SE-ATLAS

Acquired hemophilia Acquired prothrombin deficiency Acquired purpura fulminans Acquired von Willebrand syndrome Alpha delta granule deficiency Alpha granule disease Autoimmune thrombocytopenia Autosomal dominant macrothrombocytopenia Autosomal thrombocytopenia with normal platelets Bernard-Soulier syndrome Bleeding diathesis due to a collagen receptor defect Bleeding diathesis due to glycoprotein VI deficiency Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding diathesis due to thromboxane synthesis deficiency Bleeding disorder due to P2Y12 defect Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Combined deficiency of factor V and factor VIII Congenital alpha2-antiplasmin deficiency Congenital amegakaryocytic thrombocytopenia Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Congenital fibrinogen deficiency Congenital high-molecular-weight kininogen deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital prekallikrein deficiency Congenital thrombotic thrombocytopenic purpura Congenital vitamin K-dependent coagulation factors deficiency Dense granule disease East Texas bleeding disorder Epstein syndrome Essential thrombocythemia Evans syndrome Familial afibrinogenemia Familial dysfibrinogenemia Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial thrombocytosis Familial thrombomodulin anomalies Fechtner syndrome Fetal and neonatal alloimmune thrombocytopenia Gaisböck syndrome Glanzmann thrombasthenia Hemophilia Hemophilia A Hemophilia B Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Heparin-induced thrombocytopenia Hereditary combined deficiency of vitamin K-dependent clotting factors Hereditary thrombocytopenia with normal platelets Hereditary thrombophilia due to congenital antithrombin deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Immune thrombocytopenia Immune-mediated thrombotic thrombocytopenic purpura Isolated hereditary giant platelet disorder MYH9-related disease Macrothrombocytopenia with mitral valve insufficiency May-Hegglin thrombocytopenia Mediterranean macrothrombocytopenia Mild hemophilia A Mild hemophilia B Moderate hemophilia A Moderate hemophilia B Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Paris-Trousseau thrombocytopenia Protein S acquired deficiency Pseudo-von Willebrand disease Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare coagulation disorder Rare hemorrhagic disorder Rare hemorrhagic disorder due to a coagulation factors defect Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare hemorrhagic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to an acquired coagulation factor defect Rare hemorrhagic disorder due to an acquired platelet anomaly Rare hereditary thrombophilia Rare thrombotic disease of hematologic origin Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a constitutional platelet anomaly Rare thrombotic disorder due to a platelet anomaly Rare thrombotic disorder due to an acquired coagulation factors defect Rare thrombotic disorder due to an acquired platelet anomaly Scott syndrome Sebastian syndrome Severe hemophilia A Severe hemophilia B Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Simple cryoglobulinemia Stormorken-Sjaastad-Langslet syndrome Thrombocythemia with distal limb defects Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Thrombotic thrombocytopenic purpura Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 2A Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 X-linked dyserythropoietic anemia with abnormal platelets and neutropenia X-linked thrombocytopenia with normal platelets