38323006: Fetal warfarin syndrome (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Foetal finding\Fetal disorder\...
• \Disorder of fetal structure\Fetal warfarin syndrome
• \Fetus with drug damage\Fetal warfarin syndrome
• \Disease\Disorder of fetus or newborn (disorder)\fœtus ou nouveau-né affecté par une substance transmise par la mère\Fetal or neonatal effect of placental or breast transfer of anticoagulant\Fetal warfarin syndrome
• \Disease\Disorder of fetus or newborn (disorder)\Fetal disorder\Disorder of fetal structure\Fetal warfarin syndrome
• \Disease\Disorder of fetus or newborn (disorder)\Fetal disorder\Fetus with drug damage\Fetal warfarin syndrome
• \Disease\trouble du développement\Disorder of fetal structure\Fetal warfarin syndrome

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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