JSON

neuroendocrine neoplasm

Go to external page http://purl.obolibrary.org/obo/MONDO_0019496

Endocrine tumors, also referred to as neuroendocrine tumors (NETs), are defined by a common phenotype which is characterized by the expression of general markers (neuron specific enolase, chromogranin, synaptophysin) and hormone secretion products. These tumors may be localized in any part of the body and are generally discovered in non-specific situations, i.e. not immediately suggestive of NETs (tests for inherited predisposition to tumors or for a clinical syndrome caused by abnormal hormone secretion). [ Orphanet:877 ]

Synonyms: neuroendocrine tumour APUDoma neuroendocrine tumor neuroendocrine neoplasm

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0206754 (MONDO:equivalentTo)
  • SCTID:255046005 (MONDO:equivalentTo)
  • MESH:D018358 (MONDO:equivalentTo)
  • DOID:169 (MONDO:equivalentTo)
  • GARD:9316 (MONDO:GARD)
  • EFO:1001901 (MONDO:equivalentTo)
  • ICD9:239.7 (MONDO:relatedTo)
  • ICD9:209 (DOID:169)
  • MEDGEN:64652 (MONDO:equivalentTo)
  • NCIT:C3809 (MONDO:equivalentTo)
  • Orphanet:877 (MONDO:equivalentTo)
  • ICD9:209-209.99 (DOID:169)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

UK spelling synonym
neuroendocrine tumour

comment

Editor note: TODO design pattern, often NCIT uses 'neuroendocrine tumor' for particular grading with 'neuroendocrine neoplasm' as the superclass

exactMatch

http://linkedlifedata.com/resource/umls/id/C0206754

http://purl.obolibrary.org/obo/NCIT_C3809

http://identifiers.org/medgen/64652

http://identifiers.org/mesh/D018358

http://www.orpha.net/ORDO/Orphanet_877

http://purl.obolibrary.org/obo/DOID_169

http://identifiers.org/snomedct/255046005

id

MONDO:0019496