124285000: Deficiency of alanine aminotransferase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of alanine aminotransferase

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
203970019	Deficiency of glutamic-alanine transaminase	en	Synonym	Active	Case insensitive	SNOMED CT core
203971015	Deficiency of SGPT	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
203972010	Deficiency of GPT	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
203973017	Deficiency of alanine aminotransferase	en	Synonym	Active	Case insensitive	SNOMED CT core
727871016	Deficiency of alanine aminotransferase (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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