124239003: Deficiency of guanidinoacetate methyltransferase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of creatine synthesis\Deficiency of guanidinoacetate methyltransferase
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of creatine synthesis\Deficiency of guanidinoacetate methyltransferase
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of creatine synthesis\Deficiency of guanidinoacetate methyltransferase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of guanidinoacetate methyltransferase
• \Congenital disease\Inborn error of metabolism\Disorder of creatine synthesis\Deficiency of guanidinoacetate methyltransferase

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
203821017	Deficiency of guanidinoacetate methyltransferase	en	Synonym	Active	Case insensitive	SNOMED CT core
473085018	Guanidinoacetate methyltransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
727759016	Deficiency of guanidinoacetate methyltransferase (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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