OMOP Concept 36676853
Polyglucosan body myopathy type 1
StandardConditionSNOMED774148007Disorder
Maps from
0
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Polyglucosan body myopathy type 1 across source vocabularies.
- miopatía con cuerpos de poliglucosano tipo 1
- miopatía con cuerpos de poliglucosano tipo 1 (trastorno)
- PGBM1 - polyglucosan body myopathy type 1
- Polyglucosan body myopathy type 1 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cardiomyopathy
- 1Cardiovascular system hereditary disorder
- 1Glycogen storage disease
- 1Hereditary disorder of musculoskeletal system
- 1Metabolic myopathy
- 2Autosomal hereditary disorder
- 2Disorder of carbohydrate metabolism
- 2Disorder of cardiovascular system
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal muscle
- 2Hereditary disorder by system
- 2Myocardial disease
- 2Storage disease
- 3Cardiovascular finding
- 3Disorder of body system
- 3Disorder of muscle
- 3Disorder of soft tissue
- 3Heart disease
- 3Hereditary disease
- 3Inborn error of metabolism
- 3Metabolic disease
- 3Musculoskeletal finding
- 3Myocardial finding
- 4Cardiac finding
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