autosomal dominant nonsyndromic deafness 3A (DOID:0110564)
Alliance: disease page
Synonyms: autosomal dominant deafness 3A; DFNA3A
Alt IDs: OMIM:601544, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.