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hereditary mixed polyposis syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0011023

Hereditary mixed polyposis syndrome (HMPS) describes an autosomal dominantly inherited large-bowel disease characterized by the presence of a mixture of hyperplastic, atypical juvenile and adenomatous polyps that are associated with an increased risk of developing colorectal cancer if left untreated. [ Orphanet:157794 ]

Synonyms: hereditary mixed polyposis syndrome HMPS

This is just here as a test because I lose it

Term information

database cross reference
  • OMIMPS:601228 (MONDO:equivalentTo)
  • GARD:16981 (Orphanet:157794)
  • MESH:C563365 (MONDO:equivalentTo)
  • DOID:0111684 (MONDO:equivalentTo)
  • Orphanet:157794 (MONDO:equivalentTo)
  • UMLS:C5192681 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/6743

exactMatch

https://omim.org/phenotypicSeries/PS601228

http://purl.obolibrary.org/obo/DOID_0111684

http://linkedlifedata.com/resource/umls/id/C5192681

http://identifiers.org/mesh/C563365

http://www.orpha.net/ORDO/Orphanet_157794

id

MONDO:0011023

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0011023