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[X] intestinal polyposis syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0015185

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
  • SCTID:254589009 (MONDO:equivalentTo)
  • GARD:19847 (MONDO:GARD)
  • NCIT:C155954 (MONDO:equivalentTo)
  • MedDRA:10057018 (Orphanet:104010/e)
  • Orphanet:104010 (MONDO:equivalentTo)
  • UMLS:C0345891 (MONDO:equivalentTo)
  • MEDGEN:577190 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, mondo_top_grouping_syndromic_disease, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, susceptibility_mondo, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10057018

exactMatch

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

http://identifiers.org/medgen/577190

http://identifiers.org/snomedct/254589009

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

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

id

MONDO:0015185

term tracker item

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

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

Term relations