hp.md

layout	ontology_detail
id	hp
alternativePrefix	HPO
description	A structured and controlled vocabulary for the phenotypic features encountered in human hereditary and other disease.
domain	phenotype
twitter	hp_ontology
homepage	http://www.human-phenotype-ontology.org/
contact	email label sebastian.koehler@charite.de Sebastian Koehler
products	id hp.owl id hp.obo
taxon	id label NCBITaxon:9606 Homo sapiens
title	human phenotype ontology
jobs	id type https://travis-ci.org/obophenotype/human-phenotype-ontology travis-ci
build	source_url path method infallible http://compbio.charite.de/hudson/job/hpo/lastSuccessfulBuild/artifact/*zip*/archive.zip archive/hp archive 1
tracker	https://github.com/obophenotype/human-phenotype-ontology/issues/
termgenie	http://hp.termgenie.org
browsers	label title url HPO Charite HPO Browser http://www.human-phenotype-ontology.org/hpoweb/showterm?id=HP:0000118 label title url Monarch Monarch Phenotype Page http://monarchinitiative.org/phenotype/HP:0000118
publications	id title http://www.ncbi.nlm.nih.gov/pubmed/18950739 The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. id title http://www.ncbi.nlm.nih.gov/pubmed/26119816 The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease. id title http://www.ncbi.nlm.nih.gov/pubmed/24217912 The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.

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