This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Hereditary Angioedema Types I And Ii
Information about Hereditary Angioedema Types I And Ii: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Hereditary Angioedema Types I And Ii
Most recent studies have shown that Hereditary Angioedema Types I And Ii shares some biological mechanisms with abdominal-pain, allergy, anaphylaxis, angioedema, angioedemas-hereditary, asphyxia, autoimmune-diseases, complement-deficiency, edema, glomerulonephritis, hereditary-diseases, infective-disorder, laryngeal-edema, localized-edema, lupus-erythematosus-systemic, malignant-neoplasms, malnutrition, pain, urticaria.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Angioedema Types I And Ii, and have been seen in publications frequently: Anaphylaxis, Cell Activation, Coagulation, Complement Activation, Factor Xii Activation, Fibrinolysis, Hypersensitivity, Immune Response, Lactation, Localization, Mast Cell Degranulation, Menopause, Parturition, Pathogenesis, Platelet Aggregation
Quite a number of genes have been found to play important roles in Hereditary Angioedema Types I And Ii, such as ACE, AGT, BBS9, C2, C3, C4A, HNRNPC, KLK4, KLKB1, KNG1, MS4A1, PLEKHM1, PLG, SERPING1, SPANXB1, TLR9. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.