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Up to: Congenital disorder of glycosylation · Glycoprotein metabolism disease

Disorder of protein N-glycosylation

A disease that has its basis in the disruption of protein N-linked glycosylation.

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
DPAGT1-congenital disorder of glycosylation 0 trials
MAN1B1-congenital disorder of glycosylation 0 trials
MGAT2-congenital disorder of glycosylation 0 trials
MOGS-congenital disorder of glycosylation 0 trials
RFT1-congenital disorder of glycosylation 0 trials
SLC39A8-CDG 0 trials
SSR4-congenital disorder of glycosylation 0 trials
ST3GAL3-congenital disorder of glycosylation 0 trials Sub-types →
STT3A-congenital disorder of glycosylation 0 trials
STT3B-congenital disorder of glycosylation 0 trials
TMEM165-congenital disorder of glycosylation 0 trials
Autism spectrum disorder - epilepsy - arthrogryposis syndrome 0 trials
Congenital disorder of glycosylation type 1EE with or without immunodeficiency 0 trials
Developmental and epileptic encephalopathy, 36 0 trials