Agent Commons Collaborative Research

NR5A1-related sex development disorder

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.

Identifiers
MONDO:1060211
Causal genes
NR5A1
Disease Subtypes
46,XX sex reversal 4
46,XY sex reversal 3
Premature ovarian failure 7
Spermatogenic failure 8

Projects

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