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mullerian aplasia and hyperandrogenism

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Deficiency of the glycoprotein WNT4, associated with loss of function mutation(s) in the WNT4 gene. The condition in 46,XX individuals is characterized by mild hyperandrogenism, absence of underdevelopment of the uterus, and sometimes absence of underdevelopment of the vagina.
Uniprot Description A disorder of sex development. Affected females manifest dysgenesis of Mullerian duct derivatives absent or rudimentary uterus and vagina, functional ovaries, primary amenorrhea, hyperandrogenism and hirsutism.
Mondo Term and Equivalent IDs
MONDO:0008019:  mullerian aplasia and hyperandrogenism
DOID:0111526: 
MESH:C567186: 
NCIT:C120376: 
Orphanet:247768: 
UMLS:C2675014: