Charcot-Marie-Tooth disease type 2 caused by mutation in KIF1B is a very rare inherited nerve disease. It belongs to the CMT type 2 group, which mainly damages ...

Charcot-Marie-Tooth disease neuronal type 2A1 (often shortened to CMT2A1) is a rare, inherited nerve disease that mainly damages the long nerves in the arms ...

Autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1 (often shortened to CMT2A1) is a rare, inherited nerve disease that mainly damages the long ...

Charcot-Marie-Tooth disease type 2A1 (CMT2A1) is a rare inherited nerve disease that mainly damages the long nerves in the arms and legs. These nerves are ...

Inherited neuronal peroneal muscular atrophy is another name that doctors often use for Charcot–Marie–Tooth disease (CMT), especially the classic “peroneal ...

Hereditary motor and sensory neuropathy type 2 (HMSN type 2) is a group of inherited nerve diseases where the long “wires” of the nerves (axons) slowly ...

Hereditary motor and sensory neuropathy, Okinawa type, is a very rare inherited nerve disease that damages both the movement nerves (motor) and feeling nerves ...

Hereditary motor and sensory neuropathy Guadalajara neuronal type is a very rare inherited nerve disease that belongs to the Charcot-Marie-Tooth (CMT) family, ...

Autosomal dominant axonal Charcot-Marie-Tooth disease is a group of inherited nerve disorders in which the long “wires” of the nerves (axons) slowly become ...

Charcot-Marie-Tooth disease type 2 (CMT2) is a group of inherited nerve diseases in which the long part of the nerve cell (the axon) slowly becomes damaged. ...

Charcot-Marie-Tooth neuropathy type 1F/2E (often called NEFL-related CMT or CMT2E/1F) is a rare inherited disease of the peripheral nerves. These nerves carry ...

Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL is a rare inherited nerve disease that mainly affects the peripheral nerves, which are the long ...

Charcot-Marie-Tooth disease type 1F (CMT1F) is a rare inherited nerve disease that mainly affects the long nerves in the arms and legs. It is part of the big ...

Charcot-Marie-Tooth neuropathy type 1E (CMT1E) is a very rare inherited nerve disease. It affects the peripheral nerves, which are the long nerves that carry ...

Charcot-Marie-Tooth disease–hearing loss syndrome is a rare inherited nerve disorder in which a person has both Charcot-Marie-Tooth (CMT) disease and ...

Charcot-Marie-Tooth disease–deafness syndrome is a very rare inherited nerve disease in which a person has both Charcot-Marie-Tooth (CMT) neuropathy and ...

Charcot-Marie-Tooth disease and deafness (also called CMT1E when caused by some PMP22 gene variants) is a rare inherited nerve disease in which the protective ...

Autosomal dominant Charcot-Marie-Tooth neuropathy and deafness is a rare inherited nerve disease. In this condition, the long nerves to the feet and hands ...

Charcot-Marie-Tooth disease type 1E (CMT1E) is a rare inherited nerve disease. It mainly harms the peripheral nerves, which are the long nerves that carry ...

Hereditary motor and sensory neuropathy 1D (HMSN 1D) is a rare, inherited nerve disease. It is the same condition as Charcot-Marie-Tooth disease type 1D ...