Neuropathy, hereditary motor and sensory, type 6A

Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the MFN2 gene.

Also known as: Charcot-Marie-Tooth disease, type 6, neuropathy, hereditary motor and sensory, type 6, peripheral neuropathy and optic atrophy, Charcot-Marie-Tooth disease, type 6A, HMSN6A, MFN2 hereditary motor and sensory neuropathy type 6, hereditary motor and sensory neuropathy VIA, hereditary motor and sensory neuropathy type 6 caused by mutation in MFN2

9 clinical trials for this condition and its sub-types.