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congenitale afwijking van fibrinogeen (aandoening)
congenitale afwijking van fibrinogeen
congenitale afwijking van stollingsfactor I
Congenital fibrinogen abnormality
Id234456000
StatusDefined
Has interpretationafwijkend
Interpretshemostase
Occurrencecongenitaal
referentieset met complexe 'mapping' naar ICD-10
TargetD68.2
RuleTRUE
AdviceALWAYS D68.2
CorrelationSNOMED CT source code to target map code correlation not specified
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