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autosomaal dominante Alzheimer-dementie door mutatie van preseniline 1 (aandoening)
autosomaal dominante Alzheimer-dementie door mutatie van preseniline 1
autosomaal dominante ziekte van Alzheimer door mutatie van preseniline 1
Autosomal dominant Alzheimer disease due to mutation of presenilin 1
Autosomal dominant Alzheimer disease with mutation of presenilin 1
Id1156800008
StatusPrimitive
Has interpretationgestoord
Interpretscognitieve functie
Associated morphologydegeneratieve afwijking
Finding sitestructuur van cerebrum
SNOMED CT to ICD-10 extended map
TargetG30.0
RuleTRUE
AdviceALWAYS G30.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetF00.0
RuleTRUE
AdviceALWAYS F00.0 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified