| hereditaire stollingsfactor V-deficiëntie (aandoening) | | hereditaire stollingsfactor V-deficiëntie | | hereditaire factor V-deficiëntie
| | Hereditary factor V deficiency disease | | Parahemophilia
Owren's disease
Hereditary hypoproaccelerinemia
AC globulin deficiency
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| | Id | 88776002 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to Orphanet simple map | 326 |
| 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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