764999002: Non-functioning paraganglioma (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\...
• \Neuroendocrine neoplasm (disorder)\Paraganglioma\Non-functioning paraganglioma
• \Neoplastic disease of uncertain behavior\Paraganglioma\Non-functioning paraganglioma

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3656012019	Non-functioning paraganglioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3656013012	Non-functioning paraganglioma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3656014018	Non-secreting paraganglioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5404454011	A rare neuroendocrine tumor arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumors are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumor. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404455012	A rare neuroendocrine tumour arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumours are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumour. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

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