Charcot-Marie-Tooth disease axonal type 2CC

MONDO:0014836

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

Also known as: CMT2CC, Charcot-Marie-Tooth disease axonal type 2CC, Charcot-Marie-Tooth disease caused by mutation in NEFH, Charcot-Marie-Tooth disease, axonal, type 2cc, NEFH Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease, axonal, type 2CC, Charcot-Marie-Tooth neuropathy, type 2Cc

8 clinical trials for this condition and its sub-types, 0 tagged with Charcot-Marie-Tooth disease axonal type 2CC itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by