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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:Osteochondrosis
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Accession:HP:0040188 term browser browse the term
Definition:Abnormal growth ossification centers in children. Initially a degeneration/ necrosis followed by regeneration or recalcification.
Synonyms:xref: MSH:D055034;   SNOMEDCT_US:19579005;   UMLS:C0029429



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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 the musculoskeletal system 0
        Abnormality of the skeletal system 0
          Abnormality of skeletal morphology 0
            Abnormal joint morphology 0
              Osteochondrosis 0
                Osteochondritis Dissecans 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
          Abnormality of musculoskeletal physiology 0
            Avascular necrosis 0
              Juvenile aseptic necrosis 0
                Osteochondrosis 0
                  Osteochondritis Dissecans 0
paths to the root