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Concept information

disease > urinary system disease > kidney disease > tubulopathy > iminoglycinuria
disease > genetic disease > hereditary disease > aminoacid disorder > iminoglycinuria
disease > enzymopathy > aminoacid disorder > iminoglycinuria

Terme préférentiel

iminoglycinuria  

Définition

  • Iminoglycinuria, is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine, and the imino acids proline and hydroxyproline. (Wikipedia)

Concept générique

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URI

http://data.loterre.fr/ark:/67375/VH8-NPK6R515-Z

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