1186844002: Type 2B juvenile hereditary hemochromatosis (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Hereditary haemochromatosis\Juvenile haemochromatosis\Type 2B juvenile hereditary haemochromatosis
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Juvenile haemochromatosis\Type 2B juvenile hereditary haemochromatosis
• \Degenerative disorder\Juvenile haemochromatosis\Type 2B juvenile hereditary haemochromatosis
• \Metabolic disease\Hereditary metabolic disease\Hereditary haemochromatosis\Juvenile haemochromatosis\Type 2B juvenile hereditary haemochromatosis
• \Metabolic disease\Disorder of mineral metabolism\Disorder of iron metabolism\Iron overload\Haemochromatosis\Hereditary haemochromatosis\Juvenile haemochromatosis\Type 2B juvenile hereditary haemochromatosis
• \Malnutrition\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload\Haemochromatosis\Hereditary haemochromatosis\Juvenile haemochromatosis\Type 2B juvenile hereditary haemochromatosis

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4667817010	Type 2B juvenile hereditary hemochromatosis	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4667818017	Type 2B juvenile hereditary hemochromatosis (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
4667819013	Type 2B juvenile hereditary haemochromatosis	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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