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bn:02800661n
Noun Named Entity
Categories: Coagulopathies, SNPs on chromosome 11, All articles lacking reliable references
EN
prothrombin G20210A  20210A  F2 20210A  F2 G20210A  F2G20210A
EN
Prothrombin G20210A is a genetic condition that increases the risk of blood clots including from deep vein thrombosis, and of pulmonary embolism. Wikipedia
Definitions
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Sources
EN
Prothrombin G20210A is a genetic condition that increases the risk of blood clots including from deep vein thrombosis, and of pulmonary embolism. Wikipedia
Genetic condition that raises the risk of blood clots Wikidata
IS A
thrombophilia
hyperprothrombinemia
Wikipedia
EN
prothrombin G20210A
Wikidata
EN
Prothrombin G20210A
Wikipedia Redirections
EN
20210A, F2 20210A, F2 G20210A, F2G20210A, Factor 2 mutation, Factor II G20210A, factor II mutation, G20210A, Prothrombin 20210 mutation, prothrombin 20210A, Prothrombin 20210a mutation, Prothrombin 20210A variant, Prothrombin F2G20210A mutation, Prothrombin gene mutation, prothrombin mutation, Prothrombin mutation G20210A, Prothrombin thrombophilia, Rs1799963

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