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In another family previously diagnosed as having Thomsens disease , we unexpectedly found a CLCN1 14 bp deletion known to cause recessive myotonia , and a rare Trp - 118 - Gly polymorphism . .
 Disease: Thomsens disease; Disease: recessive myotonia
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: Thomsens disease, recessive myotonia 
Answer:
 Disease: Thomsens disease; Disease: recessive myotonia