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Retinitis pigmentosa 7

MONDO:0011974

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

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 7 itself.

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↑ Retinitis pigmentosa (89) ↑ PRPH2-related retinopathy (2)

Including sub-types (25) Tagged with Retinitis pigmentosa 7 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.