Monarch Disease Ontology id MONDO_0013212 (Charcot-Marie-Tooth disease axonal type 2N) can be described as follows. Autosomal dominant Charcot-Marie-Tooth disease type 2N (CMT2N) is a mild form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by distal legs sensory loss and weakness that can be asymmetric. Tendon reflexes are reduced in the knees and absent in ankles. Progression is slow. Also known as: AARS Charcot-Marie-Tooth disease type 2, CMT2N, Charcot-Marie-Tooth disease type 2 caused by mutation in AARS, Charcot-Marie-Tooth neuropathy axonal type 2N, autosomal dominant Charcot-Marie-Tooth disease type 2N, autosomal dominant axonal Charcot-Marie-Tooth disease type 2N.