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Concept information

... > Clinical finding (finding) > disease > Congenital disease > Inborn error of metabolism > Phenylketonuria > Classical phenylketonuria > Classical phenylketonuria with total deficiency of phenylalanine hydroxylase
... > Clinical finding (finding) > disease > Metabolic disease > Inborn error of metabolism > Phenylketonuria > Classical phenylketonuria > Classical phenylketonuria with total deficiency of phenylalanine hydroxylase
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Inborn error of metabolism > Phenylketonuria > Classical phenylketonuria > Classical phenylketonuria with total deficiency of phenylalanine hydroxylase
... > Clinical finding (finding) > disease > Metabolic disease > Enzymopathy > Phenylketonuria > Classical phenylketonuria > Classical phenylketonuria with total deficiency of phenylalanine hydroxylase

Preferred term

Classical phenylketonuria with total deficiency of phenylalanine hydroxylase  

Type

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

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/890436003

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