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| Term | glycogen metabolism disorder | ID (Ontology) | DOID:0050728 (Human Disease) |
| Definition | A carbohydrate metabolism disorder that is characterized by abnormal accumulation or depletion of liver glycogen. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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inherited metabolic disorder |__carbohydrate metabolic disorder |__glycogen metabolism disorder 15 rec. |__glycogen storage disease 13 rec. |__glycogen storage disease I(+) 2 rec. |__glycogen storage disease II 1 rec. |__glycogen storage disease III 2 rec. |__glycogen storage disease IV 1 rec. |__glycogen storage disease IX(+) 3 rec. |__glycogen storage disease V 1 rec. |__glycogen storage disease VI 1 rec. |__glycogen storage disease VII 1 rec. |__glycogen storage disease VIII |__glycogen storage disease XV 1 rec. |__lethal congenital glycogen storage disease of heart 1 rec. |
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| Is a | carbohydrate metabolic disorder | ||
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