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399170009: Primary hemochromatosis (disorder)


Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1767090015 Primary hemochromatosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
1773303016 Primary haemochromatosis en Synonym Active Case insensitive SNOMED CT core
1774589012 Primary hemochromatosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary hemochromatosis Is a Haemochromatosis true Inferred relationship Some
Primary hemochromatosis Finding site Body system structure false Inferred relationship Some
Primary hemochromatosis Causative agent Iron false Inferred relationship Some
Primary hemochromatosis Causative agent Iron AND/OR iron compound false Inferred relationship Some
Primary hemochromatosis Causative agent Iron and/or iron compound 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

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