About: Fetal Retinoid Syndrome     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • Fetal Retinoid Syndrome
rdfs:subClassOf
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Congenital Abnormality
  • Disease or Syndrome
Preferred_Name
  • Fetal Retinoid Syndrome
UMLS_CUI
  • C0432364
Contributing_Source
  • NICHD
FULL_SYN
  • Fetal Retinoid SyndromePTNCI
  • Retinoic Acid EmbryopathySYNCI
  • Retinoic Acid EmbryopathyPTNICHD
  • Fetal Isoretinoin SyndromeSYNICHD
DEFINITION
  • A rare syndrome that affects the fetus and is caused by the maternal use of retinoids during pregnancy. It is characterized by growth delay, skull and facial malformations, heart malformations, and central nervous system malformations.NCI
code
  • C98929
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