Human Phenotype Ontology

Metrics

Number of classes:	11785
Number of individuals:	0
Number of properties:	0
Maximum depth:	15
Maximum number of children:	36
Average number of children:	3
Classes with a single child:	997
Classes with more than 25 children:	15
Classes with no definition:	3246

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Details

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) database, for which annotations are also provided.The HPO can be browsed using:HPO Browser
Status	Alpha
Format	OBO
Contact	Sebastian Koehler, sebastian.koehler@charite.de
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Submission	Release Date	Upload Date	Downloads
releases/2016-04-01 (Parsed, Indexed, Metrics, Annotator)	12/26/2016	12/25/2016	OBO \| CSV \| RDF/XML

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5 Dong Dan San Tiao BeiJing,100005,China    Email:bmicc@pumc.edu.cn
  Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences