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Matchmaker Exchange: Join the effort to diagnose patients and identify novel disease genes

The “Matchmaker Exchange” was launched in 2013 in order to facilitate the process of matching a patient with a rare disease and a candidate gene to another to identify the gene associated with the disorder. The Exchange links multiple previously isolated databases, allowing researchers and clinicians a quick, efficient method for finding gene-phenotype matches. Watch this webinar and learn how to use the Exchange to gather evidence for novel disease-gene associations, as well as how the Exchange helps end the diagnostic odyssey for patients with rare disease by confirming the validity of novel disease genes.