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3 results for “Human Phenotype Ontology”

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dryad40/100

Mapping between Human Phenotype Ontology and phecode terminologies

Open the record for dataset details and reuse information.

publicJan 2023View details →
zenodo36/100

Data and software associated with PHENOstruct: Prediction of human phenotype ontology terms using heterogeneous data sources

<p>Data and software associated with the paper:</p> <p>PHENOstruct: Prediction of human phenotype ontology terms using heterogeneous data sources</p>

opencc-zeroJun 2015View details →
zenodo32/100

Human Phenotype Ontology: Standardized Framework Cataloging Comprehensive Phenotypic Information

<p><strong>ABSTRACT:</strong></p> <p>The Human Phenotype Ontology (HPO) is a standardized and comprehensive framework that catalogs and organizes phenotypic information related to human diseases and genetic disorders. It provides a structured vocabulary of terms to describe observable traits and abnormalities associated with various medical conditions. This dataset showcases the Human Phenotype Ontology (HPO) by including HPO IDs, names, descriptions, and additional references. The HPO IDs serve as unique identifiers for specific phenotypes. The names provide concise labels for the phenotypic traits, while the descriptions offer detailed explanations of their characteristics. In addition to the essential information, the dataset includes references that further describe and support the understanding of diverse phenotypes. These references can be used to explore the scientific literature, studies, or clinical resources associated with each phenotype. By combining HPO IDs, names, descriptions, and references, the dataset offers a comprehensive overview of different phenotypes, facilitating research, diagnostics, and the exploration of genotype-phenotype relationships.</p> <p><strong>Instructions</strong>:</p> <p>The data was downloaded as an .obo file then converted to a .csv file. Unrelated columns were removed and a references column was added.&nbsp;</p> <p><strong>Acknowledgements</strong>:</p> <p><a>Sebastian K&ouml;hler</a>,&nbsp;<a>Michael Gargano</a>,&nbsp;<a>Nicolas Matentzoglu</a>,&nbsp;<a>Leigh C Carmody</a>,&nbsp;<a>David Lewis-Smith</a>,&nbsp;<a>Nicole A Vasilevsky</a>,&nbsp;<a>Daniel Danis</a>,&nbsp;<a>Ganna Balagura</a>,&nbsp;<a>Gareth Baynam</a>,&nbsp;<a>Amy M Brower</a>,&nbsp;</p> <p><a>Tiffany J Callahan</a>,&nbsp;<a>Christopher G Chute</a>,&nbsp;<a>Johanna L Est</a>,&nbsp;<a>Peter D Galer</a>,&nbsp;<a>Shiva Ganesan</a>,&nbsp;<a>Matthias Griese</a>,&nbsp;<a>Matthias Haimel</a>,&nbsp;<a>Julia Pazmandi</a>,&nbsp;<a>Marc Hanauer</a>,&nbsp;<a>Nomi L Harris</a>,&nbsp;<a>Michael&nbsp;J Hartnett</a>,&nbsp;<a>Maximilian Hastreiter</a>,&nbsp;<a>Fabian Hauck</a>,&nbsp;<a>Yongqun He</a>,&nbsp;<a>Tim Jeske</a>,&nbsp;<a>Hugh Kearney</a>,&nbsp;<a>Gerhard Kindle</a>,&nbsp;<a>Christoph Klein</a>,&nbsp;<a>Katrin Knoflach</a>,&nbsp;<a>Roland Krause</a>,&nbsp;<a>David Lagorce</a>,&nbsp;<a>Julie A McMurry</a>,&nbsp;<a>Jillian A Miller</a>,&nbsp;<a>Monica&nbsp;C Munoz-Torres</a>,&nbsp;<a>Rebecca L Peters</a>,&nbsp;<a>Christina K Rapp</a>,&nbsp;<a>Ana M Rath</a>,&nbsp;<a>Shahmir A Rind</a>,&nbsp;<a>Avi&nbsp;Z Rosenberg</a>,&nbsp;<a>Michael M Segal</a>,&nbsp;<a>Markus G Seidel</a>,&nbsp;<a>Damian Smedley</a>,&nbsp;<a>Tomer Talmy</a>,&nbsp;<a>Yarlalu Thomas</a>,&nbsp;<a>Samuel A Wiafe</a>,&nbsp;<a>Julie Xian</a>,&nbsp;<a>Zafer Y&uuml;ksel</a>,&nbsp;<a>Ingo Helbig</a>,&nbsp;<a>Christopher J Mungall</a>,&nbsp;<a>Melissa A Haendel</a>,&nbsp;<a>Peter N Robinson</a></p> <p><em>Nucleic Acids Research</em>, Volume 49, Issue D1, 8 January 2021, Pages D1207&ndash;D1217,&nbsp;<a href="https://doi.org/10.1093/nar/gkaa1043">https://doi.org/10.1093/nar/gkaa1043</a></p> <p><strong>Human Phenotype Ontology downloads</strong> <strong>page:</strong>&nbsp;https://hpo.jax.org/app/data/ontology</p> <p><strong>U-BRITE last update:&nbsp;</strong>7/6/23</p> <p>&nbsp;</p>

opencc-by-4.0Jul 2023View details →

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