Gilbert's syndrome
hyperphenylalaninemic
glutamylase
hyaluronoglucosaminidase
hyaluronoglucuronidase
macroamylasaemia
glycomutant
hyperadiponectinemic
enzymopathic
glutaminolytic
gentobiase
hypercholanemic
elaterase
hyperargininemic
glucuronyltransferase
cellobiase
arbutinase
aminoacidopathy
metachromatic leukodystrophy
oligoglutamate
methylglyoxalase
mucopolysaccharidosis
enzymopathy
aldoketomutase
hypotransferrinemic
erythroenzymopathy
glucurolactone
Chédiak-Higashi syndrome
hyperreninemic
aspartylglucosaminuria
hyperketonemic
hyperalbuminemic
glucomannanase
hyperimmunoglobulin
cyclosophoran
hyperpipecolatemia
polyadenylase
alternan
hyperphenylalanemia
glomerulopathic
polyglutamylase
exoglucosidase
hyperhomocysteinemic
deglutarylase
enzymologic
hyperglucagonemic
glucanase
glucosamidase
histidinemia
dysglobulinemia
Hurler syndrome
hypogammaglobulinemic
glucopsychosine
glucostatic
hypoprothrombinemic
Wolman disease
hyperinsulinism
hyperproinsulinemic
phenethylglucosinolate
glutathiolation
glutaral
hyperechogenic
hypotrehalosemic
deglucuronidase
hypercholeretic
sitosterolin
nephrosis
lysine intolerance
neoglucogenic
cellobionic acid
pelitrexol
nephrotic syndrome
sialidosis
microglobulin
sizofiran
hyperglutamylation
polysaccharase
hyperphosphorylating
methylmalonic acidemia
enzymologically
foot
hypo
deoxygluconic acid
hyperheparinemic
glomeromycete
velaglucerase
lysoglobotriaosylceramide
glucoregulatory
gynandrism
gynandromorphy
glucopyranosidic
ketoacidemia
phosphoacetylglucosamine mutase
favism
hyperglutamylated
hypermethylase
monoglucosyltransferase
hypercholesteremic
proteoglycan
McArdle's disease

English words for 'A hereditary condition characterized by hyperbilirubinemia due to reduced activity of the enzyme glucuronyltransferase.'

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