SE-ATLAS

Multiple myeloma Acquired prothrombin deficiency Rare thrombotic disorder due to a constitutional platelet anomaly Acquired hemophilia Rare thrombotic disorder due to an acquired platelet anomaly Paroxysmal nocturnal hemoglobinuria Familial hypodysfibrinogenemia Hemophilia Combined deficiency of factor V and factor VIII Thrombotic thrombocytopenic purpura Primary systemic amyloidosis Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Primary localized amyloidosis AL amyloidosis Congenital fibrinogen deficiency Cystic fibrosis Congenital prekallikrein deficiency Bleeding disorder in hemophilia B carriers Bleeding disorder in hemophilia A carriers Congenital high-molecular-weight kininogen deficiency Rare hemorrhagic disorder Congenital alpha2-antiplasmin deficiency Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease Rare coagulation disorder Von Willebrand disease type 1 Von Willebrand disease type 2 Rare hemorrhagic disorder due to a platelet anomaly Hereditary combined deficiency of vitamin K-dependent clotting factors Rare aplastic anemia Rare hemorrhagic disorder due to an acquired coagulation factor defect Von Willebrand disease type 3 Rare thrombotic disease of hematologic origin Familial hypofibrinogenemia Rare hemorrhagic disorder due to an acquired platelet anomaly Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Severe hemophilia B Acquired von Willebrand syndrome Hemophilia A Mild hemophilia B Familial afibrinogenemia Hemophilia B Moderate hemophilia A Severe hemophilia A Familial dysfibrinogenemia Mild hemophilia A Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a constitutional platelet anomaly Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital vitamin K-dependent coagulation factors deficiency East Texas bleeding disorder