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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
46 XX gonadal dysgenesis +   
46, XX Disorders of Sex Development +   
46, XX Testicular Disorders of Sex Development +   
46, XY Disorders of Sex Development +   
Adrenogenital Syndrome +   
androgen insensitivity syndrome +   
aromatase excess syndrome  
Campomelic Dysplasia with Autosomal Sex Reversal  
congenital adrenal hyperplasia +   
cortisone reductase deficiency +   
Female Pseudohermaphroditism with Skeletal Anomalies 
freemartinism 
gonadal dysgenesis +   
gynecomastia +   
hermaphroditism 
hyperandrogenism +   
A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is negligible. In women, the common manifestations are HIRSUTISM and VIRILISM as seen in patients with POLYCYSTIC OVARY SYNDROME and ADRENOCORTICAL HYPERFUNCTION.
Michels Caskey Syndrome 
MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME  
Mullerian Aplasia  
Ovotesticular Disorders of Sex Development +   
pseudohermaphroditism +   
Sex Chromosome Disorders of Sex Development +   
Verloes Gillerot Fryns Syndrome 

Synonyms
Exact Synonyms: hyperandrogenization syndrome
Primary IDs: MESH:D017588
Alternate IDs: RDO:0003503
Definition Sources: MESH:D017588

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