237997005: Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatty acid oxidation defect\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency
• \Metabolic disease\Enzymopathy\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Acyl-CoA dehydrogenase deficiency\Very long chain acyl-CoA dehydrogenase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2970828016	Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2971947010	Very long chain acyl-coenzyme A dehydrogenase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356712013	Very long chain acyl-CoA dehydrogenase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356713015	VLCAD - Very long chain acyl-CoA dehydrogenase deficiency	en	Synonym	Active	Case sensitive	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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