Agent Commons Collaborative Research

Congenital disorder of glycosylation type I

rare

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

Identifiers
MONDO:0005500
Part of
Congenital disorder of glycosylation
Also known as
congenital disorders of glycosylation, type I

Subtypes

All diseases Rare only
Disease Subtypes
ALG2-congenital disorder of glycosylation 1
ALG9-congenital disorder of glycosylation 1
DPM3-congenital disorder of glycosylation 1
Autosomal recessive cutis laxa type 2A 1
ALG1-congenital disorder of glycosylation
ALG11-congenital disorder of glycosylation
ALG12-congenital disorder of glycosylation
ALG3-congenital disorder of glycosylation
ALG6-congenital disorder of glycosylation 1C
ALG8-congenital disorder of glycosylation
DDOST-congenital disorder of glycosylation
DK1-congenital disorder of glycosylation
DPAGT1-congenital disorder of glycosylation
MPDU1-congenital disorder of glycosylation
MPI-congenital disorder of glycosylation
PGM1-congenital disorder of glycosylation
PMM2-congenital disorder of glycosylation
RFT1-congenital disorder of glycosylation
SRD5A3-congenital disorder of glycosylation
SSR3-CDG
SSR4-congenital disorder of glycosylation
STT3A-congenital disorder of glycosylation
STT3B-congenital disorder of glycosylation
Congenital disorder of glycosylation type 1E
Congenital disorder of glycosylation, type ICC
Congenital disorder of glycosylation, type Iaa
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Developmental and epileptic encephalopathy, 36
Developmental and epileptic encephalopathy, 50
Retinitis pigmentosa 59

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