Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1
|
0025622 |
|
Charcot-Marie-Tooth disease, axonal, type 2EE
|
0032728 |
|
Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive
|
0011898 |
|
Charcot-Marie-Tooth disease, demyelinating, type 1G
|
0033135 |
|
Charcot-Marie-Tooth disease, dominant intermediate G
|
0036484 |
|
Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
|
0008960 |
|
Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined
|
0010553 |
|
Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita
|
0010552 |
|
Charlevoix-Saguenay spastic ataxia
|
0010041 |
|
Chiari malformation type 3
|
0022715 |
|
Chiari malformation type 4
|
0022716 |
|