Charcot-Marie-Tooth disease axonal type 2V (Q27164487)
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Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the NAGLU gene on chromosome 17q21
- CMT2V
- Charcot-Marie-Tooth neuropathy type 2V
- autosomal dominant Charcot-Marie-Tooth disease type 2V
- autosomal dominant axonal Charcot-Marie-Tooth disease type 2V
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2V
- Hereditary adult-onset painful axonal polyneuropathy
- Charcot-Marie-Tooth Neuropathy, Type 2V
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Charcot-Marie-Tooth disease axonal type 2V |
Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the NAGLU gene on chromosome 17q21 |
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