SHMARQL

Huntington's disease

<http://www.wikidata.org/entity/Q190564>

rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia
Huntington's disease
rdfs:label
"Huntington's disease"@en
skos:altLabel
"HD"@en
"Huntington Chorea"@en
"Huntington's chorea"@en
"Huntington’s disease"@en
schema:description
"rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia"@en
schema:dateModified "2026-11-05T18:03:56+00:00"^^xsd:dateTime
schema:version 2565097542
wikibase:identifiers 75
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wdt:P1036 "616.851"
wdt:P10376 "medicine-and-dentistry/huntingtons-disease"
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wdt:P10380 "huntingtons-disease"
wdt:P10565 "133276"
"57812"
wdt:P11143 "Huntington's disease"
"Huntington's_disease"
wdt:P11430 "DI-01754"
wdt:P1193 0.000123^^xsd:decimal
wdt:P1199 autosomal dominant
wdt:P12086 "Ziekte_van_Huntington"
wdt:P1325 <http://www.nanbyou.or.jp/entry/175>
wdt:P1343 The Unified Medical Dictionary (Librairie du Liban, 2009)
wdt:P13591 "concept/a4fb948d-34ae-4b97-9efd-5049d431b9cc"
wdt:P138 George Huntington
wdt:P1417 "science/Huntington-disease"
wdt:P14541 "17jBu0"
"3NTkXR"
wdt:P1461 "huntingtons-disease"
wdt:P14914 "D00399"
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wdt:P1748 "C82342"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Neuron%20with%20mHtt%20inclusion.jpg>
wdt:P1995 neurology
wdt:P2176 pimozide
ubidecarenone
tetrabenazine
(RS)-baclofen
perphenazine
wdt:P227 "4026223-6"
wdt:P2293 HTT
glucose transporter, type 3
wdt:P2347 "18497"
wdt:P244 "sh85063158"
wdt:P268 "12257151p"
wdt:P279 eye degenerative disease
trinucleotide repeat disorder
Huntington disease and related disorders
genetic neurodegenerative disease with dementia
wdt:P2841 childhood onset
juvenile onset
adult onset
late onset
wdt:P2888 <http://identifiers.org/doid/DOID:12858>
<http://purl.obolibrary.org/obo/DOID_12858>
<http://www.orpha.net/ORDO/Orphanet_248111>
<http://www.orpha.net/ORDO/Orphanet_399>
wdt:P2892 "C0020179"
wdt:P31 type of disease
symptom or sign
designated intractable/rare disease
rare disease
wdt:P3201 "10070668"
wdt:P3219 "maladie-de-huntington"
wdt:P3222 "huntingtons-sjukdom"
wdt:P3417 "Huntingtons-Disease"
wdt:P3471 "5248"
wdt:P373 "Huntington's disease"
wdt:P3827 "huntington-disease"
wdt:P3885 "huntington’s-disease"
wdt:P4229 "G10"
wdt:P4233 "huntington-s"
wdt:P4317 "6677"
wdt:P4527 "10821"
wdt:P486 "D006816"
wdt:P492 "143100"
wdt:P493 "333.4333.4,294.1294.1"
wdt:P494 "F02.2"
"G10"
wdt:P5008 WikiProject Medicine
wdt:P508 "55969"
wdt:P5082 "Huntingtons_sykdom"
wdt:P5270 "MONDO_0007739"
wdt:P557 "6060"
wdt:P575 "1872-04-13T00:00:00+00:00"^^xsd:dateTime
wdt:P604 "000770"
wdt:P61 George Huntington
wdt:P6366 "2910834379"
wdt:P646 "/m/0cvql"
wdt:P653 "PMH0001775"
wdt:P6532 hypokinesia
Inability to walk
Poor fine motor coordination
Degeneration of the striatum
Decreased body mass index
clonus
alcoholism
insomnia
compulsive behavior
abnormal reflex
depression
wdt:P665 "H00059"
wdt:P667 "P70"
wdt:P668 "NBK1305"
"NBK1529"
wdt:P672 "C10.228.140.079.545"
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"C10.574.500.497"
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"F03.615.250.400"
"F03.615.400.390"
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"289706"
"792600"
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wdt:P699 "DOID:12858"
wdt:P7033 "scot/11330"
wdt:P7329 "8A01.10"
wdt:P7464 "huntington-disease"
wdt:P780 choreatic disease
personality change
weight loss
dementia
wdt:P7807 "2132180242"
wdt:P7995 "huntingtons-disease"
wdt:P8168 "Q1213655"
wdt:P8189 "987007533753105171"
wdt:P828 trinucleotide repeat expansion
wdt:P8408 "HuntingtonsDisease"
wdt:P8669 "huntingtonova-choroba"
wdt:P910 Category:Huntington's disease
wdt:P923 genetic testing
wdt:P9322 "0324298-Huntingtonova-nemoc"
wdt:P950 "XX548572"
wdt:P973 <https://lirh.it/it/come-si-manifesta-la-malattia-di-huntington>
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