Term Name:	autosomal recessive nonsyndromic deafness 1B
Synonyms:	autosomal recessive deafness 1B, DFNB1B
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 GJB6 gene on chromosome 13q12.
Ontology:	Human Disease [DOID:0110476]   ( DOID:0110476 )