Other Names for this Disease
- CDG 2D
- Congenital disorder of glycosylation, type IId
- Congenital disorder of glycosylation type IID
- Beta-1,4-galactosyltransferase deficiency
- RareConnect has an online community for patients and families with this condition so they can connect with others and share their experiences living with a rare disease. The project is a joint collaboration between EURORDIS (European Rare Disease Organisation) and NORD (National Organization for Rare Disorders).