OMOP Concept 4047737
Facioscapulohumeral spinal muscular atrophy
StandardConditionSNOMED230249003Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Facioscapulohumeral spinal muscular atrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 230249003 | Facioscapulohumeral spinal muscular atrophy | Non-standard |
Synonyms
Alternative names recorded for Facioscapulohumeral spinal muscular atrophy across source vocabularies.
- atrofia muscular espinal facioescapulohumeral
- atrofia muscular espinal facioescapulohumeral (trastorno)
- Facioscapulohumeral spinal muscular atrophy (disorder)
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.
- 1Spinal muscular atrophy
- 2Chronic nervous system disorder
- 2Hereditary motor neuron disease
- 2Lower motor neuron disease
- 3Chronic disease
- 3Disorder of nervous system
- 3Hereditary disorder of nervous system
- 3Motor neuron disease
- 4Disease
- 4Disorder of body system
- 4Hereditary disorder by system
- 5Clinical finding
- 5Hereditary disease
- 6Genetic disease
Narrower concepts
(1)Included automatically when you query with descendants.
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