aspartylglucosaminuria
Salla disease
Hunter syndrome
Sanfilippo syndrome
Chédiak-Higashi syndrome
Fabry disease
mucolipidosis
prelysosomal
sulfatidosis
Gilbert's syndrome
methylmalonic acidemia
McArdle's disease
mucopolysaccharidosis
histidinemia
saposin
lysine intolerance
iduronidase
glomeromycete
gyrodactylid
seed bug
autophagolysosome
spastizin
acetylglucosaminephosphotransferase
Hurler syndrome
powder cap
cathepsin
nagalase
Farber disease
cellobiase
autophagolysosomal
elaterase
rhabdocoel
Andersen disease
arbutinase
erythroenzymopathy
amylopectinosis
gentobiase
cribricyath
spanin
metachromatic leukodystrophy
hyaluronoglucuronidase
Pompe disease
lysogenize
xyloglucanase
autoactivator
hapsidopareiontid
amastin
hyaluronoglucosaminidase
foxtail
Wolman disease
rhabditophoran
lystrosaurid
tussock moth
ustilaginomycetous
glucomannanase
protagrypnine
gargoylism
glomeromycetous
autophagocytotic
coccinelloid
lyssomanine
Hurler's syndrome
lipochondrodystrophy
glutamylase
kalyptorhynch
dysostosis multiplex
Hurler's disease
ascomycetous
lymexylid
methylglyoxalase
aldoketomutase
Lyme
aetosaurine
pseudolysin
foxtail clubmoss
gnomoniaceous
erythema migrans
lysozymal
lycosuchid
aminopolypeptidase
lysianassoid
allolysis
lymphangiomyomatosis
metschnikowiaceous
glucosamidase
lysosomic
rhopalid
lysianassid
sugar mite
arylamidase
hyaladherin
larentiine
rhizopus
Morquio syndrome
crinophagy
glycymeridid
atrochrysone
autophagocytosed
amygdalase
obestatin

English words for 'A rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.'

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