Main Entry: im·i·no·gly·cin·uria Pronunciation: -"glI-s&-'nur-E-& Function: noun : an abnormal inherited conditionof the kidney associated especially with hyperprolinemia and characterized by the presence of proline, hydroxyproline, and glycine in the urine
iminoglycinuria im·i·no·gly·ci·nu·ri·a (ĭm'ə-nō-glī'sə-n&oobreve;r'ē-ə, -ny&oobreve;r'-) n. A benign inborn error of amino acid transport, causing glycine, proline, and hydroxyproline to be excreted in the urine.
