1708
Expansion of a CTG trinucleotide repeat in the 3 UTR of the gene DMPK at the DM1 locus on chromosome 19 causes myotonic dystrophy , a dominantly inherited disease characterized by skeletal muscle dystrophy and myotonia , cataracts and cardiac conduction defects .
 Disease: myotonic dystrophy; Disease: dominantly inherited disease; Disease: muscle dystrophy; Disease: myotonia; Disease: cataracts; Disease: cardiac conduction defects
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, dominantly inherited disease, muscle dystrophy, myotonia, cataracts, cardiac conduction defects 
Answer:
 Disease: myotonic dystrophy; Disease: dominantly inherited disease; Disease: muscle dystrophy; Disease: myotonia; Disease: cataracts; Disease: cardiac conduction defects