has material basis in germline mutation in WNT4 hereditary disease mullerian aplasia and hyperandrogenism https://www.malacards.org/card/mullerian_aplasia_and_hyperandrogenism OMIM:158330 GARD:0017195 Mullerian duct failure and hyperandrogenism UMLS:C2675014 NORD:1858 MESH:C567186 MEDGEN:390686 mullerian aplasia and hyperandrogenism 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. NCIT:C120376 WNT4 Deficiency Orphanet:247768 WNT4 deficiency Müllerian duct failure and hyperandrogenism DOID:0111526 MONDO:0008019 partial bilateral aplasia of the mullerian ducts