OMOP Concept 3655320
Glycogen storage disease type IXB
StandardConditionSNOMED860860004Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2020
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Glycogen storage disease type IXB via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563008 | Glycogen Storage Disease IXB | Non-standard |
Synonyms
Alternative names recorded for Glycogen storage disease type IXB across source vocabularies.
- enfermedad por almacenamiento de glucógeno tipo IXB
- enfermedad por almacenamiento de glucógeno tipo IXB (trastorno)
- Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency
- Glycogen storage disease type IXB (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.
- 1Glycogen phosphorylase kinase deficiency
- 2Digestive system hereditary disorder
- 2Disease of liver
- 2Disorder of digestive system specific to fetus OR newborn
- 2Glycogen storage disease
- 3Disorder of carbohydrate metabolism
- 3Disorder of digestive system
- 3Disorder of fetus and/or newborn
- 3Disorder of liver and/or biliary tract
- 3Hereditary disorder by system
- 3Liver finding
- 3OMOP Acute Liver Failure 1
- 3OMOP Acute Liver Failure 2
- 3OMOP Acute Liver Failure 8
- 3Storage disease
- 4Abdominal organ finding
- 4Digestive system finding
- 4Disease
- 4Disorder of abdomen
- 4Disorder of body system
- 4Disorder of digestive organ
- 4Hereditary disease
- 4Inborn error of metabolism
- 4Metabolic disease
- 5Clinical finding
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