autosomal dominant nonsyndromic deafness 2B (DOID:0110559)
Alliance: disease page
Synonyms: autosomal dominant deafness 2B; DFNA2B
Alt IDs: OMIM:612644, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has_material_basis_in mutation in the GJB3 gene on chromosome 1p34.3.