726079008: Hereditary hypercarotenemia and vitamin A deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Hereditary hypercarotenemia and vitamin A deficiency
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary hypercarotenemia and vitamin A deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Hereditary hypercarotenemia and vitamin A deficiency
• \Congenital disease\Inborn error of metabolism\Hereditary hypercarotenemia and vitamin A deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3447962018	Hereditary hypercarotenemia and vitamin A deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3447963011	Hereditary hypercarotenemia and vitamin A deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3447964017	Hereditary hypercarotenaemia and vitamin A deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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