C98906Level 5
Fetal Warfarin Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** 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.
**Synonyms:** - Fetal Coumadin Syndrome
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