3347
We report the identification of a female patient with the X - linked recessive Lesch - Nyhan syndrome ( hypoxanthine phosphoribosyltransferase [ HPRT ] deficiency ) .
 Disease: Lesch - Nyhan syndrome; Disease: hypoxanthine phosphoribosyltransferase [ HPRT ] 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: Lesch - Nyhan syndrome, hypoxanthine phosphoribosyltransferase [ HPRT ] deficiency 
Answer:
 Disease: Lesch - Nyhan syndrome; Disease: hypoxanthine phosphoribosyltransferase [ HPRT ] deficiency