302835009: Pheochromocytoma (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neuroendocrine neoplasm (disorder)\Phaeochromocytoma

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

444773019 Phaeochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

444774013 Pheochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1216333014 Chromaffin tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1217832015 Chromaffin tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1227132016 Chromaffinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1227133014 Chromaffin paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1763205012 Pheochromocytoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2901271017 Adrenal medullary paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1827071000195115 feocromocitoma it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

418501000172114 phéochromocytome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

419201000172116 pheochromocytoma fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

864201000195116 Phäochromozytom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Phaeochromocytoma	Is a	tumeur neuroendocrine	false	Inferred relationship	Some
Phaeochromocytoma	Associated morphology	Neoplasm	false	Inferred relationship	Some	2
Phaeochromocytoma	Finding site	Structure of endocrine system (body structure)	false	Inferred relationship	Some	2
Phaeochromocytoma	Finding site	Anatomical structure	false	Inferred relationship	Some	3
Phaeochromocytoma	Is a	Neoplastic disease	false	Inferred relationship	Some
Phaeochromocytoma	Associated morphology	Pheochromocytoma	true	Inferred relationship	Some	1
Phaeochromocytoma	Is a	Neuroendocrine neoplasm (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign pheochromocytoma	Is a	True	Phaeochromocytoma	Inferred relationship	Some
Catecholamine secretion by pheochromocytoma	Is a	True	Phaeochromocytoma	Inferred relationship	Some
Hypermelanosis due to pheochromocytoma (disorder)	Associated etiologic finding	False	Phaeochromocytoma	Inferred relationship	Some
Hypermelanosis due to pheochromocytoma (disorder)	Due to	True	Phaeochromocytoma	Inferred relationship	Some	2
History of pheochromocytoma (situation)	Associated finding	True	Phaeochromocytoma	Inferred relationship	Some	1
A rare, hereditary, pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from any paraganglia from the skull base to the pelvic floor (paraganglioma). Clinical manifestations are often linked to excess catecholamines production causing sustained or paroxysmal elevations in blood pressure, headache, episodic profuse sweating, palpitations, pallor and apprehension or anxiety. Hereditary pheochromocytoma/paraganglioma tumors tend to present at younger ages, to be multi-focal, bilateral, and recurrent, or to have multiple synchronous neoplasms.	Is a	True	Phaeochromocytoma	Inferred relationship	Some
A potentially lethal complication of pheochromocytoma that may occur as a result of anaesthesia, surgery or during pregnancy and childbirth. The crisis is caused by excessive release of catecholamines and may be drug-induced secondary to histamine release, dopamine receptor blockade, or sympathomimetic action. Crisis may also result from mechanical factors such as squeeze of the tumour during surgery.	Is a	True	Phaeochromocytoma	Inferred relationship	Some
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.	Is a	True	Phaeochromocytoma	Inferred relationship	Some
Malignant pheochromocytoma	Is a	True	Phaeochromocytoma	Inferred relationship	Some
Tremor due to pheochromocytoma	Due to	True	Phaeochromocytoma	Inferred relationship	Some	1

Reference Sets

Description inactivation indicator reference set