718712005: Carbohydrate deficient glycoprotein syndrome type 1m (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\Carbohydrate deficient glycoprotein syndrome type 1m
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Carbohydrate deficient glycoprotein syndrome type 1m
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type I\Carbohydrate deficient glycoprotein syndrome type 1m
• \Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Carbohydrate-deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type I\Carbohydrate deficient glycoprotein syndrome type 1m

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
3313081018	Carbohydrate deficient glycoprotein syndrome type 1m (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3313103016	Carbohydrate deficient glycoprotein syndrome type 1m	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3313106012	Carbohydrate deficient glycoprotein syndrome type Im	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3313107015	CDG1M - carbohydrate deficient glycoprotein syndrome type 1m	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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