A hereditary or acquired form of generalized dysfunction of the PROXIMAL KIDNEY TUBULE without primary involvement of the KIDNEY GLOMERULUS. It is usually characterized by the tubular wasting of nutrients and salts (GLUCOSE; AMINO ACIDS; PHOSPHATES; and BICARBONATES) resulting in HYPOKALEMIA; ACIDOSIS; HYPERCALCIURIA; and PROTEINURIA.
Also Known As:
Syndrome, Fanconi; Adult Fanconi Syndrome; Fanconi Bickel Syndrome; Fanconi Renotubular Syndrome; Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance; Fanconi Syndrome without Cystinosis; Fanconi-Bickel Syndrome; Glycogen Storage Disease XI; Glycogenosis, Fanconi Type; Hepatic Glycogenosis with Amino Aciduria and Glucosuria; Hepatic Glycogenosis with Fanconi Nephropathy; Hepatorenal Glycogenosis with Renal Fanconi Syndrome; Idiopathic De Toni-Debre-Fanconi Syndrome; Luder-Sheldon Syndrome; Neonatal De Toni-Debre-Fanconi Syndrome; Primary Toni-Debre-Fanconi Syndrome; Pseudo-Phlorizin Diabetes; Toni-Debre-Fanconi Syndrome; Bickel Syndrome, Fanconi; Diabete, Pseudo-Phlorizin; Diabetes, Pseudo-Phlorizin; Fanconi Syndrome, Adult; Fanconi Syndrome, Renal; Fanconi Type Glycogenosis; Fanconi-Bickel Syndromes; Lignac Fanconi Syndrome; Luder Sheldon Syndrome; Pseudo Phlorizin Diabetes; Pseudo-Phlorizin Diabete; Renotubular Syndrome, Fanconi; Syndrome, Adult Fanconi; Syndrome, Fanconi Bickel; Syndrome, Fanconi Renotubular; Syndrome, Fanconi-Bickel; Syndrome, Lignac-Fanconi; Syndrome, Luder-Sheldon; Syndrome, Renal Fanconi; Syndromes, Fanconi-Bickel; De Toni-Debre-Fanconi Syndrome; Lignac-Fanconi Syndrome; Proximal Renal Tubular Dysfunction; Renal Fanconi Syndrome