OMOP Concept 4077298
Juvenile GM1 gangliosidosis
StandardConditionSNOMED18756002Disorder
Maps from
1
Descendants
0
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 Juvenile GM1 gangliosidosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136376 | Juvenile GM>1< gangliosidosis | Non-standard |
Synonyms
Alternative names recorded for Juvenile GM1 gangliosidosis across source vocabularies.
- gangliosidosis GM1 juvenil
- gangliosidosis GM>1< juvenil
- gangliosidosis GM1 juvenil (trastorno)
- gangliosidosis GM>1<, tipo 2
- gangliosidosis GM1, tipo 2
- gangliosidosis GM1 tipo II
- gangliosidosis GM<sub>1</sub> juvenil
- gangliosidosis GM<sub>1</sub>, tipo 2
- GM1 gangliosidosis, type 2
- GM1 Gangliosidosis type II
- Juvenile GM1 gangliosidosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1GM1 gangliosidosis
- 2Autosomal recessive hereditary disorder
- 2Developmental hereditary disorder
- 2Dysostosis multiplex group
- 2Gangliosidosis
- 2Hereditary disorder of musculoskeletal system
- 3Autosomal hereditary disorder
- 3Congenital anomaly of skeletal bone
- 3Developmental disorder
- 3Disorder of lipid storage and metabolism
- 3Disorder of lysosomal enzyme
- 3Disorder of musculoskeletal system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Inherited metabolic disorder of nervous system
- 3Lesion of bone
- 3Lysosomal storage disease
- 3Metabolic bone disease
- 3Skeletal dysplasia
- 4Congenital anomaly of musculoskeletal system
- 4Congenital disease
- 4Disease
- 4Disorder of body system
- 4Disorder of bone
- 4Disorder of bone development
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