| Acronym | HP |
| Visibility | Public |
| Description | The Human Phenotype Ontology is being developed to provide a structured and controlled vocabulary for the phenotypic features encountered in human hereditary and other disease. Our goal is to provide resource for the computational analysis of the human phenome, with a current focus on monogenic diseases listed in the Online Mendelian Inheritance in Man (OMIM) and Orphanet databases, for which annotations are also provided. Please see documentation and license information at http://www.human-phenotype-ontology.org |
| Status | Production |
| Format | OBO |
| Contact | Peter Robinson, peter.robinson@jax.org Sebastian Köhler, dr.sebastian.koehler@gmail.com |
| Categories | English |
| Version | Released | Uploaded | Downloads |
|---|---|---|---|
| releases/2018-12-21 (Parsed, Indexed, Metrics, Annotator) | 12/21/2018 | 02/25/2019 | OBO | CSV | RDF/XML |
No views of HP available
| Classes | 17,536 |
| Individuals | 0 |
| Properties | 0 |
| Maximum depth | 15 |
| Maximum number of children | 41 |
| Average number of children | 3 |
| Classes with a single child | 1,118 |
| Classes with more than 25 children | 30 |
| Classes with no definition | 6,473 |
We are still collecting data for this ontology.
No projects using HP