NR5A1-related sex development disorder

MONDO:1060211

A reproductive system disorder caused by a variation in the NR5A1 gene, and characterized by varying phenotypes, including partial or complete gonadal dysgenesis, ambiguous genitalia, and spermatogenic failure in the male, and premature ovarian failure and ovarian dysgenesis in the female.

Also known as: NR5A1-related sex development disorder

0 clinical trials for this condition and its sub-types, 0 tagged with NR5A1-related sex development disorder itself.

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↑ Hereditary disease (18187) ↑ Reproductive system disorder (8533)

Sub-types of NR5A1-related sex development disorder

46,XX sex reversal 4 0 trials
46,XY sex reversal 3 0 trials
Premature ovarian failure 7 0 trials
Spermatogenic failure 8 0 trials

Including sub-types (0) Tagged with NR5A1-related sex development disorder (0)

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