| gecombineerde deficiëntie van stollingsfactor V en VIII (aandoening) | | gecombineerde deficiëntie van stollingsfactor V en VIII | | gecombineerde FV-FVIII-deficiëntie
familiale meervoudige coagulatiefactordeficiëntie
gecombineerde deficiëntie van factor V en factor VIII
| | Combined deficiency of factor V and factor VIII | | Factor V and factor VIII combined deficiency
Familial multiple coagulation factor deficiency
| | An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in the MCFD2 gene (chromosome 2). Transmission is autosomal recessive. |
| | Id | 715559004 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to Orphanet simple map | 35909 |
| SNOMED CT to ICD-10 extended map | | Target | D68.8 | | Rule | TRUE | | Advice | ALWAYS D68.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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