SE-ATLAS

Von Willebrand disease type 3 Rare thrombotic disease of hematologic origin Rare hemorrhagic disorder due to an acquired platelet anomaly X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Familial hypofibrinogenemia Alpha granule disease Dense granule disease Severe hemophilia B Scott syndrome Sebastian syndrome Rare thrombotic disorder due to a coagulation factors defect Acquired von Willebrand syndrome Moderate hemophilia B Severe hemophilia A Hemophilia B Mild hemophilia B Hemophilia A Rare thrombotic disorder due to a constitutional coagulation factors defect Familial dysfibrinogenemia Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Familial afibrinogenemia Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Rare thrombotic disorder due to an acquired coagulation factors defect Bleeding diathesis due to glycoprotein VI deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Immune thrombocytopenia Bernard-Soulier syndrome Mild hemophilia A Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional platelet anomaly Autoimmune thrombocytopenia Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital thrombotic thrombocytopenic purpura East Texas bleeding disorder Immune-mediated thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Gaisböck syndrome Acquired prothrombin deficiency Protein S acquired deficiency Familial thrombocytosis Simple cryoglobulinemia Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Acquired hemophilia Glanzmann thrombasthenia Rare thrombotic disorder due to a constitutional platelet anomaly May-Hegglin thrombocytopenia Paris-Trousseau thrombocytopenia X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to an acquired platelet anomaly Combined deficiency of factor V and factor VIII Bleeding diathesis due to thromboxane synthesis deficiency Hemophilia Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Rare hereditary thrombophilia Essential thrombocythemia Hereditary thrombocytopenia with normal platelets Purpura, thrombotische thrombozytopenische Giant-Platelet-Syndrom, isoliertes hereditäres Angeborene amegakaryozytäre Thrombozytopenie Thrombozytopenie-Radiusaplasie-Syndrom Thrombozytopenie mit normalen Plättchen, autosomale Form Evans-Syndrom Thrombomodulin-Anomalie, genetisch bedingte Thrombozytopenie, Heparin-induzierte Alpha- und Delta-Thrombozytengranula-Mangel Faktor II-Mangel, kongenitaler Faktor V-Mangel, kongenitaler Faktor VII-Mangel, kongenitaler Faktor X-Mangel, kongenitaler Plasminogenaktivator-Inhibitor Typ 1-Mangel, kongenitaler Purpura fulminans, erworbene Thrombophilie, hereditäre, durch kongenitalen Mangel des Histidin-reichen (poly-L) Glykoproteins Faktor XI-Mangel, kongenitaler Faktor XII-Mangel, kongenitaler Faktor XIII-Mangel, kongenitaler Schwere hereditäre Thrombophilie durch kongenitalen Protein-S-Mangel Fibrinogen-Mangel, kongenitaler Schwere hereditäre Thrombophilie durch kongenitalen Protein-C-Mangel Epstein-Syndrom Makrothrombozytopenie, autosomal-dominante Stormorken-Sjaastad-Langslet-Syndrom Präkallikrein-Mangel, kongenitaler Hereditäre Thrombozytose mit transversalen Extremitätendefekt Symptomatische Form der Hämophilie A bei weiblichen Anlageträgerinnen Seltene Blutgerinnungsstörung Symptomatische Form der Hämophilie B bei weiblichen Anlageträgerinnen High-Molecular-Weight Kininogen-Mangel, kongenitaler Fechtner-Syndrom Thrombozytopenie mit kongenitaler dyserythropoetischer Anämie Blutgerinnungsstörung durch P2Y12-Defekt Alpha-2 Antiplasmin-Mangel, kongenitaler Hereditäre Thrombophilie durch kongenitalen Antithrombin-Mangel Seltene Blutgerinnungsstörung durch Gerinnungsfaktoren-Defekt Von-Willebrand-Syndrom Seltene Blutgerinnungsstörung durch qualitativen Plättchen-Defekt Seltene Blutgerinnungsstörung durch konstitutionelle Thrombozytopenie Seltene Gerinnungsstörung Von-Willebrand-Syndrom Typ 2 Radioulnar-Synostose - amegakaryozytische Thrombozytopenie Von-Willebrand-Syndrom Typ 1 Makrothrombozytopenie, mediterrane Von-Willebrand-Syndrom Typ 2A Vitamin K-abhängige Gerinnungsfaktoren, hereditärer kombinierter Mangel Seltene Blutgerinnungsstörung durch Blutplättchenanomalie Von-Willebrand-Syndrom Typ 2M Von-Willebrand-Syndrom Typ 2B Blutgerinnungsstörung, erworbene Von-Willebrand-Syndrom Typ 2N MYH9-assoziierte Krankheiten