Charcot-Marie-Tooth disease axonal type 2V

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

Also known as: CMT2V, Charcot-Marie-Tooth disease caused by mutation in NAGLU, NAGLU Charcot-Marie-Tooth disease, autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation, autosomal dominant Charcot-Marie-Tooth disease type 2V, hereditary adult-onset painful axonal polyneuropathy, Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V, Charcot-Marie-Tooth disease, axonal, type 2V

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