711412004: 3-methylglutaconic aciduria type 5 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\3-methylglutaconic aciduria type 5
• \Metabolic disease\Organic acid metabolism disorder\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 5

Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3078538012	3-methylglutaconic aciduria type 5 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3078586017	Dilated cardiomyopathy with ataxia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3078596014	3-methylglutaconic aciduria type 5	en	Synonym	Active	Case insensitive	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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