303095004: Propionyl-coenzyme A carboxylase deficiency pccBC 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 pccBC complementation group
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Organic acid metabolism disorder\Disorder of propionate AND/OR methylmalonate metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC 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 pccBC complementation group
• \Metabolic disease\Organic acid metabolism disorder\Non-amino organic acidaemia AND/OR aciduria\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Enzymopathy\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Congenital disease\Inborn error of metabolism\Propionic acidaemia\Propionyl-CoA carboxylase deficiency pccBC complementation group

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2970965018	Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2971538011	Propionyl-coenzyme A carboxylase deficiency pccBC complementation group	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
445170017	Propionyl-CoA carboxylase deficiency pccBC complementation group	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

Problem/Diagnosis reference set

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