SE-ATLAS

Congenital factor XII deficiency 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 Stormorken-Sjaastad-Langslet syndrome Congenital prekallikrein deficiency 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 Bleeding disorder in hemophilia B carriers Rare hemorrhagic disorder 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 Mediterranean macrothrombocytopenia Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome 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 Von Willebrand disease type 2M X-linked dyserythropoietic anemia with abnormal platelets and neutropenia 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 MYH9-related disease Familial hypofibrinogenemia Rare hemorrhagic disorder due to an acquired platelet anomaly Dense granule disease Alpha granule disease Scott syndrome Severe hemophilia B Sebastian syndrome Acquired von Willebrand syndrome Mild hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Hemophilia A Rare thrombotic disorder due to an acquired coagulation factors defect Familial dysfibrinogenemia Familial afibrinogenemia Severe hemophilia A Hemophilia B Mild hemophilia A Bleeding diathesis due to glycoprotein VI deficiency Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Immune thrombocytopenia Bernard-Soulier syndrome Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect 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 Familial thrombocytosis Acquired prothrombin deficiency Protein S acquired deficiency Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Glanzmann thrombasthenia Simple cryoglobulinemia Rare thrombotic disorder due to an acquired platelet anomaly May-Hegglin thrombocytopenia Bleeding diathesis due to thromboxane synthesis deficiency Acquired hemophilia Paris-Trousseau thrombocytopenia X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to a constitutional platelet anomaly Familial hypodysfibrinogenemia Macrothrombocytopenia with mitral valve insufficiency Combined deficiency of factor V and factor VIII Hemophilia Isolated hereditary giant platelet disorder Essential thrombocythemia Hereditary thrombocytopenia with normal platelets Thrombotic thrombocytopenic purpura Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Rare hereditary thrombophilia Evans syndrome Familial thrombomodulin anomalies Autosomal thrombocytopenia with normal platelets Heparin-induced thrombocytopenia Congenital factor II deficiency Alpha delta granule 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