| 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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