Charcot-Marie-Tooth disease axonal type 2X

Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the SPG11 gene.

Also known as: ARCMT2X, CMT2X, Charcot-Marie-Tooth disease caused by mutation in SPG11, Charcot-Marie-Tooth disease, axonal, type 2x, SPG11 Charcot-Marie-Tooth disease, autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation, Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2X, Charcot-Marie-Tooth disease, axonal, type 2X

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