SE-ATLAS

Primary renal tubular acidosis Simple cryoglobulinemia Bleeding diathesis due to a collagen receptor defect Glanzmann thrombasthenia Acquired hemophilia Bleeding diathesis due to thromboxane synthesis deficiency Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency TAFRO syndrome Rare thrombotic disorder due to a constitutional platelet anomaly X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Combined deficiency of factor V and factor VIII Paroxysmal nocturnal hemoglobinuria Rare thrombotic disorder due to an acquired platelet anomaly Hemophilia Hereditary thrombocytopenia with normal platelets Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Rare hereditary thrombophilia Congenital amegakaryocytic thrombocytopenia Thrombotic thrombocytopenic purpura Thrombocytopenia-absent radius syndrome Isolated hereditary giant platelet disorder Autosomal dominant polycystic kidney disease Cardiac diverticulum Evans syndrome Familial thrombomodulin anomalies Autosomal thrombocytopenia with normal platelets Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome Heparin-induced thrombocytopenia Congenital factor II deficiency Alpha delta granule deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Acquired purpura fulminans Congenital factor XI deficiency Congenital plasminogen activator inhibitor type 1 deficiency GNE myopathy Congenital factor XII deficiency Congenital factor XIII deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Alpha-1-antitrypsin deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Catastrophic antiphospholipid syndrome Congenital fibrinogen deficiency Severe hereditary thrombophilia due to congenital protein C deficiency Rare congenital non-syndromic heart malformation Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Autosomal dominant macrothrombocytopenia Bleeding disorder in hemophilia A carriers Amyloidosis Autosomal dominant thrombocytopenia with platelet secretion defect Familial short QT syndrome Congenital Gerbode defect Congenital high-molecular-weight kininogen deficiency Bleeding disorder due to CalDAG-GEFI deficiency Thrombocythemia with distal limb defects Rare hemorrhagic disorder Bleeding disorder due to P2Y12 defect Hereditary thrombocytopenia with early-onset myelofibrosis Ehlers-Danlos syndrome, fibronectinemic type STAT3-related early-onset multisystem autoimmune disease Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder in hemophilia B carriers Rare hemorrhagic disorder due to a constitutional thrombocytopenia Primary glomerular disease Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Jervell and Lange-Nielsen syndrome Von Willebrand disease Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease type 1 Atypical hemolytic uremic syndrome Romano-Ward syndrome Von Willebrand disease type 2 Rare hemorrhagic disorder due to a platelet anomaly Ectopia cordis Rare coagulation disorder Familial platelet disorder with associated myeloid malignancy 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 2B Criss-cross heart Von Willebrand disease type 2A Von Willebrand disease type 2M HELLP syndrome Heart position anomaly Hereditary isolated aplastic anemia MYH9-related disease Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect Transposition of the great arteries and conotruncal cardiac anomaly Atrioventricular valve anomaly Rare thrombotic disease of hematologic origin Familial hypofibrinogenemia Von Willebrand disease type 3 Isolated delta-storage pool disease Severe autosomal recessive macrothrombocytopenia Rare hemorrhagic disorder due to an acquired platelet anomaly Congenital anomaly of the great arteries Dense granule disease Rare congenital anomaly of ventricular septum Alpha granule disease Rare atrial defect and interatrial communication Congenital pericardium anomaly Glomerular disease Congenital anomaly of the great veins Severe hemophilia B Thrombomodulin-related bleeding disorder Scott syndrome Secondary glomerular disease Mild hemophilia B Jacobsen syndrome Coronary artery congenital malformation Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Acquired von Willebrand syndrome Rare thrombotic disorder due to an acquired coagulation factors defect Hemophilia A Severe hemophilia A Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Familial afibrinogenemia Hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a platelet anomaly Familial dysfibrinogenemia Mild hemophilia A Moderate hemophilia A Rare hemorrhagic disorder due to a constitutional coagulation factors defect Bernard-Soulier syndrome Immune thrombocytopenia Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding diathesis due to glycoprotein VI deficiency Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Rare hemorrhagic disorder due to a constitutional platelet anomaly Univentricular cardiopathy Kasabach-Merritt phenomenon Syndromic constitutional thrombocytopenia Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome East Texas bleeding disorder Pseudo-von Willebrand disease Congenital thrombotic thrombocytopenic purpura Congenital vitamin K-dependent coagulation factors deficiency Immune-mediated thrombotic thrombocytopenic purpura Genetic cystic renal disease Gaisböck syndrome Isolated constitutional thrombocytopenia Acquired prothrombin deficiency Protein S acquired deficiency Chronic myeloid leukemia Chronic neutrophilic leukemia Chronic myeloproliferative disease, unclassifiable Primary myelofibrosis Polycythemia vera Myeloproliferative neoplasm Essential thrombocythemia Hypereosinophilic syndrome