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Disease Info Card
Familial Hemophagocytic Lymphocytosis
Information about Familial Hemophagocytic Lymphocytosis: 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 Familial Hemophagocytic Lymphocytosis
Most recent studies have shown that Familial Hemophagocytic Lymphocytosis shares some biological mechanisms with anemia, histiocytosis, histiocytosis-haematophagic, histiocytosis-langerhans-cell, histiocytosis-non-langerhans-cell, hypofibrinogenemia, immunologic-deficiency-syndromes, infective-disorder, lymphatic-diseases, lymphohistiocytosis-hemophagocytic, lymphoma, malignant-paraganglionic-neoplasm, nervousness, pancytopenia, reticulosis-nos, virus-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Familial Hemophagocytic Lymphocytosis, and have been seen in publications frequently: Antibody-dependent Cellular Cytotoxicity, Cell Activation, Cell Death, Cell Killing, Coagulation, Exocytosis, Hemostasis, Immune Response, Inflammatory Response, Killer Activity, Localization, Lymphocyte Homeostasis, Lymphocyte Proliferation, Macrophage Activation, Membrane Fusion, Pathogenesis, Phagocytosis, Secretion, Secretory Pathway, Transport
Quite a number of genes have been found to play important roles in Familial Hemophagocytic Lymphocytosis, such as CD8A, CSF2, FHL2, FHL3, FHL5, HLA-DQA1, IL2, IL6, LAMC2, LAMP1, NOD2, PRF1, RAB27A, SH2D1A, STX11, STXBP2, UNC13D, XIAP, ZNF395. 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.