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Disease Info Card
Factor Vii Deficiency
Information about Factor Vii Deficiency: 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 Factor Vii Deficiency
Most recent studies have shown that Factor Vii Deficiency shares some biological mechanisms with afibrinogenemia, bleeding-tendency, blood-coagulation-disorders, blood-platelet-disorders, cerebral-hemorrhage, epistaxis, factor-v-deficiency, factor-x-deficiency, factor-xi-deficiency, hemarthrosis, hemophilia-a, hemophilia-b, hemorrhage, hemorrhagic-disorders, inherited-factor-ii-deficiency, intracranial-hemorrhages, liver-diseases, thrombosis, von-willebrand-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Factor Vii Deficiency, and have been seen in publications frequently: Blood Circulation, Blood Coagulation, Coagulation, Fibrinolysis, Hemostasis, Immune Response, Localization, Menstruation, Mrna Processing, Ossification, Pathogenesis, Platelet Activation, Platelet Aggregation, Protein Folding, Proteolysis, Response To Lipopolysaccharide, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Factor Vii Deficiency, such as EGF, EGR1, F10, F11, F2, F3, F7, F8, PLG, SERPINC1, TF, TFPI, TMSB4X, TSTA3, VWF. 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.