Informaţii despre

Nume Nephrolithiasis
Pagina Web www.malacards.org
Clasificari ICD10 Calculus of kidney with calculus of ureter
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)

Vezi şi

Boli A-Z Acute Pyelonephritis Acute Urate Nephropathy Adenine Phosphoribosyltransferase Deficiency Adenocarcinoma Adenoma Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Aminoaciduria Aniridia 1 Anorexia Nervosa 1 Anuria Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asthma Autosomal Dominant Polycystic Kidney Disease Bartter Disease Bartter Syndrome, Type 3 Beta-Thalassemia 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 Carbuncle Cerebral Palsy, Ataxic, Autosomal Recessive Cerebrotendinous Xanthomatosis Cervicitis Cholelithiasis Cohen-Gibson Syndrome Colitis Collecting Duct Carcinoma Colon Adenocarcinoma Congestive Heart Failure Cystic Angiomatosis of Bone, Diffuse Cystic Fibrosis Cystinuria Dent Disease 1 Diabetes Insipidus Diabetes Mellitus Diffuse Lymphatic Malformation Dominant Hypophosphatemia with Nephrolithiasis or Osteoporosis Endophthalmitis Fanconi Syndrome Fatty Liver Disease Gastric Cancer Gerstmann-Straussler Disease Glucose/galactose Malabsorption Glycogen Storage Disease Gout Hepatic Adenomas, Familial Hepatitis Hepatitis B Hereditary Hypophosphatemic Rickets Hereditary Xanthinuria Horseshoe Kidney Hydronephrosis Hypercalciuria, Absorptive, 2 Hyperglycinuria Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hyperuricemic Nephropathy, Familial Juvenile, 1 Hypokalemia Hypophosphatemia Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Recessive Hypouricemia, Renal, 1 Idiopathic Hypercalciuria Immunodeficiency 43 Inflammatory Bowel Disease Interstitial Nephritis Intestinal Disease Ischemic Colitis Lactic Acidosis Lesch-Nyhan Syndrome Liver Disease Lymphocele Medullary Sponge Kidney Membranous Nephropathy Microcephaly, Epilepsy, and Diabetes Syndrome Mineral Metabolism Disease Miyoshi Muscular Dystrophy 1 Multiple Sclerosis Muscular Dystrophy Myotonia Nephrocalcinosis Nephrolithiasis, Calcium Oxalate Nephrolithiasis, Uric Acid Nephrolithiasis, X-Linked Recessive, with Renal Failure Neurofibromatosis, Type Iv, of Riccardi Occipital Horn Syndrome Optic Perineuritis Osteomalacia Ovarian Cyst Overhydrated Hereditary Stomatocytosis Parathyroid Adenoma Paronychia Perinephritis Phosphorus Metabolism Disease Pica Disease Pneumonia Polycystic Kidney Disease Preauricular Sinus Primary Hyperoxaluria Primary Hyperparathyroidism Prune Belly Syndrome Pseudoxanthoma Elasticum Pulmonary Alveolar Microlithiasis Pyelonephritis Pyuria Renal Dysplasia Renal Fibrosis Renal Tubular Acidosis Rickets Sarcoidosis 2 Sialolithiasis Spinal Cord Injury Spondylitis Spondyloarthropathy 1 Squamous Cell Carcinoma Steatorrhea Systemic Mastocytosis Thalassemia Trigonitis Ulcerative Colitis Ureteral Obstruction Ureterolithiasis Urethral Calculus Urethritis Urinary Tract Obstruction Xanthinuria Xanthinuria, Type I Xanthogranulomatous Pyelonephritis Xanthomatosis