SE-ATLAS

Congenital factor XII deficiency Congenital factor XIII deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Congenital fibrinogen deficiency Autosomal dominant macrothrombocytopenia Severe hereditary thrombophilia due to congenital protein C deficiency Epstein syndrome Thrombocythemia with distal limb defects Stormorken-Sjaastad-Langslet syndrome Congenital prekallikrein deficiency Bleeding disorder in hemophilia A carriers Congenital high-molecular-weight kininogen deficiency Fechtner syndrome Bleeding disorder due to P2Y12 defect Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder in hemophilia B carriers Rare hemorrhagic disorder Rare hemorrhagic disorder due to a constitutional thrombocytopenia Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Von Willebrand disease Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease type 1 Rare coagulation disorder Mediterranean macrothrombocytopenia Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare hemorrhagic disorder due to a platelet anomaly Von Willebrand disease type 2 Von Willebrand disease type 2B Hereditary combined deficiency of vitamin K-dependent clotting factors Von Willebrand disease type 2A Von Willebrand disease type 2M X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Rare thrombotic disease of hematologic origin Von Willebrand disease type 3 Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect MYH9-related disease Familial hypofibrinogenemia Rare hemorrhagic disorder due to an acquired platelet anomaly Dense granule disease Alpha granule disease Scott syndrome Severe hemophilia B Sebastian syndrome Acquired von Willebrand syndrome Mild hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Hemophilia A Rare thrombotic disorder due to an acquired coagulation factors defect Familial dysfibrinogenemia Familial afibrinogenemia Severe hemophilia A Hemophilia B Mild hemophilia A Bleeding diathesis due to glycoprotein VI deficiency Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Immune thrombocytopenia Bernard-Soulier syndrome Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare hemorrhagic disorder due to a constitutional platelet anomaly Autoimmune thrombocytopenia East Texas bleeding disorder Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Congenital thrombotic thrombocytopenic purpura Immune-mediated thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Gaisböck syndrome Familial thrombocytosis Acquired prothrombin deficiency Protein S acquired deficiency Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Glanzmann thrombasthenia Simple cryoglobulinemia Rare thrombotic disorder due to an acquired platelet anomaly May-Hegglin thrombocytopenia Bleeding diathesis due to thromboxane synthesis deficiency Acquired hemophilia Paris-Trousseau thrombocytopenia X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to a constitutional platelet anomaly Familial hypodysfibrinogenemia Macrothrombocytopenia with mitral valve insufficiency Combined deficiency of factor V and factor VIII Hemophilia Isolated hereditary giant platelet disorder Thrombocytémie essentielle Thrombocytopénie héréditaire avec plaquettes normales Purpura thrombotique thrombocytopénique Thrombocytopénie amégacaryocytaire congénitale Syndrome de thrombocytopénie-aplasie radiale Thrombophilie héréditaire rare Syndrome d'Evans Anomalies de la thrombomoduline Thrombocytopénie autosomique avec plaquettes normales Thrombopénie induite par l'héparine Déficit congénital en facteur II Déficit en granules alpha et delta Faktor V-Mangel, kongenitaler Faktor VII-Mangel, kongenitaler Purpura fulminans, erworbene Faktor X-Mangel, kongenitaler Plasminogenaktivator-Inhibitor Typ 1-Mangel, kongenitaler Faktor XI-Mangel, kongenitaler