What does iminoglycinuria mean?
Definitions for iminoglycinuria
imino·g·lycin·uri·a
This dictionary definitions page includes all the possible meanings, example usage and translations of the word iminoglycinuria.
Wikidata
Iminoglycinuria
Iminoglycinuria, sometimes called familial iminoglycinuria, is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine, and the imino acids proline and hydroxyproline. This results in excess urinary excretion of all three acids. Iminoglycinuria is a rare and complex disorder, associated with a number of genetic mutations that cause defects in both renal and intestinal transport systems of glycine and imino acids. Imino acids typically contain an imine functional group, instead of the amino group found in amino acids. Proline is considered and usually referred to as an amino acid, but unlike others, it has a secondary amine. This feature, unique to proline, identifies proline also as an imino acid. Hydroxyproline is another imino acid, made from the naturally occurring hydroxylation of proline.
Numerology
Chaldean Numerology
The numerical value of iminoglycinuria in Chaldean Numerology is: 8
Pythagorean Numerology
The numerical value of iminoglycinuria in Pythagorean Numerology is: 8
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"iminoglycinuria." Definitions.net. STANDS4 LLC, 2024. Web. 26 Apr. 2024. <https://www.definitions.net/definition/iminoglycinuria>.
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