DISEASES

Disease-gene associations mined from literature

Human genes for autosomal dominant nonsyndromic deafness 2B

Autosomal dominant nonsyndromic deafness 2B [DOID:0110559]

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:  autosomal dominant nonsyndromic deafness 2B,  DOID:0110559,  DFNA2B,  autosomal dominant deafness 2B