autosomal recessive nonsyndromic deafness 114

An autosomal recessive nonsyndromic deafness characterized by congenital profound sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the GRAP gene on chromosome 17p11.2.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB114; autosomal recessive deafness 114