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\Organic acid metabolism disorder\Disorder of amino acid metabolism\Amino acid deficiency\Carnitine deficiency\Carnitine deficiency due to inborn error of metabolism
• \Metabolic disease\Organic acid metabolism disorder\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
• \Malnutrition\Nutritional deficiency disorder\Undernutrition\Deficiency of micronutrients\Amino acid deficiency\Carnitine deficiency\Carnitine deficiency due to inborn error of metabolism

Status: current, Defined. Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

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