Autosomal dominant Charcot–Marie–Tooth disease with focally folded myelin sheaths type 1A is a very rare form of Charcot–Marie–Tooth disease (CMT) type 1A. It is an inherited nerve disease that ...
Charcot-Marie-Tooth disease type 1A (CMT1A) is a long-lasting (chronic) nerve disease that runs in families. It mainly affects the “peripheral nerves.” These are the nerves outside the brain and ...
Charcot-Marie-Tooth disease caused by mutation in COX6A1 is a very rare, inherited nerve disease. It mainly damages the long nerves that go from the spinal cord to the feet and hands. These nerves ...
Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (often shortened to CMTRID) is a very rare inherited nerve disease. It mainly damages the long nerves that carry movement and ...
Charcot-Marie-Tooth disease recessive intermediate D (often shortened to CMTRID) is a very rare inherited disease that damages the peripheral nerves, which are the long nerves that carry signals ...
Charcot-Marie-Tooth disease caused by mutation in PLEKHG5 is a rare inherited nerve disease that mainly affects the long nerves to the feet and hands. It is classified as Charcot-Marie-Tooth disease ...
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (CMTRIC) is a very rare inherited nerve disease that mainly affects the long nerves in the arms and legs. It causes slowly ...
Charcot-Marie-Tooth disease recessive intermediate C (often shortened to CMT recessive intermediate C or CMTRIC) is a very rare inherited nerve disease. It mostly affects the long nerves that go to ...
KARS-related intermediate Charcot-Marie-Tooth neuropathy is a very rare inherited nerve disease where damage happens slowly to the long nerves in the arms and legs, causing weakness and loss of ...
Charcot-Marie-Tooth neuropathy recessive intermediate A (often shortened to CMTRIA) is a very rare, inherited nerve disease that mainly affects the nerves in the arms and legs. These nerves are ...
Charcot-Marie-Tooth disease caused by mutation in GDAP1 is a rare, inherited nerve disease. It affects the peripheral nerves, which carry signals between the brain, spinal cord, and the muscles and ...
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A (often shortened to CMTRIA) is a rare inherited nerve disease. It mainly damages the peripheral nerves, which are the long nerves ...
Charcot-Marie-Tooth disease recessive intermediate A (CMTRIA) is a rare inherited nerve disease that damages the long nerves in the arms and legs. These nerves carry signals from the brain and spinal ...
Charcot-Marie-Tooth disease dominant intermediate type F (often shortened to CMTDIF) is a very rare inherited nerve disease that slowly damages the long nerves in the arms and legs. These nerves ...
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (CMTDIF) is a very rare inherited nerve disease that affects the long nerves to the feet, legs, hands, and arms. It causes slowly ...
Charcot-Marie-Tooth disease dominant intermediate F (often shortened to CMTDIF or DI-CMTF) is a very rare inherited nerve disease that damages the peripheral nerves, which are the long nerves that ...
Charcot-marie-tooth neuropathy with focal segmental glomerulonephritis is a group of inherited nerve disorders that slowly damage the long nerves to the feet, legs, hands, and arms. It causes ...
Charcot-Marie-Tooth disease with nephropathy syndrome means a person has Charcot-Marie-Tooth (CMT) disease, which is a genetic nerve disease, together with a kidney disease (nephropathy). In most ...
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (often shortened to CMTDIE) is a very rare inherited nerve and kidney disease. It belongs to the Charcot-Marie-Tooth (CMT) group of ...
Charcot-Marie-Tooth disease dominant intermediate E (CMTDIE) is a rare inherited nerve disease that mainly affects the long nerves in the legs and arms. It belongs to the big Charcot-Marie-Tooth ...
