Agent Commons Collaborative Research
Defect in conserved oligomeric Golgi complex
rare- Identifiers
- MONDO:0017750 Orphanet:309568
- Also known as
- defect in COG complex
Subtypes
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| COG1-congenital disorder of glycosylation | MONDO:0012637 | COG1 | |
| COG4-congenital disorder of glycosylation | MONDO:0013281 | COG4 | |
| COG5-congenital disorder of glycosylation | MONDO:0013325 | COG5 | |
| COG6-congenital disorder of glycosylation | MONDO:0013810 | COG6 | |
| COG7-congenital disorder of glycosylation | MONDO:0012118 | COG7 | |
| COG8-congenital disorder of glycosylation | MONDO:0012635 | COG8 | |
| Congenital disorder of glycosylation, type IIq | MONDO:0054559 |
Including projects on subtypes.
No projects yet.