Informaţii despre

Nume Hyperuricemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Boli din aceeaşi familie Hereditary Hyperuricemia

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acquired Metabolic Disease Acute Myocardial Infarction Acute Urate Nephropathy Adenine Phosphoribosyltransferase Deficiency Adie Pupil Adult Lymphoma Aging Aland Island Eye Disease Alopecia 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 Aniridia 1 Anorexia Nervosa 1 Apnea, Obstructive Sleep Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Atherosclerosis Susceptibility Athetosis Atrial Fibrillation 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 Breast Cancer Brittle Bone Disorder Cerebrovascular Disease Childhood Leukemia Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chronic Kidney Failure Coronary Heart Disease 1 Cystic Kidney Disease Cystinuria Diabetes Mellitus Endotheliitis Epidural Abscess Epithelial Recurrent Erosion Dystrophy Fanconi-Bickel Syndrome Fatty Liver Disease Galactosemia Gastroenteritis Glomerulonephritis Glucose Intolerance Glucose Metabolism Disease Glycogen Storage Disease Glycogen Storage Disease Vii Gout Hemolytic Anemia Hemolytic-Uremic Syndrome Hepatic Adenomas, Familial Hepatitis Hepatitis C Hereditary Hyperuricemia Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hyperuricemic Nephropathy, Familial Juvenile, 1 Hypoglycemia Hypokalemia Hypokalemic Periodic Paralysis, Type 1 Hypotonia Hypouricemia, Renal, 1 Inflammatory Bowel Disease Interstitial Nephritis Isolated Optic Neuritis Lesch-Nyhan Syndrome Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipid Metabolism Disorder Liver Disease Lupus Erythematosus Lymphoma Malignant Otitis Externa Mediastinitis Megaloblastic Anemia Morbid Obesity Multiple Mitochondrial Dysfunctions Syndrome 5 Mungan Syndrome Myelodysplastic Syndrome Myeloid Leukemia Myocardial Infarction Myopathy Nephrolithiasis Nephrolithiasis, Uric Acid Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephronophthisis Nephrosclerosis Nonalcoholic Steatohepatitis Orotic Aciduria Pancreatitis Parotitis Polycythemia Polyhydramnios Postural Hypotension Prediabetes Syndrome Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Hypertension Pulmonary Tuberculosis Purine-Pyrimidine Metabolic Disorder Renal Failure, Progressive, with Hypertension Retinitis Rheumatic Disease Salt and Pepper Developmental Regression Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sleep Apnea Spondyloocular Syndrome Sveinsson Chorioretinal Atrophy Systemic Lupus Erythematosus Thalassemia Thrombophlebitis Thyroiditis Urate Oxidase, Pseudogene Uremia Urinary System Disease Vascular Disease Xanthinuria