Thrombophilia due to Activated Protein C Resistance [Supplementary Concept]
A hereditary autosomal dominant susceptibility for THROMBOSIS that is caused by mutations in the F5 gene, resulting in factor V resistant to cleavage and inactivation by activated PROTEIN C. OMIM: 188055
Date introduced: November 5, 2012
MeSH Unique ID: C566056
Heading Mapped to:
Entry Terms:
- Thrombophilia due to Deficiency of Activated Protein C Cofactor
- Hereditary Resistance To Activated Protein C
- Thrombophilia due to Factor V Leiden
- Factor V Leiden Thrombophilia
- Apc Resistance, Leiden Type
- Thrombophilia V
- Protein C Cofactor Deficiency