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Neuropathy, hereditary motor and sensory, type 6A
rareAny hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the MFN2 gene.
- Identifiers
- MONDO:0011002 OMIM:601152
- Causal genes
- MFN2
- Part of
- Charcot-Marie-Tooth diseaseHereditary motor and sensory neuropathy type 6Motor peripheral neuropathy
- 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
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