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Paper Details

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
Nucleic Acids Res
496
2014
HPO, Human, cell types, hereditary syndromes, human, mouse, zebrafish
Animals, Biological Ontologies, Databases, Factual, Genetic Diseases, Inborn, Genomics, Humans, Internet, Mice, Phenotype
Author NameAffiliation
Sebastian K??hlerInstitute for Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin, Berlin-Brandenburg Center for Regenerative Therapies, Lawrence Berkeley National Laboratory, The Wellcome Trust Sanger Institute, Cambridge University Addenbrooke's Hospital, Universite Paul Sabatier, Central Manchester University Hospitals NHS Foundation Trust, Institute of Human Development, University of Manchester, Institute of Genetic Medicine. Newcastle University, University of Toronto, Hospital for Sick Children, Leeds Teaching Hospitals NHS Trust, MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Center for Molecular and Vascular Biology, University of Leuven, University Medical Center Schleswig-Holstein, Great Ormond Street Hospital, Drexel University College of Medicine, University of Cambridge and NHS Blood and Transplant Cambridge, Autism and Developmental Medicine Institute
Sebastian K??hlerInstitute for Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin, Berlin-Brandenburg Center for Regenerative Therapies, Lawrence Berkeley National Laboratory, The Wellcome Trust Sanger Institute, Cambridge University Addenbrooke's Hospital, Universite Paul Sabatier, Central Manchester University Hospitals NHS Foundation Trust, Institute of Human Development, University of Manchester, Institute of Genetic Medicine. Newcastle University, University of Toronto, Hospital for Sick Children, Leeds Teaching Hospitals NHS Trust, MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Center for Molecular and Vascular Biology, University of Leuven, University Medical Center Schleswig-Holstein, Great Ormond Street Hospital, Drexel University College of Medicine, University of Cambridge and NHS Blood and Transplant Cambridge, Autism and Developmental Medicine Institute
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Datasets

DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink
DECIPHERDatabase of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesLink