Drive collaborative, life-saving care with a single, end-to-end, EHR-integrated solution
Next Generation phenotyping
HIPAA, GDPR, DSPT, CE+ certified & compliant
Rare disease diagnostic insights
PhenoTips digitizes more aspects of medical genetics with a unified, EHR-integrated solution
Import, export, collaborate on, and link multiple patients to a shared, gender-inclusive pedigree chart.
Leverage the Human Phenotype Ontology (HPO) to streamline laboratory test requisition and power your analysis.
Guide diagnosis with phenotype-based gene and disease suggestions. Or, use a simple search to record genes or coded diseases leveraging Orphanet and OMIM.
View additional features included in the core Genomic Health RecordLearn more
Phenotips has Genomic Health Records designed for cancer genetics, rare disease, regional health systems, and additional specialties.
Empower patients to capture their own family history with digital questionnaires that automatically generate editable pedigree charts.
Launch four simultaneous risk models within pedigrees and calculate risk scores for any family member in a pedigree with no unnecessary, redundant data re-entry.
PhenoTips is trusted by leading institutions around the world
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 allows us to click a button and save anywhere from 15 to 30 minutes in extra work.
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?”
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.
No matter your specialty, we have a complete Genomic Health Record for you
Collaboration, good charting and next-generation phenotyping are essential for accurate diagnosis. Maximize clinical resources by streamlining matchmaking and data capture and get better insights, faster.Learn more
Replace your mish-mash of tools for cancer genetics with a single, intuitive, EHR-integrated solution and never enter the same information twice, leaving you free to focus on patient care.Learn more
Stop wasting time on redundant data re-entry, simplify your workflow to focus on delivering high-quality patient care.Book a demo