has_disease_location motor neuron Charcot-Marie-Tooth disease motor neuron disorder autosomal dominant intermediate Charcot-Marie-Tooth disease type G OMIM:617882 Charcot-Marie-Tooth disease, dominant intermediate G An autosomal dominant, intermediate form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Dominant intermediate forms are characterized by clinical and pathologic features intermediate between demyelinating and axonal peripheral neuropathies, and motor median nerve conduction velocities ranging from 25 to 45 m/sec. CMTDIG is phenotypically variable. Most affected individuals have onset in the first or second decades of slowly progressive distal motor weakness and atrophy, resulting in gait instability and distal upper limb impairment, as well as distal sensory impairment. paola Rare genetic neurological disorder