congenitaal malformatiesyndroom

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embryofoetopathie door indometacine (aandoening)
	embryofoetopathie door indometacine
	Indomethacin embryofetopathy
	Foetal indomethacin syndrome Embryofetopathy caused by indomethacin Fetal indomethacin syndrome
	A group of symptoms which may be observed in the fetus or newborn when the mother has taken indomethacin, a nonsteroidal anti-inflammatory drug during pregnancy. The drug crosses the human placenta readily throughout gestation, but its effects on the embryo/fetus vary according to the stage of pregnancy.

Id	715430001
Status	Primitive

Associated morphology	morfologische afwijking
Causative agent	indometacine
Finding site	structuur van foetus
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q86.8
Term	Overige congenitale gestoorde-ontwikkelingssyndromen door bekende exogene oorzaken

SNOMED CT to Orphanet simple map

1909

SNOMED CT to ICD-10 extended map

Target	Q86.8
Rule	TRUE
Advice	ALWAYS Q86.8
Correlation	SNOMED CT source code to target map code correlation not specified