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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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

Expanded Value Set

This concept is not in any reference sets

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