Preferred Name | Huntington Disease [Disease/Finding] | |
Synonyms |
Progressive Chorea, Chronic Hereditary (Huntington) Huntington Chorea Huntington's Disease Huntington's Chorea Huntington Disease Chorea, Chronic Progressive Hereditary (Huntington) Huntington Chronic Progressive Hereditary Chorea Chronic Progressive Hereditary Chorea (Huntington) Progressive Chorea, Hereditary, Chronic (Huntington) |
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ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001558 |
|
altLabel |
Progressive Chorea, Chronic Hereditary (Huntington) Huntington Chorea Huntington's Disease Huntington's Chorea Huntington Disease Chorea, Chronic Progressive Hereditary (Huntington) Huntington Chronic Progressive Hereditary Chorea Chronic Progressive Hereditary Chorea (Huntington) Progressive Chorea, Hereditary, Chronic (Huntington) |
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cui |
C0020179 |
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May be treated by |
http://purl.bioontology.org/ontology/NDFRT/N0000164994 http://purl.bioontology.org/ontology/NDFRT/N0000186716 http://purl.bioontology.org/ontology/NDFRT/N0000146801 http://purl.bioontology.org/ontology/NDFRT/N0000186715 http://purl.bioontology.org/ontology/NDFRT/N0000152645 http://purl.bioontology.org/ontology/NDFRT/N0000148739 http://purl.bioontology.org/ontology/NDFRT/N0000163667 http://purl.bioontology.org/ontology/NDFRT/N0000163767 http://purl.bioontology.org/ontology/NDFRT/N0000152648 http://purl.bioontology.org/ontology/NDFRT/N0000154578 http://purl.bioontology.org/ontology/NDFRT/N0000154581 http://purl.bioontology.org/ontology/NDFRT/N0000177920 http://purl.bioontology.org/ontology/NDFRT/N0000178242 http://purl.bioontology.org/ontology/NDFRT/N0000162670 http://purl.bioontology.org/ontology/NDFRT/N0000152643 http://purl.bioontology.org/ontology/NDFRT/N0000161687 http://purl.bioontology.org/ontology/NDFRT/N0000146289 http://purl.bioontology.org/ontology/NDFRT/N0000186714 http://purl.bioontology.org/ontology/NDFRT/N0000191690 http://purl.bioontology.org/ontology/NDFRT/N0000178243 http://purl.bioontology.org/ontology/NDFRT/N0000146719 http://purl.bioontology.org/ontology/NDFRT/N0000188187 http://purl.bioontology.org/ontology/NDFRT/N0000152644 http://purl.bioontology.org/ontology/NDFRT/N0000153013 |
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MESH DEFINITION |
A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) |
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MESH DUI |
D006816 |
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MeSH name |
Huntington Disease |
|
MESH UI |
M0010660 |
|
NDFRT kind |
DISEASE_KIND |
|
notation |
N0000001558 |
|
NUI |
N0000001558 |
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prefLabel |
Huntington Disease [Disease/Finding] |
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SNOMED CID |
58756001 |
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tui |
T047 |
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subClassOf |