Retinitis pigmentosa 41

MONDO:0012796

Any retinitis pigmentosa in which the cause of the disease is a mutation in the PROM1 gene.

Also known as: PROM1 retinitis pigmentosa, RP41, retinitis pigmentosa 41, retinitis pigmentosa caused by mutation in PROM1, retinitis pigmentosa type 41, RP 41, retinal Degeneration, autosomal recessive, prominin-related

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 41 itself.

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Part of

↑ Retinitis pigmentosa (89) ↑ PROM1-related recessive retinopathy (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 41 (0)

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