DISEASES

Disease-gene associations mined from literature

Human genes for Mullerian aplasia and hyperandrogenism

Mullerian aplasia and hyperandrogenism [DOID:0111526]

A disorder of sexual development characterized by primary amenorrhea, an underdeveloped or absent uterus, and clinical hyperandrogenism that has_material_basis_in heterozygous mutation in WNT4 on chromosome 1p36.12.

Synonyms:  Mullerian aplasia and hyperandrogenism,  DOID:0111526,  Mullerian aplasia and hyperandrogenisms,  Mullerian duct failure and hyperandrogenism,  WNT4 deficiency ...