OMOP Concept 4041682
Late onset cerebellar ataxia
StandardConditionSNOMED230232005Disorder
Maps from
10
Descendants
19
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
10 source codes normalize to Late onset cerebellar ataxia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136031 | Late onset cerebellar ataxia | Non-standard |
| CIM10 | G11.2 | Late-onset cerebellar ataxia | Non-standard |
| ICD10 | G11.2 | Late-onset cerebellar ataxia | Non-standard |
| ICD10CM | G11.2 | Late-onset cerebellar ataxia | Non-standard |
| ICD10CN | G11.2 | Late-onset cerebellar ataxia | Non-standard |
| ICD10CN | G11.200 | Late-onset cerebellar ataxia | Non-standard |
| ICD10CN | G11.201 | Mary ataxia (machine translation) | Non-standard |
| ICD10GM | G11.2 | Late-onset cerebellar ataxia | Non-standard |
| KCD7 | G11.2 | Late-onset cerebellar ataxia | Non-standard |
| Nebraska Lexicon | 230232005 | Late onset cerebellar ataxia | Non-standard |
Synonyms
Alternative names recorded for Late onset cerebellar ataxia across source vocabularies.
- ataxia cerebelosa de inicio tardío
- ataxia cerebelosa de inicio tardío (trastorno)
- Late onset cerebellar ataxia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(19)Included automatically when you query with descendants.
- 1Autosomal recessive cerebellar ataxia Beauce type
- 1Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
- 1Azorean disease
- 1Olivopontocerebellar degeneration
- 1Periodic ataxia
- 1Progressive cerebellar ataxia
- 1Progressive cerebellar ataxia with palatal myoclonus
- 1Progressive spinocerebellar ataxia with decreased tendon reflexes
- 1Progressive spinocerebellar ataxia with retained tendon reflexes
- 1Sporadic adult-onset ataxia of unknown etiology
- 2Azorean disease, type I
- 2Azorean disease, type II
- 2Azorean disease, type III
- 2Azorean disease, type IV
- 2Olivopontocerebellar atrophy and deafness
- 2Olivopontocerebellar atrophy with blindness
- 2Olivopontocerebellar atrophy with slow eye movement
- 2Progressive cerebellar ataxia with hypogonadism
- 2Sporadic olivopontocerebellar atrophy
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