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multiple endocrine neoplasia

Go to external page http://purl.obolibrary.org/obo/MONDO_0017169

Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs. [ Orphanet:276161 ]

Synonyms: men syndromes multiple endocrine neoplasia men syndrome multiple endocrine neoplasia syndrome(s) men multiple endocrine adenomatosis multiple endocrine neoplasia syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:21044 (Orphanet:276161)
  • Orphanet:276161 (MONDO:equivalentTo)
  • MESH:D009377 (https://orcid.org/0000-0003-1967-3726)
  • MedDRA:10061299 (Orphanet:276161/e)
  • OMIMPS:131100 (MONDO:equivalentTo)
  • ICDO:8360/1 (NCIT:C6432)
  • SCTID:46724008 (MONDO:equivalentTo)
  • ICD9:258.0 (MONDO:i2s)
  • UMLS:C0027662 (Orphanet:276161/e)
  • NCIT:C6432 (MONDO:equivalentTo)
  • DOID:3125 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, nord_rare, orphanet_rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5653

closeMatch

http://identifiers.org/meddra/10061299

exactMatch

http://purl.obolibrary.org/obo/NCIT_C6432

https://omim.org/phenotypicSeries/PS131100

http://www.orpha.net/ORDO/Orphanet_276161

http://identifiers.org/mesh/D009377

http://purl.obolibrary.org/obo/DOID_3125

http://identifiers.org/snomedct/46724008

http://linkedlifedata.com/resource/umls/id/C0027662

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0021058

id

MONDO:0017169