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.

Also known as: RP 7, RP7, retinitis pigmentosa 7, retinitis pigmentosa type 7

33 clinical trials for this condition and its sub-types.