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Paper Details

The Human Phenotype Ontology in 2017.
Nucleic Acids Res
491
2017
HPO, Human, complex) disease, human, patient, phenotypic abnormalities, rare disease
Algorithms, Biological Ontologies, Computational Biology, Genetic Association Studies, Genomics, Humans, Phenotype, Precision Medicine, Rare Diseases, Software, Translational Research, Biomedical
Author NameAffiliation
Sebastian K??hlerInstitute for Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin
Sebastian K??hlerInstitute for Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin
Nicole VasilevskyLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Nicole VasilevskyLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Mark E EngelstadLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Mark E EngelstadLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Erin FosterLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Erin FosterLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Julie A McMurryLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Julie A McMurryLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
S??gol??ne Aym??Institut du Cerveau et de la Moelle epiniere-ICM, CNRS UMR 7225-Inserm U 1127-UPMC-P6 UMR S 1127
Gareth BaynamKing Edward Memorial Hospital Department of Health
Gareth BaynamUniversity of Western Australia
Gareth BaynamKing Edward Memorial Hospital Department of Health
Gareth BaynamUniversity of Western Australia
Susan M Bello
Susan M Bello
Cornelius F Boerkoel
Cornelius F Boerkoel
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Michael BrudnoUniversity of Toronto, Hospital for Sick Children
Orion J BuskeUniversity of Toronto, Hospital for Sick Children
Orion J BuskeUniversity of Toronto, Hospital for Sick Children
Patrick F ChinnerySchool of Clinical Medicine, University of Cambridge
Patrick F Chinnery
Valentina CiprianiUCL Institute of Ophthalmology
Valentina CiprianiUCL Genetics Institute, University College London
Laureen E Connell
Hugh Dawkins
Hugh Dawkins
Laura E DeMare
Andrew DevereauQueen Mary University of London
Bert B A de VriesRadboud University, University Medical Centre
Helen V FirthWellcome Trust Sanger Institute
Kathleen FresonCenter for Molecular and Vascular Biology, University of Leuven
Kathleen FresonCenter for Molecular and Vascular Biology, University of Leuven
Daniel GreeneUniversity of Cambridge
Daniel GreeneMedical Research Council Biostatistics Unit, Cambridge Institute of Public Health
Ada HamoshMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Ingo HelbigThe Children's Hospital of Philadelphia
Ingo HelbigUniversity Medical Center Schleswig-Holstein (UKSH)
Courtney HumThe Hospital for Sick Children
Johanna A J??hnUniversity Medical Center Schleswig-Holstein (UKSH)
Roger James
Roger JamesMedical Research Council Biostatistics Unit, Cambridge Institute of Public Health
Roland KrauseUniversity of Luxembourg
Stanley J F LaulederkindMedical College of Wisconsin
Stanley J F LaulederkindMedical College of Wisconsin
Hanns Lochm??llerJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, University of Newcastle
Gholson J LyonStanley Institute for Cognitive Genomics
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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