SE-ATLAS

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