SE-ATLAS

Severe hemophilia B Scott 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 Familial afibrinogenemia Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Moderate hemophilia A Rare hemorrhagic disorder due to a constitutional coagulation factors defect Bleeding diathesis due to glycoprotein VI deficiency Bernard-Soulier syndrome Mild hemophilia A Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional platelet anomaly East Texas bleeding disorder Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Familial thrombocytosis Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Glanzmann thrombasthenia Rare thrombotic disorder due to a constitutional platelet anomaly Paris-Trousseau thrombocytopenia X-linked thrombocytopenia with normal platelets Combined deficiency of factor V and factor VIII Bleeding diathesis due to thromboxane synthesis deficiency Hemophilia Hereditary thrombocytopenia with normal platelets Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Rare hereditary thrombophilia Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Isolated hereditary giant platelet disorder Autosomal thrombocytopenia with normal platelets Familial thrombomodulin anomalies 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 Congenital factor XI deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein 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 Autosomal dominant macrothrombocytopenia Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Rare genetic coagulation disorder Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Congenital high-molecular-weight kininogen deficiency Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder due to P2Y12 defect Thrombocythemia with distal limb defects Rare hemorrhagic disorder due to a constitutional thrombocytopenia Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Von Willebrand disease Von Willebrand disease type 2 Von Willebrand disease type 1 Mediterranean macrothrombocytopenia Rare hemorrhagic disorder due to a qualitative platelet defect Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Hereditary combined deficiency of vitamin K-dependent clotting factors Von Willebrand disease type 2A Von Willebrand disease type 2M Von Willebrand disease type 2B Von Willebrand disease type 2N X-linked dyserythropoietic anemia with abnormal platelets and neutropenia MYH9-related disease Von Willebrand disease type 3 Familial hypofibrinogenemia Alpha granule disease Dense granule disease