|
autosomal recessive axonal CMT4C2
|
0011901 |
|
|
autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features
|
0011901 |
|
|
autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features
|
0011901 |
|
|
axonal Charcot-Marie-Tooth disease with pyramidal involvement
|
0011901 |
|
|
Charcot-Marie-Tooth disease type 2H
|
0011901 |
|
