Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Q84807)
From determinar.ia.br - Determine suas informações
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 |
|---|---|---|---|
| default for all languages | ID_1396572570 |
||
| 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. |
Statements
CID11:ID_1396572570
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dki-india-ID_1396572570
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Concluído
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13 August 2026
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