About: Huntington's disease-like syndrome

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Huntington's disease-like syndromes (HD-like syndromes, or HDL syndromes) are a family of inherited neurodegenerative diseases that closely resemble Huntington's disease (HD) in that they typically produce a combination of chorea, cognitive decline or dementia and behavioural or psychiatric problems.

Attributes	Values
rdf:type	Thing Disease disease
rdfs:label	Chorea-Huntington-ähnliches Syndrom (de) Huntington's disease-like syndrome (en)
rdfs:comment	Das Chorea-Huntington-ähnliche Syndrom ist eine Gruppe sehr seltener angeborener Gehirnerkrankungen, die klinisch der Chorea Huntington entsprechen, aber nicht deren Mutation aufweisen. Synonyme: Chorea-Huntington-ähnliche Erkrankung; englisch Huntington’s disease-like; HDL (de) Huntington's disease-like syndromes (HD-like syndromes, or HDL syndromes) are a family of inherited neurodegenerative diseases that closely resemble Huntington's disease (HD) in that they typically produce a combination of chorea, cognitive decline or dementia and behavioural or psychiatric problems. (en)
foaf:name	Huntington's disease-like syndrome (en)
name	Huntington's disease-like syndrome (en)
dcterms:subject	Extrapyramidal and movement disorders Huntington's disease Systemic atrophies primarily affecting the central nervous system Trinucleotide repeat disorders Genetic diseases and disorders Rare syndromes Autosomal dominant disorders
Wikipage page ID	50452056 (xsd:integer)
Wikipage revision ID	1094741952 (xsd:integer)
Link from a Wikipage to another Wikipage	Benign hereditary chorea Extrapyramidal and movement disorders Neuroacanthocytosis Dementia Huntington's disease Huntington's disease CAG repeat Systemic atrophies primarily affecting the central nervous system JPH3 Chorea Trinucleotide repeat disorders Friedreich's ataxia Autosomal dominant Autosomal recessive Wilson's disease Neuroferritinopathy Phenocopy Genetic diseases and disorders Dentatorubral-pallidoluysian atrophy PRNP Rare syndromes Autosomal dominant disorders C9orf72 Spinocerebellar ataxia Neurogenetic disorders Neurology Mitochondrial diseases Neurodegenerative diseases Octapeptide Prion disease
sameAs	Huntington's disease-like syndrome Huntington's disease-like syndrome Huntington's disease-like syndrome Huntington's disease-like syndrome Huntington's disease-like syndrome Huntington's disease-like syndrome
dbp:wikiPageUsesTemplate	dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist
DiseasesDB	335203352134626 (xsd:decimal)
OMIM	606438603218604800 (xsd:decimal)
field	Neurology
synonyms	HDL syndrome (en)
has abstract	Das Chorea-Huntington-ähnliche Syndrom ist eine Gruppe sehr seltener angeborener Gehirnerkrankungen, die klinisch der Chorea Huntington entsprechen, aber nicht deren Mutation aufweisen. Synonyme: Chorea-Huntington-ähnliche Erkrankung; englisch Huntington’s disease-like; HDL (de) Huntington's disease-like syndromes (HD-like syndromes, or HDL syndromes) are a family of inherited neurodegenerative diseases that closely resemble Huntington's disease (HD) in that they typically produce a combination of chorea, cognitive decline or dementia and behavioural or psychiatric problems. (en)
prov:wasDerivedFrom	wikipedia-en:Huntington's_disease-like_syndrome?oldid=1094741952&ns=0
page length (characters) of wiki page	4289 (xsd:nonNegativeInteger)
DiseasesDB	33520, 33521, 34626
OMIM id	606438603218604800 (xsd:decimal)
foaf:isPrimaryTopicOf	wikipedia-en:Huntington's_disease-like_syndrome
is Link from a Wikipage to another Wikipage of	Neuroacanthocytosis Huntington's disease Huntington's disease-like 2 Huntington’s disease-like 2 (HDL2) JPH3 Chorea HDL HD-like HD-like syndrome HDL-1 HDL-2 HDL-3 HDL1 HDL2 HD like syndromes List of syndromes Huntington's disease like syndromes Huntington's disease–like 2 Huntington disease-like syndrome Huntington disease-like syndromes Huntington disease like Huntington’s disease–like 2 (HDL2)
is Wikipage redirect of	Huntington's disease-like 2 Huntington’s disease-like 2 (HDL2) HD-like HD-like syndrome HDL-1 HDL-2 HDL-3 HDL1 HDL2

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