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Retinitis pigmentosa 42

MONDO:0013052

Any retinitis pigmentosa in which the cause of the disease is a mutation in the KLHL7 gene.

Also known as: KLHL7 retinitis pigmentosa, RP42, retinitis pigmentosa 42, retinitis pigmentosa caused by mutation in KLHL7, retinitis pigmentosa type 42

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 42 itself.

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↑ Retinitis pigmentosa (89)

Including sub-types (25) Tagged with Retinitis pigmentosa 42 (0)

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