| dbo:complications
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- Heart problems, periods ofhigh blood calcium
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| dbo:description
|
- Krankheit (de)
- malattia umana (it)
- хвороба (uk)
- νευροαναπτυξιακή διαταραχή (el)
- neurodevelopmental disorder (en)
- trastorno genético (es)
- genetycznie uwarunkowana choroba (pl)
- وضعیت پزشکی (fa)
- תסמונת גנטית נדירה, הנגרמת בגלל פגיעה כרומוזומלית (iw)
- geneettinen häiriö (fi)
- genetická choroba (cs)
- синдром, который возникает в случае мутаций в гене (ru)
- medische conditie (nl)
- nevrorazvojni sindrom (sl)
- l’association d’un retard mental, d’une cardiopathie congénitale, d’un faciès et d’un comportement hypersocial caractéristiques de l’individu affecté (fr)
- متلازمة الحب المطلق (ar)
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| dbo:differentialDiagnosis
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| dbo:diseasesDB
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| dbo:eMedicineSubject
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| dbo:eMedicineTopic
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| dbo:geneReviewsId
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| dbo:geneReviewsName
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| dbo:icd10
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| dbo:icd9
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| dbo:medlinePlus
| |
| dbo:meshId
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| dbo:omim
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| dbo:orpha
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| dbo:symptom
| |
| dbo:thumbnail
| |
| dbo:wikiPageExternalLink
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| dbo:wikiPageWikiLink
| |
| dbp:align
| |
| dbp:alt
|
- A man with Williams syndrome making heart hands. (en)
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| dbp:caption
|
- A man with Williams syndrome (en)
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| dbp:causes
| |
| dbp:complications
|
- Heart problems, periods of high blood calcium (en)
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| dbp:differential
| |
| dbp:diseasesdb
| |
| dbp:duration
| |
| dbp:emedicinesubj
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| dbp:emedicinetopic
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| dbp:field
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| dbp:frequency
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| dbp:genereviewsname
| |
| dbp:genereviewsnbk
| |
| dbp:icd
|
- 758.900000 (xsd:double)
- (en)
- Q93.8 (en)
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| dbp:medlineplus
| |
| dbp:meshid
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| dbp:name
| |
| dbp:omim
| |
| dbp:orphanet
| |
| dbp:prognosis
|
- Shorter life expectancy (en)
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| dbp:quote
|
- (en)
- ASL (en)
- ELN (en)
- BAZ1B (en)
- CLDN3 (en)
- CLDN4 (en)
- CLIP2 (en)
- EIF4H (en)
- GTF2I (en)
- GTF2IRD1 (en)
- KCTD7 (en)
- LAT2 (en)
- LIMK1 (en)
- NSUN5 (en)
- RFC2 (en)
- STX1A (en)
- WBSCR22 (en)
- TRIM50 (en)
- FKBP6 (en)
- POR (en)
- BCL7B (en)
- FZD9 (en)
- HIP1 (en)
- MDH2 (en)
- NCF1 (en)
- TBL2 (en)
- TRIM73 (en)
- TRIM74 (en)
- WBSCR14 (en)
- WBSCR18 (en)
- WBSCR21 (en)
- WBSCR23 (en)
- WBSCR24 (en)
- WBSCR27 (en)
- WBSCR28 (en)
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| dbp:style
|
- width:30%; min-width: 20em; (en)
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| dbp:symptoms
|
- Facial changes including underdeveloped chin structure, intellectual disability, overly friendly nature, short height (en)
|
| dbp:synonyms
|
- Williams–Beuren syndrome (en)
|
| dbp:title
|
- Williams syndrome genes (en)
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| dbp:treatment
|
- Various types of therapy (en)
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| dbp:wikiPageUsesTemplate
| |
| dbp:wordnet_type
| |
| dct:subject
| |
| gold:hypernym
| |
| rdf:type
| |
| rdfs:label
|
- Williams syndrome (en)
- متلازمة ويليام (ar)
- Síndrome de Williams (ca)
- Williamsův syndrom (cs)
- Σύνδρομο Ουίλιαμς (el)
- Sindromo de Williams (eo)
- Williams-Beuren-Syndrom (de)
- Síndrome de Williams (es)
- Syndrome de Williams (fr)
- Sindrome di Williams-Beuren (it)
- Sindrom Williams (in)
- ウィリアムズ症候群 (ja)
- Síndrome de Williams (pt)
- Zespół Williamsa (pl)
- Syndroom van Williams (nl)
- Синдром Вільямса (uk)
- Синдром Вильямса (ru)
- Williams syndrom (sv)
- 威廉氏症候群 (zh)
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| owl:sameAs
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| prov:wasDerivedFrom
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| foaf:depiction
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| foaf:isPrimaryTopicOf
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| foaf:name
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| is dbo:academicDiscipline
of | |
| is dbo:knownFor
of | |
| is dbo:medicalCause
of | |
| is dbo:wikiPageDisambiguates
of | |
| is dbo:wikiPageRedirects
of | |
| is dbo:wikiPageWikiLink
of | |
| is dbp:causes
of | |
| is foaf:primaryTopic
of | |
