Retinitis pigmentosa 3

MONDO:0010227

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

Also known as: RP3, RPGR retinitis pigmentosa, retinitis pigmentosa 3, retinitis pigmentosa caused by mutation in RPGR, retinitis pigmentosa type 3, Choroidoretinal Degeneration with retinal reflex in heterozygous Women, cone-rod Degeneration, X-linked, retinitis pigmentosa 15

38 clinical trials for this condition and its sub-types.

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