4920001: Deficiency of acetyl-coenzyme A carboxylase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Acetyl-CoA carboxylase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Acetyl-CoA carboxylase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Non-amino organic acidaemia AND/OR aciduria\Acetyl-CoA carboxylase deficiency
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Acetyl-CoA carboxylase deficiency
• \Congenital disease\Inborn error of metabolism\Acetyl-CoA carboxylase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2478728017	Deficiency of acetyl-CoA carboxylase	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4697249014	Deficiency of acetyl-coenzyme A carboxylase (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
4697250014	Acetyl-CoA carboxylase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4697251013	Deficiency of acetyl-coenzyme A carboxylase	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

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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