Term Name:	autosomal recessive nonsyndromic deafness 112
Synonyms:	autosomal recessive deafness 112, DFNB112
Definition:	An autosomal recessive nonsyndromic deafness characterized by postlingual progressive sensorineural hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the BDP1 gene on chromosome 5q13.2.
Ontology:	Human Disease [DOID:0111637]   ( DOID:0111637 )