Conditions / Syndrome
Usher syndrome type 1C
info · Syndrome · ICD-10: H35.5
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15.
Signs and symptoms
- Vestibular hyporeflexia
- Rod-cone dystrophy
- Congenital sensorineural hearing impairment
Also known as: USH1C; Usher syndrome type I Acadian variety; Usher syndrome type IC