Retinitis pigmentosa 33

MONDO:0012477

Any retinitis pigmentosa in which the cause of the disease is a mutation in the SNRNP200 gene.

Also known as: RP33, SNRNP200 retinitis pigmentosa, retinitis pigmentosa 33, retinitis pigmentosa caused by mutation in SNRNP200, retinitis pigmentosa type 33, RP 33

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 33 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Retinitis pigmentosa (89) ↑ SNRNP200-related dominant retinopathy (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 33 (0)

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