Congenital Hereditary Endothelial Dystrophy Type II

About the Disease
Corneal Endothelial Dystrophy, also known as congenital hereditary endothelial dystrophy of cornea, is related to corneal dystrophy and perceptive deafness and corneal dystrophy, endothelial, x-linked. An important gene associated with Corneal Endothelial Dystrophy is SLC4A11 (Solute Carrier Family 4 Member 11). The drugs Prednisolone phosphate and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include endothelial, eye and neutrophil, and related phenotypes are corneal opacity and corneal stromal edema

Common Targets
SLC4A11

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