disorder of multiple glycosylation
MONDO:0017749Mondo
Findings
No curated finding names disorder of multiple glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Where it sits
- A kind of
- Narrower terms (19)
- B4GALT1-congenital disorder of glycosylation
- CCDC115-CDG
- congenital disorder of glycosylation type 1E
- congenital dyserythropoietic anemia type 2
- congenital muscular dystrophy with intellectual disability and severe epilepsy
- defect in conserved oligomeric Golgi complex
- defect in V-ATPase
- developmental and epileptic encephalopathy, 50
- DK1-congenital disorder of glycosylation
- DPM3-congenital disorder of glycosylation
- GNE myopathy
- immunodeficiency 23
- leukocyte adhesion deficiency type II
- 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