autosomal dominant nonsyndromic deafness 15

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Summary

Literature (0)

DOID:0110546 - autosomal dominant nonsyndromic deafness 15

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.

Synonyms: DFNA15, autosomal dominant deafness 15,

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

: pou4f3

OMIM:

MIM:602459 - deafness, autosomal dominant 15; dfna15

MIM:602459 - deafness, autosomal dominant 15; dfna15

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

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

Parent(s): autosomal dominant nonsyndromic deafness (is_a)