Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Q84807): Difference between revisions
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A deficiência de fosfoglicerato quinase é um erro inato do metabolismo caracterizado por combinações variadas de anemia hemolítica não esferocítica, miopatia e várias anormalidades do sistema nervoso central. | |||
| description / en | description / en | ||
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. | |||
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 |
|---|---|---|---|
| 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. |
