718603002: Deficiency of phosphoserine aminotransferase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Deficiency of phosphoserine aminotransferase
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of serine metabolism\Deficiency of phosphoserine aminotransferase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of aminotransferase\Deficiency of phosphoserine aminotransferase

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3312886015	Deficiency of phosphoserine aminotransferase (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3312887012	Phosphoserine aminotransferase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3312888019	Deficiency of phosphoserine aminotransferase	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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