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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1396572570 / rank | |||||||||||||||
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CID11:ID_1396572570 | |||||||||||||||
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dki-india-ID_1396572570 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest 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. |
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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