Glycogen storage disease due to muscle phosphoglycerate mutase deficiency (Q84788): Difference between revisions
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A deficiência de fosfoglicerato mutase muscular é uma miopatia metabólica caracterizada por cãimbras induzidas por exercício, mioglobinúria e presença de agregados tubulares na biópsia muscular. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/357512951 / rank | |||||||||||||||
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CID11:ID_357512951 | |||||||||||||||
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dki-india-ID_357512951 | |||||||||||||||
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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 10:08, 15 August 2026
Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_357512951 |
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| English | Glycogen storage disease due to muscle phosphoglycerate mutase deficiency |
Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy characterised by exercise-induced cramp, myoglobinuria, and presence of tubular aggregates in the muscle biopsy. |
Statements
CID11:ID_357512951
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dki-india-ID_357512951
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Concluído
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13 August 2026
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