congenitale anomalie van chromosomenpaar 21
volledige monosomie van autosoom
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syndroom van volledige monosomie 21 (aandoening)
syndroom van volledige monosomie 21
volledige monosomie 21
Complete monosomy 21
Id78740005
StatusDefined
Associated morphologymonosomie
Finding sitechromosomenpaar 21
Occurrencecongenitaal
Global Patient Set
SNOMED CT to ICD-10 extended map
TargetQ93.0
RuleTRUE
AdviceALWAYS Q93.0
CorrelationSNOMED CT source code to target map code correlation not specified