Just diagnosed with Charcot-Marie-Tooth disease?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Charcot-Marie-Tooth disease, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Charcot-Marie-Tooth disease hub →Overview
Charcot-Marie-Tooth disease is a rare condition. Also known as CMT/HMSN, Charcot-Marie-Tooth hereditary neuropathy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Charcot-Marie-Tooth disease so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:166 · GARD 0006034
Find care for Charcot-Marie-Tooth disease
Authoritative references for Charcot-Marie-Tooth disease
Research & market landscape for Charcot-Marie-Tooth disease
Following Charcot-Marie-Tooth disease for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Charcot-Marie-Tooth disease — the real-world landscape behind the condition, in one place.
- Latest Charcot-Marie-Tooth disease research on PubMed ↗
- Recruiting Charcot-Marie-Tooth disease trials on ClinicalTrials.gov ↗
- Explore the Charcot-Marie-Tooth disease research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Charcot-Marie-Tooth disease and every rare condition. See how Tomeko works with industry →
Common questions
What is Charcot-Marie-Tooth disease?
Charcot-Marie-Tooth disease is a rare condition. Also known as CMT/HMSN, Charcot-Marie-Tooth hereditary neuropathy. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Charcot-Marie-Tooth disease together in one place.
What are the symptoms of Charcot-Marie-Tooth disease?
Symptoms of Charcot-Marie-Tooth disease 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 Charcot-Marie-Tooth disease.
How is Charcot-Marie-Tooth disease treated?
Treatment for Charcot-Marie-Tooth disease depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Charcot-Marie-Tooth disease, and review current options with them.
What causes Charcot-Marie-Tooth disease — is it genetic?
The cause and inheritance of Charcot-Marie-Tooth disease are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Charcot-Marie-Tooth disease can explain what it means for you and your family.
I was just diagnosed with Charcot-Marie-Tooth disease — 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, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Charcot-Marie-Tooth disease?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Charcot-Marie-Tooth disease, filtered to your area.
Are there clinical trials for Charcot-Marie-Tooth disease?
Tomeko shows live, recruiting studies for Charcot-Marie-Tooth disease from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- Char syndrome
- Charcot-Marie-Tooth disease axonal type 2C
- Chapare hemorrhagic fever
- Charcot-Marie-Tooth disease axonal type 2CC
- Chaotic conus spinal cord lipoma
- Charcot-Marie-Tooth disease axonal type 2F
- Channelopathy-associated congenital insensitivity to pain, autosomal recessive
- Charcot-Marie-Tooth disease axonal type 2H
