autosomal recessive nonsyndromic deafness 112 (DOID:0111637)
Alliance: disease page
Synonyms: autosomal recessive deafness 112; DFNB112
Alt IDs: OMIM:618257
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.