Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 10 (HMND10)

Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 10, is also known as neuronopathy, distal hereditary motor, type x. An important gene associated with Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 10 is EMILIN1 (Elastin Microfibril Interfacer 1). Affiliated tissues include spinal cord and brain, and related phenotypes are distal lower limb muscle weakness and decreased compound muscle action potential amplitude