DPM3-CDG (CDG-Io)

Alternate names[edit | edit source]

Congenital disorder of glycosylation, type Io ; CDG Io; CDGIo; CDG1(DPM3); CDG syndrome type Io; CDG-Io; Carbohydrate deficient glycoprotein syndrome type Io; DG1O; Congenital disorder of glycosylation type Io; CDG1O; DPM3-CDG; Congenital disorder of glycosylation type 1o

Definition[edit | edit source]

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.

NIH genetic and rare disease info[edit source]

NIH info on DPM3-CDG (CDG-Io)

DPM3-CDG (CDG-Io) is a rare disease.

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v t e Rare and genetic diseases
Rare diseases - DPM3-CDG (CDG-Io)
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Also see	Comprehensive list of genetic and rare diseases
Resources	NIH GARD, US Genetic and Rare Diseases Info Rare Disease Day Undiagnosed Diseases Network Database of rare diseases at Orphanet Rare Disease UK Rare diseases search engine