Conditions / Nervous system
autosomal recessive nonsyndromic deafness 101
info · Nervous system · ICD-10: H90.3
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32.
Signs and symptoms
- Bilateral sensorineural hearing impairment
- Abnormal vestibular function
- Visual impairment
Also known as: DFNB101; autosomal recessive deafness 101