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