Charcot-Marie-Tooth disease axonal type 2L (Q27164483)
Jump to navigation
Jump to search
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 |
|---|---|---|---|
| English | Charcot-Marie-Tooth disease axonal type 2L |
Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the HSPB8 gene |
|
Statements
1 reference
1 reference
3 references
Identifiers
1 reference
2 references
1 reference
1 reference
1 reference