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bn:01363668n
Noun Concept
Categories: Nephrology, Autosomal recessive disorders, Amino acid metabolism disorders, Rare diseases
EN
iminoglycinuria  Familial iminoglycinuria  neonatal iminoglycinuria
EN
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
Definitions
Relations
Sources
EN
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
medical condition Wikidata
A rare autosomal-recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine and the imino acids proline and hydroxyproline, resulting in excess urinary excretion of all three acids. Wiktionary
IS A
Amino acid transport disorder
glycinuria
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
iminoglycinuria
Wikidata
EN
Iminoglycinuria
Wiktionary
EN
iminoglycinuria
Wikipedia Redirections
EN
Familial iminoglycinuria, neonatal iminoglycinuria
Wikidata Alias
EN
IMINOGLYCINURIA

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