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Types of Haemophilia

Hemophilia A
Hemophilia A

Hemophilia is a group of inherited blood disorders in which the blood does not clot properly. Hemophilia is the standard international spelling, also known as haemophilia in the UK, other translations include: hémophilie, hemofilie, hemofili, hemofilia, hämophilie, emofilia.

Hemophilia B
Hemophilia B

Hemophilia is a group of inherited blood disorders in which the blood does not clot properly. Hemophilia is the standard international spelling, also known as haemophilia in the UK, other translations include: hémophilie, hemofilie, hemofili, hemofilia, hämophilie, emofilia. We will use the standard international spelling for the purpose of this section.

Other Factor Deficiencies
Other Factor Deficiencies

Factor I deficiency is a collective term for three rare inherited fibrinogen deficiencies. Factor II Learn more about the symptoms, testing and treatment for factor II (FII) deficiency, or prothrombin deficiency.

Von Willebrand Disease
Von Willebrand Disease

Von Willebrand disease (VWD) is a genetic disorder caused by missing or defective von Willebrand factor (VWF), a clotting protein. VWF binds factor VIII, a key clotting protein, and platelets in blood vessel walls, which help form a platelet plug during the clotting process.

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