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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
endocrine neoplasm +     
ACTH Syndrome, Ectopic 
adrenal gland neoplasm +   
adrenal rest tumor 
benign endocrine neoplasm +   
Duodenal Gastrin-Producing Neuroendocrine Tumor 
familial tumoral calcinosis +  
functioning endocrine neoplasm +  
granulosa cell tumor +  
liver and intrahepatic bile duct neoplasm +   
malignant endocrine neoplasm +   
Malignant Paraganglioma 
neuroendocrine neoplasm +   
A benign or malignant neoplasm composed of cells of neuroendocrine origin. Representative examples include paraganglioma, carcinoid tumor, and neuroendocrine carcinoma. 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).
Non-Functional Pancreatic Neuroendocrine Tumor 
non-functioning endocrine neoplasm +  
oxyphilic adenoma +  
Pancreatic Gastrinoma 
Pancreatic Glucagonoma 
Pancreatic Vipoma 
pineal body neoplasm +  
pituitary tumor +   
thymus neoplasm +  
Thyroid Gland Mixed Medullary and Follicular Cell Carcinoma 
thyroid neoplasm +   
tumor of parathyroid gland +  

Synonyms
Exact Synonyms: APUDoma ;   NET ;   neuroendocrine tumor ;   neuroendocrine tumour
Xrefs: DOID:169 ;   GARD:9316 ;   ICD9:209 ;   ICD9:209-209.99 ;   ICD9:239.7 ;   MEDGEN:64652 ;   MESH:D018358 ;   MONDO:0019496 ;   NCI:C3809 ;   ORDO:877
Definition Sources: Orphanet:877

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