SHMARQL

Prader–Willi syndrome

<http://www.wikidata.org/entity/Q594013>

rare genetic disorder
Prader–Willi syndrome
Prader–Willi syndrome
Prader–Willi syndrome
Prader–Willi syndrome
Prader–Willi syndrome
rdfs:label
"Prader–Willi syndrome"@en
skos:altLabel
"PWS"@en
"Prader Willi syndrome"@en
"Prader-Willi syndrome"@en
"Prader–Labhart–Willi-Fanconi syndrome"@en
schema:description
"rare genetic disorder"@en
schema:dateModified "2026-11-13T12:58:39+00:00"^^xsd:dateTime
schema:version 2568689073
wikibase:identifiers 46
50
wikibase:sitelinks 43
wikibase:statements 87
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p:P7329 wd:statement/Q594013-6ed47a60-492f-17cf-7d57-dfbd4dfde17f
p:P7464 wd:statement/Q594013-1A5C5F9E-763B-4AA4-8146-C7E27AE096AB
p:P7807 wd:statement/Q594013-ca9fdd58-4298-1607-f083-fe8e5212710d
p:P7995 wd:statement/Q594013-EF403D73-D8A9-4344-BD23-2C9C28E398B0
p:P8189 wd:statement/Q594013-84B0EA75-3763-4FD5-86E0-6E943A7FFC54
p:direct-normalized/P227 <https://d-nb.info/gnd/4201277-6>
p:direct-normalized/P2347 <http://www.yso.fi/onto/yso/p18144>
p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh85106050>
p:direct-normalized/P268 <http://data.bnf.fr/ark:/12148/cb12468434q#about>
p:direct-normalized/P349 <http://id.ndl.go.jp/auth/ndlna/01179976>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D011218>
p:direct-normalized/P508 <http://purl.org/bncf/tid/67274>
p:direct-normalized/P5806 <http://snomed.info/id/89392001>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00478>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.597.606.360.690>
<http://id.nlm.nih.gov/mesh/C16.131.077.730>
<http://id.nlm.nih.gov/mesh/C16.131.260.700>
<http://id.nlm.nih.gov/mesh/C16.320.180.700>
<http://id.nlm.nih.gov/mesh/C16.320.447.500>
<http://id.nlm.nih.gov/mesh/C18.654.726.750.500.740>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:11983>
wdt:P10 <http://commons.wikimedia.org/wiki/Special:FilePath/Prader%20willi%20syndrome.webm>
wdt:P1036 "616.042"
"618.920042"
wdt:P11143 "Prader–Willi syndrome"
"Prader–Willi_syndrome"
wdt:P1193 0.00005^^xsd:decimal
wdt:P12086 "Syndroom_van_Prader-Willi"
wdt:P1325 <http://www.nanbyou.or.jp/entry/4768>
wdt:P13591 "concept/20e85c46-b52a-49ce-a2c6-bb9c0b286d72"
wdt:P13613 "170984"
wdt:P138 Heinrich Willi
Andrea Prader
wdt:P1417 "science/Prader-Willi-syndrome"
wdt:P1461 "prader-willi-syndrome-pro"
wdt:P14914 "D00739"
wdt:P1550 "739"
wdt:P1692 "759.81"
wdt:P1748 "C75463"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Juan%20Carre%C3%B1o%20de%20Miranda%20-%20La%20Monstrua%20Desnuda%20%28Eugenia%20Martinez%20Vallejo%20Unclothed%29%20-%20WGA4483.jpg>
<http://commons.wikimedia.org/wiki/Special:FilePath/Langdon%27s%20down%20PWS%20patient.jpg>
<http://commons.wikimedia.org/wiki/Special:FilePath/Mardin%20P1050311%2020080426123001.JPG>
<http://commons.wikimedia.org/wiki/Special:FilePath/PWS8.png>
<http://commons.wikimedia.org/wiki/Special:FilePath/Prader-WilliBMC.png>
wdt:P1995 medical genetics
pediatrics
neurology
wdt:P2176 somatrem
wdt:P227 "4201277-6"
wdt:P2293 NDN
OCA2
SNRPN
MKRN3
HERC2
MAGEL2
wdt:P2347 "18144"
wdt:P244 "sh85106050"
wdt:P268 "12468434q"
wdt:P2716 <http://commons.wikimedia.org/wiki/Special:FilePath/Pws.jpg>
wdt:P279 syndrome
chromosomal disease
syndromic obesity
wdt:P2841 congenital onset
neonatal onset
wdt:P2888 <http://identifiers.org/doid/DOID:11983>
<http://purl.obolibrary.org/obo/DOID_11983>
wdt:P2892 "C0032897"
"C0265222"
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P3417 "Prader-Willi-Syndrome"
wdt:P3471 "8491"
wdt:P349 "01179976"
wdt:P373 "Prader-Willi syndrome"
wdt:P3827 "prader-willi-syndrome"
wdt:P4229 "Q87.1"
wdt:P4233 "prader-willi-syndrome"
wdt:P4317 "5575"
wdt:P4839 "Entity["Disease", "ICDNine759.81"]"
"Entity["Disease", {"ICDNine759.81", "Primary"}]"
wdt:P486 "D011218"
wdt:P492 "176270"
wdt:P5008 WikiProject Medicine
wdt:P508 "67274"
wdt:P5082 "Prader-Willis_syndrom"
wdt:P5555 <http://commons.wikimedia.org/wiki/Special:FilePath/Prader-Willi%20and%20Angelman%20Syndrome%20%28Homo%20sapiens%29.svg>
<http://commons.wikimedia.org/wiki/Special:FilePath/Pws.svg>
wdt:P557 "10481"
wdt:P5806 "89392001"
wdt:P604 "001605"
wdt:P646 "/m/0fb3f"
wdt:P6532 stroke
wdt:P665 "H00478"
wdt:P668 "NBK1330"
wdt:P672 "C10.597.606.360.690"
"C16.131.077.730"
"C16.131.260.700"
"C16.320.180.700"
"C16.320.447.500"
"C18.654.726.750.500.740"
wdt:P673 "947954"
wdt:P699 "DOID:11983"
wdt:P7329 "LD90.3"
wdt:P7464 "prader-willi-syndrome"
wdt:P7807 "393773440"
wdt:P7995 "prader-willi-syndrome"
wdt:P8189 "987007531653205171"
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