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Retinitis pigmentosa 17

MONDO:0010945

Any retinitis pigmentosa caused by duplication or triplication in the chromosome 17q22-q23 region that results in disruption of topologically associated domains (TADs) and increased retinal expression of GDPD1.

Also known as: CA4 retinitis pigmentosa, RP17, retinitis pigmentosa 17, retinitis pigmentosa caused by mutation in CA4, retinitis pigmentosa type 17, RP 17

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 17 itself.

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