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:
22q11.2 deletion syndrome Acquired cystic disease-associated renal cell carcinoma Acquired hemophagocytic lymphohistiocytosis associated with malignant disease Acquired von Willebrand syndrome Acute basophilic leukemia Acute erythroid leukemia Acute megakaryoblastic leukemia Acute monoblastic/monocytic leukemia Acute myeloid leukaemia with myelodysplasia-related features 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 CEBPA somatic mutations Acute myeloid leukemia with NPM1 somatic mutations Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2) 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 myelomonocytic leukemia Acute promyelocytic leukemia Adenocarcinoma of ovary Adenocarcinoma of the cervix uteri Adenocarcinoma of the esophagus Adenocarcinoma of the penis Adenocarcinoma of the small intestine Adenoid basal carcinoma of the cervix uteri Adenoid cystic carcinoma of the cervix uteri Adenosarcoma of the cervix uteri Adenosarcoma of the corpus uteri Adrenocortical carcinoma Adrenocortical carcinoma with pure aldosterone hypersecretion Adult T-cell leukemia/lymphoma Adult hepatocellular carcinoma Aggressive NK-cell leukemia Alpha-thalassemia Alveolar soft tissue sarcoma Ameloblastic carcinoma Ameloblastoma Anaplastic ependymoma Anaplastic thyroid carcinoma Angiosarcoma Aregenerative anemia Astroblastoma Ataxia-pancytopenia syndrome Ataxia-telangiectasia Autoimmune hemolytic anemia, warm type Autoimmune lymphoproliferative syndrome Autoimmune polyendocrinopathy type 1 Autosomal dominant macrothrombocytopenia Autosomal dominant severe congenital neutropenia Autosomal dominant thrombocytopenia with platelet secretion defect Autosomal recessive malignant osteopetrosis Autosomal recessive sideroblastic anemia B-cell chronic lymphocytic leukemia B-cell prolymphocytic leukemia BAP1-related tumor predisposition syndrome Benign epithelial tumor of salivary glands Benign metanephric tumor Benign schwannoma Benign tumor of fallopian tubes Bernard-Soulier syndrome Beta-thalassemia Beta-thalassemia intermedia Beta-thalassemia major Biliary cystadenocarcinoma Bleeding disorder due to CalDAG-GEFI deficiency Borderline epithelial tumor of ovary Bronchial neuroendocrine tumor CINCA syndrome Carcinofibroma of the corpus uteri Carcinoid syndrome Carcinoma of esophagus, salivary gland type Carcinoma of the ampulla of Vater Carcinosarcoma of the cervix uteri Carcinosarcoma of the corpus uteri Cholangiocarcinoma Chondrosarcoma Choriocarcinoma of the central nervous system Choroid plexus carcinoma Chromophobe renal cell carcinoma Chronic eosinophilic leukemia Chronic granulomatous disease Chronic mucocutaneous candidiasis Chronic myeloid leukemia Chronic neutrophilic leukemia Chédiak-Higashi syndrome Class I glucose-6-phosphate dehydrogenase deficiency Classic hairy cell leukemia Clear cell adenocarcinoma of the ovary Clear cell renal carcinoma Clear cell sarcoma of kidney Cohen syndrome Collecting duct carcinoma Combined T and B cell immunodeficiency Combined deficiency of factor VII and factor X Combined hepatocellular carcinoma and cholangiocarcinoma Combined immunodeficiency due to DOCK8 deficiency Combined immunodeficiency with granulomatosis Common variable immunodeficiency Congenital amegakaryocytic thrombocytopenia Congenital autosomal recessive small-platelet thrombocytopenia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type IV Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital factor XI deficiency Congenital factor XIII deficiency Congenital fibrinogen deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital thrombotic thrombocytopenic purpura Cutaneous neuroendocrine carcinoma DDX41-related hematologic malignancy predisposition syndrome DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Deafness-lymphedema-leukemia syndrome Delta-beta-thalassemia Dendritic cell sarcoma not otherwise specified Dermatofibrosarcoma protuberans Desmoid tumor Desmoplastic small round cell tumor Diamond-Blackfan anemia Diaphyseal medullary stenosis-bone malignancy syndrome Differentiated thyroid carcinoma Drug-induced autoimmune hemolytic anemia Dysembryoplastic neuroepithelial tumor Ectopic aldosterone-producing tumor Embryonal carcinoma Endometrial stromal sarcoma Endometrioid carcinoma of ovary Ependymoblastoma Ependymoma Epithelioid sarcoma Epithelioid trophoblastic tumor Epstein-Barr virus-associated gastric carcinoma Erythropoietic uroporphyria associated with myeloid malignancy Esthesioneuroblastoma Exercise-induced malignant hyperthermia Extraskeletal Ewing sarcoma Extraskeletal myxoid chondrosarcoma Familial Mediterranean fever Familial afibrinogenemia Familial dysfibrinogenemia Familial gastric type 1 neuroendocrine tumor Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial medullary thyroid carcinoma Familial pancreatic carcinoma Familial papillary or follicular thyroid carcinoma Familial papillary thyroid carcinoma with renal papillary neoplasia Familial platelet disorder with associated myeloid malignancy Familial tumoral calcinosis Fanconi anemia Fetal and neonatal alloimmune thrombocytopenia Fibrolamellar hepatocellular carcinoma Fibrosarcoma Follicular dendritic cell sarcoma Gallbladder neuroendocrine tumor Ganglioneuroblastoma Gastric adenocarcinoma and proximal polyposis of the stomach Gastrointestinal stromal tumor Gestational choriocarcinoma Giant cell tumor of bone Glanzmann thrombasthenia Glassy cell carcinoma of the cervix uteri Glioblastoma Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome Glomus tumor Gonadoblastoma Griscelli syndrome type 2 Gynandroblastoma Hairy cell leukemia variant Hb Bart's hydrops fetalis Hemangioblastoma Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin H disease Hemoglobin Lepore-beta-thalassemia syndrome Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to diphosphoglycerate mutase deficiency Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to glutathione reductase deficiency Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hemophagocytic syndrome Hemophilia Hemophilia A Hemophilia B Hemophilia B Leyden Heparin-induced thrombocytopenia Hepatoblastoma Hereditary clear cell renal cell carcinoma Hereditary elliptocytosis Hereditary isolated aplastic anemia Hereditary neuroendocrine tumor of small intestine Hereditary papillary renal cell carcinoma Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hereditary spherocytosis Hereditary thrombocytopenia with early-onset myelofibrosis Hereditary thrombocytopenia with normal platelets Hereditary thrombophilia due to congenital antithrombin deficiency High-grade neuroendocrine carcinoma of the cervix uteri High-grade neuroendocrine carcinoma of the corpus uteri Hirschsprung disease-ganglioneuroblastoma syndrome Histiocytic sarcoma Hyper-IgE syndrome Hyperparathyroidism-jaw tumor syndrome Idiopathic CD4 lymphocytopenia Idiopathic aplastic anemia Ileal neuroendocrine tumor Immune thrombocytopenia Immunodeficiency by defective expression of MHC class I Immunodeficiency by defective expression of MHC class II Inflammatory myofibroblastic tumor Inflammatory pseudotumor of the liver Inherited acute myeloid leukemia Interdigitating dendritic cell sarcoma Intraductal papillary mucinous carcinoma of pancreas Juvenile myelomonocytic leukemia Kabuki syndrome Kaposi sarcoma Kein Name gefunden Keratocystic odontogenic tumor Klatskin tumor Langerhans cell sarcoma Laryngeal neuroendocrine tumor Leiomyosarcoma Leiomyosarcoma of the cervix uteri Leiomyosarcoma of the corpus uteri Lipoblastoma Liposarcoma Low-grade neuroendocrine tumor of the corpus uteri Lymphoepithelial-like carcinoma MITF-related melanoma and renal cell carcinoma predisposition syndrome MYH9-related disease Macrothrombocytopenia with mitral valve insufficiency Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome Malignancy diagnosed during pregnancy Malignant Sertoli-Leydig cell tumor of the ovary Malignant atrophic papulosis Malignant epithelial tumor of salivary glands Malignant germ cell tumor of the cervix uteri Malignant germ cell tumor of the corpus uteri Malignant germ cell tumor of the vagina Malignant granulosa cell tumor of the ovary Malignant melanoma of the mucosa Malignant migrating focal seizures of infancy Malignant mixed Müllerian tumor of the ovary Malignant non-dysgerminomatous germ cell tumor of ovary Malignant peripheral nerve sheath tumor Malignant peritoneal mesothelioma Malignant teratoma of ovary Malignant tumor of fallopian tubes Mast cell sarcoma Medullary thyroid carcinoma Medulloblastoma Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) Melanoma and neural system tumor syndrome Mendelian susceptibility to mycobacterial diseases Metaplastic carcinoma of the breast MiT family translocation renal cell carcinoma Microcystic stromal tumor Middle ear neuroendocrine tumor Mild hemophilia A Mild hemophilia B Mixed germ cell tumor Mixed phenotype acute leukemia Mixed-type autoimmune hemolytic anemia Moderate hemophilia A Moderate hemophilia B Monocytopenia with susceptibility to infections Mucinous adenocarcinoma of ovary Mucinous adenocarcinoma of the appendix Mucinous tubular and spindle cell renal carcinoma Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome Multiple pterygium-malignant hyperthermia syndrome Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Myeloid sarcoma Myxofibrosarcoma Myxopapillary ependymoma NUT midline carcinoma Nasopharyngeal carcinoma Neonatal autoimmune hemolytic anemia Nephroblastoma Neuroblastoma Neuroendocrine carcinoma of pancreas Neuroendocrine tumor of anal canal Neuroendocrine tumor of stomach Neuroendocrine tumor of the colon Neuroendocrine tumor of the rectum Neuroleptic malignant syndrome Neutropenia-monocytopenia-deafness syndrome Non-functioning neuroendocrine tumor of pancreas Non-papillary transitional cell carcinoma of the bladder Non-seminomatous germ cell tumor of testis Non-severe combined immunodeficiency Non-spherocytic hemolytic anemia due to hexokinase deficiency Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Osteoblastoma Osteosarcoma Ovarian dysgerminoma Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Palmoplantar keratoderma-esophageal carcinoma syndrome Pancreatoblastoma Pancytopenia due to IKZF1 mutations Papillary carcinoma of the cervix uteri Papillary glioneuronal tumor Papillary renal cell carcinoma Papillary tumor of the pineal region Paratesticular adenocarcinoma Parathyroid carcinoma Paris-Trousseau thrombocytopenia Paroxysmal nocturnal hemoglobinuria Pediatric hepatocellular carcinoma Peripheral primitive neuroectodermal tumor Phyllodes tumor of the breast Phyllodes tumor of the prostate Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome Pilomatrix carcinoma Pineal parenchymal tumor of intermediate differentiation Pineoblastoma Pituitary carcinoma Placental site trophoblastic tumor Plasma cell leukemia Pleuropulmonary blastoma Precursor B-cell acute lymphoblastic leukemia Precursor T-cell acute lymphoblastic leukemia Primary adult heart tumor Primary hepatic neuroendocrine carcinoma Primary non-gestational choriocarcinoma of ovary Primary pediatric heart tumor Primary peritoneal carcinoma Primitive neuroectodermal tumor of the cervix uteri Primitive neuroectodermal tumor of the corpus uteri Progeroid features-hepatocellular carcinoma predisposition syndrome Pseudo-von Willebrand disease Pulmonary blastoma RELA fusion-positive ependymoma Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare adenocarcinoma of the breast Rare anemia Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare immune disease Rare variants of adenocarcinoma of the corpus uteri Refractory anemia Refractory anemia with excess blasts Refractory anemia with excess blasts in transformation Renal medullary carcinoma Reticular dysgenesis Retinoblastoma Rhabdoid tumor Rhabdomyosarcoma Rhabdomyosarcoma of the cervix uteri Rhabdomyosarcoma of the corpus uteri Rosette-forming glioneuronal tumor SMARCA4-deficient sarcoma of thorax Schwartz-Jampel syndrome Serotonin-producing neuroendocrine tumor of pancreas Serous carcinoma of the corpus uteri Serous cystadenocarcinoma of pancreas Severe autosomal recessive macrothrombocytopenia Severe congenital hypochromic anemia with ringed sideroblasts Severe hemophilia A Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Sex cord-stromal tumor of testis Shwachman-Diamond syndrome Sickle cell anemia Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Skeletal Ewing sarcoma Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome Small cell carcinoma of the bladder Small cell carcinoma of the ovary Solid pseudopapillary carcinoma of pancreas Solitary fibrous tumor Squamous cell carcinoma of gallbladder and extrahepatic biliary tract Squamous cell carcinoma of liver and intrahepatic biliary tract Squamous cell carcinoma of the cervix uteri Squamous cell carcinoma of the corpus uteri Squamous cell carcinoma of the esophagus Squamous cell carcinoma of the hypopharynx Squamous cell carcinoma of the larynx Squamous cell carcinoma of the lip Squamous cell carcinoma of the nasal cavity and paranasal sinuses Squamous cell carcinoma of the oral cavity Squamous cell carcinoma of the oropharynx Squamous cell carcinoma of the penis Squamous cell carcinoma of the stomach Subependymoma Synovial sarcoma T-cell large granular lymphocyte leukemia T-cell prolymphocytic leukemia Testicular seminomatous germ cell tumor Theca steroid-producing cell malignant tumor of ovary, not further specified Thiamine-responsive megaloblastic anemia syndrome Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Thrombotic thrombocytopenic purpura Thymic carcinoma Thymic neuroendocrine carcinoma Thymic neuroendocrine tumor Thymoma Transitional cell carcinoma of the corpus uteri Tubulocystic renal cell carcinoma Tumor necrosis factor receptor 1 associated periodic syndrome Undifferentiated carcinoma of esophagus Undifferentiated carcinoma of the corpus uteri Undifferentiated carcinoma with osteoclast-like giant cells of pancreas Undifferentiated pleomorphic sarcoma Unstable hemoglobin disease Upper tract urothelial carcinoma Vaginal carcinoma Vasoproliferative tumor of the retina Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 2A Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 Vulvar carcinoma Vulvovaginal rhabdomyosarcoma Well-differentiated fetal adenocarcinoma of the lung X-linked agammaglobulinemia X-linked lymphoproliferative disease X-linked lymphoproliferative disease due to XIAP deficiency X-linked sideroblastic anemia Yolk sac tumor