1883
To determine whether PDS mutations in individuals with Pendred syndrome differ functionally from PDS mutations in individuals with non - syndromic hearing loss , we compared three common Pendred syndrome allele variants ( L236P , T416P and E384G ) , with three PDS mutations reported only in individuals with non - syndromic hearing loss ( V480D , V653A and I490L / G497S ) .
 Disease: PDS; Disease: Pendred syndrome; Disease: PDS; Disease: non - syndromic hearing loss; Disease: Pendred syndrome; Disease: PDS; Disease: non - syndromic hearing loss
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: PDS, Pendred syndrome, PDS, non - syndromic hearing loss, Pendred syndrome, PDS, non - syndromic hearing loss 
Answer:
 Disease: PDS; Disease: Pendred syndrome; Disease: PDS; Disease: non - syndromic hearing loss; Disease: Pendred syndrome; Disease: PDS; Disease: non - syndromic hearing loss