Glycogen storage disease due to glycogenin deficiency (Q84802): Difference between revisions
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Revision as of 10:09, 15 August 2026
Glycogen storage disease type 15 is an extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal muscle.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_623301128 |
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| English | Glycogen storage disease due to glycogenin deficiency |
Glycogen storage disease type 15 is an extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal muscle. |
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CID11:ID_623301128
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