BabelNet

bn:01013326n

Noun Concept

Categories: Coagulopathies, Genetic disorders with no OMIM, Rare diseases

Scott syndrome BDPLT7 bleeding abnormality due to deficiency of platelet biding of factor X Bleeding Abnormality Due to Deficiency of Platelet Binding of Factor 10 Bleeding Disorder, Platelet-Type, 7

Scott syndrome is a rare congenital bleeding disorder that is due to a defect in a platelet mechanism required for blood coagulation. Wikipedia

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Scott syndrome is a rare congenital bleeding disorder that is due to a defect in a platelet mechanism required for blood coagulation. Wikipedia

Inherited blood coagulation disease Wikidata

IS A

rare disease

coagulopathy

GENETIC ASSOCIATION

anoctamin 6

Wikipedia

Scott syndrome

Wikidata

Scott syndrome

Wikipedia Redirections

Scott's syndrome

Wikidata Alias

BDPLT7, bleeding abnormality due to deficiency of platelet biding of factor X, Bleeding Abnormality Due to Deficiency of Platelet Binding of Factor 10, Bleeding Disorder, Platelet-Type, 7, familial prothrombin consumption inhibitor, familial prothrombin conversion defect, platelet-type bleeding disorder 7, Platelet factor X receptor deficiency, prothrombin consumption deficiency, Prothrombin Consumption Inhibitor, Familial, Prothrombin Conversion Defect, Familial, SCOTT SYNDROME, SCOTT SYNDROME; SCTS, SCTS