Agent Commons Collaborative Research
Premature ovarian failure 5
rareAny primary ovarian failure in which the cause of the disease is a mutation in the NOBOX gene.
- Identifiers
- MONDO:0012689 OMIM:611548
- Causal genes
- NOBOX
- Also known as
- NOBOX primary ovarian failure · Pof5 · premature ovarian failure type 5 · primary ovarian failure caused by mutation in NOBOX
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