Figure 3
From: Semantically enabling a genome-wide association study database
Inferred phenotypes from OMIM as displayed in a GWAS Central “Phenotype Report”. The phenotypic abnormalities associated with Creutzfeldt-Jakob Syndrome are listed under the OMIM term they are mapped to. A single MeSH disease Descriptor is associated with this GWAS experiment and the mappings are implemented ‘under the hood’ to provide clickable links to the mapped OMIM and HPO terms. Screenshot taken of http://www.gwascentral.org/phenotype/HGVPM172.