SHMARQL

central nervous system vascular malformation

<http://www.wikidata.org/entity/Q54945930>

congenital, inherited, or acquired abnormalities involving arteries, veins or venous sinuses in the brain, spinal cord and meninges
rdfs:label
"central nervous system vascular malformation"@en
skos:altLabel "central nervous system vascular malformations"@en
"neurovascular malformation"@en
schema:description "congenital, inherited, or acquired abnormalities involving arteries, veins or venous sinuses in the brain, spinal cord and meninges"@en
schema:dateModified "2026-10-23T23:19:16+00:00"^^xsd:dateTime
schema:version 2560152460
wikibase:identifiers 9
wikibase:sitelinks 0
wikibase:statements 18
p:P14914 wd:statement/Q54945930-AC00EE66-F107-4BA8-A3AF-A299B2D02223
p:P1550 wd:statement/Q54945930-736D51BE-463A-40E9-8565-6D81B5A03BC8
p:P1995 wd:statement/Q54945930-02560332-8A22-48A8-9170-2402363D4CB8
wd:statement/Q54945930-1B606030-11EF-42C6-91AF-1B4CE2D39B43
p:P279 wd:statement/Q54945930-7159d1bc-4a27-8aba-2831-534ec71f42d3
wd:statement/Q54945930-92F42192-C180-4194-B203-6874DB5A4EE0
wd:statement/Q54945930-FBE24C06-D08F-44EA-A9F7-E67FBFB539EE
wd:statement/Q54945930-b8e1bfb0-4858-7ec5-65ae-ab2810818f5e
p:P2841 wd:statement/Q54945930-9784041C-3DDC-4BE7-ADC1-F139D5C2A37F
p:P2888 wd:statement/Q54945930-8FDFCDC5-CA80-4B53-A003-9B1761CC7D79
p:P2892 wd:statement/Q54945930-88E4D177-508E-4A1A-A154-0137311F15EF
p:P31 wd:statement/Q54945930-00D8A136-11C7-4828-ADAE-193F9E9271A7
p:P486 wd:statement/Q54945930-E2E551B6-7E35-4444-AD2D-2AB586C12694
p:P5270 wd:statement/Q54945930-79150EA8-71CD-4614-AE2F-550053D9ED46
p:P672 wd:statement/Q54945930-386B0374-566F-40CE-BE7D-B2331922AB4B
wd:statement/Q54945930-7B95CA55-DFAD-4C50-A245-2CC0AEFCE2D5
wd:statement/Q54945930-AE8EC7D6-B192-48C9-B405-209252282D09
wd:statement/Q54945930-E4FF9768-47C3-4C02-8450-C61AA81DDDC4
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D020785>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0015145>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.500.190>
<http://id.nlm.nih.gov/mesh/C14.240.850.875>
<http://id.nlm.nih.gov/mesh/C16.131.240.850.875>
<http://id.nlm.nih.gov/mesh/C16.131.666.190>
wdt:P14914 "D102006"
wdt:P1550 "102006"
wdt:P1995 cardiology
neurology
wdt:P279 vascular malformation
epilepsy
central nervous system and retinal vascular disease
wdt:P2841 any age
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_102006>
wdt:P2892 "C5681774"
wdt:P31 type of disease
wdt:P486 "D020785"
wdt:P5270 "MONDO_0015145"
wdt:P672 "C10.500.190"
"C14.240.850.875"
"C16.131.240.850.875"
"C16.131.666.190"
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