SE-ATLAS

Sarcome d'Ewing extrasquelettique Périneuriome intraneural Syndrome marfanoïde-neurofibromes systémiques et orbitaux douloureux Gliome angiocentrique Périneuriome extraneural Alpha-thalassémie Sarcome alvéolaire des tissus mous Tumeur épendymaire Mycosis fongoïde et variants Périneuriome sclérosant Malabsorption héréditaire de l'acide folique Cryoglobulinémie simple Lymphome B cutané primitif Séminome spermatocytaire Anémie arégénérative Alpha-thalassémie-déficience intellectuelle liée à l'X Bêta-thalassémie Syndrome hyperéosinophilique secondaire Hereditary orotic aciduria Bleeding diathesis due to a collagen receptor defect Acquired hemophilia Hemoglobinopathy Glanzmann thrombasthenia Ganglioglioma Lymphoadenopathic mastocytosis with eosinophilia OSLAM syndrome Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Primary bone lymphoma Rare thrombotic disorder due to a constitutional platelet anomaly Microcytic anemia with liver iron overload Chordoid glioma Paris-Trousseau thrombocytopenia Primary intraocular lymphoma X-linked thrombocytopenia with normal platelets Dysembryoplastic neuroepithelial tumor Fetal and neonatal alloimmune thrombocytopenia Primary central nervous system lymphoma Hereditary thrombocytopenia with normal platelets Astroblastoma Thyroid lymphoma Paroxysmal nocturnal hemoglobinuria Rare thrombotic disorder due to an acquired platelet anomaly Combined deficiency of factor V and factor VIII Bleeding diathesis due to thromboxane synthesis deficiency Craniopharyngioma Constitutional dyserythropoietic anemia Classic mast cell leukemia Hemophilia Myeloid hemopathy Anaplastic ganglioglioma Meningioma Dominant beta-thalassemia Optic pathway glioma Hepatoblastoma Myelodysplastic syndrome Inherited acute myeloid leukemia Primary organ-specific lymphoma Malignant non-dysgerminomatous germ cell tumor of ovary Angiosarcoma POEMS syndrome Transcobalamin deficiency Aleukemic mast cell leukemia Congenital dyserythropoietic anemia type IV Familial hypodysfibrinogenemia Papillary glioneuronal tumor Macrothrombocytopenia with mitral valve insufficiency Thiamine-responsive megaloblastic anemia syndrome Beta-thalassemia associated with another hemoglobin anomaly Rare hereditary thrombophilia Congenital amegakaryocytic thrombocytopenia Acute erythroid leukemia Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Embryonal carcinoma of the central nervous system Extramedullary soft tissue plasmacytoma Thrombotic thrombocytopenic purpura Bone sarcoma Skeletal Ewing sarcoma Thrombocytopenia-absent radius syndrome Isolated hereditary giant platelet disorder Primary plasmacytoma of the bone Lymphoid hemopathy Acute myeloid leukemia with CEBPA somatic mutations Extragonadal germinoma Esthesioneuroblastoma Multiple osteochondromas Hoyeraal-Hreidarsson syndrome Evans syndrome Hemoglobin H disease Rare constitutional aplastic anemia Familial thrombomodulin anomalies Primary cutaneous T-cell lymphoma Peripheral primitive neuroectodermal tumor Gamma-heavy chain disease Epignathus Heparin-induced thrombocytopenia Congenital factor II deficiency High-grade astrocytoma Alpha delta granule deficiency Post-transplant lymphoproliferative disease Congenital factor V deficiency Hemoglobinopathy Toms River Lymphoma Congenital factor VII deficiency Delta-beta-thalassemia Desmoid tumor Congenital factor X deficiency Acquired purpura fulminans Embryonal carcinoma Rare tumor of neuroepithelial tissue Congenital factor XI deficiency Congenital plasminogen activator inhibitor type 1 deficiency Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency WT limb-blood syndrome Congenital factor XII deficiency Yolk sac tumor Hemoglobin C-beta-thalassemia syndrome Congenital factor XIII deficiency Polyembryoma Congenital intrinsic factor deficiency Formiminoglutamic aciduria AL amyloidosis Constitutional deficiency anemia Severe hereditary thrombophilia due to congenital protein S deficiency Hb Bart's hydrops fetalis Congenital fibrinogen deficiency Mixed germ cell tumor Liposarcoma Severe hereditary thrombophilia due to congenital protein C deficiency Rare deficiency anemia B-cell non-Hodgkin lymphoma Rare acquired aplastic anemia Epstein syndrome Rhabdoid tumor Rhabdoid tumor predisposition syndrome Extragonadal teratoma Hypoxanthine-guanine phosphoribosyltransferase deficiency Congenital prekallikrein deficiency Hemoglobin E-beta-thalassemia syndrome Stormorken-Sjaastad-Langslet syndrome Autosomal dominant macrothrombocytopenia Beta-thalassemia with other manifestations T-cell non-Hodgkin lymphoma Bleeding disorder in hemophilia A carriers Constitutional megaloblastic anemia due to folate metabolism disorder Leiomyosarcoma Medulloblastoma Autosomal recessive sideroblastic anemia Non-central nervous system-localized embryonal carcinoma Rare acquired deficiency anemia Pancreatic insufficiency-anemia-hyperostosis syndrome Malignant germ cell tumor of ovary Malignant peripheral nerve sheath tumor with perineurial differentiation Congenital high-molecular-weight kininogen deficiency Anaplastic/large cell medulloblastoma Bleeding disorder due to P2Y12 defect Extragonadal non-dysgerminomatous germ cell tumor Rare hemorrhagic disorder Primary non-gestational choriocarcinoma of ovary X-linked sideroblastic anemia and spinocerebellar ataxia Fechtner syndrome Thrombocythemia with distal limb defects Osteoblastoma Lipoblastoma Myelodysplastic/myeloproliferative disease Vitamin B12- and folate-independent constitutional megaloblastic anemia Diaphyseal medullary stenosis-bone malignancy syndrome Ovarian dysgerminoma Hereditary methemoglobinemia Diffuse cutaneous mastocytosis IRIDA syndrome Maculopapular cutaneous mastocytosis Kaposiform hemangioendothelioma Atypical chronic myeloid leukemia Mastocytome cutané Homocystinurie sans acidurie méthylmalonique Maladie hémorragique des porteurs d'hémophilie B Tumeur embryonnaire du tissu neuroépithélial Bêta-thalassémie-thrombocytopénie liée à l'X Thrombocytopénie avec anémie dysérythropoïétique congénitale Tumeur glomique Leucémie aiguë myéloïde avec anomalie génétique récurrente Leucémie myélomonocytaire chronique Maladie hémorragique rare par thrombocytopénie constitutionnelle Syndrome d'alpha-thalassémie-syndrome myélodysplasique Tumeur des cellules germinales primitive du système nerveux central Anémie sidéroblastique autosomique récessive de l'adulte Anémie réfractaire Déficit congénital en alpha2-antiplasmine Tumeur bénine des gaines nerveuses périphériques Papillome des plexus choroïdes Maladie myélodysplasique/myéloproliférative non classée Médulloblastome à nodularité extensive Tumeur fibreuse solitaire Tumeur osseuse à cellules géantes Tératome nasopharyngé Tumeur plasmocytaire Ganglioneurome Tumeur myofibroblastique inflammatoire Syndrome myélodysplasique non-classifié Thrombophilie héréditaire due au déficit congénital en antithrombine Leucémie aiguë myéloïde associée à des anomalies en 11q23 Aplasie primaire acquise de la lignée rouge Leucémie aiguë myéloïde avec éosinophiles médullaires anormaux associée à inv(16)(p13q22) ou t(16;16)(p13;q22) Médulloblastome desmoplasique/nodulaire Maladie de Fanconi Leucémie aiguë myéloïde et syndromes myélodysplasiques liés aux agents alkylants Maladie hémorragique rare par déficit en facteurs de coagulation Leucémie myéloblastique aiguë sans maturation Maladie myéloproliférative chronique non classifiée Tumeur des histiocytes et des cellules dendritiques Anémie dysérythropoïétique congénitale Leucémie chronique à neutrophiles Maladie de von Willebrand Leucémie aiguë myéloblastique avec différenciation minimale Neuroépithéliome Hémoglobinose C Choriocarcinome gestationnel Mastocytose cutanée Leucémie aiguë non différenciée Leucémie aiguë myéloïde et syndromes myélodysplasiques liés aux inhibiteurs de la topoisomérase II Tumeur des cellules dendritiques Hémoglobinose E Syndrome de Revesz Leucémie myéloblastique aiguë avec maturation Mastocytose cutanée diffuse bulleuse Leucémie myéloïde aiguë non-classifiée Médulloblastome classique Leucémie aiguë biphénotypique Tumeur des histiocytes ou des macrophages Aplasie médullaire idiopathique Leucémie myélomonocytaire juvénile Gangliogliome nasal Syndrome lymphoprolifératif associé à un déficit immunitaire primaire Syndrome de surdité-lymphoedème-leucémie Maladie de Lhermitte-Duclos Leucémie aiguë à bi-lignée Neuroblastome Astrocytome de bas grade Leucémie chronique éosinophile Déficit immunitaire associé à un syndrome lymphoprolifératif Maladie hémorragique rare par anomalie des plaquettes Anémie mégaloblastique constitutionnelle avec neuropathie sévère Lymphome de Hodgkin Mélanome des tissus mous Coagulopathie rare Aplasie médullaire rare Cytopénie réfractaire avec dysplasie multilignée Mastocytose Anémie sidéroblastique Tumeur embryonnaire du système nerveux central Anémie réfractaire avec excès de blastes Tumeur myéloïde/lymphoïde avec éosinophiles associée à une anomalie de PDGFRA, PDGFRB, FGFR1 ou JAK2 Maladie hémorragique rare par défaut qualitatif des plaquettes Syndrome de synostose radio-ulnaire-thrombocytopénie amégacaryocytique Astrocytome Macrothrombocytopénie méditérranéenne Syndrome myélodysplasique associé à une anomalie chromosomique isolée del(5q) Déficit héréditaire combiné en facteurs de la coagulation dépendants de la vitamine K Drépanocytose Chondrosarcome Tumeur myéloïde/lymphoïde associée à un réarrangement de PDGFRB Tumeur germinale gonadique Mastocytose cutanée maculeuse télangiectasique Severe congenital hypochromic anemia with ringed sideroblasts Hemoglobin Lepore-beta-thalassemia syndrome Adamantinoma Acute panmyelosis with myelofibrosis Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement Beta-thalassemia and related diseases Primary lymphoma of the conjunctiva Acute myeloid leukaemia with myelodysplasia-related features Extragonadal germ cell tumor Indolent systemic mastocytosis Maffucci syndrome Acute myeloid leukemia and myelodysplastic syndromes related to radiation Growing teratoma syndrome Ependymoblastoma Mast cell sarcoma Choriocarcinoma of the central nervous system Lesch-Nyhan syndrome Aggressive systemic mastocytosis Primary pulmonary lymphoma Epithelioid sarcoma Therapy related acute myeloid leukemia and myelodysplastic syndrome Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement Alpha-thalassemia and related disorders Systemic mastocytosis with associated hematologic neoplasm Ganglioneuroblastoma Acute basophilic leukemia Congenital atransferrinemia Mixed germ cell tumor of central nervous system Acute lymphoblastic leukemia Mast cell leukemia X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Hypereosinophilic syndrome Germinoma of the central nervous system Acute leukemia of ambiguous lineage Medulloepithelioma of the central nervous system Rare hemorrhagic disorder due to an acquired coagulation factor defect Myeloid sarcoma Teratoma of the central nervous system Hemoglobin M disease Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Acute myelomonocytic leukemia Tumor of meninges Nephroblastoma Acute megakaryoblastic leukemia Sickle cell disease and related diseases Acute myeloid leukemia Rare thrombotic disease of hematologic origin Refractory anemia with excess blasts in transformation Oligodendroglial tumor Acute promyelocytic leukemia Plasmacytoma Composite lymphoma Rare hemorrhagic disorder due to an acquired platelet anomaly Undifferentiated pleomorphic sarcoma Primary melanocytic tumor of central nervous system Benign schwannoma Langerhans cell histiocytosis Alpha granule disease Non-amyloid monoclonal immunoglobulin deposition disease Hereditary isolated aplastic anemia Choroid plexus tumor Classic Hodgkin lymphoma Heavy chain disease Unstable hemoglobin disease Juvenile hyaline fibromatosis Diffuse leptomeningeal melanocytosis Dense granule disease Congenital dyserythropoietic anemia type I Atypical papilloma of choroid plexus Vestibular schwannoma Soft tissue sarcoma Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Severe hemophilia B Fibrosarcoma Persistent polyclonal B-cell lymphocytosis Sickle cell disease associated with another hemoglobin anomaly Transient erythroblastopenia of childhood Osteosarcoma Oligodendroglioma Methylcobalamin deficiency type cblE Idiopathic hypereosinophilic syndrome Congenital dyserythropoietic anemia type III Glial tumor Choroid plexus carcinoma Imerslund-Gräsbeck syndrome Methylcobalamin deficiency type cblG Autoimmune lymphoproliferative syndrome Scott syndrome Bloom syndrome Hypoxanthine guanine phosphoribosyltransferase partial deficiency Congenital dyserythropoietic anemia type II Aceruloplasminemia Low-grade ependymoma Sebastian syndrome Mild hemophilia B Pineal tumor of neuroepithelial tissue Germ cell tumor Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Heavy chain deposition disease Primary acquired pure red cell aplasia Sickle cell-beta-thalassemia disease syndrome Rare thrombotic disorder due to a coagulation factors defect Moderate hemophilia B Atypical teratoid rhabdoid tumor Acquired von Willebrand syndrome Anaplastic oligodendroglioma Severe hemophilia A Sickle cell-hemoglobin C disease syndrome Neurofibroma Pleomorphic liposarcoma Shwachman-Diamond syndrome Perineurioma Light chain deposition disease Adult T-cell leukemia/lymphoma Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Meningeal melanocytoma Acute myeloid leukemia with t(8;16)(p11;p13) translocation Myxoid/round cell liposarcoma Pineoblastoma Light and heavy chain deposition disease Methylcobalamin deficiency type cblDv1 Well-differentiated liposarcoma Hemophilia B Familial afibrinogenemia Primary cutaneous CD30+ T-cell lymphoproliferative disease Hemophilia A Dedifferentiated liposarcoma Rare thrombotic disorder due to a constitutional coagulation factors defect Primary cutaneous lymphoma Papillary tumor of the pineal region Desmoplastic small round cell tumor Extranodal nasal NK/T cell lymphoma Myxofibrosarcoma Rare thrombotic disorder due to a platelet anomaly Primary melanoma of the central nervous system Seltener Tumor des Nervensystems Primär kutanes Marginalzonen-B-Zell-Lymphom Primär kutanes T-Zell-Lymphom, gamma/delta-positives Pineozytom Synovialsarkom Myofibromatose, infantile Seltene thrombotische Störung durch erworbenen Gerinnungsfaktoren-Defekt Hämorrhagische Diathese durch Integrin alpha2-beta1-Mangel Hämophilie A, mittelschwere Bernard-Soulier-Syndrom Seltene Blutgerinnungsstörung durch konstitutionellen Gerinnungsfaktoren-Defekt Ependymom, anaplastisches Immunthrombozytopenie Pinealisparenchymtumor intermediärer Differenzierung Non-Hodgkin-Lymphom Anämie, sideroblastische, X-chromosomale Hämorrhagische Diathese durch Glykoprotein VI-Mangel Dyskeratosis congenita Hämangioblastom Lymphom, primär kutanes, follikuläres Hämophilie A, milde Anämie, sideroachrestische, erworbene idiopathische Sichelzellkrankheit HbSD T-Zell-Lymphom, subkutanes Pannikulitis-ähnliches Primär kutanes peripheres T-Zell-Lymphom, andernorts nicht klassifiziert Tumor, oligoastrozytischer B-Zell-Lymphom, diffuses großzelliges, primär kutanes, vom leg Typ Thrombozytopenie, autoimmune Mitochondriale Myopathie und sideroblastische Anämie Thrombopathie, konstitutionelle Tumoren der kranialen und spinalen Nerven Sichelzellkrankheit HbSE Primär kutanes T-Zell-Lymphom, indolentes Neurozytom, extraventrikuläres Schwannom, malignes Gerinnungsstörung vom Ost-Texanischen Typ Mastozytose, systemische Hereditäre Persistenz des fetalen Hämoglobins mit Sichelzellkrankheit Weichteiltumor, seltener Autosomal-dominante Aplasie und Myelodysplasie Hodgkin-Lymphom, lymphozytenprädominantes noduläres Chondrosarkom, extraskelettales myxoides Tumor, neuronaler Tumor des hämatopoetischen und lymphoiden Gewebes Sarkom, histiozytäres Schwelende systemische Mastozytose Multiple Sklerose-Ichthyose-Faktor-VIII-Mangel-Syndrom Liponeurozytom, zerebelläres Neurozytom, zentrales Dermatofibrosarcoma protuberans Pearson-Syndrom Oligoastrozytom Plummer-Vinson-Syndrom Langerhans-Zell-Sarkom Testikulärer Keimzelltumor, nicht-seminomatöser Syndrome mit Alpha-Thalassämie als Hauptmerkmal Lymphom, okulozerebrales primäres Primär kutanes T-Zell-Lymphom, aggressives Hypereosinophiles Syndrom, primäres Primär kutanes B-Zell-Lymphom, indolentes Oligoastrozytom, anaplastisches Epulis, kongenitale Pseudo-von-Willebrand-Syndrom Tumor, gemischter neuro-glialer Isolated bone marrow mastocytosis Constitutional anemia due to iron metabolism disorder Aggressive primary cutaneous B-cell lymphoma Acute myeloid leukemia with t(8;21)(q22;q22) translocation Dendritic cell sarcoma not otherwise specified Multiple myeloma Rare anemia Follicular dendritic cell sarcoma Hemoglobin D disease Familial multiple meningioma Congenital vitamin K-dependent coagulation factors deficiency Constitutional sideroblastic anemia Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Glial tumor of neuroepithelial tissue with unknown origin Desmoplastic infantile astrocytoma/ganglioglioma Familial thrombocytosis Ollier disease Testicular seminomatous germ cell tumor Methotrexate-associated lymphoproliferative disorders Gaisböck syndrome Germ cell tumor of testis Reticular perineurioma Sézary syndrome Acquired prothrombin deficiency Rare hemolytic anemia Gangliocytoma Protein S acquired deficiency Methylmalonic acidemia with homocystinuria Rosette-forming glioneuronal tumor Extracutaneous mastocytoma Diamond-Blackfan anemia Pseudoxanthomatous diffuse cutaneous mastocytosis Kaposi sarcoma Acute monoblastic/monocytic leukemia Chronic myeloid leukemia Familial hypofibrinogenemia Rhabdomyosarcoma MYH9-related disease Interdigitating dendritic cell sarcoma