720976009: Asparagine-linked glycosylation 3 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 I\Asparagine-linked glycosylation 3 congenital disorder of glycosylation
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Asparagine-linked glycosylation 3 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 I\Asparagine-linked glycosylation 3 congenital disorder of glycosylation
• \Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type I\Asparagine-linked glycosylation 3 congenital disorder of glycosylation

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
3322700017	Asparagine-linked glycosylation 3 congenital disorder of glycosylation (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3322725014	Asparagine-linked glycosylation 3 congenital disorder of glycosylation	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3322726010	ALG3 congenital disorder of glycosylation	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3322727018	Carbohydrate deficient glycoprotein syndrome type Id	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3322728011	Congenital disorder of glycosylation type 1d	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3322729015	Congenital disorder of glycosylation type Id	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3322730013	Mannosyltransferase 6 deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3322751011	ALG3-CDG - asparagine-linked glycosylation 3 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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