CDG2B (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2B has glucosidase I enzyme defect.
See also:
Congenital disorder of glycosylation type 2B:
»Introduction: Congenital disorder of glycosylation type 2B
»Symptoms of Congenital disorder of glycosylation type 2B
CDG2B: Another name for Congenital disorder of glycosylation type 2B (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 2B
»Symptoms of Congenital disorder of glycosylation type 2B
Some of the symptoms of CDG2B incude:
See full list of 11 symptoms of CDG2B (Congenital disorder of glycosylation type 2B)
These medical disease topics may be related to CDG2B:
Search to find out more about CDG2B:
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