DISEASES

Disease-gene associations mined from literature

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,  DFNA17,  autosomal dominant deafness 17