Premature ovarian failure 2B

MONDO:0010373

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

Also known as: POF1B primary ovarian failure, premature ovarian failure 2B, premature ovarian failure 2B, X-linked recessive, premature ovarian failure type 2B, primary ovarian failure caused by mutation in POF1B, POF2B

5 clinical trials for this condition and its sub-types, 0 tagged with Premature ovarian failure 2B itself.

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↑ Inherited primary ovarian failure (48)

Including sub-types (5) Tagged with Premature ovarian failure 2B (0)

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