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

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\...
• \Inborn error of metabolism\cétoacidurie à chaines ramifiées\Maple syrup urine disease, multiple dehydrogenase form
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\cétoacidurie à chaines ramifiées\Maple syrup urine disease, multiple dehydrogenase form
• \trouble métabolique\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\cétoacidurie à chaines ramifiées\Maple syrup urine disease, multiple dehydrogenase form
• \trouble métabolique\Inborn error of metabolism\cétoacidurie à chaines ramifiées\Maple syrup urine disease, multiple dehydrogenase form
• \trouble métabolique\Enzymopathy\cétoacidurie à chaines ramifiées\Maple syrup urine disease, multiple dehydrogenase form
• \Congenital disease\Inborn error of metabolism\cétoacidurie à chaines ramifiées\Maple syrup urine disease, multiple dehydrogenase form

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
119116018	Maple syrup urine disease, E3 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
811898014	Maple syrup urine disease, multiple dehydrogenase form (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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