| congenitale hypofibrinogenemie (aandoening) |   | congenitale hypofibrinogenemie  |   | aangeboren hypofibrinogenemie
   |   | Congenital hypofibrinogenemia  |  
  | | Id | 439145006 |  | Status | Primitive |  
 | SNOMED CT to ICD-10 extended map |  | Target | D68.2 |  | Rule | TRUE |  | Advice | ALWAYS D68.2 |  | Correlation | SNOMED CT source code to target map code correlation not specified |  
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