Disorder of multiple glycosylation

Part of

Sub-types of Disorder of multiple glycosylation

• GNE myopathy 3 trials
• Leukocyte adhesion deficiency type II 2 trials
• Reunion island Larsen syndrome 1 trial
• SLC35A2-congenital disorder of glycosylation 1 trial
• Congenital dyserythropoietic anemia type 2 1 trial
• Immunodeficiency 23 1 trial
• B4GALT1-congenital disorder of glycosylation 0 trials
• CCDC115-CDG 0 trials
• DK1-congenital disorder of glycosylation 0 trials
• DPM3-congenital disorder of glycosylation 0 trials
  1 sub-type

  • Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15 0 trials
• MPDU1-congenital disorder of glycosylation 0 trials
• SLC35A1-congenital disorder of glycosylation 0 trials
• SRD5A3-congenital disorder of glycosylation 0 trials
• TMEM199-CDG 0 trials
• Congenital disorder of glycosylation type 1E 0 trials
• Congenital muscular dystrophy with intellectual disability and severe epilepsy 0 trials
• Defect in V-ATPase 0 trials
• Defect in conserved oligomeric Golgi complex 0 trials
  7 sub-types

  • COG1-congenital disorder of glycosylation 0 trials
  • COG4-congenital disorder of glycosylation 0 trials
  • COG5-congenital disorder of glycosylation 0 trials
  • COG6-congenital disorder of glycosylation 0 trials
  • COG7-congenital disorder of glycosylation 0 trials
  • COG8-congenital disorder of glycosylation 0 trials
  • Congenital disorder of glycosylation, type IIq 0 trials
• Developmental and epileptic encephalopathy, 50 0 trials