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National Cancer Institute
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Version: 17.08d (Release date: 2017-08-28)
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Pierre Robin Syndrome (Code C85010)

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Terms & Properties

Preferred Name: Pierre Robin Syndrome

Definition: A rare congenital malformation characterized by micrognathia, posterior retraction of the tongue, and cleft palate.

Label: Pierre Robin Syndrome

NCI Thesaurus Code: C85010 (Search for linked caDSR metadata)  (search value sets)

NCI Metathesaurus Link: C0031900  (see NCI Metathesaurus info)

Synonyms & Abbreviations: (see Synonym Details)
Pierre Robin Sequence
Pierre Robin Syndrome
Robin Sequence

External Source Codes: 
UMLS CUI C0031900

Other Properties:
     Name Value (qualifiers indented underneath)
code C85010
Contributing_Source NICHD
NICHD_Hierarchy_Term Pierre Robin Syndrome
Semantic_Type Disease or Syndrome

Additional Concept Data: 
Defined Fully by Roles: No  

URL: https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C85010

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