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403259002: Hypermelanosis due to pheochromocytoma (disorder)


Status: current, Defined. 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 Case insensitive SNOMED CT core
1773702012 Hypermelanosis due to phaeochromocytoma en Synonym Active Case insensitive SNOMED CT core
1774988011 Hypermelanosis due to pheochromocytoma en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypermelanosis due to phaeochromocytoma Is a Hypermelanosis due to neoplasia true Inferred relationship Some
Hypermelanosis due to phaeochromocytoma Associated morphology Hyperpigmentation false Inferred relationship Some 1
Hypermelanosis due to phaeochromocytoma Finding site Structure of skin region false Inferred relationship Some 1
Hypermelanosis due to phaeochromocytoma Associated etiologic finding Phaeochromocytoma false Inferred relationship Some
Hypermelanosis due to phaeochromocytoma Due to Phaeochromocytoma true Inferred relationship Some 2
Hypermelanosis due to phaeochromocytoma Associated morphology Melanosis false Inferred relationship Some
Hypermelanosis due to phaeochromocytoma Occurrence Period of life between birth and death true Inferred relationship Some 1
Hypermelanosis due to phaeochromocytoma Finding site Skin structure true Inferred relationship Some 1
Hypermelanosis due to phaeochromocytoma Associated morphology Melanosis true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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