Illustration of doctor in front of screen displaying a pedigree

Imagine an Electronic Health Record designed for 豆荚加速器苹果.

PhenoTips is the world’s first Genomic Health Record, a complete tool for genetics that makes your work simple, efficient, and patient-focused.

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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

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Ian Stedman, Postdoctoral Fellow Researching in Artificial Intelligence Law and Ethics, Hospital for Sick Children
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Anne-Marie Laberge, MD, MPH, PhD, Researcher, CHU Sainte-Justine Research Center,Associate Clinical Professor of Medical Genetics & Paediatrics, Université de Montréal
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Dr. Marc Tischkowitz, Consultant Clinical Geneticist, Addenbrooke's Hosptial, Cambridge University Hospitals
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Lauren Bartik, Genetic Counselor, Children’s Mercy Hospitals

From first encounter to continuing care.

PhenoTips improves your workflow at every step of the patient journey.

Record family history effortlessly.

Import, export, collaborate, edit, draw and even auto-draw your patient’s family history.

over
95%
of users

agree PhenoTips is the best pedigree drawing software they have used.

Screenshot of pedigree in PhenoTips Laptop computer

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Leveraging the Human Phenotype Ontology (HPO), you can easily capture high-quality clinical symptoms to power your analysis.

almost
90%
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Screenshot of deep phenotyping in PhenoTips

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Simplify and guide diagnosis with phenotype-based gene matching and disease suggestions. Or, use a simple search to record coded rare diseases.

up to
30x
faster

for our users to reach Diagnosis.

Screenshot of pedigree in PhenoTips Laptop computer

Don't see the feature you are looking for?

View More Features

Join the movement.

PhenoTips is trusted by leading institutions around the world.

240,000+

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5,000+

Specialists

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Countries

Discover the GHR for you.

No matter where you fit in genomic medicine, we have a Genomic Health Record for you.

Doctor talking to a patient

Hospitals

Good charting and phenotyping is essential for accurate diagnosis. Maximize clinical resources by streamlining patient data capture and get better insights, faster.

Learn more
Person typing on computer

Researchers

Streamline collection of structured phenotypic data for investigative precision and efficiency. Plug into our collaborative research community today.

Learn more
Person holding test tube

Labs

Still manually transcribing your intake forms? Bring your requisition process into the digital age by streamlining the capture of high-quality intake data.

Learn more

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Stop wasting time on redundant data re-entry, simplify your workflow to focus on delivering high-quality patient care.

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