congenitale aandoening door chromosoomafwijking
|
Supernumerary der(22)t(11;22) syndrome (disorder)
Emanuel syndrome
Supernumerary der(22) syndrome
Supernumerary der(22)t(11;22) syndrome
Supernumerary derivative 22 chromosome syndrome
Der(22) syndrome due to 3:1 meiotic disjunction events
Id702417004
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van chromosoom
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ92.6
TermExtra markerchromosomen
SNOMED CT to Orphanet simple map96170
SNOMED CT to ICD-10 extended map
TargetQ92.6
RuleTRUE
AdviceALWAYS Q92.6
CorrelationSNOMED CT source code to target map code correlation not specified