SE-ATLAS

Squamous cell carcinoma of the hypopharynx Plasma cell leukemia Ataxia-telangiectasia Differentiated thyroid carcinoma Chédiak-Higashi syndrome Hereditary elliptocytosis Congenital factor VII deficiency Congenital factor XI deficiency Endometrioid carcinoma of ovary Hereditary thrombophilia due to congenital antithrombin deficiency Idiopathic aplastic anemia Diamond-Blackfan anemia Nasopharyngeal carcinoma Cohen syndrome Bernard-Soulier syndrome Combined immunodeficiency due to DOCK8 deficiency Skeletal Ewing sarcoma Congenital factor V deficiency Congenital factor X deficiency Congenital factor XIII deficiency Familial Mediterranean fever Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome Congenital fibrinogen deficiency Glioblastoma Paroxysmal nocturnal hemoglobinuria Kaposi sarcoma Adenocarcinoma of ovary Fibrolamellar hepatocellular carcinoma Chronic myeloid leukemia Rare adenocarcinoma of the breast 22q11.2 deletion syndrome Chronic granulomatous disease Hemophilia Congenital plasminogen activator inhibitor type 1 deficiency Autosomal dominant severe congenital neutropenia Malignant mixed Müllerian tumor of the ovary Metaplastic carcinoma of the breast Congenital dyserythropoietic anemia type III Immunodeficiency by defective expression of MHC class II Hemophilia A Familial dysfibrinogenemia Rare variants of adenocarcinoma of the corpus uteri Acute myeloid leukemia with t(6;9)(p23;q34) Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2) Hemophilia B Familial afibrinogenemia Reticular dysgenesis Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) Adenosarcoma of the corpus uteri Carcinofibroma of the corpus uteri Carcinosarcoma of the corpus uteri Acute myeloid leukemia with NPM1 somatic mutations Hereditary clear cell renal cell carcinoma Pediatric hepatocellular carcinoma Primitive neuroectodermal tumor of the corpus uteri Classic hairy cell leukemia Osteoblastoma Hemolytic anemia due to diphosphoglycerate mutase deficiency Squamous cell carcinoma of the corpus uteri Adenocarcinoma of the penis Mendelian susceptibility to mycobacterial diseases Squamous cell carcinoma of the oropharynx Acute myeloid leukemia with t(9;11)(p22;q23) Rhabdomyosarcoma of the corpus uteri Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome Leiomyosarcoma of the corpus uteri Neuroblastoma Nephroblastoma Thiamine-responsive megaloblastic anemia syndrome Malignant atrophic papulosis Undifferentiated carcinoma of the corpus uteri Severe hereditary thrombophilia due to congenital protein S deficiency Severe hereditary thrombophilia due to congenital protein C deficiency Squamous cell carcinoma of the penis Transitional cell carcinoma of the corpus uteri Squamous cell carcinoma of the nasal cavity and paranasal sinuses Hemolytic anemia due to red cell pyruvate kinase deficiency Rhabdomyosarcoma High-grade neuroendocrine carcinoma of the cervix uteri Carcinosarcoma of the cervix uteri Rhabdomyosarcoma of the cervix uteri Shwachman-Diamond syndrome Chronic neutrophilic leukemia Primitive neuroectodermal tumor of the cervix uteri Papillary carcinoma of the cervix uteri Acute myeloid leukaemia with myelodysplasia-related features Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Squamous cell carcinoma of the cervix uteri Adenocarcinoma of the cervix uteri Retinoblastom NUT-Karzinom Schwartz-Jampel-Syndrom Adenosarkom der Cervix uteri Purpura, thrombotische thrombozytopenische Leiomyosarkom der Cervix uteri Leukämie, juvenile myelomonozytäre Refraktäre Anämie mit Blastenexzess Myelodysplastisches Syndrom mit isolierter del(5q) Chromosomenanomalie Adenoides zystisches Karzinom der Cervix uteri Leukämie, akute basophile Myelosarkom B-Zell-Prolymphozytenleukämie Adenoides Basalzellkarzinom der Cervix uteri Testikulärer Keimzelltumor, seminomatöser Maligner Keimzelltumor der Cervix uteri Paris-Trousseau-Syndrom T-Zell-Prolymphozytenleukämie T-Zell-Leukämie mit großen granulären Lymphozyten Peritonealmesotheliom, malignes Herztumor, primärer, des Erwachsenen Glaszellkarzinom der Cervix uteri Von-Willebrand-Syndrom, erworbenes Alpha-Thalassämie Thrombasthenie Glanzmann Alloimmunthrombozytopenie, fetale und neonatale Agressive NK-Zell-Leukämie Adulte T-Zell-Leukämie/Lymphom Desmoidtumor Herztumor, primärer, des Kindes Langerhans-Zell-Sarkom Dottersacktumor Sarkom, histiozytäres Sarkom der interdigitierenden dendritischen Zellen Sarkom, follikuläres dendritisches Von-Willebrand-Syndrom Kongenitale autosomal-rezessive Thrombozytopenie der kleinen Blutplättchen Schilddrüsenkarzinom, medulläres, familiäres Transitionalzellkarzinom der Harnblase, nicht-papillär Mastzellsarkom Ösophaguskarzinom vom Speicheldrüsentyp Hämatologische Malignität-Prädispositionssyndrom, DDX41-assoziiertes Akute myeloische Leukämie und Myelodysplastische Syndrome durch Strahlung Dendritisches Zell-Sarkom, andernorts nicht klassifiziert Peritonealkarzinom, primäres Cholangiokarzinom Leukämie, chronische eosinophile Refraktäre Anämie mit Vermehrung von Blasten in Transformation Malignes Melanom der Mukosa Vasoproliferativer Tumor der Retina Ösophaguskarzinom, undifferenziertes Plattenepithelkarzinom des Magens Hepatozelluläres Karzinom, adultes Myxofibrosarkom Immundefekt, kombinierter nicht-schwerer Keratozystischer odontogener Tumor Pankreaskarzinom, familiäres Hypophysenkarzinom Kombiniertes hepatozelluläres Karzinom und Cholangiokarzinom Adrenokortikales Karzinom Thrombozytopenie mit kongenitaler dyserythropoetischer Anämie Karzinom der Ampulla Vateri Akute lymphoblastische T-Vorläuferzell-Leukämie Thymom Thymuskarzinom Schwere kongenitale hypochrome Anämie mit Ringsideroblasten Karzinom, kutanes neuroendokrines Schilddrüsenkarzinom, medulläres Candidose, chronische mukokutane Akute myeloische Leukämie mit Translokation t(8;16)(p11;p13) CINCA-Syndrom Pigmentierungsdefekte-Palmoplantarkeratose-Hautkarzinom-Syndrom Metanephrogener Tumor, benigner Hereditäre Persistenz des fetalen Hämoglobins mit Sichelzellkrankheit Rundzelltumor, desmoplastischer Akute lymphoblastische B-Vorläuferzell-Leukämie Thymuskarzinom, neuroendokrines Thrombopathie, konstitutionelle Hyperparathyreoidismus-Kiefertumor-Syndrom (HPT-JT) Maligner Granulosazelltumor des Ovars Steroid-produzierender maligner Thekazelltumor, nicht klassifizierter Hereditäre Thrombozytopenie mit früh-beginnender Myelofibrose Plazentabett-Tumor (PSST) Muzinöses Adenokarzinom des Ovars Familiäre Blutplättchen-Störungen mit assoziierter myeloischer Malignität Plattenepithelkarzinom des Ösophagus Ovarialtumor, epithelialer, Borderline-Typ Hereditärer neuroendokriner Tumor des Dünndarms Malignes Teratom des Ovars Keimzelltumor der Vagina, maligner Fetales Adenokarzinom der Lunge, gut-differenziert Tumor, neuroendokriner, des Rektums Immundefektsyndrom, variables Maligner dysgerminomatöser Keimzelltumor des Ovars Gynandroblastom Maligner Sertoli-Leydig-Zell-Tumor des Ovars Chorionkarzinom, gestationales Griscelli-Syndrom Typ 2 Radioulnar-Synostose - amegakaryozytische Thrombozytopenie Klarzelliges Adenokarzinom des Ovars Kein Name gefunden Adenokarzinom des Ösophagus Adenokarzinom des Dünndarms Klatskin-Tumor Gonadoblastom Keimzelltumor des Ovars, nicht-dysgerminomatöser maligner Tumor, neuroendokriner, des Magens Tumor, neuroendokriner, des Ileums Tumor, neuroendokriner, des Kolons Tumor, neuroendokriner, des Analkanals Subependymom Tumor, neuroendokriner, des Mittelohrs Tumor, neuroendokriner, der Gallenblase Ependymom, myxopapilläres Ependymom, anaplastisches Immundefekt durch MHC Klasse I-Expressionsdefekt Tumor, neuroendokriner, des Larynx Blasenkarzinom, kleinzelliges Tumor, neuroendokriner, primär hepatischer Progeroide Merkmale-Hepatozelluläres Karzinom-Prädispositionssyndrom Ependymom Karzinoides Syndrom Astroblastom MYH9-assoziierte Krankheiten Uroporphyrie, erythropoetische, mit assoziierter myeloischer Neoplasie Hämophilie A, schwere Haarzell-Leukämie-Variante Hämoglobin E - Beta-Thalassämie Familiärer Neuroendokriner Tumor des Magens Typ 1 Hereditary papillary renal cell carcinoma Ependymoblastoma Papillary tumor of the pineal region Pancytopenia due to IKZF1 mutations Dysembryoplastic neuroepithelial tumor Mild hemophilia B Moderate hemophilia B Hemoglobin C-beta-thalassemia syndrome Moderate hemophilia A Mild hemophilia A Lipoblastoma Undifferentiated pleomorphic sarcoma Pineoblastoma Pineal parenchymal tumor of intermediate differentiation Hereditary thrombocytopenia with normal platelets Papillary glioneuronal tumor Solitary fibrous tumor Rosette-forming glioneuronal tumor Hirschsprung disease-ganglioneuroblastoma syndrome Intraductal papillary mucinous carcinoma of pancreas Serous cystadenocarcinoma of pancreas Palmoplantar keratoderma-esophageal carcinoma syndrome Von Willebrand disease type 1 Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 Non-functioning neuroendocrine tumor of pancreas Neuroendocrine carcinoma of pancreas Benign schwannoma Melanoma and neural system tumor syndrome Hemoglobin Lepore-beta-thalassemia syndrome X-linked lymphoproliferative disease due to XIAP deficiency Choriocarcinoma of the central nervous system Solid pseudopapillary carcinoma of pancreas Hemangioblastoma Undifferentiated carcinoma with osteoclast-like giant cells of pancreas Von Willebrand disease type 2 Von Willebrand disease type 2A Adrenocortical carcinoma with pure aldosterone hypersecretion Autosomal recessive sideroblastic anemia Ectopic aldosterone-producing tumor Serotonin-producing neuroendocrine tumor of pancreas Combined immunodeficiency with granulomatosis Kabuki syndrome Malignant migrating focal seizures of infancy Hemophagocytic syndrome RELA fusion-positive ependymoma Dermatofibrosarcoma protuberans Rare anemia Clear cell sarcoma of kidney Mucinous adenocarcinoma of the appendix Epithelioid sarcoma Acquired hemophagocytic lymphohistiocytosis associated with malignant disease X-linked lymphoproliferative disease Ataxia-pancytopenia syndrome Phyllodes tumor of the prostate Epstein-Barr virus-associated gastric carcinoma Chondrosarcoma Familial hypodysfibrinogenemia Malignancy diagnosed during pregnancy Mixed phenotype acute leukemia Primary non-gestational choriocarcinoma of ovary Squamous cell carcinoma of the lip Squamous cell carcinoma of the oral cavity Combined deficiency of factor VII and factor X Familial hypofibrinogenemia Aregenerative anemia Vulvar carcinoma Lymphoepithelial-like carcinoma Neutropenia-monocytopenia-deafness syndrome Bleeding disorder due to CalDAG-GEFI deficiency BAP1-related tumor predisposition syndrome DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Thymic neuroendocrine tumor Familial papillary thyroid carcinoma with renal papillary neoplasia Squamous cell carcinoma of gallbladder and extrahepatic biliary tract Ameloblastic carcinoma Monocytopenia with susceptibility to infections Class I glucose-6-phosphate dehydrogenase deficiency Squamous cell carcinoma of the larynx Sex cord-stromal tumor of testis Bronchial neuroendocrine tumor Squamous cell carcinoma of liver and intrahepatic biliary tract Biliary cystadenocarcinoma Acquired cystic disease-associated renal cell carcinoma Ameloblastoma Malignant peripheral nerve sheath tumor Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Autoimmune lymphoproliferative syndrome Pulmonary blastoma Pseudo-von Willebrand disease Congenital thrombotic thrombocytopenic purpura Hemophilia B Leyden Deafness-lymphedema-leukemia syndrome Diaphyseal medullary stenosis-bone malignancy syndrome Leiomyosarcoma Pleuropulmonary blastoma Thrombocytopenia-absent radius syndrome Macrothrombocytopenia with mitral valve insufficiency Autoimmune polyendocrinopathy type 1 Hemoglobin H disease Giant cell tumor of bone Rare immune disease Hb Bart's hydrops fetalis Chromophobe renal cell carcinoma Renal medullary carcinoma Gastrointestinal stromal tumor Autosomal dominant thrombocytopenia with platelet secretion defect Neuroleptic malignant syndrome Microcystic stromal tumor Hemolytic anemia due to glutathione reductase deficiency Drug-induced autoimmune hemolytic anemia Severe autosomal recessive macrothrombocytopenia Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Familial papillary or follicular thyroid carcinoma Hyper-IgE syndrome Liposarcoma Combined T and B cell immunodeficiency Clear cell renal carcinoma Papillary renal cell carcinoma MiT family translocation renal cell carcinoma Tubulocystic renal cell carcinoma Mucinous tubular and spindle cell renal carcinoma Alveolar soft tissue sarcoma Inflammatory pseudotumor of the liver Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Medulloblastoma Embryonal carcinoma Mixed germ cell tumor Benign tumor of fallopian tubes Malignant tumor of fallopian tubes Vaginal carcinoma SMARCA4-deficient sarcoma of thorax Phyllodes tumor of the breast Fanconi anemia Sickle cell anemia Hereditary isolated aplastic anemia Hepatoblastoma Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type II Autosomal recessive malignant osteopetrosis Osteosarcoma Pancreatoblastoma Hemolytic anemia due to glucophosphate isomerase deficiency Endometrial stromal sarcoma Serous carcinoma of the corpus uteri High-grade neuroendocrine carcinoma of the corpus uteri Epithelioid trophoblastic tumor Low-grade neuroendocrine tumor of the corpus uteri Malignant germ cell tumor of the corpus uteri Neonatal autoimmune hemolytic anemia Hemolytic anemia due to adenylate kinase deficiency Hereditary spherocytosis Unstable hemoglobin disease Beta-thalassemia Extraskeletal myxoid chondrosarcoma Angiosarcoma Collecting duct carcinoma Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Autosomal dominant macrothrombocytopenia Benign epithelial tumor of salivary glands Small cell carcinoma of the ovary X-linked sideroblastic anemia Beta-thalassemia major Beta-thalassemia intermedia Delta-beta-thalassemia Ganglioneuroblastoma Fibrosarcoma Choroid plexus carcinoma Multiple pterygium-malignant hyperthermia syndrome Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Idiopathic CD4 lymphocytopenia Immune thrombocytopenia Congenital dyserythropoietic anemia type IV Paratesticular adenocarcinoma Non-seminomatous germ cell tumor of testis Synovial sarcoma Congenital amegakaryocytic thrombocytopenia Exercise-induced malignant hyperthermia Non-spherocytic hemolytic anemia due to hexokinase deficiency Autoimmune hemolytic anemia, warm type Mixed-type autoimmune hemolytic anemia Inherited acute myeloid leukemia Acute myeloid leukemia with CEBPA somatic mutations Extraskeletal Ewing sarcoma Vulvovaginal rhabdomyosarcoma Peripheral primitive neuroectodermal tumor Malignant epithelial tumor of salivary glands Esthesioneuroblastoma Inflammatory myofibroblastic tumor Gastric adenocarcinoma and proximal polyposis of the stomach MITF-related melanoma and renal cell carcinoma predisposition syndrome Heparin-induced thrombocytopenia Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Anaplastic thyroid carcinoma Parathyroid carcinoma Tumor necrosis factor receptor 1 associated periodic syndrome Upper tract urothelial carcinoma Acute erythroid leukemia Acute myeloid leukemia with t(8;21)(q22;q22) translocation Acute monoblastic/monocytic leukemia Acute myelomonocytic leukemia Acute megakaryoblastic leukemia Acute promyelocytic leukemia Refractory anemia Familial tumoral calcinosis B-cell chronic lymphocytic leukemia Glomus tumor Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome Rhabdoid tumor Pilomatrix carcinoma X-linked agammaglobulinemia