Conditions / Nervous system
autosomal dominant nonsyndromic deafness 4B
info · Nervous system · ICD-10: H90.3
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.
Signs and symptoms
- Sensorineural hearing impairment
- Abnormal vestibular function
- Visual impairment
Also known as: DFNA4B; autosomal dominant deafness 4B