# OnCo record nthl1-associated-polyposis (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/nthl1-associated-polyposis/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "nthl1-associated-polyposis" ;
  schema:name "NTHL1-associated polyposis"@en ;
  schema:alternateName "NTHL1 polyposis"@en, "NTHL1-related polyposis"@en ;
  schema:description "NTHL1-associated polyposis is a rare inherited condition in which a person has two faulty copies of the NTHL1 gene and develops many bowel polyps, bowel cancer and, in women, womb cancer. Care is planned at a specialist centre because there are too few patients for a fixed schedule."@en ;
  schema:url <https://onco.cc/terms/nthl1-associated-polyposis/> ;
  schema:dateModified "2026-11-04"^^xsd:date ;
  schema:citation <https://doi.org/10.1038/ng.3287>, <https://doi.org/10.1136/gutjnl-2019-319915>, <https://www.orpha.net/en/disease/detail/454840> ;
  onco:tag "gap-fill", "hereditary" ;
  onco:related <https://onco.cc/terms/mutyh-associated-polyposis/> ;
  onco:cancers <https://onco.cc/cancers/colorectal/>, <https://onco.cc/cancers/endometrial/> ;
  onco:technologies <https://onco.cc/technologies/germline-testing/> ;
  onco:targets <https://onco.cc/targets/nthl1/> ;
  onco:terms <https://onco.cc/terms/colonoscopy/>, <https://onco.cc/terms/hereditary-cancer-syndromes/> .