human phenotype ontology

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.


namespaceHP
current activityProduction and review
homewww.human-phenotype-ontology.org/
documentationwww.human-phenotype-ontology.org/
contact
help
OBO formathuman-phenotype-ontology.obo
OWL(legacy obo2owl)http://purl.org/obo/owl/HP
OWL(new obo2owl)http://purl.obolibrary.org/obo/hp.owl
trackerhttp://sourceforge.net/tracker/?atid=1112722&group_id=76834
domainphenotype
relevant_organismHomo sapiens