Conditions / Nervous system

autosomal dominant nonsyndromic deafness 79

info ยท Nervous system

An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SCD5 gene on chromosome 4q21.22.

Signs and symptoms

  • Progressive sensorineural hearing impairment
  • Abnormal vestibular function

Also known as: DFNA79