autosomal recessive nonsyndromic deafness 113

An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the CEACAM16 gene on chromosome 19q13.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal vestibular function

Also known as: DFNB113; autosomal recessive deafness 113