Label | Id |
---|
charcot-marie-tooth disease, autosomal dominant, type 2b | C537989 | |
type 2b charcot-marie-tooth neuropathy | C537989 | |
chromosome 13Q32 deletion syndrome | 7989 | |
His bundle tachycardia | 17989 | |
charcot-marie-tooth disease, neuronal, type 2b | C537989 | |
junctional ectopic tachycardia | 17989 | |
charcot-marie-tooth disease, type 2b | C537989 | |
charcot-marie-tooth neuropathy, type 2b | C537989 | |
autosomal dominant, type 2b charcot-marie-tooth disease | C537989 |