Cog5-Congenital Disorder of Glycosylation

Alias:

Carbohydrate Deficient Glycoprotein Syndrome Type Iii

Congenital Disorder of Glycosylation, Type I-Iix

Congenital Disorder of Glycosylation, Type Iii

Congenital Disorder of Glycosylation Type Iii

Cdgiii

Cdg2i

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cog5-Congenital Disorder of Glycosylation, also known as carbohydrate deficient glycoprotein syndrome type iii, is related to congenital disorder of glycosylation, type iii and congenital disorder of glycosylation, type in. An important gene associated with Cog5-Congenital Disorder of Glycosylation is COG5 (Component Of Oligomeric Golgi Complex 5). Affiliated tissues include liver and bone.

Related ID：

MALACARDS：CG5002