765143008: Sporadic pheochromocytoma and secreting paraganglioma (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Neoplasm and/or hamartoma\Neoplastic disease\...
• \Neuroendocrine tumour\Phaeochromocytoma\Sporadic phaeochromocytoma and secreting paraganglioma
• \Neuroendocrine tumour\Paraganglioma\Sporadic phaeochromocytoma and secreting paraganglioma
• \Neoplastic disease of uncertain behaviour\Paraganglioma\Sporadic phaeochromocytoma and secreting paraganglioma

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3657171012	Sporadic pheochromocytoma and secreting paraganglioma	en	Synonym	Active	Case insensitive	SNOMED CT core
3657172017	Sporadic phaeochromocytoma and secreting paraganglioma	en	Synonym	Active	Case insensitive	SNOMED CT core
3657173010	Sporadic pheochromocytoma and secreting paraganglioma (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3657174016	Isolated non-familial catecholamin-producing tumours arising from neuroendocrine chromaffin cells in the adrenal medulla or in extra-adrenal chromaffin tissue, respectively. 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	Case sensitive	SNOMED CT core
3657175015	Isolated non-familial catecholamin-producing tumors arising from neuroendocrine chromaffin cells in the adrenal medulla or in extra-adrenal chromaffin tissue, respectively. 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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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