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Nume Hemosiderosis
Pagina Web www.malacards.org
Clasificare globală Malacards Metabolic diseases; Rare diseases

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Ablepharon-Macrostomia Syndrome Acatalasemia Aceruloplasminemia Acute Leukemia Acute Leukemia of Ambiguous Lineage Adenocarcinoma Adenoma Adenosine Deaminase Deficiency Adult Respiratory Distress Syndrome Adult T-Cell Leukemia Aging Alcohol Abuse Alcoholic Hepatitis Allergic Asthma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-1-Antitrypsin Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Amyloidosis Analbuminemia Ancylostomiasis Anemia, Congenital Dyserythropoietic, Type Ii Anemia, Sideroblastic, 1 Aneurysm Aniridia 1 Anorexia Nervosa 1 Anterior Segment Dysgenesis 4 Aortic Aneurysm Aplastic Anemia Apparent Mineralocorticoid Excess Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atransferrinemia Autoimmune Hepatitis Autosomal Recessive Sideroblastic Anemia Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bowen-Conradi Syndrome Brain Edema Bronchiolitis Bronchiolitis Obliterans Bronchopulmonary Dysplasia Burns Cardiac Tamponade Cartilage-Hair Hypoplasia Cataract Cerebritis Childhood Leukemia Cholestasis Chorioamnionitis Choroiditis Chronic Granulomatous Disease Chronic Meningitis Cleft Palate, Isolated Colon Adenocarcinoma Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Corneal Dystrophy, Avellino Type Cor Triatriatum Cor Triatriatum Sinister Cutaneous Porphyria Cyanosis, Transient Neonatal Cystic Fibrosis Deficiency Anemia Dementia Diabetes Mellitus Diamond-Blackfan Anemia Diarrhea Diffuse Alveolar Hemorrhage Dilated Cardiomyopathy Down Syndrome Dubin-Johnson Syndrome Duodenitis Encephalopathy Endotheliitis Epilepsy Epileptic Encephalopathy, Early Infantile, 36 Fanconi Anemia, Complementation Group E Fanconi Syndrome Fatty Liver Disease Ferro-Cerebro-Cutaneous Syndrome Folic Acid Deficiency Anemia Frontotemporal Dementia, Chromosome 3-Linked Glomerulonephritis Gracile Syndrome Graft-Versus-Host Disease Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemochromatosis, Type 4 Hemochromatosis, Type 5 Hemoglobin E-Beta-Thalassemia Syndrome Hemoglobin E Disease Hemoglobin H Disease Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hepatic Adenomas, Familial Hepatic Veno-Occlusive Disease Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis D Hepatocellular Adenoma Hepatocellular Carcinoma Hepatopulmonary Syndrome Hereditary Spherocytosis Hfe-Associated Hereditary Hemochromatosis Human Coronavirus Sensitivity Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hyperferritinemia with or Without Cataract Hyper Ige Syndrome Hyperinsulinism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoascorbemia Hypochromic Microcytic Anemia Hypochromic Microcytic Anemia with Iron Overload Hypogonadism Hypoparathyroidism Immune-Complex Glomerulonephritis Immunoglobulin Alpha Deficiency Infertility Inherited Metabolic Disorder Iron Deficiency Anemia Iron Metabolism Disease Iron Overload in Africa Juvenile Rheumatoid Arthritis Kwashiorkor Lactic Acidosis Leukemia Listeriosis Liver Cirrhosis Liver Disease Long Qt Syndrome Lupus Erythematosus Lymphadenitis Lymphoblastic Leukemia Lymphoma Macrophage Activation Syndrome Malignant Hypertension Megaloblastic Anemia Melioidosis Meningitis Metal Metabolism Disorder Microcytic Anemia Microscopic Polyangiitis Miller-Dieker Lissencephaly Syndrome Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Sclerosis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Nasopharyngitis Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neuropathy Neutrophilic Dermatosis, Acute Febrile Nevus Comedonicus Nonalcoholic Steatohepatitis Nutritional Deficiency Disease Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Pancreatitis Pancreatitis, Hereditary Paroxysmal Nocturnal Hemoglobinuria Pellagra Pericardial Effusion Peritonitis Pernicious Anemia Pneumoconiosis Pneumonia Porphyria Porphyria Cutanea Tarda Portal Hypertension Premature Chromatid Separation Trait Prostate Cancer Prostatitis Protoporphyria, Erythropoietic Protoporphyria, Erythropoietic, X-Linked Psoriasis Psoriasis 13 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonic Stenosis Pure Red-Cell Aplasia Purpura Pyelonephritis Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Pyruvate Kinase Deficiency of Red Cells Rapidly Progressive Glomerulonephritis Rapp-Hodgkin Syndrome Refractory Anemia Retinal Degeneration Retinitis Retinitis Pigmentosa Rheumatic Heart Disease Rheumatoid Arthritis Rh Isoimmunization Rhizomelic Chondrodysplasia Punctata, Type 2 Ring Chromosome 2 Scott Syndrome Secondary Pulmonary Hemosiderosis Septic Arthritis Sickle Cell Anemia Sickle Cell Disease Sideroblastic Anemia Siderosis Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Stachybotrys Chartarum Superficial Siderosis Swayback Systemic Lupus Erythematosus T-Cell Leukemia Tfr2-Related Hereditary Hemochromatosis Thalassemia Thrombocytopenia Thrombosis Tyrosinemia Vaginitis Vascular Disease Vasculitis Ventricular Septal Defect Vibrio Vulnificus Infection Viral Hepatitis Vitamin B12 Deficiency Warfarin Syndrome Wilson Disease Wilson-Mikity Syndrome X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Zellweger Syndrome Zygomycosis