DPM3-congenital disorder of glycosylation

MONDO:0013049

DPM3-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case by muscle weakness, waddling gait and dilated cardiomyopathy.

Also known as: CDG syndrome type Io, CDG-Io, CDG1O, DPM3-CDG, DPM3-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type Io, congenital disorder of glycosylation type 1o, congenital disorder of glycosylation type Io

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