| 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
人类表型本体的开发，目的是为人类遗传和其他疾病中遇到的表型特征提供结构化和可控的词汇。我们的目标是为人类表型的计算分析提供资源，目前的重点是人类孟德尔遗传(OMIM)数据库中列出的单基因疾病，该数据库也提供了注释。请参阅http://www.human-phenotype-ontology.org上的文档和许可信息。 |
| Status | Production |
| Format | OBO |
| Contact | Peter Robinson, peter.robinson@jax.org Sebastian Köhler, dr.sebastian.koehler@gmail.com |
| Categories | English |
| Version | Released | Uploaded | Downloads |
|---|---|---|---|
| hp/releases/2022-06-11 (Parsed, Indexed, Metrics, Annotator) | 06/11/2022 | 06/27/2022 | OBO | CSV | RDF/XML | Diff |
| hp/releases/2022-02-14 (Archived) | 02/14/2022 | 04/13/2022 | OBO | Diff |
| 2021-02-08 (Archived) | 02/08/2021 | 02/24/2021 | OBO | Diff |
| releases/2018-12-21 (Archived) | 12/21/2018 | 02/25/2019 | OBO |
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