PhenoTips is the world’s first Genomic Health Record, a complete tool for genetics that makes your work simple, efficient, and patient-focused.
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.
32 years and 180+ visits to my GP without a diagnosis. PhenoTips would now suggest a differential by the sixth visit.
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?”
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.
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.
PhenoTips improves your workflow at every step of the patient journey.
Import, export, collaborate, edit, draw and even auto-draw your patient’s family history.
Leveraging the Human Phenotype Ontology (HPO), you can easily capture high-quality clinical symptoms to power your analysis.
Simplify and guide diagnosis with phenotype-based gene matching and disease suggestions. Or, use a simple search to record coded rare diseases.
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PhenoTips is trusted by leading institutions around the world.
No matter where you fit in genomic medicine, we have a GHR for you.
Good charting and phenotyping is essential for accurate diagnosis. Maximize clinical resources by streamlining patient data capture and get better insights, faster.
Replace your mish-mash of add-on tools for oncology with one, streamlined solution and never enter the same information twice, leaving you free to focus on patient care.