Preferred Label : Charcot-Marie-Tooth disease type 2G;
ICD-11 definition : 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.;
Origin ID : 1279608482;
Currated CISMeF NLP mapping
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.
