Informaţii despre

Nume Lymphoblastic Leukemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Lymphoid leukaemia, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
Boli din aceeaşi familie Leukemia, Acute Lymphoblastic; Leukemia, Acute Lymphoblastic 2; Leukemia, Acute Lymphoblastic 3

Vezi şi

Boli A-Z 8p11 Myeloproliferative Syndrome Abducens Nerve Disease Acalculous Cholecystitis Acanthosis Nigricans Acinar Cell Carcinoma Acth Deficiency, Isolated Acute Biphenotypic Leukemia Acute Graft Versus Host Disease Acute Leukemia Acute Liver Failure Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Monoblastic Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Non Lymphoblastic Leukemia Acute Pancreatitis Acute T Cell Leukemia Adie Pupil Agammaglobulinemia Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Al Amyloidosis Aleukemic Leukemia Cutis Alopecia Alopecia Areata 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 Alstrom Syndrome Alzheimer Disease 3 Amyloidosis Anaplastic Large Cell Lymphoma Anaplastic Oligoastrocytoma Anaplastic Oligodendroglioma Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aphasia Aplastic Anemia Apocrine Gland Secretion, Variation in Appendicitis Argyria Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Aseptic Meningitis Asparagine Synthetase Deficiency Aspergillosis Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Atypical Chronic Myeloid Leukemia Atypical Teratoid Rhabdoid Tumor Autoimmune Lymphoproliferative Syndrome, Type V B-Cell Adult Acute Lymphocytic Leukemia B-Cell Childhood Acute Lymphoblastic Leukemia B-Cell Growth Factor B Cell Linker Protein Deficiency B-Cell Lymphomas Bilateral Breast Cancer Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Boerhaave Syndrome Bone Marrow Cancer Bone Marrow Necrosis Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Breast Cancer Bronchiolitis Bronchiolitis Obliterans Brucellosis Burkitt Lymphoma Calcinosis Candidiasis Capillary Leak Syndrome Cavernous Sinus Thrombosis Cellulitis Central Nervous System Disease Central Nervous System Leukemia Central Pontine Myelinolysis Central Serous Chorioretinopathy Cerebellar Degeneration-Related Autoantigen 3 Cerebral Atrophy Cerebral Sinovenous Thrombosis Cerebritis Charcot-Marie-Tooth Disease Childhood Leukemia Cholecystitis Choroiditis Chromosomal Triplication Chromosome 11q Duplication Chromosome 5q Deletion Syndrome Chromosome Xq Duplication Chronic Enteropathy Associated with Slco2a1 Gene Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Myelomonocytic Leukemia Chronic Recurrent Multifocal Osteomyelitis Classic Phenylketonuria Cleft Lip/palate with Abnormal Thumbs and Microcephaly Clostridium Difficile Colitis Cohen-Gibson Syndrome Colitis Colorblindness, Partial, Protan Series Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Disorder of Glycosylation, Type Iic Conidiobolomycosis Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Critical Illness Polyneuropathy Cryptosporidiosis Cutaneous Mastocytosis Cystic Fibrosis Cystinuria Cystitis Cytochrome P450 2d6 Variant Cytomegalovirus Infection Cytomegalovirus Retinitis Darier-White Disease Demodicidosis Desmoplastic Small Round Cell Tumor Diphtheria Discitis Disseminated Intravascular Coagulation Down Syndrome Dwarfism Dyskeratosis Congenita Eating Disorder Ecthyma Ectopic Thymus Empty Sella Syndrome Encephalitis Encephalopathy Endocarditis Endomyocardial Fibrosis Endophthalmitis Endotheliitis Eosinophilic Meningitis Epidermolysis Bullosa Pruriginosa Epididymo-Orchitis Epiglottitis Epilepsy Epithelial Recurrent Erosion Dystrophy Erdheim-Chester Disease Esotropia Essential Thrombocythemia Ewing Sarcoma Exanthem Extrapontine Myelinolysis Facial Paralysis Fanconi Anemia, Complementation Group D2 Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasciitis Fasting Hypoglycemia Fibrous Histiocytoma Fibular Hypoplasia and Complex Brachydactyly Filariasis Follicular Lymphoma Follicular Mucinosis Folliculitis Friedreich Ataxia 1 Fundus Albipunctatus Fusariosis Ganglioneuroma Gastroenteritis Genitopatellar Syndrome Gilbert Syndrome Glioblastoma Glomerulonephritis Glucocorticoid Resistance, Generalized Graft-Versus-Host Disease Granulocytopenia Granulomatous Amebic Encephalitis Growth Hormone Deficiency Guillain-Barre Syndrome Gynecomastia Hairy Cell Leukemia Headache Headache Associated with Sexual Activity Helix Syndrome Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 2a Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemorrhagic Cystitis Hepatic Adenomas, Familial Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatoblastoma Hereditary Hemorrhagic Telangiectasia Hereditary Multiple Exostoses Hereditary Wilms' Tumor Herpes Simplex Herpes Zoster Hhv-6 Encephalitis Histiocytic Sarcoma Histiocytoma Histiocytosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypereosinophilic Syndrome Hyperglycemia Hyperostosis Hyperphenylalaninemia Hyperphenylalaninemia, Bh4-Deficient, C Hyperphosphatemia Hyperreflexia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoglycemia Hypokalemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hypopituitarism Hypopyon Hypoxia Ichthyosis Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Infant Gynecomastia Influenza Insulin-Like Growth Factor I Intellectual Disability-Developmental Delay-Contractures Syndrome Intestinal Perforation Intracranial Hypertension Invasive Aspergillosis Iridocyclitis Juvenile Myelomonocytic Leukemia Juvenile Pilocytic Astrocytoma Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome Juvenile Rheumatoid Arthritis Juvenile Xanthogranuloma Knobloch Syndrome Lactic Acidosis Langerhans Cell Histiocytosis Large Granular Lymphocyte Leukemia Laryngitis Leber Hereditary Optic Neuropathy Legionellosis Leishmaniasis Leopard Syndrome Leukemia Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphoblastic 3 Leukemia, Acute Myeloid Leukemia, Chronic Myeloid Lipodystrophy Lipoid Nephrosis Liposarcoma Listeriosis Loeffler Endocarditis Long Qt Syndrome Luscan-Lumish Syndrome Lymphoblastic Leukemia, Acute, with Lymphomatous Features Lymphoblastic Lymphoma Lymphocytic Vasculitis Lymphoid Leukemia Lymphoma Lymphomatoid Granulomatosis Macroglobulinemia Malignant Histiocytosis Malignant Triton Tumor Mannose-Binding Lectin Deficiency Mckusick-Kaufman Syndrome Measles Mediastinitis Megacolon Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency Meningitis Meningoencephalitis Menkes Disease Meralgia Paresthetica Methemoglobinemia Microcephalic Osteodysplastic Primordial Dwarfism, Type I Miller-Dieker Lissencephaly Syndrome Mirage Syndrome Mn1 Molluscum Contagiosum Monocytic Leukemia Mucoepidermoid Carcinoma Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Mumps Myasthenia Gravis Mycobacterium Chelonae Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloproliferative Neoplasm Myeloproliferative Syndrome, Transient Myopathy Myxoid Liposarcoma Necrotizing Fasciitis Nephrocalcinosis Nervous System Disease Neuroblastoma Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuropathy Neutropenia Neutrophil Actin Dysfunction Nicolaides-Baraitser Syndrome Niemann-Pick Disease Niemann-Pick Disease, Type C1 Nijmegen Breakage Syndrome Nocardiosis Noma Non-Involuting Congenital Hemangioma Obstructive Jaundice Oculotrichodysplasia Oligoastrocytoma Oligodendroglioma Oral Cancer Orchitis Osteomyelitis Osteonecrosis Otitis Externa Paine Syndrome Pancreatitis Pancytopenia Panniculitis Papillary Carcinoma Papilledema Paraplegia Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Parotitis Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Pericardial Effusion Pericoronitis Perivascular Epithelioid Cell Tumor Phelan-Mcdermid Syndrome Phenylketonuria Philadelphia-Negative Chronic Myeloid Leukemia Pick Disease of Brain Pilocytic Astrocytoma Platelet Disorder, Familial, with Associated Myeloid Malignancy Pleuropneumonia Pneumatosis Cystoides Intestinalis Pneumonia Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polyneuropathy Polyradiculoneuropathy Polyradiculopathy Porokeratosis Porphyria Porphyria Cutanea Tarda Precocious Puberty Precursor Lymphoblastic Lymphoma/leukemia Precursor T-Cell Acute Lymphoblastic Leukemia Prostatitis Ptosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Purpura Pyomyositis Rapadilino Syndrome Rapp-Hodgkin Syndrome Recurrent Acute Pancreatitis Refractory Anemia Retinal Detachment Retinitis Retinoblastoma Rett Syndrome Reversible Cerebral Vasoconstriction Syndrome Rhabdomyosarcoma Rheumatoid Arthritis Richter's Syndrome Ring Chromosome 16 Ring Chromosome 21 Roberts Syndrome Rosai-Dorfman Disease Rubella Sagittal Sinus Thrombosis Sarcoma Satb2-Associated Syndrome Seminoma Septic Arthritis Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Severe Combined Immunodeficiency Severe Congenital Neutropenia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sideroblastic Anemia Siderosis Sinusitis Sjogren-Larsson Syndrome Skin Disease Small Non-Cleaved Cell Lymphoma Soft Tissue Sarcoma Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spindle Cell Carcinoma Spiradenoma Splenic Infarction Spondylocarpotarsal Synostosis Syndrome Stenotrophomonas Maltophilia Infection Steroid-Induced Glaucoma Subleukemic Leukemia Sveinsson Chorioretinal Atrophy Systemic Mastocytosis Systemic Onset Juvenile Idiopathic Arthritis T-Cell Large Granular Lymphocyte Leukemia T-Cell Leukemia T-Cell Lymphoma 1a Temporal Lobe Epilepsy Testicular Disease Testicular Leukemia Testicular Seminoma Tetanus Tetraploidy Thalassemia Thiopurines, Poor Metabolism of, 1 Three M Syndrome 1 Thrombasthenia Thrombocytopenia Thrombophilia Thrombosis Thymoma Thyroid Cancer Thyroid Cancer, Nonmedullary, 1 Thyroiditis Tonsillitis Tooth Disease Toxic Encephalopathy Toxic Megacolon Toxoplasmoză Tracheoesophageal Fistula Trigeminal Neuralgia Triploidy Tuberculous Meningitis Ureteral Obstruction Urticaria Urticaria Pigmentosa Vasculitis Virus Associated Hemophagocytic Syndrome Visceral Leishmaniasis Vitamin B12 Deficiency Vogt-Koyanagi-Harada Disease Weaver Syndrome West Nile Virus Whim Syndrome Wilms Tumor 1 Wilms Tumor 6 Wilson Disease Zinc-Responsive Necrolytic Acral Erythema Zygomycosis