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Ontology Browser

Parent Terms Term With Siblings Child Terms
hypogonadism +     
46, XX Disorders of Sex Development +   
46, XY Disorders of Sex Development +   
Adrenogenital Syndrome +   
Alopecia, Hypogonadism, Extrapyramidal Disorder 
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism 
androgen insensitivity syndrome +   
Bassoe Syndrome 
Biemond Syndrome II 
Borjeson-Forssman-Lehmann syndrome  
Boucher-Neuhauser syndrome  
Campomelic Dysplasia with Autosomal Sex Reversal  
Cantalamessa Baldini Ambrosi Syndrome 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Chang Davidson Carlson Syndrome 
Chudley-Rozdilsky Syndrome 
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
De Sanctis-Cacchione Syndrome  
Deafness-Hypogonadism Syndrome 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome  
Encephalopathy, Spastic Tetraparesis, and Hypogonadism 
eunuchism +   
gonadal dysgenesis +   
A number of syndromes with defective gonadal developments such as streak GONADS and dysgenetic testes or ovaries. The spectrum of gonadal and sexual abnormalities is reflected in their varied sex chromosome (SEX CHROMOSOMES) constitution as shown by the karyotypes of 45,X monosomy (TURNER SYNDROME); 46,XX (GONADAL DYSGENESIS, 46XX); 46,XY (GONADAL DYSGENESIS, 46,XY); and sex chromosome MOSAICISM; (GONADAL DYSGENESIS, MIXED). Their phenotypes range from female, through ambiguous, to male. This concept includes gonadal agenesis.
gynecomastia +   
hyperandrogenism +   
Hypergonadotropic Hypogonadism And Partial Alopecia 
Hypogonadism and Testicular Atrophy 
Hypogonadism with Low-Grade Mental Deficiency and Microcephaly 
hypogonadotropic hypogonadism +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Ichthyosis and Male Hypogonadism 
Isolated Mineralocorticoid Deficiency  
Johnson Neuroectodermal Syndrome 
Klinefelter's syndrome  
Lubinsky Syndrome 
Male Hypogonadism with Mental Retardation and Skeletal Anomalies 
Martsolf syndrome  
MEHMO syndrome  
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Moebius Axonal Neuropathy Hypogonadism 
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism  
Myopathy, Cataract, Hypogonadism Syndrome 
Ovotesticular Disorders of Sex Development +   
Progressive External Ophthalmoplegia with Hypogonadism 
pseudohermaphroditism +   
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Richards-Rundle Syndrome 
Rud Syndrome 
Scholte Syndrome 
Seemanova Lesny Syndrome 
Sex Chromosome Disorders of Sex Development +   
Sexual Infantilism  
Slti Salem Syndrome 
syndromic X-linked intellectual disability Cabezas type  
Vasquez Hurst Sotos Syndrome 
Verloes Gillerot Fryns Syndrome 
Warburg micro syndrome +   
Weinstein Kliman Scully Syndrome 
Woodhouse-Sakati Syndrome  
Young Hughes Syndrome 

Exact Synonyms: Gonadal Agenesis ;   gonadal dysgenesis syndrome
Primary IDs: MESH:D006059
Alternate IDs: RDO:0000821
Xrefs: GARD:2538 ;   ICD9CM:758.6 ;   NCI:C61420
Definition Sources: MESH:D006059,

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.