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125376006: Exogenous hemosiderin pigmentation (morphologic abnormality)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
193866011 Exogenous hemosiderin pigmentation en Synonym Active Case insensitive SNOMED CT core
473502013 Exogenous haemosiderin pigmentation en Synonym Active Case insensitive SNOMED CT core
729195010 Exogenous hemosiderin pigmentation (morphologic abnormality) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Exogenous haemosiderin pigmentation Is a Haemosiderin pigmentation true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Body structure foundation reference set

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