SE-ATLAS

Myelom, multiples Faktor II-Mangel, erworbener Seltene thrombotische Störung durch konstitutionelle Blutplättchenanomalie Hämophilie, erworbene Seltene thrombotische Störung durch erworbene Blutplättchenanomalie Hämoglobinurie, nächtliche paroxysmale Hypodysfibrinogenämie, familiäre Hämophilie Kombinierter Mangel an Faktor V und Faktor VIII Purpura, thrombotische thrombozytopenische Amyloidose, primäre systemische Faktor II-Mangel, kongenitaler Faktor V-Mangel, kongenitaler Faktor VII-Mangel, kongenitaler Faktor X-Mangel, kongenitaler 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