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isolated Pierre-Robin syndrome

^ http://purl.obolibrary.org/obo/MONDO_0009869

Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. [ Orphanet:718 ]

Term info

database cross reference
  • SCTID:4602007 (MONDO:equivalentTo)
  • NCIT:C85010 (MONDO:equivalentTo)
  • GARD:0004354 (MONDO:equivalentTo)
  • GARD:0004347 (MONDO:equivalentTo)
  • MESH:D010855 (MONDO:equivalentTo)
  • OMIM:261800 (Orphanet:718/e)
  • Orphanet:718 (OMIM:261800)
Subsets

gard_rare, ordo_malformation_syndrome

abbreviation
PRBNS [ MESH:D010855 MONDO:Lexical OMIM:261800 ]

definition

Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft.

exactMatch

https://omim.org/entry/261800, http://purl.obolibrary.org/obo/NCIT_C85010, http://purl.obolibrary.org/obo/Orphanet_718, http://identifiers.org/snomedct/4602007, http://identifiers.org/mesh/D010855

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015501, http://purl.obolibrary.org/obo/MONDO_0002254

has exact synonym

isolated Pierre-Robin syndrome, isolated Pierre Robin sequence

has related synonym

sequence, Pierre Robin's, Robin sequence, Pierre Robin's sequence, isolated Pierre Robin syndrome, sequence, Robin, Pierre Robin syndrome, PRBNS, sequence, Pierre Robin, Pierre Robin sequence, Pierre-Robin syndrome, Robin syndrome, Pierre, glossoptosis, micrognathia, and cleft palate, syndrome, Pierre-Robin, syndrome, Pierre Robin, Pierre Robin syndrome skeletal dysplasia polydactyly, Pierre Robins sequence

id

MONDO:0009869

Term relations

Subclass of: