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Glycogen storage disease, type II

Just diagnosed with Glycogen storage disease, type II?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Glycogen storage disease, type II, look for clinical trials, and connect with others living with it — all in one place.

Open the full Glycogen storage disease, type II hub →

Overview

Glycogen storage disease, type II is a rare condition. Also known as Alpha-1,4-glucosidase acid deficiency, GSD due to acid maltase deficiency, GSD type 2, GSD type II, Glycogen storage disease type 2, Glycogen storage disease type II, Glycogenosis due to acid maltase deficiency, Glycogenosis type 2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glycogen storage disease, type II so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:365 · OMIM 232300 · ICD-10 E74.0 · GARD 0005714

Find care for Glycogen storage disease, type II

Authoritative references for Glycogen storage disease, type II

Common questions

I was just diagnosed with Glycogen storage disease, type II — 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 II, and connect with a patient organization. Tomeko brings these together on one hub.

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

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

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

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

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com