71702000: Maple syrup urine disease, multiple dehydrogenase form (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Maple syrup urine disease\Maple syrup urine disease, multiple dehydrogenase form
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Maple syrup urine disease\Maple syrup urine disease, multiple dehydrogenase form
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Maple syrup urine disease\Maple syrup urine disease, multiple dehydrogenase form
• \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\Maple syrup urine disease\Maple syrup urine disease, multiple dehydrogenase form
• \Metabolic disease\Enzymopathy\Maple syrup urine disease\Maple syrup urine disease, multiple dehydrogenase form
• \Congenital disease\Inborn error of metabolism\Maple syrup urine disease\Maple syrup urine disease, multiple dehydrogenase form

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
119115019	Maple syrup urine disease, multiple dehydrogenase form	en	Synonym	Active	Case insensitive	SNOMED CT core
119116018	Maple syrup urine disease, E3 deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
811898014	Maple syrup urine disease, multiple dehydrogenase form (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

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