5226
The mutation causing myotonic dystrophy ( DM ) has recently been identified as an unstable CTG trinucleotide repeat located in the 3 untranslated region of a gene encoding for a protein with putative serine - threonine protein kinase activity .
 Disease: myotonic dystrophy; 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 
Answer:
 Disease: myotonic dystrophy; Disease: DM