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embryopathie door retinoïd (aandoening)
embryopathie door retinoïd
Retinoid embryopathy
Embryopathy caused by retinoid
A rare teratogenic disorder due to acitretin or etretinate exposure during the first trimester of pregnancy, carrying a risk of fetal malformations of approximately 20%, including central nervous system, craniofacial, ear, thymic, cardiac and limb anomalies.
Id725287006
StatusDefined
Associated morphologymorfologische afwijking
Causative agentretinoïd
Occurrencefoetale periode
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ86.8
TermOverige congenitale gestoorde-ontwikkelingssyndromen door bekende exogene oorzaken
SNOMED CT to Orphanet simple map40366
SNOMED CT to ICD-10 extended map
TargetQ86.8
RuleTRUE
AdviceALWAYS Q86.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
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