RLBP1-related retinopathy

MONDO:0100444

A retinopathy caused by bialleleic variants in the RLBP1 gene, often involving flecks in the retina.

Also known as: RLBP1 retinopathy, Bothnia retinal dystrophy, NFRCD, Newfoundland ROD-cone dystrophy, Newfoundland rod-cone dystrophy, RLBP1 cone-rod dystrophy, Vasterbotten dystrophy, Västerbotten dystrophy

36 clinical trials for this condition and its sub-types.

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