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Paper Details

The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human disease.
Med
1
2023
HPO, Human, MAxO, NHGRI 1U24HG011449, NHGRI 5RM1HG010860-04, POET, human, patients, phenotypic abnormalities, rare diseases
Author NameAffiliation
Leigh C Carmody
Leigh C Carmody
Michael Gargano
Sabrina ToroUniversity of Colorado Anschutz Medical Campus
Nicole VasilevskyCritical Path Institute
Nicole VasilevskyCritical Path Institute
Michael J AdamUniversity of Washington School of Medicine
Hannah Blau
Lauren E ChanOregon State University
David G??mez-Andr??sVall d'Hebron Institut de Recerca (VHIR), Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus
Rita HorvathUniversity of Cambridge
Markus S LadewigUniversity of Colorado Anschutz Medical Campus
David Lewis-Smith
Hanns Lochm??llerTranslational and Clinical Research Institute, Newcastle University
Hanns Lochm??llerChildren's Hospital of Eastern Ontario Research Institute, The Ottawa Hospital, Canada Brain and Mind Research Institute, University of Ottawa, Medical Center - University of Freiburg
Manuel Mu??oz-Torres
Manuel Mu??oz-Torres
Monica C Munoz-TorresUniversity of Colorado Anschutz Medical Campus
Monika KrausTechnische Universitat Dresden
Berthold SeitzSaarland University Medical Center UKS
Morgan SimilukNational Institute of Allergy and Infectious Diseases, National Institutes of Health
Teresa N SparksUniversity of California san francisco
Timmy StraussTechnische Universitat Dresden
Emilia M SwietlikUniversity of Cambridge, Heart and Lung Research Institute
Rachel ThompsonChildren's Hospital of Eastern Ontario Research Institute
Xingmin Aaron Zhang
Christopher J MungallLawrence Berkeley National Laboratory
Christopher J MungallLawrence Berkeley National Laboratory
Melissa A HaendelUniversity of Colorado Anschutz Medical Campus
Melissa A HaendelUniversity of Colorado Anschutz Medical Campus
Peter N Robinson
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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