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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:Morbus Scheuermann
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Accession:HP:0010891 term browser browse the term
Definition:A developmental growth retardation of the vertebral end plates that may lead to secondary destruction of the vertebral end plates and protrusion of the nucleus pulposus into the vertebral body (so called Schmorl's nodes as seen on x-rays).
Comment:Scheuermann's disease usually manifests during the 2nd decade and leads to the appearance of the so called adolescence kyphosis. Late manifestations may be wedge-shaped vertebrae, platyspondyly and arthrosis affecting the verterbal collum.
Synonyms:exact_synonym: Calve disease;   Juvenile Osteochondrosis of the spine;   Scheuermann disease;   Scheuermann kyphosis;   Sherman's Disease
 xref: SNOMEDCT_US:53406005;   UMLS:C0036310


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Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the musculoskeletal system 0
        Abnormal musculoskeletal physiology 0
          Avascular necrosis 0
            Juvenile aseptic necrosis 0
              Morbus Scheuermann 0
                Scheuermann-like vertebral changes 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 axial skeleton morphology 0
              Abnormality of the vertebral column 0
                Abnormal vertebral morphology 0
                  Morbus Scheuermann 0
                    Scheuermann-like vertebral changes 0
paths to the root