Informaţii despre

Nume Uremia
Pagina Web www.malacards.org
Clasificari ICD10 Unspecified kidney failure
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)

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Boli A-Z Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acrocallosal Syndrome Acromegaly Acute Pancreatitis Acute Poststreptococcal Glomerulonephritis Adenoma Aging Alcoholic Liver Cirrhosis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amyloidosis Analbuminemia Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Anuria Aortic Atherosclerosis Aortic Valve Disease 2 Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Arterial Calcification, Generalized, of Infancy, 1 Arteries, Anomalies of Arteriosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autonomic Dysfunction Autonomic Neuropathy Bipolar Disorder Bladder Cancer Bladder Neck Obstruction 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 Remodeling Disease Bone Resorption Disease Brain Edema Bronchopneumonia Bulimia Nervosa 2 Calciphylaxis Cardiac Tamponade Carotid Stenosis Carpal Tunnel Syndrome Cerebral Atrophy Cerebritis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chronic Pyelonephritis Cohen-Gibson Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Generalized Lipodystrophy Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Cough Headache Critical Limb Ischemia Diabetes Mellitus Diabetic Angiopathy Diabetic Autonomic Neuropathy Dysentery Encephalopathy Endocarditis Endotheliitis End Stage Renal Failure Epstein-Barr Virus Hepatitis Familial Hyperlipidemia Familial Hypocalciuric Hypercalcemia Fanconi Anemia, Complementation Group E Fanconi-Like Syndrome Fanconi Syndrome Fatty Liver Disease Fetal Erythroblastosis Fibrogenesis Imperfecta Ossium Folic Acid Deficiency Anemia Gestational Diabetes Glomerulonephritis Glucose Intolerance Glucose Metabolism Disease Headache Hemarthrosis Hemolytic Anemia Hemopericardium Hemorrhagic Fever with Renal Syndrome Hepatic Coma Hepatitis Hepatitis B Hepatocellular Carcinoma Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 2 Hyperglycemia Hyperlipoproteinemia, Type V Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertriglyceridemia, Familial Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoglycemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia, Adult Hypoxia Idiopathic Recurrent Pericarditis Immune System Disease Immunodeficiency 43 Infective Endocarditis Insulin-Like Growth Factor I Intermittent Claudication Iron Deficiency Anemia Ischemia Kidney Disease Kidney Hypertrophy Kwashiorkor Lecithin:cholesterol Acyltransferase Deficiency Leukoencephalopathy, Hereditary Diffuse, with Spheroids Limb Ischemia Lipid Metabolism Disorder Lipodystrophy, Familial Partial, Type 2 Liver Cirrhosis Liver Disease Lutheran Suppressor, X-Linked Lymphopenia Malignant Hypertension Malignant Otitis Externa Marasmus Median Rhomboid Glossitis Mediastinitis Melancholia Metabolic Acidosis Miliary Tuberculosis Mineral Metabolism Disease Mononeuropathy of the Median Nerve, Mild Morbid Obesity Mucositis Multiple Endocrine Neoplasia Mungan Syndrome Myocardial Infarction Myoma Myopathy Nephrolithiasis, Calcium Oxalate Nephronophthisis Nephrosclerosis Neuronitis Neuropathy Nonalcoholic Steatohepatitis Nutritional Deficiency Disease Obesity-Hypoventilation Syndrome Occipital Horn Syndrome Ocular Motor Apraxia Osteitis Fibrosa Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteomalacia Ovarian Cyst Overhydrated Hereditary Stomatocytosis Overnutrition Paget's Disease of Bone Pancreatitis Parathyroid Carcinoma Parathyroid Gland Disease Pericardial Effusion Pericarditis Peripheral Artery Disease Peritonitis Phosphorus Metabolism Disease Pitt-Hopkins Syndrome Platelet Membrane Fluidity Polyhydramnios Prediabetes Syndrome Primary Hyperparathyroidism Prurigo Nodularis Ptosis Pure Red-Cell Aplasia Purpura Pyelonephritis Pyuria Renal Hypertension Renal Osteodystrophy Rheumatoid Arthritis Rickets Scleredema Adultorum Secondary Hyperparathyroidism of Renal Origin Sensorineural Hearing Loss Sheehan Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialolithiasis Sleep Apnea Spondyloocular Syndrome Status Epilepticus Sudden Sensorineural Hearing Loss Sveinsson Chorioretinal Atrophy Testicular Yolk Sac Tumor Thrombasthenia Thrombocytopenia Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Tuberous Sclerosis Uremic Neuropathy Ureteral Obstruction Urinary System Disease Vascular Disease Xanthinuria, Type I