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 Thrombotic thrombocytopenic purpura Isolated hereditary giant platelet disorder Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Autosomal thrombocytopenia with normal platelets Evans syndrome Familial thrombomodulin anomalies Heparin-induced thrombocytopenia Alpha delta granule deficiency Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital plasminogen activator inhibitor type 1 deficiency Acquired purpura fulminans Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Congenital fibrinogen deficiency Severe hereditary thrombophilia due to congenital protein C deficiency Epstein syndrome Autosomal dominant macrothrombocytopenia Stormorken-Sjaastad-Langslet syndrome Congenital prekallikrein deficiency Thrombocythemia with distal limb defects Bleeding disorder in hemophilia A carriers Rare hemorrhagic disorder Bleeding disorder in hemophilia B carriers Congenital high-molecular-weight kininogen deficiency Fechtner syndrome Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder due to P2Y12 defect 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 qualitative platelet defect Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare coagulation disorder Von Willebrand disease type 2 Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Von Willebrand disease type 1 Mediterranean macrothrombocytopenia Von Willebrand disease type 2A Hereditary combined deficiency of vitamin K-dependent clotting factors Rare hemorrhagic disorder due to a platelet anomaly Von Willebrand disease type 2M Von Willebrand disease type 2B Rare hemorrhagic disorder due to an acquired coagulation factor defect Von Willebrand disease type 2N MYH9-related disease