MeSH 搜索器

Fanconi Syndrome

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.
推出的年份: 1965
副标题
树号: C12.050.351.968.419.815.450, C12.200.777.419.815.450, C12.950.419.815.450, C16.320.831.450
MeSH 单一 ID: D005198
进入的组:
  • Syndrome, Fanconi
  • Proximal Renal Tubular Dysfunction
  • Toni-Debre-Fanconi Syndrome
  • Idiopathic De Toni-Debre-Fanconi Syndrome
  • Primary Toni-Debre-Fanconi Syndrome
  • De Toni-Debre-Fanconi Syndrome
  • Neonatal De Toni-Debre-Fanconi Syndrome
  • Fanconi Bickel Syndrome
  • Bickel Syndrome, Fanconi
  • Syndrome, Fanconi Bickel
  • Glycogen Storage Disease XI
  • Glycogenosis, Fanconi Type
  • Fanconi Type Glycogenosis
  • Fanconi-Bickel Syndrome
  • Fanconi-Bickel Syndromes
  • Syndrome, Fanconi-Bickel
  • Syndromes, Fanconi-Bickel
  • Pseudo-Phlorizin Diabetes
  • Diabete, Pseudo-Phlorizin
  • Diabetes, Pseudo-Phlorizin
  • Pseudo Phlorizin Diabetes
  • Pseudo-Phlorizin Diabete
  • Lignac-Fanconi Syndrome
  • Lignac Fanconi Syndrome
  • Syndrome, Lignac-Fanconi
  • Hepatic Glycogenosis with Amino Aciduria and Glucosuria
  • Hepatic Glycogenosis with Fanconi Nephropathy
  • Hepatorenal Glycogenosis with Renal Fanconi Syndrome
  • Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
  • Fanconi Syndrome without Cystinosis
  • Renal Fanconi Syndrome
  • Fanconi Syndrome, Renal
  • Syndrome, Renal Fanconi
  • Adult Fanconi Syndrome
  • Fanconi Syndrome, Adult
  • Syndrome, Adult Fanconi
  • Fanconi Renotubular Syndrome
  • Renotubular Syndrome, Fanconi
  • Syndrome, Fanconi Renotubular
  • Luder-Sheldon Syndrome
  • Luder Sheldon Syndrome
  • Syndrome, Luder-Sheldon

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