Informaţii despre

Nume Hemoglobinopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Other haemoglobinopathies
Clasificare anatomică Malacards Boli de sânge

Vezi şi

Boli A-Z Acrocallosal Syndrome Acute Erythroid Leukemia Aging Alpha-Thalassemia Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Anemia, Sideroblastic, 1 Angioid Streaks Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Asthma Atransferrinemia Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Bone Marrow Necrosis Cardiac Conduction Defect Cerebritis Choledocholithiasis Cholelithiasis Color Blindness Congenital Disorder of Glycosylation, Type Ia Congenital Hemolytic Anemia Cystic Fibrosis Deficiency Anemia Diabetes Mellitus Diabetes Mellitus, Insulin-Dependent, 24 Extrinsic Allergic Alveolitis Fetal Hemoglobin Quantitative Trait Locus 1 Folic Acid Deficiency Anemia Galactosemia Gilbert Syndrome Glucosephosphate Dehydrogenase Deficiency Glutathione Peroxidase Deficiency Haemophilus Influenzae Heinz Body Anemias Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemoglobin C Disease Hemoglobin D Disease Hemoglobin E Disease Hemoglobinemia Hemoglobin H Disease Hemoglobin Lepore-Beta-Thalassemia Syndrome Hemolytic Anemia Hemosiderosis Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hereditary Elliptocytosis Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hydrops Fetalis Hydrops Fetalis, Nonimmune Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperferritinemia with or Without Cataract Hyper Ige Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypochromic Microcytic Anemia Hypophosphatemic Bone Disease Immature Cataract Immune Hydrops Fetalis Influenza Inherited Metabolic Disorder Iron Deficiency Anemia Iron Metabolism Disease Iron Overload in Africa Ischemia Kidney Papillary Necrosis Kluver-Bucy Syndrome Lissencephaly 1 Lupus Erythematosus Malaria Malignant Secondary Hypertension Melancholia Meningitis Metal Metabolism Disorder Methemoglobinemia Methemoglobinemia, Beta-Globin Type Methemoglobin Reductase Deficiency Microcytic Anemia Neonatal Anemia Neutrophilic Dermatosis, Acute Febrile Nutritional Deficiency Disease Osgood-Schlatter's Disease Osteomyelitis Osteonecrosis Plasmodium Falciparum Malaria Pneumococcal Meningitis Pneumonia Polycythemia Porphyria Porphyria Cutanea Tarda Priapism Pulmonary Hypertension Purpura Purpura Fulminans Pythiosis Renal Glucosuria Renal Tubular Acidosis Retinal Detachment Retinitis Satb2-Associated Syndrome Schimmelpenning-Feuerstein-Mims Syndrome Schnyder Corneal Dystrophy Shprintzen-Goldberg Craniosynostosis Syndrome Sickle Cell Anemia Sickle Cell Disease Siderosis Spherocytosis, Type 2 Splenic Sequestration Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Subacute Cerebellar Degeneration Superior Semicircular Canal Dehiscence Tetanus Thalassemia Type 1 Diabetes Mellitus 11 Type 1 Diabetes Mellitus 7 Vitamin B12 Deficiency