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The Orphan Diseasome web site allows investigators to explore the orphan disease (OD) or rare disease relationships based on shared genes and shared enriched features (e.g., Gene Ontology Biological Process, Cellular Component, Pathways, Mammalian Phenotype). Additionally, users can also explore the networks of orphan disease causal genes where the nodes are orphan disease genes (ODG) while the edge represents shared OD or a protein-protein interaction.


To start exploring the Orphan Diseasome, click on the "Networks/Maps" (top navigation bar).