MeSH Browser

MeSH Supplementary: Hyperheparinemia
Unique ID: C562723
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562723
Registry Number: 0
Heading Mapped to: *Blood Coagulation Disorders
Frequency: 17
Note: A congenital susceptibility to hemmorhage due to an excess of clotting inhibitor. The blood clotting defected may be corrected in vitro by PROTAMINE SULFATE and TOLUIDINE BLUE. OMIM: 144050
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Hyperheparinemia MeSH Supplementary Concept Data 2023