Informaţii despre

Nume Gout
Pagina Web www.malacards.org
Clasificari ICD10 Gout due to impairment of renal function; Gout, unspecified; Gouty arthropathy due to enzyme defects and other inherited disorders
Clasificare anatomică Malacards Boli osoase

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Boli A-Z Acute Myocardial Infarction Acute Respiratory Distress Syndrome Acute Urate Nephropathy Adenine Phosphoribosyltransferase Deficiency Adenocarcinoma Adie Pupil Aging Aland Island Eye Disease Alkaptonuria Allopurinol Toxicity Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Totalis Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Atrial Fibrillation Back Pain 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 Bursitis Calcific Tendinitis Calcifying Aponeurotic Fibroma Calcinosis Carpal Tunnel Syndrome Central Nervous System Origin Vertigo Cerebral Palsy, Ataxic, Autosomal Recessive Cervical Adenitis Cervicitis Chondrocalcinosis Chondrocalcinosis 2 Chromate Resistance Chronic Recurrent Multifocal Osteomyelitis Collagen Disease Congenital Dyserythropoietic Anemia Corneal Dystrophy, Band-Shaped Coronary Heart Disease 1 Crouzon Syndrome with Acanthosis Nigricans Crystal Arthropathies Cystic Kidney Disease Diabetes Mellitus Diabetic Neuropathy Diffuse Idiopathic Skeletal Hyperostosis Dilated Cardiomyopathy Discitis Enthesopathy Epidural Abscess Epilepsy Factor Xii Deficiency Familial Adenomatous Polyposis Familial Cold Autoinflammatory Syndrome 1 Foot Drop Genitopatellar Syndrome Gitelman Syndrome Glycogen Storage Disease Hantavirus Pulmonary Syndrome Hawkinsinuria Hemarthrosis Hemoglobin C Disease Hepatic Adenomas, Familial Hepatitis Hereditary Xanthinuria Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperostosis Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia Hyperuricemic Nephropathy, Familial Juvenile, 1 Hypervitaminosis a Hypouricemia, Renal, 1 Kearns-Sayre Syndrome Kelley-Seegmiller Syndrome Keratopathy Lesch-Nyhan Syndrome Lissencephaly 1 Lung Disease Lupus Erythematosus Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Mevalonic Aciduria Mononeuropathy of the Median Nerve, Mild Motor Neuron Disease Mucinous Adenocarcinoma Multicentric Reticulohistiocytosis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mycobacterium Kansasii Myocardial Infarction Myopathy Natural Killer Cell Leukemia Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nephrolithiasis, Uric Acid Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephronophthisis Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neuropathy Ochronosis Olecranon Bursitis Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteomyelitis Pancreatitis Panniculitis Paraplegia Parkinson Disease 15, Autosomal Recessive Early-Onset Peroxisome Biogenesis Disorder 1a Phosphoribosylpyrophosphate Synthetase Superactivity Pituitary Adenoma 1, Multiple Types Prediabetes Syndrome Primary Biliary Cirrhosis Prostate Cancer Prostatitis Pseudoainhum Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Tuberculosis Purine-Pyrimidine Metabolic Disorder Radiculopathy Retinitis Rheumatic Disease Rheumatoid Arthritis Rheumatoid Nodulosis Rheumatoid Vasculitis Salt and Pepper Developmental Regression Syndrome Schnitzler Syndrome Septic Arthritis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sickle Cell Disease Skin Disease Sleep Apnea Sleep Disorder Spinal Meningioma Spinal Stenosis Spondyloarthropathy Spondylolisthesis Spondyloocular Syndrome Sporotrichosis Sveinsson Chorioretinal Atrophy Synovitis Systemic Lupus Erythematosus Tendinitis Tendinopathy Tenosynovitis Thalassemia Thyroiditis Tinea Favosa Undifferentiated Pleomorphic Sarcoma Urate Oxidase, Pseudogene Vascular Disease Vasculitis Xanthinuria Xanthinuria, Type I