47719001: Hypervalinemia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Hypervalinaemia
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hypervalinaemia
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Hypervalinaemia
• \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\Disorder of valine metabolism\Hypervalinaemia
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidaemia\Hypervalinaemia
• \Metabolic disease\Enzymopathy\Hypervalinaemia
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Aminoacidaemia\Hypervalinaemia
• \Congenital disease\Inborn error of metabolism\Hypervalinaemia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
494905018	Valinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
494906017	Hypervalinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
785208014	Hypervalinemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
79521012	Hypervalinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
79522017	Valine transaminase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
79523010	Valinemia	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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