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