SE-ATLAS

Bernard-Soulier syndrome Immune thrombocytopenia Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding diathesis due to glycoprotein VI deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Autoimmune thrombocytopenia Rare hemorrhagic disorder due to a constitutional platelet anomaly Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome East Texas bleeding disorder Congenital thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Congenital vitamin K-dependent coagulation factors deficiency Immune-mediated thrombotic thrombocytopenic purpura Familial thrombocytosis Acquired prothrombin deficiency Gaisböck syndrome Protein S acquired deficiency Simple cryoglobulinemia Bleeding diathesis due to a collagen receptor defect Glanzmann thrombasthenia May-Hegglin thrombocytopenia Bleeding diathesis due to thromboxane synthesis deficiency Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Acquired hemophilia Paris-Trousseau thrombocytopenia Rare thrombotic disorder due to a constitutional platelet anomaly X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Hereditary thrombocytopenia with normal platelets Combined deficiency of factor V and factor VIII Hemophilia Rare thrombotic disorder due to an acquired platelet anomaly Isolated hereditary giant platelet disorder Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Essential thrombocythemia Rare hereditary thrombophilia Congenital amegakaryocytic thrombocytopenia Thrombocytopenia-absent radius syndrome Thrombotic thrombocytopenic purpura Evans syndrome Familial thrombomodulin anomalies Heparin-induced thrombocytopenia Congenital factor II deficiency Autosomal thrombocytopenia with normal platelets Alpha delta granule deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Acquired purpura fulminans Congenital plasminogen activator inhibitor type 1 deficiency Congenital factor XI deficiency 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 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 Thrombocythemia with distal limb defects Rare hemorrhagic disorder Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder in hemophilia B carriers 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 coagulation factors defect Von Willebrand disease type 1 Mediterranean macrothrombocytopenia Von Willebrand disease type 2 Rare hemorrhagic disorder due to a platelet anomaly Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare coagulation disorder Seltene Blutgerinnungsstörung durch qualitativen Plättchen-Defekt 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 MYH9-assoziierte Krankheiten Blutgerinnungsstörung, erworbene Von-Willebrand-Syndrom Typ 2N Hypofibrinogenämie, familiäre Thrombotische Krankheit hämatologischen Ursprungs, seltene Von-Willebrand-Syndrom Typ 3 Seltene Blutgerinnungsstörung durch erworbene Blutplättchenanomalie Delta-Thrombozytengranula-Mangel Alpha-Granula-Defekt der Thrombozyten Hämophilie B, schwere Scott-Syndrom Seltene thrombotische Störung durch konstitutionellen Gerinnungsfaktoren-Defekt Sebastian-Syndrom Hämophilie B, milde Seltene thrombotische Störung durch Gerinnungsfaktoren-Defekt Hämophilie B, mittelschwere Von-Willebrand-Syndrom, erworbenes Hämophilie A Seltene thrombotische Störung durch erworbenen Gerinnungsfaktoren-Defekt Hämophilie A, schwere Hämorrhagische Krankheit durch Alpha-1-Antitrypsin Pittsburgh-Mutation Afibrinogenämie, familiäre Hämophilie B Hämophilie A, milde Seltene thrombotische Störung durch Blutplättchenanomalie Dysfibrinogenämie, familiäre Hämophilie A, mittelschwere