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You searched for “X” in All. RX Search found 56,119 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Charcot-Marie-Tooth neuropathy X type 2 (often written as CMTX2) is a very rare, inherited nerve disease. It affects the peripheral nerves. These are the long nerves...
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 from the...
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 and feet....
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 feet, legs,...
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, called peripheral nerves....
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, which carry messages...
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 nerves.” These are...
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 nerves that carry...
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 carry...
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 outside...
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 legs slowly...
Charcot-Marie-Tooth disease type 4 caused by mutation in PRX is a rare inherited nerve disease. Doctors usually call it Charcot-Marie-Tooth disease type 4F (CMT4F). It mainly...
