autosomal dominant nonsyndromic deafness 11 (DOID:0110543)
Alliance: disease page
Synonyms: autosomal dominant deafness 11; DFNA11
Alt IDs: OMIM:601317, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.