3720
Since sporadic variants of G6PD causing HNSHA show no special racial predilection , the diagnosis of G6PD deficiency should always be considered in patients with this syndrome . .
 Disease: HNSHA; Disease: G6PD 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: HNSHA, G6PD deficiency 
Answer:
 Disease: HNSHA; Disease: G6PD deficiency