congenitale anomalie van chromosomenpaar 11
paternale uniparentale disomie
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paternale uniparentale disomie van chromosoom 11 (aandoening)
paternale uniparentale disomie van chromosoom 11
Paternal uniparental disomy of chromosome 11
Uniparental disomy of paternal origin of chromosome 11
Id1003873008
StatusDefined
Associated morphologyverandering van chromosoomstructuur
Finding sitechromosomenpaar 11
Occurrencecongenitaal
SNOMED CT to ICD-10 extended map
TargetQ99.8
RuleTRUE
AdviceALWAYS Q99.8
CorrelationSNOMED CT source code to target map code correlation not specified