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 ]
Term information
- 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)
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders
https://github.com/monarch-initiative/mondo/issues/6877
https://github.com/monarch-initiative/mondo/issues/6878
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