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53836006: Secondary hemochromatosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
496776011 Secondary haemochromatosis en Synonym Active Case insensitive SNOMED CT core
792000016 Secondary hemochromatosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
89480016 Secondary hemochromatosis en Synonym Active Case insensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Secondary haemochromatosis Is a Haemochromatosis true Inferred relationship Some
Secondary haemochromatosis Finding site Body system structure false Inferred relationship Some
Secondary haemochromatosis Is a Haemochromatosis false Inferred relationship Some
Secondary haemochromatosis Causative agent Iron AND/OR iron compound false Inferred relationship Some
Secondary haemochromatosis Causative agent Iron false Inferred relationship Some
Secondary haemochromatosis Finding site Liver structure false Inferred relationship Some
Secondary haemochromatosis Causative agent Iron and/or iron compound true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
African nutritional haemochromatosis Is a True Secondary haemochromatosis Inferred relationship Some
Erythropoietic haemochromatosis Is a True Secondary haemochromatosis Inferred relationship Some
Haemochromatosis following repeated red blood cell transfusion Is a True Secondary haemochromatosis Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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