Neuropathy, hereditary motor and sensory, type 6A

Definition

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 6A, hereditary motor and sensory neuropathy type 6 caused by mutation in MFN2, hereditary motor and sensory neuropathy VIA, HMSN6A, MFN2 hereditary motor and sensory neuropathy type 6, neuropathy, hereditary motor and sensory, type VIA — per MONDO

Also identified as

• OMIM 601152 per MONDO