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\Deficiency of acetyl-coenzyme A carboxylase
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Deficiency of acetyl-coenzyme A carboxylase
• \Metabolic disease\Disorder of organic acid metabolism\Non-amino organic acidemia AND/OR aciduria\Deficiency of acetyl-coenzyme A carboxylase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of acetyl-coenzyme A carboxylase
• \Congenital disease\Inborn error of metabolism\Deficiency of acetyl-coenzyme A carboxylase

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
9212012	Acetyl-CoA: carboxylase deficiency	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
9213019	ACC deficiency	en	Synonym	Inactive	Entire term case sensitive	SNOMED CT core module
786853014	Acetyl-CoA: carboxylase deficiency (disorder)	en	Fully specified name	Inactive	Only initial character case insensitive	SNOMED CT core module
2478728017	Deficiency of acetyl-CoA carboxylase	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4697249014	Deficiency of acetyl-coenzyme A carboxylase (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
4697250014	Acetyl-CoA carboxylase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4697251013	Deficiency of acetyl-coenzyme A carboxylase	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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