MeSH Browser

MeSH Supplementary: Hyperprothrombinemia
Unique ID: C566755
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566755
Entry Term(s): Prothrombin G20210a Thrombophilia; Prothrombin Thrombophilia
Registry Number: 0
Heading Mapped to: *Thrombophilia
Frequency: 22
Note: Increased PROTHROMBIN levels and risk of THROMBOSIS due to a G20210A mutation in the prothrombin gene.
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Hyperprothrombinemia MeSH Supplementary Concept Data 2024