1271
We identified two heterozygous insertion mutations in exon 1 of TNFRSF11A in affected members of four families with FEO or familial Paget disease of bone ( PDB ) .
 Disease: FEO; Disease: familial Paget disease of bone; Disease: PDB
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: FEO, familial Paget disease of bone, PDB 
Answer:
 Disease: FEO; Disease: familial Paget disease of bone; Disease: PDB