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 DeCS Categories

C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.100 Blood Coagulation Disorders, Inherited .
C15.378.100.100.325 Factor XI Deficiency .
C15.378.100.141 Coagulation Protein Disorders .
C15.378.100.141.325 Factor XI Deficiency .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.325 Factor XI Deficiency .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.099 Blood Coagulation Disorders, Inherited .
C16.320.099.325 Factor XI Deficiency .
D08 Enzymes and Coenzymes .
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 .
D08.811.277.656.300.760.320 Factor XIa .
D08.811.277.656.959 Serine Proteases .
D08.811.277.656.959.350 Serine Endopeptidases .
D08.811.277.656.959.350.320 Factor XIa .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.125 Blood Coagulation Factors .
D12.776.124.125.425 Factor XI .
D12.776.124.125.425.320 Factor XIa .
D23 Biological Factors .
D23.119 Blood Coagulation Factors .
D23.119.425 Factor XI .
D23.119.425.320 Factor XIa .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
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. .
1.00
61062
 
Factor XIa .
Activated Factor XI .
Blood Coagulation Factor XI, Activated .
Contact Activation Product .
Factor 11A .
Factor Eleven A .
Factor XIa, Coagulation .
Factor XI, Activated .
Coagulation Factor XIa .
Activated form of factor XI. In the intrinsic pathway, Factor XI is activated to XIa by factor XIIa in the presence of cofactor HMWK; (HIGH MOLECULAR WEIGHT KININOGEN). Factor XIa then activates factor IX to factor IXa in the presence of calcium. .
0.81
1317
 
Factor XI Deficiency .
Deficiency, Factor 11 .
Deficiency, Factor Eleven .
Deficiency, Factor XI .
Factor 11 Deficiency .
Factor Eleven Deficiency .
Plasma Thromboplastin Antecedent Deficiency .
Rosenthal's Syndrome .
Deficiencies, Factor 11 .
Deficiencies, Factor Eleven .
Deficiencies, Factor XI .
Factor 11 Deficiencies .
Factor Eleven Deficiencies .
Factor XI Deficiencies .
Rosenthal Syndromes .
Rosenthal's Syndromes .
Rosenthals Syndrome .
Syndrome, Rosenthal .
Syndrome, Rosenthal's .
Hemophilia C .
Rosenthal Syndrome .
PTA Deficiency .
A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia. .
0.76
12663