Heritable and acquired thrombophilias in arterial disease

Heritable	Acquired
Prothrombin G20210A mutation Factor V Leiden Factor deficiency Protein C Protein S Antithrombin	Antiphospholipid syndrome Heparin-induced thrombocytopenia Myeloproliferative neoplasms Primary myelofibrosis Polycythemia vera Essential thrombocythemia Hypereosinophilic syndrome Systemic mastocytosis Paroxysmal nocturnal hemoglobinuria

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