1187534001: Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Glutaric aciduria\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Non-amino organic acidaemia AND/OR aciduria\Glutaric aciduria\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Glutaric aciduria, type 2\Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency

Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4674097019	Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
4674098012	Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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