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

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

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