MONDO_0014866 (Charcot-Marie-Tooth disease axonal type 2T) is a Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25. Also known as: CMT2T, Charcot-Marie-Tooth disease, axonal, type 2T, Charcot-Marie-Tooth neuropathy type 2T, DNAJB2-related CMT2.