Search Ontology:
Human Disease
primary ovarian insufficiency 9
- Term ID
- DOID:0080866
- Synonyms
-
- Definition
- A primary ovarian insufficiency that has_material_basis_in compound heterozygous mutation in the HFM1 gene on chromosome 1p22. https://pubmed.ncbi.nlm.nih.gov/24597873/
- References
- Ontology
- Human Disease ( DOID:0080866 )
- is a type of
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