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\Organic acid metabolism disorder\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, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3316394019	Deficiency of dimethylglycine dehydrogenase (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3316395018	Deficiency of dimethylglycine dehydrogenase	en	Synonym	Active	Case insensitive	SNOMED CT core
3316396017	Dimethylglycine dehydrogenase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3316397014	An extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor.	en	Definition	Active	Case sensitive	SNOMED CT core
3316398016	An extremely rare autosomal recessive glycine metabolism disorder characterised clinically in the single reported case to date by muscle fatigue and a fish-like odour.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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