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1186847009: Hemochromatosis type 1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4668225019 Haemochromatosis type 1 en Synonym Active Entire term case insensitive SNOMED CT core module
4668226018 Hemochromatosis type 1 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4668227010 Hemochromatosis type 1 en Synonym Active Entire term case insensitive SNOMED CT core module
4668470013 HFE related haemochromatosis en Synonym Active Entire term case sensitive SNOMED CT core module
4668471012 HFE related hemochromatosis en Synonym Active Entire term case sensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemochromatosis type 1 Causative agent Iron and/or iron compound true Inferred relationship Existential restriction modifier 1
Hemochromatosis type 1 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hemochromatosis type 1 Is a Hereditary hemochromatosis true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Symptomatic form of hemochromatosis type 1 Is a True Hemochromatosis type 1 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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