You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Congenital disorder of glycosylation type 1E, look for clinical trials, and connect with others living with it — all in one place.
Open the full Congenital disorder of glycosylation type 1E hub →Congenital disorder of glycosylation type 1E is a rare condition. Also known as CDG syndrome type Ie, CDG-Ie, CDG1E, Carbohydrate deficient glycoprotein syndrome type Ie, Congenital disorder of glycosylation type 1e, Congenital disorder of glycosylation type Ie, Dol-P-mannosyltransferase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital disorder of glycosylation type 1E so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79322 · OMIM 608799 · ICD-10 E77.8 · GARD 0009831
Start by learning the basics from an authoritative source, find a specialist or center that sees Congenital disorder of glycosylation type 1E, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Congenital disorder of glycosylation type 1E, filtered to your area.
Tomeko shows live, recruiting studies for Congenital disorder of glycosylation type 1E from ClinicalTrials.gov on the hub.