Chemical abnormalities associated with muscle disease.
D006008:Glycogen Storage Disease / Q000378:metabolism*; D005953:Glycogen Storage Disease Type I; D006801:Humans; D008928:Mitochondria; D009119:Muscle Contraction; D009124:Muscle Proteins / Q000378:metabolism; D009132:Muscles / Q000166:cytology; D009135:Muscular Diseases / Q000378:metabolism*; D009136:Muscular Dystrophies; D010243:Paralysis / Q000378:metabolism