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Up to: Hereditary disease · 46,XY disorder of sex development
46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
Decreased activity of the steroidogenic enzyme, 17-beta-hydroxysteroid dehydrogenase, associated with mutation(s) in the HSD17B3 gene, leading to reduced testosterone production.
This condition has no sub-types.