| ernstige hereditaire stollingsfactor VIII-deficiëntieziekte (aandoening) | | ernstige hereditaire stollingsfactor VIII-deficiëntieziekte | | ernstige hereditaire factor VIII-deficiëntieziekte
ernstige erfelijke factor VIII-deficiëntieziekte
ernstige hemofilie A
ernstige genetische factor VIII-deficiëntieziekte
| | Severe hereditary factor VIII deficiency disease | | Severe hemophilia A
| | A severe form of hemophilia A characterized by a large deficiency of factor VIII (biological activity <1 IU/dL) leading to frequent spontaneous hemorrhage and abnormal bleeding as a result of minor injuries, or following trauma, surgery or tooth extraction. It primarily affects males but may also be observed in female carriers of disease-causing mutations. |
| | Id | 16872008 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 169802 |
| SNOMED CT to ICD-10 extended map | | Target | D66 | | Rule | TRUE | | Advice | ALWAYS D66 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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