Conditions / Genetic
retinitis pigmentosa 9
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the RP9 gene on chromosome 7p14.
Signs and symptoms
- Constriction of peripheral visual field
- Spicular pigmentation of the retina
- Nyctalopia
- Rod-cone dystrophy
- Undetectable light- and dark-adapted electroretinogram
- Macular edema
- Cataract
- Macular atrophy
Also known as: RP9