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1186847009: Hemochromatosis type 1 (disorder)


Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

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


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemochromatosis type 1 Causative agent Iron and/or iron compound true Inferred relationship Some 1
Haemochromatosis type 1 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Haemochromatosis type 1 Is a Hereditary haemochromatosis true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Symptomatic form of haemochromatosis type 1 Is a True Haemochromatosis type 1 Inferred relationship Some

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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