Glycogen storage disease due to glucose-6-phosphate system deficiency (Q84780): Difference between revisions
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Revision as of 10:08, 15 August 2026
Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b (see these terms), and characterised by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_523888904 |
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| English | Glycogen storage disease due to glucose-6-phosphate system deficiency |
Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b (see these terms), and characterised by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver. |
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CID11:ID_523888904
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dki-india-ID_523888904
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Concluído
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