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Paper Details

The Human Phenotype Ontology in 2021.
Nucleic Acids Res
519
2021
Epilepsy, HPO, Human, human, phenotypic abnormalities
Animals, Biological Ontologies, Computational Biology, Databases, Factual, Disease, Disease Models, Animal, Genome, Genotype, Humans, Infant, Newborn, International Cooperation, Internet, Neonatal Screening, Pharmacogenetics, Phenotype, Software, Terminology as Topic
Author NameAffiliation
Sebastian K??hler
Sebastian K??hler
Sebastian K??hler
Sebastian K??hler
Michael Gargano
Michael Gargano
Nicolas Matentzoglu
Nicolas MatentzogluSemanticly Ltd
Nicolas MatentzogluEuropean Bioinformatics Institute (EMBL-EBI).
Leigh C Carmody
Leigh C Carmody
Leigh C Carmody
Leigh C Carmody
David Lewis-SmithTranslational and Clinical Research Institute, Newcastle University
David Lewis-SmithClinical Neurosciences, Newcastle upon Tyne Hospitals NHS Foundation Trust
Nicole Vasilevsky
Nicole VasilevskyOregon Clinical & Translational Research Institute, Oregon Health & Science University.
Nicole Vasilevsky
Nicole VasilevskyOregon Clinical & Translational Research Institute, Oregon Health & Science University.
Ganna BalaguraUniversity of Genoa
Ganna BalaguraIRCCS 'G. Gaslini' Institute
Gareth BaynamKing Edward memorial Hospital
Gareth BaynamTelethon Kids Institute and the Division of Paediatrics, University of Western Australia
Gareth BaynamKing Edward memorial Hospital
Gareth BaynamTelethon Kids Institute and the Division of Paediatrics, University of Western Australia
Amy BrowerAmerican College of Medical Genetics and Genomics (ACMG)
Tiffany J CallahanUniversity of Colorado Anschutz Medical Campus
Christopher G ChuteJohns Hopkins University Schools of Medicine
Johanna L EstDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat Munchen
Peter D GalerChildren's Hospital of Philadelphia
Peter D GalerChildren's Hospital of Philadelphia
Shiva GanesanChildren's Hospital of Philadelphia
Shiva GanesanChildren's Hospital of Philadelphia
Matthias GrieseDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat Munchen
Matthias GrieseLudwig-Maximilians University, German Center for Lung Research (DZL)
Matthias HaimelLudwig Boltzmann Institute for Rare and Undiagnosed Diseases
Matthias HaimelCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Julia PazmandiLudwig Boltzmann Institute for Rare and Undiagnosed Diseases
Julia PazmandiCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Julia PazmandiInstitute for Systems Genomics, University of Connecticut
Marc HanauerINSERM
Nomi L Harris
Nomi L Harris
Nomi L HarrisLawrence Berkeley National Laboratory
Nomi L HarrisLawrence Berkeley National Laboratory
Michael J HartnettAmerican College of Medical Genetics and Genomics (ACMG)
Maximilian HastreiterDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat Munchen
Fabian HauckDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat Munchen
Fabian HauckGerman Centre for Infection Research (DZIF)
Yongqun HeCenter for Computational Medicine and Bioinformatics, University of Michigan Medical School ann arbor
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Datasets

Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink