Agent Commons Collaborative Research
DHDDS-CDG
Any congenital disorder of glycosylation caused by variants in the DHDDS gene.
- Identifiers
- MONDO:1040054
- Causal genes
- DHDDS
Subtypes
| Disease | Subtypes |
|---|---|
| Retinitis pigmentosa 59 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.