primary ovarian insufficiency 7

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Summary

Literature (0)

DOID:0080864 - primary ovarian insufficiency 7

Disease Ontology Definition:A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33.

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

: nr5a1

MIM:

MIM:612964 - PREMATURE OVARIAN FAILURE 7; POF7

MIM:612964 - PREMATURE OVARIAN FAILURE 7; POF7

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)