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Glycogen storage disease, type I

Specialists and centers, recruiting clinical trials, patient organizations, research, and community for Glycogen storage disease, type I — brought together in one place.

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Just diagnosed with Glycogen storage disease, type I?

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.

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Overview

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

Find care for Glycogen storage disease, type I

Authoritative references for Glycogen storage disease, type I

Research & market landscape for Glycogen storage disease, type I

Following Glycogen storage disease, type I for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Glycogen storage disease, type I — the real-world landscape behind the condition, in one place.

Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Glycogen storage disease, type I and every rare condition. See how Tomeko works with industry →

Common questions

What is Glycogen storage disease, type I?

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. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Glycogen storage disease, type I together in one place.

What are the symptoms of Glycogen storage disease, type I?

Symptoms of Glycogen storage disease, type I vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Glycogen storage disease, type I.

How is Glycogen storage disease, type I treated?

Treatment for Glycogen storage disease, type I depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Glycogen storage disease, type I, and review current options with them.

What causes Glycogen storage disease, type I — is it genetic?

The cause and inheritance of Glycogen storage disease, type I are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Glycogen storage disease, type I can explain what it means for you and your family.

I was just diagnosed with Glycogen storage disease, type I — what should I do first?

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.

Where can I find a specialist for Glycogen storage disease, type I?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Glycogen storage disease, type I, filtered to your area.

Are there clinical trials for Glycogen storage disease, type I?

Tomeko shows live, recruiting studies for Glycogen storage disease, type I from ClinicalTrials.gov on the hub.

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