2054
Mutations in the brain specific P / Q type Ca2 + channel alpha1 subunit gene , CACNA1A , have been identified in three clinically distinct disorders , viz . episodic ataxia type 2 ( EA - 2 ) , familial hemiplegic migraine ( FHM ) and spinocerebellar ataxia 6 ( SCA6 ) .
 Disease: episodic ataxia type 2; Disease: EA - 2; Disease: familial hemiplegic migraine; Disease: FHM; Disease: spinocerebellar ataxia 6; Disease: SCA6
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: episodic ataxia type 2, EA - 2, familial hemiplegic migraine, FHM, spinocerebellar ataxia 6, SCA6 
Answer:
 Disease: episodic ataxia type 2; Disease: EA - 2; Disease: familial hemiplegic migraine; Disease: FHM; Disease: spinocerebellar ataxia 6; Disease: SCA6