| iminoglycinuria | A defect in amino acid transport leading to abnormal excretion of glycine, proline and hydroxyproline in the urine: more seriously, absorption in the intestine may be inadequate. See: Hartnup disease. Origin: Gr. Ouron = urine (18 Nov 1997) |
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| iminoglycinuria |
a benign hereditary disorder of renal tubular reabsorption of glycine and the imino acids proline and hydroxyproline, marked by excessive levels of all three substances in the urine.
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