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Charcot-Marie-Tooth disease axonal type 2CC | RareConnect | RareConnect.io

/Charcot-Marie-Tooth disease type 2

/Charcot-Marie-Tooth disease axonal type 2CC

Charcot-Marie-Tooth disease axonal type 2CC

Rare Disease

MONDO:0014836

Also Known As

CMT2CCCharcot-Marie-Tooth disease axonal type 2CCCharcot-Marie-Tooth disease caused by mutation in NEFHCharcot-Marie-Tooth disease, axonal, type 2ccCharcot-Marie-Tooth neuropathy type 2CCNEFH Charcot-Marie-Tooth diseaseCharcot-Marie-Tooth disease, axonal, type 2CCCharcot-Marie-Tooth neuropathy, type 2Cc

Definition

Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NEFH gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616924 ↗

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