124257002: Deficiency of carnitine acetyltransferase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Deficiency of carnitine acetyltransferase
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Deficiency of carnitine acetyltransferase
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Deficiency of carnitine acetyltransferase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of carnitine acetyltransferase
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Deficiency of carnitine acetyltransferase
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Deficiency of carnitine acetyltransferase

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
203869019	Deficiency of carnitine acetyltransferase	en	Synonym	Active	Case insensitive	SNOMED CT core
727816017	Deficiency of carnitine acetyltransferase (disorder)	en	Fully specified name	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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