# OnCo record birt-hogg-dube-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/birt-hogg-dube-syndrome/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "birt-hogg-dube-syndrome" ;
  schema:name "Birt-Hogg-Dubé syndrome"@en ;
  schema:alternateName "BHD"@en, "BHD syndrome"@en, "FLCN syndrome"@en ;
  schema:description "Birt-Hogg-Dubé syndrome is an inherited condition, caused by a fault in the FLCN gene, that causes small skin bumps, lung cysts that can collapse a lung, and a raised risk of kidney cancer. Kidney scans every one to two years from age 20 are recommended to find kidney tumours early."@en ;
  schema:url <https://onco.cc/terms/birt-hogg-dube-syndrome/> ;
  schema:dateModified "2026-11-04"^^xsd:date ;
  schema:sameAs <https://en.wikipedia.org/wiki/Birt–Hogg–Dubé_syndrome> ;
  schema:citation <https://doi.org/10.1038/s41431-024-01671-2>, <https://doi.org/10.1136/jmg-2022-109104>, <https://www.cancer.gov/types/kidney/hp/kidney-genetics-pdq>, <https://www.orpha.net/en/disease/detail/122>, <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/rcc/> ;
  onco:technologies <https://onco.cc/technologies/germline-testing/> ;
  onco:targets <https://onco.cc/targets/flcn/> ;
  onco:terms <https://onco.cc/terms/hereditary-cancer-syndromes/> .