Human genes for autosomal dominant nonsyndromic deafness 22
Autosomal dominant nonsyndromic deafness 22 [DOID:0110552]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.
Synonyms: autosomal dominant nonsyndromic deafness 22, DOID:0110552, autosomal dominant deafness 22, DFNA22