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Nume Myelodysplastic Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Myelodysplastic syndromes
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge

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Boli A-Z 8p11 Myeloproliferative Syndrome Aarskog-Scott Syndrome Acquired Amegakaryocytic Thrombocytopenia Acquired Hemophilia Acquired Hemophilia a Acquired Idiopathic Sideroblastic Anemia Acquired Polycythemia Acral Lentiginous Melanoma Acrodermatitis Acute Adrenal Insufficiency Acute Basophilic Leukemia Acute Biphenotypic Leukemia Acute Erythroid Leukemia Acute Graft Versus Host Disease Acute Leukemia Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Monoblastic 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 T(8;21)(q22;q22) Translocation Acute Myocardial Infarction Acute Non Lymphoblastic Leukemia Acute Panmyelosis with Myelofibrosis Acute Promyelocytic Leukemia Adenocarcinoma Adult Mesoblastic Nephroma Adult Xanthogranuloma Agammaglobulinemia Aggressive Systemic Mastocytosis Aging Aleukemic Leukemia Cutis Alk-Negative 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 Alpha-Thalassemia Alpha-Thalassemia Myelodysplasia Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amegakaryocytic Thrombocytopenia, Congenital Analbuminemia Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Anemia of Prematurity Aniridia 1 Anorexia Nervosa 1 Antithrombin Iii Deficiency Aortitis Aplastic Anemia Aquagenic Pruritus Arterial Thoracic Outlet Syndrome Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atypical Chronic Myeloid Leukemia Atypical Neurofibroma Autoimmune Disease Autoimmune Hepatitis Autoimmune Pancreatitis Autosomal Recessive Sideroblastic Anemia Axenfeld-Rieger Syndrome B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beta-Thalassemia Blastic Plasmacytoid Dendritic Cell Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group Incompatibility 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 Breast Cancer Brucellosis Bullous Pemphigoid Cd4 Deficiency Cellular Neurofibroma Cellulitis Cerebral Artery Occlusion Cerebritis Childhood Leukemia Chromosomal Triplication Chromosome 5q Deletion Syndrome Chronic Active Epstein-Barr Virus Infection Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Colon Adenocarcinoma Colorblindness, Partial, Protan Series Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Mesoblastic Nephroma Core Binding Factor Acute Myeloid Leukemia Crescentic Glomerulonephritis Cryofibrinogenemia Cryptococcosis Cutaneous Polyarteritis Nodosa Cyclic Neutropenia Cytogenetically Normal Acute Myeloid Leukemia Demyelinating Polyneuropathy Dermatitis Dermatomyositis Diabetes Insipidus Diamond-Blackfan Anemia Diffuse Large B-Cell Lymphoma Disseminated Intravascular Coagulation Dyskeratosis Congenita Dyskeratosis Congenita, Autosomal Dominant 6 Ecthyma Endocarditis Endotheliitis Engraftment Syndrome Eosinophilic Pneumonia Eosinophilic Pustular Folliculitis Epidermodysplasia Verruciformis Erosive Pustular Dermatosis of the Scalp Erythema Elevatum Diutinum Erythrocytosis, Familial, 1 Erythroleukemia, Familial Essential Thrombocythemia Ewing's Family of Tumors Ewing Sarcoma Exanthem Exophthalmos Extracutaneous Mastocytoma Familial Mediterranean Fever Fanconi Anemia, Complementation Group D2 Fasciitis Felty Syndrome Focal Segmental Glomerulosclerosis Folic Acid Deficiency Anemia Folliculitis Friedreich Ataxia 1 Fundus Albipunctatus Galactose Epimerase Deficiency Gallbladder Leiomyoma Gastrointestinal Stromal Tumor Gingivitis Glomerulonephritis Glucagonoma Glucose/galactose Malabsorption Gonadal Dysgenesis Graft-Versus-Host Disease Granuloma Annulare Granulomatous Dermatitis Griscelli Syndrome Headache Helix Syndrome Hemangioma-Thrombocytopenia Syndrome Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia a Hemopoietic Proliferation Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis E Hepatosplenic T-Cell Lymphoma Hereditary Wilms' Tumor Hermaphroditism Herpes Zoster Histiocytoma Histiocytosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hyperostosis Hyperthyroidism Hyperuricemia Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypoplastic Left Heart Syndrome 1 Hypoxia Ichthyosis Prematurity Syndrome Indolent B Cell Lymphoma Infantile Sialic Acid Storage Disease Infective Dermatitis Associated with Htlv-1 Inherited Bone Marrow Failure Syndromes Insulin-Like Growth Factor I Intermediate Uveitis Intervertebral Disc Disease Intestinal Perforation Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Intravascular Large B-Cell Lymphoma Invasive Aspergillosis Iridocyclitis Ischemic Optic Neuropathy Juvenile Myelomonocytic Leukemia Kabuki Syndrome 1 Kikuchi Disease Langerhans Cell Histiocytosis Large Granular Lymphocyte Leukemia Leukemia Leukemia, Acute Lymphoblastic Leukemia, Acute Lymphoblastic 3 Leukemia, Acute Myeloid Leukemia, Chronic Lymphocytic Leukemia, Chronic Myeloid Leukocyte Disease Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Lipomatosis Liposarcoma Littoral Cell Angioma of the Spleen Liver Angiosarcoma Lung Cancer Lung Leiomyosarcoma Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoid Leukemia Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphomatoid Granulomatosis Macrocytic Anemia Macroglobulinemia Macs Syndrome Malakoplakia Malignant Histiocytosis Malignant Spindle Cell Melanoma Mast Cell Disease Mediastinal Cancer Megakaryocytic Leukemia Megaloblastic Anemia Melanoma Melanoma, Cutaneous Malignant 1 Melanomatosis Meningoencephalitis Merkel Cell Carcinoma Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Mirage Syndrome Miyoshi Muscular Dystrophy 1 Mn1 Monocytic Leukemia Mononeuritis Multiplex Monosomy 7 of Bone Marrow Mosaic Trisomy 8 Mucoepithelial Dysplasia, Hereditary Mucosal Melanoma Muir-Torre Syndrome Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Mitochondrial Dysfunctions Syndrome 5 Mutagen Sensitivity Mycobacterium Kansasii Mycobacterium Malmoense Myelodysplastic Myeloproliferative Cancer Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloperoxidase Deficiency Myelophthisic Anemia Myeloproliferative Disorder, Chronic, with Eosinophilia Myeloproliferative Neoplasm Myocardial Infarction Myoclonic Epilepsy of Lafora Myoclonus, Familial Cortical Myositis Myxoid Liposarcoma Necrotizing Fasciitis Neuritis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuropathy Neutropenia Neutropenia, Severe Congenital, 3, Autosomal Recessive Neutrophilia, Hereditary Neutrophilic Dermatosis, Acute Febrile Neutrophil Migration Nevus, Epidermal Nonarteritic Anterior Ischemic Optic Neuropathy Non-Involuting Congenital Hemangioma Non-Secretory Myeloma Noonan Syndrome 1 Optic Neuritis Orbital Cellulitis Ovarian Cancer Pancreatitis Pancytopenia Panniculitis Paraneoplastic Syndromes Parkinsonism with Spasticity, X-Linked Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Peliosis Hepatis Perinephritis Peripheral Artery Disease Pernicious Anemia Phelan-Mcdermid Syndrome Pigmented Villonodular Synovitis Plantar Wart Platelet Disorder, Familial, with Associated Myeloid Malignancy Pleural Empyema Pneumonia Polyarteritis Nodosa Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polyneuropathy Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes Porokeratosis Porphyria Porphyria Cutanea Tarda Premature Chromatid Separation Trait Primary Ciliary Dyskinesia Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma Primary Polycythemia Progressive Multifocal Leukoencephalopathy Prostatitis Pulmonary Alveolar Proteinosis Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonic Stenosis Pure Red-Cell Aplasia Purpura Pyoderma Pyoderma Gangrenosum Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Pyruvate Kinase Deficiency of Red Cells Rapp-Hodgkin Syndrome Reactive Angioendotheliomatosis Refractory Anemia Refractory Anemia with Excess Blasts Refractory Anemia with Excess Blasts in Transformation Relapsing Polychondritis Reticular Dysgenesis Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Retinoblastoma Retinoschisis 1, X-Linked, Juvenile Reye Syndrome Rheumatic Disease Ring Chromosome 1 Ring Chromosome 21 Ring Chromosome 7 Rosai-Dorfman Disease Rothmund-Thomson Syndrome Sagittal Sinus Thrombosis Sarcoidosis 2 Sarcoma Schimmelpenning-Feuerstein-Mims Syndrome Scleritis Sclerosing Cholangitis, Neonatal Scott Syndrome Sea-Blue Histiocyte Disease Secondary Pulmonary Alveolar Proteinosis Sensorineural Hearing Loss Severe Combined Immunodeficiency Severe Congenital Neutropenia Shwachman-Diamond Syndrome Sickle Cell Anemia Sideroblastic Anemia Sinusitis Spinal Cord Infarction Spiradenoma Splenic Abscess Splenomegaly Spondylocarpotarsal Synostosis Syndrome Storage Pool Platelet Disease Stroke, Ischemic Subleukemic Leukemia Sudden Sensorineural Hearing Loss Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Synovitis Systemic Mastocytosis Systemic Scleroderma T-Cell Large Granular Lymphocyte Leukemia Tenosynovial Giant Cell Tumor Testicular Gonadoblastoma Tetraploidy Tetrasomy 21 Tetrasomy 5p Thalassemia Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Tn Polyagglutination Syndrome Triploidy Trisomy 1q Trisomy 22 Trisomy 2 Mosaicism Tuberculous Uveitis Unclassified Myelodysplastic Syndrome Uruguay Faciocardiomusculoskeletal Syndrome Uveitis Van Der Woude Syndrome 1 Vasculitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vulvar Melanoma Whim Syndrome Wilms Tumor 1 Wilms Tumor 6 Witkop Syndrome Zygomycosis