1920
Congenital afibrinogenemia is a rare , autosomal , recessive disorder characterized by the complete absence of detectable fibrinogen .
 Disease: Congenital afibrinogenemia; Disease: autosomal , recessive disorder
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: Congenital afibrinogenemia, autosomal , recessive disorder 
Answer:
 Disease: Congenital afibrinogenemia; Disease: autosomal , recessive disorder