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Retinitis pigmentosa 56

MONDO:0013314

Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPG2 gene.

Also known as: IMPG2 retinitis pigmentosa, RP56, retinitis pigmentosa 56, retinitis pigmentosa caused by mutation in IMPG2, retinitis pigmentosa type 56, maculopathy, Impg2-related

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 56 itself.

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Part of

↑ Retinitis pigmentosa (89) ↑ IMPG2-related recessive retinopathy (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 56 (0)

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