| hereditaire dysfibrinogenemie (aandoening) | | hereditaire dysfibrinogenemie | | Hereditary dysfibrinogenemia | | Congenital dysfibrinogenemia
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| | Id | 45366001 | | 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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