warfarin syndrome

Preferred Label : warfarin syndrome;

MeSH synonym : coumarin syndrome; warfarin embryopathy; fetal anticoagulant syndrome; congenital warfarin syndrome; DiSala syndrome;

Details

Origin ID

C536683;

UMLS CUI

C0265374;

Currated CISMeF NLP mapping
- Dysmorphism due to warfarin [ICD-10 Sub-category]
- Dysmorphism due to warfarin [ICD-10 Sub-category (who)]
- Embryofetopathy due to oral anticoagulant therapy [ICD-11 Sub-sub category]
- Fetal Warfarin Syndrome [NCIt concept]
- Fetal warfarin syndrome [MedDRA LLT]
- Fetal warfarin syndrome (disorder) [SNOMED CT concept]
- Foetal warfarin syndrome [MedDRA Preferred Term]
- Vitamin K antagonist embryofetopathy [ORDO Disease]
- fetal warfarin syndrome [SNOMED Notion]
MeSH term(s) associated for indexing
- abnormalities, drug-induced [MeSH Descriptor]
- nasal bone [MeSH Descriptor]
- warfarin [MeSH Descriptor]
Record concept(s)
- Warfarin syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dysmorphism due to warfarin [ICD-10 Sub-category (who)]
- Dysmorphism due to warfarin [ICD-10 Sub-category]
- Embryofetopathy due to oral anticoagulant therapy [ICD-11 Sub-sub category]
- Fetal Warfarin Syndrome [NCIt concept]
- Fetal warfarin syndrome [MedDRA LLT]
- Fetal warfarin syndrome (disorder) [SNOMED CT concept]
- Foetal warfarin syndrome [MedDRA Preferred Term]
- Vitamin K antagonist embryofetopathy [ORDO Disease]
- fetal warfarin syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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