Informaţii despre

Nume Thalassemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Thalassaemia, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli endocrine; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Alpha-Thalassemia; Beta-Thalassemia

Vezi şi

Boli A-Z Aceruloplasminemia Achalasia-Addisonianism-Alacrima Syndrome Acquired Amegakaryocytic Thrombocytopenia Acrocallosal Syndrome Acute Chest Syndrome Acute Erythroid Leukemia Acute Graft Versus Host Disease Adenoma Adrenocortical Carcinoma, Hereditary Aging Aland Island Eye Disease 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/mental Retardation Syndrome, Chromosome 16-Related Alpha-Thalassemia/mental Retardation Syndrome, X-Linked Alpha-Thalassemia Myelodysplasia Syndrome Alpha Thalassemia-X-Linked Intellectual Disability Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Angel-Shaped Phalangoepiphyseal Dysplasia Angioid Streaks Angiomatous Meningioma Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia Neuropathy Spectrum Atransferrinemia Atrial Fibrillation Atrial Standstill Aural Atresia, Congenital Autism X-Linked 2 Autoimmune Disease Autoimmune Lymphoproliferative Syndrome, Type V Autoinflammation with Infantile Enterocolitis Autonomic Dysfunction Autosomal Recessive Sideroblastic Anemia Beta-Thalassemia Beta-Thalassemia, Dominant Inclusion Body Type Biliary Tract Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Kidd System Bone Marrow Necrosis Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Ischemia Budd-Chiari Syndrome Cardiac Conduction Defect Cardiogenic Shock Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Carotid Intimal Medial Thickness 2 Cataract Cataract 40 Cataract, Total Congenital Cerebritis Cerebrovascular Disease Childhood Myocerebrohepatopathy Spectrum Cholelithiasis Choroiditis Chromosomal Triplication Cleidocranial Dysplasia Cohen-Gibson Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Conjunctivitis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cystic Fibrosis Cystitis Cytomegalovirus Infection Deficiency Anemia Dengue Hemorrhagic Fever Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Insulin-Dependent, 24 Diamond-Blackfan Anemia Dna, Satellite, Iii Down Syndrome Dubin-Johnson Syndrome Dubowitz Syndrome Echo Virus 11 Sensitivity Eclampsia Ectodermal Dysplasia Eisenmenger Syndrome Elliptocytosis 2 Encephalopathy, Ethylmalonic Endotheliitis Enterocolitis Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica, Pretibial Epidermolysis Bullosa Pruriginosa Esophagitis, Eosinophilic, 1 Ewing's Family of Tumors Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor V Deficiency Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fetal Erythroblastosis Fetal Hemoglobin Quantitative Trait Locus 1 Fetal Hemoglobin Quantitative Trait Locus 6 Folic Acid Deficiency Anemia Gastric Lymphoma Genitopatellar Syndrome Gilbert Syndrome Gingivitis Glucose Intolerance Glucosephosphate Dehydrogenase Deficiency Glutathione Peroxidase Deficiency Glycogen Storage Disease V Goblet Cell Carcinoid Gout Graft-Versus-Host Disease Growth Hormone Deficiency Gynecomastia Headache Associated with Sexual Activity Heinz Body Anemias Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 1 Hemoglobin C-Beta-Thalassemia Syndrome Hemoglobin C Disease Hemoglobin D Disease Hemoglobin E-Beta-Thalassemia Syndrome Hemoglobin E Disease Hemoglobinemia Hemoglobin H Disease Hemoglobin Lepore-Beta-Thalassemia Syndrome Hemoglobinopathy Hemoglobin Se Disease Hemoglobinuria Hemoglobin Zurich Hemolytic Anemia Hemophilia Hemorrhagic Cystitis Hemorrhagic Fever Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatocellular Adenoma Hepatocellular Carcinoma Hereditary Elliptocytosis Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hereditary Spherocytosis Hereditary Xanthinuria Hinman Syndrome Histiocytosis Human Coronavirus Sensitivity Hydrops Fetalis Hydrops Fetalis, Nonimmune Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperbilirubinemia, Rotor Type Hypercholesterolemia, Autosomal Dominant, 3 Hyperferritinemia with or Without Cataract Hyper Ige Syndrome Hyperproinsulinemia Hyperprolinemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia Hypoascorbemia Hypochromic Microcytic Anemia Hypogonadism Hypoparathyroidism Hypophosphatemic Bone Disease Hypospadias Hypoxia Ichthyosis Prematurity Syndrome Immune Hydrops Fetalis Incontinentia Pigmenti Infant Gynecomastia Inherited Metabolic Disorder Insulin-Like Growth Factor I Iron Deficiency Anemia Iron Metabolism Disease Iron Overload in Africa Ischemia Jejunal Atresia Juvenile Myelomonocytic Leukemia Klebsiella Infection Lactose Intolerance Left Ventricular Noncompaction Leukemia Limb Reduction Defect Linear Iga Disease Lissencephaly 1 Liver Cirrhosis Liver Disease Long Qt Syndrome Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome Lutheran Suppressor, X-Linked Lymphoblastic Leukemia Lymphoma Major Affective Disorder 8 Major Affective Disorder 9 Malaria Malignant Secondary Hypertension Maxillary Sinusitis Mediastinitis Megaloblastic Anemia Melioidosis Metabolic Acidosis Metal Metabolism Disorder Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcytic Anemia Mosaic Trisomy 7 Moyamoya Disease 1 Multiple Mitochondrial Dysfunctions Syndrome 5 Myelodysplastic Syndrome Myelofibrosis Myocardial Infarction Myopathy Neonatal Anemia Neonatal Jaundice Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neutrophilic Dermatosis, Acute Febrile Nevus Comedonicus Niemann-Pick Disease Obsessive-Compulsive Disorder Osgood-Schlatter's Disease Osteochondroma Osteogenesis Imperfecta, Type Ii Osteomalacia Osteomyelitis Osteonecrosis Ovalocytosis, Southeast Asian Pancreatitis Pancytopenia Paraplegia Paroxysmal Nocturnal Hemoglobinuria Pellagra Penis Agenesis Periodontitis Pernicious Anemia Persistent Generalized Lymphadenopathy Pheochromocytoma Pica Disease Pick Disease of Brain Pituitary Hormone Deficiency, Combined, 2 Plastic Bronchitis Pneumonia Polycystic Kidney Disease Polycythemia Polycythemia Vera Polymorphic Reticulosis Polyneuropathy Porphyria Porphyria Cutanea Tarda Portal Vein Thrombosis Posttransplant Acute Limbic Encephalitis Pre-Eclampsia Priapism Prieto X-Linked Mental Retardation Syndrome Protein C Deficiency Pseudohermaphroditism Pseudoxanthoma Elasticum Puerperal Pulmonary Embolism Pulmonary Embolism Pulmonary Embolism and Infarction Pulmonary Hypertension Pure Red-Cell Aplasia Purpura Pycnodysostosis Pyomyositis Pyruvate Kinase Deficiency of Red Cells Pythiosis Rapp-Hodgkin Syndrome Refractive Error Renal Glucosuria Retinitis Retinitis Pigmentosa Retinitis Pigmentosa and Erythrocytic Microcytosis Ring Chromosome 2 Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Sarcoma Schimmelpenning-Feuerstein-Mims Syndrome Schizophrenia Schnyder Corneal Dystrophy Sea-Blue Histiocyte Disease Septic Arthritis Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Severe Combined Immunodeficiency Sickle Beta Thalassemia Sickle Cell Anemia Sickle Cell Disease Sideroblastic Anemia Siderosis Sinusitis Sleep Apnea Spasticity Spastic Paraparesis Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spherocytosis, Type 1 Spherocytosis, Type 2 Spherocytosis, Type 3 Spherocytosis, Type 4 Splenic Abscess Splenic Infarction Splenic Sequestration Splenomegaly Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Storage Pool Platelet Disease Subacute Cerebellar Degeneration Suppressor of Tumorigenicity 3 Tarsal-Carpal Coalition Syndrome Tay-Sachs Disease Temple-Baraitser Syndrome Testicular Microlithiasis Thoracoabdominal Syndrome Thrombocytopenia Thrombocytosis Thrombophilia Thrombosis Thrombotic Thrombocytopenic Purpura Thyroid Cancer Thyroiditis Townes-Brocks Syndrome Traumatic Avascular Necrosis Treacher Collins Syndrome 1 Valproate Embryopathy Viral Hepatitis Vitamin B12 Deficiency Wandering Spleen Wilson Disease Xanthinuria X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome