syndromic disease vitamin K-antagonist embryofetopathy https://rarediseases.info.nih.gov/diseases/8580/warfarin-syndrome https://www.malacards.org/card/vitamin_k_antagonist_embryofetopathy NCIT:C98906 Orphanet:1914 warfarin syndrome foetal warfarin syndrome coumarin syndrome vitamin K-antagonist embryofetopathy fetal warfarin syndrome di Sala syndrome embryofetopathy due to oral anticoagulant therapy coumarin embryopathy ICD9:759.89 MEDGEN:75570 fetal Coumadin syndrome vitamin K antagonists embryofetopathy foetal Coumadin syndrome icd11.foundation:71579696 warfarin embryopathy warfarin embryofetopathy MedDRA:10051445 congenital warfarin syndrome vitamin K antagonist embryofetopathy MESH:C536683 SCTID:38323006 MONDO:0016010 UMLS:C0265374 vitamin K antagonist embryopathy vitamin K-antagonist embryopathy 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. fetal anticoagulant syndrome foetal anticoagulant syndrome DiSala syndrome toxic or drug-related embryofetopathy