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Cell Culture Ontology
Last uploaded:
July 23, 2014
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| Id | http://www.orpha.net/ORDO/Orphanet_399
http://www.orpha.net/ORDO/Orphanet_399
|
|---|---|
| Preferred Name | obsolete_Huntington disease |
| Definitions |
Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.
|
| Synonyms |
Huntington chorea
Huntington's disease
|
| Obsolete | true |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition_citation | orphanet |
|---|---|
| definition | Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia. |
| preferred label |
obsolete_Huntington disease
|
| label |
obsolete_Huntington disease
|
| prefLabel |
obsolete_Huntington disease
|
| database_cross_reference |
OMIM:143100
UMLS:C0020179
MedDRA:10070668
MeSH:D006816
ICD10:G10
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| reason_for_obsolescence |
Replaced with Mondo term.
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| subClassOf | |
| obsoleted_in_version |
3.41.0
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| deprecated |
true
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| type | |
| term replaced by | |
| has_exact_synonym |
Huntington chorea
Huntington's disease
|
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