FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

125375005: Endogenous hemosiderin pigmentation (morphologic abnormality)


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

Descriptions:

Id Description Lang Type Status Case? Module
193865010 Endogenous hemosiderin pigmentation en Synonym Active Case insensitive SNOMED CT core
473501018 Endogenous haemosiderin pigmentation en Synonym Active Case insensitive SNOMED CT core
729194014 Endogenous 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
Endogenous 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

Australian dialect reference set

Description inactivation indicator reference set

Back to Start