Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NAGLU gene. The disease is Monarch Disease Ontology entry MONDO_0014665 (Charcot-Marie-Tooth disease axonal type 2V). Also known as: CMT2V, Charcot-Marie-Tooth disease caused by mutation in NAGLU, Charcot-Marie-Tooth neuropathy type 2V, 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, autosomal dominant axonal Charcot-Marie-Tooth disease type 2V, hereditary adult-onset painful axonal polyneuropathy.