SE-ATLAS

Von Willebrand disease type 3 Rare thrombotic disease of hematologic origin Rare hemorrhagic disorder due to an acquired platelet anomaly X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Familial hypofibrinogenemia Alpha granule disease Dense granule disease Severe hemophilia B Scott syndrome Sebastian syndrome Rare thrombotic disorder due to a coagulation factors defect Acquired von Willebrand 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 Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Familial afibrinogenemia Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Rare thrombotic disorder due to an acquired coagulation factors defect Bleeding diathesis due to glycoprotein VI deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Immune thrombocytopenia Bernard-Soulier syndrome Mild hemophilia A Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional platelet anomaly Autoimmune thrombocytopenia Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital thrombotic thrombocytopenic purpura East Texas bleeding disorder Immune-mediated thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Gaisböck syndrome Acquired prothrombin deficiency Protein S acquired deficiency Familial thrombocytosis Simple cryoglobulinemia Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Acquired hemophilia Glanzmann thrombasthenia Rare thrombotic disorder due to a constitutional platelet anomaly May-Hegglin thrombocytopenia Paris-Trousseau thrombocytopenia X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to an acquired platelet anomaly Combined deficiency of factor V and factor VIII Bleeding diathesis due to thromboxane synthesis deficiency Hemophilia Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Rare hereditary thrombophilia Essential thrombocythemia Hereditary thrombocytopenia with normal platelets Thrombotic thrombocytopenic purpura Isolated hereditary giant platelet disorder Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Autosomal thrombocytopenia with normal platelets Evans syndrome Familial thrombomodulin anomalies Heparin-induced thrombocytopenia 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 Acquired purpura fulminans Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Congenital factor XI 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 Epstein syndrome Autosomal dominant macrothrombocytopenia Syndrome de Stormorken-Sjaastad-Langslet Déficit congénital en prékallicréine Thrombocytémie avec anomalies distales des membres Maladie hémorragique des porteurs d'hémophilie A Maladie hémorragique rare Maladie hémorragique des porteurs d'hémophilie B Déficit congénital en kininogène de haut poids moléculaire Syndrome de Fechtner Thrombocytopénie avec anémie dysérythropoïétique congénitale Troubles hémorragiques par anomalie du récepteur P2Y12 Déficit congénital en alpha2-antiplasmine Thrombophilie héréditaire due au déficit congénital en antithrombine Maladie hémorragique rare par déficit en facteurs de coagulation Maladie de von Willebrand Maladie hémorragique rare par défaut qualitatif des plaquettes Maladie hémorragique rare par thrombocytopénie constitutionnelle Coagulopathie rare Maladie de von Willebrand type 2 Syndrome de synostose radio-ulnaire-thrombocytopénie amégacaryocytique Maladie de von Willebrand type 1 Macrothrombocytopénie méditérranéenne Maladie de von Willebrand type 2A Déficit héréditaire combiné en facteurs de la coagulation dépendants de la vitamine K Maladie hémorragique rare par anomalie des plaquettes Maladie de von Willebrand type 2M Maladie de von Willebrand type 2B Maladie hémorragique rare par déficit acquis en facteurs de coagulation Maladie de von Willebrand type 2N Syndrome MYH9