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

5 clinical trials for this condition and its sub-types, 0 tagged with DPM3-congenital disorder of glycosylation itself.

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Part of

↑ Disorder of multiple glycosylation (9) ↑ Congenital disorder of glycosylation type I (7) ↑ Muscular dystrophy-dystroglycanopathy (1)

Sub-types of DPM3-congenital disorder of glycosylation

Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15 0 trials

Including sub-types (5) Tagged with DPM3-congenital disorder of glycosylation (0)

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