Diseases Associated with Clotting Factor Dysfunction


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Afibrinogenemia, complete loss of fibrinogen, Factor I
Dysfibrinogenemia, dysfunctional fibrinogen, Factor I
Factor II Disorders
Factor III (tissue factor) is the only coagulation factor for which a congenital defect has not been identified

Factor V Leiden thrombophilia

Factor VII Deficiency

Hemophilia A Factor VIII deficiency

Hemophilia B Factor IX deficiency

Factor X Deficiency

Factor XI Deficiency Rosenthal Syndrome, Plasma Thromboplastin Antecedent (PTA) deficiency

Factor XII Deficiency Hageman factor deficiency

Factor XIII Deficiency

Protein C Deficiency

Protein S Deficiency
Thrombophilia: Antithrombin III deficiency

Glanzmann thrombasthenia platelet glycoprotein IIb-IIIa complex deficiency

Giant Platelet Syndrome: Bernard-Soulier Syndrome platelet glycoprotein Ib complex deficiency

von Willebrand Disease

Fletcher Factor Deficiency: Prekallikrein deficiency

 

 

 

 

 

 

 

 

 

 

 


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Michael W King, PhD | © 1996–2017 themedicalbiochemistrypage.org, LLC | info @ themedicalbiochemistrypage.org

Last modified: February 13, 2016