OMOP Concept 4239176
Dentatorubropallidoluysian degeneration
StandardConditionSNOMED68116008Disorder
Maps from
3
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Dentatorubropallidoluysian degeneration via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142579 | Dentatorubral-pallidoluysian atrophy | Non-standard |
| CIEL | 153958 | Dentatorubropallidoluysian atrophy | Non-standard |
| Nebraska Lexicon | 68116008 | Myoclonic epilepsy with choreoathetosis | Non-standard |
Synonyms
Alternative names recorded for Dentatorubropallidoluysian degeneration across source vocabularies.
- atrofia dentatorrubropalidoluisiana
- degeneración dentatorrubropalidoluisiana
- degeneración dentatorrubropalidoluisiana (trastorno)
- Dentatorubral-pallidoluysian atrophy
- Dentatorubral-pallidoluysian atrophy (DRPLA)
- Dentatorubropallidoluysian atrophy
- Dentatorubropallidoluysian degeneration (disorder)
- DRPLA - Dentatorubropallidoluysian atrophy
- Haw river syndrome
- Myoclonic epilepsy with choreoathetosis
- Naito-Oyanagi disease
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Cerebellar ataxia
- 1Chorea
- 1Hereditary ataxia
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Cerebellar disorder
- 2Disorder of basal ganglia
- 2Extrapyramidal disease
- 2Hereditary disorder of nervous system
- 2Involuntary movement
- 3Disorder of brain
- 3Disorder of nervous system
- 3Finding of head region
- 3Finding of movement
- 3Finding related to coordination / incoordination
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Movement disorder
- 4Clinical finding
- 4Disease
- 4Disorder of body system
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
Narrower concepts
(1)Included automatically when you query with descendants.
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