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HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.
Term:Pierre-Robin sequence
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Accession:HP:0000201 term browser browse the term
Definition:Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate.
Synonyms:exact_synonym: Pierre-robin anomaly;   Pierre-robin deformity;   Pierre-robin malformation;   Robin sequence
 xref: MESH:D010855;   SNOMEDCT_US:4602007;   UMLS:C0031900


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  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of head or neck 0
        Abnormality of the head 0
          Abnormality of the face 0
            Abnormality of the mouth 0
              Abnormal oral morphology 0
                Pierre-Robin sequence 0
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