serw-MX  [xml]  

 DeCS Categories

D08 Enzymes and Coenzymes .
D08.622 Enzyme Precursors .
D08.622.355 Factor IX .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.125 Blood Coagulation Factors .
D12.776.124.125.350 Factor VIII .
D12.776.124.125.375 Factor IX .
D12.776.124.125.425 Factor XI .
D12.776.124.125.900 Thromboplastin .
D23 Biological Factors .
D23.119 Blood Coagulation Factors .
D23.119.350 Factor VIII .
D23.119.375 Factor IX .
D23.119.425 Factor XI .
D23.119.965 Thromboplastin .
E01 Diagnosis .
E01.370 Diagnostic Techniques and Procedures .
E01.370.225 Clinical Laboratory Techniques .
E01.370.225.625 Hematologic Tests .
E01.370.225.625.115 Blood Coagulation Tests .
E01.370.225.625.115.600 Partial Thromboplastin Time .
E05 Investigative Techniques .
E05.200 Clinical Laboratory Techniques .
E05.200.625 Hematologic Tests .
E05.200.625.115 Blood Coagulation Tests .
E05.200.625.115.600 Partial Thromboplastin Time .
G09 Circulatory and Respiratory Physiological Phenomena .
G09.188 Blood Physiological Phenomena .
G09.188.660 Partial Thromboplastin Time .
 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. .
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). .
Partial Thromboplastin Time .
Coagulation Time, Cephalin-Kaolin .
Cephalin Kaolin Coagulation Time .
Coagulation Time, Cephalin Kaolin .
Coagulation Time, Kaolin-Cephalin .
Kaolin Cephalin Coagulation Time .
Activated Partial Thromboplastin Time .
Cephalin-Kaolin Coagulation Time .
Kaolin-Cephalin Coagulation Time .
Thromboplastin Time, Partial .
The time required for the appearance of FIBRIN strands following the mixing of PLASMA with phospholipid platelet substitute (e.g., crude cephalins, soybean phosphatides). It is a test of the intrinsic pathway (factors VIII, IX, XI, and XII) and the common pathway (fibrinogen, prothrombin, factors V and X) of BLOOD COAGULATION. It is used as a screening test and to monitor HEPARIN therapy. .
Factor XI .
Blood Coagulation Factor XI .
Factor 11 .
Factor Eleven .
Antecedent, Plasma Thromboplastin .
Factor XI, Coagulation .
Thromboplastin Antecedent, Plasma .
Plasma Thromboplastin Antecedent .
Coagulation Factor XI .
Stable blood coagulation factor involved in the intrinsic pathway. The activated form XIa activates factor IX to IXa. Deficiency of factor XI is often called hemophilia C. .