62578003: Congenital defect of folate absorption (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of folate metabolism\Congenital defect of folate absorption
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of folate metabolism\Congenital defect of folate absorption
• \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\Congenital defect of folate absorption
• \Metabolic disease\Organic acid metabolism disorder\Inherited disorder of folate metabolism\Congenital defect of folate absorption
• \Congenital disease\Inborn error of metabolism\Inherited disorder of folate metabolism\Congenital defect of folate absorption

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
104006016	Congenital defect of folate absorption	en	Synonym	Active	Case insensitive	SNOMED CT core
104007013	Congenital malabsorption of folic acid	en	Synonym	Active	Case insensitive	SNOMED CT core
104008015	Folic acid transport defect	en	Synonym	Active	Case insensitive	SNOMED CT core
1232350015	Hereditary folate malabsorption	en	Synonym	Active	Case insensitive	SNOMED CT core
1232351016	Folate transport defect	en	Synonym	Active	Case insensitive	SNOMED CT core
801765019	Congenital defect of folate absorption (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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