| Disease Browser
|
Parent Node:
 Alopecia (D000505) |
Parent Node:
Hypogonadism (D007006) |
..Starting node
.. Slti Salem syndrome (C536673)
|
Child Nodes:
|
Sister Nodes: |
..Alopecia hypogonadism extrapyramidal disorder (C537053)
|
..Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism (C563370)
|
..Bassoe syndrome (C537661)
|
..Biemond syndrome type 2 (C535439)
|
..Borjeson-Forssman-Lehmann syndrome (C536575)
|
..Cantalamessa Baldini Ambrosi syndrome (C537981)
|
..Cardiomyopathy hypogonadism collagenoma syndrome (C535582)
|
..Cerebellar Ataxia and Hypergonadotropic Hypogonadism (C565308)
|
..Cerebellar Ataxia and Hypogonadotropic Hypogonadism (C565870)
|
..Chang Davidson Carlson syndrome (C538075)
|
..Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism (C565850)
|
..Chudley-Rozdilsky syndrome (C535458)
|
..De Sanctis-Cacchione syndrome (C535992)
|
..Deafness-Hypogonadism Syndrome (C564435)
|
..Encephalopathy, Spastic Tetraparesis, and Hypogonadism (C565722)
|
..Eunuchism (D005058)  2
|
..Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis (C565295)
|
..Hypergonadotropic Hypogonadism And Partial Alopecia (C567109)
|
..Hypogonadism and Testicular Atrophy (C567108)
|
..Hypogonadism with Low-Grade Mental Deficiency and Microcephaly (C565482)
|
..Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies (C564406)
|
..Ichthyosis and male hypogonadism (C537365)
|
..Idiopathic Hypogonadotropic Hypogonadism (C562785)
|
..Johnson neuroectodermal syndrome (C535882)
|
..Kallmann Syndrome (D017436) 9
|
..Klinefelter Syndrome (D007713)
|
..Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
|
..Lubinsky syndrome (C543092)
|
..Malouf syndrome (C535703)
|
..Martsolf syndrome (C536028)
|
..MEHMO syndrome (C537451)
|
..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
|
..Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457)
|
..Mineralocorticoid Deficiency, Isolated (C567596)
|
..Moebius axonal neuropathy hypogonadism (C535806)
|
..MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM (OMIM:300845)
|
..Muscular dystrophy, congenital, infantile with cataract and hypogonadism (C537385)
|
..Myopathy, Cataract, Hypogonadism Syndrome (C563578)
|
..Progressive External Ophthalmoplegia With Hypogonadism (C563576)
|
..Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
|
..Richards-Rundle syndrome (C535674)
|
..Rud Syndrome (C535878)
|
..Scholte syndrome (C536638)
|
..Seemanova Lesny syndrome (C537536)
|
..Sexual Infantilism (D050035)
|
..Slti Salem syndrome (C536673)
|
..Vasquez Hurst Sotos syndrome (C536533)
|
..Warburg Sjo Fledelius syndrome (C536681)
|
..Weinstein Kliman Scully syndrome (C536688)
|
..Woodhouse Sakati syndrome (C536742)
|
..Young Hughes syndrome (C536715)
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
