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Charcot-Marie-Tooth disease type 2B1

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The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Disease Overview

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

Synonyms

  • AR-CMT2B1
  • CMT 2B1
  • CMT2B1
  • Charcot Marie Tooth disease type 2B1
  • Charcot-Marie-Tooth disease neuronal type 2B1
  • Charcot-Marie-Tooth disease type 2 caused by mutation in LMNA
  • Charcot-Marie-Tooth disease, axonal, autosomal recessive, 2B1
  • Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B1
  • Charcot-Marie-Tooth disease, axonal, type 2B1
  • Charcot-Marie-Tooth disease, neuronal, type 2B1
  • Charcot-Marie-Tooth disease, type 2B1
  • Charcot-Marie-Tooth neuropathy type 2B1
  • Charcot-Marie-Tooth neuropathy, type 2B1
  • LMNA Charcot-Marie-Tooth disease type 2
  • autosomal recessive Charcot-Marie-Tooth disease type 2B1
  • autosomal recessive axonal CMT4C1
  • autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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