Conditions / Nervous system

autosomal dominant nonsyndromic deafness 2A

info · Nervous system · ICD-10: H90.3

An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2.

Signs and symptoms

Hearing impairment
Tinnitus

Also known as: DFNA2A; autosomal dominant deafness 2A