autosomal dominant nonsyndromic deafness 6

Summary

DOID:0110584 - autosomal dominant nonsyndromic deafness 6

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.

Synonyms: autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6, DFNA14, DFNA38, DFNA6, DFNA6/14/38

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

: wfs1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010963 - trunk and cervical myotome group

MONDO:0010963 - trunk and cervical myotome group

MIM:

MIM:600965 - DEAFNESS, AUTOSOMAL DOMINANT 6; DFNA6

MIM:600965 - DEAFNESS, AUTOSOMAL DOMINANT 6; DFNA6

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)