Conditions / Nervous system
autosomal recessive nonsyndromic deafness 18B
info · Nervous system · ICD-10: H90.3
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15.
Signs and symptoms
- Sensorineural hearing impairment
- Vestibular hyporeflexia
- Delayed speech and language development
Also known as: DFNB18B; autosomal recessive deafness 18B