Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Q84807): Difference between revisions
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Revision as of 10:09, 15 August 2026
Phosphoglycerate kinase (PGK) deficiency is an inborn error of metabolism characterised by variable combinations of nonspherocytic haemolytic anaemia, myopathy, and various central nervous system abnormalities.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1396572570 |
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| English | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency |
Phosphoglycerate kinase (PGK) deficiency is an inborn error of metabolism characterised by variable combinations of nonspherocytic haemolytic anaemia, myopathy, and various central nervous system abnormalities. |
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CID11:ID_1396572570
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