The complete Genomic Health Record
Drive collaborative, life-saving care with a single, end-to-end, EHR-integrated solution
Genomic Health Record Core Features
PhenoTips digitizes more aspects of medical genetics with a unified, EHR-integrated solution
Complex, inclusive pedigree charts.
Import, export, collaborate on, and link multiple patients to a shared, gender-inclusive pedigree chart.
of users agree that PhenoTips is the best pedigree drawing software they have used.
Next-generation phenotyping made easy.
Leverage the Human Phenotype Ontology (HPO) to streamline laboratory test requisition and power your analysis.
of our users use PhenoTips in their daily practice.
Diagnose with confidence
Guide diagnosis with phenotype-based gene and disease suggestions. Or, use a simple search to record genes or coded diseases leveraging Orphanet and OMIM.
up to 30x for our users to reach diagnosis
Plus Add-on Features
Phenotips has Genomic Health Records designed for cancer genetics, rare disease, regional health systems, and additional specialties.
Automate pedigree drawing
Empower patients to capture their own family history with digital questionnaires that automatically generate editable pedigree charts.
Pedigree-embedded cancer risk assessment.
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.
Join the Movement
PhenoTips is trusted by leading institutions around the world
+ Patient Records
+ Specialists
+ Countries
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?”
32 years and 180+ visits to my GP without a diagnosis. PhenoTips would now suggest a differential by the sixth visit.
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.
Discover the Genomic Health Record for you
No matter your specialty, we have a complete Genomic Health Record for you
[**Rare Disease**
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](https://phenotips.com/rare-disease)
[**Cancer Genetics**
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](https://phenotips.com/cancer-genetics)
[**Health Systems**
Unify your regional health system with a single, intuitive solution for genetics. Prepare for the scaling of genomics as whole genome and exome sequencing become routine clinical practice.
Learn more](https://phenotips.com/health-systems)
Simplify your workflow today.
Stop wasting time on redundant data re-entry, simplify your workflow to focus on delivering high-quality patient care.
Empowering genomic medicine.