The Human Phenotype Ontology

被引:243
作者
Robinson, P. N. [1 ,2 ]
Mundlos, S. [1 ,2 ]
机构
[1] Charite Univ Med Berlin, Inst Med Genet, D-13353 Berlin, Germany
[2] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
关键词
biomedical ontologies; differential diagnosis; diseasome; Human Phenotype Ontology; Phenomizer; MORPHOLOGY STANDARD TERMINOLOGY; GENE-EXPRESSION; ELEMENTS; TOOL; NETWORK; DISORDERS; SEQUENCE; DATABASE; GENOME; INTERACTOME;
D O I
10.1111/j.1399-0004.2010.01436.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A standardized, controlled vocabulary allows phenotypic information to be described in an unambiguous fashion in medical publications and databases. The Human Phenotype Ontology (HPO) is being developed in an effort to provide such a vocabulary. The use of an ontology to capture phenotypic information allows the use of computational algorithms that exploit semantic similarity between related phenotypic abnormalities to define phenotypic similarity metrics, which can be used to perform database searches for clinical diagnostics or as a basis for incorporating the human phenome into large-scale computational analysis of gene expression patterns and other cellular phenomena associated with human disease. The HPO is freely available at http://www.human-phenotype-ontology.org.
引用
收藏
页码:525 / 534
页数:10
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