765143008: Sporadic pheochromocytoma and secreting paraganglioma (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\...
• \Neuroendocrine neoplasm (disorder)\Phaeochromocytoma\A rare, isolated, non-familial pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from extra-adrenal chromaffin tissue (paraganglioma). The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.
• \Neuroendocrine neoplasm (disorder)\Paraganglioma\A rare, isolated, non-familial pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from extra-adrenal chromaffin tissue (paraganglioma). The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.
• \Neoplastic disease of uncertain behavior\Paraganglioma\A rare, isolated, non-familial pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from extra-adrenal chromaffin tissue (paraganglioma). The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.

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
5404492012	A rare, isolated, non-familial pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from extra-adrenal chromaffin tissue (paraganglioma). The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404493019	A rare, isolated, non-familial phaeochromocytoma/paraganglioma tumour arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from extra-adrenal chromaffin tissue (paraganglioma). The majority of these tumours are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumour, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3657171012	Sporadic pheochromocytoma and secreting paraganglioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3657172017	Sporadic phaeochromocytoma and secreting paraganglioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3657173010	Sporadic pheochromocytoma and secreting paraganglioma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1013391000172111	phéochromocytome/paragangliome sécrétant sporadique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3443021001000118	Sporadisches Phaeochromozytom/sezernierendes Paragangliom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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