1362
The genetic defect is a CTG triplet repeat expansion in the 3 - untranslated region of the myotonic dystrophy protein kinase ( DMPK ) gene , consisting of 15 exons .
 Disease: genetic defect; Disease: myotonic dystrophy
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: genetic defect, myotonic dystrophy 
Answer:
 Disease: genetic defect; Disease: myotonic dystrophy