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1186847009: Hemochromatosis type 1 (disorder)


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

Descriptions:

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


0 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 est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Haemochromatosis type 1 est un(e) (attribut) hémochromatose héréditaire (trouble) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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