autosomal dominant nonsyndromic deafness 15

Summary

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: autosomal dominant deafness 15, autosomal dominant deafness 52, autosomal dominant nonsyndromic deafness 52, DFNA15, DFNA52

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

: pou4f3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011226 - autosomal dominant nonsyndromic hearing loss 15

MONDO:0011226 - autosomal dominant nonsyndromic hearing loss 15

MIM:

MIM:602459 - DEAFNESS, AUTOSOMAL DOMINANT 15; DFNA15

MIM:602459 - DEAFNESS, AUTOSOMAL DOMINANT 15; DFNA15

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

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

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