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At Mendelian, we build digital tools that help doctors find and diagnose rare disease patients faster. We see a future where doctors are enabled to transform lives at the earliest opportunity; where every rare disease patient can expect, rather than hope for an answer.

At Mendelian, we have developed a platform called MendelScan, our flagship product and primary care's solution to early disease discovery. Our algorithm search Electronic Health Records for indicators of rare diseases, which then identifies clinical patterns associated with rare diseases. Once a patient is flagged, MendelScan generates a clinical report which is sent to the clinician, outlining information about the patient, the suspected disease and the next clinical steps in the pathway. By collecting large amounts of diseases on a single platform, MendelScan becomes a crucial tool for healthcare providers and is ending the diagnostic odyssey for millions of patients, by bringing rapid rare disease discovery to primary care.

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