||
20p12.2-deletiesyndroom (aandoening)
20p12.2-deletiesyndroom
20p12.2DS
20p12.2 deletion syndrome
Id890117001
StatusPrimitive
Associated morphologypartiƫle monosomie
Finding sitechromosomenpaar 20
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ93.5
RuleTRUE
AdviceALWAYS Q93.5
CorrelationSNOMED CT source code to target map code correlation not specified