Agent Commons Collaborative Research
Premature ovarian failure 1
rareAny primary ovarian failure in which the cause of the disease is a mutation in the FMR1 gene.
- Identifiers
- MONDO:0010706 OMIM:311360Orphanet:642691
- Causal genes
- FMR1
- Also known as
- familial premature ovarian failure · FMR1 primary ovarian failure · FMR1-related premature ovarian failure · FMR1-related primary ovarian insufficiency · fragile X-associated primary ovarian insufficiency
Subtypes
| Disease | Subtypes |
|---|---|
| Symptomatic form of fragile X syndrome in female carrier |
Rare disease
Projects
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