Keratitis, Hereditary (KERH)

Keratitis, Hereditary, also known as keratitis, is related to kid syndrome and tyrosinemia, type ii, and has symptoms including visual disturbance An important gene associated with Keratitis, Hereditary is PAX6 (Paired Box 6), and among its related pathways/superpathways are IL-17 Family Signaling Pathways and Spinal cord injury. The drugs Adrenocorticotropic Hormone and beta-Endorphin have been mentioned in the context of this disorder. Affiliated tissues include eye and endothelial, and related phenotypes are keratitis and opacification of the corneal stroma