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LCA5-related retinopathy

MONDO:0100445

A retinopathy caused by biallelic variants in the LCA5 gene.

Also known as: LCA5 retinopathy, LCA5-related retinopathy, LCA5, LCA5 Leber congenital amaurosis, Leber congenital amaurosis 5, Leber congenital amaurosis caused by mutation in LCA5, Leber congenital amaurosis type 5, amaurosis congenita of Leber, type 5

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

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Sub-types

Leber congenital amaurosis 5 (2)

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! 22 Not yet recruiting 4 Not yet finished but already full! 1 Completed 6 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