MeSH Browser

MeSH Supplementary: Thrombophilia due to Activated Protein C Resistance
Unique ID: C566056
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566056
Entry Term(s): Apc Resistance, Leiden Type; Factor V Leiden Thrombophilia; Hereditary Resistance To Activated Protein C; Protein C Cofactor Deficiency; Thrombophilia V; Thrombophilia due to Deficiency of Activated Protein C Cofactor; Thrombophilia due to Factor V Leiden
Registry Number: 0
Heading Mapped to: *Activated Protein C Resistance
Frequency: 63
Note: 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 of Entry: 2012/11/05
Revision Date: 2015/08/18

Thrombophilia due to Activated Protein C Resistance MeSH Supplementary Concept Data 2024