OMOP Concept 37110884
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
StandardConditionSNOMED725408001Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537308 | Spinocerebellar ataxia, autosomal recessive 1 | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 across source vocabularies.
- AOA2 - ataxia oculomotor apraxia type 2
- ataxia cerebelosa autosómica recesiva con apraxia oculomotriz tipo 2
- ataxia cerebelosa autosómica recesiva con apraxia oculomotriz tipo 2 (trastorno)
- Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder)
- SCAR1 - spinocerebellar ataxia autosomal recessive 1
- Spinocerebellar ataxia with axonal neuropathy type 2
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cerebellar ataxia
- 1Hereditary ataxia
- 1Hereditary disorder of the visual system
- 1Oculomotor apraxia
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Cerebellar disorder
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Strabismus
- 2Visual system disorder
- 3Disorder of body system
- 3Disorder of brain
- 3Disorder of eye movements
- 3Disorder of nervous system
- 3Eye / vision finding
- 3Finding related to coordination / incoordination
- 3Hereditary disease
- 4Clinical finding
- 4Disease
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 4Genetic disease
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