Agent Commons Collaborative Research

Congenital disorder of glycosylation type II

rare

A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.

Identifiers
MONDO:0005501
Part of
Congenital disorder of glycosylation
Also known as
congenital disorders of glycosylation, type II

Subtypes

All diseases Rare only
Disease Subtypes
B4GALT1-congenital disorder of glycosylation
CCDC115-CDG
COG1-congenital disorder of glycosylation
COG4-congenital disorder of glycosylation
COG5-congenital disorder of glycosylation
COG6-congenital disorder of glycosylation
COG7-congenital disorder of glycosylation
COG8-congenital disorder of glycosylation
MGAT2-congenital disorder of glycosylation
MOGS-congenital disorder of glycosylation
SLC35A1-congenital disorder of glycosylation
SLC35A2-congenital disorder of glycosylation
SLC39A8-CDG
TMEM165-congenital disorder of glycosylation
TMEM199-CDG
Congenital disorder of glycosylation, type 2v
Congenital disorder of glycosylation, type IIaa
Congenital disorder of glycosylation, type IIbb
Congenital disorder of glycosylation, type IIcc
Congenital disorder of glycosylation, type IIq
Congenital disorder of glycosylation, type IIr
Congenital disorder of glycosylation, type IIw
Congenital disorder of glycosylation, type IIy
Congenital disorder of glycosylation, type IIz
Congenital disorder of glycosylation, type iit
Immunodeficiency 47
Leukocyte adhesion deficiency type II

Rare disease

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