MeSH Browser

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
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

Concept UI: M0531144
Terms: Warfarin syndrome Preferred Term
Term UI T740108
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Warfarin embryopathy
Term UI T740109
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Fetal anticoagulant syndrome
Term UI T740110
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); DiSala syndrome
Term UI T740111
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Congenital warfarin syndrome
Term UI T740112
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Coumarin syndrome
Term UI T740113
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Warfarin syndrome MeSH Supplementary Concept Data 2024