(Q27164492)
English
Charcot-Marie-Tooth disease axonal type 2C
Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the TRPV4 gene on chromosome 12q24
- CMT2C
- Charcot-Marie-Tooth neuropathy type 2C
- HMSN2C
- autosomal cominant axonal Charcot-Marie-Tooth disease type 2C
- autosomal dominant Charcot-Marie-Tooth disease type 2C
- hereditary motor and sensory neuropathy type IIc
- Hereditary motor and sensory neuropathy 2 C
- Charcot Marie Tooth disease type 2C
- HMSN 2 C
- Charcot-Marie-Tooth Neuropathy, Type 2C
- HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C
- HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2C
- Charcot-Marie-Tooth disease, axonal, Type 2C
- Hmsn 2C
- Charcot-Marie-Tooth disease type 2C
- CMT 2C
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Identifiers
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