Early-onset Severe Retinal Dystrophy

About the Disease
Leber Congenital Amaurosis 14, also known as lca14, is related to stargardt disease 1 and severe early-childhood-onset retinal dystrophy, and has symptoms including photophobia An important gene associated with Leber Congenital Amaurosis 14 is LRAT (Lecithin Retinol Acyltransferase), and among its related pathways/superpathways are Visual phototransduction and Ciliary landscape. Affiliated tissues include retina, eye and bone, and related phenotypes are nystagmus and photophobia

Common Targets
PRPH2 | PRPF8 | CEP290 | RP1 | RPGR

Note: If you'd like to get a target analysis report for Early-onset Severe Retinal Dystrophy, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Early-onset Severe Retinal Dystrophy at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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