2140
Lesch - Nyhan syndrome caused by a complete deficiency of hypoxanthine guanine phosphoribosyltransferase ( HPRT ) is the result of a heterogeneous group of germ line mutations .
 Disease: Lesch - Nyhan syndrome; Disease: complete deficiency of hypoxanthine guanine phosphoribosyltransferase
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, complete deficiency of hypoxanthine guanine phosphoribosyltransferase 
Answer:
 Disease: Lesch - Nyhan syndrome; Disease: complete deficiency of hypoxanthine guanine phosphoribosyltransferase