763720007: Hypermethioninemia due to deficiency of glycine N-methyltransferase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hypermethioninemia due to deficiency of glycine N-methyltransferase
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of sulfur-bearing amino acid metabolism\Hypermethioninemia\Hypermethioninemia due to deficiency of glycine N-methyltransferase
• \Congenital disease\Hypermethioninemia due to deficiency of glycine N-methyltransferase

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3643478017	Hypermethioninemia due to deficiency of glycine N-methyltransferase	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3643479013	Hypermethioninaemia due to GNMT (glycine N-methyltransferase) deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3643480011	Hypermethioninemia due to GNMT (glycine N-methyltransferase) deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3643481010	Hypermethioninemia due to deficiency of glycine N-methyltransferase (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3643482015	Hypermethioninaemia due to deficiency of glycine N-methyltransferase	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3643483013	Glycine N-methyltransferase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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