility to included
|
|
D056844||renal colic
|
|
D056844||acute renal colic
|
|
D056844||acute renal colics
|
|
D056844||colic acute renal
|
|
D056844||colic renal
|
|
D056844||colics acute renal
|
|
D056844||colics renal
|
|
D056844||colics ureteral
|
|
D056844||colic ureteral
|
|
D056844||renal colic acute
|
|
D056844||renal colics
|
|
D056844||renal colics acute
|
|
D056844||ureteral colic
|
|
D056844||ureteral colics
|
|
D001745||urinary bladder diseases
|
|
D001745||bladder disease
|
|
D001745||bladder diseases
|
|
D001745||urinary bladder disease
|
|
D001744||urinary bladder calculi
|
|
D001744||bladder calculi
|
|
D001744||bladder calculi urinary
|
|
D001744||bladder calculus
|
|
D001744||bladder calculus urinary
|
|
D001744||bladder stone
|
|
D001744||bladder stones
|
|
D001744||bladder stones urinary
|
|
D001744||bladder stone urinary
|
|
D001744||calculi bladder
|
|
D001744||calculi of urinary bladder
|
|
D001744||calculi urinary bladder
|
|
D001744||calculi vesical
|
|
D001744||calculus bladder
|
|
D001744||calculus urinary bladder
|
|
D001744||calculus vesical
|
|
D001744||cystolith
|
|
D001744||cystoliths
|
|
D001744||stone bladder
|
|
D001744||stones bladder
|
|
D001744||stones urinary bladder
|
|
D001744||stone urinary bladder
|
|
D001744||urinary bladder calculus
|
|
D001744||urinary bladder stone
|
|
D001744||urinary bladder stones
|
|
D001744||vesical calculi
|
|
D001744||vesical calculus
|
|
D001742||blackwater fever
|
|
D001742||black water fever
|
|
D001742||blackwater fevers
|
|
D001742||black water fevers
|
|
D001742||fever blackwater
|
|
D001742||fever black water
|
|
D001742||fevers blackwater
|
|
D001742||fevers black water
|
|
D001742||hemolytic malaria
|
|
D001742||hemolytic malarias
|
|
D001742||malaria hemolytic
|
|
D001742||malarias hemolytic
|
|
D001748||urinary bladder neck obstruction
|
|
D001748||bladder neck obstruction
|
|
D001748||bladder outlet obstruction
|
|
D000417||albinism
|
|
D001747||urinary bladder fistula
|
|
D001747||fistulas urinary bladder
|
|
D001747||fistulas vesical
|
|
D001747||fistula urinary bladder
|
|
D001747||fistula vesical
|
|
D001747||urinary bladder fistulas
|
|
D001747||vesical fistula
|
|
D001747||vesical fistulas
|
|
157700||mitral valve prolapse familial
|
|
157700||click murmur syndrome mitral valve prolapse myxomatous 1 included
|
|
157700||mmvp1 included
|
|
157700||mvp
|
|
157700||myxomatous mitral valve prolapse 1 included
|
|
157700||pmv
|
|
D001746||bladder exstrophy
|
|
D001746||bladder exstrophies
|
|
D001746||bladder extrophies
|
|
D001746||bladder extrophy
|
|
D001746||exstrophies bladder
|
|
D001746||exstrophies urinary bladder
|
|
D001746||exstrophy bladder
|
|
D001746||exstrophy of bladder
|
|
D001746||exstrophy of the bladder
|
|
D001746||exstrophy urinary bladder
|
|
D001746||extrophies bladder
|
|
D001746||extrophy bladder
|
|
D001746||urinary bladder exstrophies
|
|
D001746||urinary bladder exstrophy
|
|
D013724||teratoma
|
|
D013724||benign teratoma
|
|
D013724||benign teratomas
|
|
D013724||dysembryoma
|
|
D013724||dysembryomas
|
|
D013724||immature teratoma
|
|
D013724||immature teratomas
|
|
D013724||malignant teratoma
|
|
D013724||malignant teratomas
|
|
D013724||teratoid tumor
|
|
D013724||teratoid tumors
|
|
D013724||teratoma benign
|
|
D013724||teratoma cystic
|
|
D013724||teratoma immature
|
|
D013724||teratoma malignant
|
|
D013724||teratoma mature
|
|
D013724||teratomas
|
|
D013724||teratomas benign
|
|
D013724||teratomas immature
|
|
D013724||teratomas malignant
|
|
D013724||tumors teratoid
|
|
D013724||tumor teratoid
|
|
C565275|605913||bleeding disorder east texas type
|
|
C565275|605913||bdet
|
|
607095|C538256||anauxetic dysplasia
|
|
607095|C538256||spondylometaepiphyseal dysplasia anauxetic type
|
|
607095|C538256||spondylometaepiphyseal dysplasia menger type
|
|
C567216|612642||deafness autosomal dominant 59
|
|
C567216|612642||dfna59
|
|
C565406|249500||mental retardation autosomal recessive 1
|
|
C565406|249500||mrt1
|
|
102600||adenine phosphoribosyltransferase
|
|
102600||aprt
|
|
D000419||albuminuria
|
|
D000419||albuminurias
|
|
C567506|611879||cardiomyopathy dilated 1z
|
|
C567506|611879||cmd1z
|
|
C562695|609304||epileptic encephalopathy early infantile 3
|
|
C562695|609304||early myoclonic encephalopathy
|
|
C562695|609304||eiee3
|
|
C562695|609304||myoclonic epilepsy neonatal with suppression burst pattern
|
|
D044882||glucose metabolism disorders
|
|
D044882||disorder glucose metabolic
|
|
D044882||disorder glucose metabolism
|
|
D044882||disorders glucose metabolic
|
|
D044882||disorders glucose metabolism
|
|
D044882||glucose metabolic disorder
|
|
D044882||glucose metabolic disorders
|
|
D044882||glucose metabolism disorder
|
|
D044882||metabolic disorder glucose
|
|
D044882||metabolic disorders glucose
|
|
D044882||metabolism disorder glucose
|
|
D044882||metabolism disorders glucose
|
|
D001716||bird fancier apos s lung
|
|
D001716||avian hypersensitivity pneumonitides
|
|
D001716||avian hypersensitivity pneumonitis
|
|
D001716||bird fancier lung
|
|
D001716||bird fanciers lung
|
|
D001716||bird fancier apos s lungs
|
|
D001716||budgerigar fancier lung
|
|
D001716||budgerigar fancier apos s lung
|
|
D001716||budgerigar fanciers lung
|
|
D001716||budgerigar fancier apos s lungs
|
|
D001716||hypersensitivity pneumonitides avian
|
|
D001716||hypersensitivity pneumonitis avian
|
|
D001716||lung bird fancier apos s
|
|
D001716||lung budgerigar fancier apos s
|
|
D001716||lung pigeon breeder apos s
|
|
D001716||lungs bird fancier apos s
|
|
D001716||lungs budgerigar fancier apos s
|
|
D001716||lungs pigeon breeder apos s
|
|
D001716||pigeon breeder lung
|
|
D001716||pigeon breeder apos s lung
|
|
D001716||pigeon breeders lung
|
|
D001716||pigeon breeder apos s lungs
|
|
D001716||pneumonitides avian hypersensitivity
|
|
D001716||pneumonitis avian hypersensitivity
|
|
D001716||pneumonitis hypersensitivity avian
|
|
D001715||bird diseases
|
|
D001715||avian disease
|
|
D001715||avian diseases
|
|
D001715||bird disease
|
|
D001715||disease avian
|
|
D001715||disease bird
|
|
D001715||diseases avian
|
|
D001715||diseases bird
|
|
D001714||bipolar disorder
|
|
D001714||affective psychosis bipolar
|
|
D001714||bipolar affective psychosis
|
|
D001714||bipolar depression
|
|
D001714||bipolar disorders
|
|
D001714||depression bipolar
|
|
D001714||disorder bipolar
|
|
D001714||disorder manic
|
|
D001714||mania
|
|
D001714||manias
|
|
D001714||manic depressive psychoses
|
|
D001714||manic disorder
|
|
D001714||manic disorders
|
|
D001714||manic state
|
|
D001714||manic states
|
|
D001714||psychoses bipolar affective
|
|
D001714||psychoses manic depressive
|
|
D001714||psychosis bipolar affective
|
|
D001714||psychosis manic depressive
|
|
D001714||state manic
|
|
D001714||states manic
|
|
207750|D008072||hyperlipoproteinemia type i
|
|
207750|D008072||anapolipoproteinemia c ii
|
|
207750|D008072||anapolipoproteinemias c ii
|
|
207750|D008072||apoc2 deficiency
|
|
207750|D008072||apolipoprotein c ii deficiencies
|
|
207750|D008072||apolipoprotein c ii deficiency
|
|
207750|D008072||burger grutz syndrome
|
|
207750|D008072||burger grutz syndromes
|
|
207750|D008072||chylomicronemias familial
|
|
207750|D008072||c ii anapolipoproteinemia
|
|
207750|D008072||c ii anapolipoproteinemias
|
|
207750|D008072||deficiencies apolipoprotein c ii
|
|
207750|D008072||deficiencies familial lpl
|
|
207750|D008072||deficiencies lipase d
|
|
207750|D008072||deficiencies lipd
|
|
207750|D008072||deficiencies lipoprotein lipase
|
|
207750|D008072||deficiency apolipoprotein c ii
|
|
207750|D008072||deficiency familial lpl
|
|
207750|D008072||deficiency lipase d
|
|
207750|D008072||deficiency lipd
|
|
207750|D008072||deficiency lipoprotein lipase
|
|
207750|D008072||essential familial hyperlipemia
|
|
207750|D008072||essential familial hyperlipemias
|
|
207750|D008072||familial chylomicronemia
|
|
207750|D008072||familial chylomicronemias
|
|
207750|D008072||familial fat induced hypertriglyceridemia
|
|
207750|D008072||familial fat induced hypertriglyceridemias
|
|
207750|D008072||familial hyperchylomicronemia
|
|
207750|D008072||familial hyperchylomicronemias
|
|
207750|D008072||familial hyperlipemia essential
|
|
207750|D008072||familial hyperlipemias essential
|
|
207750|D008072||familial hyperlipoproteinemia type 1
|
|
207750|D008072||familial lipoprotein lipase deficiency
|
|
207750|D008072||familial lpl deficiencies
|
|
207750|D008072||familial lpl deficiency
|
|
207750|D008072||fat induced hypertriglyceridemia familial
|
|
207750|D008072||fat induced hypertriglyceridemias familial
|
|
207750|D008072||hyperchylomicronemias familial
|
|
207750|D008072||hyperlipemias essential familial
|
|
207750|D008072||hyperlipoproteinemias type i
|
|
207750|D008072||hyperlipoproteinemias type ia
|
|
207750|D008072||hyperlipoproteinemias type ib
|
|
207750|D008072||hyperlipoproteinemia type ias
|
|
207750|D008072||hyperlipoproteinemia type ib
|
|
207750|D008072||hyperlipoproteinemia type ibs
|
|
207750|D008072||hyperlipoproteinemia type is
|
|
207750|D008072||hypertriglyceridemia familial fat induced
|
|
207750|D008072||hypertriglyceridemias familial fat induced
|
|
207750|D008072||lipase d deficiencies
|
|
207750|D008072||lipase deficiencies lipoprotein
|
|
207750|D008072||lipd deficiencies
|
|
207750|D008072||lipoprotein lipase deficiencies
|
|
207750|D008072||lipoprotein lipase deficiency
|
|
207750|D008072||lipoprotein lipase deficiency familial
|
|
207750|D008072||lpl deficiencies familial
|
|
207750|D008072||lpl deficiency familial
|
|
207750|D008072||syndrome burger grutz
|
|
207750|D008072||syndromes burger grutz
|
|
207750|D008072||type ia hyperlipoproteinemia
|
|
207750|D008072||type ia hyperlipoproteinemias
|
|
207750|D008072||type ib hyperlipoproteinemia
|
|
207750|D008072||type ib hyperlipoproteinemias
|
|
207750|D008072||type i hyperlipoproteinemia
|
|
207750|D008072||type i hyperlipoproteinemias
|
|
137600|C535536||iridogoniodysgenesis dominant type
|
|
137600|C535536||igds
|
|
137600|C535536||ihga
|
|
137600|C535536||irid2
|
|
137600|C535536||iridogoniodysgenesis syndrome
|
|
137600|C535536||iridogoniodysgenesis type 2
|
|
137600|C535536||iris hypoplasia with early onset glaucoma autosomal dominant
|
|
C567447|611959||prostate cancer hereditary 15
|
|
C567447|611959||hpc15
|
|
C567115|233650||combined cellular and humoral immune defects with granulomas
|
|
C567115|233650||cchidg
|
|
120430|C535970||coloboma of optic nerve
|
|
120430|C535970||congenital coloboma of the optic nerve
|
|
120430|C535970||morning glory disc included
|
|
120430|C535970||optic nerve coloboma
|
|
120430|C535970||optic nerve head pits bilateral congenital
|
|
120430|C535970||optic nerve head pits bilateral congenital included
|
|
D015518|312750||rett syndrome
|
|
D015518|312750||autism dementia ataxia and loss of purposeful hand use
|
|
D015518|312750||autism dementia ataxia and loss of purposeful hand use rett syndrome zappella variant included
|
|
D015518|312750||autism dementia ataxia loss of purposeful hand use syndrome
|
|
D015518|312750||cerebroatrophic hyperammonemia
|
|
D015518|312750||cerebroatrophic hyperammonemias
|
|
D015518|312750||hyperammonemia cerebroatrophic
|
|
D015518|312750||hyperammonemias cerebroatrophic
|
|
D015518|312750||rett disorder
|
|
D015518|312750||rett apos s disorder
|
|
D015518|312750||rett apos s syndrome
|
|
D015518|312750||retts syndrome
|
|
D015518|312750||rett syndrome atypical included
|
|
D015518|312750||rett syndrome preserved speech variant included
|
|
D015518|312750||rtt
|
|
D015518|312750||syndrome rett
|
|
D015518|312750||syndrome rett apos s
|
|
C544351||idiopathic orthostatic hypotension
|
|
D055538||delta thalassemia
|
|
D055538||delta thalassemias
|
|
D055534||bulbo spinal atrophy x linked
|
|
D055534||atrophies x linked bulbo spinal
|
|
D055534||atrophy x linked bulbo spinal
|
|
D055534||bulbo spinal atrophies x linked
|
|
D055534||disease kennedy
|
|
D055534||disease kennedy apos s
|
|
D055534||kennedy apos s disease
|
|
D055534||kennedys disease
|
|
D055534||kennedy syndrome
|
|
D055534||syndrome kennedy
|
|
D055534||x linked bulbo spinal atrophies
|
|
D055534||x linked bulbo spinal atrophy
|
|
D055534||x linked bulbospinal muscular atrophy
|
|
D055534||x linked spinal and bulbar muscular atrophy
|
|
D055535||morgellons disease
|
|
D055535||disease morgellons
|
|
D055535||morgellon
|
|
D055535||morgellons
|
|
D055535||morgellon apos s
|
|
D055535||morgellons syndrome
|
|
D055535||syndrome morgellons
|
|
C567764|613087||atrial septal defect 6
|
|
C567764|613087||asd6
|
|
C567887|154230||46 xy sex reversal 4
|
|
C567887|154230||46 xy gonadal dysgenesis complete or partial with 9p24 3 deletion
|
|
C567887|154230||chromosome 9p24 3 deletion syndrome
|
|
C567887|154230||srxy4
|
|
D001720||birth injuries
|
|
D001720||birth injury
|
|
D001720||injuries birth
|
|
D001720||injury birth
|
|
C537352|156500||metaphyseal chondrodysplasia schmid type
|
|
C537352|156500||mcds
|
|
C537352|156500||spondylometaphyseal dysplasia japanese type
|
|
D001724||birth weight
|
|
D001724||birth weights
|
|
D001724||weight birth
|
|
D001724||weights birth
|
|
C563678|610356||retinal cone dystrophy 3b
|
|
C563678|610356||cdsrr
|
|
C563678|610356||cone dystrophy with night blindness and supernormal rod responses kcnv2 related
|
|
C563678|610356||cone dystrophy with supernormal rod responses
|
|
C563678|610356||rcd3b
|
|
D013708||tendon injuries
|
|
D013708||injuries tendon
|
|
D013708||injury tendon
|
|
D013708||tendon injury
|
|
D013700||giant cell arteritis
|
|
D013700||aortic arteritis giant cell
|
|
D013700||aortitides giant cell
|
|
D013700||aortitis giant cell
|
|
D013700||arteritides cranial
|
|
D013700||arteritides giant cell
|
|
D013700||arteritides juvenile temporal
|
|
D013700||arteritides temporal
|
|
D013700||arteritis cranial
|
|
D013700||arteritis giant cell
|
|
D013700||arteritis giant cell horton
|
|
D013700||arteritis giant cell horton apos s
|
|
D013700||arteritis juvenile temporal
|
|
D013700||arteritis temporal
|
|
D013700||cranial arteritides
|
|
D013700||cranial arteritis
|
|
D013700||giant cell aortic arteritis
|
|
D013700||giant cell aortitides
|
|
D013700||giant cell aortitis
|
|
D013700||giant cell aortitis horton apos s
|
|
D013700||giant cell arteritides
|
|
D013700||giant cell arteritis horton
|
|
D013700||horton disease
|
|
D013700||horton giant cell arteritis
|
|
D013700||horton apos s disease
|
|
D013700||hortons disease
|
|
D013700||horton apos s giant cell arteritis
|
|
D013700||juvenile temporal arteritides
|
|
D013700||juvenile temporal arteritis
|
|
D013700||temporal arteritides
|
|
D013700||temporal arteritides juvenile
|
|
D013700||temporal arteritis
|
|
D013700||temporal arteritis juvenile
|
|
D013705||temporomandibular joint disorders
|
|
D013705||diseases temporomandibular joint
|
|
D013705||diseases tmj
|
|
D013705||disease temporomandibular joint
|
|
D013705||disease tmj
|
|
D013705||disorders temporomandibular
|
|
D013705||disorders temporomandibular joint
|
|
D013705||disorders tmj
|
|
D013705||disorder temporomandibular
|
|
D013705||disorder temporomandibular joint
|
|
D013705||disorder tmj
|
|
D013705||joint diseases temporomandibular
|
|
D013705||joint disease temporomandibular
|
|
D013705||joint disorders temporomandibular
|
|
D013705||joint disorder temporomandibular
|
|
D013705||temporomandibular disorder
|
|
D013705||temporomandibular disorders
|
|
D013705||temporomandibular joint disease
|
|
D013705||temporomandibular joint diseases
|
|
D013705||temporomandibular joint disorder
|
|
D013705||tmj disease
|
|
D013705||tmj diseases
|
|
D013705||tmj disorder
|
|
D013705||tmj disorders
|
|
278300|C562584||xanthinuria type i
|
|
278300|C562584||xanthine dehydrogenase deficiency
|
|
278300|C562584||xanthine oxidase deficiency
|
|
278300|C562584||xdh deficiency
|
|
D013706||temporomandibular joint dysfunction syndrome
|
|
D013706||costen apos s syndrome
|
|
D013706||costens syndrome
|
|
D013706||costen syndrome
|
|
D013706||joint syndrome temporomandibular
|
|
D013706||myofascial pain dysfunction syndrome temporomandibular joint
|
|
D013706||syndrome costen apos s
|
|
D013706||syndrome temporomandibular joint
|
|
D013706||syndrome tmj
|
|
D013706||temporomandibular joint syndrome
|
|
D013706||tmj syndrome
|
|
C537143|602475||ossification of the posterior longitudinal ligament of the spine
|
|
C537143|602475||opll
|
|
C537143|602475||ossification of the posterior longitudinal ligament of spine
|
|
C563440|600802||severe combined immunodeficiency autosomal recessive t cell negative b cell positive nk cell negative
|
|
C563440|600802||scid t cell negative b cell positive nk cell negative
|
|
D054219||neoplasms plasma cell
|
|
D054219||neoplasm plasma cell
|
|
D054219||plasma cell neoplasm
|
|
D054219||plasma cell neoplasms
|
|
D054218||precursor t cell lymphoblastic leukemia lymphoma
|
|
D054218||acute t cell leukemia
|
|
D054218||acute t cell leukemias
|
|
D054218||acute t lymphocytic leukemia
|
|
D054218||acute t lymphocytic leukemias
|
|
D054218||leukemia acute t cell
|
|
D054218||leukemia acute t lymphocytic
|
|
D054218||leukemia lymphoblastic acute t cell
|
|
D054218||leukemia lymphocytic acute t cell
|
|
D054218||leukemias acute t cell
|
|
D054218||leukemias acute t lymphocytic
|
|
D054218||leukemia t cell acute
|
|
D054218||lymphoblastic leukemia acute t cell
|
|
D054218||lymphocytic leukemia t cell acute
|
|
D054218||precursor t cell lymphoblastic leukemia
|
|
D054218||precursor t cell lymphoblastic lymphoma
|
|
D054218||t all
|
|
D054218||t cell acute lymphocytic leukemia
|
|
D054218||t cell leukemia acute
|
|
D054218||t cell leukemias acute
|
|
D054218||t lymphocytic leukemia acute
|
|
D054218||t lymphocytic leukemias acute
|