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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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Sub-types

Fundus albipunctatus (1) Retinitis punctata albescens (1) Bothnia retinal dystrophy (0) Newfoundland cone-rod dystrophy (0)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Eye disorder (97) Retinal disorder (79) Inherited retinal dystrophy (40) Retinal degeneration (40) Perceptual disorders (21) Human disease (14) Hereditary neurological disease (5)

Trials to join now! 23 Not yet recruiting 3 Not yet finished but already full! 1 Completed 7 Terminated 2

Free eye tests aim to catch vision loss early in harlem and washington heights

Knowledge-focused Ongoing

This study offers free vision screenings to underserved adults over 40 living in affordable housing in Harlem and Washington Heights. The goal is to find eye problems like glaucoma, cataracts, and diabetic retinopathy early and connect people with follow-up care. About 749 partic…

Phase: NA • Sponsor: Columbia University • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:54 UTC