Scott syndrome (Q7437571)
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inherited blood coagulation disease
- familial prothrombin consumption inhibitor
- familial prothrombin conversion defect
- prothrombin consumption deficiency
- bleeding abnormality due to deficiency of platelet biding of factor X
- BDPLT7
- platelet-type bleeding disorder 7
- SCTS
- Bleeding Disorder, Platelet-Type, 7
- SCOTT SYNDROME
- Platelet factor X receptor deficiency
- SCOTT SYNDROME; SCTS
- Bleeding Abnormality Due to Deficiency of Platelet Binding of Factor 10
- Prothrombin Consumption Inhibitor, Familial
- Prothrombin Conversion Defect, Familial
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Scott syndrome |
inherited blood coagulation disease |
|
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Identifiers
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Sitelinks
Wikipedia(4 entries)
- arwiki متلازمة سكوت
- dewiki Scott-Syndrom
- enwiki Scott syndrome
- plwiki Zespół Scotta