Global Code Book Ontology

Last uploaded: May 2, 2024
Preferred Name

neuroendocrine neoplasm
Synonyms

neuroendocrine neoplasm

neuroendocrine tumour

neuroendocrine tumor

APUDoma

Definitions

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

ID

http://purl.obolibrary.org/obo/MONDO_0019496

comment

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

disease has feature

http://purl.obolibrary.org/obo/HP_0002027

http://purl.obolibrary.org/obo/MONDO_0001517

exactMatch

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

http://identifiers.org/mesh/D018358

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

http://identifiers.org/snomedct/255046005

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

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

hasDbXref

MESH:D018358

UMLS:C0206754

Orphanet:877

EFO:1001901

ICD9:209-209.99

SCTID:255046005

DOID:169

GARD:9316

ICD9:209

ICD9:239.7

NCIT:C3809

hasExactSynonym

neuroendocrine neoplasm

neuroendocrine tumour

neuroendocrine tumor

APUDoma

IAO_0000115

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).

id

MONDO:0019496

inSubset

http://purl.obolibrary.org/obo/mondo#rare

http://purl.obolibrary.org/obo/mondo#orphanet_rare

http://purl.obolibrary.org/obo/mondo#gard_rare

http://purl.obolibrary.org/obo/mondo#disease_grouping

http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders

label

neuroendocrine neoplasm

notation

MONDO:0019496

prefLabel

neuroendocrine neoplasm

subClassOf

http://purl.obolibrary.org/obo/MONDO_0002082

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