SE-ATLAS

Faktor XII-Mangel, kongenitaler Faktor XIII-Mangel, kongenitaler Thrombophilie, hereditäre, durch kongenitalen Mangel des Histidin-reichen (poly-L) Glykoproteins Schwere hereditäre Thrombophilie durch kongenitalen Protein-S-Mangel Fibrinogen-Mangel, kongenitaler Makrothrombozytopenie, autosomal-dominante Schwere hereditäre Thrombophilie durch kongenitalen Protein-C-Mangel Epstein-Syndrom Hereditäre Thrombozytose mit transversalen Extremitätendefekt Stormorken-Sjaastad-Langslet-Syndrom Präkallikrein-Mangel, kongenitaler Symptomatische Form der Hämophilie A bei weiblichen Anlageträgerinnen High-Molecular-Weight Kininogen-Mangel, kongenitaler Fechtner-Syndrom Blutgerinnungsstörung durch P2Y12-Defekt Thrombozytopenie mit kongenitaler dyserythropoetischer Anämie Symptomatische Form der Hämophilie B bei weiblichen Anlageträgerinnen Seltene Blutgerinnungsstörung Seltene Blutgerinnungsstörung durch konstitutionelle Thrombozytopenie Alpha-2 Antiplasmin-Mangel, kongenitaler Hereditäre Thrombophilie durch kongenitalen Antithrombin-Mangel Von-Willebrand-Syndrom Seltene Blutgerinnungsstörung durch qualitativen Plättchen-Defekt Seltene Blutgerinnungsstörung durch Gerinnungsfaktoren-Defekt Von-Willebrand-Syndrom Typ 1 Seltene Gerinnungsstörung Makrothrombozytopenie, mediterrane Radioulnar-Synostose - amegakaryozytische Thrombozytopenie Seltene Blutgerinnungsstörung durch Blutplättchenanomalie Von-Willebrand-Syndrom Typ 2 Von-Willebrand-Syndrom Typ 2B Vitamin K-abhängige Gerinnungsfaktoren, hereditärer kombinierter Mangel Von-Willebrand-Syndrom Typ 2A Von-Willebrand-Syndrom Typ 2M X-chromosomale dyserythropoetische Anämie mit abnormen Blutplättchen und Neutropenie Thrombotische Krankheit hämatologischen Ursprungs, seltene Von-Willebrand-Syndrom Typ 3 Von-Willebrand-Syndrom Typ 2N Blutgerinnungsstörung, erworbene MYH9-assoziierte Krankheiten 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 Essential thrombocythemia Hereditary thrombocytopenia with normal platelets Thrombotic thrombocytopenic purpura Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Rare hereditary thrombophilia Evans syndrome Familial thrombomodulin anomalies Autosomal thrombocytopenia with normal platelets Heparin-induced thrombocytopenia Congenital factor II deficiency Alpha delta granule deficiency Congenital factor V deficiency Congenital factor VII deficiency Acquired purpura fulminans Congenital factor X deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital factor XI deficiency