303094000: Propionyl-coenzyme A carboxylase deficiency pccA complementation group (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Organic acid metabolism disorder\Disorder of propionate AND/OR methylmalonate metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of branched-chain amino acid metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Organic acid metabolism disorder\Non-amino organic acidaemia AND/OR aciduria\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Enzymopathy\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Congenital disease\Inborn error of metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccA complementation group

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2971280014	Propionyl-coenzyme A carboxylase deficiency pccA complementation group (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2971976013	Propionyl-coenzyme A carboxylase deficiency pccA complementation group	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
445169018	Propionyl-CoA carboxylase deficiency pccA complementation group	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
699271014	Propionyl-CoA carboxylase deficiency pccA complementation group (disorder)	en	Fully specified name	Inactive	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

Unit of use quantity reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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