Rare disease relations through common genes and protein interactions

Mol Cell Probes. 2016 Jun;30(3):178-81. doi: 10.1016/j.mcp.2016.03.004. Epub 2016 Mar 16.

Abstract

ODCs (Orphan Disease Connections), available at http://csbg.cnb.csic.es/odcs, is a novel resource to explore potential molecular relations between rare diseases. These molecular relations have been established through the integration of disease susceptibility genes and human protein-protein interactions. The database currently contains 54,941 relations between 3032 diseases.

Keywords: Biomedical databases; Disease relations; Protein interactions; Rare diseases.

MeSH terms

  • Databases as Topic
  • Humans
  • Phenotype
  • Protein Interaction Maps / genetics*
  • Rare Diseases / genetics*