908
Existence of the P16INK4A mutation and the hereditary TP53 mutation with or without loss of heterozygosity in the TP53 gene ( seminoma / medulloblastoma ) may be evidence for a common mechanism involved in tumorogenesis .
 Disease: seminoma; Disease: medulloblastoma; Disease: tumorogenesis
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: seminoma, medulloblastoma, tumorogenesis 
Answer:
 Disease: seminoma; Disease: medulloblastoma; Disease: tumorogenesis