Charcot-Marie-Tooth disease axonal type 2O

Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the DYNC1H1 gene.

Also known as: CMT2O, Charcot-Marie-Tooth disease caused by mutation in DYNC1H1, Charcot-Marie-Tooth disease, axonal, type 20, DYNC1H1 Charcot-Marie-Tooth disease, autosomal dominant Charcot-Marie-Tooth disease type 2O, Charcot-Marie-Tooth disease type 2O, Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2O, Charcot-Marie-Tooth disease, axonal, type 2O

27 clinical trials for this condition and its sub-types, 1 tagged with Charcot-Marie-Tooth disease axonal type 2O itself.