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One of the homozygotes for the 442D G mutation was the patient previously described by us as having hyperalphalipoproteinemia with corneal opacity and coronary heart disease .
 Disease: hyperalphalipoproteinemia; Disease: corneal opacity; Disease: coronary heart disease
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, corneal opacity, coronary heart disease 
Answer:
 Disease: hyperalphalipoproteinemia; Disease: corneal opacity; Disease: coronary heart disease