dysfibrinogenemie
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dysfibrinogenemie door defect in gammaketen (aandoening)
dysfibrinogenemie door defect in gammaketen
Gamma chain defect dysfibrinogenemia
Id234461003
StatusPrimitive
Occurrencecongenitaal
Has interpretationafwijkend
Interpretshemostase
SNOMED CT to ICD-10 extended map
TargetD68.2
RuleTRUE
AdviceALWAYS D68.2
CorrelationSNOMED CT source code to target map code correlation not specified