DISEASES

Disease-gene associations mined from literature

Human genes for autosomal dominant nonsyndromic deafness 3A

Autosomal dominant nonsyndromic deafness 3A [DOID:0110564]

An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.

Synonyms:  autosomal dominant nonsyndromic deafness 3A,  DOID:0110564,  autosomal dominant deafness 3A,  DFNA3A