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 Neoplasie, endokrine multiple, Typ 2 Nephroblastom Extraskelettales Ewing-Sarkom Retinoblastom, familiäres Peripherer primitiver neuroektodermaler Tumor Anämie, refraktäre, mit Blastenexzess-1 DICER1-Tumorprädispositionssyndrom Anämie, refraktäre, mit Blastenexzess-2 Neoplasie, endokrine multiple, Typ 4 Schwannom, isoliertes melanotisches Polycythaemia vera Polyposis, adenomatöse familiäre Schwannomatose Anämie, aregenerative Dyskeratosis congenita Transientes myeloproliferatives Syndrom Rhabdomyosarkom Rubinstein-Taybi-Syndrom Schinzel-Giedion-Syndrom Perlman-Syndrom Tuberöse Sklerose Komplex Shwachman-Diamond-Syndrom Leukämie, chronische neutrophile Anämie, sideroachrestische, erworbene idiopathische Myeloproliferative Krankheit, nicht klassifizierbare Zytopenie, refraktäre mit multilineärer Dysplasie Peutz-Jeghers-Syndrom Sotos-Syndrom Refraktäre Anämie mit Blastenexzess Myelodysplastisches Syndrom mit isolierter del(5q) Chromosomenanomalie Primäre Myelofibrose Akute myeloische Leukämie mit Myelodysplasie-assoziierten Veränderungen Therapiebedingte akute myeloische Leukämie und myelodysplastische Syndrome Leukämie, akute basophile Leukämie, akute, gemischter Linienzugehörigkeit Myelosarkom RASopathie Rothmund-Thomson-Syndrom 14q32-Duplikationssyndrom MIRAGE-Syndrom Weichteilsarkom, alveoläres Polyposis, gastrointestinale juvenile Akute myeloische Leukämie und Myelodysplastische Syndrome durch Strahlung Von-Hippel-Lindau-Krankheit WAGR-Syndrom Xeroderma pigmentosum Myeloproliferative Neoplasie Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Sarkom, undifferenziertes pleomorphes Akute myeloische Leukämie und myelodysplastische Syndrome durch alkylierende Agenzien Akute myeloische Leukämie und myelodysplastische Syndrome durch Topoisomerase Typ II-Inhibitor Akute myeloische Leukämie, vererbte Leukämie, chronische eosinophile Fibrosarkom MUTYH-abhängige adenomatöse attenuierte familiäre Polyposis Hypereosinophile Syndrome Chondrosarkom, extraskelettales myxoides