Klinik und Poliklinik für Pädiatrische Hämatologie und Onkologie am Universitätsklinikum Hamburg-Eppendorf Assigned 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