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