35400008: Hereditary hemochromatosis (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary haemochromatosis
• \Metabolic disease\Hereditary metabolic disease\Hereditary haemochromatosis
• \Metabolic disease\Disorder of mineral metabolism\Disorder of iron metabolism\Iron overload\Haemochromatosis\Hereditary haemochromatosis
• \Malnutrition\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload\Haemochromatosis\Hereditary haemochromatosis

Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
486146014	Primary haemochromatosis	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
486147017	Hereditary haemochromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
486148010	Familial haemochromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
486149019	Idiopathic haemochromatosis	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
59062011	Hereditary hemochromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
59063018	Primary hemochromatosis	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
59064012	Idiopathic hemochromatosis	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
59065013	Familial hemochromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
767034016	Hereditary hemochromatosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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