Monarch Disease Ontology id MONDO_0009885 (Scott syndrome) is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity. Also known as: BDPLT7, SCTS, bleeding abnormality due to deficiency of platelet biding of factor X, familial prothrombin consumption inhibitor, familial prothrombin conversion defect, platelet-type bleeding disorder 7, prothrombin consumption deficiency.