Informaţii despre

Nume Iron Deficiency Anemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice
Clasificari ICD10 Iron deficiency anaemia
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge

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Boli A-Z Acute Cholangitis Adenocarcinoma Adenoma Adie Pupil 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 Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Analbuminemia Anemia of Prematurity Anemia, Sideroblastic, 1 Angiodysplasia Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Arteriovenous Fistula 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 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 Bornholm Eye Disease Branch Retinal Artery Occlusion Candidiasis Capillary Hemangioma Cardiogenic Shock Castleman Disease Cataract Cavernous Hemangioma Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cholangiocarcinoma Choroiditis Chromate Resistance Cold Agglutinin Disease Collagenous Gastritis Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hemolytic Anemia Congestive Heart Failure Constipation Cranioectodermal Dysplasia 1 Cryopyrin-Associated Periodic Syndrome Deficiency Anemia Diabetes Mellitus Diabetic Foot Ulcers Diaphragmatic Hernia, Congenital Duodenitis Dwarfism Dysentery End Stage Renal Failure Essential Thrombocythemia Fascioliasis Febrile Seizures 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 Glossodynia Helicobacter Pylori Infection Hemangioma Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemochromatosis, Type 3 Hemochromatosis, Type 4 Hemoglobin H Disease Hemoglobinopathy Hemolytic Anemia Hemosiderosis Hepatic Adenomas, Familial Hepatocellular Adenoma Hereditary Hemorrhagic Telangiectasia Hernia, Hiatus Hfe-Associated Hereditary Hemochromatosis Hyperferritinemia with or Without Cataract Hyperostosis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoascorbemia Hypochromic Microcytic Anemia Hypogonadism Hypophosphatemia Hypoxia Immune System Disease Inflammatory Bowel Disease Inherited Metabolic Disorder Intussusception 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 Malaria Median Arcuate Ligament Syndrome Megaloblastic Anemia Melancholia Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Metal Metabolism Disorder Microcytic Anemia Miliary Tuberculosis Moyamoya Disease 1 Mungan Syndrome Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neutrophilia, Hereditary Nutritional Deficiency Disease Oral Submucous Fibrosis Pancytopenia Papilledema Peliosis Hepatis Perinatal Necrotizing Enterocolitis Periodontitis Peroxisome Biogenesis Disorder 1a Peutz-Jeghers Syndrome Pica Disease Plummer Vinson Syndrome Polycythemia Polycythemia Vera Porphyria Cutanea Tarda Portal Hypertension Posttransplant Acute Limbic Encephalitis Pouchitis Prediabetes Syndrome Protein-Losing Enteropathy Pulmonary Embolism Pulmonary Hemosiderosis Purpura Pyogenic Granuloma Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Refractory Anemia Relapsing Polychondritis Restless Legs Syndrome Retinal Artery Occlusion Retinal Vein Occlusion Retinitis Rheumatoid Arthritis Sagittal Sinus Thrombosis Satb2-Associated Syndrome Sensorineural Hearing Loss Sickle Cell Anemia Sickle Cell Disease Siderosis Somatostatinoma Spinal Disease Splenomegaly Spondyloocular Syndrome Subacute Thyroiditis Superficial Siderosis Superficial Siderosis of the Central Nervous System Tenosynovitis Thalassemia Three M Syndrome 1 Thrombocytopenia Thrombocytosis Thrombosis Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tracheopathia Osteoplastica Trichuriasis Uremia Vasculitis Vibrio Vulnificus Infection Viral Pneumonia Vitamin B12 Deficiency Vulvovaginal Candidiasis Vulvovaginitis