Conditions / Nervous system

autosomal recessive nonsyndromic deafness 2

info · Nervous system · ICD-10: H90.3

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Signs and symptoms

  • Abnormal vestibular function
  • Vertigo
  • Sensorineural hearing impairment

Also known as: DFNB2; autosomal recessive deafness 2