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.

Descriptor ID	D005198
MeSH Number(s)	C12.777.419.250 C12.777.419.815.450 C13.351.968.419.250 C13.351.968.419.815.450 C16.320.565.861.450 C18.452.648.861.450
Concept/Terms	Fanconi Syndrome Fanconi Syndrome Syndrome, Fanconi Fanconi Renotubular Syndrome Syndrome, Fanconi Renotubular Idiopathic De Toni-Debre-Fanconi Syndrome Idiopathic De Toni Debre Fanconi Syndrome Lignac-Fanconi Syndrome Lignac Fanconi Syndrome Syndrome, Lignac-Fanconi Neonatal De Toni-Debre-Fanconi Syndrome Neonatal De Toni Debre Fanconi Syndrome Primary Toni-Debre-Fanconi Syndrome Primary Toni Debre Fanconi Syndrome Toni-Debre-Fanconi Syndrome, Primary Proximal Renal Tubular Dysfunction Renal Fanconi Syndrome Toni-Debre-Fanconi Syndrome Toni Debre Fanconi Syndrome Fanconi Bickel syndrome Fanconi syndrome with intestinal malabsorption and galactose intolerance 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 Pseudo-phlorizin diabetes De Toni-Debre-Fanconi Syndrome De Toni Debre Fanconi Syndrome Syndrome, De Toni-Debre-Fanconi

Below are MeSH descriptors whose meaning is more general than "Fanconi Syndrome".

Below are MeSH descriptors whose meaning is related to "Fanconi Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Fanconi Syndrome".