Retinitis pigmentosa 23

MONDO:0010320

Any retinitis pigmentosa in which the cause of the disease is a mutation in the OFD1 gene.

Also known as: OFD1 retinitis pigmentosa, RP23, retinitis pigmentosa 23, retinitis pigmentosa 23, X-linked recessive, retinitis pigmentosa caused by mutation in OFD1, retinitis pigmentosa type 23, RP 23

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 23 itself.

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Part of

↑ Retinitis pigmentosa (89) ↑ Retinal ciliopathy (2) ↑ OFD1-related ciliopathy (1)

Including sub-types (25) Tagged with Retinitis pigmentosa 23 (0)

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