SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


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