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

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

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