Cone Dystrophy

About the Disease
Cone Dystrophy, also known as retinal cone dystrophy, is related to retinal cone dystrophy 3b and progressive cone dystrophy, and has symptoms including photophobia An important gene associated with Cone Dystrophy is GUCY2D (Guanylate Cyclase 2D, Retinal), and among its related pathways/superpathways are Visual phototransduction and Visual Cycle in Retinal Rods. The drugs Anti-Infective Agents and interferons have been mentioned in the context of this disorder. Affiliated tissues include retina, eye and liver, and related phenotypes are no effect and no effect

Common Targets
KCNV2 | GUCY2D | PRPH2 | CLN3 | CRX | NMNAT1 | CEP290 | GUCA1A | ABCA4 | POC1B | TULP1 | OPN1LW | PROM1 | IMPG1 | RAB28 | PITPNM3 | CDHR1 | RPGR | TTLL5 | VAX2 | OPN1MW | RP1L1 | AIPL1

Note: If you'd like to get a target analysis report for Cone 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 Cone Dystrophy at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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