autosomal dominant nonsyndromic deafness 20 (DOID:0110550)
Alliance: disease page
Synonyms: autosomal dominant deafness 20; DFNA20; DFNA26
Alt IDs: OMIM:604717, 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 ACTG1 gene on chromosome 17q25.