2266
This finding confirms that the fragile X phenotype can exist , without amplification of the CCG repeat or cytogenetic expression of the fragile X , and that fragile X syndrome is a genetically homogeneous disorder involving FMR1 .
 Disease: fragile X; Disease: fragile X; Disease: fragile X syndrome
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: fragile X, fragile X, fragile X syndrome 
Answer:
 Disease: fragile X; Disease: fragile X; Disease: fragile X syndrome