276426004: Ornithine oxo-acid aminotransferase deficiency (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\Disorder of the urea cycle metabolism\Ornithine metabolism disorder\Ornithine aminotransferase deficiency
• \Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Ornithine aminotransferase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2476096010	Deficiency of ornithine-oxo-acid aminotransferase	en	Synonym	Active	Case insensitive	SNOMED CT core
2669599018	Ornithine oxo-acid aminotransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
412550019	Ornithine aminotransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
412551015	Ornithine ketoacid transaminase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
412552010	OKT deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
412553017	Ornithine-oxo-acid amino acid transferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
412554011	Ornithine-delta-aminotransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
412555012	OAT - Ornithine oxo-acid aminotransferase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
412556013	OAT deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
669339011	Ornithine oxo-acid aminotransferase deficiency (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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