303095004: Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of propionate AND/OR methylmalonate metabolism\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of branched-chain amino acid metabolism\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Metabolic disease\Disorder of organic acid metabolism\Non-amino organic acidemia AND/OR aciduria\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Metabolic disease\Enzymopathy\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Metabolic disease\Disorder of acid-base balance\Acidemia\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)
• \Congenital disease (disorder)\Inborn error of metabolism\Propionic acidemia\Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (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
445170017	Propionyl-CoA carboxylase deficiency pccBC complementation group	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2970965018	Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2971538011	Propionyl-coenzyme A carboxylase deficiency pccBC complementation group	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
844181000052114	propionyl-CoA-karboxylasbrist, komplementeringsgrupp pccBC	sv	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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