| | | | | Genetic variants - ATIII-deficiency
- Protein C deficiency
- Protein S deficiency
- increased levels of Factor I
- G2021A mutation (increased Prothrombin)
- Factor V Leiden Mutation (Resistance to activated protein C)
- increased levels of factor VII
- factor VII Genotype H6H6
- paroxysmal nocturnal hemoglobinuria (PNH)
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