Conditions / Genetic
Usher syndrome type 1D
info · Genetic · ICD-10: H35.5
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.
Signs and symptoms
- Abnormal vestibular function
- Hearing impairment
- Rod-cone dystrophy
Also known as: USH1D; Usher syndrome type ID