neuroendocrine neoplasm
http://purl.obolibrary.org/obo/MONDO_0019496
Endocrine tumours, also referred to as neuroendocrine tumours (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 tumours 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 tumours or for a clinical syndrome caused by abnormal hormone secretion). [ Orphanet:877 ]
Term info
- MESH:D018358 (MONDO:equivalentTo)
- Orphanet:877 (MONDO:equivalentTo)
- DOID:169 (MONDO:equivalentTo)
- ICD9:209 (DOID:169)
- NCIT:C3809 (MONDO:equivalentTo)
- UMLS:CN206284 (MONDO:equivalentTo)
- UMLS:C0003650 (Orphanet:877)
- EFO:1001901 (MONDO:equivalentTo)
- SCTID:255046005 (MONDO:equivalentTo)
- UMLS:C0206754 (Orphanet:877)
- ICD9:209-209.99 (DOID:169)
- ICD9:239.7 (MONDO:relatedTo)
disease_grouping, ordo_group_of_disorders
Editor note: TODO design pattern, often NCIT uses 'neuroendocrine tumor' for particular grading with 'neuroendocrine neoplasm' as the superclass
Endocrine tumours, also referred to as neuroendocrine tumours (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 tumours 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 tumours or for a clinical syndrome caused by abnormal hormone secretion).
http://linkedlifedata.com/resource/umls/id/C0206754, http://purl.obolibrary.org/obo/NCIT_C3809, http://identifiers.org/mesh/D018358, http://purl.obolibrary.org/obo/DOID_169, http://linkedlifedata.com/resource/umls/id/CN206284, http://identifiers.org/snomedct/255046005, http://purl.obolibrary.org/obo/Orphanet_877, http://linkedlifedata.com/resource/umls/id/C0003650
APUDoma, neuroendocrine tumor, neuroendocrine neoplasm
MONDO:0019496