Cardiologists and other cardiovascular medical staff struggle with access to live data at the point of care. Rummaging through files to find out if certain genetic tests or diagnostic procedures were performed is not uncommon. Further challenges stem from the ability to extract and analyze the raw text data that is typically provided as part of generalized EMR solutions. This raw data represents lab and test results from other sources but is not actionable for clinicians when seeing patients.

Aurora for Cardiomyopathy provides the following key features for clinicians and investigators

  • One location for all pertinent data about patient
  • Data includes phenotype, genotype, tests, and family history and pedigrees
  • Data is searchable across all patient and family members
  • Find people with similar genetic variants or discover who has similar phenotypes within 2 degrees of an affected patient




Browse the screenshots below to see our cardiomyopathy views


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