SHMARQL
Docs
Query
Entity
Story editor
Moyamoya syndrome
<http:/
/
www.wikidata.org/
entity/
Q55788342>
human disease
rdfs:
label
en
fr
ja
pt
pt-br
"Doença rara com angiopatia de Moyamoya"
@pt
"Doença rara com angiopatia de Moyamoya"
@pt-br
"Moyamoya syndrome"
@en
"syndrome de Moyamoya"
@fr
"もやもや症候群"
@ja
schema:
description
en
uk
"human disease"
@en
"хвороба людини"
@uk
schema:
date
Modified
"2026-10-24T00:22:42+00:00"
^^xsd:dateTime
schema:
version
2560165258
wikibase:
identifiers
6
wikibase:
sitelinks
0
wikibase:
statements
10
p:
P14914
wd:
statement/Q55788342-6ABAD4C4-290F-4CFF-ADA4-E9AC3C7BCCBB
p:
P1550
wd:
statement/Q55788342-C02C9020-6B93-42FD-9C47-6268426C024D
p:
P279
wd:
statement/Q55788342-54D7F456-FB88-4FDC-9722-B2E74E5419F2
wd:
statement/Q55788342-6B2361C1-D631-4C11-A847-06D9855F0A1E
p:
P2888
wd:
statement/Q55788342-BF3FC971-B814-4C98-A105-8A8D5121094E
p:
P2892
wd:
statement/Q55788342-E76D7040-1A70-4456-9B8B-C22979E2E525
p:
P31
wd:
statement/Q55788342-8D495C6E-6DBC-4D8F-B146-0D33692E088A
p:
P5270
wd:
statement/Q55788342-12DA50E7-CD7E-4C0A-9FE0-9E3069EA01D2
p:
P7329
wd:
statement/Q55788342-91b2a8ac-f220-4eca-98b2-2cd67fe0209d
p:
P7807
wd:
statement/Q55788342-AA93BC3F-1FC3-4F37-A1C8-37EF86BBBDF0
p:
direct-
normalized/
P5270
<http:/
/
purl.obolibrary.org/
obo/
MONDO_0018792>
wdt:
P14914
"D477771"
wdt:
P1550
"477771"
wdt:
P279
genetic central nervous system and retinal vascular disease
Moyomoya angiopathy
wdt:
P2888
<http:/
/
www.orpha.net/
ORDO/
Orphanet_477771>
wdt:
P2892
"C5681260"
wdt:
P31
type of disease
wdt:
P5270
"MONDO_0018792"
wdt:
P7329
"8B22.B"
wdt:
P7807
"1746892088"
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