Retinitis pigmentosa 51

MONDO:0013274

Any retinitis pigmentosa in which the cause of the disease is a mutation in the TTC8 gene.

Also known as: RP51, TTC8 retinitis pigmentosa, retinitis pigmentosa 51, retinitis pigmentosa caused by mutation in TTC8, retinitis pigmentosa type 51

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 51 itself.

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Part of

↑ Retinitis pigmentosa (89) ↑ Retinal ciliopathy (2) ↑ TTC8-related ciliopathy (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 51 (0)

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