OMOP Concept 4046079
Distal spinal muscular atrophy
StandardConditionSNOMED230247001Disorder
Maps from
2
Descendants
8
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Distal spinal muscular atrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141876 | Distal spinal muscular atrophy | Non-standard |
| Nebraska Lexicon | 230247001 | Distal spinal muscular atrophy | Non-standard |
Synonyms
Alternative names recorded for Distal spinal muscular atrophy across source vocabularies.
- atrofia muscular espinal distal
- atrofia muscular espinal distal (trastorno)
- Distal 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
(8)Included automatically when you query with descendants.
- 1Autosomal dominant congenital benign spinal muscular atrophy
- 1Autosomal recessive lower motor neuron disease with childhood onset
- 1Distal hereditary motor neuropathy type 1
- 1Distal hereditary motor neuropathy type 7
- 1Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
- 1Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
- 1Spinal muscular atrophy with respiratory distress type 2
- 1X-linked distal spinal muscular atrophy type 3
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