Pädiatrie 5 – Onkologie, Hämatologie und Immunologie am Klinikum Stuttgart Assigned diseases:
In the following you will find the diseases that are treated in this facility:
AL amyloidosis
Aceruloplasminemia
Acquired hemophilia
Acquired idiopathic sideroblastic anemia
Acquired prothrombin deficiency
Acquired purpura fulminans
Acquired von Willebrand syndrome
Acute basophilic leukemia
Acute biphenotypic leukemia
Acute erythroid leukemia
Acute leukemia of ambiguous lineage
Acute lymphoblastic leukemia
Acute megakaryoblastic leukemia
Acute monoblastic/monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myeloid leukaemia with myelodysplasia-related features
Acute myeloid leukemia
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 11q23 abnormalities
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with minimal differentiation
Acute myeloid leukemia with recurrent genetic anomaly
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute myelomonocytic leukemia
Acute panmyelosis with myelofibrosis
Acute promyelocytic leukemia
Acute undifferentiated leukemia
Adamantinoma
Adult T-cell leukemia/lymphoma
Adult-onset autosomal recessive sideroblastic anemia
Aggressive primary cutaneous B-cell lymphoma
Aggressive primary cutaneous T-cell lymphoma
Aggressive systemic mastocytosis
Aleukemic mast cell leukemia
Alpha delta granule deficiency
Alpha granule disease
Alpha-heavy chain disease
Alpha-thalassemia
Alpha-thalassemia and related disorders
Alpha-thalassemia-X-linked intellectual disability syndrome
Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
Alpha-thalassemia-myelodysplastic syndrome
Alveolar rhabdomyosarcoma
Alveolar soft tissue sarcoma
Anaplastic ependymoma
Anaplastic ganglioglioma
Anaplastic oligoastrocytoma
Anaplastic oligodendroglioma
Anaplastic/large cell medulloblastoma
Angiocentric glioma
Angiosarcoma
Aregenerative anemia
Astroblastoma
Astrocytoma
Atypical chronic myeloid leukemia
Atypical papilloma of choroid plexus
Atypical teratoid rhabdoid tumor
Autoimmune lymphoproliferative syndrome
Autoimmune thrombocytopenia
Autosomal dominant aplasia and myelodysplasia
Autosomal dominant macrothrombocytopenia
Autosomal recessive sideroblastic anemia
Autosomal thrombocytopenia with normal platelets
B-cell non-Hodgkin lymphoma
Benign peripheral nerve sheath tumor
Benign schwannoma
Bernard-Soulier syndrome
Beta-thalassemia
Beta-thalassemia and related diseases
Beta-thalassemia associated with another hemoglobin anomaly
Beta-thalassemia intermedia
Beta-thalassemia major
Beta-thalassemia with other manifestations
Beta-thalassemia-X-linked thrombocytopenia syndrome
Bilineal acute leukemia
Bleeding diathesis due to a collagen receptor defect
Bleeding diathesis due to glycoprotein VI deficiency
Bleeding diathesis due to integrin alpha2-beta1 deficiency
Bleeding diathesis due to thromboxane synthesis deficiency
Bleeding disorder due to P2Y12 defect
Bleeding disorder in hemophilia A carriers
Bleeding disorder in hemophilia B carriers
Bloom syndrome
Bone sarcoma
Bullous diffuse cutaneous mastocytosis
Central nervous system embryonal tumor
Central neurocytoma
Cerebellar liponeurocytoma
Chondrosarcoma
Chordoid glioma
Choriocarcinoma of the central nervous system
Choroid plexus carcinoma
Choroid plexus tumor
Chronic eosinophilic leukemia
Chronic myeloid leukemia
Chronic myelomonocytic leukemia
Chronic myeloproliferative disease, unclassifiable
Chronic neutrophilic leukemia
Classic Hodgkin lymphoma
Classic mast cell leukemia
Classic medulloblastoma
Combined deficiency of factor V and factor VIII
Composite lymphoma
Congenital alpha2-antiplasmin deficiency
Congenital amegakaryocytic thrombocytopenia
Congenital atransferrinemia
Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia type I
Congenital dyserythropoietic anemia type II
Congenital dyserythropoietic anemia type III
Congenital dyserythropoietic anemia type IV
Congenital epulis
Congenital factor II deficiency
Congenital factor V deficiency
Congenital factor VII deficiency
Congenital factor X deficiency
Congenital factor XI deficiency
Congenital factor XII deficiency
Congenital factor XIII deficiency
Congenital fibrinogen deficiency
Congenital high-molecular-weight kininogen deficiency
Congenital intrinsic factor deficiency
Congenital plasminogen activator inhibitor type 1 deficiency
Congenital prekallikrein deficiency
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
Congenital thrombotic thrombocytopenic purpura
Congenital vitamin K-dependent coagulation factors deficiency
Constitutional anemia due to iron metabolism disorder
Constitutional deficiency anemia
Constitutional dyserythropoietic anemia
Constitutional megaloblastic anemia due to folate metabolism disorder
Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder
Constitutional megaloblastic anemia with severe neurologic disease
Constitutional sideroblastic anemia
Craniopharyngioma
Cutaneous mastocytoma
Cutaneous mastocytosis
Deafness-lymphedema-leukemia syndrome
Dedifferentiated liposarcoma
Delta-beta-thalassemia
Dendritic cell sarcoma not otherwise specified
Dendritic cell tumor
Dense granule disease
Dermatofibrosarcoma protuberans
Desmoid tumor
Desmoplastic infantile astrocytoma/ganglioglioma
Desmoplastic small round cell tumor
Desmoplastic/nodular medulloblastoma
Diamond-Blackfan anemia
Diaphyseal medullary stenosis-bone malignancy syndrome
Diffuse cutaneous mastocytosis
Diffuse leptomeningeal melanocytosis
Dominant beta-thalassemia
Dysembryoplastic neuroepithelial tumor
Dyskeratosis congenita
East Texas bleeding disorder
Embryonal carcinoma
Embryonal carcinoma of the central nervous system
Embryonal rhabdomyosarcoma
Embryonal tumor of neuroepithelial tissue
Ependymal tumor
Ependymoblastoma
Epignathus
Epithelioid sarcoma
Epstein syndrome
Essential thrombocythemia
Esthesioneuroblastoma
Evans syndrome
Extracutaneous mastocytoma
Extragonadal germ cell tumor
Extragonadal germinoma
Extragonadal non-dysgerminomatous germ cell tumor
Extragonadal teratoma
Extramedullary soft tissue plasmacytoma
Extraneural perineurioma
Extranodal nasal NK/T cell lymphoma
Extraskeletal Ewing sarcoma
Extraskeletal myxoid chondrosarcoma
Extraventricular neurocytoma
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial multiple meningioma
Familial thrombocytosis
Familial thrombomodulin anomalies
Fanconi anemia
Fechtner syndrome
Fetal and neonatal alloimmune thrombocytopenia
Fibrosarcoma
Follicular dendritic cell sarcoma
Formiminoglutamic aciduria
Gaisböck syndrome
Gamma-heavy chain disease
Gangliocytoma
Ganglioglioma
Ganglioneuroblastoma
Ganglioneuroma
Germ cell tumor
Germ cell tumor of testis
Germinoma of the central nervous system
Gestational choriocarcinoma
Giant cell tumor of bone
Glanzmann thrombasthenia
Glial tumor
Glial tumor of neuroepithelial tissue with unknown origin
Glomus tumor
Gonadal germ cell tumor
Growing teratoma syndrome
Hb Bart's hydrops fetalis
Heavy chain deposition disease
Heavy chain disease
Hemangioblastoma
Hemoglobin C disease
Hemoglobin C-beta-thalassemia syndrome
Hemoglobin D disease
Hemoglobin E disease
Hemoglobin E-beta-thalassemia syndrome
Hemoglobin H disease
Hemoglobin Lepore-beta-thalassemia syndrome
Hemoglobin M disease
Hemoglobinopathy
Hemoglobinopathy Toms River
Hemophilia
Hemophilia A
Hemophilia B
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Heparin-induced thrombocytopenia
Hepatoblastoma
Hereditary combined deficiency of vitamin K-dependent clotting factors
Hereditary folate malabsorption
Hereditary isolated aplastic anemia
Hereditary methemoglobinemia
Hereditary orotic aciduria
Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
Hereditary thrombocytopenia with normal platelets
Hereditary thrombophilia due to congenital antithrombin deficiency
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
High-grade astrocytoma
Histiocytic and dendritic cell tumor
Histiocytic sarcoma
Hodgkin lymphoma
Homocystinuria without methylmalonic aciduria
Hoyeraal-Hreidarsson syndrome
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
Hypereosinophilic syndrome
Hypoxanthine guanine phosphoribosyltransferase partial deficiency
Hypoxanthine-guanine phosphoribosyltransferase deficiency
IRIDA syndrome
Idiopathic aplastic anemia
Idiopathic hypereosinophilic syndrome
Imerslund-Gräsbeck syndrome
Immune thrombocytopenia
Immune-mediated thrombotic thrombocytopenic purpura
Immunodeficiency-associated lymphoproliferative disease
Indolent primary cutaneous B-cell lymphoma
Indolent primary cutaneous T-cell lymphoma
Indolent systemic mastocytosis
Infantile myofibromatosis
Inflammatory myofibroblastic tumor
Inherited acute myeloid leukemia
Interdigitating dendritic cell sarcoma
Intraneural perineurioma
Isolated bone marrow mastocytosis
Isolated hereditary giant platelet disorder
Juvenile hyaline fibromatosis
Juvenile myelomonocytic leukemia
Kaposi sarcoma
Kaposiform hemangioendothelioma
Langerhans cell histiocytosis
Langerhans cell sarcoma
Leiomyosarcoma
Lesch-Nyhan syndrome
Lhermitte-Duclos disease
Light and heavy chain deposition disease
Light chain deposition disease
Lipoblastoma
Liposarcoma
Low-grade astrocytoma
Low-grade ependymoma
Lymphoadenopathic mastocytosis with eosinophilia
Lymphoid hemopathy
Lymphoma
Lymphoproliferative disease associated with primary immune disease
MYH9-related disease
Macrophage or histiocytic tumor
Macrothrombocytopenia with mitral valve insufficiency
Maculopapular cutaneous mastocytosis
Maffucci syndrome
Malignant germ cell tumor of ovary
Malignant non-dysgerminomatous germ cell tumor of ovary
Malignant peripheral nerve sheath tumor
Malignant peripheral nerve sheath tumor with perineurial differentiation
Malignant triton tumor
Mast cell leukemia
Mast cell sarcoma
Mastocytosis
May-Hegglin thrombocytopenia
Mediterranean macrothrombocytopenia
Medulloblastoma
Medulloblastoma with extensive nodularity
Medulloepithelioma of the central nervous system
Melanoma of soft tissue
Meningeal melanocytoma
Meningioma
Methotrexate-associated lymphoproliferative disorders
Methylcobalamin deficiency type cblDv1
Methylcobalamin deficiency type cblE
Methylcobalamin deficiency type cblG
Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia with homocystinuria type cblF
Methylmalonic acidemia with homocystinuria, type cblC
Methylmalonic acidemia with homocystinuria, type cblD
Methylmalonic acidemia with homocystinuria, type cblJ
Methylmalonic acidemia with homocystinuria, type cblX
Microcytic anemia with liver iron overload
Mild hemophilia A
Mild hemophilia B
Mitochondrial myopathy and sideroblastic anemia
Mixed germ cell tumor
Mixed germ cell tumor of central nervous system
Mixed neuronal-glial tumor
Moderate hemophilia A
Moderate hemophilia B
Mu-heavy chain disease
Multiple myeloma
Multiple osteochondromas
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
Mycosis fungoides and variants
Myelodysplastic syndrome
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Myelodysplastic/myeloproliferative disease
Myeloid hemopathy
Myeloid sarcoma
Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement
Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement
Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement
Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
Myeloproliferative neoplasm
Myxofibrosarcoma
Myxoid/round cell liposarcoma
Nasal ganglioglioma
Nasopharyngeal teratoma
Nephroblastoma
Neuroblastoma
Neuroepithelioma
Neurofibroma
Neuronal tumor
Nodular lymphocyte predominant Hodgkin lymphoma
Nodular urticaria pigmentosa
Non-Hodgkin lymphoma
Non-amyloid monoclonal immunoglobulin deposition disease
Non-central nervous system-localized embryonal carcinoma
Non-seminomatous germ cell tumor of testis
OSLAM syndrome
Oligoastrocytic tumor
Oligoastrocytoma
Oligodendroglial tumor
Oligodendroglioma
Ollier disease
Optic pathway glioma
Osteoblastoma
Osteosarcoma
Ovarian dysgerminoma
POEMS syndrome
Painful orbital and systemic neurofibromas-marfanoid habitus syndrome
Pancreatic insufficiency-anemia-hyperostosis syndrome
Papillary glioneuronal tumor
Papillary tumor of the pineal region
Papilloma of choroid plexus
Paris-Trousseau thrombocytopenia
Paroxysmal nocturnal hemoglobinuria
Pearson syndrome
Perineurioma
Peripheral primitive neuroectodermal tumor
Persistent polyclonal B-cell lymphocytosis
Pineal parenchymal tumor of intermediate differentiation
Pineal tumor of neuroepithelial tissue
Pineoblastoma
Pineocytoma
Plaque-form urticaria pigmentosa
Plasma cell tumor
Plasmacytoma
Pleomorphic liposarcoma
Pleomorphic rhabdomyosarcoma
Plummer-Vinson syndrome
Polycythemia vera
Polyembryoma
Post-transplant lymphoproliferative disease
Primary acquired pure red cell aplasia
Primary acquired red cell aplasia
Primary bone lymphoma
Primary central nervous system lymphoma
Primary cutaneous B-cell lymphoma
Primary cutaneous CD30+ T-cell lymphoproliferative disease
Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma
Primary cutaneous T-cell lymphoma
Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
Primary cutaneous diffuse large B-cell lymphoma, leg type
Primary cutaneous follicle center lymphoma
Primary cutaneous gamma/delta-positive T-cell lymphoma
Primary cutaneous lymphoma
Primary cutaneous marginal zone B-cell lymphoma
Primary cutaneous peripheral T-cell lymphoma not otherwise specified
Primary germ cell tumor of central nervous system
Primary hypereosinophilic syndrome
Primary intraocular lymphoma
Primary localized amyloidosis
Primary lymphoma of the conjunctiva
Primary melanocytic tumor of central nervous system
Primary melanoma of the central nervous system
Primary myelofibrosis
Primary non-gestational choriocarcinoma of ovary
Primary oculocerebral lymphoma
Primary organ-specific lymphoma
Primary plasmacytoma of the bone
Primary pulmonary lymphoma
Primary systemic amyloidosis
Protein S acquired deficiency
Pseudo-von Willebrand disease
Pseudoxanthomatous diffuse cutaneous mastocytosis
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
Rare acquired aplastic anemia
Rare acquired deficiency anemia
Rare anemia
Rare aplastic anemia
Rare bone tumor
Rare coagulation disorder
Rare constitutional aplastic anemia
Rare deficiency anemia
Rare hemolytic anemia
Rare hemorrhagic disorder
Rare hemorrhagic disorder due to a coagulation factors defect
Rare hemorrhagic disorder due to a constitutional coagulation factors defect
Rare hemorrhagic disorder due to a constitutional platelet anomaly
Rare hemorrhagic disorder due to a constitutional thrombocytopenia
Rare hemorrhagic disorder due to a platelet anomaly
Rare hemorrhagic disorder due to a qualitative platelet defect
Rare hemorrhagic disorder due to an acquired coagulation factor defect
Rare hemorrhagic disorder due to an acquired platelet anomaly
Rare hereditary thrombophilia
Rare nervous system tumor
Rare soft tissue tumor
Rare thrombotic disease of hematologic origin
Rare thrombotic disorder due to a coagulation factors defect
Rare thrombotic disorder due to a constitutional coagulation factors defect
Rare thrombotic disorder due to a constitutional platelet anomaly
Rare thrombotic disorder due to a platelet anomaly
Rare thrombotic disorder due to an acquired coagulation factors defect
Rare thrombotic disorder due to an acquired platelet anomaly
Rare tumor of neuroepithelial tissue
Refractory anemia
Refractory anemia with excess blasts
Refractory anemia with excess blasts in transformation
Refractory anemia with excess blasts type 1
Refractory anemia with excess blasts type 2
Refractory cytopenia with multilineage dysplasia
Reticular perineurioma
Revesz syndrome
Rhabdoid tumor
Rhabdoid tumor predisposition syndrome
Rhabdomyosarcoma
Rosette-forming glioneuronal tumor
Sclerosing perineurioma
Scott syndrome
Sebastian syndrome
Secondary hypereosinophilic syndrome
Severe congenital hypochromic anemia with ringed sideroblasts
Severe hemophilia A
Severe hemophilia B
Severe hereditary thrombophilia due to congenital protein C deficiency
Severe hereditary thrombophilia due to congenital protein S deficiency
Shwachman-Diamond syndrome
Sickle cell anemia
Sickle cell disease and related diseases
Sickle cell disease associated with another hemoglobin anomaly
Sickle cell-beta-thalassemia disease syndrome
Sickle cell-hemoglobin C disease syndrome
Sickle cell-hemoglobin D disease syndrome
Sickle cell-hemoglobin E disease syndrome
Sideroblastic anemia
Simple cryoglobulinemia
Skeletal Ewing sarcoma
Smoldering systemic mastocytosis
Soft tissue sarcoma
Solitary fibrous tumor
Spermatocytic seminoma
Stormorken-Sjaastad-Langslet syndrome
Subcutaneous panniculitis-like T-cell lymphoma
Syndrome with alpha-thalassemia as a major feature
Synovial sarcoma
Systemic mastocytosis
Systemic mastocytosis with associated hematologic neoplasm
Sézary syndrome
T-cell non-Hodgkin lymphoma
Telangiectasia macularis eruptiva perstans
Teratoma of the central nervous system
Testicular seminomatous germ cell tumor
Therapy related acute myeloid leukemia and myelodysplastic syndrome
Thiamine-responsive megaloblastic anemia syndrome
Thrombocythemia with distal limb defects
Thrombocytopenia with congenital dyserythropoietic anemia
Thrombocytopenia-absent radius syndrome
Thrombotic thrombocytopenic purpura
Thyroid lymphoma
Transcobalamin deficiency
Transient erythroblastopenia of childhood
Tumor of cranial and spinal nerves
Tumor of hematopoietic and lymphoid tissues
Tumor of meninges
Typical urticaria pigmentosa
Unclassified acute myeloid leukemia
Unclassified myelodysplastic syndrome
Unclassified myelodysplastic/myeloproliferative disease
Undifferentiated pleomorphic sarcoma
Unstable hemoglobin disease
Vestibular schwannoma
Vitamin B12- and folate-independent constitutional megaloblastic anemia
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
WT limb-blood syndrome
Well-differentiated liposarcoma
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
X-linked sideroblastic anemia
X-linked sideroblastic anemia and spinocerebellar ataxia
X-linked thrombocytopenia with normal platelets
Yolk sac tumor
Yolk sac tumor of central nervous system