Scott Syndrome [Supplementary Concept]
Date introduced: November 5, 2012
MeSH Unique ID: C563120
Heading Mapped to:
Entry Terms:
- Bleeding Abnormality due to Deficiency of Platelet Binding of Factor X
- Prothrombin Conversion Defect, Familial
- Prothrombin Consumption Deficiency
- Prothrombin Consumption Inhibitor, Familial