SNRNP200-related dominant retinopathy

MONDO:0800098

A retinopathy caused by heterozygous variants in the SNRNP200 gene.

Also known as: SNRNP200-related dominant retinopathy, 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 SNRNP200-related dominant retinopathy itself.

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↑ Inherited retinal dystrophy (513)

Sub-types of SNRNP200-related dominant retinopathy

Retinitis pigmentosa 33 0 trials

Including sub-types (25) Tagged with SNRNP200-related dominant retinopathy (0)

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