Cardiovascular Diseases

Thrombophilia represents a predisposition to form clots inappropriately. It is caused by abnormalities in blood consistency, determined by modified levels and activity of coagulation factors that participate in the “coagulation cascade”.

Thrombotic events are increasingly recognized as a significant source of mortality and morbidity. Predisposition to form clots is a multifactorial disease: it derives from genetic factors, acquired changes in the clotting mechanism, or, more commonly, an interaction between genetic and acquired factors.

A significant proportion of the population has a detectable abnormality, but most of these only develop thrombosis in the presence of additional environmental risk factors. Clonit’s assays provide a complete coverage of frequent as well as rare mutations in genes related to the coagulation pathway reported to constitute risk factors for thrombophilia.

Cardiovascular Diseases
ProductCodeCE MarkDescription
Factor V CambridgeEER024032EER024032

32 Tests - R306T

Factor V Y1702CEER047032EER047032

32 Tests

Factor V H1299R EER041032EER041032

32 Tests - A4070G

Available for QiaSymphony SP/AS - Ref: EER31032QS

Factor V LeidenEER038032EER038032

32 Tests - G1691A 

Available for QiaSymphony SP/AS - Ref: EER027032QS

Factor II EER037032EER037032

32 Tests - G20210A Mut

Available for QiaSymphony SP/AP - Ref. EER028032QS

MTHFR C677TEER039032EER039032

32 Tests - C677T

Available for QiaSymphony SP/AS - Ref: EER029032QS

MTHFR A1298CEER040032EER040032

32 Tests - A1298C

Available for QiaSymphony SP/AS - Ref: EER030032QS

PAI-1 EER053032EER053032

32 Tests - 675 Promoter 4G/5G

Factor XIII EER22032EER22032

32 Tests - V34L

HPA-1 a/bEER048050EER048050

50 Tests - HPA-1 a/b

Available for QiaSymphony SP/AS - Ref: EER048032QS

MTRREER042032EER042032

32 Tests - A66G

MTREER043032EER043032

32 Tests - A2756G

Beta FibrinogenEER049050EER049050

50 Tests  

Available for QiaSymphony SP/AS - Ref: EER049032QS