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
for our users to reach diagnosis
Join groundbreaking rare disease organizations
Hospital features
From pre-visit through continuing care
Designed for rare disease at every stage of the patient journey.
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.
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.
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.
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.
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.
Symptom capture that counts
More than simply listing symptoms, your standardized symptoms power your analysis.
Diagnose 30 times faster
Built-in diagnoses suggestions help you reach diagnosis sooner, even for rare diseases.
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.
Empowering genomic medicine.