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

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