Conditions / Syndrome
Usher syndrome type 2D
info · Syndrome · ICD-10: H35.5
An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32.
Signs and symptoms
- Hearing impairment
- Nyctalopia
- Rod-cone dystrophy
- Abnormal vestibular function
Also known as: USH2D; Usher syndrome type IID