35400008: Hereditary hemochromatosis (disorder)

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\hémochromatose héréditaire (trouble)

\trouble métabolique\troubles du métabolisme des minéraux (trouble)\trouble du métabolisme du fer\Iron overload\Hemochromatosis (disorder)\hémochromatose héréditaire (trouble)

\Nutritional disorder\trouble lié à la suralimentation\Excess intake of micronutrients\Mineral excess\Iron overload\Hemochromatosis (disorder)\hémochromatose héréditaire (trouble)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

420671000241119 hémochromatose héréditaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

486147017 Hereditary haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

486148010 Familial haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

59062011 Hereditary hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

59065013 Familial hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

767034016 Hereditary hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

90131000172116 hémochromatose héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
hémochromatose héréditaire (trouble)	est un(e) (attribut)	maladie héréditaire	true	Inferred relationship	Some
hémochromatose héréditaire (trouble)	est un(e) (attribut)	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	est un(e) (attribut)	Digestive system hereditary disorder	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	est un(e) (attribut)	Hemochromatosis	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	est un(e) (attribut)	Hemochromatosis (disorder)	true	Inferred relationship	Some
hémochromatose héréditaire (trouble)	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	Causative agent	Iron AND/OR iron compound	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	localisation d'une constatation (attribut)	foie	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	Causative agent	fer (substance)	false	Inferred relationship	Some
hémochromatose héréditaire (trouble)	Causative agent	Iron and/or iron compound	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Juvenile haemochromatosis	est un(e) (attribut)	True	hémochromatose héréditaire (trouble)	Inferred relationship	Some
Haemochromatosis type 1	est un(e) (attribut)	True	hémochromatose héréditaire (trouble)	Inferred relationship	Some
FTH1-related iron overload	est un(e) (attribut)	True	hémochromatose héréditaire (trouble)	Inferred relationship	Some
Hemochromatosis type 3 (disorder)	est un(e) (attribut)	True	hémochromatose héréditaire (trouble)	Inferred relationship	Some
Autosomal dominant hereditary hemochromatosis (disorder)	est un(e) (attribut)	True	hémochromatose héréditaire (trouble)	Inferred relationship	Some

This concept is not in any reference sets