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Disease Info Card
Uveomeningoencephalitic Syndrome
Information about Uveomeningoencephalitic Syndrome: 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 Uveomeningoencephalitic Syndrome
Most recent studies have shown that Uveomeningoencephalitic Syndrome shares some biological mechanisms with anterior-uveitis, autoimmune-diseases, autoimmune-reaction, behcet-syndrome, cataract, disorder-of-eye, edema, endophthalmitis, headache, inflammation, ophthalmia-sympathetic, panuveitis, pigmentation-disorders, retinal-detachment, retinal-diseases, sarcoidosis, serous-retinal-detachment, uveitis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Uveomeningoencephalitic Syndrome, and have been seen in publications frequently: Aging, Cell Activation, Cell Death, Cell Proliferation, Cytokine Production, Cytokine Secretion, Enucleation, Hypersensitivity, Immune Response, Inflammatory Response, Leukocyte Migration, Lymphocyte Proliferation, Pathogenesis, Phagocytosis, Pigmentation, Programmed Cell Death, Proteolysis, Reflex, Secretion, Sensitization
Quite a number of genes have been found to play important roles in Uveomeningoencephalitic Syndrome, such as CD4, CSF2, CTLA4, HLA-A, HLA-B, HLA-DQA1, HLA-DRB1, HLA-DRB4, HLA-DRB5, IFNG, IL17A, IL2, IL4, LAMC2, NOD2, RPE, TNF, TNFRSF10A, TYR, TYRP1. 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.