autosomal recessive nonsyndromic deafness 112

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.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB112; autosomal recessive deafness 112