Preferred Label : Charcot-Marie-Tooth disease type 2F;
ICD-11 definition : Autosomal dominant Charcot-Marie-Tooth disease type 2F (CMT2F) is a form of axonal
Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2F is characterized
by symmetric weakness primarily occurring in the lower limbs (distal muscles in a
majority of cases) and reaching the arms only after 5 to 10 years, occasional and
predominantly distal sensory loss and reduced tendon reflexes. CMT2F presents with
gait anomaly between the 1st and 6th decade and early onset is generally associated
to a more severe phenotype which may include foot drop.;
Origin ID : 1970894933;
Automatic exact mappings (from CISMeF team)
Autosomal dominant Charcot-Marie-Tooth disease type 2F (CMT2F) is a form of axonal
Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2F is characterized
by symmetric weakness primarily occurring in the lower limbs (distal muscles in a
majority of cases) and reaching the arms only after 5 to 10 years, occasional and
predominantly distal sensory loss and reduced tendon reflexes. CMT2F presents with
gait anomaly between the 1st and 6th decade and early onset is generally associated
to a more severe phenotype which may include foot drop.
