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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models