SE-ATLAS

Tumeur triton maligne Syndrome de persistance familiale de l'hémoglobine foetale-bêta-thalassémie Purpura thrombotique thrombocytopénique d'origine immunitaire Gangliocytome Thrombocytose familiale Tumeur testiculaire germinale séminomateuse Oligoastrocytome anaplasique Syndrome de Gaisböck Déficit acquis en facteur II Séminome spermatocytaire Périneuriome sclérosant Déficit acquis en protéine S Lymphome oculo-cérébral primitif Périneuriome réticulé Tumeur germinale des testicules Alpha-thalassémie Périneuriome intraneural Troubles hémorragiques par déficit en récepteur du collagène Tumeur gliale du tissu neuroépithélial d'origine inconnue Astrocytome/gangliogliome desmoplasique infantile Tumeur épendymaire Alpha-thalassémie-déficience intellectuelle liée à l'X Périneuriome extraneural Bêta-thalassémie Syndrome d'hypercoagulabilité par déficit héréditaire en glycosyl phosphatidyl inositol Maladie thrombotique rare par anomalie constitutionnelle des plaquettes Gliome chordoïde Tumeur neuroépithéliale dysembryoplasique Thrombasthénie de Glanzmann Cryoglobulinémie simple Sarcome alvéolaire des tissus mous Thrombopénie de May-Hegglin Bêta-thalassémie majeure Maladie de Letterer-Siwe Thrombocytopénie type Paris-Trousseau Hémophilie acquise Gliome angiocentrique Astroblastome Thrombocytopénie liée à l'X avec plaquettes normales Syndrome de Hashimoto-Pritzker Thrombopénie materno-foetale et néonatale allo-immune Maladie thrombotique rare par anomalie acquise des plaquettes Syndrome marfanoïde-neurofibromes systémiques et orbitaux douloureux Lymphome primitif du système nerveux central Troubles hémorragiques par déficit de synthèse de la thromboxane Gangliogliome Sarcome d'Ewing extrasquelettique Déficit combiné en facteurs V et VIII Craniopharyngiome Angiosarcome Tumeur germinale maligne non dysgerminomateuse de l'ovaire Hémophilie Macrothrombocytopenie avec insuffisance mitrale Thrombocytopénie héréditaire avec plaquettes normales Hépatoblastome Bêta-thalassémie intermédiaire Méningiome Gliome des voies optiques Hypodysfibrinogénémie familiale Tumeur neuroectodermique primitive périphérique Germinome extragonadique Sarcome osseux Syndrome d'alpha-thalassémie-déficience intellectuelle associée au chromosome 16 Thrombocytémie essentielle Carcinome embryonnaire du système nerveux central Macrothrombocytopénie héréditaire isolée Purpura thrombotique thrombocytopénique Bêta-thalassémie dominante Thrombocytopénie amégacaryocytaire congénitale Gangliogliome anaplasique Tératome épignathe Sarcome d'Ewing squelettique Syndrome de thrombocytopénie-aplasie radiale Esthésioneuroblastome Thrombocytopénie autosomique avec plaquettes normales Tumeur glioneuronale papillaire Thrombophilie héréditaire rare Syndrome d'Evans Bêta-thalassémie associée à une autre anomalie de l'hémoglobine Carcinome embryonnaire Delta-bêta-thalassémie Hémoglobinose H Anomalies de la thrombomoduline Thrombopénie induite par l'héparine Déficit en granules alpha et delta Tumeur rare du tissu neuroépithélial Déficit congénital en facteur II Rhabdomyosarcome alvéolaire Déficit congénital en facteur V Déficit congénital en facteur VII Déficit congénital en facteur X Hémoglobine C-bêta-thalassémie Rhabdomyosarcome embryonnaire Déficit congénital en inhibiteur 1 de l'activateur du plasminogène Purpura fulminans acquis Déficit congénital en facteur XI Déficit congénital en facteur XII Tumeur du sac vitellin Déficit congénital en facteur XIII Astrocytome de haut grade Polyembryome Tumeur germinale maligne mixte Syndrome de prédisposition aux tumeurs rhabdoïdes Hydrops fetalis de Bart Thrombophilie héréditaire sévère due au déficit congénital en protéine S Tumeur glioneuronale formant des rosettes Tumeur rhabdoïde Déficit congénital en fibrinogène Thrombophilie héréditaire due au déficit congénital en histidine-rich (poly-L) glycoprotéine Severe hereditary thrombophilia due to congenital protein C deficiency Beta-thalassemia with other manifestations Epstein syndrome Extragonadal teratoma Liposarcoma Hemoglobin E-beta-thalassemia syndrome Thrombocythemia with distal limb defects Primary non-gestational choriocarcinoma of ovary Autosomal dominant macrothrombocytopenia Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Leiomyosarcoma Medulloblastoma Non-central nervous system-localized embryonal carcinoma Malignant germ cell tumor of ovary Rare hemorrhagic disorder Bleeding disorder in hemophilia B carriers Ovarian dysgerminoma Congenital high-molecular-weight kininogen deficiency Embryonal tumor of neuroepithelial tissue Fechtner syndrome Bleeding disorder in hemophilia A carriers Beta-thalassemia-X-linked thrombocytopenia syndrome Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder due to P2Y12 defect Extragonadal non-dysgerminomatous germ cell tumor Medulloblastoma with extensive nodularity Nasopharyngeal teratoma Benign peripheral nerve sheath tumor Congenital alpha2-antiplasmin deficiency Ganglioneuroma Papilloma of choroid plexus Malignant peripheral nerve sheath tumor with perineurial differentiation Anaplastic/large cell medulloblastoma Solitary fibrous tumor Rare hemorrhagic disorder due to a coagulation factors defect Hereditary thrombophilia due to congenital antithrombin deficiency Alpha-thalassemia-myelodysplastic syndrome Fanconi anemia Primary germ cell tumor of central nervous system Von Willebrand disease Neuroepithelioma Rare hemorrhagic disorder due to a constitutional thrombocytopenia Low-grade astrocytoma Giant cell tumor of bone Gestational choriocarcinoma Desmoplastic/nodular medulloblastoma Nasal ganglioglioma Lhermitte-Duclos disease Rare coagulation disorder Neuroblastoma Growing teratoma syndrome Pleomorphic rhabdomyosarcoma Central nervous system embryonal tumor Von Willebrand disease type 2 Yolk sac tumor of central nervous system Mediterranean macrothrombocytopenia Extragonadal germ cell tumor Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Von Willebrand disease type 1 Classic medulloblastoma Epithelioid sarcoma Rare hemorrhagic disorder due to a qualitative platelet defect Von Willebrand disease type 2A Astrocytoma Chondrosarcoma Sickle cell anemia Rare hemorrhagic disorder due to a platelet anomaly Hereditary combined deficiency of vitamin K-dependent clotting factors Beta-thalassemia and related diseases Hemoglobin Lepore-beta-thalassemia syndrome Rhabdomyosarcoma Choriocarcinoma of the central nervous system Ganglioneuroblastoma Sickle cell disease and related diseases Von Willebrand disease type 2B Medulloepithelioma of the central nervous system Gonadal germ cell tumor MYH9-related disease Alpha-thalassemia and related disorders Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect Teratoma of the central nervous system Von Willebrand disease type 2M Ependymoblastoma Rare thrombotic disease of hematologic origin Germinoma of the central nervous system Nephroblastoma Mixed germ cell tumor of central nervous system Von Willebrand disease type 3 Oligodendroglial tumor Primary melanocytic tumor of central nervous system Familial hypofibrinogenemia Benign schwannoma X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Undifferentiated pleomorphic sarcoma Tumor of meninges Choroid plexus tumor Dense granule disease Diffuse leptomeningeal melanocytosis Rare hemorrhagic disorder due to an acquired platelet anomaly Alpha granule disease Sickle cell disease associated with another hemoglobin anomaly Glial tumor Oligodendroglioma Choroid plexus carcinoma Fibrosarcoma Soft tissue sarcoma Severe hemophilia B Osteosarcoma Pineal tumor of neuroepithelial tissue Moderate hemophilia B Sickle cell-beta-thalassemia disease syndrome Scott syndrome Rare thrombotic disorder due to a coagulation factors defect Langerhans cell histiocytosis specific to childhood Sebastian syndrome Anaplastic oligodendroglioma Acquired von Willebrand syndrome Vestibular schwannoma Germ cell tumor Atypical papilloma of choroid plexus Myxoid/round cell liposarcoma Pineoblastoma Severe hemophilia A Atypical teratoid rhabdoid tumor Hemophilia A Rare thrombotic disorder due to a constitutional coagulation factors defect Pleomorphic liposarcoma Mild hemophilia B Perineurioma Low-grade ependymoma Rare nervous system tumor Familial afibrinogenemia Well-differentiated liposarcoma Primary melanoma of the central nervous system Moderate hemophilia A Kaposi sarcoma Hemophilia B Dedifferentiated liposarcoma Pineocytoma Rare thrombotic disorder due to an acquired coagulation factors defect Desmoplastic small round cell tumor Familial dysfibrinogenemia Neurofibroma Sickle cell-hemoglobin C disease syndrome Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Meningeal melanocytoma Myxofibrosarcoma Hemangioblastoma Synovial sarcoma Bernard-Soulier syndrome Immune thrombocytopenia Sickle cell-hemoglobin D disease syndrome Papillary tumor of the pineal region Bleeding diathesis due to glycoprotein VI deficiency Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a platelet anomaly Mild hemophilia A Sickle cell-hemoglobin E disease syndrome Tumor of cranial and spinal nerves Autoimmune thrombocytopenia Non-seminomatous germ cell tumor of testis Anaplastic ependymoma Rare hemorrhagic disorder due to a constitutional platelet anomaly Pineal parenchymal tumor of intermediate differentiation Extraskeletal myxoid chondrosarcoma Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Neuronal tumor Oligoastrocytic tumor Malignant peripheral nerve sheath tumor Central neurocytoma Oligoastrocytoma Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Dermatofibrosarcoma protuberans Syndrome with alpha-thalassemia as a major feature Extraventricular neurocytoma Congenital vitamin K-dependent coagulation factors deficiency East Texas bleeding disorder Mixed neuronal-glial tumor Pseudo-von Willebrand disease Familial multiple meningioma Congenital thrombotic thrombocytopenic purpura Cerebellar liponeurocytoma