# OnCo record beckwith-wiedemann-syndrome (term). Data CC BY-NC 4.0, attribute "Data from OnCo (onco.cc)". Whole corpus: https://onco.cc/api/v1/onco.nt
@prefix schema: <https://schema.org/> .
@prefix onco: <https://onco.cc/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://onco.cc/terms/beckwith-wiedemann-syndrome/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "beckwith-wiedemann-syndrome" ;
  schema:name "Beckwith-Wiedemann syndrome"@en ;
  schema:alternateName "BWS"@en, "Beckwith-Wiedemann spectrum"@en, "BWSp"@en, "11p15 overgrowth"@en ;
  schema:description "Beckwith-Wiedemann syndrome is an overgrowth condition, caused by changes in a region of chromosome 11, that raises the risk of childhood kidney and liver tumours. Most children are offered a tummy ultrasound every three months until their seventh birthday so that any tumour is found small."@en ;
  schema:url <https://onco.cc/terms/beckwith-wiedemann-syndrome/> ;
  schema:dateModified "2026-11-04"^^xsd:date ;
  schema:sameAs <https://en.wikipedia.org/wiki/Beckwith–Wiedemann_syndrome> ;
  schema:citation <https://doi.org/10.1038/nrendo.2017.166>, <https://doi.org/10.1158/1078-0432.ccr-17-0710>, <https://www.orpha.net/en/disease/detail/116>, <https://www.england.nhs.uk/wp-content/uploads/2018/08/rare-and-inherited-disease-national-genomics-test-directory-v9.xlsx> ;
  onco:tag "gap-fill", "hereditary" ;
  onco:cancers <https://onco.cc/cancers/wilms-tumor/>, <https://onco.cc/cancers/hepatoblastoma/>, <https://onco.cc/cancers/neuroblastoma/> ;
  onco:technologies <https://onco.cc/technologies/germline-testing/> ;
  onco:terms <https://onco.cc/terms/hereditary-cancer-syndromes/> .