NIH GARD Information: SLC35A2-CDG
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- CDG syndrome type IIm
- Congenital disorder of glycosylation type 2m
- Congenital disorder of glycosylation type IIm
- Congenital disorder of glycosylation, type IIm
- EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 22; EIEE22
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.