SE-ATLAS

Plattenepithelkarzinom des Hypopharynx Plasmazell-Leukämie Ataxia-Teleangiectasia Schilddrüsenkarzinom, differenziertes Chédiak-Higashi-Syndrom Elliptozytose, hereditäre Faktor VII-Mangel, kongenitaler Faktor XI-Mangel, kongenitaler Endometriumskarzinom des Ovars Hereditäre Thrombophilie durch kongenitalen Antithrombin-Mangel Aplastische Anämie, idiopathische Diamond-Blackfan-Anämie Nasopharynxkarzinom Cohen-Syndrom Bernard-Soulier-Syndrom Immundefekt, kombinierter schwerer, durch DOCK8-Mangel Ewing-Sarkom, skelettales Faktor V-Mangel, kongenitaler Faktor X-Mangel, kongenitaler Faktor XIII-Mangel, kongenitaler Mittelmeerfieber, familiäres Makrothrombozytopenie-Lymphödem-Entwicklungsverzögerung-Gesichtsdysmorphien-Kamptodaktylie-Syndrom Fibrinogen-Mangel, kongenitaler Glioblastom Hämoglobinurie, nächtliche paroxysmale Kaposi-Sarkom Adenokarzinom des Ovars Hepatozelluläres Karzinom, fibrolamelläres Leukämie, chronische myeloische Seltenes Adenokarzinom der Brust Deletion 22q11 Granulomatose, chronische Hämophilie Plasminogenaktivator-Inhibitor Typ 1-Mangel, kongenitaler Neutropenie, kongenitale schwere, autosomal-dominante Maligner Müllerscher Mischtumor des Ovars Metaplastisches Karzinom der Brust Anämie, dyserythropoetische, kongenitale, Typ III Immundefekt durch MHC Klasse II-Expressionsdefekt Hämophilie A Dysfibrinogenämie, familiäre Seltene Varianten des Adenokarzinoms des Corpus uteri Akute myeloische Leukämie mit t(6;9)(p23;q34) Akute myeloische Leukämie mit inv3(q21q26.2) oder t(3;3)(q21;q26.2) Hämophilie B Afibrinogenämie, familiäre Retikuläre Dysgenesie Megakaryoblastische akute myeloische Leukämie mit t(1;22)(p13;q13) Adenosarkom des Corpus uteri Karzinofibrom des Corpus uteri Karzinosarkom des Corpus uteri Akute myeloische Leukämie mit somatischen NPM1-Genmutationen Nierenzellkarzinom, klarzelliges, hereditäre Form Karzinom, hepatozelluläres, des Kindes Primitiver neuroektodermaler Tumor des Corpus uteri Haarzell-Leukämie, klassische Osteoblastom Hämolytische Anämie durch Diphosphoglycerat-Mutase-Mangel Plattenepithelkarzinom des Corpus uteri Adenokarzinom des Penis Suszeptibilität für Mykobakteriosen, familiäre Form Plattenepithelkarzinom des Oropharynx Akute myeloische Leukämie mit t(9;11)(p22;q23) Rhabdomyosarkom des Corpus uteri Skelettdysplasie-T-Zell-Immundefekt-Entwicklungsverzögerung-Syndrom Leiomyosarkom des Corpus uteri Neuroblastom Nephroblastom Thiamin-responsive megaloblastäre Anämie mit Diabetes mellitus und sensorineuraler Schwerhörigkeit Papulose, atrophische maligne Undifferenziertes Karzinom des Corpus uteri Schwere hereditäre Thrombophilie durch kongenitalen Protein-S-Mangel Schwere hereditäre Thrombophilie durch kongenitalen Protein-C-Mangel Plattenepithelkarzinom des Penis Transitionalzellkarzinom des Corpus uteri Plattenepithelkarzinom der Nasenhöhle und Nasennebenhöhlen Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Rhabdomyosarkom High-grade-NET der Cervix uteri Karzinosarkom der Cervix uteri Rhabdomyosarkom der Cervix uteri Shwachman-Diamond-Syndrom Leukämie, chronische neutrophile Primitiver neuroektodermaler Tumor der Cervix uteri Papilläres Karzinom der Cervix uteri Akute myeloische Leukämie mit Myelodysplasie-assoziierten Veränderungen Hämolytische Anämie durch erythrozytäre Adenosin-Desaminase-Überproduktion Plattenepithelkarzinom der Cervix uteri Adenokarzinom der 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 Malignant melanoma of the mucosa Vasoproliferative tumor of the retina Undifferentiated carcinoma of esophagus Squamous cell carcinoma of the stomach Adult hepatocellular carcinoma Myxofibrosarcoma Non-severe combined immunodeficiency Keratocystic odontogenic tumor Familial pancreatic carcinoma Pituitary carcinoma Combined hepatocellular carcinoma and cholangiocarcinoma Adrenocortical carcinoma Thrombocytopenia with congenital dyserythropoietic anemia Carcinoma of the ampulla of Vater Precursor T-cell acute lymphoblastic leukemia Thymoma Thymic carcinoma Severe congenital hypochromic anemia with ringed sideroblasts Cutaneous neuroendocrine carcinoma Medullary thyroid carcinoma Chronic mucocutaneous candidiasis Acute myeloid leukemia with t(8;16)(p11;p13) translocation CINCA syndrome Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome Benign metanephric tumor Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Desmoplastic small round cell tumor Precursor B-cell acute lymphoblastic leukemia Thymic neuroendocrine carcinoma Rare hemorrhagic disorder due to a constitutional platelet anomaly Hyperparathyroidism-jaw tumor syndrome Malignant granulosa cell tumor of the ovary Theca steroid-producing cell malignant tumor of ovary, not further specified Hereditary thrombocytopenia with early-onset myelofibrosis Placental site trophoblastic tumor Mucinous adenocarcinoma of ovary Familial platelet disorder with associated myeloid malignancy Squamous cell carcinoma of the esophagus Borderline epithelial tumor of ovary Hereditary neuroendocrine tumor of small intestine Malignant teratoma of ovary Malignant germ cell tumor of the vagina Well-differentiated fetal adenocarcinoma of the lung Neuroendocrine tumor of the rectum Common variable immunodeficiency Ovarian dysgerminoma Gynandroblastoma Malignant Sertoli-Leydig cell tumor of the ovary Gestational choriocarcinoma Griscelli syndrome type 2 Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Clear cell adenocarcinoma of the ovary Kein Name gefunden Adenocarcinoma of the esophagus Adenocarcinoma of the small intestine Klatskin tumor Gonadoblastoma Malignant non-dysgerminomatous germ cell tumor of ovary Neuroendocrine tumor of stomach Ileal neuroendocrine tumor Neuroendocrine tumor of the colon Neuroendocrine tumor of anal canal Subependymoma Middle ear neuroendocrine tumor Gallbladder neuroendocrine tumor Myxopapillary ependymoma Anaplastic ependymoma Immunodeficiency by defective expression of MHC class I Laryngeal neuroendocrine tumor Small cell carcinoma of the bladder Primary hepatic neuroendocrine carcinoma Progeroid features-hepatocellular carcinoma predisposition syndrome Ependymoma Carcinoid syndrome Astroblastoma MYH9-related disease Erythropoietic uroporphyria associated with myeloid malignancy Severe hemophilia A Hairy cell leukemia variant Hemoglobin E-beta-thalassemia syndrome Familial gastric type 1 neuroendocrine tumor 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 Syndrome de persistance familiale de l'hémoglobine foetale-bêta-thalassémie Syndrome de lymphangioendothéliomatose multifocale-thrombocytopénie Drépanocytose-bêta-thalassémie Drépanocytose-hémoglobinose C Drépanocytose-hémoglobinose D Macrothrombocytopénie autosomique dominant Tumeur épithéliale bénigne des glandes salivaires Carcinome à petites cellules de l'ovaire Anémie sidéroblastique liée à l'X Bêta-thalassémie majeure Bêta-thalassémie intermédiaire Delta-bêta-thalassémie Ganglioneuroblastome Fibrosarcome Carcinome des plexus choroïdes Syndrome des ptérygiums multiples-hyperthermie maligne Anémie hémolytique par déficit en pyrimidine 5' nucléotidase Lymphocytopénie CD4 idiopathique Thrombopénie immune Anémie dysérythropoïétique congénitale type IV Adénocarcinome paratesticulaire Tumeur germinale non séminomateuse des testicules Sarcome synovial Thrombocytopénie amégacaryocytaire congénitale Hyperthermie maligne induite par l'exercice Anémie hémolytique non sphérocytique par déficit en hexokinase Anémie hémolytique auto-immune à auto-anticorps chauds Anémie hémolytique auto-immune mixte Leucémie aiguë myéloïde héréditaire Leucémie aiguë myéloïde avec mutations somatiques de CEBPA Sarcome d'Ewing extrasquelettique Rhabdomyosarcome vulvo-vaginal Tumeur neuroectodermique primitive périphérique Tumeur épithéliale maligne des glandes salivaires Esthésioneuroblastome Tumeur myofibroblastique inflammatoire Adénocarcinome gastrique et polypose proximale de l'estomac Syndrome de prédisposition au carcinome rénal et mélanome associé à MITF Thrombopénie induite par l'héparine Syndrome Noonan-like avec leucémie myélomonocytaire juvénile Cancer anaplasique de la thyroïde Carcinome parathyroidien Syndrome périodique associé au récepteur 1 du facteur de nécrose tumorale Cancer urothélial des voies supérieures Leucémie érythroblastique Leucémie myéloblastique aiguë type associée à une translocation t(8;21)(q22;q22) Leucémie aiguë monoblastique/monocytaire Leucémie aiguë myélomonocytaire Leucémie aiguë mégacaryoblastique Leucémie aiguë promyélocytaire Anémie réfractaire Calcinose tumorale familiale Leucémie lymphocytaire chronique à cellules B Tumeur glomique Syndrome de retard de développement-kystes pulmonaires-croissance excessive-tumeur de Wilms Tumeur rhabdoïde Carcinome pilomatriciel Agammaglobulinémie liée à l'X