OMOP Concept 373747
Extrapyramidal disease
StandardConditionSNOMED76349003Disorder
Maps from
10
Descendants
359
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 Extrapyramidal disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 118407 | Extrapyramidal syndrome | Non-standard |
| Nebraska Lexicon | 76349003 | Extrapyramidal disorder | Non-standard |
| Read | F13..00 | Other extrapyramidal disease and abnormal movement disorders | Non-standard |
| Read | F13..11 | Extrapyramidal disease excluding Parkinson's disease | Non-standard |
| Read | F13z.00 | Other and unspecified extrapyramidal diseases and abnormal movement disorders | Non-standard |
| Read | F13z000 | Unspecified extrapyramidal disease | Non-standard |
| Read | F13zz00 | Extrapyramidal disease and abnormal movement disorder NOS | Non-standard |
| Read | Fyu2.00 | [X]Extrapyramidal and movement disorders | Non-standard |
| Read | Fyu2700 | [X]Other specified extrapyramidal and movement disorders | Non-standard |
| Read | Fyu2800 | [X]Extrapyramidal and movement disorders in diseases classified elsewhere | Non-standard |
Synonyms
Alternative names recorded for Extrapyramidal disease across source vocabularies.
- enfermedad extrapiramidal
- enfermedad extrapiramidal (trastorno)
- Extrapyramidal disease (disorder)
- Extrapyramidal disorder
- trastorno extrapiramidal
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
Narrower concepts
(359)Included automatically when you query with descendants.
- 1Aase Smith type 1 syndrome
- 1Athetosis
- 1Benedikt's syndrome
- 1Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
- 1Chorea
- 1Combined pyramidal-extrapyramidal syndrome
- 1Congenital pontocerebellar hypoplasia type 12
- 1Corticobasal degeneration
- 1Diffuse Lewy body disease
- 1Dyssynergia cerebellaris myoclonica
- 1Dystonia
- 1Electric chorea
- 1Exacerbation of extrapyramidal disease
- 1Familial essential myoclonus
- 1Gilles de la Tourette's syndrome
- 1Hemiballism
- 1Juvenile cerebellar degeneration AND myoclonus
- 1Macrocephaly, short stature, paraplegia syndrome
- 1McLeod neuroacanthocytosis syndrome
- 1Myoclonus, cerebellar ataxia, deafness syndrome
- 1Neuroleptic malignant syndrome
- 1Non-spastic cerebral palsy
- 1Olivopontocerebellar degeneration
- 1Opticocochleodentate degeneration
- 1Orofacial dyskinesia
- 1Pallidonigroluysian degeneration
- 1Paramyoclonus multiplex
- 1Parkinsonism
- 1Progressive cerebellar tremor
- 1Progressive pyramidopallidal degeneration
- 1Progressive supranuclear ophthalmoplegia
- 1Proximal myopathy with extrapyramidal signs
- 1Woodhouse Sakati syndrome
- 2Acquired choreiform dyspraxia
- 2Adult-onset dystonia parkinsonism
- 2Amyotrophic lateral sclerosis, parkinsonism, dementia complex
- 2Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula
- 2Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea
- 2Amyotrophic lateral sclerosis with parkinsonism
- 2Ataxia telangiectasia variant
- 2Ataxic cerebral palsy
- 2Athetoid cerebral palsy
- 2Athetosis with rigidity
- 2Athetosis with spastic paraplegia
- 2ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
- 2Atypical Parkinsonism
- 2Autosomal dominant striatal neurodegeneration
- 2Basal ganglia degeneration with calcification
- 2Benign hereditary chorea
- 2Birnbaum's syndrome
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