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Myotonic dystrophy type 2

Just diagnosed with Myotonic dystrophy type 2?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Myotonic dystrophy type 2, look for clinical trials, and connect with others living with it — all in one place.

Open the full Myotonic dystrophy type 2 hub →

Overview

Myotonic dystrophy type 2 is a rare condition. Also known as Myotonic dystrophy type 2, Proximal myotonic dystrophy, Ricker disease, Ricker syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Myotonic dystrophy type 2 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:606 · OMIM 602668 · ICD-10 G71.1 · GARD 0009728

Find care for Myotonic dystrophy type 2

Authoritative references for Myotonic dystrophy type 2

Common questions

I was just diagnosed with Myotonic dystrophy type 2 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Myotonic dystrophy type 2, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Myotonic dystrophy type 2?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Myotonic dystrophy type 2, filtered to your area.

Are there clinical trials for Myotonic dystrophy type 2?

Tomeko shows live, recruiting studies for Myotonic dystrophy type 2 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