autosomal dominant nonsyndromic deafness 22 (DOID:0110552)
Alliance: disease page
Synonyms: autosomal dominant deafness 22; DFNA22
Alt IDs: OMIM:606346, 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 MYO6 gene on chromosome 6q14.