About: Fetal Warfarin Syndrome     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Fetal Warfarin Syndrome
rdfs:subClassOf
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Fetal Warfarin Syndrome
UMLS_CUI
  • C0265374
Contributing_Source
  • NICHD
FULL_SYN
  • Fetal Warfarin SyndromePTNCI
  • Fetal Coumadin SyndromeSYNICHD
  • Fetal Warfarin SyndromePTNICHD
DEFINITION
  • A rare syndrome characterized by congenital abnormalities caused by fetal exposure to the administration of warfarin to the mother during pregnancy. The congenital abnormalities include nasal bridge depression, nasal bones hypoplasia, microcephaly, congenital heart disorders, and brachydactyly.NCI
code
  • C98906
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