congenital disorder of glycosylation type I
A congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor. [ url:http://en.wikipedia.org/wiki/Congenital_disorder_of_glycosylation#Classification ]
Synonyms: DPM3-CDG, DOLK-CDG, PMM2-CDG, MPI-CDG, DPAGT1-CDG, ALG3-CDG, DPM1-CDG, ALG2-CDG, ALG11-CDG, ALG8-CDG, ALG6-CDG, ALG9-CDG, ALG12-CDG, DPM2-CDG, ALG1-CDG, MPDU1-CDG, RFT1-CDG, SRD5A3-CDG
OMIM mapping confirmed by DO. [SN].