Charcot-Marie-Tooth disease axonal type 2L (Q27164483)
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Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the HSPB8 gene
- CMT2L
- Charcot-Marie-Tooth neuropathy axonal type 2L
- autosomal dominant Charcot-Marie-Tooth disease type 2L
- autosomal dominant axonal Charcot-Marie-Tooth disease type 2L
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2L
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L
- Charcot-Marie-Tooth Neuropathy, Axonal, Type 2L
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L
Language | Label | Description | Also known as |
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English | Charcot-Marie-Tooth disease axonal type 2L |
Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the HSPB8 gene |
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