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Up to: Congenital disorder of glycosylation

Congenital disorder of glycosylation type I

A congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor.

0 trials tagged with this condition →

PMM2-congenital disorder of glycosylation 5 trials
MPI-congenital disorder of glycosylation 1 trial
PGM1-congenital disorder of glycosylation 1 trial
ALG1-congenital disorder of glycosylation 0 trials
ALG11-congenital disorder of glycosylation 0 trials
ALG12-congenital disorder of glycosylation 0 trials
ALG2-congenital disorder of glycosylation 0 trials Sub-types →
ALG3-congenital disorder of glycosylation 0 trials
ALG6-congenital disorder of glycosylation 1C 0 trials
ALG8-congenital disorder of glycosylation 0 trials
ALG9-congenital disorder of glycosylation 0 trials Sub-types →
DDOST-congenital disorder of glycosylation 0 trials
DK1-congenital disorder of glycosylation 0 trials
DPAGT1-congenital disorder of glycosylation 0 trials
DPM3-congenital disorder of glycosylation 0 trials Sub-types →
MPDU1-congenital disorder of glycosylation 0 trials
RFT1-congenital disorder of glycosylation 0 trials
SRD5A3-congenital disorder of glycosylation 0 trials
SSR3-CDG 0 trials
SSR4-congenital disorder of glycosylation 0 trials
STT3A-congenital disorder of glycosylation 0 trials
STT3B-congenital disorder of glycosylation 0 trials
Congenital disorder of glycosylation type 1E 0 trials
Congenital disorder of glycosylation, type IAA 0 trials
Congenital disorder of glycosylation, type ICC 0 trials
Congenital muscular dystrophy with intellectual disability and severe epilepsy 0 trials
Developmental and epileptic encephalopathy, 36 0 trials
Developmental and epileptic encephalopathy, 50 0 trials