SE-ATLAS

Acquired hemophilia Acquired prothrombin deficiency Acquired purpura fulminans Acquired von Willebrand syndrome Alpha delta granule deficiency Alpha granule disease Alpha-1-antitrypsin deficiency Amyloidosis Atrioventricular valve anomaly Atypical hemolytic uremic syndrome Autosomal dominant macrothrombocytopenia Autosomal dominant polycystic kidney disease Autosomal dominant thrombocytopenia with platelet secretion defect 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 CalDAG-GEFI deficiency Bleeding disorder due to P2Y12 defect Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Cardiac diverticulum Catastrophic antiphospholipid syndrome Chronic myeloid leukemia Chronic myeloproliferative disease, unclassifiable Chronic neutrophilic leukemia Combined deficiency of factor V and factor VIII Congenital Gerbode defect Congenital alpha2-antiplasmin deficiency Congenital amegakaryocytic thrombocytopenia Congenital anomaly of the great arteries Congenital anomaly of the great veins 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 pericardium anomaly Congenital plasminogen activator inhibitor type 1 deficiency Congenital prekallikrein deficiency Congenital thrombotic thrombocytopenic purpura Congenital vitamin K-dependent coagulation factors deficiency Coronary artery congenital malformation Criss-cross heart Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Dense granule disease East Texas bleeding disorder Ectopia cordis Ehlers-Danlos syndrome, fibronectinemic type Essential thrombocythemia Evans syndrome Familial afibrinogenemia Familial dysfibrinogenemia Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial platelet disorder with associated myeloid malignancy Familial short QT syndrome Familial thrombomodulin anomalies Fetal and neonatal alloimmune thrombocytopenia GNE myopathy Gaisböck syndrome Genetic cystic renal disease Glanzmann thrombasthenia Glomerular disease HELLP syndrome Heart position anomaly Hemophilia Hemophilia A Hemophilia B Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Heparin-induced thrombocytopenia Hereditary combined deficiency of vitamin K-dependent clotting factors Hereditary isolated aplastic anemia Hereditary thrombocytopenia with early-onset myelofibrosis 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 Hypereosinophilic syndrome Immune thrombocytopenia Immune-mediated thrombotic thrombocytopenic purpura Isolated constitutional thrombocytopenia Isolated delta-storage pool disease Isolated hereditary giant platelet disorder Jacobsen syndrome Jervell and Lange-Nielsen syndrome Kasabach-Merritt phenomenon MYH9-related disease Macrothrombocytopenia with mitral valve insufficiency Mild hemophilia A Mild hemophilia B Moderate hemophilia A Moderate hemophilia B Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Myeloproliferative neoplasm Paroxysmal nocturnal hemoglobinuria Polycythemia vera Primary glomerular disease Primary myelofibrosis Primary renal tubular acidosis Protein S acquired deficiency Pseudo-von Willebrand disease Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare atrial defect and interatrial communication Rare coagulation disorder Rare congenital anomaly of ventricular septum Rare congenital non-syndromic heart malformation Rare hemorrhagic disorder Rare hemorrhagic disorder due to a coagulation factors defect 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 platelet anomaly Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to an acquired coagulation factor defect Rare hemorrhagic disorder due to an acquired platelet anomaly Rare hereditary thrombophilia Rare thrombotic disease of hematologic origin Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a constitutional platelet anomaly Rare thrombotic disorder due to a platelet anomaly Rare thrombotic disorder due to an acquired coagulation factors defect Rare thrombotic disorder due to an acquired platelet anomaly Romano-Ward syndrome STAT3-related early-onset multisystem autoimmune disease Scott syndrome Secondary glomerular disease Severe autosomal recessive macrothrombocytopenia Severe hemophilia A Severe hemophilia B Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Simple cryoglobulinemia Stormorken-Sjaastad-Langslet syndrome Syndromic constitutional thrombocytopenia TAFRO syndrome Thrombocythemia with distal limb defects Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Thrombomodulin-related bleeding disorder Thrombotic thrombocytopenic purpura Transposition of the great arteries and conotruncal cardiac anomaly Univentricular cardiopathy 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 thrombocytopenia with normal platelets