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Disease Info Card
Hereditary Autoinflammatory Diseases
Information about Hereditary Autoinflammatory Diseases: 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 Autoinflammatory Diseases
Most recent studies have shown that Hereditary Autoinflammatory Diseases shares some biological mechanisms with amyloidosis, arthritis, autoimmune-diseases, autoimmune-reaction, brucellosis, cryopyrin-associated-periodic-syndromes, deficiency-of-mevalonate-kinase, exanthema, familial-cold-urticaria, familial-mediterranean-fever, hyper-igd-syndrome, hypergammaglobulinemia, inflammation, muckle-wells-syndrome, pain, relapsing-fever, tnf-receptor-associated-periodic-fever-syndrome-(traps).
Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Autoinflammatory Diseases, and have been seen in publications frequently: Acute Inflammatory Response, Acute-phase Response, B Cell Activation, Cell Activation, Cell Death, Cell Differentiation, Cell Maturation, Cell Migration, Cytokine Production, Cytokine Secretion, Hypersensitivity, Immune Response, Inflammatory Response, Innate Immune Response, Ossification, Pathogenesis, Phagocytosis, Proteolysis, Regulation Of Cytokine Production, Secretion
Quite a number of genes have been found to play important roles in Hereditary Autoinflammatory Diseases, such as CADPS, CAPS, CASP1, GDI1, IL18, IL1B, IL1RN, MEFV, MVK, NLRP12, NLRP3, NOD2, PSTPIP1, PYCARD, TEAD1, TNF, TNFRSF1A. 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.