SE-ATLAS

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 Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome 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 Rare hemorrhagic disorder Bleeding disorder in hemophilia B carriers 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 Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Mediterranean macrothrombocytopenia 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 MYH9-related disease X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Von Willebrand disease type 2M 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 Familial hypofibrinogenemia Rare hemorrhagic disorder due to an acquired platelet anomaly Alpha granule disease Dense granule disease Moderate hemophilia B Scott syndrome Sebastian syndrome Severe hemophilia B Mild hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Acquired von Willebrand syndrome Rare thrombotic disorder due to a coagulation factors defect Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Hemophilia B Rare thrombotic disorder due to an acquired coagulation factors defect Hemophilia A Familial dysfibrinogenemia Familial afibrinogenemia Severe hemophilia A Mild hemophilia A Bleeding diathesis due to glycoprotein VI deficiency Rare thrombotic disorder due to a platelet anomaly Hämophilie A, mittelschwere Bernard-Soulier-Syndrom Immunthrombozytopenie Seltene Blutgerinnungsstörung durch konstitutionellen Gerinnungsfaktoren-Defekt Hämorrhagische Diathese durch Integrin alpha2-beta1-Mangel Thrombopathie, konstitutionelle Thrombozytopenie, autoimmune Gerinnungsstörung vom Ost-Texanischen Typ Multiple Sklerose-Ichthyose-Faktor-VIII-Mangel-Syndrom Thrombotisch-thrombozytopenische Purpura, kongenitale Form Thrombotisch-thrombozytopenische Purpura, immun-vermittelte Pseudo-von-Willebrand-Syndrom Vitamin K-abhängige Gerinnungsfaktoren, kongenitaler Mangel Gaisböck-Syndrom Faktor II-Mangel, erworbener Thrombozytose, familiäre Protein-S-Mangel, erworbener Hämorrhagische Diathese durch Kollagen-Rezeptor-Mangel Hyperkoagulabilitätssyndrom durch Glykosylphosphatidyl-Inositol-Mangel Thrombasthenie Glanzmann Kryoglobulinämie, einfache Thrombozytopenie May-Hegglin Seltene thrombotische Störung durch erworbene Blutplättchenanomalie Paris-Trousseau-Syndrom Hämophilie, erworbene Hämorrhagische Diathese durch Thromboxan-Synthetase-Mangel Thrombozytopenie, X-chromosomale, mit normalen Plättchen Alloimmunthrombozytopenie, fetale und neonatale Seltene thrombotische Störung durch konstitutionelle Blutplättchenanomalie Makrothrombozytopenie mit Mitralklappeninsuffizienz Hypodysfibrinogenämie, familiäre Hämophilie Kombinierter Mangel an Faktor V und Faktor VIII Giant-Platelet-Syndrom, isoliertes hereditäres Essentielle Thrombozythämie Thrombozytopenie, hereditäre, mit normalen Plättchen Angeborene amegakaryozytäre Thrombozytopenie Purpura, thrombotische thrombozytopenische Thrombozytopenie-Radiusaplasie-Syndrom Thrombophilie, hereditäre, seltene Evans-Syndrom Thrombomodulin-Anomalie, genetisch bedingte Thrombozytopenie mit normalen Plättchen, autosomale Form Thrombozytopenie, Heparin-induzierte Alpha- und Delta-Thrombozytengranula-Mangel Faktor II-Mangel, kongenitaler 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 Faktor XII-Mangel, kongenitaler