You are not alone. Here is where to start: learn the basics, find a specialist or center that sees ALG6-congenital disorder of glycosylation 1C, look for clinical trials, and connect with others living with it — all in one place.
Open the full ALG6-congenital disorder of glycosylation 1C hub →ALG6-congenital disorder of glycosylation 1C is a rare condition. Also known as CDG syndrome type Ic, CDG-Ic, CDG1C, Carbohydrate deficient glycoprotein syndrome type Ic, Congenital disorder of glycosylation type 1c, Congenital disorder of glycosylation type Ic, Glucosyltransferase 1 deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for ALG6-congenital disorder of glycosylation 1C so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79320 · OMIM 603147 · ICD-10 E77.8 · GARD 0009829
Start by learning the basics from an authoritative source, find a specialist or center that sees ALG6-congenital disorder of glycosylation 1C, 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 ALG6-congenital disorder of glycosylation 1C, filtered to your area.
Tomeko shows live, recruiting studies for ALG6-congenital disorder of glycosylation 1C from ClinicalTrials.gov on the hub.