autosomal dominant nonsyndromic deafness 6 (DOID:0110584)
Alliance: disease page
Synonyms: autosomal dominant deafness 6; autosomal dominant deafness 14; autosomal dominant deafness 38; DFNA6; DFNA14; DFNA38
Alt IDs: OMIM:600965, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.