719449007: Deficiency of dimethylglycine dehydrogenase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Deficiency of dimethylglycine dehydrogenase
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of glycine metabolism\Deficiency of dimethylglycine dehydrogenase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of dimethylglycine dehydrogenase

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
3316394019	Deficiency of dimethylglycine dehydrogenase (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3316395018	Deficiency of dimethylglycine dehydrogenase	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3316396017	Dimethylglycine dehydrogenase deficiency	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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