MONDO_0011903 (Charcot-Marie-Tooth disease type 2J) can be described as follows. Autosomal dominant Charcot-Marie-Tooth disease type 2J (CMT2J) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a relatively late onset, pupillary abnormalities and deafness, in most patients, associated with distal weakness and muscle atrophy. Also known as: CMT2J, Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities, Charcot-Marie-Tooth disease, type 2J, Charcot-Marie-Tooth neuropathy type 2J.