SE-ATLAS

Primary renal tubular acidosis Simple cryoglobulinemia Bleeding diathesis due to a collagen receptor defect Glanzmann thrombasthenia Acquired hemophilia Bleeding diathesis due to thromboxane synthesis deficiency Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency TAFRO syndrome Rare thrombotic disorder due to a constitutional platelet anomaly X-linked thrombocytopenia with normal platelets Fetal and neonatal alloimmune thrombocytopenia Combined deficiency of factor V and factor VIII Paroxysmal nocturnal hemoglobinuria Rare thrombotic disorder due to an acquired platelet anomaly Hemophilia Hereditary thrombocytopenia with normal platelets Macrothrombocytopenia with mitral valve insufficiency Familial hypodysfibrinogenemia Rare hereditary thrombophilia Congenital amegakaryocytic thrombocytopenia Thrombotic thrombocytopenic purpura Thrombocytopenia-absent radius syndrome Isolated hereditary giant platelet disorder Autosomal dominant polycystic kidney disease Cardiac diverticulum Evans syndrome Familial thrombomodulin anomalies Autosomal thrombocytopenia with normal platelets Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome Heparin-induced thrombocytopenia Congenital factor II deficiency Alpha delta granule deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Acquired purpura fulminans Congenital factor XI deficiency Congenital plasminogen activator inhibitor type 1 deficiency GNE myopathy Congenital factor XII deficiency Congenital factor XIII deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Alpha-1-antitrypsin deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Catastrophic antiphospholipid syndrome Congenital fibrinogen deficiency Severe hereditary thrombophilia due to congenital protein C deficiency Rare congenital non-syndromic heart malformation Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Autosomal dominant macrothrombocytopenia Bleeding disorder in hemophilia A carriers Amyloidosis Autosomal dominant thrombocytopenia with platelet secretion defect Familial short QT syndrome Congenital Gerbode defect Congenital high-molecular-weight kininogen deficiency Bleeding disorder due to CalDAG-GEFI deficiency Thrombocythemia with distal limb defects Rare hemorrhagic disorder Bleeding disorder due to P2Y12 defect Hereditary thrombocytopenia with early-onset myelofibrosis Ehlers-Danlos syndrome, fibronectinemic type STAT3-related early-onset multisystem autoimmune disease Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder in hemophilia B carriers Rare hemorrhagic disorder due to a constitutional thrombocytopenia Primary glomerular disease Congenital alpha2-antiplasmin deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Jervell and Lange-Nielsen syndrome Von Willebrand disease Rare hemorrhagic disorder due to a coagulation factors defect Von Willebrand disease type 1 Atypical hemolytic uremic syndrome Romano-Ward syndrome Von Willebrand disease type 2 Rare hemorrhagic disorder due to a platelet anomaly Ectopia cordis Rare coagulation disorder Familial platelet disorder with associated myeloid malignancy Rare hemorrhagic disorder due to a qualitative platelet defect Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Hereditary combined deficiency of vitamin K-dependent clotting factors Von Willebrand disease type 2B Criss-cross heart Von Willebrand disease type 2A Von Willebrand disease type 2M HELLP syndrome Heart position anomaly Hereditary isolated aplastic anemia MYH9-related disease Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect Transposition of the great arteries and conotruncal cardiac anomaly Atrioventrikulären Klappe, Anomalie der Thrombotische Krankheit hämatologischen Ursprungs, seltene Hypofibrinogenämie, familiäre Von-Willebrand-Syndrom Typ 3 Delta-Storage-Pool-Krankheit, isolierte Makrothrombozytopenie, schwere, autosomal-rezessive Seltene Blutgerinnungsstörung durch erworbene Blutplättchenanomalie Kongenitale Anomalie der großen Arterien Delta-Thrombozytengranula-Mangel Seltene kongenitale Anomalie des Ventrikelseptums Alpha-Granula-Defekt der Thrombozyten Seltener Vorhofdefekt und interatriale Kommunikation Perikardfehlbildungen, kongenitale Glomerulopathie Großen Venen, kongenitale Anomalie der Hämophilie B, schwere Thrombomodulin-abhängige Blutgerinnungsstörung Scott-Syndrom Glomerulopathie, sekundäre Hämophilie B, milde Jacobsen-Syndrom Fehlbildung der Koronararterien, kongenitale Hämophilie B, mittelschwere Seltene thrombotische Störung durch Gerinnungsfaktoren-Defekt Von-Willebrand-Syndrom, erworbenes Seltene thrombotische Störung durch erworbenen Gerinnungsfaktoren-Defekt Hämophilie A Hämophilie A, schwere Hämorrhagische Krankheit durch Alpha-1-Antitrypsin Pittsburgh-Mutation Afibrinogenämie, familiäre Hämophilie B Seltene thrombotische Störung durch konstitutionellen Gerinnungsfaktoren-Defekt Seltene thrombotische Störung durch Blutplättchenanomalie Dysfibrinogenämie, familiäre Hämophilie A, milde Hämophilie A, mittelschwere Seltene Blutgerinnungsstörung durch konstitutionellen Gerinnungsfaktoren-Defekt Bernard-Soulier-Syndrom Immunthrombozytopenie Hämorrhagische Diathese durch Integrin alpha2-beta1-Mangel Hämorrhagische Diathese durch Glykoprotein VI-Mangel Blutungskrankheit mit assoziiertem Mangel der zytosolischen Phospholipase-A2 alpha Thrombopathie, konstitutionelle Kardiopathie, univentrikuläre Kasabach-Merritt-Syndrom Konstitutionelle Thrombozytopenie, syndromale Multiple Sklerose-Ichthyose-Faktor-VIII-Mangel-Syndrom Gerinnungsstörung vom Ost-Texanischen Typ Pseudo-von-Willebrand-Syndrom Thrombotisch-thrombozytopenische Purpura, kongenitale Form Vitamin K-abhängige Gerinnungsfaktoren, kongenitaler Mangel Thrombotisch-thrombozytopenische Purpura, immun-vermittelte Zystische Nierenerkrankung, genetisch bedingte Gaisböck-Syndrom Konstitutionelle Thrombozytopenie, isolierte Faktor II-Mangel, erworbener Protein-S-Mangel, erworbener Leukämie, chronische myeloische Leukämie, chronische neutrophile Myeloproliferative Krankheit, nicht klassifizierbare Primäre Myelofibrose Polycythaemia vera Myeloproliferative Neoplasie Essentielle Thrombozythämie Hypereosinophile Syndrome