Familial glycinuria

[MIM*138500] a metabolic disorder believed to be due to defective renal glycine reabsorption; it may or may not be accompanied by oxalate urolithiasis; may be the heterozygous state of iminoglycinuria; autosomal dominant inheritance.

Chemwatch
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.