SHMARQL

Waardenburg's syndrome

<http://www.wikidata.org/entity/Q1151801>

genetic condition involving hearing loss and depigmentation
Waardenburg's syndrome
Waardenburg's syndrome
rdfs:label
"Waardenburg's syndrome"@en
skos:altLabel
"Klein–Waardenburg syndrome (type 3)"@en
"Shah–Waardenburg syndrome (type 4)"@en
"Waardenburg Shah syndrome"@en
"Waardenburg syndrome"@en
"Waardenburg, types I and/or II"@en
"Waardenburg-Klein syndrome"@en
"van der Hoeve Halbertsona Waardenburg syndrome"@en
schema:description
"genetic condition involving hearing loss and depigmentation"@en
schema:dateModified "2026-11-02T01:41:02+00:00"^^xsd:dateTime
schema:version 2563678797
wikibase:identifiers 30
33
wikibase:sitelinks 27
wikibase:statements 59
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p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh85072629>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D014849>
p:direct-normalized/P6366 <https://makg.org/entity/2777259899>
<https://makg.org/entity/2910933322>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00759>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C16.131.077.938>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:9258>
p:direct-normalized/P8408 <http://kbpedia.org/kko/rc/WaardenburgSyndrome>
wdt:P10283 "C2777259899"
wdt:P10376 "agricultural-and-biological-sciences/waardenburg-syndrome"
wdt:P10565 "463449"
wdt:P11143 "Waardenburg syndrome"
wdt:P1193 0.00005^^xsd:decimal
wdt:P13204 "d24gvh6p"
wdt:P138 Petrus Johannes Waardenburg
wdt:P14541 "27Bx9U"
wdt:P14914 "D03440"
wdt:P1550 "3440"
wdt:P1748 "C85222"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Outdoor%20selfie%20shushugah%202020.jpg>
<http://commons.wikimedia.org/wiki/Special:FilePath/Waardenburg%20syndrome.jpg>
wdt:P1995 medical genetics
wdt:P2293 TYR
MITF
KITLG
PAX3
EDN3
SNAI2
SOX10
EDNRB
wdt:P244 "sh85072629"
wdt:P279 syndrome
autosomal dominant disease
genetic deafness
wdt:P2841 neonatal onset
infantile onset
wdt:P2888 <http://identifiers.org/doid/DOID:9258>
<http://purl.obolibrary.org/obo/DOID_9258>
<http://www.orpha.net/ORDO/Orphanet_3440>
wdt:P2892 "C0079661"
"C1847800"
"C3266898"
wdt:P31 type of disease
rare disease
wdt:P3417 "Waardenburg-Syndrome"
wdt:P373 "Waardenburg syndrome"
wdt:P4317 "5525"
wdt:P486 "D014849"
wdt:P493 "270.2270.2"
wdt:P5008 WikiProject Medicine
wdt:P557 "14021"
"33475"
wdt:P604 "001428"
wdt:P6366 "2777259899"
"2910933322"
wdt:P646 "/m/02w_x_"
wdt:P665 "H00759"
wdt:P672 "C16.131.077.938"
wdt:P673 "1113314"
"950277"
wdt:P699 "DOID:9258"
wdt:P7464 "waardenburg-syndrome"
wdt:P7500 premature greying of hair
wdt:P7807 "304883627"
wdt:P8189 "987007545796205171"
wdt:P8408 "WaardenburgSyndrome"
wdt:P9513 "waardenburgs-syndrome"
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data from SPARQL profile: Wikidata