CLiX focus

Enabling a new approach to the diagnosis of rare disease and the management of health around the globe


CLiX focus for healthcare


By rapidly identifying the phenotypic variations for rare disease, by helping physicians speed up diagnosis, and by expediting correct treatment, CLiX focus, with its understanding of SNOMED terminology, is saving lives.

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 of millions can be brought to an end.


Refocus your view of the rare disease landscape with CLiX focus.

Read 2 million clinical documents in one hour
Search 12,000 phenotype descriptions in seconds
Extract 28 times more phenotypes than with manual review

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What CLiX focus users say

“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.”

Stephen Kingsmore, President & CEO, Rady Children’s Institute for Genomic Medicine, San Diego