SE-ATLAS

Acidose tubulaire rénale primitive Cryoglobulinémie simple Troubles hémorragiques par déficit en récepteur du collagène Thrombasthénie de Glanzmann Hémophilie acquise Troubles hémorragiques par déficit de synthèse de la thromboxane Syndrome d'hypercoagulabilité par déficit héréditaire en glycosyl phosphatidyl inositol Syndrome de TAFRO Maladie thrombotique rare par anomalie constitutionnelle des plaquettes Thrombocytopénie liée à l'X avec plaquettes normales Thrombopénie materno-foetale et néonatale allo-immune Déficit combiné en facteurs V et VIII Hémoglobinurie paroxystique nocturne Maladie thrombotique rare par anomalie acquise des plaquettes Hémophilie Thrombocytopénie héréditaire avec plaquettes normales Macrothrombocytopenie avec insuffisance mitrale Hypodysfibrinogénémie familiale Thrombophilie héréditaire rare Thrombocytopénie amégacaryocytaire congénitale Purpura thrombotique thrombocytopénique Syndrome de thrombocytopénie-aplasie radiale Macrothrombocytopénie héréditaire isolée Polykystose rénale autosomique dominante Diverticule du coeur Syndrome d'Evans Anomalies de la thrombomoduline Thrombocytopénie autosomique avec plaquettes normales Syndrome de lymphangioendothéliomatose multifocale-thrombocytopénie Thrombopénie induite par l'héparine Déficit congénital en facteur II Déficit en granules alpha et delta Déficit congénital en facteur V Déficit congénital en facteur VII Déficit congénital en facteur X Purpura fulminans acquis Déficit congénital en facteur XI Déficit congénital en inhibiteur 1 de l'activateur du plasminogène Myopathie liée à GNE Déficit congénital en facteur XII Déficit congénital en facteur XIII Thrombophilie héréditaire due au déficit congénital en histidine-rich (poly-L) glycoprotéine Déficit en alpha-1-antitrypsine Thrombophilie héréditaire sévère due au déficit congénital en protéine S Syndrome catastrophique des antiphospholipides Déficit congénital en fibrinogène 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 Atrioventricular valve anomaly Rare thrombotic disease of hematologic origin Familial hypofibrinogenemia Von Willebrand disease type 3 Isolated delta-storage pool disease Severe autosomal recessive macrothrombocytopenia Rare hemorrhagic disorder due to an acquired platelet anomaly Congenital anomaly of the great arteries Dense granule disease Rare congenital anomaly of ventricular septum Alpha granule disease Rare atrial defect and interatrial communication Congenital pericardium anomaly Glomerular disease Congenital anomaly of the great veins Severe hemophilia B Thrombomodulin-related bleeding disorder Scott syndrome Secondary glomerular disease Mild hemophilia B Jacobsen syndrome Coronary artery congenital malformation Moderate hemophilia B Rare thrombotic disorder due to a coagulation factors defect Acquired von Willebrand syndrome Rare thrombotic disorder due to an acquired coagulation factors defect Hemophilia A Severe hemophilia A Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Familial afibrinogenemia Hemophilia B Rare thrombotic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a platelet anomaly Familial dysfibrinogenemia Mild hemophilia A Moderate hemophilia A Rare hemorrhagic disorder due to a constitutional coagulation factors defect Bernard-Soulier syndrome Immune thrombocytopenia Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding diathesis due to glycoprotein VI deficiency Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Rare hemorrhagic disorder due to a constitutional platelet anomaly Univentricular cardiopathy Kasabach-Merritt phenomenon Syndromic constitutional thrombocytopenia Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome East Texas bleeding disorder Pseudo-von Willebrand disease Congenital thrombotic thrombocytopenic purpura Congenital vitamin K-dependent coagulation factors deficiency Immune-mediated thrombotic thrombocytopenic purpura Genetic cystic renal disease Gaisböck syndrome Isolated constitutional thrombocytopenia Acquired prothrombin deficiency Protein S acquired deficiency Chronic myeloid leukemia Chronic neutrophilic leukemia Chronic myeloproliferative disease, unclassifiable Primary myelofibrosis Polycythemia vera Myeloproliferative neoplasm Essential thrombocythemia Hypereosinophilic syndrome