440009: Persistent hyperphenylalaninemia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidemia\Hyperphenylalaninemia\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \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\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \Metabolic disease\Enzymopathy\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \Metabolic disease\Disorder of acid-base balance\Acidemia\Aminoacidemia\Hyperphenylalaninemia\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia
• \Congenital disease\Inborn error of metabolism\Phenylketonuria\Classical phenylketonuria\Persistent hyperphenylalaninemia

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
1815015	Persistent hyperphenylalaninemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1816019	Essential hyperphenylalaninemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1817011	Hyperphenylalaninemia, type II	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
493753017	Persistent hyperphenylalaninaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
493754011	Essential hyperphenylalaninaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
493755012	Hyperphenylalaninaemia, type II	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
781079017	Persistent hyperphenylalaninemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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