Illustration of doctor in front of screen displaying a pedigree

Empowering life-saving care with workflows for genomic medicine.

Capture patient symptoms and family history with intuitive tools that make your data standardized and interoperable.

PhenoTips has made the most impact in the phenotyping space. The tool allows symptoms to be collected in a standardized way, which enables case matching and downstream analysis. PhenoTips software is used on a daily basis by UDN clinicians and researchers.

Kimberly LeBlanc, Associate Director of Research Operations, Undiagnosed Diseases Network, Boston, MA, USA

32 years and 180+ visits to my GP without a diagnosis. PhenoTips would now suggest a differential by the sixth visit.

Ian Stedman, Postdoctoral Fellow Researching in Artificial Intelligence Law and Ethics, Hospital for Sick Children

In terms of collaboration, PhenoTips has made it much better than what we had before! It’s easier to know which cases are complete and much easier for us to go back to a case and know where it is in the process. Before, we had to ask others on the team questions like “When are we going to get results?”, “Are you analyzing this case?”

Anne-Marie Laberge, MD, MPH, PhD, Researcher, CHU Sainte-Justine Research Center,Associate Clinical Professor of Medical Genetics & Paediatrics, Université de Montréal

There’s a lot of different pedigree drawing programs out there. I’ve found them clunky and not very useful. But with PhenoTips I’ve never had any problems - it just works. You don’t want to think about the IT behind it, you just want something that works.

Dr. Marc Tischkowitz, Consultant Clinical Geneticist, Addenbrooke's Hosptial, Cambridge University Hospitals

Phenotips has become an indispensable asset to our research team. We are now able to securely store data including medical history, genetic test results, and family histories all in one location outside of the EMR. This has improved our genomic analysts’ ability to locate necessary data to inform results interpretation. In addition, the ease of use has prompted our clinical Genetics team to adopt the pedigree tool for daily utilization.

Lauren Bartik, Genetic Counselor, Children’s Mercy Hospitals

Modernize your genomics workflow.

PhenoTips is the leading solution for capturing the essential phenotype and family history data for genome analysis.

Deep Phenotyping with the HPO.

Leveraging the Human Phenotype Ontology (HPO), you can easily capture high quality clinical symptoms and physical findings for your analysis.

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HPO users since the beginning

PhenoTips was one of the first tools to make it practical to store patient records coded with HPO terms.

Screenshot of deep phenotyping in PhenoTips

Ditch pen and paper for a Pedigree solution that works.

Create comprehensive family history trees in seconds to tell each family’s unique story.

Screenshot of pedigree in PhenoTips Laptop computer

Join the movement.

PhenoTips is trusted by leading institutions around the world.

240,000+

Patient records

5,000+

Specialists

60+

Countries

Discover how PhenoTips can help you.

No matter where you fit into genomic medicine, we have a solution for you.

Digitize your genomic workflow today.

Stop wasting time trying to transcribe patient data with pen and paper. PhenoTips is fast, accurate and saves you time and resources so you can help more patients.

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