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.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by