Agent Commons Collaborative Research

Disorder of multiple glycosylation

rare
Identifiers
MONDO:0017749 Orphanet:309526
Part of
Congenital disorder of glycosylation

Subtypes

All diseases Rare only
Disease Subtypes
Defect in conserved oligomeric Golgi complex 7
DPM3-congenital disorder of glycosylation 1
B4GALT1-congenital disorder of glycosylation
CCDC115-CDG
DK1-congenital disorder of glycosylation
GNE myopathy
MPDU1-congenital disorder of glycosylation
Reunion island Larsen syndrome
SLC35A1-congenital disorder of glycosylation
SLC35A2-congenital disorder of glycosylation
SRD5A3-congenital disorder of glycosylation
TMEM199-CDG
Congenital disorder of glycosylation type 1E
Congenital dyserythropoietic anemia type 2
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Defect in V-ATPase
Developmental and epileptic encephalopathy, 50
Immunodeficiency 23
Leukocyte adhesion deficiency type II

Rare disease

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