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Disease Info Card
Erdheim-chester Disease
Information about Erdheim-chester Disease: 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 Erdheim-chester Disease
Most recent studies have shown that Erdheim-chester Disease shares some biological mechanisms with bone-diseases, diabetes-mellitus, exophthalmos, farber-lipogranulomatosis, fibrosis, granuloma, histiocytosis, histiocytosis-langerhans-cell, histiocytosis-non-langerhans-cell, lipogranuloma, lipoidosis, neoplasms, nervousness, orbit-(eye-disorders), osteosclerosis, pain, sclerosis, xanthomatosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Erdheim-chester Disease, and have been seen in publications frequently: Blood Coagulation, Bone Remodeling, Bone Resorption, Cell Proliferation, Coagulation, Cytokine Production, Granuloma Formation, Innervation, Intramembranous Ossification, Lipid Storage, Localization, Macrophage Activation, Ossification, Pathogenesis, Pigmentation, Transposition, Tropism
Quite a number of genes have been found to play important roles in Erdheim-chester Disease, such as AR, ASAH1, CD163, CD1A, CD1B, CD1C, CD68, CRP, CTLA4, ECD, HLA-DQA1, IL1RN, IL6, NOD2, POMC, S100A1, S100B. 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.