SE-ATLAS

Multiple endocrine neoplasia Unclassified acute myeloid leukemia Follicular dendritic cell sarcoma Multiple endocrine neoplasia type 2A Acute panmyelosis with myelofibrosis Multiple endocrine neoplasia type 2B Acute myeloid leukemia with CEBPA somatic mutations Costello syndrome Refractory anemia with excess blasts in transformation Bohring-Opitz syndrome SMARCA4-deficient sarcoma of thorax Malignant peripheral nerve sheath tumor Solitary fibrous tumor Fanconi anemia Ataxia-telangiectasia Beckwith-Wiedemann syndrome Birt-Hogg-Dubé syndrome Diamond-Blackfan anemia Bloom syndrome Acute myeloid leukemia with t(9;22)(q34.1;q11.2) Lynch syndrome B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality B-lymphoblastic leukemia/lymphoma with t(v;11q23.3) B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2) B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1) Synovial sarcoma Cowden syndrome Leiomyosarcoma B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3) B-lymphoblastic leukemia/lymphoma with hyperdiploidy Denys-Drash syndrome B-lymphoblastic leukemia/lymphoma with hypodiploidy B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3) Angiosarcoma Essential thrombocythemia Myxofibrosarcoma Kabuki syndrome Constitutional mismatch repair deficiency syndrome Familial monosomy 7 syndrome Acute erythroid leukemia Soft tissue sarcoma Acute myeloid leukemia with t(8;21)(q22;q22) translocation PTEN hamartoma tumor syndrome Epithelioid sarcoma Frasier syndrome Acute myeloid leukemia with t(8;16)(p11;p13) translocation Simpson-Golabi-Behmel syndrome Weaver syndrome Gorlin syndrome Dermatofibrosarcoma protuberans Hereditary pheochromocytoma-paraganglioma Kostmann syndrome Coffin-Siris syndrome Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Myelodysplastic syndrome Rhabdoid tumor Liposarcoma Kaposi sarcoma Acute lymphoblastic leukemia Acute monoblastic/monocytic leukemia Acute myelomonocytic leukemia Acute megakaryoblastic leukemia Acute myeloid leukemia Acute promyelocytic leukemia Chronic myeloid leukemia Unclassified myelodysplastic syndrome Refractory anemia Desmoplastic small round cell tumor Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Li-Fraumeni syndrome Acute myeloid leukemia with 11q23 abnormalities Acute myeloblastic leukemia without maturation Mulibrey nanism Acute myeloid leukemia with minimal differentiation Acute undifferentiated leukemia Acute myeloblastic leukemia with maturation Precursor T-cell acute lymphoblastic leukemia Acute biphenotypic leukemia Precursor B-cell acute lymphoblastic leukemia Bilineal acute leukemia Ataxia-pancytopenia syndrome Mixed phenotype acute leukemia Hereditary thrombocytopenia with early-onset myelofibrosis Acute myeloid leukemia with t(6;9)(p23;q34) Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2) Acute myeloid leukemia with t(9;11)(p22;q23) Acute myeloid leukemia with NPM1 somatic mutations Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome Neuroblastoma Neurofibromatosis type 1 Full NF2-related schwannomatosis Nijmegen breakage syndrome Noonan syndrome Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Nephroblastoma Extraskeletal Ewing sarcoma Hereditary retinoblastoma Peripheral primitive neuroectodermal tumor Refractory anemia with excess blasts type 1 DICER1 tumor-predisposition syndrome Refractory anemia with excess blasts type 2 Multiple endocrine neoplasia type 4 Isolated melanotic schwannoma Polycythemia vera Familial adenomatous polyposis Full schwannomatosis Aregenerative anemia Dyskeratosis congenita Transient myeloproliferative syndrome Rhabdomyosarcoma Rubinstein-Taybi syndrome Schinzel-Giedion syndrome Perlman syndrome Tuberous sclerosis complex Shwachman-Diamond syndrome Chronic neutrophilic leukemia Acquired idiopathic sideroblastic anemia Chronic myeloproliferative disease, unclassifiable Refractory cytopenia with multilineage dysplasia Peutz-Jeghers syndrome Sotos syndrome Refractory anemia with excess blasts Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Primary myelofibrosis Acute myeloid leukaemia with myelodysplasia-related features Therapy related acute myeloid leukemia and myelodysplastic syndrome Acute basophilic leukemia Acute leukemia of ambiguous lineage Myeloid sarcoma RASopathy Rothmund-Thomson syndrome 14q32 duplication syndrome MIRAGE syndrome Alveolar soft tissue sarcoma Juvenile polyposis syndrome Acute myeloid leukemia and myelodysplastic syndromes related to radiation Von Hippel-Lindau disease WAGR syndrome Xeroderma pigmentosum Myeloproliferative neoplasm Acute myeloid leukemia with recurrent genetic anomaly Undifferentiated pleomorphic sarcoma Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Inherited acute myeloid leukemia Chronic eosinophilic leukemia Fibrosarcoma MUTYH-related attenuated familial adenomatous polyposis Hypereosinophilic syndrome Extraskeletal myxoid chondrosarcoma