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Results 1 - 10 of 28 for Thrombophilia
  1. Prothrombin thrombophilia is an inherited disorder of blood clotting. Thrombophilia is an increased tendency to form abnormal blood clots in blood vessels. People ...
  2. Factor V Leiden thrombophilia is an inherited disorder of blood clotting. Factor V Leiden is the name of a specific gene mutation that results in thrombophilia, ...
  3. Learning about Factor V Leiden Thrombophilia From the National Institutes of Health (National Human Genome Research Institute)  
    Blood Clots/Genetics ... Blood Clots ... National Human Genome Research Institute ... From the National Institutes of Health ... Factor V Leiden thrombophilia is an inherited ...
  4. ... history of the condition in their family. Hereditary thrombophilia due to protein S deficiency Thrombophilia due to protein S deficiency, autosomal dominant Thrombophilia ...
  5. ... each cell have severe protein C deficiency. Hereditary thrombophilia due to protein C deficiency PROC deficiency Genetic Testing Registry: Thrombophilia due to protein C deficiency, autosomal dominant Protein ...
  6. Thrombophlebitis is swelling (inflammation) of a vein. A blood clot (thrombus) in the vein is the most common cause of this swelling.
  7. ... that can block blood vessels is known as thrombophilia.The presence of the factor V Leiden variant ... both copies of the F5 gene can cause thrombophilia; two copies of the variant lead to a ...
  8. Blood Clots (National Library of Medicine)  
    What is a blood clot? A blood clot is a mass of blood that forms when platelets, proteins, and cells in the blood stick together. When you get hurt, your ...
  9. ... called G6PD deficiency Hereditary hemochromatosis Transthyretin amyloidosis Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden thrombophilia Alzheimer' ...
  10. ... The mutation that causes most cases of prothrombin thrombophilia changes one DNA building block (nucleotide) in the ... 3' end processing of the prothrombin mRNA in thrombophilia. Acta Haematol. 2006;115(3-4):192-7. ...
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