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Nume Deficiency Anemia
Pagina Web www.malacards.org
Clasificari ICD10 Anaemia, unspecified
Clasificare anatomică Malacards Boli de sânge

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Boli A-Z Acatalasemia Acquired Angioedema Acquired Methemoglobinemia Acquired Polycythemia Acquired Thrombocytopenia Acute Erythroid Leukemia Acute Pyelonephritis Adenocarcinoma Adenoma Adie Pupil Agammaglobulinemia Aging Al Amyloidosis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Amegakaryocytic Thrombocytopenia, Congenital Amyloidosis Analbuminemia Androgen Insensitivity Syndrome, Mild Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Anemia of Prematurity Anemia, Sideroblastic, 1 Angiodysplasia Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atransferrinemia Atrophic Gastritis Autism Autoimmune Atrophic Gastritis Basal Cell Carcinoma Benign Idiopathic Neonatal Seizures Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Rubber Bleb Nevus 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 Bornholm Eye Disease Branch Retinal Artery Occlusion Candidiasis Capillary Hemangioma Castleman Disease Cataract Cavernous Hemangioma Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cholangiocarcinoma Choroiditis Chromate Resistance Cleft Palate, Isolated Cold Agglutinin Disease Collagenous Gastritis Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hemolytic Anemia Congenital Hypoplastic Anemia Congenital Methemoglobinemia Congestive Heart Failure Constipation Coronary Stenosis Cranioectodermal Dysplasia 1 Diabetes Mellitus Diaphragmatic Hernia, Congenital Dirofilariasis Duodenitis Dwarfism Dysentery Eales Disease End Stage Renal Failure Epileptic Encephalopathy, Early Infantile, 36 Erythrocytosis, Familial, 1 Erythrocytosis, Familial, 2 Essential Thrombocythemia Ewing's Family of Tumors Fanconi Anemia, Complementation Group a Fanconi Anemia, Complementation Group B Fanconi Anemia, Complementation Group D2 Fanconi Anemia, Complementation Group E Fanconi Anemia, Complementation Group F Fascioliasis Febrile Seizures Fetal Erythroblastosis Fetal Hemoglobin Quantitative Trait Locus 1 Focal Cortical Dysplasia, Type Ii Folic Acid Deficiency Anemia Frontotemporal Dementia, Chromosome 3-Linked Gastric Antral Vascular Ectasia Gastric Ulcer Gastritis Gastroduodenitis Gastroesophageal Reflux Gestational Diabetes Giardioză Glossitis Glossodynia Glucosephosphate Dehydrogenase Deficiency Glutathione Peroxidase Deficiency Granulocytopenia Headache Heinz Body Anemias Helicobacter Pylori Infection Hemangioma Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemochromatosis, Type 3 Hemochromatosis, Type 4 Hemoglobinemia Hemoglobin H Disease Hemoglobinopathy Hemolytic Anemia Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemosiderosis Hepatic Adenomas, Familial Hepatocellular Adenoma Hereditary Hemorrhagic Telangiectasia Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hernia, Hiatus Hfe-Associated Hereditary Hemochromatosis Hyperferritinemia with or Without Cataract Hyperostosis Hyperpigmentation with or Without Hypopigmentation, Familial Progressive Hypersensitivity Reaction Type Iii Disease Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoascorbemia Hypochromic Microcytic Anemia Hypogonadism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hypoxia Immune System Disease Inflammatory Bowel Disease Inherited Metabolic Disorder Intermittent Claudication Intestinal Disease Intrinsic Factor Deficiency Intussusception Iron Deficiency Anemia Iron Metabolism Disease Iron Overload in Africa Iron-Refractory Iron Deficiency Anemia Ischemic Optic Neuropathy Kleine-Levin Hibernation Syndrome Lactic Acidosis Lateral Sinus Thrombosis Leiomyoma Lice Infestation Liver Cirrhosis Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome Lymphocytic Gastritis Macs Syndrome Malaria Malignant Spiradenoma Mastitis Meckel Syndrome, Type 1 Median Arcuate Ligament Syndrome Megaloblastic Anemia Melancholia Meningitis and Encephalitis Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Metal Metabolism Disorder Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcytic Anemia Moyamoya Disease 1 Mungan Syndrome Myelofibrosis Neonatal Anemia Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Nutmeg Liver Nutritional Deficiency Disease Oral Submucous Fibrosis Ovarian Squamous Cell Carcinoma Pancreatitis, Hereditary Pancytopenia Papilledema Peliosis Hepatis Pericardial Effusion Perinatal Necrotizing Enterocolitis Periodontitis Peroxisome Biogenesis Disorder 1a Peutz-Jeghers Syndrome Pica Disease Plummer Vinson Syndrome Polycythemia Polycythemia Vera Porphyria Porphyria Cutanea Tarda Portal Hypertension Posttransplant Acute Limbic Encephalitis Pouchitis Prediabetes Syndrome Primary Polycythemia Protein-Deficiency Anemia Protein-Energy Malnutrition Protein-Losing Enteropathy Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pure Red-Cell Aplasia Purpura Pyogenic Granuloma Pyridoxine Deficiency Pyridoxine Deficiency Anemia Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Pyridoxine-Responsive Sideroblastic Anemia Pyruvate Kinase Deficiency of Red Cells Refractory Anemia Restless Legs Syndrome Retinal Artery Occlusion Retinal Vein Occlusion Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rheumatoid Arthritis Rhizomelic Chondrodysplasia Punctata, Type 2 Sagittal Sinus Thrombosis Satb2-Associated Syndrome Sensorineural Hearing Loss Sickle Cell Anemia Sickle Cell Disease Siderosis Skeletal Tuberculosis Sleeping Sickness Somatostatinoma Splenic Disease Splenic Sequestration Splenomegaly Spondyloocular Syndrome Swayback Thalassemia Three M Syndrome 1 Thrombocytopenia Thrombocytosis Thrombosis Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxic Optic Neuropathy Tracheoesophageal Fistula Tracheopathia Osteoplastica Transient Erythroblastopenia of Childhood Trichuriasis Trypanosomiasis Typhoid Fever Uncombable Hair Syndrome 1 Uremia Vasculitis Vibrio Vulnificus Infection Vitamin B12 Deficiency Vulvovaginal Candidiasis Vulvovaginitis Wilson Disease