Factor XII D005174

Related MeSH Hierarchy (4)

Chemicals and Drugs [D] » Enzymes and Coenzymes [D08] » Enzyme Precursors » Factor XII

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Blood Proteins » Blood Coagulation Factors » Factor XII

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Protein Precursors » Enzyme Precursors » Factor XII

Chemicals and Drugs [D] » Biological Factors [D23] » Blood Coagulation Factors » Factor XII

Description

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.   MeSH

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