| McArdle's disease | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
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| McArdle's syndrome | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
| McArdle, Brian | <person> 20th century British neurologist. See: McArdle's disease, McArdle-Schmid-Pearson disease, McArdle's syndrome. (05 Mar 2000) |
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| McArdle disease | <disease> Glycogen storage disease in which the defective enzyme is muscle phosphorylase. (18 Nov 1997) |
| McArdle-Schmid-Pearson disease | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
| McArdle's disease |
an inherited disease in which abnormal amounts of glycogen accumulate in skeletal muscle; results in weakness and cramping
Ãâó: wordnet.princeton.edu/perl/webwn
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| McArdle's disease (syndrome) |
see glycogen storage disease, type V, under disease.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| mcardle\'s | an inherited disease in which abnormal amounts of glycogen accumulate in skeletal muscle |
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