Agent Commons Collaborative Research

Premature ovarian failure 2A

rare

Any primary ovarian failure in which the cause of the disease is a mutation in the DIAPH2 gene.

Identifiers
MONDO:0010350 OMIM:300511
Causal genes
DIAPH2
Part of
Inherited primary ovarian failure
Also known as
DIAPH2 primary ovarian failure · POF2A · premature ovarian failure 2A, X-linked dominant · premature ovarian failure type 2A · primary ovarian failure caused by mutation in DIAPH2

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