OMOP Concept 36715523
Huntington disease-like 2
StandardConditionSNOMED721228006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Huntington disease-like 2 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564708 | Huntington Disease-Like 2 | Non-standard |
| Nebraska Lexicon | 721228006 | Huntington disease-like 2 | Non-standard |
Synonyms
Alternative names recorded for Huntington disease-like 2 across source vocabularies.
- enfermedad similar a Huntington tipo 2
- enfermedad similar a Huntington tipo 2 (trastorno)
- Huntington disease-like 2 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Cerebral degeneration
- 1Hereditary degenerative disease of central nervous system
- 1Huntington disease-like syndrome
- 2Autosomal hereditary disorder
- 2Chorea
- 2Degenerative brain disorder
- 2Degenerative disease of the central nervous system
- 2Hereditary disorder of nervous system
- 3Degenerative disorder
- 3Disorder of basal ganglia
- 3Disorder of brain
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Extrapyramidal disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Involuntary movement
- 4Central nervous system finding
- 4Disease
- 4Disorder of body system
- 4Disorder of head
- 4Finding of brain
- 4Finding of head region
- 4Finding of movement
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