Congenital disorder of glycosylation type 1F
Other Names for this Disease
- Carbohydrate-deficient glycoprotein syndrome type 1F
- CDG 1F
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).