primary ovarian insufficiency 5

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Summary

Literature (0)

DOID:0080862 - primary ovarian insufficiency 5

Disease Ontology Definition:A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NOBOX gene on chromosome 7q35.

Synonyms:

Xenbase 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

MIM:

MIM:611548 - PREMATURE OVARIAN FAILURE 5; POF5

MIM:611548 - PREMATURE OVARIAN FAILURE 5; POF5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), primary ovarian insufficiency (is_a)