124122005: Deficiency of 3-hydroxyacyl-CoA dehydrogenase (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\Deficiency of 3-hydroxyacyl-CoA dehydrogenase
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatty acid oxidation defect\Deficiency of 3-hydroxyacyl-CoA dehydrogenase
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Deficiency of 3-hydroxyacyl-CoA dehydrogenase
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Deficiency of 3-hydroxyacyl-CoA dehydrogenase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of 3-hydroxyacyl-CoA dehydrogenase
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Deficiency of 3-hydroxyacyl-CoA dehydrogenase
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Deficiency of 3-hydroxyacyl-CoA dehydrogenase

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
203527011	Deficiency of beta-keto-reductase	en	Synonym	Active	Case insensitive	SNOMED CT core
203528018	Deficiency of beta-hydroxyacyl dehydrogenase	en	Synonym	Active	Case insensitive	SNOMED CT core
203529014	Deficiency of 3-hydroxyacyl-CoA dehydrogenase	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
727608012	Deficiency of 3-hydroxyacyl-CoA dehydrogenase (disorder)	en	Fully specified name	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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