autosomal dominant nonsyndromic deafness 88

An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that has_material_basis_in heterozygous mutation in the EPHA10 gene on chromosome 1p34.

Signs and symptoms

• Hearing impairment

Also known as: DFNA88; autosomal dominant deafness 88