National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Charcot-Marie-Tooth disease type 2


Other Names:
Autosomal dominant Charcot-Marie-Tooth disease type 2; Hereditary motor and sensory neuropathy type 2; CMT2; Autosomal dominant Charcot-Marie-Tooth disease type 2; Hereditary motor and sensory neuropathy type 2; CMT2; Charcot-Marie-Tooth type 2; Autosomal dominant axonal Charcot-Marie-Tooth disease See More
Subtypes:
Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons; Charcot-Marie-Tooth disease type 2A; Charcot-Marie-Tooth disease type 2B; Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons; Charcot-Marie-Tooth disease type 2A; Charcot-Marie-Tooth disease type 2B; Charcot-Marie-Tooth disease type 2B1; Charcot-Marie-Tooth disease type 2B2; Charcot-Marie-Tooth disease type 2C; Charcot-Marie-Tooth disease type 2D; Charcot-Marie-Tooth disease type 2E; Charcot-Marie-Tooth disease type 2F; Charcot-Marie-Tooth disease type 2G; Charcot-Marie-Tooth disease type 2H; Charcot-Marie-Tooth disease type 2I; Charcot-Marie-Tooth disease type 2J; Charcot-Marie-Tooth disease type 2K; Charcot-Marie-Tooth disease type 2L; Charcot-Marie-Tooth disease type 2N; Charcot-Marie-Tooth disease type 2O; Charcot-Marie-Tooth disease type 2P; Charcot-Marie-Tooth disease type 2Q See More
This disease is grouped under:

Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.

Organizations Supporting this Disease

Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.

Community Resources

  • The Job Accommodation Network (JAN) has information on workplace accommodations and disability employment issues related to this condition. JAN is a service of the Office of Disability Employment Policy in the U.S. Department of Labor.

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.

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