OMOP Concept 435242
Cerebellar ataxia
StandardConditionSNOMED85102008Disorder
Maps from
7
Descendants
150
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Cerebellar ataxia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 118792 | Cerebellar Dysmetria | Non-standard |
| CIEL | 120816 | Cerebellar ataxia | Non-standard |
| ICD10CM | G32.81 | Cerebellar ataxia in diseases classified elsewhere | Non-standard |
| ICD9CM | 334.3 | Other cerebellar ataxia | Non-standard |
| MeSH | D002524 | Cerebellar Ataxia | Non-standard |
| OXMIS | 3479AF | CEREBELLAR ATAXIA | Non-standard |
| Read | F143.00 | Cerebellar ataxia NOS | Non-standard |
Synonyms
Alternative names recorded for Cerebellar ataxia across source vocabularies.
- ataxia cerebelosa
- ataxia cerebelosa (trastorno)
- Cerebellar ataxia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
Narrower concepts
(150)Included automatically when you query with descendants.
- 1Acute cerebellar ataxia
- 1Acute cerebellar ataxia caused by varicella
- 1Ataxia pancytopenia syndrome
- 1Ataxia with deafness and intellectual disability syndrome
- 1Ataxia with tapetoretinal degeneration syndrome
- 1Ataxic cerebral palsy
- 1Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
- 1Autosomal dominant cerebellar ataxia type 2
- 1Autosomal recessive ataxia due to ubiquinone deficiency
- 1Autosomal recessive cerebellar ataxia Beauce type
- 1Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
- 1Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
- 1Autosomal recessive cerebellar ataxia with late-onset spasticity
- 1Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
- 1Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
- 1Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
- 1Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
- 1Autosomal recessive spastic ataxia with leukoencephalopathy
- 1Boucher Neuhäuser syndrome
- 1Cerebellar ataxia and ectodermal dysplasia
- 1Cerebellar ataxia associated with another disorder
- 1Cerebellar ataxia caused by chemical
- 1Cerebellar ataxia Cayman type
Showing 25 of 150. Retrieve the full set via the API.
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