Current Data About
Scott syndrome
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q890200)
(Q18555031)
(Q55786859)
|
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| (P2293) |
(Q18053079)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0111052
http://identifiers.org/doid/DOID:0111052
http://www.orpha.net/ORDO/Orphanet_806 |
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| (P5008) |
(Q4099686)
|
other details
| aliases |
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 |
| description | inherited blood coagulation disease |
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