Charcot-Marie-Tooth disease axonal type 2N (Q27164486)
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Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the AARS gene on chromosome 16q21
- CMT2N
- Charcot-Marie-Tooth neuropathy axonal type 2N
- autosomal dominant Charcot-Marie-Tooth disease type 2N
- autosomal dominant axonal Charcot-Marie-Tooth disease type 2N
- Charcot-Marie-Tooth Neuropathy, Axonal, Type 2N
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2N
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N; CMT2N
Language | Label | Description | Also known as |
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English | Charcot-Marie-Tooth disease axonal type 2N |
Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the AARS gene on chromosome 16q21 |
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