(Q27164484)
English
Charcot-Marie-Tooth disease axonal type 20
Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32
- Charcot-Marie-Tooth neuropathy axonal type 2O
- autosomal dominant Charcot-Marie-Tooth disease type 2O
- autosomal dominant axonal Charcot-Marie-Tooth disease type 2O
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O
- Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2O
- CMT2O
- Charcot-Marie-Tooth Neuropathy, Axonal, Type 2O
- Charcot-Marie-Tooth disease axonal type 2O
Statements
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Identifiers
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