A syndrome associated with the development of multiple polyps throughout the intestine. It includes familial adenomatous polyposis , hamartomatous polyposis syndromes, and other rare polyposis syndromes. [ NCIT:C155954 ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:19847 (Orphanet:104010)
  • UMLS:C0345891 (Orphanet:104010/e)
  • SCTID:254589009 (MONDO:equivalentTo)
  • NCIT:C155954 (MONDO:equivalentTo)
  • Orphanet:104010 (MONDO:equivalentTo)
  • MedDRA:10057018 (Orphanet:104010/e)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/6877

https://github.com/monarch-initiative/mondo/issues/6878

closeMatch

http://identifiers.org/meddra/10057018

exactMatch

http://linkedlifedata.com/resource/umls/id/C0345891

http://identifiers.org/snomedct/254589009

http://purl.obolibrary.org/obo/NCIT_C155954

http://www.orpha.net/ORDO/Orphanet_104010

id

MONDO:0015185

Term relations