38323006: Fetal warfarin syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Fetal finding\Fetal disorder\...
• \Disorder of fetal structure\Fetal warfarin syndrome
• \Fetus with drug damage\Fetal warfarin syndrome
• \Disease\Disorder of fetus or newborn\Fetal or neonatal effect of maternal transmission of substance\Fetal or neonatal effect of placental or breast transfer of anticoagulant\Fetal warfarin syndrome
• \Disease\Disorder of fetus or newborn\Fetal disorder\Disorder of fetal structure\Fetal warfarin syndrome
• \Disease\Disorder of fetus or newborn\Fetal disorder\Fetus with drug damage\Fetal warfarin syndrome
• \Disease\Developmental disorder\Disorder of fetal structure\Fetal warfarin syndrome

Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1229413014	Dysmorphism due to warfarin	en	Synonym	Active	Case insensitive	SNOMED CT core
3011848011	Foetal warfarin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
64136018	Fetal warfarin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
773275016	Fetal warfarin syndrome (disorder)	en	Fully specified name	Active	Case insensitive	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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