has material basis in autosomal dominant disease 46,XY sex reversal 11 disease_ontology A 46 XY sex reversal characterized by a genital phenotype that may range from predominantly female to predominantly male, including marked sex ambiguity depending on the duration of normal testicular function prior to the loss of testicular tissue and that has_material_basis_in heterozygous mutation in the DHX37 gene on chromosome 12q24.31. DOID:0061369 MIM:273250 SRXY11 TRS embryonic testicular regression familial anorchia testicular regression syndrome xy gonadal agenesis/dysgenesis syndrome 46,XY complete gonadal dysgenesis autosomal dominant inheritance