4623
The mutation causing myotonic dystrophy ( DM ) has been identified as an amplification of an unstable trinucleotide ( CTG ) n repeat in over 99 % of the global DM population .
 Disease: myotonic dystrophy; Disease: DM; Disease: DM
Given options, please tell me the categories of all the listed entity words.Output format is "type1: word1; type2: word2". 
Option: Disease 
Text: {0} 
 Entities: myotonic dystrophy, DM, DM 
Answer:
 Disease: myotonic dystrophy; Disease: DM; Disease: DM