Enabling a new approach to the diagnosis of rare disease
CLiX focus, based on rich and detailed SNOMED terminology, can rapidly identify specific phenotypic variations associated individual rare diseases, helping physicians speed up diagnosis, and expediting correct treatment,
And if CLiX focus is used to take a Phenotype First approach to the analysis of population-wide clinical data, then transformational national screening programs become a reality and the diagnostic odyssey endured by many sufferers of rare disease can be brought to an end.
“Some people call this artificial intelligence, we call it augmented intelligence. Patient care will always begin and end with the doctor and by harnessing the power of technology we can quickly and accurately determine the root cause of genetic diseases.”