autosomaal dominante hereditaire aandoening
hereditair tumorpredispositiesyndroom
hereditaire aandoening van spijsverteringsstelsel
syndroom van intestinale poliepose
||||
AXIN2-gerelateerde 'attenuated' familiaire adenomateuze polyposis (aandoening)
AXIN2-gerelateerde 'attenuated' familiaire adenomateuze polyposis
AXIN2-gerelateerde 'attenuated' FAP
AXIN2-gerelateerde AFAP
AXIN2-gerelateerde milde vorm van familiaire adenomateuze poliepose
AXIN2-related attenuated familial adenomatous polyposis
AXIN2-related AFAP (attenuated familial adenomatous polyposis)
AXIN2-related attenuated familial polyposis coli
AXIN2-related attenuated FAP (familial adenomatous polyposis)
Id1367882008
StatusPrimitive
Associated morphologymultipele poliepen
Finding sitestructuur van intestinum
SNOMED CT to ICD-10 extended map
TargetD12.6
RuleTRUE
AdviceALWAYS D12.6 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified