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Hemosiderosis
Informaţii despre
Nume
Hemosiderosis
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli metabolice
;
Boli rare
Vezi şi
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
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