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... > Clinical finding (finding) > disease > Congenital disease > Inborn error of metabolism > Propionic acidemia > Propionyl-CoA carboxylase deficiency pccBC complementation group
... > Clinical finding (finding) > disease > Metabolic disease > Inborn error of metabolism > Propionic acidemia > Propionyl-CoA carboxylase deficiency pccBC complementation group
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Inborn error of metabolism > Propionic acidemia > Propionyl-CoA carboxylase deficiency pccBC complementation group
... > Clinical finding (finding) > disease > Metabolic disease > Enzymopathy > Propionic acidemia > Propionyl-CoA carboxylase deficiency pccBC complementation group

Preferred term

Propionyl-CoA carboxylase deficiency pccBC complementation group  

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  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Broader concept

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/303095004

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