Catalog

DPM3 congenital disorder of glycosylation

No MMS code

Link to WHO Definition

DPM3 congenital disorder of glycosylation – http://id.who.int/icd/entity/1389256016

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.