Human genes for autosomal dominant nonsyndromic deafness 17
Autosomal dominant nonsyndromic deafness 17 [DOID:0110548]
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 MYH9 gene on chromosome 22q12.
Synonyms: autosomal dominant nonsyndromic deafness 17, DOID:0110548, autosomal dominant deafness 17, DFNA17