Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the MFN2 gene.
Comprehensive, easy-to-understand information about this condition
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motor nerve neuritis
MONDO:0004004
glossopharyngeal motor neuropathy
MONDO:0004279
Charcot-Marie-Tooth disease, Guadalajara neuronal type
MONDO:0007310
Charcot-Marie-Tooth disease with ptosis and parkinsonism
MONDO:0007312
Charcot-Marie-Tooth disease type 3
MONDO:0007790
neuronopathy, distal hereditary motor, autosomal dominant 1
MONDO:0008451