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Summary Literature (0)
DOID:0080866 - primary ovarian insufficiency 9

Disease Ontology Definition:A primary ovarian insufficiency that has_material_basis_in compound heterozygous mutation in the HFM1 gene on chromosome 1p22.

Synonyms:

Xenbase Genes : hfm1


MIM:
MIM:615724 - PREMATURE OVARIAN FAILURE 9; POF9

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), primary ovarian insufficiency (is_a)