38323006: Fetal warfarin syndrome (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Fetal finding\Fetal disorder\...
• \Disorder of fetal structure\Fetal warfarin syndrome
• \Foetal disorder caused by chemicals\Fetal warfarin syndrome
• \Fetus with drug damage\Fetal warfarin syndrome
• \Disease\Disorder of foetus and/or newborn\Fetal disorder\Disorder of fetal structure\Fetal warfarin syndrome
• \Disease\Disorder of foetus and/or newborn\Fetal disorder\Foetal disorder caused by chemicals\Fetal warfarin syndrome
• \Disease\Disorder of foetus and/or newborn\Fetal disorder\Fetus with drug damage\Fetal warfarin syndrome
• \Disease\Developmental disorder\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
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
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

Expanded Value Set

This concept is not in any reference sets

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