725028009: Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
• \Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437640019	Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3437641015	Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3437642010	Carbohydrate deficient glycoprotein syndrome type IIb	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3437643017	Congenital disorder of glycosylation type 2b	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3437644011	Congenital disorder of glycosylation type IIb	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3437645012	Glucosidase 1 deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3437646013	MOGS CDG - mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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