OMOP Concept 4246087
Glycogen storage disease, hepatic form
StandardConditionSNOMED6075009Disorder
Maps from
2
Descendants
7
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Glycogen storage disease, hepatic form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139366 | Glycogen storage disease, hepatic form | Non-standard |
| HPO | HP_0500030 | Abnormal hepatic glycogen storage | Non-standard |
Synonyms
Alternative names recorded for Glycogen storage disease, hepatic form across source vocabularies.
- glucogenosis, forma hepática
- glucogenosis, forma hepática (trastorno)
- Glycogen storage disease, hepatic form (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Digestive system hereditary disorder
- 1Disorder of digestive system specific to fetus OR newborn
- 1Glycogen storage disease
- 1Metabolic and genetic disorder affecting the liver
- 2Disease of liver
- 2Disorder of carbohydrate metabolism
- 2Disorder of digestive system
- 2Fetal and/or neonatal disorder
- 2Hereditary disorder by system
- 2Metabolic disease
- 2Storage disease
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of liver and/or biliary tract
- 3Hereditary disease
- 3Inborn error of metabolism
- 3Liver finding
- 3OMOP Acute Liver Failure 1
- 3OMOP Acute Liver Failure 2
- 3OMOP Acute Liver Failure 8
- 4Abdominal organ finding
- 4Clinical finding
- 4Congenital disease
- 4Disorder of abdomen
Showing 25 of 34. Retrieve the full set via the API.
Narrower concepts
(7)Included automatically when you query with descendants.
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