Pierre Robin syndrome (Q1756040)

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a congenital condition with micrognathia and glossoptosis
  • Pierre Robin sequence
  • Pierre Robin malformation
  • Pierre Robin anomaly
  • Pierre Robin anomalad
  • PRS
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Language Label Description Also known as
English
Pierre Robin syndrome
a congenital condition with micrognathia and glossoptosis
  • Pierre Robin sequence
  • Pierre Robin malformation
  • Pierre Robin anomaly
  • Pierre Robin anomalad
  • PRS

Statements

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C85010
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Identifiers

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LA56
Pierre Robin syndrome
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