SE-ATLAS

Extraskeletal Ewing sarcoma Intraneural perineurioma Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Angiocentric glioma Extraneural perineurioma Alpha-thalassemia Alveolar soft tissue sarcoma Ependymal tumor Mycosis fungoides and variants Sclerosing perineurioma Hereditary folate malabsorption Simple cryoglobulinemia Primary cutaneous B-cell lymphoma Spermatocytic seminoma Aregenerative anemia Alpha-thalassemia-X-linked intellectual disability syndrome Beta-thalassemia Secondary hypereosinophilic syndrome 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 Cutaneous mastocytoma Homocystinuria without methylmalonic aciduria Bleeding disorder in hemophilia B carriers Embryonal tumor of neuroepithelial tissue Beta-thalassemia-X-linked thrombocytopenia syndrome Thrombocytopenia with congenital dyserythropoietic anemia Glomus tumor Acute myeloid leukemia with recurrent genetic anomaly Chronic myelomonocytic leukemia Rare hemorrhagic disorder due to a constitutional thrombocytopenia Alpha-thalassemia-myelodysplastic syndrome Primary germ cell tumor of central nervous system Adult-onset autosomal recessive sideroblastic anemia Refractory anemia Congenital alpha2-antiplasmin deficiency Benign peripheral nerve sheath tumor Papilloma of choroid plexus Unclassified myelodysplastic/myeloproliferative disease Medulloblastoma with extensive nodularity Solitary fibrous tumor Giant cell tumor of bone Nasopharyngeal teratoma Plasma cell tumor Ganglioneuroma Inflammatory myofibroblastic tumor Unclassified myelodysplastic syndrome Hereditary thrombophilia due to congenital antithrombin deficiency Acute myeloid leukemia with 11q23 abnormalities Primary acquired red cell aplasia Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Desmoplastic/nodular medulloblastoma Fanconi anemia Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Rare hemorrhagic disorder due to a coagulation factors defect Acute myeloblastic leukemia without maturation Chronic myeloproliferative disease, unclassifiable Histiocytic and dendritic cell tumor Congenital dyserythropoietic anemia Chronic neutrophilic leukemia Von Willebrand disease Acute myeloid leukemia with minimal differentiation Neuroepithelioma Hemoglobin C disease Gestational choriocarcinoma Cutaneous mastocytosis Acute undifferentiated leukemia Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Dendritic cell tumor Hemoglobin E disease Revesz syndrome Acute myeloblastic leukemia with maturation Bullous diffuse cutaneous mastocytosis Unclassified acute myeloid leukemia Classic medulloblastoma Acute biphenotypic leukemia Macrophage or histiocytic tumor Idiopathic aplastic anemia Juvenile myelomonocytic leukemia Nasal ganglioglioma Lymphoproliferative disease associated with primary immune disease Deafness-lymphedema-leukemia syndrome Lhermitte-Duclos disease Bilineal acute leukemia Neuroblastoma Low-grade astrocytoma Chronic eosinophilic leukemia Immunodeficiency-associated lymphoproliferative disease Rare hemorrhagic disorder due to a platelet anomaly Constitutional megaloblastic anemia with severe neurologic disease Hodgkin lymphoma Melanoma of soft tissue Rare coagulation disorder Rare aplastic anemia Refractory cytopenia with multilineage dysplasia Mastocytosis Sideroblastic anemia Central nervous system embryonal tumor Refractory anemia with excess blasts Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 Rare hemorrhagic disorder due to a qualitative platelet defect Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Astrocytoma Mediterranean macrothrombocytopenia Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Hereditary combined deficiency of vitamin K-dependent clotting factors Sickle cell anemia Chondrosarcoma Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement Gonadal germ cell tumor Telangiectasia macularis eruptiva perstans 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 Maladie de dépôt des chaînes légères Leucémie/lymphome T de l'adulte Hémorragie due à la mutation Pittsburgh de l'alpha-1-antitrypsine Mélanocytome méningé Leucémie myéloblastique aiguë associée à une translocation t(8;16)(p11;p13) Liposarcome myxoïde/à cellules rondes Pinéoblastome Maladie de dépôt des chaînes légères et lourdes Déficit en méthylcobalamine type cblDv1 Liposarcome bien différencié Hémophilie B Afibrinogénémie familiale Lymphoprolifération T cutanée primitive CD30+ Hémophilie A Liposarcome dédifférencié Maladie thrombotique rare par déficit constitutionnel en facteurs de coagulation Lymphome cutané primitif Tumeur papillaire de la région pinéale Tumeur desmoplastique à petites cellules Lymphome NK/T extranodulaire type nasal Myxofibrosarcome Maladie thrombotique rare par anomalie des plaquettes Mélanome primitif du système nerveux central Tumeur rare du système nerveux Lymphome B cutané de la zone marginale Lymphome T cutané primitif de phénotype TCRgamma/delta Pinéocytome Sarcome synovial Myofibromatose infantile Maladie thrombotique rare par déficit acquis en facteurs de coagulation Troubles hémmoragiques par déficit en intégrine alpha2-bêta1 Hémophilie A modérée Syndrome de Bernard-Soulier Maladie hémorragique rare par déficit constitutionnel en facteurs de coagulation Ependymome anaplasique Thrombopénie immune Tumeur du parenchyme pinéal à différenciation intermédiaire Lymphome malin non-hodgkinien Anémie sidéroblastique liée à l'X Troubles hémorragiques par déficit en glycoprotéine VI Dyskératose congénitale Hémangioblastome Lymphomes B centrofolliculaire cutané primitif Hémophilie A mineure Anémie sidéroblastique idiopathique acquise Drépanocytose-hémoglobinose D Lymphome T sous-cutané type panniculite Lymphome cutané primitif à cellules T périphérique sans autre indication Tumeur oligoastrocytaire Lymphome cutané à grandes cellules de type jambe Thrombocytopénie auto-immune Myopathie mitochondriale et anémie sidéroblastique Maladie hémorragique rare par anomalie constitutionnelle des plaquettes Tumeur des nerfs crâniens et spinaux Drépanocytose-hémoglobinose E Lymphome T cutané primitif d'évolution indolente Neurocytome extraventriculaire Tumeur maligne des gaines nerveuses périphériques Maladie hémorragique de l'est du Texas Mastocytose systémique Syndrome de persistance familiale de l'hémoglobine foetale-drépanocytose Tumeur rare des tissus mous Aplasie et myélodysplasie autosomiques dominantes Lymphome de Hodgkin nodulaire à prédominance lymphocytaire Chondrosarcome myxoïde extrasquelettique Tumeur neuronale Tumeur des tissus lymphoïde et hématopoïétique Sarcome histiocytaire Mastocytose systémique type smoldering Syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII Liponeurocytome cérébelleux Neurocytome central Dermatofibrosarcome de Darier-Ferrand Syndrome de Pearson Oligoastrocytome Syndrome de Plummer-Vinson Sarcome des cellules de Langerhans Tumeur germinale non séminomateuse des testicules Syndrome avec alpha-thalassémie comme manifestation majeure Lymphome oculo-cérébral primitif Lymphome T cutané primitif d'évolution agressive Syndrome hyperéosinophilique primitif Lymphome B cutané primitif d'évolution indolente Oligoastrocytome anaplasique Epulis congénital Maladie de von Willebrand type plaquette Tumeur mixte neuronale-gliale Mastocytose isolée de la moelle osseuse Anémie constitutionnelle due à une anomalie du métabolisme du fer Lymphome B cutané primitif d'évolution agressive Leucémie myéloblastique aiguë type associée à une translocation t(8;21)(q22;q22) Sarcome des cellules dendritiques sans autre spécification Myélome multiple Anémie rare Sarcome des cellules folliculaires dendritiques Hémoglobinose D Méningiomes multiples familiaux Déficit congénital en facteurs Vitamino-K dépendants Anémie sidéroblastique constitutionnelle Syndrome de persistance familiale de l'hémoglobine foetale-bêta-thalassémie Tumeur gliale du tissu neuroépithélial d'origine inconnue Astrocytome/gangliogliome desmoplasique infantile Thrombocytose familiale Maladie d'Ollier Tumeur testiculaire germinale séminomateuse Troubles lymphoprolifératifs associés au méthotréxate Syndrome de Gaisböck Tumeur germinale des testicules Périneuriome réticulé Syndrome de Sézary Déficit acquis en facteur II Anémie hémolytique rare Gangliocytome Déficit acquis en protéine S Acidémie méthylmalonique avec homocystinurie Tumeur glioneuronale formant des rosettes Mastocytome extra-cutané Anémie de Blackfan-Diamond Mastocytose cutanée diffuse pseudoxanthomateuse Sarcome de Kaposi Leucémie aiguë monoblastique/monocytaire Leucémie myéloïde chronique Hypofibrinogénémie familiale Rhabdomyosarcome Syndrome MYH9 Sarcome des cellules dendritiques interdigitées