Conditions / Genetic
retinitis pigmentosa 35
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the SEMA4A gene on chromosome 1q22.
Signs and symptoms
- Nyctalopia
- Blindness
- Reduced visual acuity
- Rod-cone dystrophy
Also known as: RP35