Informaţii despre

Nume Acute Leukemia
Pagina Web www.malacards.org
Clasificare globală Malacards Bolile canceroase
Clasificari ICD10 Acute leukaemia of unspecified cell type
Clasificare anatomică Malacards Boli ale sistemului imunitar
Boli din aceeaşi familie Chronic Leukemia; Subacute Leukemia

Vezi şi

Boli A-Z 8p11 Myeloproliferative Syndrome Acquired Idiopathic Sideroblastic Anemia Acute Biphenotypic Leukemia Acute Erythroid Leukemia Acute Graft Versus Host Disease Acute Leukemia of Ambiguous Lineage Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Myeloblastic Leukemia with Maturation 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 T(8;21)(q22;q22) Translocation Acute Myeloid Leukemia with T(9;11)(p22;q23) Acute Promyelocytic Leukemia Adult Mesoblastic Nephroma Adult T-Cell Leukemia Aging Aleukemic Leukemia Cutis 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 Anaplastic Oligodendroglioma Angiomatosis Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Appendicitis Arbitrary Restriction Polymorphism 1 Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aryl Hydrocarbon Hydroxylase Inducibility Aspergillosis Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autoimmune Disease Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Polyendocrine Syndrome Autoinflammation with Infantile Enterocolitis Bacillary Angiomatosis B- and T-Cell Mixed Leukemia B-Cell Lymphomas Blastic Plasmacytoid Dendritic Cell Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen 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 Bone Marrow Cancer Bone Marrow Necrosis Breast Cancer Budd-Chiari Syndrome Candidiasis Cardiac Arrest Carotidynia Cataract 5, Multiple Types Central Nervous System Leukemia Cerebellar Astrocytoma Cerebral Degeneration Cerebritis Cervical Cancer Cervicitis Chediak-Higashi Syndrome Childhood Leukemia Choroiditis Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Mesoblastic Nephroma Core Binding Factor Acute Myeloid Leukemia Cortical Blindness Cytochrome P450 2d6 Variant Cytogenetically Normal Acute Myeloid Leukemia Cytomegalic Inclusion Disease Deep Leiomyoma Diffuse Large B-Cell Lymphoma Diphtheria Discitis Disseminated Intravascular Coagulation Down Syndrome Ecthyma Ectopic Pregnancy Endocarditis Endotheliitis Enterocolitis Enterovesical Fistula Epiglottitis Epithelial Recurrent Erosion Dystrophy Erythroleukemia, Familial Essential Thrombocythemia Extracutaneous Mastocytoma Fanconi Anemia, Complementation Group D2 Fanconi Syndrome Friedreich Ataxia 1 Fusariosis Gallbladder Leiomyoma Gastrointestinal Stromal Tumor Genitopatellar Syndrome Germ Cells Tumors Graft-Versus-Host Disease Granulocytopenia Granulomatous Hepatitis Headache Associated with Sexual Activity Helix Syndrome Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hepatic Adenomas, Familial Hepatic Vascular Disease Hepatitis Hepatitis C Hepatosplenic T-Cell Lymphoma Hereditary Wilms' Tumor Histiocytosis Hydronephrosis Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hyperglycemia Hyperphosphatemia Hyperreflexia Hypersplenism Hypophosphatemia Hypopyon Hypoxia Immunodeficiency 43 Infective Endocarditis Influenza Interleukin-7 Receptor Alpha Deficiency Intervertebral Disc Disease Invasive Aspergillosis Ischemia Juvenile Xanthogranuloma Kaposiform Hemangioendothelioma Lactic Acidosis Langerhans Cell Histiocytosis Leukemia Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphoblastic 3 Leukemia, Acute Monocytic Leukemia, Acute Myeloid Leukemia, Chronic Lymphocytic Leukemia, Chronic Myeloid Leukocyte Disease Leukostasis Liposarcoma Liver Leiomyoma Lung Leiomyosarcoma Lymphedema Lymphoblastic Leukemia Lymphoblastic Leukemia, Acute, with Lymphomatous Features Lymphoblastic Lymphoma Lymphoid Leukemia Lymphoma Lymphosarcoma Macrocytic Anemia Macroglobulinemia Malignant Histiocytosis Malignant Teratoma Malignant Triton Tumor Mantle Cell Lymphoma Mast-Cell Sarcoma Mediastinal Cancer Mediastinitis Medulloblastoma Megakaryocytic Leukemia Megaloblastic Anemia Melanoma Miller-Dieker Lissencephaly Syndrome Mn1 Mononeuritis Multiplex Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mycetoma Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myelophthisic Anemia Myeloproliferative Neoplasm Myeloproliferative Syndrome, Transient Myoclonic Epilepsy of Lafora Myxoid Liposarcoma Neonatal Leukemia Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neutropenia Neutrophil Actin Dysfunction Occipital Horn Syndrome Ocular Melanoma Olfactory Neuroblastoma Oligodendroglioma Oral Candidiasis Osteomyelitis Ovarian Cancer Overhydrated Hereditary Stomatocytosis Panniculitis Parainfluenza Virus Type 3 Parkinsonism with Spasticity, X-Linked Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Pernicious Anemia Plasma Cell Neoplasm Platelet Disorder, Familial, with Associated Myeloid Malignancy Pneumatosis Cystoides Intestinalis Pneumonia Pneumothorax Polykaryocytosis Inducer Polysubstance Abuse Prolymphocytic Leukemia Protein C Deficiency Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pustulosis Palmaris Et Plantaris Pyelonephritis Pyoderma Pyoderma Gangrenosum Pyomyositis Pyruvate Kinase Deficiency of Red Cells Refractory Anemia Respiratory Syncytial Virus Infectious Disease Retina Lymphoma Retinitis Pigmentosa and Erythrocytic Microcytosis Retinoblastoma Rett Syndrome Rhabdomyosarcoma Ring Chromosome 1 Ring Chromosome 21 Roberts Syndrome Sarcoma Scedosporiosis Scott Syndrome Septic Arthritis Severe Combined Immunodeficiency Severe Congenital Neutropenia Sideroblastic Anemia Sinusitis Sjogren-Larsson Syndrome Small Cell Carcinoma Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spindle Cell Liposarcoma Spiradenoma Splenic Abscess Splenic Tuberculosis Splenomegaly Spondylocarpotarsal Synostosis Syndrome Subacute Leukemia Suppression of Tumorigenicity 12 Sveinsson Chorioretinal Atrophy Systemic Mastocytosis T-Cell Leukemia Teratoma Testicular Disease Testicular Gonadoblastoma Tetraploidy Tetrasomy 21 Thrombocytopenia Thrombocytosis Thrombosis Thyroid Cancer Thyroiditis Trigonitis Trisomy 22 Uterine Sarcoma Weber Syndrome Whim Syndrome Wilms Tumor 1 Wilms Tumor 6 Xanthogranulomatous Pyelonephritis Zygomycosis