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Charcot-Marie-Tooth disease, type IA

Just diagnosed with Charcot-Marie-Tooth disease, type IA?

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

Open the full Charcot-Marie-Tooth disease, type IA hub →

Overview

Charcot-Marie-Tooth disease, type IA is a rare condition. Also known as CMT1A, Microduplication 17p12. Tomeko brings together the specialists, research, clinical trials, treatments and community for Charcot-Marie-Tooth disease, type IA so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:101081 · OMIM 118220 · ICD-10 G60.0 · GARD 0001245

Find care for Charcot-Marie-Tooth disease, type IA

Authoritative references for Charcot-Marie-Tooth disease, type IA

Common questions

I was just diagnosed with Charcot-Marie-Tooth disease, type IA — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Charcot-Marie-Tooth disease, type IA, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Charcot-Marie-Tooth disease, type IA?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Charcot-Marie-Tooth disease, type IA, filtered to your area.

Are there clinical trials for Charcot-Marie-Tooth disease, type IA?

Tomeko shows live, recruiting studies for Charcot-Marie-Tooth disease, type IA 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