715430001: Embryofetopathy caused by indomethacin (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Indomethacin embryofetopathy
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Indomethacin embryofetopathy

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3302597019	Fetal indomethacin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3302598012	Foetal indomethacin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3302602014	Embryofetopathy caused by indomethacin (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3302603016	Embryofetopathy caused by indomethacin	en	Synonym	Active	Case insensitive	SNOMED CT core
3302622013	Indomethacin embryofetopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
3302600018	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.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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