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autosomaal dominante plasminogeendeficiƫntie (aandoening)
autosomaal dominante plasminogeendeficiƫntie
autosomaal dominante deficiƫntie van profibrinolysine
Autosomal dominant deficiency of plasminogen
Autosomal dominant deficiency of profibrinolysin
Id95842004
StatusPrimitive
Has interpretationafwijkend
Interpretshemostase
SNOMED CT to ICD-10 extended map
TargetD68.2
RuleTRUE
AdviceALWAYS D68.2 | MAPPED FOLLOWING WHO GUIDANCE
CorrelationSNOMED CT source code to target map code correlation not specified