primary ovarian insufficiency 9

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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:

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hfm1

MIM:

MIM:615724 - premature ovarian failure 9; pof9

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)