OMOP Concept 37205065
Autosomal recessive spastic ataxia with leukoencephalopathy
StandardConditionSNOMED784343003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive spastic ataxia with leukoencephalopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566956 | Ataxia, Spastic, 3, Autosomal Recessive | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive spastic ataxia with leukoencephalopathy across source vocabularies.
- ARSAL - autosomal recessive spastic ataxia with leucoencephalopathy
- ARSAL - autosomal recessive spastic ataxia with leukoencephalopathy
- ataxia espástica autosómica recesiva con leucoencefalopatía
- ataxia espástica autosómica recesiva con leucoencefalopatía (trastorno)
- Autosomal recessive spastic ataxia type 3
- Autosomal recessive spastic ataxia with leucoencephalopathy
- Autosomal recessive spastic ataxia with leukoencephalopathy (disorder)
- SPAX3 - autosomal recessive spastic ataxia type 3
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cerebellar ataxia
- 1Hereditary ataxia
- 1Leukoencephalopathy
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Cerebellar disorder
- 2Disorder of brain
- 2Finding of head region
- 2Hereditary disorder of nervous system
- 3Disorder of head
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Finding related to coordination / incoordination
- 3Head finding
- 3Hereditary disease
- 3Hereditary disorder by system
- 4Central nervous system finding
- 4Clinical finding
- 4Disease
- 4Disorder of body system
- 4Genetic disease
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