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Disease Info Card
Chediak-higashi Syndrome
Information about Chediak-higashi 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 Chediak-higashi Syndrome
Most recent studies have shown that Chediak-higashi Syndrome shares some biological mechanisms with albinism, albinism-oculocutaneous, bacterial-infections, bleeding-tendency, cattle-diseases, granulomatous-disease-chronic, granulomatous-disorder, hematological-disease, hemorrhage, hereditary-diseases, hermanski-pudlak-syndrome, hypopigmentation-disorder, hypopigmentation-immunodeficiency-disease, immunologic-deficiency-syndromes, infective-disorder, leukemia, lymphohistiocytosis-hemophagocytic, phagocyte-bactericidal-dysfunction, piebaldism, wiskott-aldrich-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Chediak-higashi Syndrome, and have been seen in publications frequently: Chemotaxis, Coagulation, Cytolysis, Endocytosis, Exocytosis, Granulocyte Chemotaxis, Hemostasis, Immune Response, Killer Activity, Leukocyte Chemotaxis, Localization, Locomotion, Macrophage Activation, Pathogenesis, Phagocytosis, Pigmentation, Platelet Aggregation, Secretion, Secretory Pathway, Transport
Quite a number of genes have been found to play important roles in Chediak-higashi Syndrome, such as ACSBG1, AP3B1, APOH, C4B, CAT, CTLA4, CTSG, GUSB, HPS1, IL2, KCNE1, LAMP1, LYST, MINK1, MPO, RAB27A, TNFSF14, TYR, VPS13B, WAS. 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.