767
As this mutation leads to a loss of protein function its frequency makes it the most common cause of Zellweger syndrome , helping to explain the high percentage of patients that belong to CG1 .
 Disease: Zellweger syndrome
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: Zellweger syndrome 
Answer:
 Disease: Zellweger syndrome