SE-ATLAS

Epstein syndrome Thrombocythemia with distal limb defects Autosomal dominant macrothrombocytopenia Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Bleeding disorder in hemophilia B carriers Rare hemorrhagic disorder Congenital high-molecular-weight kininogen deficiency Bleeding disorder due to P2Y12 defect Fechtner syndrome Bleeding disorder in hemophilia A carriers Thrombocytopenia with congenital dyserythropoietic anemia Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare coagulation disorder Von Willebrand disease type 2 Von Willebrand disease type 1 Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Mediterranean macrothrombocytopenia Von Willebrand disease type 2A Rare hemorrhagic disorder due to a qualitative platelet defect Hereditary combined deficiency of vitamin K-dependent clotting factors Rare hemorrhagic disorder due to a platelet anomaly 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 Faktor VII-Mangel, kongenitaler Faktor X-Mangel, kongenitaler Plasminogenaktivator-Inhibitor Typ 1-Mangel, kongenitaler Faktor XI-Mangel, kongenitaler Purpura fulminans, erworbene Faktor XII-Mangel, kongenitaler Faktor XIII-Mangel, kongenitaler Schwere hereditäre Thrombophilie durch kongenitalen Protein-S-Mangel Thrombophilie, hereditäre, durch kongenitalen Mangel des Histidin-reichen (poly-L) Glykoproteins Fibrinogen-Mangel, kongenitaler Schwere hereditäre Thrombophilie durch kongenitalen Protein-C-Mangel