serw-MX  [xml]  

 DeCS Categories

D08 Enzymes and Coenzymes .
D08.622 Enzyme Precursors .
D08.622.355 Factor IX .
D08.622.432 Factor VII .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.656 Peptide Hydrolases .
D08.811.277.656.300 Endopeptidases .
D08.811.277.656.300.760 Serine Endopeptidases .
D08.811.277.656.300.760.300 Factor VIIa .
D08.811.277.656.300.760.315 Factor Xa .
D08.811.277.656.959 Serine Proteases .
D08.811.277.656.959.350 Serine Endopeptidases .
D08.811.277.656.959.350.300 Factor VIIa .
D08.811.277.656.959.350.315 Factor Xa .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.125 Blood Coagulation Factors .
D12.776.124.125.325 Factor VII .
D12.776.124.125.325.300 Factor VIIa .
D12.776.124.125.350 Factor VIII .
D12.776.124.125.350.300 Factor VIIIa .
D12.776.124.125.375 Factor IX .
D12.776.124.125.400 Factor X .
D12.776.124.125.400.315 Factor Xa .
D12.776.124.125.450 Factor XII .
D12.776.124.125.691 Platelet Factor 3 .
D12.776.124.125.900 Thromboplastin .
D23 Biological Factors .
D23.119 Blood Coagulation Factors .
D23.119.325 Factor VII .
D23.119.325.300 Factor VIIa .
D23.119.350 Factor VIII .
D23.119.350.300 Factor VIIIa .
D23.119.375 Factor IX .
D23.119.400 Factor X .
D23.119.400.315 Factor Xa .
D23.119.450 Factor XII .
D23.119.932 Platelet Factor 3 .
D23.119.965 Thromboplastin .
 Synonyms & Historicals
Thromboplastin .
Blood Coagulation Factor III .
Coagulin .
Glomerular Procoagulant Activity .
Prothrombinase .
Tissue Factor Procoagulant .
Urothromboplastin .
Activity, Glomerular Procoagulant .
Factor III, Coagulation .
Procoagulant Activity, Glomerular .
Procoagulant, Tissue Factor .
Thromboplastin, Tissue .
Factor III .
Tissue Factor .
Tissue Thromboplastin .
Coagulation Factor III .
Antigens, CD142 .
CD142 Antigens .
Constituent composed of protein and phospholipid that is widely distributed in many tissues. It serves as a cofactor with factor VIIa to activate factor X in the extrinsic pathway of blood coagulation. .
Factor VIII .
Blood Coagulation Factor VIII .
Factor 8 .
Factor 8 C .
Factor Eight .
Factor VIIIC .
Hyate-C .
Hyatt-C .
Hyate C .
HyateC .
Hyatt C .
HyattC .
Thromboplastinogen .
Factor VIII Clotting Antigen .
Factor VIII Coagulant Antigen .
Factor VIII Procoagulant Activity .
Coagulation Factor VIII .
Antihemophilic Factor VIII .
Antihemophilic Factor .
Factor VIII of blood coagulation. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin. .
Platelet Factor 3 .
Factor 3, Platelet .
PF 3 12320 .
A phospholipid from the platelet membrane that contributes to the blood clotting cascade by forming a phospholipid-protein complex (THROMBOPLASTIN) which serves as a cofactor with FACTOR VIIA to activate FACTOR X in the extrinsic pathway of BLOOD COAGULATION. .
Factor Xa .
Activated Factor X .
Blood Coagulation Factor X, Activated .
Factor 10A .
Factor Ten A .
Factor Xa, Coagulation .
Autoprothrombin C .
Factor X, Activated .
Thrombokinase .
Coagulation Factor Xa .
Activated form of factor X that participates in both the intrinsic and extrinsic pathways of blood coagulation. It catalyzes the conversion of prothrombin to thrombin in conjunction with other cofactors. .
Factor VIIa .
Blood Coagulation Factor VII, Activated .
Factor 7A .
Factor Seven A .
Activated Factor VII .
Factor VIIa, Coagulation .
Factor VII, Activated .
Coagulation Factor VIIa .
Activated form of factor VII. Factor VIIa activates factor X in the extrinsic pathway of blood coagulation. .
Factor VIIIa .
Blood Coagulation Factor VIII, Activated .
Factor 8A .
Factor Eight A .
Factor VIIIa Heavy Chain, 200 kDa Isoform .
Factor VIIIa Heavy Chain, 92 kDa Isoform .
Factor VIIIa Light Chain .
Activated Factor VIII .
Factor VIII, Thrombin Activated .
Factor VIIIa, Coagulation .
Thrombin-Activated Factor VIII .
Factor VIII, Activated .
Factor VIII, Thrombin-Activated .
Coagulation Factor VIIIa .
Activated form of factor VIII. The B-domain of factor VIII is proteolytically cleaved by thrombin to form factor VIIIa. Factor VIIIa exists as a non-covalent dimer in a metal-linked (probably calcium) complex and functions as a cofactor in the enzymatic activation of factor X by factor IXa. Factor VIIIa is similar in structure and generation to factor Va. .
Factor VII .
Blood Coagulation Factor VII .
Factor 7 .
Factor Seven .
Factor VII, Coagulation .
Proconvertin .
Stable Factor .
Coagulation Factor VII .
Heat- and storage-stable plasma protein that is activated by tissue thromboplastin to form factor VIIa in the extrinsic pathway of blood coagulation. The activated form then catalyzes the activation of factor X to factor Xa. .
Factor IX .
Blood Coagulation Factor IX .
Factor 9 .
Factor IX Complex .
Factor IX Fraction .
Factor Nine .
Factor IX, Coagulation .
Christmas Factor .
Plasma Thromboplastin Component .
Autoprothrombin II .
Coagulation Factor IX .
Storage-stable blood coagulation factor acting in the intrinsic pathway of blood coagulation. Its activated form, IXa, forms a complex with factor VIII and calcium on platelet factor 3 to activate factor X to Xa. Deficiency of factor IX results in HEMOPHILIA B (Christmas Disease). .
Factor XII .
Factor 12 .
Factor Twelve .
Hageman Factor .
Coagulation Factor XII .
Stable blood coagulation factor activated by contact with the subendothelial surface of an injured vessel. Along with prekallikrein, it serves as the contact factor that initiates the intrinsic pathway of blood coagulation. Kallikrein activates factor XII to XIIa. Deficiency of factor XII, also called the Hageman trait, leads to increased incidence of thromboembolic disease. Mutations in the gene for factor XII that appear to increase factor XII amidolytic activity are associated with HEREDITARY ANGIOEDEMA TYPE III. .