717774004: Component of oligomeric golgi complex 8 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\Component of oligomeric golgi complex 8 congenital disorder of glycosylation
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Component of oligomeric golgi complex 8 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\Component of oligomeric golgi complex 8 congenital disorder of glycosylation
• \Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\Component of oligomeric golgi complex 8 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
3322952010	Component of oligomeric golgi complex 8 congenital disorder of glycosylation (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3323499018	COG8 congenital disorder of glycosylation	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3323512014	COG8 (component of oligomeric golgi complex 8) congenital disorder of glycosylation	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3323513016	Carbohydrate deficient glycoprotein syndrome type IIh	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3323514010	Component of oligomeric golgi complex 8 congenital disorder of glycosylation	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3323515011	Congenital disorder of glycosylation type 2h	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3323516012	Congenital disorder of glycosylation type IIh	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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