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RPGR-related retinopathy

MONDO:0100437

A retinopathy caused by a variant in the X-linked gene, RPGR.

Also known as: RPGR retinopathy, RPGR-related retinopathy with or without sino-oto-pulmonary symptoms, COD1, CORDX1, RP3, RPGR retinitis pigmentosa, X-linked cone dystrophy 1, X-linked cone-rod dystrophy 1

32 clinical trials for this condition and its sub-types, 0 tagged with RPGR-related retinopathy itself.

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Where it sits in the disease tree

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Part of

↑ Inherited retinal dystrophy (513)

Sub-types of RPGR-related retinopathy

Retinitis pigmentosa 3 7 trials
X-linked cone-rod dystrophy 1 0 trials
Macular degeneration, X-linked atrophic 0 trials

Including sub-types (32) Tagged with RPGR-related retinopathy (0)

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