autosomal recessive nonsyndromic deafness 76

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has_material_basis_in mutation in the SYNE4 gene on chromosome 19q13.

Signs and symptoms

• Progressive sensorineural hearing impairment

Also known as: DFNB76; autosomal recessive deafness 76