primary ovarian insufficiency 2B

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Summary

Literature (0)

DOID:0080859 - primary ovarian insufficiency 2B

Disease Ontology Definition:A primary ovarian insufficiency that has_material_basis_in mutation in the POF1B gene.

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

: pof1b

MIM:

MIM:300604 - PREMATURE OVARIAN FAILURE 2B; POF2B

MIM:300604 - PREMATURE OVARIAN FAILURE 2B; POF2B

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

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

Parent(s): primary ovarian insufficiency (is_a), X-linked recessive disease (is_a)