OMOP Concept 37162949
Amyotrophic lateral sclerosis type 1
StandardConditionSNOMED1201863001Disorder
Maps from
1
Descendants
2
Valid from
28 Feb 2022
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Amyotrophic lateral sclerosis type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C531617 | Amyotrophic lateral sclerosis 1 | Non-standard |
Synonyms
Alternative names recorded for Amyotrophic lateral sclerosis type 1 across source vocabularies.
- ALS1 - amyotrophic lateral sclerosis type 1
- ALS (amyotrophic lateral sclerosis) type 1
- Amyotrophic lateral sclerosis type 1 (disorder)
- ELA (esclerosis lateral amiotrófica) tipo 1
- ELA tipo 1
- esclerosis lateral amiotrófica tipo 1
- esclerosis lateral amiotrófica tipo 1 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Amyotrophic lateral sclerosis
- 1Autosomal hereditary disorder
- 1Chronic nervous system disorder
- 1Degenerative disorder
- 1Hereditary disorder of nervous system
- 2Chronic disease
- 2Disease
- 2Disorder of nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Motor neuron disease
- 3Clinical finding
- 3Disorder of body system
- 3Genetic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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