loading...| Preferred Name |
neuroendocrine neoplasm |
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| Synonyms |
APUDoma neuroendocrine neoplasm neuroendocrine tumor |
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| Definitions |
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). |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0019496 |
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| comment |
Editor note: TODO design pattern, often NCIT uses 'neuroendocrine tumor' for particular grading with 'neuroendocrine neoplasm' as the superclass |
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| closeMatch | ||
| database_cross_reference |
ICD9:209-209.99 SCTID:255046005 ICD9:209 COHD:434300 EFO:1001901 MESH:D018358 NCIT:C3809 DOID:169 UMLS:C0003650 UMLS:CN206284 ICD9:239.7 UMLS:C0206754 ICD10:D3A.8 Orphanet:877 |
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| disease has feature | ||
| exactMatch |
http://purl.obolibrary.org/obo/NCIT_C3809 http://linkedlifedata.com/resource/umls/id/C0003650 http://linkedlifedata.com/resource/umls/id/CN206284 http://identifiers.org/mesh/D018358 http://linkedlifedata.com/resource/umls/id/C0206754 http://identifiers.org/snomedct/255046005 |
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| has exact synonym |
APUDoma neuroendocrine neoplasm neuroendocrine tumor |
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| id |
MONDO:0019496 |
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| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
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| label |
neuroendocrine neoplasm |
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| notation |
MONDO:0019496 |
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| prefLabel |
neuroendocrine neoplasm |
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| textual definition |
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). |
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| subClassOf |