Display Settings:

Format

Send to:

Choose Destination
    Am J Hum Genet. 2008 Nov;83(5):610-5. Epub 2008 Oct 23.

    The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease.

    Source

    Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany. peter.robinson@charite.de

    Abstract

    There are many thousands of hereditary diseases in humans, each of which has a specific combination of phenotypic features, but computational analysis of phenotypic data has been hampered by lack of adequate computational data structures. Therefore, we have developed a Human Phenotype Ontology (HPO) with over 8000 terms representing individual phenotypic anomalies and have annotated all clinical entries in Online Mendelian Inheritance in Man with the terms of the HPO. We show that the HPO is able to capture phenotypic similarities between diseases in a useful and highly significant fashion.

    PMID:
    18950739
    [PubMed - indexed for MEDLINE]
    PMCID: PMC2668030
    Free PMC Article

    Images from this publication.See all images (2) Free text

    Figure 1
    Figure 2

      Supplemental Content

      Click here to read Click here to read

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk