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399053004: Idiopathic hemochromatosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1766973015 Idiopathic hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1773292017 Idiopathic haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
1774578017 Idiopathic hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic hemochromatosis Is a Hemochromatosis true Inferred relationship Existential restriction modifier
Idiopathic hemochromatosis Causative agent Iron false Inferred relationship Existential restriction modifier
Idiopathic hemochromatosis Finding site Body system structure false Inferred relationship Existential restriction modifier
Idiopathic hemochromatosis Causative agent Iron AND/OR iron compound false Inferred relationship Existential restriction modifier
Idiopathic hemochromatosis Causative agent Iron and/or iron compound true Inferred relationship Existential restriction modifier 1
Idiopathic hemochromatosis Is a Idiopathic disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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