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

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\Inborn error of metabolism\Deficiency of acetyl-coenzyme A carboxylase (disorder)
• \trouble métabolique\Disorder of organic acid metabolism\Non-amino organic acidemia AND/OR aciduria\Deficiency of acetyl-coenzyme A carboxylase (disorder)
• \trouble métabolique\Inborn error of metabolism\Deficiency of acetyl-coenzyme A carboxylase (disorder)
• \trouble métabolique\Enzymopathy\Specific enzyme deficiency\Deficiency of acetyl-coenzyme A carboxylase (disorder)
• \Congenital disease\Inborn error of metabolism\Deficiency of acetyl-coenzyme A carboxylase (disorder)

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

Descriptions:

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

Expanded Value Set

Reference Sets

Canada French language reference set (foundation metadata concept)

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