Factor v leiden mutation. Medical search. Frequent questions

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Diseases21

Activated Protein C Resistance Thrombophilia Blood Coagulation Disorders, Inherited Venous Thrombosis Pregnancy Complications, Hematologic Protein S Deficiency Livedo Reticularis Thrombosis Factor V Deficiency Thrombophlebitis Thromboembolism Budd-Chiari Syndrome Blood Coagulation Disorders Protein C Deficiency Antithrombin III Deficiency Venous Thromboembolism Genetic Predisposition to Disease Abortion, Habitual Pulmonary Embolism Abruptio Placentae Skin Diseases, Vascular

Chemicals and Drugs12

Factor V Prothrombin Protein C Protein S Anticoagulants Methylenetetrahydrofolate Reductase (NADPH2)Oxidoreductases Acting on CH-NH Group Donors Apolipoprotein E3 Blood Coagulation Factor Inhibitors Factor VIII Factor Va Contraceptives, Oral

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Risk Factors Case-Control Studies Polymerase Chain Reaction Partial Thromboplastin Time Genetic Testing Blood Coagulation Tests Heterozygote Detection DNA Mutational Analysis Pedigree

Psychiatry and Psychology1

Rationalization

Phenomena and Processes12

Point Mutation Heterozygote Mutation Homozygote Pregnancy Mutation, Missense Blood Coagulation Genotype Genetic Predisposition to Disease Partial Thromboplastin Time Frameshift Mutation Polymorphism, Genetic

Health Care3

Risk Factors Case-Control Studies Genetic Testing

Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Health Care

Factor V Activated Protein C Resistance Thrombophilia Blood Coagulation Disorders, Inherited Prothrombin Venous Thrombosis Point Mutation Pregnancy Complications, Hematologic Protein S Deficiency Livedo Reticularis Protein C Thrombosis Heterozygote Factor V Deficiency Thrombophlebitis Mutation Thromboembolism Budd-Chiari Syndrome Blood Coagulation Disorders Protein S Homozygote Protein C Deficiency Risk Factors Case-Control Studies Anticoagulants Polymerase Chain Reaction Methylenetetrahydrofolate Reductase (NADPH2)Pregnancy Mutation, Missense Blood Coagulation Antithrombin III Deficiency Venous Thromboembolism Genotype Rationalization Oxidoreductases Acting on CH-NH Group Donors Genetic Predisposition to Disease Abortion, Habitual Apolipoprotein E3 Blood Coagulation Factor Inhibitors Pulmonary Embolism Partial Thromboplastin Time Genetic Testing Blood Coagulation Tests Abruptio Placentae Factor VIII Factor Va Heterozygote Detection Frameshift Mutation DNA Mutational Analysis Contraceptives, Oral Polymorphism, Genetic Pedigree Skin Diseases, Vascular

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