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Iminoglycinuria
Iminoglycinuria
meaning
ĭm′ə-nō-glī′sə-no͝or
′
ē-ə
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A benign inborn error of amino acid transport, causing glycine, proline, and hydroxyproline to be excreted in the urine.
noun
0
0
(medicine) 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.
noun
0
0
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iminodipeptidases
iminoester
iminoesters
iminoethyl
iminoglycinuria
iminoglycinurias
iminoglycinuric
iminolactone
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