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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:Foot oligodactyly
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Accession:HP:0001849 term browser browse the term
Definition:A developmental defect resulting in the presence of fewer than the normal number of toes.
Synonyms:exact_synonym: Missing toes;   Oligodactyly of feet
 alt_id: HP:0001777
 xref: SNOMEDCT_US:249820005;   UMLS:C0426934


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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of limbs 0
        Abnormality of limb bone 0
          Abnormal limb bone morphology 0
            Abnormal digit morphology 0
              Oligodactyly 0
                Foot oligodactyly 0
                  Foot monodactyly 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the musculoskeletal system 0
        Abnormality of the skeletal system 0
          Abnormal skeletal morphology 0
            Abnormal appendicular skeleton morphology 0
              Abnormal limb bone morphology 0
                Aplasia/hypoplasia involving bones of the extremities 0
                  Aplasia/hypoplasia involving bones of the lower limbs 0
                    Aplasia/Hypoplasia involving bones of the feet 0
                      Aplasia/Hypoplasia of toe 0
                        Absent toe 0
                          Foot oligodactyly 0
                            Foot monodactyly 0
paths to the root