Search Ontology:
Human Disease
primary ovarian insufficiency 3
- Term ID
- DOID:0080860
- Synonyms
-
- Definition
- A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22. https://pubmed.ncbi.nlm.nih.gov/12149404/
- References
- Ontology
- Human Disease ( DOID:0080860 )
- is a type of
-
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