Urticaria
About the Disease
Urticaria, also known as urticaria nos, is related to physical urticaria and chronic spontaneous urticaria, and has symptoms including abdominal pain, chest pain and constipation. An important gene associated with Urticaria is F12 (Coagulation Factor XII), and among its related pathways/superpathways are NF-kappaB Signaling and "Agents Acting on the Renin-Angiotensin System Pathway, Pharmacodynamics". The drugs Levoleucovorin and Dapsone have been mentioned in the context of this disorder. Affiliated tissues include upper dermis, skin and thyroid, and related phenotype is immune system.
Common Targets / Biomarkers
G7006 | G2826 | G3557 | G3491 | G1845 | G1776 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G5142 | G7376 | G1600 | G10800 | G84876 | G5465 | G148 | G2312 | G10 | G5321 | G3106 | G10280 | G239 | G660 | G27181 | G3274 | G3497 | G5535 | G6530 | Protein Tyrosine Phosphatase (PTP) (nonspecified subtype) | G5533 | G5481 | G3357 | G3067 | P5561 | G7124 | G3105 | G6850 | G3702 | G2908 | G3630 | G85480 | G54578 | 15-Lipoxygenase (nonspecified subtype) | G140 | G367 | G3554 | G931 | G5734 | G30817 | G26762 | G3567 | G11251 | G7421 | G83985 | G8792 | G10203 | P43029 | G131450 | G5147 | G5335 | G26 | Serine protease (nonspecified subtype) | G51751 | G6532 | G6361 | G64806 | G3568 | G3269 | G11314 | G9570 | G1559 | G5532 | G5534 | G213 | G64109 | alpha1-Adrenoceptor (nonspecified subtype) | G728 | Histamine Receptor (HR) (nonspecified subtype) | G940 | G27040 | G10333 | G6915 | G117194 | G3565 | G4056 | G3569 | G240 | G1401 | G2740 | G3107 | G3596 | G2205 | G3576 | G59340 | G9343 | G7294 | G5724 | G7096 | G246 | G5144 | G3815 | G3176 | G6097 | P16683 | G4157 | G5478 | G11255 | G695
Other Diseases
Usher Syndrome | Usher Syndrome Type II | Usher Syndrome Type IIC | Usher Syndrome Type III | Uterine Leiomyoma | Uveitis | Uveitis, Anterior | VACTERL Association | VACTERL/VATER Association | Vaginitis | Van Der Knaap Disease | Varicocele | Vascular Calcification | Vascular Cognitive Impairment | Vasculitis | Veno-occlusive Disease | Venous Insufficiency | Ventricular Septal Defect | Vertebrobasilar Insufficiency | Vertigo | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Vestibular Disease | VEXAS Syndrome | Vici Syndrome | Viral Meningitis | Vitamin A Deficiency | Vitamin B12 Deficiency | Vitamin D Deficiency | Vitamin K Deficiency | Vitelliform Macular Dystrophy | Vitiligo | Vitreoretinal Degeneration, Snowflake Type | Vitreoretinopathy, Proliferative | Vogt-Koyanagi-Harada Syndrome | 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
