Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency (Q100848)
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Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_273845529 |
||
| English | Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency |
Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance. |
Statements
CID11:ID_273845529
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dki-india-ID_273845529
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Concluído
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15 August 2026
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