You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Glycogen storage disease type X, look for clinical trials, and connect with others living with it — all in one place.
Open the full Glycogen storage disease type X hub →Glycogen storage disease type X is a rare condition. Also known as DiMauro disease, GSD due to phosphoglycerate mutase 2 deficiency, GSD type 10, Glycogen storage disease due to PGAM2 deficiency, Glycogen storage disease due to phosphoglycerate mutase 2 deficiency, Glycogen storage disease, type 10, Glycogen storage disease, type X, Glycogenosis due to phosphoglycerate mutase 2 deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glycogen storage disease type X so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:97234 · OMIM 261670 · ICD-10 E74.0 · GARD 0009964
Start by learning the basics from an authoritative source, find a specialist or center that sees Glycogen storage disease type X, 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 X, filtered to your area.
Tomeko shows live, recruiting studies for Glycogen storage disease type X from ClinicalTrials.gov on the hub.