PHENOTIPS FOR health systems

A future-forward solution for NHS health systems
PhenoTips is a proud partner of the NHS, helping trusts and regional alliances collaborate, engage patients, and offer consistent, accessible genomic care through a single, centralised Genomic Health Record
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NHS trusts have adopted PhenoTips
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Join the NHS trusts reimagining regional genomics and unifying nationwide care

The logo for NHS Cambridge University Hospitals NHS Foundation Trust
The logo for London North West University Healthcare. London North West University Healthcare is written in black and NHS in blue. NHS foundation trust is written below in blue.
NHS East Genomics logo.
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The logo for NHS Foundation Trust: Guy's and St Thomas'
The logo for the NHS Foundation Trust: Oxford University Hosptials.
The logo for NHS Great Ormond Street Hospital for Children, NHS Foundation Trust
The logo for the NHS Royal Devon and Exeter NHS Foundation Trust.
The logo for the NHS University Hospitals Birmingham, NHS Foundation Trust.
lighting talk by dr.pawel buczkowicz

PhenoTips and the East Genomic Service Alliance Partner in Regional Transformation Project

PhenoTips’ COO Dr. Pawel Buczkowicz presents the project making genomic expansion possible by equitably embedding and centralising genomics in the East Midlands and East of England region.
Hospital features

From pre-visit through continuing care

Designed for genomic mainstreaming and digitisation at every stage of the patient journey.

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

Seamless integrations

Unite EPRs, laboratory hubs, and Trusts

Avoid redundant data re-entry while uniting your health system. Your Genomic Health Record can integrate with any existing data management systems for seamless communication between systems, hospitals, labs, and trusts.

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Test requisition generation

Streamline WGS test ordering

Take advantage of patient records populated with detailed Human Phenotype Ontology (HPO) terms. With a single click, generate a pre-populated WGS test ordering form, ready to send to your GLH.

An image of a laptop open to a patient record in PhenoTips. On top of the record is a pre-populated NHS WGS ordering form ready to be printed or sent to the respective GLH laboratory hub.
A GIF shows a PhenoTips user entering free text clinic notes in one section of the software, and then scrolling down to select the HPO terms pulled from the free text that apply to their patient.

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.

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Patient Entered Data Draws Pedigrees

Automate pedigree drawing

Improve patient engagement and save time during the first patient encounter by sending your patient a gender-inclusive digital family history questionnaire that automatically draws their pedigree.

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A patient using the Cardiac Pre-Visit Patient Questionnaire enters their cardiovascular family medical history into the platform. A provider opens the pedigree maker where, without having to create a pedigree, a family pedigree is already automatically generated.
A PhenoTips user selects an individual in the pedigree and launches the risk assessment tool within the pedigree. With a few clicks they choose which models to run and then press one button to run them all. They then download and scroll through their PDF report of the findings.

Pedigree-Embedded Risk Assessment Tool

One click cancer risk assessments

Streamline cancer risk assessment by running four risk models simultaneously for any family member with a simple click of a button in pedigrees, saving time wasted on re-entering information already in other models and pedigrees.

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Individual and Family Centric Data Capture

Holistic family care

Build complex and inclusive pedigrees with a tool that understands the concept of family members, harnessing the latest standards to collect and link both patient and family level data.

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A screen capture of PhenoTips' pedigree maker shows a user clicking on the linked patient record within a pedigree. The user also unlinks a member of the family's patient record and their node becomes blank. The user then drags that patient record link, now in the sidebar key, and drops it on a different node, and the node becomes automatically populated with the information of the patient record.
A GIF showing a PhenoTips' user browsing their entire database of patient and family records. Showing the complete list, they scroll down to filter based on one of the many available filtration options. They specify a phenotype to search by and then scroll up, revealing the database narrowed down to three patients.

Comprehensive Searchable Database

Search, import, and export in bulk

Harness the power of computable data to create cohorts and search your database. Search and filter for patients and families based on phenotypic presentation, diagnosis, genotype and much more.

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Plus PhenoTips Core Features

Inclusive pedigree charts

Build complex, standardized, and gender-inclusive pedigree charts with a user-friendly tool.

Symptom capture that counts

Easily store and capture rich clinical datasets with standard data models and HPO nomenclature.

Better insights, faster

Gene and diagnosis suggestions help you reach diagnosis sooner, even for rare diseases.

Secure workflows

PhenoTips' Genomic Health Record is GDPR, DSPT, HIPAA, and CE+ certified and compliant.

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The entire clinical genetics team, inherited cardiovascular team, and some other specialties such as Ophthalmology use PhenoTips on a daily basis. We save time as we no longer have to re-enter information for cancer risk calculations. It is easier to share and helps avoid unnecessary duplication of work. When requesting Whole exome/genome testing, we attach a printout from PhenoTips, rather than re-entering the data.

Dr. Ajith Kumar, Consultant in Clinical Genetics, Great Ormond Street Hospital for Children Foundation Trust, London, UK

PhenoTips looks good and it’s just so easy to use. You really want something that people who are not IT savvy can pick up quickly, this is perfect, it’s so easy to pick up.

Marc Tischkowitz, Consultant Clinical Geneticist, CUH Addenbrookes, Cambridge, UK

Prepare your health system

Receive an assessment from our experts to discover how PhenoTips can prepare your regional centre for the scaling of genomics.

Book a demo
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SOLUTIONS

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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.
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