Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (CMT2A2) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as se...

Autosomal dominant Charcot-Marie-Tooth disease type 2B (AD-CMT2B) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as s...

Autosomal dominant Charcot-Marie-Tooth disease type 2C (CMT2C) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2D (CMT2D) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2DD (CMT2DD) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as se...

Autosomal dominant Charcot-Marie-Tooth disease type 2E (CMT2E) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2F (CMT2F) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2G (CMT2G) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2I (AD-CMT2I) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as s...

Autosomal dominant Charcot-Marie-Tooth disease type 2J (CMT2J) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by slowly progressive muscle weakness and wasting (atrophy) of the lower legs, feet, a...

Autosomal dominant Charcot-Marie-Tooth disease type 2K (CMT2K) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting, sensory loss, and foot deformities. CMT2K ...

Autosomal dominant Charcot-Marie-Tooth disease type 2L (CMT2L) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs, feet, and hands, as well...

Autosomal dominant Charcot-Marie-Tooth disease type 2M (CMT2M) is a rare inherited neurological disorder that affects the peripheral nerves. It is caused by mutations in the SH3TC2 gene, which is responsible for the production of a protein that he...

Autosomal dominant Charcot-Marie-Tooth disease type 2N (CMT2N) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2O (CMT2O) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...

Autosomal dominant Charcot-Marie-Tooth disease type 2Q (CMT2Q) is a rare inherited neurological disorder that affects the peripheral nerves. It is caused by mutations in the GARS gene, which is responsible for the production of the protein glycine...

Autosomal dominant Charcot-Marie-Tooth disease type 2U (CMT2U) is a rare inherited neurological disorder that affects the peripheral nerves. It is characterized by progressive muscle weakness and wasting in the lower legs and feet, as well as sens...