Illustration of doctor in front of screen displaying a pedigree

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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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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
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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.

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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.

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Screenshot of pedigree in PhenoTips Laptop computer

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Doctor talking to a patient

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Person typing on computer

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Person holding test tube

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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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