64852002: Sarcosine dehydrogenase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Sarcosine dehydrogenase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Sarcosine dehydrogenase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Sarcosine dehydrogenase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of glycine metabolism\Sarcosine dehydrogenase deficiency
• \Metabolic disease\Enzymopathy\Sarcosine dehydrogenase deficiency
• \Congenital disease\Inborn error of metabolism\Sarcosine dehydrogenase deficiency

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
107791015	Sarcosine dehydrogenase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
107792010	Sarcosinuria	en	Synonym	Active	Case insensitive	SNOMED CT core
107793017	Sarcosinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
107794011	Hypersarcosinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
107795012	Deficiency of the sarcosine dehydrogenase complex	en	Synonym	Active	Case insensitive	SNOMED CT core
107796013	Demethylation defect of N-methylglycine	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
499975015	Sarcosinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
499976019	Hypersarcosinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
804291015	Sarcosine dehydrogenase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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