Retinitis pigmentosa 7, digenic

MONDO:1060144

A digenic form of retinitis pigmentosa resulting from a mutation in the PRPH2 gene and a null mutation of the ROM1 gene, leading to progressive degeneration of the retina and vision loss.

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

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

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

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