1237181009: Symptomatic form of hemochromatosis type 1 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Hereditary hemochromatosis\Hemochromatosis type 1\Symptomatic form of hemochromatosis type 1
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hemochromatosis type 1\Symptomatic form of hemochromatosis type 1
• \Metabolic disease\Hereditary metabolic disease\Hereditary hemochromatosis\Hemochromatosis type 1\Symptomatic form of hemochromatosis type 1
• \Metabolic disease\Disorder of mineral metabolism\Disorder of iron metabolism\Iron overload\Hemochromatosis\Hereditary hemochromatosis\Hemochromatosis type 1\Symptomatic form of hemochromatosis type 1
• \Nutritional disorder\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload\Hemochromatosis\Hereditary hemochromatosis\Hemochromatosis type 1\Symptomatic form of hemochromatosis type 1

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Aug 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5090967013	Symptomatic form of hemochromatosis type 1 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
5090968015	Symptomatic form of classic hemochromatosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5090969011	Symptomatic form of hemochromatosis type 1	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5090970012	Symptomatic form of classic haemochromatosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5090971011	Symptomatic form of haemochromatosis type 1	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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