1492
The observation of typical mutations in STM7 / X25 ( GAA expansions ) in this patient demonstrates that the two genetically different forms of FRDA cannot be distinguished clinically . .
 Disease: FRDA
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: FRDA 
Answer:
 Disease: FRDA