OMOP Concept 4050057
Glycogen storage disease, muscular form
StandardConditionSNOMED15978003Disorder
Maps from
1
Descendants
6
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Glycogen storage disease, muscular form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139365 | Glycogen Storage Disease, Muscular Form | Non-standard |
Synonyms
Alternative names recorded for Glycogen storage disease, muscular form across source vocabularies.
- glucogenosis, forma muscular
- glucogenosis, forma muscular (trastorno)
- Glycogen storage disease, muscular form (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Glycogen storage disease
- 1Hereditary disorder of musculoskeletal system
- 1Metabolic myopathy
- 2Disorder of carbohydrate metabolism
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal muscle
- 2Hereditary disorder by system
- 2Storage disease
- 3Disorder of body system
- 3Disorder of muscle
- 3Disorder of soft tissue
- 3Hereditary disease
- 3Inborn error of metabolism
- 3Metabolic disease
- 3Musculoskeletal finding
- 4Clinical finding
- 4Congenital disease
- 4Disease
- 4General finding of soft tissue
- 4Genetic disease
- 4Hereditary metabolic disease
- 4Muscle finding
- 5Fetal and/or neonatal disorder
Narrower concepts
(6)Included automatically when you query with descendants.
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