721187005: Methylcobalamin deficiency type cbl G (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Homocystinuria without methylmalonic aciduria\Methylcobalamin deficiency type cbl G
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of sulfur-bearing amino acid metabolism\...
• \Functional defects of methionine synthase\Homocystinuria without methylmalonic aciduria\Methylcobalamin deficiency type cbl G
• \Homocystinuria\Homocystinuria without methylmalonic aciduria\Methylcobalamin deficiency type cbl G

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3324559012	Methylcobalamin deficiency type cbl G (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3324560019	Methylcobalamin deficiency type cbl G	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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