OMOP Concept 36713480
Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
StandardConditionSNOMED717821004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 717821004 | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | Non-standard |
Synonyms
Alternative names recorded for Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency across source vocabularies.
- enfermedad por almacenamiento de glucógeno con miocardiopatía severa debida a deficiencia de glucogenina
- enfermedad por almacenamiento de glucógeno con miocardiopatía severa debida a deficiencia de glucogenina (trastorno)
- enfermedad por almacenamiento de glucógeno tipo 15
- Glycogenosis with severe cardiomyopathy due to glycogenin deficiency
- Glycogen storage disease type 15
- Glycogen storage disease type XV
- Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Glycogen storage disease
- 2Autosomal hereditary disorder
- 2Disorder of carbohydrate metabolism
- 2Storage disease
- 3Hereditary disease
- 3Inborn error of metabolism
- 3Metabolic disease
- 4Congenital disease
- 4Disease
- 4Genetic disease
- 4Hereditary metabolic disease
- 5Clinical finding
- 5Disorder of fetus and/or newborn
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