Informaţii despre

Nume Neuroblastoma
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Malignant neoplasm: Adrenal gland, unspecified
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Neuroblastoma 2; Neuroblastoma 3; Neuroblastoma 4; Neuroblastoma 5; Neuroblastoma 6; Neuroblastoma 7

Vezi şi

Boli A-Z Achondroplasia Acute Leukemia Acute Promyelocytic Leukemia Adenocarcinoma Adenoma Adie Pupil Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Neuroblastoma Adult Medulloblastoma Aging Aland Island Eye Disease Alkaptonuria Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anaplastic Ganglioglioma Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Angel-Shaped Phalangoepiphyseal Dysplasia Angiomatosis Angiomyoma Aniridia 1 Anorexia Nervosa 1 Aortic Valve Disease 2 Aromatic Alpha-Keto Acid Reductase Aromatic L-Amino Acid Decarboxylase Deficiency Arterial Tortuosity Syndrome Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 5 Askin's Tumor Astroblastoma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Autonomic Nervous System Neoplasm Autonomic Neuropathy Baroreflex Failure Beckwith-Wiedemann Syndrome Bilateral Retinoblastoma Biliary Atresia Bipolar Disorder Bjornstad Syndrome Bladder Transitional Cell Papilloma Bleeding Disorder, Platelet-Type, 11 Blepharocheilodontic Syndrome 1 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Mineral Density Quantitative Trait Locus 1 Borna Disease Brain Cancer Breast Adenocarcinoma Breast Cancer Bronchogenic Cyst Budd-Chiari Syndrome Burns C3 Glomerulopathy Capillary Hemangioma Carcinoid Syndrome Carpal Tunnel Syndrome Caspase 8 Deficiency Cataract 5, Multiple Types Cat-Scratch Disease Cellulitis Central Nervous System Disease Central Neurocytoma Cerebellar Ataxia, Cayman Type Cerebral Hypoxia Cerebral Neuroblastoma Cerebral Primitive Neuroectodermal Tumor Cerebritis Cerebrum Cancer Cervical Cancer Cervical Neuroblastoma Cervicitis Charles Bonnet Syndrome Chikungunya Cholera Chorea, Benign Hereditary Choroiditis Chromosomal Deletion Syndrome Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 1p Deletion Chromosome 2p Duplication Clear Cell Sarcoma Cohen-Gibson Syndrome Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Congenital Disorder of Glycosylation, Type Iic Conn's Syndrome Conventional Fibrosarcoma Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Cutaneous Ganglioneuroma Cystathioninuria Cystic Nephroma Cystic Teratoma Cytomegalovirus Infection Deafness, Autosomal Recessive 74 Delayed Sleep Phase Disorder Dengue Virus Desmoplastic Small Round Cell Tumor Diabetes Mellitus Diabetes Mellitus, Transient Neonatal, 1 Diabetic Autonomic Neuropathy Diabetic Neuropathy Diabetic Polyneuropathy Diarrhea Differentiating Neuroblastoma Dihydropyrimidinase Deficiency Dilated Cardiomyopathy Disseminated Intravascular Coagulation Dysautonomia Dysphagia Dystonia Ectodermal Dysplasia Ectopic Cushing Syndrome Elastosis Perforans Serpiginosa Embryonal Rhabdomyosarcoma Embryonal Tumor with Multilayered Rosettes Encephalitis Encephalopathy Endometrial Small Cell Carcinoma Endotheliitis Ependymoblastoma Epidermolysis Bullosa Pruriginosa Epilepsy, Pyridoxine-Dependent Epithelial Recurrent Erosion Dystrophy Epithelioid Malignant Peripheral Nerve Sheath Tumor Esophageal Varix Ewing Sarcoma Extracranial Neuroblastoma Facial Paralysis Femoral-Facial Syndrome Fetal Erythroblastosis Fetal Hydantoin Syndrome Fetal Retinoid Syndrome Friedreich Ataxia 1 Fundus Albipunctatus Fusariosis Galactosialidosis Gallbladder Small Cell Carcinoma Gangliocytoma Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Gardner-Diamond Syndrome Gastric Teratoma Gastrointestinal Neuroendocrine Tumor Gastrointestinal Stromal Tumor Gastrointestinal System Cancer Gastroschisis Gaucher Disease, Type Ii Gaucher Disease, Type Iii Generalized Epilepsy with Febrile Seizures Plus, Type 7 Genitopatellar Syndrome Germ Cells Tumors Gerstmann Syndrome Gianotti Crosti Syndrome Giardioză Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Glucose Transporter Type 1 Deficiency Syndrome Griscelli Syndrome Hajdu-Cheney Syndrome Harlequin Syndrome Heart and Brain Malformation Syndrome Helix Syndrome Hemangioma Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 1 Hemophagocytic Lymphohistiocytosis Hemophagocytic Lymphohistiocytosis, Familial, 2 Hemorrhagic Disease Hepatic Adenomas, Familial Hepatic Fibrosis, Severe Due to Schistosoma Mansoni Infection Hepatic Veno-Occlusive Disease Hepatitis Hepatitis C Hepatitis C Virus Hepatoblastoma Hereditary Wilms' Tumor Herpes Simplex High Pressure Neurological Syndrome Histiocytoma Histiocytosis Horner Syndrome, Congenital Horseshoe Kidney Human Immunodeficiency Virus Type 1 Huntington Disease Hydrocele Hydrocephalus Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperaldosteronism, Familial, Type I Hyperaldosteronism, Familial, Type Ii Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 5 Hyperphenylalaninemia, Bh4-Deficient, C Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypervitaminosis a Hypoglycemia Hypophosphatemia Hypoplastic Left Heart Syndrome 1 Hypotonia-Cystinuria Syndrome Hypoxia Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Immunoglobulin E Concentration, Serum Inappropriate Adh Syndrome Incontinentia Pigmenti Infant Botulism Infantile Scoliosis Infratentorial Cancer Insulin-Like Growth Factor I Insulinoma Intervertebral Disc Disease Ischemia Isolated Optic Neuritis Isotretinoin Syndrome Jacobsen Syndrome Japanese Encephalitis Kawasaki Disease Kwashiorkor Lambert-Eaton Myasthenic Syndrome Langerhans Cell Histiocytosis Large Cell Neuroendocrine Carcinoma Lateral Sclerosis Leiomyosarcoma Lesch-Nyhan Syndrome Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Limbic Encephalitis Lung Cancer Lyme Disease Lymphadenitis Lymphangiectasia, Intestinal Lymphoblastic Leukemia Lymphoma Macs Syndrome Malignant Peripheral Nerve Sheath Tumor Malignant Spiradenoma Malignant Teratocarcinosarcoma Manganese Poisoning Marcus Gunn Phenomenon Mature Teratoma Measles Meckel Syndrome, Type 1 Mediastinitis Medulloblastoma Medullomyoblastoma Megacolon Megaesophagus Melanoma Meningeal Melanomatosis Meningioma, Familial Meningitis Merkel Cell Carcinoma Microphthalmia Migraine with or Without Aura 1 Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Mirage Syndrome Mismatch Repair Cancer Syndrome Mixed Germ Cell Tumor Monocytic Leukemia Morphine Dependence Mucoepidermoid Carcinoma Mucopolysaccharidosis-Plus Syndrome Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Mumps Muscular Atrophy Myelitis Myelodysplastic Syndrome Myoclonic Encephalopathy of Infants Myoclonus Myoclonus and Ataxia Myopathy with Lactic Acidosis, Hereditary Narcolepsy Neonatal Hypoxic and Ischemic Brain Injury Nephrogenic Adenoma Nervous System Cancer Nervous System Disease Nestor-Guillermo Progeria Syndrome Netherton Syndrome Neural Crest Tumor Neuroblastoma 2 Neuroblastoma 3 Neuroblastoma 4 Neuroblastoma 5 Neuroblastoma 6 Neuroblastoma 7 Neuroblastoma Breakpoint Family, Member 17, Pseudogene Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type V Neutropenia Neutrophil Actin Dysfunction Newcastle Disease Nicolaides-Baraitser Syndrome Nijmegen Breakage Syndrome Nodular Ganglioneuroblastoma Non-Involuting Congenital Hemangioma Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 Obstructive Hydrocephalus Ocular Dominance Olfactory Neuroblastoma Oligodendroglioma Opsoclonus-Myoclonus Syndrome Oral Squamous Cell Carcinoma Orbital Cancer Orbital Cellulitis Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Osteochondroma Ovarian Cancer Ovarian Cystic Teratoma Pancreatic Cancer Pancreatitis Pancreatitis, Hereditary Pancreatoblastoma Paraganglioma Paragangliomas 4 Parameningeal Embryonal Rhabdomyosarcoma Parametritis Paraneoplastic Syndromes Paraplegia Pelger-Huet Anomaly Peripheral Nervous System Neoplasm Perivascular Epithelioid Cell Tumor Pertussis Phaeochromocytoma Phelan-Mcdermid Syndrome Pheochromocytoma Pituitary Adenoma Pleurisy Pneumonia Poland Syndrome Polyneuropathy Porphyria Variegata Postpartum Depression Primary Effusion Lymphoma Prostate Cancer Prostate Small Cell Carcinoma Prostatitis Protein-Losing Enteropathy Protoporphyria, Erythropoietic Psoriasis 2 Psoriasis 7 Pulmonary Sequestration Rabies Rapp-Hodgkin Syndrome Renal Cell Carcinoma Associated with Neuroblastoma Renal Glucosuria Renovascular Hypertension Renpenning Syndrome 1 Retinitis Retinoblastoma Retroperitoneal Neuroblastoma Rett Syndrome Rhabdomyosarcoma Rhabdomyosarcoma 2 Rhabdomyosarcoma, Embryonal, 1 Right Atrial Isomerism Roberts Syndrome Sacrococcygeal Teratoma Salivary Gland Adenoma, Pleomorphic Salt and Pepper Developmental Regression Syndrome Sarcoma Schistosoma Mansoni Infection, Susceptibility/ Scoliosis Scrapie Severe Combined Immunodeficiency Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sinonasal Undifferentiated Carcinoma Skin Melanoma Small Cell Cancer of the Lung Small Cell Carcinoma Small Cell Neuroendocrine Carcinoma Smith-Kingsmore Syndrome Smith-Magenis Syndrome Smith-Mccort Dysplasia 2 Soft Tissue Sarcoma Sotos Syndrome 1 Spastic Diplegia Spasticity Spastic Paraplegia 20, Autosomal Recessive Spindle Cell Carcinoma Spiradenoma Spondyloocular Syndrome Status Epilepticus Stomatitis Subependymal Giant Cell Astrocytoma Suppression of Tumorigenicity 12 Suppressor of Tumorigenicity 3 Supratentorial Cancer Syndrome of Inappropriate Antidiuretic Hormone Syringocystadenoma Papilliferum Teratocarcinoma Teratoma Testicular Regression Syndrome Tetraploidy Thrombosis Thymic Hyperplasia Thymoma Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tolosa-Hunt Syndrome Toxic Encephalopathy Toxocariasis Transverse Myelitis Treacher Collins Syndrome 1 Tuberous Sclerosis Tubulin, Beta Unilateral Retinoblastoma Urethral Diverticulum Urethritis Vacterl Association, X-Linked, with or Without Hydrocephalus Vitamin B12 Deficiency Weaver Syndrome Wernicke Encephalopathy West Nile Virus Whim Syndrome Wilms Tumor 6 Wolf-Hirschhorn Syndrome