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Nume Myeloid Leukemia
Pagina Web
Clasificare globală Malacards Cancer diseases; Genetic diseases; Rare diseases
Clasificari ICD10 Myeloid leukaemia, unspecified
Clasificare anatomică Malacards Blood diseases; Immune diseases
Boli din aceeaşi familie Acute Myeloid Leukemia with T(6;9)(p23;q34); Acute Myeloid Leukemia with T(9;11)(p22;q23); Leukemia, Acute Myeloid; Leukemia, Chronic Myeloid

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Boli A-Z 8p11 Myeloproliferative Syndrome Abdominal Tuberculosis Ablepharon-Macrostomia Syndrome Achondroplasia Acquired Hemophilia Acquired Immunodeficiency Syndrome Acromegaly Acute Biphenotypic Leukemia Acute Disseminated Encephalomyelitis Acute Generalized Exanthematous Pustulosis Acute Graft Versus Host Disease Acute Leukemia Acute Leukemia of Ambiguous Lineage Acute Lymphocytic Leukemia Acute Myeloblastic Leukemia with Maturation Acute Myeloblastic Leukemia Without 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(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 Myocardial Infarction Acute Panmyelosis with Myelofibrosis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Adenocarcinoma Adenomatoid Tumor Adenosquamous Carcinoma Adie Pupil Adult T-Cell Leukemia Agammaglobulinemia Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Aleukemic Leukemia Cutis Aleukemic Mast Cell Leukemia Alk-Positive Anaplastic Large Cell Lymphoma 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 Amenorrhea Anaplastic Ganglioglioma Anaplastic Large Cell Lymphoma Anaplastic Oligoastrocytoma Anauxetic Dysplasia 1 Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Antigen Defined by Monoclonal Antibody Aj9 Aplastic Anemia Apparent Mineralocorticoid Excess Appendicitis Arterial Thoracic Outlet Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Aspergillus Niger Infection Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Atypical Chronic Myeloid Leukemia Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Pancreatitis Autoinflammation with Infantile Enterocolitis Autonomic Neuropathy Back Pain Baraitser-Winter Cerebrofrontofacial Syndrome Baraitser-Winter Syndrome 1 B-Cell Lymphomas Beckwith-Wiedemann Syndrome Bernard-Soulier Syndrome Bjornstad Syndrome Bladder Cancer Blastic Plasmacytoid Dendritic Cell Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group Incompatibility Blood Group, I System Blood Platelet Disease 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 Brain Edema Breast Cancer Brugada Syndrome C3 Glomerulopathy Calcinosis Candida Glabrata Candidiasis Cardiac Tamponade Cardiomyopathy, Familial Hypertrophic, 1 Cataract 5, Multiple Types Cauda Equina Syndrome Cellulitis Central Nervous System Disease Central Nervous System Leukemia Central Nervous System Origin Vertigo Central Retinal Vein Occlusion Cerebellar Degeneration-Related Autoantigen 3 Cerebritis Cervicitis Childhood Leukemia Chops Syndrome Choriocarcinoma Chromosomal Triplication Chromosome 3q29 Deletion Syndrome Chromosome 5q Deletion Syndrome Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Leukemia Chronic Meningitis Chronic Monocytic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Cleidocranial Dysplasia Coccidiosis Colitis Colon Adenocarcinoma Colorblindness, Partial, Protan Series Colorectal Cancer Colorectal Cancer 3 Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Mesoblastic Nephroma Conjunctivitis Conversion Disorder Core Binding Factor Acute Myeloid Leukemia Corneal Dystrophy, Avellino Type Coumarin Resistance Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cytogenetically Normal Acute Myeloid Leukemia Dacryoadenitis Demyelinating Polyneuropathy Dengue Virus Dermatitis Diabetes Insipidus Diabetes Mellitus Diarrhea 2, with Microvillus Atrophy Diffuse Alveolar Hemorrhage Diffuse Large B-Cell Lymphoma Diphtheria Disseminated Intravascular Coagulation Down Syndrome Duane Retraction Syndrome 1 Duodenitis Dyschromatosis Symmetrica Hereditaria Ecthyma Elliptocytosis 1 Encephalitis Endocarditis Endotheliitis End Stage Renal Failure Enterocolitis Epidermodysplasia Verruciformis Epidermolysis Bullosa Pruriginosa Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Elderly Esophageal Candidiasis Essential Thrombocythemia Ewing Sarcoma Exfoliative Dermatitis Exophthalmos Factor Vii Deficiency Fanconi Syndrome Fibrosarcoma Fibrous Dysplasia Follicular Dendritic Cell Sarcoma Follicular Mucinosis Foot Drop Friedreich Ataxia 1 Fructose Utilization Fundus Albipunctatus Fusariosis Galactorrhea Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Gastric Antral Vascular Ectasia Gastritis Gastrointestinal Stromal Tumor Germ Cells Tumors Gingival Hypertrophy Gingivitis Glanzmann Thrombasthenia Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioma Glomerulonephritis Glucose/galactose Malabsorption Glucose Transporter Type 1 Deficiency Syndrome Glycogen Storage Disease Graft-Versus-Host Disease Granulomatous Gastritis Granulomatous Rosacea Grover's Disease Growing Teratoma Syndrome Gynecomastia Hairy Cell Leukemia Hansen's Disease Headache Associated with Sexual Activity Helix Syndrome Hellp Syndrome Hemarthrosis Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemophilia Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatoblastoma Hepatosplenic T-Cell Lymphoma Hereditary Multiple Exostoses Hereditary Wilms' Tumor Herpes Zoster Hhv-6 Encephalitis Histiocytosis Histoplasmosis Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hyperglycemia Hyperostosis Hyperreflexia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia Hypokalemia Hypophosphatemia Hypopyon Hypoxia Idiopathic Neutropenia Immune Suppression Immunodeficiency 21 Immunoglobulin E Concentration, Serum Inclusion Body Myositis Indeterminate Cell Histiocytosis Infant Gynecomastia Infective Dermatitis Associated with Htlv-1 Insulin-Like Growth Factor I Intussusception Invasive Aspergillosis Ischemia Juvenile Myelomonocytic Leukemia Juvenile Xanthogranuloma Kallmann Syndrome Keratoacanthoma Kikuchi Disease Langerhans Cell Histiocytosis Laryngitis Leiomyosarcoma Leishmaniasis Lepromatous Leprosy Leukemia Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphoblastic 3 Leukemia, Acute Monocytic Leukemia, Acute Myeloid Leukemia, Chronic Lymphocytic Leukemia, Chronic Myeloid Leukoplakia Leukostasis Leukotriene C4 Synthase Deficiency Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Limb-Girdle Muscular Dystrophy Limbic Encephalitis Limb Ischemia Liposarcoma Lissencephaly 1 Lung Cancer Lutheran Suppressor, X-Linked Lymphadenitis Lymphedema Lymphoblastic Leukemia Lymphoblastic Leukemia, Acute, with Lymphomatous Features Lymphoblastic Lymphoma Lymphocytic Vasculitis Lymphoid Leukemia Lymphoma Lymphomatoid Granulomatosis Lymphosarcoma Macroglobulinemia Malaria Malignant Spiradenoma Malignant Teratoma Malignant Triton Tumor Mantle Cell Lymphoma Mast Cell Disease Mast-Cell Leukemia Measles Meckel Syndrome, Type 1 Meconium Ileus Mediastinitis Medulloblastoma Megakaryocytic Leukemia Megaloblastic Anemia Melanoma Melanoma-Astrocytoma Syndrome Melanoma, Cutaneous Malignant 8 Membranoproliferative Glomerulonephritis Meningioma, Familial Meningitis Microcephaly, Epilepsy, and Diabetes Syndrome Microphthalmia Miller-Dieker Lissencephaly Syndrome Mismatch Repair Cancer Syndrome Mitochondrial Import-Stimulating Factor Mn1 Monocytic Leukemia Muenke Syndrome Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Cranial Nerve Palsy Multiple Enchondromatosis, Maffucci Type Multiple Mitochondrial Dysfunctions Syndrome 5 Mumps Mungan Syndrome Muscular Dystrophy Muscular Dystrophy, Limb-Girdle, Type 1a Mycobacterium Chelonae Mycobacterium Kansasii Mycosis Fungoides Myelitis Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Sarcoma Myeloma, Multiple Myeloproliferative Neoplasm Myeloproliferative Syndrome, Transient Myocardial Infarction Myopathy Myopathy, Tubular Aggregate, 1 Myopathy with Lactic Acidosis, Hereditary Myositis Myxoid Liposarcoma Nasopharyngeal Carcinoma Nasopharyngitis Neonatal Leukemia Nervous System Disease Neuritis Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuropathy Neutropenia Neutropenia, Nonimmune Chronic Idiopathic, of Adults Neutrophil Actin Dysfunction Neutrophil Migration Nijmegen Breakage Syndrome Obstructive Jaundice Occipital Horn Syndrome Oligoastrocytoma Optic Neuritis Oral Candidiasis Oral Hairy Leukoplakia Overhydrated Hereditary Stomatocytosis Pancreatitis Pancreatitis, Hereditary Pancytopenia Panniculitis Paraneoplastic Pemphigus Paraneoplastic Syndromes Paraplegia Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Parotitis Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Pelger-Huet Anomaly Pemphigus Pericardial Effusion Pericarditis Periodontal Ehlers-Danlos Syndrome Peripartum Cardiomyopathy Phaeohyphomycosis Philadelphia-Negative Chronic Myeloid Leukemia Pineal Gland Cancer Pituitary Apoplexy Pituitary Hormone Deficiency, Combined, 2 Pityriasis Rotunda Plasma Cell Leukemia Plasmacytoma Platelet Disorder, Familial, with Associated Myeloid Malignancy Plexopathy Pneumonia Poems Syndrome Polyclonal Hypergammaglobulinemia Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polymorphic Reticulosis Polymyositis Polyneuropathy Porphyria Porphyria Cutanea Tarda Porphyria Variegata Portal Hypertension Portal Vein Thrombosis Precursor T-Cell Acute Lymphoblastic Leukemia Priapism Prieto X-Linked Mental Retardation Syndrome Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Polycythemia Prostatitis Protein C Deficiency Pseudo Pelger-Huet Anomaly Psoriasis 2 Psoriasis 7 Pulmonary Alveolar Proteinosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Sarcoidosis Pulmonary Sequestration Pure Red-Cell Aplasia Pyoderma Pyoderma Gangrenosum Pyomyositis Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Quadriplegia Radiculopathy Ramer Ladda Syndrome Reactive Arthritis Refractory Anemia Refractory Anemia with Excess Blasts Refractory Anemia with Excess Blasts in Transformation Retinal Detachment Retinal Vasculitis Retinal Vein Occlusion Retinitis Retinoblastoma Rett Syndrome Rhabdomyosarcoma Rheumatoid Arthritis Ring Chromosome 11 Ring Chromosome 2 Ring Chromosome 21 Ring Chromosome 5 Ring Chromosome 7 Ring Chromosome 8 Rosacea Sagittal Sinus Thrombosis Sarcoidosis 2 Sarcoma Satb2-Associated Syndrome Schizophrenia Scleromalacia Perforans Scott Syndrome Secondary Pulmonary Alveolar Proteinosis Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Severe Combined Immunodeficiency Severe Congenital Neutropenia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sickle Cell Anemia Sickle Cell Disease Sideroblastic Anemia Sinusitis Situs Inversus Skin Disease Soft Tissue Sarcoma Spinal and Bulbar Muscular Atrophy, X-Linked 1 Splenic Abscess Splenic Infarction Splenomegaly Spondylitis Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Subleukemic Leukemia Sveinsson Chorioretinal Atrophy Syncope Syndrome of Inappropriate Antidiuretic Hormone Systemic Mastocytosis Tarsal-Carpal Coalition Syndrome Tatton-Brown-Rahman Syndrome T-Cell Leukemia Temporal Arteritis Teratoma Testicular Cancer Testicular Gonadoblastoma Tetraploidy Tetrasomy 21 Tetrasomy 5p Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome Thiopurines, Poor Metabolism of, 1 Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophlebitis Thrombosis Thymic Hyperplasia Thyroiditis Tonsillitis Treacher Collins Syndrome 1 Trichosporonosis Trisomy 1q Trisomy 22 Uveitis Van Der Woude Syndrome 1 Vasculitis Velocardiofacial Syndrome Visceral Leishmaniasis Vogt-Koyanagi-Harada Disease Weaver Syndrome Whim Syndrome Wilms Tumor 1 Wilms Tumor 6 Wilson-Turner X-Linked Mental Retardation Syndrome Zygomycosis