OMOP Concept 4266669
Infantile GM2 gangliosidosis
StandardConditionSNOMED62440002Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Infantile GM2 gangliosidosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 137545 | Infantile GM2 gangliosidosis | Non-standard |
Synonyms
Alternative names recorded for Infantile GM2 gangliosidosis across source vocabularies.
- gangliosidosis GM 2 infantil
- gangliosidosis GM 2 infantil (trastorno)
- Infantile GM2 gangliosidosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1GM2 gangliosidosis
- 2Gangliosidosis
- 3Disorder of lipid storage and metabolism
- 3Disorder of lysosomal enzyme
- 3Inherited metabolic disorder of nervous system
- 3Lysosomal storage disease
- 4Congenital disease
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Enzymopathy
- 4Hereditary disorder of nervous system
- 4Inborn error of metabolism
- 4Storage disease
- 5Disorder of nervous system
- 5Fetal and/or neonatal disorder
- 5Hereditary disorder by system
- 5Hereditary metabolic disease
- 5Metabolic disease
- 6Disease
- 6Disorder of body system
- 6Hereditary disease
- 7Clinical finding
- 7Genetic disease
Narrower concepts
(1)Included automatically when you query with descendants.
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