Keratitis

About the Disease
Keratitis, Hereditary, also known as keratitis, is related to keratitis-ichthyosis-deafness syndrome, autosomal dominant and aspergillosis, 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 IL27-mediated signaling events and IL-17 Family Signaling Pathways. The drugs Amphotericin B and Liposomal amphotericin B have been mentioned in the context of this disorder. Affiliated tissues include eye, endothelial and t cells, and related phenotypes are keratitis and opacification of the corneal stroma

Common Targets
Interleukin-1 receptor-associated kinase (IRAK) (nonspecified subtype) | Protein Phosphatase 2B | PPIA | G114548 | JAK1 | G3576 | IL12B | PLA2G4A | FLG | G3569 | Mucin (nonspecified subtype) | PPP3R2 | AIM2 | PPID | PPP3CC | Neurotrophic Factor (nonspecified subtype) | CNR1 | Phospholipase A2, Cytosolic (nonspecified subtype) | SYK | CXCL1 | NTRK1 | AP-1 Transcription Factor Complex | AIM2 Inflammasome | PPP3CB | NR3C1 | PPP3R1 | IRAK1 | NLRP3 Inflammasome | CYP51A1 | ADAR

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