SE-ATLAS

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