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Human Phenotype Ontology / 人类表型本体

Last uploaded: January 9, 2023
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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
Submissions
Version Released Uploaded Downloads
2022-12-15 (Parsed, Indexed, Metrics, Annotator) 12/15/2022 01/09/2023 OBO | CSV | RDF/XML | Diff
hp/releases/2022-10-05 (Archived) 10/05/2022 11/07/2022 OBO | Diff
hp/releases/2022-06-11 (Archived) 06/11/2022 06/27/2022 OBO | 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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Metrics
Classes 20,625
Individuals 0
Properties 3
Maximum depth 16
Maximum number of children 161
Average number of children 3
Classes with a single child 1,169
Classes with more than 25 children 32
Classes with no definition 6,384
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