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• Clinical Diagnostic Decision  Support: Uses signs, symptoms, and clinical knowledge from a peer-reviewed database to suggest tests and present a differential diagnosis as shown in

  Caption reference
  CapRefId clinical-findings-and-diseases-can-be-represented-using-snomed-ct-content-in-simulconsult CapRefType Figure

   below.
• Loss of Heterozygosity: Supports the analysis of microarrays.
• Genome-Phenome Analyzer: Analyzes and reports on whole exome and genome testing.

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Clinical findings and diseases can be represented using SNOMED CT content in SimulConsult.

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