McArdle's disease
Pompe disease
Andersen disease
amylopectinosis
glycogenosis
glycolipidosis
Hurler syndrome
Morquio syndrome
mucopolysaccharidosis
glycobiological
syndrome X
Hunter syndrome
dysmetabolism
glycosphingolipidosis
dystroglycan
glycoregulatory
glycotope
phosphoglycoprotein
glycophenotype
glycophenotypic
saccharidosis
glycogenotic
glycosylglycoside
glycoproteic
amidohydrolytic
glycosylic
metabolopathy
histidinemia
glycogenic
transglycosylase
glycerine
elacridar
glycogene
glycogenation
glycophosphatidylinositol
mycoyltransferase
microglycoprotein
glycosomal
reglycosylation
dextrinosis
glycomarker
arthro-series
mucosubstance
sulfatidosis
sialoglycoproteome
glycophytic
glycosyllipid
tyrosinemia
glycoproteinaceous
lipoglycoprotein
podoplanin
glycohydrolytic
glycostructure
glycopeptidolipid
Sandhoff disease
fructopyranoside
methylmalonic acidemia
clusterin
hunger knock
glycosecretory
phosphoglycolipid
neoglucogenic
metabasis
glyco-
galactosemia
plurimetabolic
glucosylase
wogonoside
moroctocog alfa
velaglucerase
acetylgalactosaminidase
glycoproteomics
myotilinopathy
hyperglyceridemia
glucocerebrosidase
adipomyokine
macroglycopeptide
metaflammation
sialoglycosylation
glucosaminoglycan
inborn error of metabolism
isoamylase
acylglycerol
glycosuric
lysine intolerance
glycogenated
glycobiochemical
phosphoglycerolipid
glycophospholipoprotein
glucopyranoside
glyconeogenic
mucolipidosis
lysoglobotriaosylceramide
glycylase
fucolipid
galactoglycerolipid
glucoside
glycoxidation
cerebrosidase

English words for 'Glycogen storage disease type V, a metabolic disorder caused by a deficiency of myophosphorylase.'

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