About: nervous system heredodegenerative disease

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human disease

Attributes	Values
rdf:type	Item
description	Human disease (en) хвороба людини (uk) مرض يصيب الإنسان (ar)
exact match	wds:Q19001236-BDC6F848-415D-4694-BE71-A0881D2AB469
health specialty	wds:Q19001236-7D6EC269-C473-4B63-9F78-D27E2EE3C2A3
Mondo ID	wds:Q19001236-746D2D6A-D5DB-4A9E-94D0-5325DF1D6115
Disease Ontology ID	wds:Q19001236-6E6DB53C-0373-433F-A09E-BF748BC2D4D2
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0024237
health specialty	neurology
Mondo ID	MONDO_0024237
rdfs:label	مرض الجهاز العصبي الوراثي التنكسي (ar) enfermedad genética neurodegenerativa (es) heredebla neŭrodegenera malsano (eo) heredodegenerativ sjukdom i nervesystemet (nn) heterodegenerativna bolezen živčevja (sl) maladies neurodégénératives héréditaires (fr) malaltia neurodegenerativa hereditària (ca) nervous system heredodegenerative disease (en)
skos:prefLabel	مرض الجهاز العصبي الوراثي التنكسي (ar) enfermedad genética neurodegenerativa (es) heredebla neŭrodegenera malsano (eo) heredodegenerativ sjukdom i nervesystemet (nn) heterodegenerativna bolezen živčevja (sl) maladies neurodégénératives héréditaires (fr) malaltia neurodegenerativa hereditària (ca) nervous system heredodegenerative disease (en)
name	مرض الجهاز العصبي الوراثي التنكسي (ar) enfermedad genética neurodegenerativa (es) heredebla neŭrodegenera malsano (eo) heredodegenerativ sjukdom i nervesystemet (nn) heterodegenerativna bolezen živčevja (sl) maladies neurodégénératives héréditaires (fr) malaltia neurodegenerativa hereditària (ca) nervous system heredodegenerative disease (en)
instance of	wds:Q19001236-F838B82D-E9D9-4066-AADD-EB873E52AC5B
instance of	class of disease
subclass of	wds:Q19001236-0F8397B5-95F1-493B-B10B-FC6B9B86E58C wds:Q19001236-57A4F635-8C32-4FAA-B8BC-096DB3B2E6D0 wds:Q19001236-7C7A54DD-BAC8-40C5-B3CE-F8ECA51A6338
subclass of	genetic disease neurodegeneration genetic nervous system disorder
Orphanet ID	wds:Q19001236-E2267B21-9A02-4A63-B1DE-F57BE697883F
Orphanet ID	183500
skos:altLabel	affections dégénératives héréditaires du système nerveux (fr) Hereditary Neurodegenerative Disorder (en) Heredodegenerative Disorders, Nervous System (en) arveleg nevrodegenerativ sjukdom (nn) enfermedad neurodegenerativa genética (es) genetic neurodegenerative disease (en) hereditary neurodegenerative disease (en) hereditær nevrogenerativ sjukdom (nn) heredonevrodegenerativ sjukdom (nn) inherited neurodegenerative disorder (en) maladie neurodégénérative génétique (fr)
NCI Thesaurus ID	wds:Q19001236-00029890-5A4A-4206-9E26-E70BB2ED61BF
UMLS CUI	wds:Q19001236-1216D45A-2B92-4DF2-A4F1-185994A049E7 wds:Q19001236-16F893A5-E694-4F9E-8824-C17C44295199 wds:Q19001236-E0FB23C3-A526-40E5-A8A4-CF5A5D41CA8F
MeSH descriptor ID	wds:Q19001236-6A84B75F-84AA-403B-BE54-6E337F3ED28C
on focus list of Wikimedia project	wds:Q19001236-C5B45152-6687-42D9-A0C3-90887CDB7483
MeSH tree code	wds:Q19001236-43848C8C-E2C0-4933-86D1-8DD942635036 wds:Q19001236-E3248A3B-0F54-4EA0-84DC-73BDC9A6C50D
KBpedia ID	wds:Q19001236-C1FD8596-7E94-4EFE-BDAD-EEB77BAE0930
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D020271
MeSH tree code	http://id.nlm.nih.gov/mesh/C10.574.500 http://id.nlm.nih.gov/mesh/C16.320.400
KBpedia ID	rc:NervousSystemHeredodegenerativeDisease
NCI Thesaurus ID	C97073
UMLS CUI	C0751870 C3273225 C5680568
MeSH descriptor ID	D020271
on focus list of Wikimedia project	WikiProject Medicine
MeSH tree code	C10.574.500 C16.320.400
KBpedia ID	NervousSystemHeredodegenerativeDisease
is owl:sameAs of	nervous system heredodegenerative disease nervous system heredodegenerative disease nervous system heredodegenerative disease
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q19001236
is subclass of of	myoclonic cerebellar dyssynergia hereditary spastic paraplegia Huntington's disease-like syndrome Lafora disease spinocerebellar ataxia X-linked adrenoleukodystrophy Niemann–Pick disease, type C EAST syndrome Allan-Herndon-Dudley syndrome normal pressure hydrocephalus Stickler syndrome autosomal recessive distal spinal muscular atrophy 2 autosomal recessive cerebellar ataxia PEHO syndrome pantothenate kinase-associated neurodegeneration non-syndromic pontocerebellar hypoplasia Kennedy disease lateral sclerosis

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