Glycogen storage disease due to acid maltase deficiency, juvenile onset (Q100841): Difference between revisions
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15 August 2026
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Latest revision as of 17:37, 16 August 2026
Glycogen storage disease due to acid maltase deficiency, non-classical infantile onset, is form of glycogen storage disease due to acid maltase deficiency, a metabolic myopathy affecting respiratory and skeletal muscles that may fatally impede respiratory function during childhood.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1193859896 |
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| English | Glycogen storage disease due to acid maltase deficiency, juvenile onset |
Glycogen storage disease due to acid maltase deficiency, non-classical infantile onset, is form of glycogen storage disease due to acid maltase deficiency, a metabolic myopathy affecting respiratory and skeletal muscles that may fatally impede respiratory function during childhood. |
Statements
CID11:ID_1193859896
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dki-india-ID_1193859896
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Concluído
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15 August 2026
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