autosomal dominant nonsyndromic deafness 20

Summary

DOID:0110550 - autosomal dominant nonsyndromic deafness 20

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 ACTG1 gene on chromosome 17q25.

Synonyms: DFNA26, autosomal dominant deafness 20, DFNA20

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

: actg1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011480 - autosomal dominant nonsyndromic hearing loss 20

MONDO:0011480 - autosomal dominant nonsyndromic hearing loss 20

MIM:

MIM:604717 - DEAFNESS, AUTOSOMAL DOMINANT 20; DFNA20

MIM:604717 - DEAFNESS, AUTOSOMAL DOMINANT 20; DFNA20

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

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

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