CDGS4 (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1D has a ?1,3-Mannosyl transferase enzyme defect.
See also:
Congenital disorder of glycosylation type 1D:
»Introduction: Congenital disorder of glycosylation type 1D
»Symptoms of Congenital disorder of glycosylation type 1D
CDGS4: Another name for Congenital disorder of glycosylation type 1D (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 1D
»Symptoms of Congenital disorder of glycosylation type 1D
Some of the symptoms of CDGS4 incude:
See full list of 7 symptoms of CDGS4 (Congenital disorder of glycosylation type 1D)
These medical disease topics may be related to CDGS4:
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