You are not alone. Here is where to start: learn the basics, find a specialist or center that sees TMEM199-CDG, look for clinical trials, and connect with others living with it — all in one place.
Open the full TMEM199-CDG hub →TMEM199-CDG is a rare condition. Also known as CDG syndrome type IIp, CDG-IIp, CDG2P, Carbohydrate deficient glycoprotein syndrome type IIp, Congenital disorder of glycosylation type 2p, Congenital disorder of glycosylation type IIp. Tomeko brings together the specialists, research, clinical trials, treatments and community for TMEM199-CDG so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:466703 · OMIM 616829 · ICD-10 E77.8 · GARD 0017825
Start by learning the basics from an authoritative source, find a specialist or center that sees TMEM199-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 TMEM199-CDG, filtered to your area.
Tomeko shows live, recruiting studies for TMEM199-CDG from ClinicalTrials.gov on the hub.