You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Glycogen storage disease, type VI, look for clinical trials, and connect with others living with it — all in one place.
Open the full Glycogen storage disease, type VI hub →Glycogen storage disease, type VI is a rare condition. Also known as GSD due to liver glycogen phosphorylase deficiency, GSD type 6, GSD type VI, Glycogen storage disease type 6, Glycogen storage disease type VI, Glycogenosis due to liver glycogen phosphorylase deficiency, Glycogenosis type 6, Glycogenosis type VI. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glycogen storage disease, type VI so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:369 · OMIM 232700 · ICD-10 E74.0 · GARD 0006529
Start by learning the basics from an authoritative source, find a specialist or center that sees Glycogen storage disease, type VI, 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 VI, filtered to your area.
Tomeko shows live, recruiting studies for Glycogen storage disease, type VI from ClinicalTrials.gov on the hub.