autosomal dominant nonsyndromic deafness 2B

Summary

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 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

: gjb3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012976 - autosomal dominant nonsyndromic hearing loss 2B

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)