premature ovarian failure 1
Findings
No curated finding names premature ovarian failure 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any primary ovarian failure in which the cause of the disease is a mutation in the FMR1 gene.
Definition from the Mondo Disease Ontology (MONDO:0010706), read 2026-09-29. CC BY 4.0.
- Inheritance
- X-linked inheritance
- Onset and course
- Adult onset
HPO, annotations 2026-09-02
Features
1 feature
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Premature ovarian insufficiencyHPOHP:0008209
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- A kind of
- Narrower terms (1)
Other names
4 names
Resolves to: premature ovarian failure 1
- Also called
- FMR1 primary ovarian failurefragile x-associated primary ovarian insufficiencypremature ovarian failure type 1primary ovarian failure caused by mutation in FMR1