Autosomal dominant Charcot-Marie-Tooth disease type 2W

Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the HARS gene.

Also known as: CMT2W, Charcot-Marie-Tooth disease type 2 caused by mutation in HARS, Charcot-Marie-Tooth disease, axonal, type 2w, HARS Charcot-Marie-Tooth disease type 2, autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation, Charcot-Marie-Tooth disease, axonal type 2W, Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2W, Charcot-Marie-Tooth disease, axonal, type 2W

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