obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2G true http://purl.obolibrary.org/obo/MONDO_0013753 ICD10:G60.0 orphanet OMIM:608591 Autosomal dominant Charcot-Marie-Tooth disease type 2G (CMT2G) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2G [has only been described in 1 familly and] onset is associated to development of foot deformity and walking difficulties between the 1st and the 8th decades, with a median range in the 2nd one. Weakness and sensory loss involve primarily the legs and ankles tendon reflexes are reduced. CMT2G has a slowly progressive course. CMT2G 3.41.0 Replaced with Mondo term.