Charcot-Marie-Tooth disease X-linked recessive 2 (often shortened to CMTX2) is a very rare inherited nerve disease. It mainly damages the long nerves that go ...

Charcot-Marie-Tooth neuropathy X-linked dominant 6 (often called CMTX6) is a very rare, inherited nerve disease that mainly affects the long nerves in the legs ...

Charcot-Marie-Tooth disease X-linked dominant 6 (often shortened to CMTX6) is a very rare, inherited nerve disease that mainly affects the long nerves to the ...

Charcot-Marie-Tooth neuropathy X-linked dominant 1 (often called CMTX1) is a rare inherited nerve disease that mainly affects the “long wires” of the body, ...

Charcot-Marie-Tooth disease X-linked dominant type 1 (often called CMTX1 or CMT1X) is a rare inherited nerve disease. It mainly damages the peripheral nerves, ...

Charcot-Marie-Tooth disease type X caused by mutation in GJB1 (often called CMTX1) is a rare, inherited nerve disease. It mainly damages the “peripheral ...

Charcot-Marie-Tooth disease X-linked dominant 1 (often called CMTX1) is a genetic nerve disease. It mainly affects the peripheral nerves, which are the long ...

X-linked hereditary motor and sensory neuropathy is a long-term nerve disease that mainly damages the nerves in the legs, feet, hands, and arms. These nerves ...

Charcot-Marie-Tooth disease type X (often written as CMTX or CMTX1) is a genetic nerve disease. It mainly affects the peripheral nerves, which are the nerves ...

Hereditary motor and sensory neuropathy with pyramidal features is a very rare nerve disease that runs in families. It affects the long nerves that move the ...

Hereditary motor and sensory neuropathy type V (HMSN V) is a very rare inherited nerve disease. It affects both the motor nerves (that move muscles) and the ...

Hereditary motor and sensory neuropathy type 5 (HMSN type 5) is a very rare form of Charcot–Marie–Tooth (CMT) disease. Doctors also call it ...

Charcot-Marie-Tooth (CMT) disease–pyramidal features syndrome is a rare, inherited nerve disease in which a person has both signs of CMT (damage to the long ...

Charcot-Marie-Tooth disease type 5 (CMT type 5) is a rare inherited nerve disease that mainly damages the long nerves to the feet, legs, hands, and arms and ...

Cytochrome c oxidase assembly factor–related Charcot-Marie-Tooth disease type 4 is a very rare inherited nerve disease where the long nerves in the arms and ...

Surf1-related severe demyelinating Charcot-Marie-Tooth (CMT) disease is a very rare inherited nerve disease. It mainly damages the long nerves that go from the ...

Charcot–Marie–Tooth disease type 4 caused by mutation in SURF1 is a group of inherited nerve diseases that slowly damage the peripheral nerves. These nerves ...

Autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K (often shortened to CMT4K) is a very rare inherited disease that affects the ...

Autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K (CMT4K) is a very rare inherited nerve disease that mainly affects the long nerves of the ...

Charcot-Marie-Tooth disease type 4K (CMT4K) is a rare inherited nerve disease that mainly damages the long nerves in the arms and legs. It is an autosomal ...