iminoglycinuria
hyperaminoaciduria
aminoaciduria
Fanconi syndrome
glycinuria
proteinuria
Hartnup disease
albuminuria
macroproteinuria
hyperuricosuria
guanylin
hyperproteinuria
eosinophiluria
hypoalbuminuria
uraturia
glyceroluria
vesicorenal
nephrocalcin
kallidin
oxoprolinuria
isouric acid
collectrin
normoalbuminuric
uromucoid
uricaciduria
methylmalonic acidemia
uratolytic
uricosuria
dopasensitivity
ureterorenal reflux
hyperaminoacidemia
hyperalbuminuria
uridylyltransferase
oxonic acid
uricosuric
transpeptidation
uropoiesis
renourinary
urinary tract
pronephritic
renointestinal
glycocapture
iduronic acid
nephrourinary
hyperuricemia
peptidyltransferase
indacrinone
uricemia
hydronephrosis
hyperoxaluria
anuria
hydroureteronephrosis
ornithine
hypercalcinuric
uricacidemia
urosis
uricostatic
biliuria
tubuloglomerular
uricolysis
renotubular
Lesch-Nyhan syndrome
lantanuric acid
neer
aminoterminus
proteinic
normoproteinuria
ureolysis
ureterorenal
proteinous
renal pelvis
nephrosis
lysine intolerance
aminotranspeptidase
microproteinuria
urobilinogenuria
oxaluria
hyperhomocysteinuria
glomerulocystic
polyuria
macroalbuminuria
citrullinemia
hyperglycosuria
glutamine
peptonuria
aciduria
uricogenesis
urodynamics
peptide bond
glomerulotubular
enzymuria
glycinamide
mannuronic acid
natriuretic
aminuria
carboxyglutamic acid
urocanic acid

English words for '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.'

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