Monarch Disease Ontology id MONDO_0011002 (neuropathy, hereditary motor and sensory, type 6A) is 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, 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, neuropathy, hereditary motor and sensory, type VIA.