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Up to: Inherited lipid metabolism disorder · Developmental anomaly of metabolic origin · 46,XY disorder of sex development
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
A rare disorder of sex development (DSD) due to a defect in metabolizing testosterone to dihydrotestosterone and characterized by incomplete intrauterine masculinization which ranges from a female genitalia with a blind vaginal pouch to a fully male phenotype with pseudovaginal posterior hypospadias and micropenis.
This condition has no sub-types.