Informaţii despre

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

Vezi şi

Boli A-Z Acquired Methemoglobinemia Acute Chest Syndrome Acute Erythroid Leukemia Adenoma Aging 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 Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Anemia, Sideroblastic, 1 Angel-Shaped Phalangoepiphyseal Dysplasia Angioid Streaks Angiomatous Meningioma Aniridia 1 Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Atransferrinemia Atrial Fibrillation Beta-Thalassemia, Dominant Inclusion Body Type Biliary Tract Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group Incompatibility Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Cardiac Conduction Defect Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cataract Cerebritis Childhood Myocerebrohepatopathy Spectrum Cholelithiasis Cleidocranial Dysplasia Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Congenital Methemoglobinemia Cystic Fibrosis Deficiency Anemia Diabetes Mellitus, Insulin-Dependent, 24 Diamond-Blackfan Anemia Down Syndrome Endotheliitis Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica, Pretibial Fanconi Anemia, Complementation Group E Fetal Erythroblastosis Fetal Hemoglobin Quantitative Trait Locus 1 Fetal Hemoglobin Quantitative Trait Locus 6 Folic Acid Deficiency Anemia Gilbert Syndrome Gingivitis Glucosephosphate Dehydrogenase Deficiency Glutathione Peroxidase Deficiency Goblet Cell Carcinoid Heinz Body Anemias Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemochromatosis, Type 3 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 Hemolytic Anemia Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Adenoma Hereditary Elliptocytosis Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hereditary Spherocytosis Hereditary Xanthinuria Hfe-Associated Hereditary Hemochromatosis 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 Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoascorbemia Hypochromic Microcytic Anemia Hypogonadism Hypoparathyroidism Hypophosphatemic Bone Disease Inherited Metabolic Disorder Insulin-Like Growth Factor I Iron Deficiency Anemia Iron Metabolism Disease Iron Overload in Africa Ischemia Juvenile Myelomonocytic Leukemia Lactose Intolerance Leukemia Liver Disease Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome Lymphoma Major Affective Disorder 8 Major Affective Disorder 9 Malaria Maxillary Sinusitis Mediastinitis Megaloblastic Anemia Metabolic Acidosis Metal Metabolism Disorder Methemoglobinemia, Beta-Globin Type Microcytic Anemia Moyamoya Disease 1 Myelodysplastic Syndrome Myopathy Neonatal Anemia Neonatal Jaundice Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neurodegeneration with Brain Iron Accumulation 2a Niemann-Pick Disease Nutritional Deficiency Disease Osteomalacia Osteonecrosis Pancreatitis Pancytopenia Paraplegia Pellagra Periodontitis Pernicious Anemia Persistent Generalized Lymphadenopathy Pheochromocytoma Pick Disease of Brain Plastic Bronchitis Pneumonia Polycythemia Polyneuropathy Porphyria Porphyria Cutanea Tarda Portal Vein Thrombosis Posttransplant Acute Limbic Encephalitis Priapism Protein C Deficiency Pseudoxanthoma Elasticum Pulmonary Hypertension Pure Red-Cell Aplasia Purpura Pycnodysostosis Pyruvate Kinase Deficiency of Red Cells Renal Glucosuria Retinitis Pigmentosa and Erythrocytic Microcytosis Sarcoidosis 2 Schizophrenia Schnyder Corneal Dystrophy Sea-Blue Histiocyte Disease 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 Splenic Infarction Splenic Sequestration Splenomegaly Storage Pool Platelet Disease Subacute Cerebellar Degeneration Tarsal-Carpal Coalition Syndrome Tay-Sachs Disease Thalassemia Thrombocytopenia Thrombocytosis Thrombophilia Thrombosis Thyroiditis Vitamin B12 Deficiency Wilson Disease Xanthinuria