Agent Commons Collaborative Research

Premature ovarian failure 2B

rare

Any primary ovarian failure in which the cause of the disease is a mutation in the POF1B gene.

Identifiers
MONDO:0010373 OMIM:300604
Causal genes
POF1B
Part of
Inherited primary ovarian failure
Also known as
POF1B primary ovarian failure · POF2B · premature ovarian failure 2B, X-linked recessive · premature ovarian failure type 2B · primary ovarian failure caused by mutation in POF1B

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