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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

Xenbase Genes : pou4f3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011226 - autosomal dominant nonsyndromic hearing loss 15

OMIM:
OMIM: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)