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.
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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.
agree PhenoTips is the best pedigree drawing software they have used.
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use PhenoTips in their daily practice.
Simplify and guide diagnosis with phenotype-based gene matching and disease suggestions. Or, use a simple search to record coded rare diseases.
for our users to reach Diagnosis.
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Patient records
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No matter where you fit in genomic medicine, we have a Genomic Health Record for you.
Good charting and phenotyping is essential for accurate diagnosis. Maximize clinical resources by streamlining patient data capture and get better insights, faster.
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Streamline collection of structured phenotypic data for investigative precision and efficiency. Plug into our collaborative research community today.
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Still manually transcribing your intake forms? Bring your requisition process into the digital age by streamlining the capture of high-quality intake data.
Learn moreStop wasting time on redundant data re-entry, simplify your workflow to focus on delivering high-quality patient care.
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