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The hyperalphalipoproteinemia caused by CETP deficiency is fairly common in Japan and one of the most common mutations in the CETP gene is the splicing defect of the intron 14 , the allelic frequency of which has been shown to be 0 .
 Disease: hyperalphalipoproteinemia; Disease: CETP deficiency
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: hyperalphalipoproteinemia, CETP deficiency 
Answer:
 Disease: hyperalphalipoproteinemia; Disease: CETP deficiency