Charcot-Marie-Tooth disease type 2B1 (Q27164462)
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Charcot-Marie-Tooth disease type 2 that has material basis in homozygous mutation in the lamin A/C gene (LMNA) on chromosome 1q22
- CMT2B1
- Charcot-Marie-Tooth disease neuronal type 2B1
- Charcot-Marie-Tooth neuropathy type 2B1
- autosomal recessive Charcot-Marie-Tooth disease type 2B1
- autosomal recessive axonal CMT4C1
- autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1
- Charcot-Marie-Tooth disease, axonal, Type 2B1
- Charcot Marie Tooth disease type 2B1
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, 2B1
- Charcot-Marie-Tooth Neuropathy, Type 2B1
- Charcot-Marie-Tooth Disease, Neuronal, Type 2B1
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1
- AR-CMT2B1
- CMT 2B1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Charcot-Marie-Tooth disease type 2B1 |
Charcot-Marie-Tooth disease type 2 that has material basis in homozygous mutation in the lamin A/C gene (LMNA) on chromosome 1q22 |
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