Vogt-Koyanagi-Harada Syndrome
About the Disease
Vogt-Koyanagi-Harada Disease, also known as uveomeningoencephalitic syndrome, is related to uveitis and pars planitis. An important gene associated with Vogt-Koyanagi-Harada Disease is PTPN22 (Protein Tyrosine Phosphatase Non-Receptor Type 22), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Bevacizumab and Triamcinolone have been mentioned in the context of this disorder. Affiliated tissues include eye, skin and retina, and related phenotypes are sensorineural hearing impairment and cognitive impairment
Common Targets / Biomarkers
G137196 | Tyrosine-Protein Kinases Src (nonspecified subtype) | G101928791 | G284825 | G1235 | G54665 | G102467213 | G107986764 | G10533 | G105377441 | G3426 | G3932 | G3105 | G400867 | G10866 | G283575 | G101929019 | G105375523 | G201266 | G107987121 | G7188 | G1611 | G121838 | G105370982 | G30009 | G3605 | G958 | G4846 | G105371006 | G960 | G100874048 | G102659288 | G9474 | G3586 | G55054 | G728597 | G105369325 | G285484 | G105375746 | G400952 | G101928136 | G400957 | G11116 | G105375911 | P5867 | G105369568 | G7010 | G221178 | G100130476 | G9448 | G406958 | G285577 | G150577 | G284119 | G3458 | G11184 | G729993 | G4843 | G7128 | G3717 | G51300 | G107984118 | G23130 | G55191 | G152225 | G102724900 | G105369735 | G105374364 | G105374410 | G404663 | G285626 | G26191 | G2842 | G3716 | G102724940 | G105376230 | G283876 | G406938 | G4282 | G3565 | G103689918 | G23274 | G3119 | G105371887 | G3107 | G2625 | G8927 | G107984764 | G6347 | G105374624 | G100507267 | G105376481 | G7040 | G105369850 | G107984884 | G100505566 | G107984903 | G101927324 | G6774 | G10318 | G6890 | G101927334 | G105376626 | G149233 | G83734 | G101927354 | G101930275 | G285834 | G10758 | G50943 | G3123 | G6097 | G101927592 | G105379031 | G3106 | G6696 | G2113 | G8408 | G100132677 | G7248 | G101927650 | G27 | G102723828 | G5820 | G100506023 | G105370401 | G101927745 | G400757
Other Diseases
Von Hippel-Lindau Disease | Von Willebrand Disease | Vulvovaginitis | Waardenburg Syndrome | Waardenburg Syndrome Type 1 | Waardenburg Syndrome Type 2 | Waardenburg Syndrome Type 2A | Waardenburg Syndrome Type 2E | Waardenburg Syndrome Type 4 | Waardenburg Syndrome Type 4A | Wagner Disease | WAGR Syndrome | Waldenstrom Macroglobulinemia | Walker-Warburg Syndrome | Warsaw Breakage Syndrome | Weill-Marchesani Syndrome | Werner's Syndrome | Whipple's Disease | Wieacker-Wolff Syndrome | Wiedemann-Steiner Syndrome | Williams Syndrome | Wilson's Disease | Wiskott-Aldrich Syndrome | Withdrawal Syndrome | Wolcott-Rallison Syndrome | Wolff-Parkinson-White Syndrome | Wolfram Syndrome | Wolfram Syndrome 2 | Wolman Disease | Woodhouse-Sakati Syndrome | X-linked Acrogigantism | X-linked Charcot-Marie-Tooth Disease | X-linked Creatine Transporter Deficiency | X-linked Myotubular Myopathy | X-linked Sideroblastic Anemia | Xeroderma Pigmentosum | Xeroderma Pigmentosum Variant Type | Yellow Fever | Zellweger Syndrome | Zimmermann-Laband Syndrome | Zollinger-Ellison Syndrome | Zygomycosis
