Human genes for autosomal recessive nonsyndromic deafness 1B
Autosomal recessive nonsyndromic deafness 1B [DOID:0110476]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.
Synonyms: autosomal recessive nonsyndromic deafness 1B, DOID:0110476, autosomal recessive deafness 1B, DFNB1B