(Q27677646)
English
Charcot-Marie-Tooth disease type 1E
Charcot-Marie-Tooth disease type 1 that has material basis in autosomal dominant mutation in the peripheral myelin protein-22 gene (PMP22)
- CMT1E
- Charcot-Marie-Tooth disease and deafness
- Charcot-Marie-Tooth disease demyelinating type 1E
- Charcot-Marie-Tooth disease-deafness
- autosomal dominant Charcot-Marie-Tooth neuropathy and deafness
- Charcot-Marie-Tooth disease-deafness syndrome
- Charcot-Marie-Tooth Disease, Demyelinating, Type 1E
- Charcot-Marie-Tooth Neuropathy and Deafness, Autosomal Dominant
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