| hereditaire stollingsfactor I-deficiëntie (aandoening) | | hereditaire stollingsfactor I-deficiëntie | | erfelijke fibrinogeendeficiëntie
hereditaire factor I-deficiëntie
| | Hereditary factor I deficiency disease | | Hereditary hypofibrinogenemia
Congenital fibrinogen deficiency
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| | Id | 31925001 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to Orphanet simple map | 335 |
| 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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