OMOP Concept 37162961
Amyotrophic lateral sclerosis type 3
StandardConditionSNOMED1201950008Disorder
Maps from
1
Descendants
0
Valid from
28 Feb 2022
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Amyotrophic lateral sclerosis type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564688 | Amyotrophic Lateral Sclerosis 3 | Non-standard |
Synonyms
Alternative names recorded for Amyotrophic lateral sclerosis type 3 across source vocabularies.
- ALS3 - amyotrophic lateral sclerosis type 3
- Amyotrophic lateral sclerosis type 3 (disorder)
- ELA (esclerosis lateral amiotrófica) tipo 3
- ELA tipo 3
- esclerosis lateral amiotrófica tipo 3
- esclerosis lateral amiotrófica tipo 3 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Amyotrophic lateral sclerosis
- 1Autosomal dominant hereditary disorder
- 1Chronic nervous system disorder
- 1Degenerative disorder
- 1Hereditary disorder of nervous system
- 2Autosomal hereditary disorder
- 2Chronic disease
- 2Disease
- 2Disorder of nervous system
- 2Hereditary disorder by system
- 2Motor neuron disease
- 3Clinical finding
- 3Disorder of body system
- 3Hereditary disease
- 4Genetic disease
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