12066005: Citrullinemia, late-onset type (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Citrullinaemia\Citrullinaemia, late-onset type
• \Metabolic disease\Hereditary metabolic disease\Citrullinaemia\Citrullinaemia, late-onset type
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidaemia\Citrullinaemia\Citrullinaemia, late-onset type
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of the urea cycle metabolism\Citrullinaemia\Citrullinaemia, late-onset type
• \Metabolic disease\Enzymopathy\Citrullinaemia\Citrullinaemia, late-onset type
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Aminoacidaemia\Citrullinaemia\Citrullinaemia, late-onset type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
20796016	Citrullinemia, late-onset type	en	Synonym	Active	Case insensitive	SNOMED CT core
464689019	Citrullinaemia, late-onset type	en	Synonym	Active	Case insensitive	SNOMED CT core
717195017	Citrullinemia, late-onset type (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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