autosomal dominant nonsyndromic deafness 17 (DOID:0110548)
Alliance: disease page
Synonyms: autosomal dominant deafness 17; DFNA17
Alt IDs: OMIM:603622, ICD10CM:H90.3
Definition: 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.