238004006: Succinyl-coenzyme A acetoacetate transferase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Succinyl-CoA acetoacetate transferase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Succinyl-CoA acetoacetate transferase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Succinyl-CoA acetoacetate transferase deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Succinyl-CoA acetoacetate transferase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Succinyl-CoA acetoacetate transferase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2971157012	Succinyl-coenzyme A acetoacetate transferase deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2971960016	Succinyl-coenzyme A acetoacetate transferase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356731019	Succinyl-CoA acetoacetate transferase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356732014	Succinyl-CoA 3-ketoacid transferase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356733016	3-Ketoacid CoA transferase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
356734010	Thioacyl transferase deficiency	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

Description inactivation indicator reference set

REPLACED BY association reference set

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