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Congenital myasthenic syndrome

Just diagnosed with Congenital myasthenic syndrome?

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

Open the full Congenital myasthenic syndrome hub →

Overview

Congenital myasthenic syndrome is a rare condition. Also known as CMS. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital myasthenic syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:590 · OMIM 254190, 254210, 254300 · ICD-10 G70.2 · GARD 0011902

Find care for Congenital myasthenic syndrome

Authoritative references for Congenital myasthenic syndrome

Common questions

I was just diagnosed with Congenital myasthenic syndrome — what should I do first?

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

Where can I find a specialist for Congenital myasthenic syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Congenital myasthenic syndrome, filtered to your area.

Are there clinical trials for Congenital myasthenic syndrome?

Tomeko shows live, recruiting studies for Congenital myasthenic syndrome 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