Hunter syndrome
sulfatidosis
aspartylglucosaminuria
McArdle's disease
Fabry disease
enzymopathic
mucolipidosis
lysine intolerance
mucopolysaccharidosis
prelysosomal
glucosamidase
hyaluronoglucosaminidase
elosulfase
Pompe disease
synzyme
hyaluronoglucuronidase
acetylgalactosaminidase
sitosterolin
erythroenzymopathy
tyrase
aldoketomutase
amylopectinosis
Andersen disease
methylglyoxalase
pseudolysin
acetylglucosaminephosphotransferase
biocatalyzator
maltohydrolase
Farber disease
-in
enzymologic
TYRP1
glycosphingolipidosis
glucosidase
oligopeptidase
necroenzyme
metachromatic leukodystrophy
propionylcholinesterase
glucomannanase
enzymeless
glycolipidosis
Sanfilippo syndrome
sulfonase
exozyme
azymia
Wolman disease
halidohydrolase
malonaldehyde
neoenzyme
phenylketonuria
alpha-d-galactosidase
chylomicron
nonenzyme
heparan
glutamylase
thermitase
oligoribonuclease
lysogenize
digalactosidase
foldase
acylphosphatase
dihydropyrimidinase
exostosin
reductase
aldonolactonase
heparanase
saposin
glycogenosis
enzymologist
histidinemia
maltooligosyl
sterol esterase
antienzymatic
maltase
enzymologically
adipophilin
autocleavage
antiproteinuric
sulfohydrolase
arylsulfatase
glycophosphatidylinositol
Sandhoff disease
oligoadenylase
phosphoenzyme
metalloelastase
phosphoglucoseisomerase
chorismatase
glucose-6-phosphate isomerase
polyglutamylase
Lyme
idursulfase
glucosaccharide
microglycoprotein
Gilbert's syndrome
pectolyase
dihydroceramidase
alginase
polysaccharidase
insulinase
ketoacidemia

English words for 'A lysosomal storage disease caused by a deficient (or absent) enzyme, iduronate-2-sulfatase.'

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