SE-ATLAS

Acquired hemophilia Acquired prothrombin deficiency Acquired purpura fulminans Acquired von Willebrand syndrome Afibrinogénémie familiale Alpha delta granule deficiency Alpha granule disease Alpha-thalassemia Alpha-thalassemia and related disorders Alpha-thalassemia-X-linked intellectual disability syndrome Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Alpha-thalassemia-myelodysplastic syndrome Alveolar rhabdomyosarcoma Alveolar soft tissue sarcoma Anaplastic ganglioglioma Anaplastic oligoastrocytoma Anaplastic oligodendroglioma Anaplastic/large cell medulloblastoma Angiocentric glioma Angiosarcoma Astroblastoma Astrocytoma Atypical papilloma of choroid plexus Atypical teratoid rhabdoid tumor Autosomal dominant macrothrombocytopenia Autosomal thrombocytopenia with normal platelets Benign peripheral nerve sheath tumor Benign schwannoma Beta-thalassemia Beta-thalassemia and related diseases Beta-thalassemia associated with another hemoglobin anomaly Beta-thalassemia intermedia Beta-thalassemia major Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Bleeding diathesis due to a collagen receptor defect Bleeding diathesis due to thromboxane synthesis deficiency Bleeding disorder due to P2Y12 defect Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Bone sarcoma Central nervous system embryonal tumor Chondrosarcoma Chondrosarcome myxoïde extrasquelettique Chordoid glioma Choriocarcinoma of the central nervous system Choroid plexus carcinoma Choroid plexus tumor Classic medulloblastoma Combined deficiency of factor V and factor VIII Congenital alpha2-antiplasmin deficiency Congenital amegakaryocytic thrombocytopenia Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Congenital fibrinogen deficiency Congenital high-molecular-weight kininogen deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital prekallikrein deficiency Craniopharyngioma Delta-beta-thalassemia Dense granule disease Dermatofibrosarcome de Darier-Ferrand Desmoplastic infantile astrocytoma/ganglioglioma Desmoplastic/nodular medulloblastoma Diffuse leptomeningeal melanocytosis Dominant beta-thalassemia Drépanocytose-hémoglobinose C Drépanocytose-hémoglobinose D Drépanocytose-hémoglobinose E Dysembryoplastic neuroepithelial tumor Dysfibrinogénémie familiale Déficit congénital en facteurs Vitamino-K dépendants Embryonal carcinoma Embryonal carcinoma of the central nervous system Embryonal rhabdomyosarcoma Embryonal tumor of neuroepithelial tissue Ependymal tumor Ependymoblastoma Ependymome anaplasique Ependymome de bas grade Epignathus Epithelioid sarcoma Epstein syndrome Essential thrombocythemia Esthesioneuroblastoma Evans syndrome Extragonadal germ cell tumor Extragonadal germinoma Extragonadal non-dysgerminomatous germ cell tumor Extragonadal teratoma Extraneural perineurioma Extraskeletal Ewing sarcoma Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial thrombocytosis Familial thrombomodulin anomalies Fanconi anemia Fechtner syndrome Fetal and neonatal alloimmune thrombocytopenia Fibrosarcoma Gaisböck syndrome Gangliocytoma Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Germ cell tumor Germ cell tumor of testis Germinoma of the central nervous system Gestational choriocarcinoma Giant cell tumor of bone Glanzmann thrombasthenia Glial tumor Glial tumor of neuroepithelial tissue with unknown origin Gonadal germ cell tumor Growing teratoma syndrome Hashimoto-Pritzker syndrome Hb Bart's hydrops fetalis Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin H disease Hemoglobin Lepore-beta-thalassemia syndrome Hemophilia Heparin-induced thrombocytopenia Hepatoblastoma Hereditary combined deficiency of vitamin K-dependent clotting factors Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Hereditary thrombocytopenia with normal platelets Hereditary thrombophilia due to congenital antithrombin deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency High-grade astrocytoma Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Hémangioblastome Hémophilie A Hémophilie A mineure Hémophilie A modérée Hémophilie B Hémophilie B mineure Hémorragie due à la mutation Pittsburgh de l'alpha-1-antitrypsine Immune-mediated thrombotic thrombocytopenic purpura Intraneural perineurioma Isolated hereditary giant platelet disorder Langerhans cell histiocytosis specific to childhood Leiomyosarcoma Letterer-Siwe disease Lhermitte-Duclos disease Liponeurocytome cérébelleux Liposarcoma Liposarcome bien différencié Liposarcome dédifférencié Liposarcome pléiomorphe Low-grade astrocytoma MYH9-related disease Macrothrombocytopenia with mitral valve insufficiency Maladie de von Willebrand type plaquette Maladie hémorragique de l'est du Texas Maladie hémorragique rare par anomalie constitutionnelle des plaquettes Maladie hémorragique rare par déficit constitutionnel en facteurs de coagulation Maladie thrombotique rare par anomalie des plaquettes Maladie thrombotique rare par déficit acquis en facteurs de coagulation Maladie thrombotique rare par déficit constitutionnel en facteurs de coagulation Malignant germ cell tumor of ovary Malignant non-dysgerminomatous germ cell tumor of ovary Malignant peripheral nerve sheath tumor with perineurial differentiation Malignant triton tumor May-Hegglin thrombocytopenia Mediterranean macrothrombocytopenia Medulloblastoma Medulloblastoma with extensive nodularity Medulloepithelioma of the central nervous system Meningioma Mixed germ cell tumor Mixed germ cell tumor of central nervous system Moderate hemophilia B Myxofibrosarcome Myxoid/round cell liposarcoma Mélanocytome méningé Mélanome primitif du système nerveux central Méningiomes multiples familiaux Nasal ganglioglioma Nasopharyngeal teratoma Nephroblastoma Neuroblastoma Neurocytome central Neurocytome extraventriculaire Neuroepithelioma Neurofibrome Non-central nervous system-localized embryonal carcinoma Oligoastrocytome Oligodendroglial tumor Oligodendroglioma Optic pathway glioma Osteosarcoma Ovarian dysgerminoma Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Papillary glioneuronal tumor Papilloma of choroid plexus Paris-Trousseau thrombocytopenia Peripheral primitive neuroectodermal tumor Pineal tumor of neuroepithelial tissue Pineoblastoma Pinéocytome Pleomorphic rhabdomyosarcoma Polyembryoma Primary central nervous system lymphoma Primary germ cell tumor of central nervous system Primary melanocytic tumor of central nervous system Primary non-gestational choriocarcinoma of ovary Primary oculocerebral lymphoma Protein S acquired deficiency Purpura thrombotique thrombocytopénique congénital Périneuriome Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare coagulation disorder Rare hemorrhagic disorder Rare hemorrhagic disorder due to a coagulation factors defect Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare hemorrhagic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to an acquired coagulation factor defect Rare hemorrhagic disorder due to an acquired platelet anomaly Rare hereditary thrombophilia Rare thrombotic disease of hematologic origin Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to a constitutional platelet anomaly Rare thrombotic disorder due to an acquired platelet anomaly Rare tumor of neuroepithelial tissue Reticular perineurioma Rhabdoid tumor Rhabdoid tumor predisposition syndrome Rhabdomyosarcoma Rosette-forming glioneuronal tumor Sarcome de Kaposi Sarcome synovial Sclerosing perineurioma Scott syndrome Sebastian syndrome Severe hemophilia A Severe hemophilia B Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Sickle cell anemia Sickle cell disease and related diseases Sickle cell disease associated with another hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Simple cryoglobulinemia Skeletal Ewing sarcoma Soft tissue sarcoma Solitary fibrous tumor Spermatocytic seminoma Stormorken-Sjaastad-Langslet syndrome Syndrome avec alpha-thalassémie comme manifestation majeure Syndrome de Bernard-Soulier Syndrome de persistance familiale de l'hémoglobine foetale-drépanocytose Syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII Teratoma of the central nervous system Testicular seminomatous germ cell tumor Thrombocythemia with distal limb defects Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Thrombocytopénie auto-immune Thrombopénie immune Thrombotic thrombocytopenic purpura Troubles hémmoragiques par déficit en intégrine alpha2-bêta1 Troubles hémorragiques par déficit en glycoprotéine VI Tumeur des nerfs crâniens et spinaux Tumeur desmoplastique à petites cellules Tumeur du parenchyme pinéal à différenciation intermédiaire Tumeur germinale non séminomateuse des testicules Tumeur maligne des gaines nerveuses périphériques Tumeur mixte neuronale-gliale Tumeur neuronale Tumeur oligoastrocytaire Tumeur papillaire de la région pinéale Tumeur rare du système nerveux Tumor of meninges Undifferentiated pleomorphic sarcoma Vestibular schwannoma Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 2A Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 X-linked dyserythropoietic anemia with abnormal platelets and neutropenia X-linked thrombocytopenia with normal platelets Yolk sac tumor Yolk sac tumor of central nervous system