302835009: phéochromocytome (trouble)

SNOMED CT Concept\constatation clinique\Disease\néoplasme et/ou hamartome\maladie néoplasique\Neuroendocrine tumour\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

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

418501000172114 phéochromocytome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

419201000172116 pheochromocytoma fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

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

602331000241115 phéochromocytome (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pheochromocytoma (disorder)	est un(e) (attribut)	Neuroendocrine tumour	true	Inferred relationship	Some
Pheochromocytoma (disorder)	morphologie associée (attribut)	Neoplasm	false	Inferred relationship	Some	2
Pheochromocytoma (disorder)	localisation d'une constatation (attribut)	Structure of endocrine system (body structure)	false	Inferred relationship	Some	2
Pheochromocytoma (disorder)	localisation d'une constatation (attribut)	Anatomical structure	false	Inferred relationship	Some	3
Pheochromocytoma (disorder)	est un(e) (attribut)	maladie néoplasique	false	Inferred relationship	Some
Pheochromocytoma (disorder)	morphologie associée (attribut)	Pheochromocytoma	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Malignant pheochromocytoma	est un(e) (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some
Tremor due to pheochromocytoma	Due to	True	Pheochromocytoma (disorder)	Inferred relationship	Some	1
Benign pheochromocytoma	est un(e) (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some
Catecholamine secretion by pheochromocytoma	est un(e) (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some
Hypermelanosis due to pheochromocytoma (disorder)	Associated aetiologic finding	False	Pheochromocytoma (disorder)	Inferred relationship	Some
Hypermelanosis due to pheochromocytoma (disorder)	Due to	True	Pheochromocytoma (disorder)	Inferred relationship	Some	2
History of pheochromocytoma (situation)	constatation associée (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some	1
Hereditary pheochromocytoma and paraganglioma (disorder)	est un(e) (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some
Phaeochromocytoma crisis	est un(e) (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some
phéochromocytome/paragangliome sécrétant sporadique	est un(e) (attribut)	True	Pheochromocytoma (disorder)	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Description inactivation indicator reference set