MeSH Browser

MeSH Supplementary: Scott Syndrome
Unique ID: C563120
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563120
Entry Term(s): Bleeding Abnormality due to Deficiency of Platelet Binding of Factor X; Prothrombin Consumption Deficiency; Prothrombin Consumption Inhibitor, Familial; Prothrombin Conversion Defect, Familial
Registry Numbers: 0
Heading Mapped to: *Blood Coagulation Disorders
Frequency: 19
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Scott Syndrome MeSH Supplementary Concept Data 2025