Congenital disorder of glycosylation type 1G
Other Names for this Disease
- ALG12-CDG (CDG-Ig)
- ALG12-congenital disorder of glycosylation
- CDG 1G
On this page
- 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).