89579000: Tetrahydrofolate methyltransferase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of folate metabolism\Tetrahydrofolate methyltransferase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of folate metabolism\Tetrahydrofolate methyltransferase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of sulfur-bearing amino acid metabolism\Tetrahydrofolate methyltransferase deficiency
• \Metabolic disease\Organic acid metabolism disorder\Inherited disorder of folate metabolism\Tetrahydrofolate methyltransferase deficiency
• \Metabolic disease\Enzymopathy\Tetrahydrofolate methyltransferase deficiency
• \Congenital disease\Inborn error of metabolism\Inherited disorder of folate metabolism\Tetrahydrofolate methyltransferase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
148520014	Tetrahydrofolate methyltransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
148521013	THF methyltransferase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
832501014	Tetrahydrofolate methyltransferase 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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