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

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of propionate AND/OR methylmalonate metabolism\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of amino acid metabolism (disorder)\Disorder of amino acid and organic acid metabolism\Disorder of branched-chain amino acid metabolism\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Disorder of organic acid metabolism (disorder)\Non-amino organic acidemia AND/OR aciduria\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Enzymopathy\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA complementation group
• \Metabolic disease\Disorder of acid-base balance\Acidemia\Propionic acidemia (disorder)\Propionyl-CoA carboxylase deficiency pccA 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
445169018	Propionyl-CoA carboxylase deficiency pccA complementation group	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2971280014	Propionyl-coenzyme A carboxylase deficiency pccA complementation group (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2971976013	Propionyl-coenzyme A carboxylase deficiency pccA complementation group	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5314972016	PCCA-gene related propionyl-coenzyme A carboxylase deficiency pccA complementation group	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
445169018	Propionyl-CoA carboxylase deficiency pccA complementation group	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
699271014	Propionyl-CoA carboxylase deficiency pccA complementation group (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2971280014	Propionyl-coenzyme A carboxylase deficiency pccA complementation group (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2971976013	Propionyl-coenzyme A carboxylase deficiency pccA complementation group	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5314972016	PCCA-gene related propionyl-coenzyme A carboxylase deficiency pccA complementation group	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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