Fetal Warfarin Syndrome

Preferred Label : Fetal Warfarin Syndrome;

NCIt related terms : Fetal Coumadin Syndrome;

Alternative definition : NICHD: A teratogenic disorder observed in a newborn or child of a mother who was exposed to warfarin during pregnancy. Manifestations include nasal bridge depression, nasal bones hypoplasia, microcephaly, congenital heart disorders, and brachydactyly.;

Détails

Origin ID

C98906;

UMLS CUI

C0265374;

Automatic exact mappings (from CISMeF team)
- Fetal warfarin syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- 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 [MedDRA LLT]
- Fetal warfarin syndrome (disorder) [SNOMED CT concept]
- Foetal warfarin syndrome [MedDRA Preferred Term]
- Vitamin K antagonist embryofetopathy [ORDO Disease]
- Warfarin syndrome [MeSH concept]
- fetal warfarin syndrome [SNOMED Notion]
- warfarin syndrome [MeSH Supplementary 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 [MedDRA LLT]
- Fetal warfarin syndrome (disorder) [SNOMED CT concept]
- Foetal warfarin syndrome [MedDRA Preferred Term]
- Vitamin K antagonist embryofetopathy [ORDO Disease]
- Warfarin syndrome [MeSH concept]
- fetal warfarin syndrome [SNOMED Notion]
- warfarin syndrome [MeSH Supplementary Concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
- Perinatal Terminology [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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