Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Retinitis pigmentosa · PRPH2-related retinopathy
Retinitis pigmentosa 7
A retinitis pigmentosain which the cause of the disease is a variation in the RDS gene (PRPH2). A digenic form of retinitis pigmentosa, resulting from a mutation in the RDS gene and a null mutation of the ROM1 gene, has also been reported.
This condition has no sub-types.