Conditions / Nervous system

autosomal dominant nonsyndromic deafness 89

info ยท Nervous system

An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ATOH1 gene on chromosome 4q22.

Signs and symptoms

  • Hearing impairment

Also known as: DFNA89; autosomal dominant deafness 89