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Warfarin syndrome MeSH Supplementary Concept Data 2022


MeSH Supplementary
Warfarin syndrome
Unique ID
C536683
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C536683
Entry Term(s)
Congenital warfarin syndrome
Coumarin syndrome
DiSala syndrome
Fetal anticoagulant syndrome
Warfarin embryopathy
Registry Number
0
Heading Mapped to
*Abnormalities, Drug-Induced
Nasal Bone / *abnormalities
Warfarin / *adverse effects
Frequency
13
Date of Entry
2010/08/25
Revision Date
2013/11/06
Warfarin syndrome Preferred
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