Retinitis pigmentosa 18

MONDO:0011075

Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF3 gene.

Also known as: PRPF3 retinitis pigmentosa, RP18, retinitis pigmentosa 18, retinitis pigmentosa caused by mutation in PRPF3, retinitis pigmentosa type 18, RP 18

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 18 itself.

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↑ Retinitis pigmentosa (89)

Including sub-types (25) Tagged with Retinitis pigmentosa 18 (0)

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