Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110571 - autosomal dominant nonsyndromic deafness 48

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14.

Synonyms: autosomal dominant deafness 48, DFNA48

Xenbase Genes : myo1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011920 - autosomal dominant nonsyndromic hearing loss 48


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)