You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Glycogen storage disease due to glucose-6-phosphatase deficiency type IA, look for clinical trials, and connect with others living with it — all in one place.
Open the full Glycogen storage disease due to glucose-6-phosphatase deficiency type IA hub →Glycogen storage disease due to glucose-6-phosphatase deficiency type IA is a rare condition. Also known as G6P deficiency type 1a, GSD due to G6P deficiency type 1a, GSD due to G6P deficiency type Ia, GSD type 1a, GSDIa, Glycogen storage disease due to G6P deficiency type Ia, Glycogen storage disease type 1a, Glycogenosis due to glucose-6-phosphatase deficiency type 1a. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glycogen storage disease due to glucose-6-phosphatase deficiency type IA so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79258 · OMIM 232200 · ICD-10 E74.0 · GARD 0007864
Start by learning the basics from an authoritative source, find a specialist or center that sees Glycogen storage disease due to glucose-6-phosphatase deficiency type IA, and connect with a patient organization. Tomeko brings these together on one hub.
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