autosomal dominant nonsyndromic deafness 5

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life and high frequency progressive hearing loss, and has_material_basis_in heterozygous mutation in the gasdermin E (GSDME) gene on chromosome 7p15.

Signs and symptoms

• Progressive sensorineural hearing impairment

Also known as: DFNA5; autosomal dominant deafness 5