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:0110559 - autosomal dominant nonsyndromic deafness 2B

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has_material_basis_in mutation in the GJB3 gene on chromosome 1p34.3.

Synonyms: DFNA2B, autosomal dominant deafness 2B

Xenbase Genes : gjb3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012976 - autosomal dominant nonsyndromic hearing loss 2B

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)