764860006: 3-methylglutaconic aciduria type 7 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\3-methylglutaconic aciduria type 7
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of branched-chain amino acid metabolism\3-Methylglutaconic aciduria\3-methylglutaconic aciduria type 7

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
3655424014	MGA7 - 3-methylglutaconic aciduria type 7	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3655425010	3-methylglutaconic aciduria type VII	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3655426011	3-methylglutaconic aciduria type 7 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3655427019	3-methylglutaconic aciduria type 7	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3655428012	3-methylglutaconic aciduria, cataract, neurologic involvement, neutropenia syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3655429016	CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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