SE-ATLAS

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 Präkallikrein-Mangel, kongenitaler Stormorken-Sjaastad-Langslet-Syndrom 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 Seltene Blutgerinnungsstörung Symptomatische Form der Hämophilie B bei weiblichen Anlageträgerinnen 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 Radioulnar-Synostose - amegakaryozytische Thrombozytopenie Makrothrombozytopenie, mediterrane 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 MYH9-assoziierte Krankheiten X-chromosomale dyserythropoetische Anämie mit abnormen Blutplättchen und Neutropenie Von-Willebrand-Syndrom Typ 2M Thrombotische Krankheit hämatologischen Ursprungs, seltene Von-Willebrand-Syndrom Typ 3 Von-Willebrand-Syndrom Typ 2N Blutgerinnungsstörung, erworbene Hypofibrinogenämie, familiäre Seltene Blutgerinnungsstörung durch erworbene Blutplättchenanomalie Alpha-Granula-Defekt der Thrombozyten Delta-Thrombozytengranula-Mangel Hämophilie B, mittelschwere Scott-Syndrom Sebastian-Syndrom Hämophilie B, schwere Mild hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Acquired von Willebrand syndrome Rare thrombotic disorder due to a coagulation factors defect Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Hemophilia B Rare thrombotic disorder due to an acquired coagulation factors defect Hemophilia A Familial dysfibrinogenemia Familial afibrinogenemia Severe hemophilia A Mild hemophilia A Bleeding diathesis due to glycoprotein VI deficiency Rare thrombotic disorder due to a platelet anomaly Moderate hemophilia A Bernard-Soulier syndrome Immune thrombocytopenia Rare hemorrhagic disorder due to a constitutional coagulation factors defect Bleeding diathesis due to integrin alpha2-beta1 deficiency 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 Acquired prothrombin deficiency Familial thrombocytosis Protein S acquired deficiency Bleeding diathesis due to a collagen receptor defect Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Glanzmann thrombasthenia Simple cryoglobulinemia May-Hegglin thrombocytopenia Rare thrombotic disorder due to an acquired platelet anomaly Paris-Trousseau thrombocytopenia Acquired hemophilia Bleeding diathesis due to thromboxane synthesis deficiency X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to a constitutional platelet anomaly Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Hemophilia Combined deficiency of factor V and factor VIII Isolated hereditary giant platelet disorder Essential thrombocythemia Hereditary thrombocytopenia with normal platelets Congenital amegakaryocytic thrombocytopenia Thrombotic thrombocytopenic purpura Thrombocytopenia-absent radius syndrome Rare hereditary thrombophilia Evans syndrome Familial thrombomodulin anomalies Autosomal thrombocytopenia with normal platelets Heparin-induced thrombocytopenia Alpha delta granule deficiency Congenital factor II 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 Congenital factor XII deficiency