Neuropathy, hereditary motor and sensory, type 6A

MONDO:0011002

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, 0 tagged with Neuropathy, hereditary motor and sensory, type 6A itself.

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↑ Charcot-Marie-Tooth disease (77) ↑ Motor peripheral neuropathy (1) ↑ Hereditary motor and sensory neuropathy type 6 (0)

Including sub-types (9) Tagged with Neuropathy, hereditary motor and sensory, type 6A (0)

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