| Disease Browser
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Parent Node:
 Cerebellar Ataxia (D002524) |
Parent Node:
Hearing Loss, Sensorineural (D006319) |
Parent Node:
Hypogonadism (D007006) |
..Starting node
.. Cerebellar Ataxia and Hypergonadotropic Hypogonadism (C565308)
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Child Nodes:
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Sister Nodes: |
..Alopecia hypogonadism extrapyramidal disorder (C537053)
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..Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism (C563370)
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..Bassoe syndrome (C537661)
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..Biemond syndrome type 2 (C535439)
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..Borjeson-Forssman-Lehmann syndrome (C536575)
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..Cantalamessa Baldini Ambrosi syndrome (C537981)
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..Cardiomyopathy hypogonadism collagenoma syndrome (C535582)
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..Cerebellar Ataxia and Hypergonadotropic Hypogonadism (C565308)
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..Cerebellar Ataxia and Hypogonadotropic Hypogonadism (C565870)
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..Chang Davidson Carlson syndrome (C538075)
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..Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism (C565850)
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..Chudley-Rozdilsky syndrome (C535458)
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..De Sanctis-Cacchione syndrome (C535992)
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..Deafness-Hypogonadism Syndrome (C564435)
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..Encephalopathy, Spastic Tetraparesis, and Hypogonadism (C565722)
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..Eunuchism (D005058)  2
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..Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis (C565295)
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..Hypergonadotropic Hypogonadism And Partial Alopecia (C567109)
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..Hypogonadism and Testicular Atrophy (C567108)
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..Hypogonadism with Low-Grade Mental Deficiency and Microcephaly (C565482)
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..Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies (C564406)
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..Ichthyosis and male hypogonadism (C537365)
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..Idiopathic Hypogonadotropic Hypogonadism (C562785)
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..Johnson neuroectodermal syndrome (C535882)
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..Kallmann Syndrome (D017436) 9
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..Klinefelter Syndrome (D007713)
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..Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
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..Lubinsky syndrome (C543092)
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..Malouf syndrome (C535703)
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..Martsolf syndrome (C536028)
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..MEHMO syndrome (C537451)
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..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
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..Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457)
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..Mineralocorticoid Deficiency, Isolated (C567596)
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..Moebius axonal neuropathy hypogonadism (C535806)
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..MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM (OMIM:300845)
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..Muscular dystrophy, congenital, infantile with cataract and hypogonadism (C537385)
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..Myopathy, Cataract, Hypogonadism Syndrome (C563578)
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..Progressive External Ophthalmoplegia With Hypogonadism (C563576)
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..Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
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..Richards-Rundle syndrome (C535674)
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..Rud Syndrome (C535878)
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..Scholte syndrome (C536638)
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..Seemanova Lesny syndrome (C537536)
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..Sexual Infantilism (D050035)
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..Slti Salem syndrome (C536673)
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..Vasquez Hurst Sotos syndrome (C536533)
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..Warburg Sjo Fledelius syndrome (C536681)
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..Weinstein Kliman Scully syndrome (C536688)
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..Woodhouse Sakati syndrome (C536742)
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..Young Hughes syndrome (C536715)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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