Retinitis pigmentosa 49

MONDO:0013405

Any retinitis pigmentosa in which the cause of the disease is a mutation in the CNGA1 gene.

Also known as: CNGA1 retinitis pigmentosa, RP49, retinitis pigmentosa 49, retinitis pigmentosa caused by mutation in CNGA1, retinitis pigmentosa type 49

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 49 itself.

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Where it sits in the disease tree

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Part of

↑ Retinitis pigmentosa (89) ↑ CNGA1-related retinopathy (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 49 (0)

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