890435004: Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Inborn error of metabolism\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidemia\Hyperphenylalaninemia\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of phenylalanine metabolism\Hyperphenylalaninemia\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Metabolic disease\Inborn error of metabolism\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Metabolic disease\Enzymopathy\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Metabolic disease\Disorder of acid-base balance\Acidemia\Aminoacidemia\Hyperphenylalaninemia\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
• \Congenital disease (disorder)\Inborn error of metabolism\Classical phenylketonuria\Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4029832018	Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4029833011	Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4824691000052113	klassisk fenylketonuri med partiell brist på fenylalanin 4-monooxigenas	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Reference Sets

Description inactivation indicator reference set

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