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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
Familial multiple coagulation factor deficiency
Factor V and factor VIII combined 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.
Id715559004
StatusPrimitive
Has interpretationafwijkend
Interpretshemostase
referentieset met complexe 'mapping' naar ICD-10
TargetD68.8
RuleTRUE
AdviceALWAYS D68.8
CorrelationSNOMED CT source code to target map code correlation not specified