4691
CETP deficiency , reflecting two prevalent mutations ( D442G and Int14 A ) , is the first example of a genetic deficiency state which is sufficiently common to explain a significant fraction of the variation in HDL - C in the general population . .
 Disease: CETP deficiency; Disease: genetic 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: CETP deficiency, genetic deficiency 
Answer:
 Disease: CETP deficiency; Disease: genetic deficiency