| Combined deficiency of factor V and factor VIII (disorder) |
| Combined deficiency of factor V and factor VIII |
| Factor V and factor VIII combined deficiency
Familial multiple coagulation factor deficiency
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| 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. |
| gecombineerde deficiëntie van stollingsfactor V en VIII |
| gecombineerde FV-FVIII-deficiëntie
familiale meervoudige coagulatiefactordeficiëntie
gecombineerde deficiëntie van factor V en factor VIII
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