MONDO_0011909 (Charcot-Marie-Tooth disease dominant intermediate D) can be described as follows. Autosomal dominant intermediate Charcot-Marie-Tooth disease type D is a rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies. It presents with usual Charcot-Marie-Tooth disease clinical features of variable severity (progressive muscle weakness and atrophy of the distal extremities, distal sensory loss, reduced or absent deep tendon reflexes, and feet deformities). Other findings in some of the families include debilitating neuropathic pain and mild postural/kinetic upper limb tremor. Also known as: CMTDID, Charcot-Marie-Tooth disease caused by mutation in MPZ, Charcot-Marie-Tooth disease dominant intermediate type D, Charcot-Marie-Tooth disease, dominant Intermediate type D, Charcot-Marie-Tooth neuropathy dominant intermediate D, DI-CMTD, MPZ Charcot-Marie-Tooth disease, autosomal dominant intermediate Charcot-Marie-Tooth disease type D.