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, autosomal dominant deafness 2B, DFNA2B