OMOP Concept 4284550
Glycogen storage disease type III
StandardConditionSNOMED66937008Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Glycogen storage disease type III via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139369 | Glycogen storage disease type III | Non-standard |
| ICD10CM | E74.03 | Cori disease | Non-standard |
| MeSH | D006010 | Glycogen Storage Disease Type III | Non-standard |
| Nebraska Lexicon | 66937008 | Amylo-1,6-glucosidase deficiency | Non-standard |
Synonyms
Alternative names recorded for Glycogen storage disease type III across source vocabularies.
- Amylo-1,6-glucosidase deficiency
- Cori disease
- Cori's disease
- Debrancher deficiency glycogen storage disease
- Debrancher enzyme deficiency
- dextrinosis límite
- enfermedad de Cori
- enfermedad de Forbes
- enfermedad por depósito de glucógeno de tipo III
- enfermedad por depósito de glucógeno de tipo III (trastorno)
- glucogenosis tipo III
- Glycogen storage disease type 3
- Glycogen storage disease, type III
- Glycogen storage disease, type III (disorder)
- GSD III
- Limit dextrin - glycogen
- Limit dextrinosis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Glycogen storage disease, hepatic form
- 1Glycogen storage disease, muscular form
- 2Digestive system hereditary disorder
- 2Disorder of digestive system specific to fetus OR newborn
- 2Glycogen storage disease
- 2Hereditary disorder of musculoskeletal system
- 2Metabolic and genetic disorder affecting the liver
- 2Metabolic myopathy
- 3Disease of liver
- 3Disorder of carbohydrate metabolism
- 3Disorder of digestive system
- 3Disorder of fetus and/or newborn
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal muscle
- 3Hereditary disorder by system
- 3Metabolic disease
- 3Storage disease
- 4Digestive system finding
- 4Disease
- 4Disorder of body system
- 4Disorder of liver and/or biliary tract
- 4Disorder of muscle
- 4Disorder of soft tissue
- 4Hereditary disease
- 4Inborn error of metabolism
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