SE-ATLAS

Alpha delta granule deficiency Alpha granule disease 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 Familial afibrinogenemia Familial dysfibrinogenemia Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial thrombocytosis Familial thrombomodulin anomalies Glanzmann thrombasthenia Hemophilia Hemophilia A Hemophilia B Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation 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 Isolated hereditary giant platelet disorder MYH9-related disease Macrothrombocytopenia with mitral valve insufficiency Mediterranean macrothrombocytopenia Mild hemophilia A Mild hemophilia B Moderate hemophilia A Moderate hemophilia B Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Paris-Trousseau thrombocytopenia Pseudo-von Willebrand disease Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare genetic coagulation disorder 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 qualitative platelet defect Rare hereditary thrombophilia Rare thrombotic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a constitutional platelet anomaly Scott 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 Stormorken-Sjaastad-Langslet syndrome Thrombocythemia with distal limb defects Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome 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