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Disease Info Card
Congenital Combined Immunodeficiency
Information about Congenital Combined Immunodeficiency: 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 Congenital Combined Immunodeficiency
Most recent studies have shown that Congenital Combined Immunodeficiency shares some biological mechanisms with adenosine-deaminase-deficiency, agammaglobulinemia, autoimmune-reaction, carcinoma, graft-vs-host-disease, immunologic-deficiency-syndromes, infective-disorder, inflammation, leukemia, lymphoma, lymphopenia, malignant-neoplasms, malignant-paraganglionic-neoplasm, neoplasms, pneumonia, primary-immune-deficiency-disorder, severe-combined-immunodeficiency, x-linked-severe-combined-immunodeficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Combined Immunodeficiency, and have been seen in publications frequently: Angiogenesis, Cell Activation, Cell Adhesion, Cell Cycle, Cell Death, Cell Development, Cell Differentiation, Cell Growth, Cell Proliferation, Cytokine Production, Dna Repair, Hypersensitivity, Immune Response, Induction Of Apoptosis, Inflammatory Response, Localization, Pathogenesis, Regeneration, Secretion, V(d)j Recombination
Quite a number of genes have been found to play important roles in Congenital Combined Immunodeficiency, such as ADA, ATN1, CD34, CD4, CD8A, CTLA4, DCLRE1C, HLA-DQA1, IFNG, IL2, IL2RG, IL4, IL6, IL7, JAK3, NOD2, TNF. 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.