autosomal recessive nonsyndromic deafness 1A (DOID:0110475)
Alliance: disease page
Synonyms: autosomal recessive deafness 1A; DFNB1A
Alt IDs: OMIM:220290, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.