@prefix p: <http://www.wikidata.org/prop/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix schema1: <http://schema.org/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix wd: <http://www.wikidata.org/entity/> .
@prefix wds: <http://www.wikidata.org/entity/statement/> .
@prefix wdt: <http://www.wikidata.org/prop/direct/> .
@prefix wdtn: <http://www.wikidata.org/prop/direct-normalized/> .
@prefix wikibase: <http://wikiba.se/ontology#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

wd:Q558077 rdfs:label "متلازمة وليم"@ar,
        "Vilyams sindromu"@az,
        "Williamsov sindrom"@bs,
        "síndrome de Williams"@ca,
        "Williamsův syndrom"@cs,
        "Syndrom Williams"@cy,
        "Williams syndrom"@da,
        "Williams-Beuren-Syndrom"@de,
        "σύνδρομο Ουίλιαμς"@el,
        "Williams-Beuren syndrome"@en,
        "sindromo de Williams"@eo,
        "síndrome de Williams"@es,
        "Williamsi sündroom"@et,
        "نشانگان ویلیامز"@fa,
        "Williamsin oireyhtymä"@fi,
        "syndrome de Williams"@fr,
        "Williams-Beuren syndrome"@gpe,
        "תסמונת ויליאמס"@he,
        "Williams-szindróma"@hu,
        "Ուիլյամսի համախտանիշ"@hy,
        "Sindrom Williams"@id,
        "Williams-heilkenni"@is,
        "sindrome di Williams-Beuren"@it,
        "ウィリアムズ症候群"@ja,
        "ვილიამსის სინდრომი"@ka,
        "윌리엄스 증후군"@ko,
        "Viljamso sindromas"@lt,
        "Вилијамсов синдром"@mk,
        "sindrom Williams"@ms,
        "Williams syndrom"@nb,
        "syndroom van Williams"@nl,
        "ଉଇଲିଅମସ ସିଣ୍ଡ୍ରୋମ"@or,
        "zespół Williamsa"@pl,
        "síndrome de Williams"@pt,
        "синдром Вильямса"@ru,
        "Umukoresha:RebeccaRwanda/Indwara ya Williams"@rw,
        "Williams-Beurenov sindrom"@sl,
        "Вилијамсов синдром"@sr,
        "Williams syndrom"@sv,
        "வில்லியம்ஸ் நோய்க்கூட்டறிகுறி"@ta,
        "విలియమ్స్ సిండ్రోమ్"@te,
        "กลุ่มอาการวิลเลียม"@th,
        "Williams-Beuren sendromu"@tr,
        "синдром Вільямса"@uk,
        "hội chứng Williams"@vi,
        "威廉氏綜合症"@yue,
        "威廉氏症候群"@zh ;
    schema1:dateModified "2026-10-24T00:41:55+00:00"^^xsd:dateTime ;
    schema1:description "متلازمة الحب المطلق"@ar,
        "متلازمة الحب المطلق"@ary,
        "un trastorn genètic multisistèmic originat per una deleció heterozigòtica d’entre 1,5 i 1,8 Mb i quasi sempre espontània en el braç llarg d’un cromosoma 7"@ca,
        "genetická choroba"@cs,
        "Krankheit"@de,
        "νευροαναπτυξιακή διαταραχή"@el,
        "neurodevelopmental disorder caused by a deletion of around 27 genes in chromosome 7, characterized by a broad forehead, underdeveloped chin, short nose, full cheeks, challenges with visual tasks, increased empathy and decreased aggression"@en,
        "genetika neŭrodisvolva malsano kaŭzata de la foriĝo de ĉ. 27 genoj en kromosomo 7, karakterizita de «elfeca» vizaĝo, intelekta malkapablo, kaj agrableco"@eo,
        "trastorno genético"@es,
        "وضعیت پزشکی"@fa,
        "geneettinen häiriö"@fi,
        "l’association d’un retard mental, d’une cardiopathie congénitale, d’un faciès et d’un comportement hypersocial caractéristiques de l’individu affecté"@fr,
        "genetic disorder"@gpe,
        "תסמונת גנטית נדירה, הנגרמת בגלל פגיעה כרומוזומלית"@he,
        "genetikai rendellenesség"@hu,
        "malattia umana"@it,
        "まれな遺伝子疾患"@ja,
        "medische conditie"@nl,
        "genetycznie uwarunkowana choroba"@pl,
        "синдром, который возникает в случае мутаций в гене"@ru,
        "nevrorazvojni sindrom"@sl,
        "хвороба"@uk ;
    schema1:version 2560168092 ;
    wikibase:identifiers 48,
        51 ;
    wikibase:sitelinks 48 ;
    wikibase:statements 120 ;
    skos:altLabel "WBS"@cs,
        "WS"@cs,
        "Williams-Beurenův syndrom"@cs,
        "Williamsův-Beurenův syndrom"@cs,
        "Elfin-face-Syndrom"@de,
        "Fanconi-Schlesiner-Syndrom"@de,
        "Williams Syndrom"@de,
        "Williams-Syndrom"@de,
        "idiopathische Hyperkalzämie"@de,
        "σύνδρομο Williams"@el,
        "Fanconi Schlesinger syndrome"@en,
        "WBS"@en,
        "WS"@en,
        "Williams syndrome"@en,
        "chromosome 7Q11.23 Deletion Syndrome, 1.5- to 1.8-Mb"@en,
        "deletion 7q11.23"@en,
        "monosomy 7q11.23"@en,
        "sindromo de Williams-Beuren"@eo,
        "sindromo de elfa vizaĝo"@eo,
        "sindrome de Williams"@es,
        "sindrome de Williams Beuren"@es,
        "sindrome de Williams-Beuren"@es,
        "síndrome de Williams Beuren"@es,
        "síndrome de Williams-Beuren"@es,
        "WBS"@et,
        "WS"@et,
        "Williams-Beureni sündroom"@et,
        "Williamsi-Beureni sündroom"@et,
        "Williams-Beurenin oireyhtymä"@fi,
        "Williams-Beurenin syndrooma"@fi,
        "Williamsin syndrooma"@fi,
        "syndrome de Williams Beuren"@fr,
        "syndrome de Williams-Beuren"@fr,
        "Fanconi Schlesinger syndrome"@gpe,
        "WBS"@gpe,
        "WILLIAMS-BEUREN SYNDROME"@gpe,
        "WILLIAMS-BEUREN SYNDROME; WBS"@gpe,
        "WS"@gpe,
        "Williams Syndrome"@gpe,
        "Williams syndrome"@gpe,
        "Williams-Beuren Syndrome (WBS)"@gpe,
        "Williams–Beuren syndrome, WBS"@gpe,
        "chromosome 7Q11.23 Deletion Syndrome, 1.5- to 1.8-Mb"@gpe,
        "deletion 7q11.23"@gpe,
        "monosomy 7q11.23"@gpe,
        "תסמונת וויליאמס"@he,
        "sindrome di Williams"@it,
        "ウィリアムズ・ボイレン症候群"@ja,
        "Viljamso Beureno sindromas"@lt,
        "Viljamso beureno"@lt,
        "Williams syndroom"@nl,
        "Williams-Beuren syndroom"@nl,
        "Williams-Beuren-Syndroom"@nl,
        "Williams-Beurensyndroom"@nl,
        "Williams-syndroom"@nl,
        "Williamssyndroom"@nl,
        "Williamssyndrooom"@nl,
        "zespół Williamsa i Beurena"@pl,
        "zespół Williamsa-Beurena"@pl,
        "Вильямса синдром"@ru,
        "лицо эльфа"@ru,
        "синдром Уильямса"@ru,
        "синдром лица эльфа"@ru,
        "Fanconi-Schlesingerjev sindrom"@sl,
        "monosomija 7q11.23"@sl,
        "வில்லியம் நோய்க்கூட்டறிகுறி"@ta,
        "Вільямса синдром"@uk ;
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    wdtn:P8408 <http://kbpedia.org/kko/rc/WilliamsSyndrome> ;
    wdtn:P9827 <http://purl.obolibrary.org/obo/GSSO_006997> ;
    wdt:P10 <http://commons.wikimedia.org/wiki/Special:FilePath/Spontaneous-and-cued-gaze-following-in-autism-and-Williams-syndrome-1866-1955-5-13-S4.ogv> ;
    wdt:P10283 "C2781240822" ;
    wdt:P1036 "616.042",
        "618.920042" ;
    wdt:P11143 "Williams syndrome" ;
    wdt:P1193 0.0003 ;
    wdt:P1325 <http://www.nanbyou.or.jp/entry/4765> ;
    wdt:P13591 "concept/8c65753b-43b7-4268-afcf-861aa6c59f98" ;
    wdt:P138 wd:Q6103955 ;
    wdt:P14914 "D00904" ;
    wdt:P1550 "904" ;
    wdt:P1617 "9a0a1967-183c-411a-9b45-b8bddb482854" ;
    wdt:P1692 "759.89" ;
    wdt:P1748 "C85232" ;
    wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Four%20kids%20with%20Williams%20syndrome.jpg> ;
    wdt:P1995 wd:Q1071953,
        wd:Q123028 ;
    wdt:P2013 "Williams.Syndrome.Israel" ;
    wdt:P2163 "1175481" ;
    wdt:P227 "4323165-2" ;
    wdt:P2293 wd:Q14864092,
        wd:Q18026642,
        wd:Q18028572,
        wd:Q18031097,
        wd:Q18031771,
        wd:Q18032347,
        wd:Q18032349,
        wd:Q18032958,
        wd:Q18033772,
        wd:Q18034388,
        wd:Q18038318,
        wd:Q18047437,
        wd:Q18047525,
        wd:Q18048944,
        wd:Q18050644,
        wd:Q18052312,
        wd:Q18052314,
        wd:Q18060600 ;
    wdt:P2347 "38846" ;
    wdt:P244 "sh98004230" ;
    wdt:P268 "13540439d" ;
    wdt:P2716 <http://commons.wikimedia.org/wiki/Special:FilePath/Williams%20syndromeCCBY.jpg> ;
    wdt:P279 wd:Q16874615,
        wd:Q16918398,
        wd:Q18553439,
        wd:Q55785288,
        wd:Q55785336,
        wd:Q55785400,
        wd:Q55785518,
        wd:Q55785524,
        wd:Q55785601,
        wd:Q55785866,
        wd:Q55786608,
        wd:Q55787256,
        wd:Q55789170 ;
    wdt:P2841 wd:Q21953121,
        wd:Q21953125 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:1928>,
        <http://purl.obolibrary.org/obo/DOID_1928>,
        <http://www.orpha.net/ORDO/Orphanet_904> ;
    wdt:P2892 "C0175702" ;
    wdt:P31 wd:Q112193867,
        wd:Q42303753,
        wd:Q929833 ;
    wdt:P3417 "Williams-Beuren-Syndrome" ;
    wdt:P3471 "17874" ;
    wdt:P349 "01196757" ;
    wdt:P373 "Williams syndrome" ;
    wdt:P3827 "williams-syndrome" ;
    wdt:P4229 "Q87.8" ;
    wdt:P4233 "williams-syndrome" ;
    wdt:P4317 "7891" ;
    wdt:P4527 "434614" ;
    wdt:P486 "D018980" ;
    wdt:P492 "194050" ;
    wdt:P493 "758.9" ;
    wdt:P494 "Q93.8" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P508 "5062" ;
    wdt:P5270 "MONDO_0008678" ;
    wdt:P557 "859" ;
    wdt:P604 "001116" ;
    wdt:P61 wd:Q6103955 ;
    wdt:P6366 "2781240822",
        "2908753905" ;
    wdt:P646 "/m/01dwrw" ;
    wdt:P6532 wd:Q11088,
        wd:Q110938491,
        wd:Q141814981,
        wd:Q141815153,
        wd:Q141815885,
        wd:Q141815986,
        wd:Q1471642,
        wd:Q1549421,
        wd:Q2735907,
        wd:Q2856379,
        wd:Q30016719,
        wd:Q468207,
        wd:Q515376,
        wd:Q54973951 ;
    wdt:P665 "H01439" ;
    wdt:P668 "NBK1249" ;
    wdt:P672 "C10.597.606.360.970",
        "C14.280.484.150.535.960",
        "C16.131.260.970",
        "C16.320.180.970" ;
    wdt:P673 "893149" ;
    wdt:P691 "ph637817" ;
    wdt:P699 "DOID:1928" ;
    wdt:P7464 "williams-syndrome" ;
    wdt:P780 wd:Q16874615 ;
    wdt:P7807 "1644383468" ;
    wdt:P8189 "987007532654405171" ;
    wdt:P8313 "Williams_syndrom" ;
    wdt:P8408 "WilliamsSyndrome" ;
    wdt:P8885 "윌리엄스 증후군" ;
    wdt:P9827 "006997" .