autosomal recessive nonsyndromic deafness 110

An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal vestibular function

Also known as: DFNB110; autosomal recessive deafness 110