You are not alone. Here is where to start: learn the basics, find a specialist or center that sees SLC39A8-CDG, look for clinical trials, and connect with others living with it — all in one place.
Open the full SLC39A8-CDG hub →SLC39A8-CDG is a rare condition. Also known as CDG syndrome type IIn, CDG-IIn, CDG2N, Carbohydrate deficient glycoprotein syndrome type IIn, Congenital disorder of glycosylation type 2n, Congenital disorder of glycosylation type IIn, SLC39A8 deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for SLC39A8-CDG so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:468699 · OMIM 616721 · ICD-10 E77.8 · GARD 0017846
Start by learning the basics from an authoritative source, find a specialist or center that sees SLC39A8-CDG, 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 SLC39A8-CDG, filtered to your area.
Tomeko shows live, recruiting studies for SLC39A8-CDG from ClinicalTrials.gov on the hub.