55341000119107: Carnitine deficiency due to inborn error of metabolism (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Carnitine deficiency due to inborn error of metabolism
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Carnitine deficiency due to inborn error of metabolism
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Amino acid deficiency\Carnitine deficiency\Carnitine deficiency due to inborn error of metabolism
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of fatty acid metabolism\Carnitine deficiency due to inborn error of metabolism
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Carnitine deficiency due to inborn error of metabolism
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Carnitine deficiency due to inborn error of metabolism
• \Nutritional disorder\Nutritional deficiency disorder\Undernutrition\Deficiency of micronutrients\Amino acid deficiency\Carnitine deficiency\Carnitine deficiency due to inborn error of metabolism

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3011519013	Carnitine deficiency due to inborn error of metabolism (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3012236016	Carnitine deficiency due to inborn error of metabolism	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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