Charcot-Marie-Tooth disease type 2B1

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Charcot-Marie-Tooth disease type 2B1

Synonyms: AR-CMT2B1 | Autosomal recessive Charcot-Marie-Tooth disease type 2B1 | Autosomal recessive axonal CMT4C1

Charcot-Marie-Tooth disease type 2B1 (CMT2B1 also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version April 2024

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Charcot-Marie-Tooth disease type 2B1?

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Advocacy Organizations

Hereditary Neuropathy Foundation

Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth (CMT) and related inherited neuropathies, support patients and families with critical information to improve quality of life, and fund research that will lead to treatments and cures.

Clinical Trials

For a list of clinical trials in this disease area, please click here.