# Williams-Beuren syndrome

> 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

**Wikidata**: [Q558077](https://www.wikidata.org/wiki/Q558077)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Williams_syndrome)  
**Source**: https://4ort.xyz/entity/williams-beuren-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. [Source](https://ddrare.nibiohn.go.jp/)
3. [Nuovo soggettario](https://thes.bncf.firenze.sbn.it/termine.php?id=5062)
4. Disease Ontology
5. Engineered zinc-finger proteins can compensate genetic haploinsufficiency by transcriptional activation of the wild-type allele: application to Willams-Beuren syndrome and supravalvular aortic stenosis
6. Nuovo soggettario
7. Freebase Data Dumps. 2013
8. Integrated Authority File
9. BBC Things
10. YSO-Wikidata mapping project
11. [Identifiers.org](https://registry.identifiers.org/registry/doid)
12. Quora
13. National Library of Israel
14. KBpedia
15. [OpenAlex](https://docs.openalex.org/download-snapshot/snapshot-data-format)