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IMPDH1-related retinopathy
MONDO:1040051Any retinopathy caused by a variant in the IMPDH1 gene.
Also known as: IMPDH1-related retinopathy
25 clinical trials for this condition and its sub-types, 0 tagged with IMPDH1-related retinopathy itself.
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Browse by category →Sub-types of IMPDH1-related retinopathy
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Leber congenital amaurosis 11 0 trials
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Retinitis pigmentosa 10 0 trials
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.