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 Retinoblastoma NUT midline carcinoma Schwartz-Jampel syndrome Adenosarcoma of the cervix uteri Thrombotic thrombocytopenic purpura Leiomyosarcoma of the cervix uteri Juvenile myelomonocytic leukemia Refractory anemia with excess blasts Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Adenoid cystic carcinoma of the cervix uteri Acute basophilic leukemia Myeloid sarcoma B-cell prolymphocytic leukemia Adenoid basal carcinoma of the cervix uteri Testicular seminomatous germ cell tumor Malignant germ cell tumor of the cervix uteri Paris-Trousseau thrombocytopenia T-cell prolymphocytic leukemia T-cell large granular lymphocyte leukemia Malignant peritoneal mesothelioma Primary adult heart tumor Glassy cell carcinoma of the cervix uteri Acquired von Willebrand syndrome Alpha-thalassemia Glanzmann thrombasthenia Fetal and neonatal alloimmune thrombocytopenia Aggressive NK-cell leukemia Adult T-cell leukemia/lymphoma Desmoid tumor Primary pediatric heart tumor Langerhans cell sarcoma Yolk sac tumor Histiocytic sarcoma Interdigitating dendritic cell sarcoma Follicular dendritic cell sarcoma Von Willebrand disease Congenital autosomal recessive small-platelet thrombocytopenia Familial medullary thyroid carcinoma Non-papillary transitional cell carcinoma of the bladder Mast cell sarcoma Carcinoma of esophagus, salivary gland type DDX41-related hematologic malignancy predisposition syndrome Acute myeloid leukemia and myelodysplastic syndromes related to radiation Dendritic cell sarcoma not otherwise specified Primary peritoneal carcinoma Cholangiocarcinoma Chronic eosinophilic leukemia Refractory anemia with excess blasts 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 Vulvakarzinom Karzinom, lymphoepitheliom-artiges Neutropenie - Monozytopenie - Schwerhörigkeit Blutungskrankheit durch CalDAG-GEFI-Mangel BAP1-abhängiges Tumorprädispositionssyndrom Sensorineuraler Hörverlust-Thrombozytopenie-Syndrom, DIAPH1-assoziiertes Neuroendokriner Tumor des Thymus Papilläres Schilddrüsenkarzinom mit papillärem Nierenzellkarzinom Plattenepithelkarzinom der Gallenblase und extrahepatischen Gallengänge Karzinom, ameloblastisches Monozytopenie mit erhöhter Infektionsanfälligkeit Glukose-6-Phosphat-Dehydrogenase-Mangel der Klasse I Plattenepithelkarzinom des Larynx Keimstrang-Stromatumor, testikulärer Tumor, neuroendokriner, bronchialer Plattenepithelkarzinom der Leber und intrahepatischen Gallengänge Biliäres Zystadenokarzinom der Leber Erworbene Nierenkrankheit mit assoziiertem Nierenzellkarzinom Ameloblastom Schwannom, malignes Palmoplantarkeratose-XX-Geschlechtsumkehr-Prädisposition für Plattenepithelkarzinom-Syndrom Autoimmun-lymphoproliferatives Syndrom Pulmonales Blastom Pseudo-von-Willebrand-Syndrom Thrombotisch-thrombozytopenische Purpura, kongenitale Form Hämophilie B Leyden Taubheit-Lymphödem-Leukämie-Syndrom Diaphysäre medulläre Stenose - maligne Knochentumore Leiomyosarkom Pleuro-pulmonales Blastom Thrombozytopenie-Radiusaplasie-Syndrom Makrothrombozytopenie mit Mitralklappeninsuffizienz Autoimmun-Polyendokrinopathie Typ 1 Hämoglobin-H-Krankheit Riesenzell-Tumor des Knochens Immunkrankheit, seltene Hb-Bart´s Hydrops fetalis-Syndrom Nierenzellkarzinom, chromophobes Nierenkarzinom, medulläres Stroma-Tumor, gastrointestinaler Autosomal-dominante Thrombozytopenie mit Defekt der Plättchensekretion Malignes neuroleptisches Syndrom Mikrozystischer Stromatumor Anämie, hämolytische durch Glutathion-Reduktase-Mangel Anämie, autoimmun-hämolytische, Medikamenten-induzierte Makrothrombozytopenie, schwere, autosomal-rezessive Akute myeloische Leukämie und myelodysplastische Syndrome durch Topoisomerase Typ II-Inhibitor Schilddrüsenkarzinom, papilläres oder follikuläres, familiäre Form Hyper IgE-Syndrom Liposarkom T- und B-Zell-Immundefekt, kombinierter Nierenzellkarzinom, klarzelliges Nierenzellkarzinom, papilläres Translokationsassoziiertes Nierenzellkarzinom der MiT-Familie Nierenzellkarzinom, tubulozystisches Muzinöses tubuläres und spindelzelliges Karzinom Weichteilsarkom, alveoläres Pseudotumor der Leber, inflammatorischer Akute myeloische Leukämie und myelodysplastische Syndrome durch alkylierende Agenzien Medulloblastom Embryonales Karzinom Keimzelltumor, gemischter Benigner Tumor der Eileiter Maligner Tumor der Eileiter Vaginalkarzinom Sarkom des Thorax bei SMARCA4-Mangel Phylloidestumor der Brust Fanconi-Anämie Sichelzellanämie Hereditäre Aplastische Anämie, isolierte Form Hepatoblastom Anämie, dyserythropoetische, kongenitale, Typ I Anämie, dyserythropoetische, kongenitale, Typ II Osteopetrose, maligne, autosomal-rezessive Form Osteosarkom Pankreasblastom Hämolytische Anämie durch Glukosephosphat-Isomerase-Mangel Stromasarkom des Corpus uteri Seröses Karzinom des Corpus uteri High-grade-NET des Corpus uteri Trophoblasttumor, epitheloider Low-grade-NET des Corpus uteri Maligner Keimzelltumor des Corpus uteri Neonatale autoimmune hämolytische Anämie Anämie, hämolytische durch Adenylat-Kinase-Mangel Sphärozytose, hereditäre Hämolytische Anämie durch Instabiles Hämoglobin Beta-Thalassämie Chondrosarkom, extraskelettales myxoides Angiosarkom Sammelgangkarzinom Hereditäre Persistenz des fetalen Hämoglobins - beta-Thalassämie Multifokale Lymphangioendotheliomatose-Thrombozytopenie-Syndrom Sichelzellkrankheit HbSbeta-Thal Sichelzellkrankheit HbSC Sichelzellkrankheit HbSD Makrothrombozytopenie, autosomal-dominante Speicheldrüsentumor, epithelialer benigner Ovarialkarzinom, kleinzelliges Anämie, sideroblastische, X-chromosomale Beta-Thalassämie major Beta-Thalassämie intermedia Delta-beta-Thalassämie Ganglioneuroblastom Fibrosarkom Choroid-Plexuskarzinom Multiples Pterygium-maligne Hyperthermie-Syndrom Hämolytische Anämie durch Pyrimidin-5'-Nukleotidase-Mangel CD4-Lymphozytopenie, idiopathische Immunthrombozytopenie Anämie, dyserythropoetische kongenitale, Typ IV Adenokarzinom, paratestikuläres Testikulärer Keimzelltumor, nicht-seminomatöser Synovialsarkom Angeborene amegakaryozytäre Thrombozytopenie Maligne Hyperthermie, anstrengungsinduzierte Anämie, hämolytische, nicht-sphärozytäre durch Hexokinase-Mangel Anämie, autoimmun-hämolytische, Wärme-Typ Anämie, autoimmun-hämolytische, gemischter Typ Akute myeloische Leukämie, vererbte Akute myeloische Leukämie mit somatischen CEBPA-Genmutationen Extraskelettales Ewing-Sarkom Rhabdomyosarkom, vulvovaginales Peripherer primitiver neuroektodermaler Tumor Maligner epithelialer Tumor der Speicheldrüsen Ästhesioneuroblastom Tumor, inflammatorischer myofibroblastischer Gastrisches Adenokarzinom und proximale Polyposis des Magens MITF-assoziiertes Melanom und Nierenzellkarzinom-Prädispositionssyndrom Thrombozytopenie, Heparin-induzierte Noonan-ähnliches Syndrom mit juveniler myelomonozytischer Leukämie Schilddrüsenkarzinom, anaplastisches Nebenschilddrüsen-Karzinom Tumornekrosefaktor-Rezeptor 1-assoziiertes periodisches Fieber-Syndrom Urothelkarzinom des oberen Harntraktes Akute Erythroleukämie Akute myeloische Leukämie mit Translokation t(8;21)(q22;q22) Leukämie, akute monoblastische Myelomonozytenleukämie, akute Akute Megakaryoblastenleukämie Promyelozytenleukämie, akute Anämie, refraktäre Tumorale Kalzinose, familiäre B-Zell-Leukämie, chronische lymphatische Glomustumor Allgemeine Entwicklungsverzögerung-Lungenzysten-Großwuchs-Wilms-Tumor-Syndrom Rhabdoidtumor Pilomatrixkarzinom Agammaglobulinämie, X-chromosomale