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\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\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, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
119115019	Maple syrup urine disease, multiple dehydrogenase form	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
119116018	Maple syrup urine disease, E3 deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
811898014	Maple syrup urine disease, multiple dehydrogenase form (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start