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302835009: Pheochromocytoma (disorder)

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
444773019 Phaeochromocytoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
698994011 Phaeochromocytoma [Ambiguous] en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1187709019 Phaeochromocytoma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216333014 Chromaffin tumour en Synonym (core metadata concept) Active Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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
864201000195116 Phäochromozytom de 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
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

12 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pheochromocytoma (disorder) Is a tumeur neuroendocrine false Inferred relationship Existential restriction modifier (core metadata concept)
Pheochromocytoma (disorder) Associated morphology Neoplasm false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pheochromocytoma (disorder) Finding site Structure of endocrine system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pheochromocytoma (disorder) Finding site Anatomical structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Pheochromocytoma (disorder) Is a Neoplastic disease false Inferred relationship Existential restriction modifier (core metadata concept)
Pheochromocytoma (disorder) Associated morphology Pheochromocytoma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pheochromocytoma (disorder) Is a Neuroendocrine neoplasm (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Benign pheochromocytoma Is a True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Catecholamine secretion by pheochromocytoma Is a True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypermelanosis due to pheochromocytoma (disorder) Associated etiologic finding False Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypermelanosis due to pheochromocytoma (disorder) Due to True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 2
History of pheochromocytoma (situation) Associated finding True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare, hereditary, phaeochromocytoma/paraganglioma tumour arising from neuroendocrine chromaffin cells of the adrenal medulla (phaeochromocytoma) 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 phaeochromocytoma/paraganglioma tumours tend to present at younger ages, to be multi-focal, bilateral, and recurrent, or to have multiple synchronous neoplasms. Is a True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Phaeochromocytoma crisis Is a True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic pheochromocytoma and secreting paraganglioma Is a True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Malignant pheochromocytoma Is a True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tremor due to pheochromocytoma (disorder) Due to True Pheochromocytoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set

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