autosomal dominant nonsyndromic deafness 4A

Summary

DOID:0110573 - autosomal dominant nonsyndromic deafness 4A

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has_material_basis_in mutation in the MYH14 gene on chromosome 19q13.33.

Synonyms: DFNA4A, autosomal dominant deafness 4A,

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

: myh14

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A

MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A

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)