hp: alias: description: The Human Phenotype Ontology (HPO) aims to provide a standardized vocabulary of phenotypic abnormalities encountered in human disease. Each term in the HPO describes a phenotypic abnormality, such as atrial septal defect. The HPO is currently being developed using the medical literature, Orphanet, DECIPHER, and OMIM. forward: http://compbio.charite.de/hpoweb/showterm?id=HP:${ac} institution: Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin, Berlin location: Germany more: http://human-phenotype-ontology.github.io/ name: Human Phenotype Ontology at Institute for Medical Genetics and Human Genetics pattern: ^HP:\d{7}$ prefixed: true primary: true probe: http://compbio.charite.de/hpoweb/showterm?id=HP:0000118 provider: provider_id: MIR:00100753 redirect: http://compbio.charite.de/hpoweb/showterm?id=HP:$id sort_score: 6 state: 97:Probably up subject: human; phenotype; ontology synonym: HPO test: 0000118 type: scheme ols/hp: alias: description: The Human Phenotype Ontology (HPO) aims to provide a standardized vocabulary of phenotypic abnormalities encountered in human disease. Each term in the HPO describes a phenotypic abnormality, such as atrial septal defect. The HPO is currently being developed using the medical literature, Orphanet, DECIPHER, and OMIM. forward: https://www.ebi.ac.uk/ols/ontologies/hp/terms?obo_id=HP:${ac} institution: European Bioinformatics Institute, Hinxton, Cambridge location: UK more: https://www.ebi.ac.uk/ols/ontologies/hp name: Human Phenotype Ontology through OLS pattern: ^HP:\d{7}$ prefixed: true primary: false probe: https://www.ebi.ac.uk/ols/ontologies/hp/terms?obo_id=HP:0000118 provider: ols provider_id: MIR:00100754 redirect: https://www.ebi.ac.uk/ols/ontologies/hp/terms?obo_id=HP:$id sort_score: 2 state: 99:Up subject: human; phenotype; ontology synonym: HPO test: 0000118 type: scheme