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403259002: Hypermelanosis due to pheochromocytoma (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771185014 Hypermelanosis due to pheochromocytoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773702012 Hypermelanosis due to phaeochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774988011 Hypermelanosis due to pheochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1771185014 Hypermelanosis due to pheochromocytoma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771185014 Hypermelanosis due to pheochromocytoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773702012 Hypermelanosis due to phaeochromocytoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1773702012 Hypermelanosis due to phaeochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774988011 Hypermelanosis due to pheochromocytoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1774988011 Hypermelanosis due to pheochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6264541000241111 hypermélanose due à un phéochromocytome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6264541000241111 hypermélanose due à un phéochromocytome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypermelanosis due to pheochromocytoma (disorder) Is a Hypermelanosis due to neoplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Hypermelanosis due to pheochromocytoma (disorder) Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypermelanosis due to pheochromocytoma (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypermelanosis due to pheochromocytoma (disorder) Associated etiologic finding Pheochromocytoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hypermelanosis due to pheochromocytoma (disorder) Due to Pheochromocytoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypermelanosis due to pheochromocytoma (disorder) Associated morphology Melanosis false Inferred relationship Existential restriction modifier (core metadata concept)
Hypermelanosis due to pheochromocytoma (disorder) Occurrence Period of life between birth and death false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypermelanosis due to pheochromocytoma (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypermelanosis due to pheochromocytoma (disorder) Associated morphology Melanosis true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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