Catalog
Glycogen storage disease
Link to WHO Definition
Glycogen storage disease – http://id.who.int/icd/entity/1187107383
The term Glycogen storage disease characterises a group of heterogeneous diseases resulting from defects in the process of glycogen synthesis or breakdown within muscles, liver, and other cell types.
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Children
- Glycogen storage disease due to aldolase A deficiency
- Glycogen storage disease due to lactate dehydrogenase deficiency
- Glycogen storage disease due to muscle pyruvate kinase deficiency
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- Glycogen storage disease due to acid maltase deficiency
- Glycogen storage disease due to glycogen phosphorylase kinase deficiency
- Glycogen storage liver disease
- Glycogen storage disease due to liver glycogen phosphorylase deficiency
- Glycogen storage disease due to glycogen synthase deficiency
- Glycogen storage disease due to muscle glycogen phosphorylase deficiency
- Glycogen storage disease due to muscle phosphofructokinase deficiency
- Glycogen storage disease due to LAMP-2 deficiency
- Glycogen storage disease due to muscle phosphoglycerate mutase deficiency
- Glycogen storage disease due to branching-transferase deficiency
- Glycogen storage disease due to GLUT2 deficiency
- Glycogen storage disease due to glucose-6-phosphate system deficiency
- Glycogen storage disease due to glycogen debranching enzyme deficiency
- Glycogen storage disease due to phosphoglucomutase deficiency
- Glycogen storage disease due to glycogenin deficiency
- Glycogen storage disease due to muscle beta-enolase deficiency