4292
Among 117 Japanese hyperalphalipoproteinemic subjects ( HDL - cholesterol ; 116 . 7 + / - 16 . 5 mg / dl , mean + / - S . D . ) without the intron 14 splice defect , three homozygotes ( 2 . 5 % ) and 34 heterozygotes ( 29 . 1 % ) were found to have the 442D G mutation .
 Disease: hyperalphalipoproteinemic
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: hyperalphalipoproteinemic 
Answer:
 Disease: hyperalphalipoproteinemic