# OnCo record carney-complex (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/carney-complex/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "carney-complex" ;
  schema:name "Carney complex"@en ;
  schema:alternateName "PRKAR1A Carney complex"@en ;
  schema:description "Carney complex is a rare inherited condition that causes spotty pigmentation of the skin and lining of the mouth, heart tumours called myxomas, and tumours of the hormone glands, skin and nerves. Children with it are offered regular checks under recommendations updated in 2025."@en ;
  schema:url <https://onco.cc/terms/carney-complex/> ;
  schema:dateModified "2026-11-04"^^xsd:date ;
  schema:sameAs <https://en.wikipedia.org/wiki/Carney_complex> ;
  schema:citation <https://doi.org/10.1210/jcem.86.9.7903>, <https://doi.org/10.1158/1078-0432.ccr-24-3860>, <https://www.orpha.net/en/disease/detail/1359>, <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/sertoli-cell-tumour/> ;
  onco:technologies <https://onco.cc/technologies/germline-testing/> ;
  onco:targets <https://onco.cc/targets/prkar1a/> ;
  onco:terms <https://onco.cc/terms/hereditary-cancer-syndromes/> .
