You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Glycogen storage disease, type I, look for clinical trials, and connect with others living with it — all in one place.
Open the full Glycogen storage disease, type I hub →Glycogen storage disease, type I is a rare condition. Also known as G6P deficiency, GSD due to G6P deficiency, GSD type 1, GSD type I, Glycogen storage disease due to G6P deficiency, Glycogen storage disease type 1, Glycogen storage disease type I, Glycogenosis type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glycogen storage disease, type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:364 · OMIM 232200, 232220, 232240 · ICD-10 E74.0 · GARD 0016523
Start by learning the basics from an authoritative source, find a specialist or center that sees Glycogen storage disease, type I, 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 Glycogen storage disease, type I, filtered to your area.
Tomeko shows live, recruiting studies for Glycogen storage disease, type I from ClinicalTrials.gov on the hub.