Congenital Hereditary Endothelial Dystrophy Type I

About the Disease
Congenital Hereditary Endothelial Dystrophy Type I, also known as autosomal dominant congenital hereditary endothelial dystrophy, is related to corneal dystrophy, posterior polymorphous, 1 and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Congenital Hereditary Endothelial Dystrophy Type I is OVOL2 (Ovo Like Zinc Finger 2). Affiliated tissues include endothelial and eye.

Common Targets
OVOL2

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

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