30287008: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Metabolic disease\...
• \Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\...
• \Aminoacidaemia\Hyperornithinaemia\Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome
• \Disorder of the urea cycle metabolism\Ornithine metabolism disorder\Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome
• \Disorder of the urea cycle metabolism\Hyperornithinaemia\Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome
• \Disorder of the urea cycle metabolism\Hyperammonaemia\Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome
• \Disorder of acid-base balance\Acidaemia\Aminoacidaemia\Hyperornithinaemia\Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1216334015	HHH - Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
1217833013	HHH - Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
484534018	Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
50692013	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
761274013	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (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

Problem/Diagnosis reference set

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