Other genetic bleeding disorders
Many proteins are involved in the cascade of the clotting process. Each genetic malformation in a protein can cause a bleeding disorder. But the expression of the disorder is more rare than haemophilia or Von Willebrand. Each disorder has to be treated by its own specific therapy.
This is a list of the most common other hereditary rare bleeding disorders:
- F I = Fibrinogen Deficiencies: afibrinogenemia; hypofibrinogenemia; dysfibrinogenemia; hypodysfibrinogenemia
- F II = Prothrombin Deficiency
- F V = Factor V-deficiency
- F V-VIII = Combined Factor V-VIII deficiency
- F VII = Factor VII deficiency
- F X = Factor X deficiency
- F XI = Factor XI deficiency
- F XIII = Factor XIII deficiency
- Vit K + ... = Combined deficiency of Vitamin K-dependent Clotting Factors (II, VII, IX, X)
- Glanzman Thrombastenia
- Bernard-Soulier
For short introduction see 
coagulation
Have also a look at the website of Rare Bleeding disorders:
www.rbdd.org