Human Phenotype Ontology
type: https://bioregistry.io/schema/#0000001
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.
is part of: bioregistry
git repository: human-phenotype-ontology
keyword: biomedical science
keyword: disease phenotype
keyword: disorder
keyword: fair data spaces
keyword: genetics
keyword: genome/gene
keyword: health/disease
keyword: life sciences, biology
keyword: medicine
keyword: obo
keyword: omics
keyword: ontology
keyword: ontology/terminology/nomenclature
keyword: pathology
keyword: phenomics
keyword: phenotype
keyword: preclinical studies
0000005: 0011140
0000006: http://purl.obolibrary.org/obo/HP_$1
0000008: ^\d{7}$
0000010: hp.owl
0000012: false
0000018: chiro
0000018: maxo
0000018: scdo
0000019: Sebastian Koehler
0000023: hpo
0000024: http://purl.obolibrary.org/obo/HP_
0000027: HP_0011140
0000029: hp