Informaţii despre

Nume Leukemia, Chronic Myeloid
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Chronic myeloid leukaemia [CML], BCR/ABL-positive
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
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

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Boli A-Z 8p11 Myeloproliferative Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achondroplasia Acquired Polycythemia Acromegaly Acute Generalized Exanthematous Pustulosis Acute Graft Versus Host Disease Acute Leukemia 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 T(6;9)(p23;q34) Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation Acute Myeloid Leukemia with T(9;11)(p22;q23) Acute Promyelocytic Leukemia Adenocarcinoma Adenomatoid Tumor Adult Fibrosarcoma Adult Mesoblastic Nephroma Aggressive Systemic Mastocytosis Aging Aleukemic Leukemia Cutis Alk-Positive Anaplastic Large Cell Lymphoma 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 Amegakaryocytic Thrombocytopenia, Congenital Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Anemia of Prematurity Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arthrochalasia Ehlers-Danlos Syndrome Asthma Atypical Chronic Myeloid Leukemia Autoimmune Hepatitis Autonomic Nervous System Neoplasm B-Cell Lymphomas Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Ewing's Sarcoma Bone Marrow Cancer Bone Marrow Necrosis Breast Cancer Brugada Syndrome Budd-Chiari Syndrome C3 Glomerulopathy Calcinosis Candida Glabrata Cardiac Tamponade Cardiomyopathy, Familial Hypertrophic, 1 Cataract 5, Multiple Types Cauda Equina Syndrome Cellular Congenital Mesoblastic Nephroma Cellular Neurofibroma Central Nervous System Leukemia Central Nervous System Origin Vertigo Central Retinal Vein Occlusion Cerebellar Degeneration-Related Autoantigen 3 Choriocarcinoma Chromosomal Triplication Chromosome 22q11.2 Deletion Syndrome, Distal Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Leukemia Chronic Monocytic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Colitis Colon Adenocarcinoma 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 Conventional Fibrosarcoma Core Binding Factor Acute Myeloid Leukemia Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cryoglobulinemia, Familial Mixed Cutaneous Solitary Mastocytoma Cyclic Neutropenia Deep Leiomyoma Demyelinating Polyneuropathy Dengue Virus Dermatitis Desmoid Tumor Diabetes Insipidus Diabetes Mellitus Dyschromatosis Symmetrica Hereditaria Dyskeratosis Congenita, Autosomal Dominant 6 Endotheliitis End Stage Renal Failure Engraftment Syndrome Epidermodysplasia Verruciformis Epidermolysis Bullosa Pruriginosa Erythrocytosis, Familial, 1 Essential Thrombocythemia Ewing's Family of Tumors Ewing Sarcoma Exfoliative Dermatitis Extracutaneous Mastocytoma Felty Syndrome Fibrosarcoma of Bone Fibrous Dysplasia Follicular Dendritic Cell Sarcoma Foot Drop Friedreich Ataxia 1 Fundus Albipunctatus Gallbladder Leiomyoma Ganglioneuroma Gastric Antral Vascular Ectasia Gastrointestinal Stromal Tumor Glanzmann Thrombasthenia Glomerulonephritis Graft-Versus-Host Disease Granulocytopenia Gynecomastia Hairy Cell Leukemia Hantavirus Pulmonary Syndrome Headache Associated with Sexual Activity Heart Sarcoma Hemarthrosis Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatoblastoma Hereditary Wilms' Tumor Herpes Zoster Hydronephrosis Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypophosphatemia Hypopyon Inclusion Body Myositis Infant Gynecomastia Isolated Growth Hormone Deficiency, Type Ii Juvenile Myelomonocytic Leukemia Juvenile Xanthogranuloma Kallmann Syndrome Keratoacanthoma Leiomyosarcoma Leishmaniasis Leukemia Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphoblastic 3 Leukemia, Acute Myeloid Leukemia, Chronic Lymphocytic Leukocyte Disease Leukostasis Leukotriene C4 Synthase Deficiency Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Liver Leiomyoma Loeffler Endocarditis Lung Adenoid Cystic Carcinoma Lung Cancer Lung Leiomyosarcoma Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoid Leukemia Lymphoma Lymphomatoid Granulomatosis Lymphoproliferative Syndrome 2 Lymphosarcoma Malaria Malignant Conjunctival Melanoma Malignant Dermis Tumor Malignant Skin Fibrous Histiocytoma Marcus Gunn Phenomenon Mast Cell Disease Mast Cell Neoplasm Mediastinitis Medulloblastoma Megakaryocytic Leukemia Megaloblastic Anemia Melanocytic Nevus Syndrome, Congenital Melanomatosis Membranoproliferative Glomerulonephritis Mesenchymal Cell Neoplasm Microcephaly, Epilepsy, and Diabetes Syndrome Mn1 Muenke Syndrome Multiple Cranial Nerve Palsy Mungan Syndrome Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 Myeloid Leukemia Myeloid Sarcoma Myeloproliferative Disorder, Chronic, with Eosinophilia Myeloproliferative Neoplasm Myeloproliferative Syndrome, Transient Myocardial Infarction Myopathy Myositis Nasopharyngeal Carcinoma Nasopharyngitis Neuritis Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neutropenia Nutmeg Liver Optic Neuritis Orbital Granuloma Ovarian Angiosarcoma Ovarian Melanoma Ovary Sarcoma Pallister-Hall Syndrome Pancreatitis, Hereditary Pancytopenia Paraneoplastic Syndromes Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Pelger-Huet Anomaly Pemphigus Pericardial Effusion Periodontal Ehlers-Danlos Syndrome Peripheral Nervous System Neoplasm Philadelphia-Negative Chronic Myeloid Leukemia Piebald Trait Pitt-Hopkins Syndrome Plasmacytoma Platelet Disorder, Familial, with Associated Myeloid Malignancy Pneumonia Poems Syndrome Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymyositis Polyneuropathy Porphyria Porphyria Cutanea Tarda Portal Hypertension Portal Vein Thrombosis Precursor T-Cell Acute Lymphoblastic Leukemia Priapism Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Effusion Lymphoma Primary Hypereosinophilic Syndrome Primary Polycythemia Pseudo Pelger-Huet Anomaly Pulmonary Alveolar Proteinosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Sarcoidosis Pure Red-Cell Aplasia Pyomyositis Refractory Anemia Refractory Anemia with Excess Blasts Reticular Perineurioma Retinal Vein Occlusion Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rett Syndrome Sarcoidosis 2 Sarcoma Sarcomatoid Renal Cell Carcinoma Satb2-Associated Syndrome Scott Syndrome Seborrheic Infantile Dermatitis Secondary Pulmonary Alveolar Proteinosis Severe Combined Immunodeficiency Severe Congenital Neutropenia Sickle Cell Disease Sideroblastic Anemia Situs Inversus Small Cell Sarcoma Spindle Cell Liposarcoma Splenic Abscess Splenic Infarction Splenomegaly Spondylitis Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Stomatitis Syncope Systemic Mastocytosis Tarsal-Carpal Coalition Syndrome Testicular Cancer Testicular Gonadoblastoma Tetraploidy Tetrasomy 21 Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombosis Transient Erythroblastopenia of Childhood Uterine Sarcoma Uveitis Van Der Woude Syndrome 1 Venous Hemangioma Visceral Leishmaniasis Vogt-Koyanagi-Harada Disease Vulvar Melanoma Wilms Tumor 1 Wilms Tumor 6