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-CoA carboxylase deficiency pccBC complementation group
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Fetal and/or neonatal disorder\Congenital disease\Inborn error of metabolism\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of propionate AND/OR methylmalonate metabolism\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Disorder of 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 acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Disorder of organic acid metabolism (disorder)\Non-amino organic acidemia AND/OR aciduria\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Enzymopathy\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group
• \Metabolic disease\Disorder of acid-base balance\Acidemia\Propionic acidemia\Propionyl-CoA carboxylase deficiency pccBC complementation group

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
5314975019	PCCB-gene related propionyl-coenzyme A carboxylase deficiency pccBC complementation group	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
7410261000241115	glycinémie cétosique, groupe de complémentation pccBC	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
7410271000241111	acidémie propionique, groupe de complémentation pccBC	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
7410281000241113	déficit en propionyl coenzyme A carboxylase, groupe de complémentation pccBC	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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