SE-ATLAS

Congenital factor XII deficiency Congenital factor XIII deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Congenital fibrinogen deficiency Autosomal dominant macrothrombocytopenia Severe hereditary thrombophilia due to congenital protein C deficiency Epstein syndrome Thrombocythemia with distal limb defects Stormorken-Sjaastad-Langslet syndrome Congenital prekallikrein deficiency Bleeding disorder in hemophilia A carriers Congenital high-molecular-weight kininogen deficiency Fechtner syndrome Bleeding disorder due to P2Y12 defect Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder in hemophilia B carriers Rare hemorrhagic disorder Rare hemorrhagic disorder due to a constitutional thrombocytopenia Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Von Willebrand disease Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease type 1 Rare coagulation disorder Mediterranean macrothrombocytopenia Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare hemorrhagic disorder due to a platelet anomaly Von Willebrand disease type 2 Von Willebrand disease type 2B Hereditary combined deficiency of vitamin K-dependent clotting factors Von Willebrand disease type 2A Von Willebrand disease type 2M X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Rare thrombotic disease of hematologic origin Von Willebrand disease type 3 Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect MYH9-related disease Familial hypofibrinogenemia Rare hemorrhagic disorder due to an acquired platelet anomaly Dense granule disease Alpha granule disease Scott syndrome Severe hemophilia B Sebastian syndrome Acquired von Willebrand syndrome Mild hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Hemophilia A Rare thrombotic disorder due to an acquired coagulation factors defect Familial dysfibrinogenemia Familial afibrinogenemia Severe hemophilia A Hemophilia B Mild hemophilia A Bleeding diathesis due to glycoprotein VI deficiency Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Immune thrombocytopenia Bernard-Soulier syndrome Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare hemorrhagic disorder due to a constitutional platelet anomaly Autoimmune thrombocytopenia East Texas bleeding disorder Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital thrombotic thrombocytopenic purpura Immune-mediated thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Gaisböck-Syndrom Thrombozytose, familiäre Faktor II-Mangel, erworbener Protein-S-Mangel, erworbener Hämorrhagische Diathese durch Kollagen-Rezeptor-Mangel Hyperkoagulabilitätssyndrom durch Glykosylphosphatidyl-Inositol-Mangel Thrombasthenie Glanzmann Kryoglobulinämie, einfache Seltene thrombotische Störung durch erworbene Blutplättchenanomalie Thrombozytopenie May-Hegglin Hämorrhagische Diathese durch Thromboxan-Synthetase-Mangel Hämophilie, erworbene Paris-Trousseau-Syndrom Thrombozytopenie, X-chromosomale, mit normalen Plättchen Alloimmunthrombozytopenie, fetale und neonatale Seltene thrombotische Störung durch konstitutionelle Blutplättchenanomalie Hypodysfibrinogenämie, familiäre Makrothrombozytopenie mit Mitralklappeninsuffizienz Kombinierter Mangel an Faktor V und Faktor VIII Hämophilie Giant-Platelet-Syndrom, isoliertes hereditäres Essentielle Thrombozythämie Thrombozytopenie, hereditäre, mit normalen Plättchen Purpura, thrombotische thrombozytopenische Angeborene amegakaryozytäre Thrombozytopenie Thrombozytopenie-Radiusaplasie-Syndrom Thrombophilie, hereditäre, seltene Evans-Syndrom Thrombomodulin-Anomalie, genetisch bedingte Thrombozytopenie mit normalen Plättchen, autosomale Form Thrombozytopenie, Heparin-induzierte Faktor II-Mangel, kongenitaler Alpha- und Delta-Thrombozytengranula-Mangel Faktor V-Mangel, kongenitaler Faktor VII-Mangel, kongenitaler Purpura fulminans, erworbene Faktor X-Mangel, kongenitaler Plasminogenaktivator-Inhibitor Typ 1-Mangel, kongenitaler Faktor XI-Mangel, kongenitaler