IMPG1-related recessive retinopathy

MONDO:1040037

Any retinopathy caused by autosomal recessive variants in the IMPG1 gene.

Also known as: IMPG1-related recessive retinopathy

25 clinical trials for this condition and its sub-types, 0 tagged with IMPG1-related recessive retinopathy itself.

Where it sits in the disease tree

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Sub-types of IMPG1-related recessive retinopathy

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