SE-ATLAS

Epstein-Syndrom Hereditäre Thrombozytose mit transversalen Extremitätendefekt Makrothrombozytopenie, autosomal-dominante Präkallikrein-Mangel, kongenitaler Stormorken-Sjaastad-Langslet-Syndrom Symptomatische Form der Hämophilie B bei weiblichen Anlageträgerinnen Seltene Blutgerinnungsstörung High-Molecular-Weight Kininogen-Mangel, kongenitaler Blutgerinnungsstörung durch P2Y12-Defekt Fechtner-Syndrom Symptomatische Form der Hämophilie A bei weiblichen Anlageträgerinnen Thrombozytopenie mit kongenitaler dyserythropoetischer Anämie Alpha-2 Antiplasmin-Mangel, kongenitaler Hereditäre Thrombophilie durch kongenitalen Antithrombin-Mangel Seltene Blutgerinnungsstörung durch Gerinnungsfaktoren-Defekt Von-Willebrand-Syndrom Seltene Blutgerinnungsstörung durch konstitutionelle Thrombozytopenie Seltene Gerinnungsstörung Von-Willebrand-Syndrom Typ 2 Von-Willebrand-Syndrom Typ 1 Radioulnar-Synostose - amegakaryozytische Thrombozytopenie Makrothrombozytopenie, mediterrane Von-Willebrand-Syndrom Typ 2A Seltene Blutgerinnungsstörung durch qualitativen Plättchen-Defekt Vitamin K-abhängige Gerinnungsfaktoren, hereditärer kombinierter Mangel Seltene Blutgerinnungsstörung durch Blutplättchenanomalie Von Willebrand disease type 2B MYH9-related disease Rare hemorrhagic disorder due to an acquired coagulation factor defect Von Willebrand disease type 2N Von Willebrand disease type 2M Rare thrombotic disease of hematologic origin Von Willebrand disease type 3 X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Familial hypofibrinogenemia Dense granule disease Rare hemorrhagic disorder due to an acquired platelet anomaly Alpha granule disease Severe hemophilia B Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Scott syndrome Sebastian syndrome Acquired von Willebrand syndrome Severe hemophilia A Rare thrombotic disorder due to a constitutional coagulation factors defect Hemophilia A Mild hemophilia B Moderate hemophilia A Familial afibrinogenemia Hemophilia B Rare thrombotic disorder due to an acquired coagulation factors defect Familial dysfibrinogenemia Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Bleeding diathesis due to glycoprotein VI deficiency Immune thrombocytopenia Bernard-Soulier syndrome Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Mild hemophilia A Rare thrombotic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a constitutional platelet anomaly Autoimmune thrombocytopenia Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome East Texas bleeding disorder Congenital vitamin K-dependent coagulation factors deficiency Pseudo-von Willebrand disease Immune-mediated thrombotic thrombocytopenic purpura Congenital thrombotic thrombocytopenic purpura Familial thrombocytosis Acquired prothrombin deficiency Gaisböck syndrome Protein S acquired deficiency Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Rare thrombotic disorder due to a constitutional platelet anomaly Glanzmann thrombasthenia Simple cryoglobulinemia May-Hegglin thrombocytopenia Paris-Trousseau thrombocytopenia Acquired hemophilia X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to an acquired platelet anomaly Bleeding diathesis due to thromboxane synthesis deficiency Combined deficiency of factor V and factor VIII Hemophilia Familial hypodysfibrinogenemia Macrothrombocytopenia with mitral valve insufficiency Hereditary thrombocytopenia with normal platelets Essential thrombocythemia Isolated hereditary giant platelet disorder Thrombotic thrombocytopenic purpura Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Autosomal thrombocytopenia with normal platelets Evans syndrome Rare hereditary thrombophilia Familial thrombomodulin anomalies Alpha delta granule deficiency Heparin-induced thrombocytopenia 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 Acquired purpura fulminans Congenital factor XII deficiency Congenital factor XIII deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Congenital fibrinogen deficiency Severe hereditary thrombophilia due to congenital protein C deficiency