238070003: Glutaryl-coenzyme A oxidase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Glutaryl-CoA oxidase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Glutaryl-CoA oxidase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Glutaryl-CoA oxidase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2970955012	Glutaryl-coenzyme A oxidase deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2971456013	Glutaryl-coenzyme A oxidase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356855018	Glutaryl-CoA oxidase deficiency	en	Synonym	Active	Initial character 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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