(Q27164465)
English
Charcot-Marie-Tooth disease type 2B
Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the RAB7 gene on chromosome 3q21
- CMT2B
- Charcot-Marie-Tooth neuropathy type 2B
- HMSN IIB
- HMSN2B
- autosomal dominant Charcot-Marie-Tooth disease type 2B
- hereditary motor and sensory nueropathy IIB
- Hereditary Motor and Sensory Neuropathy 2B
- Charcot-Marie-Tooth disease, axonal, Type 2B
- Hereditary motor and sensory neuropathy 2 B (HMSN 2 B)
- Charcot Marie Tooth disease type 2B
- CMT 2B
- Peripheral sensory neuropathy, autosomal dominant (PSN)
- Charcot-Marie-Tooth disease, neuronal, Type 2B
- Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2B
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B
- Charcot-Marie-Tooth Neuropathy, Type 2B
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