OBO ID: DOID:0080866
Term Name: primary ovarian insufficiency 9 Search Ontology:
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)
OTHER primary ovarian insufficiency 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HFM1 Premature ovarian failure 9 615724
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None