CDGS1B (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1B has a phosphomannose isomerase enzyme defect.
See also:
Congenital disorder of glycosylation type 1B:
»Introduction: Congenital disorder of glycosylation type 1B
»Symptoms of Congenital disorder of glycosylation type 1B
CDGS1B: Another name for Congenital disorder of glycosylation type 1B (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 1B
»Symptoms of Congenital disorder of glycosylation type 1B
Some of the symptoms of CDGS1B incude:
See full list of 8 symptoms of CDGS1B (Congenital disorder of glycosylation type 1B)
These medical disease topics may be related to CDGS1B:
Search to find out more about CDGS1B:
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