Rx Autoimmune, Genetic and Rare Diseases (A – Z)
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Charcot-Marie-Tooth Disease Type 4 Caused by Mutation in SBF1
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Charcot-Marie-Tooth disease type 4 caused by mutation in SBF1 is a very rare inherited nerve disease that mainly affects the peripheral nerves, which carry ...

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Charcot-Marie-Tooth Disease Type 4B3 (CMT4B3)
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Charcot-Marie-Tooth disease type 4B3 (CMT4B3) is a very rare inherited nerve disease. It mainly damages the peripheral nerves, which are the long nerves that ...

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Charcot-Marie-Tooth Neuropathy Type 4B2 (CMT4B2)
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Charcot-Marie-Tooth neuropathy type 4B2 (CMT4B2) is a rare, inherited nerve disease that mainly damages the long nerves to the feet, legs, hands and sometimes ...

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Charcot-Marie-Tooth Disease Demyelinating Type 4B2 (CMT4B2)
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Charcot-Marie-Tooth disease, demyelinating, type 4B2 (CMT4B2) is a very rare inherited nerve disease that mainly affects the “peripheral nerves,” the long ...

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Charcot-Marie-Tooth Disease Type 4 Caused by Mutation in the SBF2 Gene (CMT4B2)
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Charcot-Marie-Tooth disease type 4 caused by mutation in the SBF2 gene (often called CMT4B2) is a rare inherited nerve disease that mainly affects the long ...

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Autosomal Recessive Charcot-Marie-Tooth Disease with Focally Folded Myelin Sheaths Type 4b2
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Autosomal recessive Charcot-Marie-Tooth disease type 4B2 (CMT4B2) is a rare inherited nerve disease. It mainly damages the peripheral nerves, which carry ...

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Charcot-Marie-Tooth Disease Type 4B2 (CMT4B2)
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Charcot-Marie-Tooth disease type 4B2 (CMT4B2) is a very rare inherited nerve disease. It mainly damages the peripheral nerves, which are the “wires” that carry ...

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Charcot-Marie-Tooth Neuropathy Type 4B1 (CMT4B1)
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Charcot-Marie-Tooth neuropathy type 4B1 (CMT4B1) is a very rare inherited nerve disease that mainly affects the peripheral nerves, which carry signals to and ...

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Charcot-Marie-Tooth Disease Demyelinating Type 4B1 (CMT4B1)
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Charcot-Marie-Tooth disease, demyelinating, type 4B1 (often shortened to CMT4B1) is a rare, inherited nerve disease that mainly affects the peripheral nerves, ...

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Autosomal Recessive Charcot-Marie-Tooth Disease with Focally Folded Myelin Sheaths Type 4B1
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Autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1 (usually shortened to CMT4B1) is a very rare inherited nerve ...

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Charcot-Marie-Tooth Disease Type 4B1 (CMT4B1)
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Charcot-Marie-Tooth disease type 4B1 (CMT4B1) is a rare inherited nerve disease. It mainly damages the long nerves that go from the spinal cord to the feet and ...

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Charcot-Marie-Tooth Neuropathy Type 4A (CMT4A)
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Charcot-Marie-Tooth neuropathy type 4A (CMT4A) is a rare inherited nerve disease. It mainly damages the long nerves in the legs and arms (the peripheral ...

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Charcot-Marie-Tooth Disease Type 4 Caused by Mutation in GDAP1
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Charcot-Marie-Tooth disease type 4 caused by mutation in GDAP1 (often called CMT4A) is a rare, inherited nerve disease. It mainly damages the peripheral ...

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Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease Type 4A (CMT4A)
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Autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A (CMT4A) is a rare, inherited nerve disease. It mainly damages the peripheral nerves. ...

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Charcot–Marie–Tooth Disease Type 4A (CMT4A)
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Charcot–Marie–Tooth disease type 4A (CMT4A) is a rare inherited nerve disease. It mainly damages the peripheral nerves, which are the long nerves that carry ...

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Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease, Type IV ( CMT4)
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Autosomal recessive demyelinating Charcot-Marie-Tooth disease, type IV (often called CMT4) is a rare inherited nerve disease. It mainly damages the peripheral ...

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Charcot-Marie-Tooth Disease Type 4 (CMT4)
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Charcot-Marie-Tooth disease type 4 (CMT4) is a rare inherited nerve disease that mainly damages the “wires” that carry signals between the spinal cord and the ...

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Charcot-Marie-Tooth Neuropathy Type 2Y (CMT2Y)
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Charcot-Marie-Tooth neuropathy type 2Y (CMT2Y) is a very rare, inherited nerve disease that mainly affects the long nerves of the arms and legs. It is an ...

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Charcot-Marie-Tooth Disease Type 2 Caused by Mutation in the VCP Gene
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Charcot-Marie-Tooth disease type 2 caused by mutation in the VCP gene is a rare inherited nerve disease in which the long nerves to the feet and hands slowly ...

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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to VCP Mutation (CMT2Y)
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Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation (often called CMT2Y) is a rare inherited nerve disease. It damages the long nerves ...

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