733450008: Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Glycoprotein metabolism disorder\Carbohydrate deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Glycoprotein metabolism disorder\Carbohydrate deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation
• \Congenital disease\Inborn error of metabolism\Glycoprotein metabolism disorder\Carbohydrate deficient glycoprotein syndrome\Carbohydrate-deficient glycoprotein syndrome type II\MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3499448014	Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3499449018	MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation	en	Synonym	Active	Case sensitive	SNOMED CT core
3499450018	Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3499451019	Congenital disorder of glycosylation type II due to MAN1B1 deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3499452014	Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3499997013	A form of congenital disorders of N-linked glycosylation with characteristics of intellectual disability, delayed motor development, hypotonia and truncal obesity. Additional features include slight facial dysmorphism (hypertelorism, downslanting palpebral fissures, large, low-set ears, hypoplastic nasolabial fold, thin upper lip), hypermobility of the joints and skin laxity. The disease is caused by mutations in the gene MAN1B1 (9q34.3).	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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