Other Names for this Disease
- Prothrombin 20210G>A thrombophilia
- Prothrombin-related thrombophilia
- Prothrombin G20210A thrombophilia
- Factor II-related thrombophilia
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deep venous thrombosis, which typically occur in the deep veins of the legs. Affected people also have an increased risk of developing a pulmonary embolism. However, most people with prothrombin thrombophilia never develop abnormal blood clots. Prothrombin thrombophilia is the second most common inherited form of thrombophilia after factor V Leiden thrombophilia. It is more common in Caucasian populations. This condition is caused by a particular mutation (written G20210A or 20210G>A) in the F2 gene. People can inherit one or two copies of the gene mutation from their parents.Prothrombin thrombophilia is an inherited disorder of blood clotting. Thrombophilia is an increased tendency to form abnormal blood clots in blood vessels. People who have prothrombin thrombophilia are at somewhat higher than average risk for a type of clot called a
Last updated: 12/5/2011
- Prothrombin thrombophilia. Genetics Home Reference. August 2008; http://ghr.nlm.nih.gov/condition/prothrombin-thrombophilia. Accessed 8/8/2011.
- Genetics Home Reference (GHR) contains information on Prothrombin thrombophilia. This website is maintained by the National Library of Medicine.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Prothrombin thrombophilia. Click on the link to view a sample search on this topic.