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Fanconi renotubular syndrome

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The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Disease Overview

A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.

Synonyms

  • De toni-Fanconi syndrome
  • De toni-debre-Fanconi syndrome
  • Fanconi syndrome
  • Fanconi's syndrome
  • Fanconi-de toni syndrome
  • Fanconi-de-toni syndrome
  • Lignac-Fanconi syndrome
  • adult Fanconi syndrome
  • congenital Fanconi syndrome
  • deToni Fanconi syndrome
  • infantile nephropathic cystinosis
  • toni-debre-Fanconi syndromeDe toni-Fanconi syndrome
  • De toni-debre-Fanconi syndrome
  • Fanconi syndrome
  • Fanconi's syndrome
  • Fanconi-de toni syndrome
  • Fanconi-de-toni syndrome
  • Lignac-Fanconi syndrome
  • adult Fanconi syndrome
  • congenital Fanconi syndrome
  • deToni Fanconi syndrome
  • infantile nephropathic cystinosis
  • toni-debre-Fanconi syndrome
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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