DPM3 congenital disorder of glycosylation (Q94040)

Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy.

Language	Label	Description	Also known as
default for all languages	ID_1389256016
English	DPM3 congenital disorder of glycosylation	Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy.