Autosomal dominant hereditary disorder
Familial Alzheimer's disease of early onset
Hereditary degenerative disease of central nervous system
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Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder)
Autosomal dominant Alzheimer disease due to mutation of presenilin 1
Autosomal dominant Alzheimer disease with mutation of presenilin 1
autosomaal dominante Alzheimer-dementie door mutatie van preseniline 1
autosomaal dominante ziekte van Alzheimer door mutatie van preseniline 1
Id1156800008
StatusPrimitive
Has interpretationImpaired
InterpretsCognitive functions
Associated morphologyDegenerative abnormality
Finding siteCerebrum
ICD-10 complex map reference set
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