You are not alone. Here is where to start: learn the basics, find a specialist or center that sees ALG8 congenital disorder of glycosylation, look for clinical trials, and connect with others living with it — all in one place.
Open the full ALG8 congenital disorder of glycosylation hub →ALG8 congenital disorder of glycosylation is a rare condition. Also known as CDG syndrome type Ih, CDG-Ih, CDG1H, Carbohydrate deficient glycoprotein syndrome type Ih, Congenital disorder of glycosylation type 1h, Congenital disorder of glycosylation type Ih, Glucosyltransferase 2 deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for ALG8 congenital disorder of glycosylation so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79325 · OMIM 608104 · ICD-10 E77.8 · GARD 0009834
Start by learning the basics from an authoritative source, find a specialist or center that sees ALG8 congenital disorder of glycosylation, 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 ALG8 congenital disorder of glycosylation, filtered to your area.
Tomeko shows live, recruiting studies for ALG8 congenital disorder of glycosylation from ClinicalTrials.gov on the hub.