PHENOTIPS FOR health systems

Lifesaving answers at your fingertips
With deep phenotyping, diagnostic insights, and seamless collaboration, PhenoTips enhances care and diagnosis for even the rarest conditions
up to
30x
faster

for our users to reach diagnosis

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Join groundbreaking rare disease organizations

Care for Rare (Care4Rare) Canada logo in blue, green, red, and black.
Genomics4rd logo, the dot over the I in "genomics" is a blue cloud "Canada's rare disease research platform", in blue and black.
Children's Mercy Kansas City logo in blue next to a blue outline of an adult figure holding a child.
The Hospital for Sick Children logo with the word "Sick" written in light blue, and "Kids" in dark blue.
Children's Hospital of Eastern Ontario logo, CHEO written in purple.
The University of Alabama at Birmingham. UAB logo written in green and the University of Alabama at Birmingham in black.
The logo for School of Medicine and Public Health University of Wisconsin-Madison with a red 'W' inside a gold crest on the left and red and black text on the right
Hospital features

From pre-visit through continuing care

Designed for rare disease at every stage of the patient journey.
A sequence of screenshots from a digital health questionnaire platform, showing a user entering family medical history, confirming data, and preparing to submit the form. The interface includes fields for names, health conditions, and status of relatives.

Patient entered data

Increase efficiency by up to 50%

Save time during the first patient encounter. Increase efficiency by up to 50% by sending your patient a survey that auto-draws their pedigree.

EHR Integration

Automate your admin work

Never enter the same information twice. Embedded directly into your clinic’s electronic health record, information is shared between patient charts and PhenoTips automatically.

A screen captured video of a PhenoTips user opening PhenoTips' pedigree maker tool within their Epic interface. PhenoTips is embedded within their EHR.

Concept Recognition

Messy clinical notes read themselves

Focus on patient care instead of deciphering clinical notes. Standardized HPO terms are suggested from large chunks of free text for effortless symptom capture.

Smart Charting

Automate charting and interpretation

Forget graphing and interpreting growth curves, PhenoTips instantly creates quantiles from clinical measurements and reports abnormal values as standardized HPO terms.

Push to other instances

Effortless collaboration

Effortlessly share de-identified patient data with other PhenoTips instances or PhenomeCentral to find similar cases and work collaboratively with researchers and clinicians around the world.

Plus Phenotips Core Features

In addition to our rare disease suite, all Genomic Health Records™ come equipped with the necessities of genomic medicine.

Superior pedigree drawing

Over 95% of users agree PhenoTips is the best pedigree drawing software they’ve used.

Learn more

Symptom capture that counts

More than simply listing symptoms, your standardized symptoms power your analysis.

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Diagnose 30 times faster

Built-in diagnoses suggestions help you reach diagnosis sooner, even for rare diseases.

Learn more
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Discover your Genomic Health Record™

Our GHRs are customized to your rare disease needs with additional cross department functionality. Discover your complete genomic solution today.
Book a demo
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Empowering genomic medicine.
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SOLUTIONS

Rare DiseaseCancer GeneticsHealth Systems

PRODUCTS

Core Genomic Health RecordPedigree MakerStructured Patient Data & Clinical InsightsCancer risk assessmentPre-visit patient questionnairesSeamless Integrations

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By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
By entering your email you are agreeing to periodic relevant communications from PhenoTips.
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